1. Genetics and Genomics
  2. Microbiology and Infectious Disease

An analog to digital converter controls bistable transfer competence development of a widespread bacterial integrative and conjugative element

  1. Nicolas Carraro
  2. Xavier Richard
  3. Sandra Sulser
  4. François Delavat
  5. Christian Mazza
  6. Jan Roelof van der Meer  Is a corresponding author
  1. Department of Fundamental Microbiology, University of Lausanne, Switzerland
  2. Department of Mathematics, University of Fribourg, Switzerland
  3. UMR CNRS 6286 UFIP, University of Nantes, France
https://doi.org/10.7554/eLife.57915
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  1. Nicolas Carraro
  2. Xavier Richard
  3. Sandra Sulser
  4. François Delavat
  5. Christian Mazza
  6. Jan Roelof van der Meer
(2020)
An analog to digital converter controls bistable transfer competence development of a widespread bacterial integrative and conjugative element
eLife 9:e57915.
https://doi.org/10.7554/eLife.57915
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Abstract

Conjugative transfer of the integrative and conjugative element ICEclc in Pseudomonas requires development of a transfer competence state in stationary phase, which arises only in 3–5% of individual cells. The mechanisms controlling this bistable switch between non-active and transfer competent cells have long remained enigmatic. Using a variety of genetic tools and epistasis experiments in P. putida, we uncovered an ‘upstream’ cascade of three consecutive transcription factor-nodes, which controls transfer competence initiation. One of the uncovered transcription factors (named BisR) is representative for a new regulator family. Initiation activates a feedback loop, controlled by a second hitherto unrecognized heteromeric transcription factor named BisDC. Stochastic modelling and experimental data demonstrated the feedback loop to act as a scalable converter of unimodal (population-wide or ‘analog’) input to bistable (subpopulation-specific or ‘digital’) output. The feedback loop further enables prolonged production of BisDC, which ensures expression of the ‘downstream’ functions mediating ICE transfer competence in activated cells. Phylogenetic analyses showed that the ICEclc regulatory constellation with BisR and BisDC is widespread among Gamma- and Beta-proteobacteria, including various pathogenic strains, highlighting its evolutionary conservation and prime importance to control the behaviour of this wide family of conjugative elements.

eLife digest

Mobile DNA elements are pieces of genetic material that can jump from one bacterium to another, and even across species. They are often useful to their host, for example carrying genes that allow bacteria to resist antibiotics.

One example of bacterial mobile DNA is the ICEclc element. Usually, ICEclc sits passively within the bacterium’s own DNA, but in a small number of cells, it takes over, hijacking its host to multiply and to get transferred to other bacteria. Cells that can pass on the elements cannot divide, and so this ability is ultimately harmful to individual bacteria. Carrying ICEclc can therefore be positive for a bacterium but passing it on is not in the cell’s best interest. On the other hand, mobile DNAs like ICEclc have evolved to be disseminated as efficiently as possible. To shed more light on this tense relationship, Carraro et al. set out to identify the molecular mechanisms ICEclc deploys to control its host.

Experiments using mutant bacteria revealed that for ICEclc to successfully take over the cell, a number of proteins needed to be produced in the correct order. In particular, a protein called BisDC triggers a mechanism to make more of itself, creating a self-reinforcing ‘feedback loop’.

Mathematical simulations of the feedback loop showed that it could result in two potential outcomes for the cell. In most of the ‘virtual cells’, ICEclc ultimately remained passive; however, in a few, ICEclc managed to take over its hosts. In this case, the feedback loop ensured that there was always enough BisDC to maintain ICEclc’s control over the cell. Further analyses suggested that this feedback mechanism is also common in many other mobile DNA elements, including some that help bacteria to resist drugs.

These results are an important contribution to understand how mobile DNAs manipulate their bacterial host in order to propagate and disperse. In the future, this knowledge could help develop new strategies to combat the spread of antibiotic resistance.

Introduction

Biological bistability refers to the existence of two mutually exclusive stable states within a population of genetically identical individuals, leading to two distinct phenotypes or developmental programs (Shu et al., 2011). The basis for bistability lies in a stochastic regulatory decision resulting in cells following one of two possible specific genetic programs that determine their phenotypic differentiation (Norman et al., 2015). Bistability has been considered as a bet-hedging strategy leading to an increased fitness of the genotype by ensuring survival of one of both phenotypes depending on environmental conditions (Veening et al., 2008). A number of bistable differentiation programs is well known in microbiology, notably competence formation and sporulation in Bacillus subtilis (Xi et al., 2013; Schultz et al., 2007), colicin production and persistence in Escherichia coli (Lewis, 2007), virulence development of Acinetobacter baumannii (Chin et al., 2018), or the lysogenic/lytic switch of phage lambda (Sepúlveda et al., 2016; Arkin et al., 1998).

Bistability may also be pervasive among many bacterial DNA conjugative systems, leading to the formation of specific conjugating donor cells at low frequency in the population (Delavat et al., 2017). The best described case of this is the dual lifestyle of the Pseudomonas integrative and conjugative element (ICE) ICEclc (Figure 1A; Minoia et al., 2008). In the majority of cells ICEclc is maintained in the integrated state, but a small proportion of cells (3–5%) in stationary phase activates the ICE transfer competence program (Minoia et al., 2008; Delavat et al., 2016). Upon resuming growth, transfer competent (tc) donor cells excise and replicate the ICE (Delavat et al., 2019), which can conjugate to a recipient cell, where the ICE can integrate (Delavat et al., 2016). ICEclc transfer competence comprises a differentiated stable state, because initiated tc cells do not transform back to the ICE-quiescent state. Although tc cells divide a few times, their division is compromised by the ICE and eventually arrests completely (Takano et al., 2019; Reinhard et al., 2013).

Figure 1 with 4 supplements see all
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ICEclc and postulated regulation network for transfer competence formation.

(A) Schematic representation of the genetic organization of ICEclc (GenBank accession number AJ617740.2). Loci of interest (a, b and c) are detailed below the general map and drawn to scale. Note the ~7 kb left-end region, which is the major focus of the study. Genes are represented by coloured arrows with their name below (former names shown in lighter font inside brackets). Promoters are represented by hooked arrows pointing towards the transcription orientation. Those marked with an asterisk are known to be expressed only in the subpopulation of transfer competent cells. attL and attR, attachment sites; clc genes: 3-chlorocatechol degradation, amn genes: 2-aminophenol degradation. (B) Known steps in ICEclc transfer competence regulation. An ‘upstream’ cascade, with MfsR autorepressing its own transcription and that of tciR; TciR overexpression leading to transfer competence in almost all cells (Pradervand et al., 2014). Bistable expression of ‘downstream’ genes from PinR and Pint in the subpopulation of transfer competent cells, and further roles of additional factors RpoS (Miyazaki et al., 2012) and InrR (Minoia et al., 2008).

ICEs have attracted wide general interest because of the large variety of adaptive functions they can confer to their host, including resistance to multiple antibiotics (Waldor et al., 1996; Johnson and Grossman, 2015; Burrus et al., 2002), or metabolism of xenobiotic compounds, such as encoded by ICEclc (Miyazaki et al., 2015; Zamarro et al., 2016). ICEclc stands model for a ubiquitous family of genomic islands found by bacterial genome sequencing, occurring in important opportunistic pathogens such as Pseudomonas aeruginosa, Bordetella bronchiseptica, Xylella fastidiosa or Xanthomonas campestris (Miyazaki et al., 2015). The ICEclc family of elements is characterized by a consistent ‘core’ region of some 50 kb (Figure 1A), predicted to encode conjugative functions, and a highly diverse set of variable genes with adaptive benefit (Miyazaki et al., 2015). Strong core similarities between ICEclc and the PAGI-2 family of pathogenicity islands in P. aeruginosa clinical isolates have been noted previously (Miyazaki, 2011a; Klockgether et al., 2007).

Although the existence and the fitness consequences of the ICEclc bistable transfer competence pathway have been studied in quite some detail, the regulatory basis for its activation has remained largely elusive (Delavat et al., 2017). In terms of its genetic makeup, ICEclc seems very distinct from the well-known SXT/R391 family of ICEs (Wozniak and Waldor, 2010) and from ICESt1/ICESt3 of Streptococcus thermophilus (Carraro and Burrus, 2014). These carry analogous genetic regulatory circuitry to the lambda prophage, which is characterized by a typical double-negative feedback control (Poulin-Laprade and Burrus, 2015; Bellanger et al., 2007). Transcriptomic studies indicated that the core region of ICEclc (Figure 1A) is higher expressed in stationary than exponential phase cultures grown on 3-chlorobenzoate (3-CBA), and organized in at least half a dozen transcriptional units (Gaillard et al., 2010). A group of three consecutive regulatory genes precludes ICEclc activation in exponentially growing cells, with the first gene (mfsR) constituting a negative autoregulatory feedback (Figure 1B; Pradervand et al., 2014). Overexpression of the most distal of the three genes (tciR), leads to a dramatic increase of the proportion of cells activating the ICEclc transfer competence program (Pradervand et al., 2014). Despite this initial discovery, however, the nature of the regulatory network architecture leading to bistability and controlling further expression of the ICEclc genes in tc cells has remained enigmatic.

The primary goal of this work was to dissect the regulatory factors and nodes underlying the activation of ICEclc transfer competence. Secondly, given that transfer competence only arises in a small proportion of cells in a population, we aimed to understand how the regulatory architecture yields and maintains ICE bistability. We essentially followed two experimental strategies and phenotypic readouts. First, known and suspected regulatory elements were seamlessly deleted from ICEclc in P. putida and complemented with inducible plasmid-cloned copies to study their epistasis in transfer of the ICE. Secondly, individual and combinations of suspected regulatory elements were expressed in a P. putida host without ICE, to study their capacity to activate the ICEclc promoters Pint and PinR, which normally only express in wild-type tc cells (Figure 1B; Minoia et al., 2008). As readout for their activation we quantified fluorescent reporter expression from single copy chromosomally integrated transcriptional fusions, as well as the proportion of cells expressing the reporters using subpopulation statistics as previously described (Reinhard and van der Meer, 2013). On the basis of the discovered key regulators and nodes, we then developed a conceptual mathematical model to show by stochastic simulations how bistability is generated and maintained. This suggested that the ICEclc transfer competence regulatory network essentially converts a unimodal (analog) input signal from the ‘upstream’ regulatory branch occurring in all cells (Figure 1B) to a bistable (digital) output in a subset, and in scalable manner. We experimentally verified this scalable analog-digital conversion in a P. putida without ICEclc but with the reconstructed bistability generator. The key ICEclc bistability regulatory elements involve new previously unrecognized transcription factors, which are conserved among a wide range of Proteobacteria, illustrating their importance for the behaviour of this conglomerate of related ICEs.

Results

Activation of ICEclc starts with the LysR-type transcription regulator TciR

Previous work had implied an ICEclc-located operon of three consecutive regulatory genes (mfsR, marR and tciR, Figure 1B) in control of transfer competence formation (Pradervand et al., 2014). That work had shown that mfsR codes for an autorepressor, whose deletion yielded unhindered production of the LysR-type activator TciR. As a result, the proportion of tc cells is largely increased in P. putida UWC1 bearing ICEclc-∆mfsR (Delavat et al., 2016; Pradervand et al., 2014). We reproduced this state of affairs here by cloning tciR under control of the IPTG-inducible Ptac promoter on a plasmid (pMEtciR) in P. putida UWC1-ICEclc. In absence of cloned tciR, transfer of wild-type ICEclc from succinate-grown P. putida to an ICEclc-free isogenic P. putida was below detection limit, indicating that spontaneous ICE activation under those conditions is negligible (Figure 2A). In contrast, inducing tciR expression by IPTG addition triggered ICEclc transfer from succinate-grown cells up to frequencies close to those observed under wild-type growth conditions with 3-CBA (Miyazaki and van der Meer, 2011b) (10–2 transconjugant colony-forming units (CFU) per donor CFU, Figure 2A). Transfer frequencies were lower in the absence of IPTG, which indicated that leaky expression of tciR from Ptac was sufficient to trigger ICEclc transfer (Figure 2A). These results confirmed the implication of TciR and thus we set out to identify its potential activation targets on ICEclc.

Figure 2
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The LysR-type regulator TciR links to a single node in the regulation network.

(A) Ectopic overexpression of tciR induces ICEclc wild-type conjugative transfer under non-permissive conditions. Bars show the means (+ one standard deviation) of transconjugant formation after 48 hr in triplicate matings using P. putida UWC1 donors carrying the indicated ICEclc or plasmids, in absence (-) or presence (+) of 0.1 mM IPTG, and with a GmR-derivative of P. putida as recipient. Dots represent individual transfer; nd: not detected (<10−7 for the three replicates). p-value derives from one-sided t-test comparison (n = 3). (B) Reporter expression from single copy chromomosomal PbisR, PinR, Pint, or PalpA transcriptional egfp fusions in P. putida UWC1 without ICEclc as a function of ectopically expressed TciR, in comparison to strains carrying the empty vector pME6032. Bars show means of the 75th percentile fluorescence of 500–1000 individual cells each per triplicate culture grown on succinate, induced with 0.05 mM IPTG. Error bars denote standard deviation from the means from biological triplicates (dots show individual 75th percentiles). AU, arbitrary units of brightness at 500 ms exposure. p-values derive from pair-wise comparisons in t-tests between cultures expressing TciR and not. (C) Proportion of cells expressing eCherry from a single-copy chromosomal insertion of Pint in P. putida with ICEclc in presence of induced TciR (pMEtciR, 0.05 mM IPTG) or with empty vector (pME6032). Fluorescence images scaled to same brightness (300–2000). Diagrams show quantile-quantile plots of individual cell fluorescence levels, with n denoting the number of analysed cells and the shaded part indicating the subpopulation size expressing Pint-echerry. (D) Fluorescence images of P. putida without ICEclc with a single-copy chromosomal PbisR-egfp fusion in presence of empty vector or of induced TciR. Images scaled to same brightness (300–1200).

Figure 2—source data 1

Figure 2 panel A: ICEclc transfer data.

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Figure 2—source data 2

Figure 2 panel B: 75th percentile fluorescence data.

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Figure 2—source data 3

Figure 2 panel C: qq-plot single cell fluorescence data.

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Induction of tciR from pMEtciR in P. putida without ICEclc was insufficient to trigger eGFP production from a single-copy Pint promoter, which is a hallmark of induction of ICEclc transfer competence (Figure 2B; Minoia et al., 2008; Delavat et al., 2016). In contrast, in presence of ICEclc, similar induction of tciR yielded a clear increased subpopulation of activated cells (Figure 2C). This suggested, therefore, that TciR does not directly activate Pint, but only through one or more other ICE-located factors. To search for such potential factors, we examined in more detail the genes in a 7 kb region at the left end of ICEclc (close to the attL site, Figure 1A), where transposon mutations had previously been shown to influence Pint expression (Sentchilo et al., 2003). In addition, three promoters had been characterized in this region (Figure 1A; Gaillard et al., 2010), which we tested individually for potential activation by TciR (Figure 2B).

Promoters were fused with a promoterless egfp gene and inserted in single copy into the chromosome of P. putida UWC1 without ICEclc (Materials and methods). Induction of tciR from Ptac on pMEtciR did not yield any eGFP fluorescence in P. putida UWC1 containing a single-copy PalpA- or PinR-egfp transcriptional fusion (Figure 2B). In contrast, the PbisR-egfp fusion was activated upon induction of TciR compared to a vector-only control (p=0.0042, paired t-test, Figure 2B & D). This suggested that the link between TciR and ICEclc transfer competence proceeds through transcription activation of the promoter upstream of the gene bisR (previously designated orf101284). This transcript has previously been mapped and covers a single gene (Gaillard et al., 2010). We renamed this gene as bisR, or bistability regulator, for its presumed implication in ICEclc bistability control (Figure 1—figure supplement 1, see further below).

BisR is the second step in the cascade of ICEclc transfer competence initiation

bisR is predicted to encode a 251-aa protein of unknown function with no detectable Pfam-domains. Further structural analysis using Phyre2 (Kelley et al., 2015) suggested three putative domains with low confidence (between 38% and 53%, Figure 1—figure supplement 2). One of these is a predicted DNA-binding domain, which hinted at the possible function of BisR as a transcriptional regulator itself. BlastP analysis showed that BisR homologs are widely distributed and well conserved among Beta-, Alpha- and Gammaproteobacteria, with homologies ranging from 43–100% amino acid identity over the (quasi) full sequence length (Figure 1—figure supplement 2).

In order to investigate its potential regulatory function, bisR was cloned on a plasmid (pMEbisR) and introduced into P. putida UWC1-ICEclc. Inducing bisR by IPTG addition from Ptac triggered high rates of ICEclc transfer on succinate media (Figure 3A). Deletion of bisR on ICEclc abolished its transfer, even upon overexpression of tciR, but could be restored upon ectopic expression of bisR (Figure 3A). This showed that the absence of transfer was due to the lack of intact bisR, and not to a polar effect of bisR deletion on a downstream gene (Figure 1A). In addition, transfer of an ICEclc deleted for tciR (Pradervand et al., 2014) could be restored by ectopic bisR expression (Figure 3A). This indicated that TciR is ‘upstream’ in the regulatory cascade of BisR, and that TciR does not act anywhere else on the expression of components crucial for ICEclc transfer.

Figure 3
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Identification of BisR as a new intermediary regulator for PalpA activation.

(A) Ectopic overexpression of bisR induces ICEclc conjugative transfer under non-permissive conditions and from ICEclc deleted of key regulatory genes. For explanation of bar diagram meaning, see Figure 2A legend. BisR (+), plasmid with bisR; TciR, pMEtciR; –, empty vector pME6032. nd: not detected (<10−7 for the three replicates). Letters indicate significance groups in ANOVA followed by post-hoc Tukey testing (e.g., a-b: p-values between groups a and b; b-c: p-values between groups b and c). (B) Absence of direct induction by BisR of Pint or PinR fluorescence reporters in P. putida without ICE. For explanation of bars, see Figure 2B legend. (C) Population-wide expression of Pint-echerry in P. putida with ICEclc upon ectopic induction of plasmid-located BisR (pMEbisR, 0.05 mM IPTG). Image brightness scale: 300–2000. For vector control, see Figure 2C. (D) Induced BisR from plasmid leads to reporter expression from the alpA-promoter in all cells of P. putida without ICEclc. Image brightness scales: 300–1200. Bars show means and standard deviation from median fluorescence intensity of single cells (n = 500–1000, summed from 6 to 12 images per replicate) of biological triplicates. p-value derives from pair-wise t-test between cultures with empty vector (–) and those with induced BisR (+).

Figure 3—source data 1

Figure 3 panel A: ICEclc transfer frequencies.

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Figure 3—source data 2

Figure 3 panel C: qq plot single cell fluorescence values.

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Figure 3—source data 3

Figure 3 panel B and panel D: 75th percentile fluorescence data.

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IPTG induction of bisR in P. putida without ICE again did not yield activation of the single-copy Pint or PinR transcriptional reporter fusions, whereas some repression was observed on Pint itself (Figure 3B). In contrast, BisR induction in P. putida UWC1 with ICEclc led to a massive activation of the same reporter constructs in virtually all cells (Figure 3C), compared to a vector-only control (Figure 2C, pME6032). This suggested that BisR was an(other) intermediate regulator step in the complete cascade of activation of ICEclc transfer competence. Of the tested ICE–promoters within this 7 kb region, BisR induction triggered very strong expression from a single copy PalpA–egfp transcriptional fusion in all cells (Figure 3D). This indicated that BisR is a transcription activator, and an intermediate regulator between TciR and further factors encoded downstream of the alpA-promoter (Figure 1—figure supplement 1).

A new regulator BisDC is the last step in the activation cascade

Next, we thus focused our attention on the genes downstream of the alpA-promoter. Cloning the genes from alpA all the way to inrR (Figure 1A) on plasmid pME6032 under control of Ptac and inducing that construct with IPTG resulted in activation of PinR–egfp and Pint–echerry expression in P. putida without ICEclc (Figure 4A). Both these promoters had been silent upon activation of TciR or BisR (Figure 2B and Figure 3B). This indicated that one or more regulatory factors directly controlling expression of PinR and/or Pint were encoded in this region, which we tried to identify by subcloning different gene configurations.

Figure 4 with 2 supplements see all
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A new regulatory factor BisDC for activation of downstream ICEclc functions.

(A) IPTG (0.05 mM) induction of a plasmid with the cloned ICEclc left-end gene region (as depicted on top) leads to reporter expression from the ‘downstream’ PinR- and Pint-promoters in P. putida without ICEclc. Fluorescence images scaled to same brightness (300–1200). (B) Pint-echerry reporter expression upon IPTG induction (0.05 mM) of different plasmid-subcloned left-end region fragments (grey shaded area on the left) in P. putida without ICEclc. Bars show means of median cell fluorescence levels with one standard deviation, from triplicate biological cultures (n = 500–1000 cells, summed from 6 to 12 images per replicate). Asterisks denote significance groups in ANOVA followed by post-hoc Tukey testing. (C) Population response of Pint-echerry induction in P. putida with ICEclc in presence of plasmid constructs expressing bisD, bisC or both (fluorescence images scaled to 300–2000 brightness). Quantile-quantile plots (n = number of cells) below show the estimated size of the responding subpopulation. (D) Effect of bisDC induction from cloned plasmid (0.05 mM IPTG) on conjugative transfer of ICEclc wild-type or mutant derivatives. Transfer assays as in legend to Figure 2A. ND, below detection limit (10–7).

Figure 4—source data 1

Figure 4 panel B: median fluorescence values.

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Figure 4—source data 2

Figure 4 panel C: qq plot single cell fluorescence data.

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Figure 4—source data 3

Figure 4 panel D: ICEclc transfer data.

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Removing alpA from the initial construct had no measurable effect on expression of the fluorescent reporters, but replacing Ptac by the native PalpA promoter abolished all Pint reporter activation (Figure 4B, Figure 4—figure supplement 1). This suggested that PalpA is silent without activation by BisR (see below) and no spontaneous production of regulatory factors occurred. Removing three genes at the 3’ extremity (i.e., orf96323, orf95213 and inrR) reduced Pint–echerry reporter expression, but a fragment with a further deletion into the bisC gene was unable to activate Pint (Figure 4B). Induction of inrR alone did not result in Pint activation (Figure 4B). Deletion of parA and shi at the 5’ end of the fragment still enabled reporter expression from Pint, narrowing the activator factor regions down to two genes, previously named parB and orf97571, but renamed here to bisD and bisC (Figure 4B). Neither bisC or bisD alone, but only the combination of bisDC resulted in reporter expression from Pint in P. putida UWC1 without ICEclc (Figure 4B), and similarly, of PinR (Figure 4—figure supplement 1). In the presence of ICEclc, inducing either bisC or bisD from a plasmid yielded a small proportion of cells expressing the Pint reporters (Figure 4C). This was not the case in a P. putida carrying an ICEclc with a deletion of bisD (Figure 4—figure supplement 2), suggesting there was some sort of feedback mechanism of BisDC on itself (see further below). In contrast, induction of bisDC in combination caused a majority of cells to express fluorescence from Pint in P. putida containing ICEclc (Figure 4C) or ICEclc-∆bisD (Figure 4—figure supplement 2). These results indicated that BisDC acts as an ensemble to activate transcription, and this pointed to bisDC as the last step in the regulatory cascade, since it was the minimum unit sufficient for activation of the Pint–promoter, which is exclusively expressed in the subpopulation of tc cells of wild-type P. putida with ICEclc (Delavat et al., 2016; Figure 1—figure supplement 1).

Induction of bisDC from plasmid pMEbisDC yielded high frequencies of ICEclc transfer from P. putida UWC1 under succinate-growth conditions (Figure 4D). Expression of BisDC also induced transfer of ICEclc-variants deleted for tciR or for bisR (Figure 4D). This confirmed that both tciR and bisR relay activation steps to PbisR and PalpA, respectively, but not to further downstream ICE promoters (Figure 1—figure supplement 1). Moreover, an ICEclc deleted for bisD could not be restored for transfer by overexpression of tciR or bisR, but only by complementation with bisDC (Figure 4D). Interestingly, the frequency of transfer of an ICEclc lacking bisD complemented by expression of bisDC in trans was two orders of magnitude lower than that of similarly complemented wild-type ICEclc, ICEclc with tciR- or bisR-deletion (Figure 4D). This was similar as the reduction in reporter expression observed in P. putida ICEclc-∆bisD complemented with pMEbisDC compared to wild-type ICEclc (Figure 4—figure supplement 2), and suggested the necessity of some ‘reinforcement’ occurring in the wild-type configuration that was lacking in the bisD deletion and could not be restored by in trans induction of plasmid-cloned bisDC.

BisDC is part of a positive autoregulatory feedback loop

To investigate this potential ‘reinforcement’ in wild-type configuration, we revisited the potential for activation of the alpA promoter. Induction by IPTG of the plasmid-cloned fragment encompassing the gene region parA-shi-bisDC caused strong activation of reporter gene expression from PalpA in P. putida without ICEclc (Figure 5A). The minimal region that still maintained PalpA induction encompassed bisDC, although much lower than with a cloned parA-shi-bisDC fragment (Figure 5A). Interestingly, when the parA-shi-bisDC fragment was extended by alpA itself, reporter expression from PalpA was abolished, whereas also a fragment containing only alpA caused significant repression of the alpA promoter (Figure 5A). The alpA gene is predicted to encode a 70-amino acid DNA binding protein with homology to phage regulators (Trempy et al., 1994; Figure 1—figure supplement 2). These results would imply feedback control on activation of PalpA, since its previously mapped transcript covers the complete region from alpA to orf96323 on ICEclc, including bisDC (Figure 1A; Gaillard et al., 2010). Although induction of BisDC was sufficient for activation of transcription from PalpA, this effectively only yielded a small subpopulation of cells with high reporter fluorescence values (Figure 5B & C), in contrast to induction of the larger cloned gene region encompassing parA-shi-bisDC that activated all cells (Figure 5B & C). The feedback loop, therefore, seemed to consist of a positive forward part that includes BisDC (reinforced by an as yet unknown other mechanism) and a modulatory repressive branch including AlpA (Figure 1—figure supplement 1).

Figure 5
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Autoregulatory feedbacks on the alpA promoter.

(A) PalpA-reporter expression upon IPTG induction (0.05 mM) of plasmid-cloned individual genes or gene combinations (as depicted in the shaded area on the left) in P. putida without ICEclc. Bars represent means of median cell fluorescence plus one standard deviation, as in legend to Figure 2B. p-values stem from pair-wise comparisons between triplicate cultures carrying the empty vector pME6032 and the indicated plasmid-cloned gene(s). (B) Cell images of P. putida PalpA-egfp without ICEclc expressing plasmid-cloned combinations with bisDC (fluorescence brightness scaled to 300–1200, 0.05 mM IPTG). (C) Quantile-quantile estimation of subpopulation expression of the PalpA-egfp reporter, showing the sufficiency of bisDC induction for autoregulatory feedback and the reinforcement from upstream elements (n denotes the number of cells used for the quantile-quantile plot, summed from 6 to 12 images of a single replicate culture).

Figure 5—source data 1

Figure 5 panel A: Median fluorescence values.

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Figure 5—source data 2

Figure 5 panel C : qq plot single cell fluorescence values.

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Modelling suggests positive feedback loop to generate and maintain ICEclc bistable output

The results so far thus indicated that ICEclc transfer competence is initiated by TciR activating transcription of the promoter upstream of bisR. BisR then kickstarts expression from the alpA-promoter, leading to (among others) expression of BisDC. This is sufficient to induce the ‘downstream’ ICEclc transfer competence pathway (Figure 1—figure supplement 1), exemplified here by activation of the Pint and PinR promoters that become exclusively expressed in the subpopulation of transfer competent cells under wild-type conditions (Minoia et al., 2008). In addition, BisDC reinforces transcription from the same alpA-promoter.

In order to understand the importance of this regulatory architecture for generating bistability, for initiating and maintaining (downstream) transfer competence, we developed a conceptual mathematical model (Figure 6A, Materials and methods, SI model). The model assumes the regulatory factors TciR, BisR and BisDC, typical oligomerization (Tropel and van der Meer, 2004), as well as binding of the oligomerized forms to and unbinding from their respective nodes (i.e., the linked promoters PbisR, PalpA and Pint). Binding is assumed to lead to protein synthesis and finally, protein degradation (Figure 6A). We varied and explored the outcomes of different regulatory network architectures and parts, testing their effect on production of intermediary and downstream elements in stochastic simulations, with each individual simulation corresponding to events taking place in an individual cell (Figure 6A,SI model).

Figure 6
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Stochastic simulations of ICEclc regulatory network configurations.

(A) Conceptual model of the ICEclc regulatory cascade producing bistable output. Ellipses indicate the three major regulatory factors (TciR, BisR and BisDC) interacting with their target promoters (PbisR, PalpA), and BisDC-regulated downstream output (here schematically as Plate and a late gene). Relevant simulated processes include: production (combination of transcription and translation, with corresponding rates: C5, A3), oligomerization (assumed number of protein monomers in the binding complex), binding and unbinding to the target promoter, and degradation. All processes are simulated as stochastic events across 100 time steps, and protein output levels are summarized from 10,000 individual stochastic simulations (curly bracket in B; detailed parametrization in Supplementary file 4; one simulation being equivalent to an individual cell). (B) Behaviour of a BisDC autoregulatory feedback loop on the distribution of BisDC protein levels per cell (histograms, n = 10,000 simulated cells) as a function of different binding (A1), unbinding (A2), production (A3) and degradation (A4) rate constants, starting from a uniformly distributed set of BisDC levels (input, in green). Black bar indicates the proportion of cells with zero output (i.e., non-activated circuit). Light blue: simulation example where BisDC levels go to zero and loop would die out. Dark blue: BisDC levels remain positive. (C) As for A, but for an architecture of BisR initiating bisDC expression, with different input distributions (uniformly low to high mean, or bimodal BisR input). Note how higher or bimodal BisR input is not expected to change the median BisDC quantity in active cells, but only the proportion of ‘cells’ with positive (magenta, bars) and zero state (black bars; n = 10,000 simulated cells; note different ordinate scales). (D) As for A, but for the complete cascade starting with TciR. Shown are regulatory factor level distributions from two different TciR starting distributions across 10,000 simulations; for BisR integrated between time points 10 and 20 (t10-20), and for BisDC after 100 time steps (t100). Bimodal expression of zero and positive states arises at the bisR node, but is further maintained to constant BisDC output as a result of the feedback loop. (E) Importance of the BisDC-feedback on the output of a downstream (‘late’) BisDC-dependent expressed protein, for a case of a stable and an unstable protein (n = 10,000 simulated cells).

Figure 6—source data 1

Figure 6 panels B–E: Model simulations and histogram data.

https://cdn.elifesciences.org/articles/57915/elife-57915-fig6-data1-v2.xlsx

First we simulated the cellular output of BisDC in a subnetwork configuration with only BisDC activating PalpA (i.e., in absence of TciR or BisR, Figure 6B). Stochastic simulations (n = 10,000) of this bare feedback loop with an arbitrary start of binomially distributed BisDC quantities (mean = 8 molecules per cell, Figure 6B, INPUT), yielded a bimodal population with two BisDC output states after 100 time steps, one of which is zero (black bar in histograms) and the other with a mean positive BisDC value (magenta) (Figure 6B). The output zero results when BisDC levels stochastically fall to 0 (as in case of the light blue line in the panel STOCHASTIC of Figure 6B), since in that case there is no BisDC to stimulate its own production. Parameter variation showed that the proportion of cells with output zero from the loop is dependent on the binding and unbinding constants of BisDC to the alpA promoter, and the BisDC degradation rate (Figure 6B, different A1, A2 and A4-values). In addition, BisDC unbinding and degradation rates can influence the median BisDC output quantity in cells with positive state (Figure 6B, case of A2 = 5 or A4 = 0.3). This simulation thus indicated that a BisDC feedback loop can produce bimodal output, once BisDC is present.

Since the feedback loop cannot start without BisDC, it is imperative to kickstart the alpA promoter by BisR (Figure 6C). Simulations of a configuration that includes activation by BisR, showed how upon a single pulse of BisR, the feedback loop again leads to a bimodal population with zero and positive BisDC levels (Figure 6C). Increasing the (uniformly distributed) mean quantity of BisR in the simulations, within a per-cell range that is typically measured for transcription factors (Li et al., 2014), increased the proportion of cells with positive BisDC state, but did not influence their mean BisDC quantity (Figure 6C). Even bimodally distributed BisR input also gave rise to bimodal BisCD output, but with a higher proportion of zero BisDC state (Figure 6C, bimodal). In contrast to the BisDC loop alone, therefore, activation by BisR only influences the proportion of zero and positive BisDC states in the population, but not the mean resulting BisDC quantity in cells with positive state.

In the full regulatory hierarchy of the ICE, production of BisR is controlled by TciR. Simulation of this configuration showed that bimodality already appeared at the level of BisR (Figure 6D). The proportions of zero and positive states of both BisR and BisDC varied depending on the mean of uniformly distributed amounts of TciR among all cells, again sampled to within regular empiric transcription regulator quantities in individual cells (Li et al., 2014; Figure 6D). Bimodal BisDC levels are propagated by the network architecture to downstream (‘late’) promoters, as a consequence of them being under BisDC control (Figure 6A & E). Importantly, simulations of an architecture without the BisDC feedback loop consistently resulted in lower protein output from BisDC–regulated promoters in activated cells than with feedback (Figure 6E). This suggests two crucial functions for the ICE regulatory network: first, to convert unimodal or stochastic (‘analog’) expression of TciR and BisR among all cells to a consistent subpopulation of cells with positive (‘digital’) BisDC state, and secondly, to ensure sufficient BisDC levels to activate downstream promoters within the positive cell population (Figure 6E). Through the kickstart by BisR and reinforcement by BisDC itself, bimodal expression at the alpA-promoter node can thus yield a stably expressed transfer competence pathway in a subpopulation of cells.

ICEclc regulatory architecture exemplifies a faithful analog-to-digital converter

Simulations thus predicted that the ICE regulatory network faithfully transmits and stabilizes analog input (e.g., a single regulatory factor uniformly or stochastically expressed at moderately low levels in all cells [Li et al., 2014]) to bistable output (e.g., a subset of cells with transfer competence and the remainder silent). To demonstrate this experimentally, we engineered a P. putida without ICEclc, but with a single copy chromosomally inserted IPTG-inducible bisR, a plasmid with alpA-parA-shi-bisDC under control of PalpA, and a single-copy dual Pint-echerry and PinR-egfp reporter (Figure 7A). Induction from Ptac by IPTG addition yields unimodal (analog) production of BisR, the mean level of which can be controlled by the IPTG concentration (Figure 7—figure supplement 1). In the presence of all components of the system, IPTG induction of BisR led to bistable activation of both reporters (Figure 7B, ABC). Increasing BisR induction was converted by the feedback loop into an increased proportion of fluorescent cells (Figure 7C). This effectively created a scalable bimodal (digital) output from unimodal input, dependent on the used IPTG concentration (Figure 7C, Figure 7—figure supplement 1). The proportion of fluorescent cells was in line with predictions from stochastic simulations as a function of the relative strength of Ptac activation (Figure 7D). Furthermore, in agreement with model predictions (Figure 6C), the median fluorescence of activated cells remained the same at different IPTG (and thus BisR) concentrations (Figure 7E). These results confirmed that the feedback loop architecture transforms a unimodal (analog) regulatory factor concentration (BisR) into a stabilized bimodal (digital) output.

Figure 7 with 1 supplement see all
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The ICEclc bistability generator is a scalable analog-digital converter.

(A) Schematic representation of the three ICEclc components used to generate scalable bistable output in P. putida UWC1 without ICE. (B) Cell images of P. putida with the different bistability-generator components as indicated, induced in presence or absence of IPTG (0.1 mM). Fluorescence brightness scaled to between 300–1200. (C) Proportion of active cells (estimated from quantile-quantile plotting as in Figure 2C) as a function of IPTG concentration (same induction time for all). Lines correspond to the means from three biological replicates with transparent areas representing the standard deviation. (D) Modelled proportion of cells with positive output in the architecture of Figure 6C as a function of the relative BisR starting levels from Ptac. (E) Measured distributions (as normalized probability density) of eCherry fluorescence among the subpopulations of activated (magenta bars) and non-activated cells (black bars) at different IPTG concentrations, showing same subpopulation fluorescence median (dotted grey lines), as predicted in the stochastic model. AU, arbitrary units of fluorescence brightness at 500 ms exposure. n denotes the number of cells used to produce the histograms, summed from 6 to 12 images from a single replicate culture. Panels autoscaled to maximum ordinate.

Figure 7—source data 1

Figure 7 panel C: Mean fluorescence data.

https://cdn.elifesciences.org/articles/57915/elife-57915-fig7-data1-v2.xlsx
Figure 7—source data 2

Figure 7 panel E: Single cell and histogram fluorescence data of IPTG induction.

https://cdn.elifesciences.org/articles/57915/elife-57915-fig7-data2-v2.xlsx

BisDC-elements are widespread in other presumed ICEs

Pfam analysis detected a DUF2857-domain in the BisC protein, and further structural analysis using Phyre2 indicated significant similarities of BisC to FlhC (Figure 1—figure supplement 2). FlhC is a subunit of the master flagellar activator FlhDC of E. coli and Salmonella (Claret and Hughes, 2000; Liu and Matsumura, 1994). BisD carries a ParB domain, with a predicted DNA binding domain in the C-terminal portion of the protein (Figure 1—figure supplement 2). Although no FlhD domain was detected in BisD, in analogy to FhlDC we named the ICEclc activator complex BisDC, for bistability regulator subunits D and C.

Database searches showed that bisDC loci are also widespread among pathogenic and environmental Gamma- and Beta-proteobacteria, and are also found in some Alphaproteobacteria (Figure 1—figure supplement 3). Phylogenetic analysis using the more distantly related sequence from Dickeya zeae MS2 as an outgroup indicated several clear clades, encompassing notably bisDC homologs within genomes of P. aeruginosa and Xanthomonas (Figure 1—figure supplement 4). Several genomes contained more than one bisDC homolog, the most extreme case being Bordetella petrii DSM12804 with up to four homologs belonging to four different clades (Figure 1—figure supplement 4).

The gene synteny from bisR to inrR of ICEclc was maintained in several genomes (Figure 1—figure supplement 3), suggesting them being part of related ICEs with similar regulatory architecture. Notably, some of those are opportunistic pathogens, such as P. aeruginosa, B. petrii, B. bronchiseptica, or X. citri, and regions of high similarity to the ICEclc regulatory core extended to the well-known pathogenicity islands of the PAGI-2 (Klockgether et al., 2007) and PAGI-16 families (Hong et al., 2016; Figure 1—figure supplement 3). Several of the ICEclc core homologs carry genes suspected in virulence (e.g., filamentous hemagglutinin [Sun et al., 2016] encoded on the P. aeruginosa HS9 and Carb01-63 genomic islands), or implicated in acquired antibiotic resistance (e.g, multidrug efflux pump on the A. xylosoxidans NH44784-1996 element (Miyazaki et al., 2015), and carbapenem resistance on the PAGI-16 elements [Hong et al., 2016]). This indicates the efficacy of the ICEclc type regulatory control on the dissemination of this type of mobile elements, and consequently, on the distribution and selection of adaptive gene functions they carry.

Discussion

ICEs operate a dual life style in their host, which controls their overall fitness as the integral of vertical descent (i.e., maintenance of the integrated state and replication with the host chromosome) and horizontal transfer (i.e., excision from the host cell, transfer and reintegration into a new host) (Delavat et al., 2017; Delavat et al., 2016; Johnson and Grossman, 2015). The decision for horizontal transfer is costly and potentially damages the host cell (Delavat et al., 2016; Pradervand et al., 2014), which is probably why its frequency of occurrence in most ICEs is fairly low (<10–5 per cell in a host cell population) (Delavat et al., 2017). Consequently, the mechanisms that initiate and ensure ICE horizontal transfer must have been selected to operate under extremely low opportunity with high success. In other words, they have been selected to maximize faithful maintenance of transfer competence development, once this process has been triggered in a host cell. One would thus expect such mechanisms to impinge on rare, perhaps stochastic cellular events, yielding robust output despite cellular gene expression and pathway noise. ICEclc is further particular in the sense that its transfer competence is initiated in cells during stationary phase conditions (Miyazaki et al., 2012), which restricts global transcription and activity, and may even profoundly alter the cytoplasmic state of the cell (Parry et al., 2014).

The results of our work here reveal that the basis for initiation and maintenance of ICEclc transfer competence in a minority of cells in a stationary phase population (Reinhard et al., 2013), originates in a multinode regulatory network that further includes a positive feedback loop. Genetic dissection, epistasis experiments and expression of individual components in P. putida devoid of the ICE showed that the network consists of a number of regulatory factors, composed of MfsR, TciR, BisR and BisDC, acting sequentially on singular (TciR, BisR) or multiple nodes (BisDC). The network has an ‘upstream’ branch controlling the initiation of transfer competence, a ‘bistability generator’ that confines the input signal, and maintains the ‘downstream’ path of transfer competence to a dedicated subpopulation of cells (Figure 1—figure supplement 1).

The previously characterized mfsR-marR-tciR operon (Pradervand et al., 2014), whose transcription is controlled through autorepression by MfsR, is probably the main break on activation of the upstream branch. This was concluded from effects of deleting mfsR, which resulted in overexpression of TciR, and massively increased and deregulated ICE transfer even in exponentially growing cells (Pradervand et al., 2014). We showed here that TciR activates the transcription of a hitherto unrecognized transcription factor gene named bisR, but not of any further critical ICEclc promoters. Autorepression by MfsR in wild-type ICEclc results in low unimodal transcription from PmfsR (Pradervand et al., 2014) and therefore, likely, to low TciR levels in all cells. TciR appeared here as a weak activator of the bisR promoter, suggesting that only in a small proportion of cells it manages to trigger bisR transcription, as our model simulations further attested.

The BisR amino acid sequence revealed only very weak homology to known functional domains, thus making it the prototype of a new family of transcriptional regulators. In contrast to TciR, BisR was a very potent activator of its target, the alpA promoter. Model simulations suggested that BisR triggers and transmits the response in a scalable manner to the bistability generator, encoded by the genes downstream of PalpA. Triggering of PalpA stimulated expression of (among others) two consecutive genes bisD and bisC, which code for subunits of an activator complex that weakly resembles the known regulator of flagellar synthesis FlhDC (Claret and Hughes, 2000; Liu and Matsumura, 1994). BisDC production was sufficient to activate the previously characterized bistable ICEclc promoters Pint and PinR, making it the key regulator for the ‘downstream’ branch (Figure 1—figure supplement 1). Importantly, BisDC was also part of a feedback mechanism activating transcription from PalpA, and therefore, regulates its own production. Simulations and experimental data indicated that the feedback loop acts as a scalable analog-to-digital converter, transforming any positive input received from BisR into a dedicated cell that can regenerate sufficiently high BisDC levels to activate the complete downstream transfer competence pathway.

Bistable gene network architectures are characterized by the fact that expression variation is not resulting in a single mean phenotype, but can lead to two (or more) stable phenotypes - mostly resulting in individual cells displaying either one or the other phenotype (Ferrell, 2012; Ferrell, 2002; Dubnau and Losick, 2006). Importantly, such bistable states are an epigenetic result of the network functioning and do not involve modifications or mutations on the DNA (Kussell and Leibler, 2005; Balázsi et al., 2011). Bistable phenotypes may endure for a particular time in individual cells and their offspring, or erode over time as a result of cell division or other mechanism, after which the ground state of the network reappears. One can thus distinguish different steps in a bistable network: (i) the bistability switch that is at the origin of producing the different states, (ii) a propagation or maintenance mechanism and (iii) a degradation mechanism [11].

Some of the most well characterized bistable processes in bacteria include competence formation and sporulation in Bacillus subtilis (Dubnau and Losick, 2006). Differentiation of vegetative cells into spores only takes place when nutrients become scarce or environmental conditions deteriorate (Veening et al., 2008; Veening et al., 2006). Sporulation is controlled by a set of feedback loops and protein phosphorylations, which culminate in levels of the key regulator SpoOA ~P being high enough to activate the sporulation genes (Dubnau and Losick, 2006). In contrast, bistable competence formation in B. subtilis is generated by feedback transcription control from the major competence regulator ComK. Stochastic variations among ComK levels in individual cells, ComK degradation and inhibition by ComS, and noise at the comK promoter determine the onset of comK transcription, which then reinforces itself because of the feedback mechanism (Süel et al., 2006; Maamar et al., 2007). Initiation and maintenance of the ICEclc transfer competence pathway thus resembles DNA transformation competence in B. subtilis in its architecture of an auto-feedback loop (BisDC vs ComK). However, the switches leading to bistability are different, with ICEclc depending on a hierarchy of transcription factors (MfsR, TciR and BisR), and transformation competence being a balance of ComK degradation and inhibition of such degradation (Süel et al., 2006; Maamar et al., 2007). ICEclc bistability architecture is clearly different from the well-known double negative feedback control exerted by, for example the phage lambda lysogeny/lytic phase decision in E. coli (Arkin et al., 1998; Bednarz et al., 2014). That switch entails essentially a balance of the counteracting transcription factors CI, CII and Cro (Arkin et al., 1998; Bednarz et al., 2014). Interestingly, other ICEs of the SXT/R391 family carry this typical double negative feedback loop architecture, which may therefore control their (bistable) activation (Poulin-Laprade and Burrus, 2015; Bellanger et al., 2008; Beaber and Waldor, 2004; Poulin-Laprade et al., 2015). Given the low frequencies of conjugative transfer of many different elements (Delavat et al., 2017), bistability activation mechanisms may be much more widespread than assumed.

Mathematically speaking, the ICEclc transfer competence regulatory architecture has two states, one of which is zero (inactive) and the other with a positive value (activation of transfer competence). Stochastic modelling suggested that the feedback loop maintains positive output during a longer time period than in its absence (although it will drop to zero at infinite time). Previous experimental data suggested that the tc cells indeed do not return to a silent ICEclc state, but become irreparably damaged, arrest their division (Takano et al., 2019) and wither (Reinhard et al., 2013). However, because their number is proportionally low, there is no fitness cost on the population carrying the ICE (Delavat et al., 2016; Gaillard et al., 2008). The advantage of prolonged feedback output seems that constant levels of the BisCD regulator can be maintained, allowing coordinated and organized production of the components necessary for the ICEclc transfer itself. This would consist of, for example, the relaxosome complex responsible for DNA processing at the origin(s) of transfer, and the mating pore formation complex (Carraro and Burrus, 2015). Because Pseudomonas cells activate ICEclc transfer competence upon entry in stationary phase, the feedback loop may have a critical role to ensure faithful completion of the transfer competence pathway during this period of limiting nutrients, and to allow the ICE to excise and transfer from tc cells once new nutrients become available (Delavat et al., 2016).

Although our results were conclusive on the roles of the key regulatory factors (MfsR, TciR, BisR, BisDC), there may be further auxiliary and modulary factors, and environmental cues that influence the transfer competence network. For example, we previously found that deletions in the gene inrR drastically decreased ICEclc transfer capability by 45–fold and reduced reporter gene expression from Pint (Minoia et al., 2008). Expression of InrR alone, however, did not show any direct activation of Pint, PinR or PalpA, and InrR is thus unlikely to be a direct transcription activator protein. Our results also indicated that induction of AlpA may repress output from the PalpA promoter, and modulate the feedback loop that is initiated by BisR and maintained by BisDC. Furthermore, although induction of bisDC was sufficient to activate expression from PalpA, it was enhanced through an as yet uncharacterized mechanism involving its upstream regions. Previous results also highlighted the implication of the stationary phase sigma factor RpoS for PinR activation (Figure 1B; Miyazaki et al., 2012), which may be more generally important for other ICEclc regulatory promoters as well. Unraveling these details in future work will be important for a full understanding of the generation and maintenance of bistability of the ICEclc family of elements, and its role in effective horizontal dissemination.

Phylogenetic analyses showed the different ICEclc regulatory loci (i.e., bisR-alpA-bisDC-inrR) to be widely conserved in Beta- and Gammaproteobacteria, with only few small variations in regulatory gene configurations. Most likely, these regions are part of ICEclc-like elements in these organisms, several of which have been detected previously (Miyazaki et al., 2015; Miyazaki, 2011a; Gaillard et al., 2006). They are further part of PAGI-2 (Klockgether et al., 2007) and PAGI-16 family genomic islands in P. aeruginosa clinical isolates (Hong et al., 2016) that have been implicated in the distribution of virulence factors and antibiotic resistance elements. The ICEclc regulatory cascade for transfer competence thus seems widely conserved, controlling horizontal dissemination of this important class of bacterial conjugative elements.

Materials and methods

Key resources table
Reagent type
(species)
or resource		DesignationSource or referenceIdentifiersAdditional information
Gene (Pseudomonas knackmussii ICEclc)ICEclcPMID:16484212GenBank: AJ617740.2Full ICEclc sequence
Gene (Pseudomonas knackmussii ICEclc)tciRPMID:24945944GenBank: CAE92867.2Transcriptional regulator of ICEclc
Gene (Pseudomonas knackmussii ICEclc)bisR; orf101284this paperGenBank: CAE92957.1Transcriptional regulator of ICEclc
Gene (Pseudomonas knackmussii ICEclc)bisD; parB; orf98147this paperGenBank: CAE92953.1Subunit D of the transcriptional regulator complex BisCD of ICEclc
Gene (Pseudomonas knackmussii ICEclc)bisC; orf97571this paperGenBank: CAE92952.1Subunit C of the transcriptional regulator complex BisCD of ICEclc
Gene
(plasmid pZS2FUNR)		echerryPMID:19098098Red fluorescent protein gene used for the miniTn7:Ptac-echerry reporter
Strain, strain background (Pseudomonas putida)UWC1PMID:2604401NCBI: txid1407054Background strain for ICEclc transfer and mutagenesis experiments
Strain, strain background (Pseudomonas putida)2737PMID:21255116UWC1 carrying ICEclc in tRNAGly
Strain, strain background (Pseudomonas putida)UWCGCPMID:21255116Recipient strain used for conjugation transfer experiments
Strain, strain background (Escherichia coli)DH5αλpirPMID:10610816Cloning strain
Recombinant DNA reagentpME6032; pME
(plasmid)		PMID:11807065GenBank: DQ645594.1Broad-host range cloning vector, lacIq-Ptac expression
Recombinant DNA reagentminiTn5 (plasmid; transposon)PMID:21342504
(RRID:Addgene_60487)		GenBank: HQ908071.1Transposon suicide vector for gene reporter constructs
Recombinant DNA reagentminiTn7 (plasmid; transposon)PMID:15908923
(RRID:Addgene_63121)		GenBank: AY619004.1Transposon suicide vector for single copy insertions
Recombinant DNA reagentminiTn7:Ptac
(plasmid; transposon)		PMID:15908923GenBank: AY599234.1Transposon vector used for miniTn7:Ptac-echerry reporter
Recombinant DNA reagentminiTn5:PinR-egfp/Pint-echerryPMID:19098098Dual single copy insertion reporter system for ICEclc bistable activity
Sequence-based reagentDNA fragment containingPalpA, alpA, parA, shi and the 5’ part of bisDThermoFisher ScientificSynthetic DNA fragment
Commercial assay or kitNucleospin Plasmid KitMacherey-NagelMacherey-Nagel: 740588.50Plasmid purification
Commercial assay or kitNucleospin Gel and PCR Clean-up KitMacherey-NagelMacherey-Nagel: 740609.50PCR fragment purification
Commercial assay or kitQuick-Fusion Cloning KitBimakeBimake: B22611Generation of recombinant vectors
Chemical compound, drugIPTG; isopropyl β-D-1-thiogalactopyranosideSigma-AldrichSigma-Aldrich: I5502Used for induction of Ptac promoter
Chemical compound, drug3-CBA; 3-chlorobenzoate
(3-chlorobenzoic acid)		Sigma-AldrichSigma-Aldrich: C24604Specific carbon source for selection of ICEclc in Pseudomonas
Chemical compound, drugSodium succinate; succinate
(Sodium succinate dibasic hexahydrate)		Sigma-AldrichSigma-Aldrich:14170General carbon source for growth of Pseudomonas
Software, algorithmMEGA7PMID:27004904Phylogenetic analysis
Software, algorithmVisiviewVisitron systems GMbHhttps://www.visitron.de/products/visiviewr-software.htmlMicroscopy images acquisition
Software, algorithmImageJPMID:22930834Image processing
Software, algorithmMatLab
(v 2016a)		MathworksData treatment
Software, algorithmR ggplotHadley Wickhamhttps://ggplot2.tidyverse.org/Data visualization
Software, algorithmJulia; DifferentialEquations.jl packageDOI:http://doi.org/10.5334/jors.151Mathematical model
OtherMinimum media; MM
(culture media)		PMCID:PMC494262Supplementary file 2Carbon source-free base for minimal media
OtherBio-Rad GenePulser XcellBioradBiorad: 165–2660Device used for electro-transformation of bacterial strains
OtherZeiss Axioplan II microscope (Carl Zeiss); EC ‘Plan-Neofluar’ 100x/1.3 Oil Pol Ph3 M27
objective lens (Carl Zeiss); SOLA SE light engine (Lumencor); SPOT Xplorer slow-can charge coupled device camera 1.4 Megapixels monochrome w/o IR (Diagnostic Instruments)		Carl Zeiss; Lumencor; Diagnostic instrumentsCarl Zeiss: Axioplan II;Carl Zeiss: 420491-9910-000; Lumencor: SOLA 6-LCR-SC; Diagnostic instrument: XP2400Microscope for single cell phase contrast and epifluorescence imaging
Other0.2–μm cellulose acetate filtersSartoriusSartorius:11107–25 Nfilters for conjugative transfer

Strains and growth conditions

Request a detailed protocol

Bacterial strains and plasmid constructions used in this study are shortly described in Table 1 and with more detail in Supplementary file 1. Strains were routinely grown in Luria broth (10 g l–1 Tryptone, 10 g l–1 NaCl and 5 g l–1 Yeast extract, LB Miller, Sigma Aldrich) at 30°C for P. putida and 37°C for E. coli in an orbital shaker incubator, and were preserved at –80°C in LB broth containing 15% (v/v) glycerol. Reporter assays and transfer experiments were carried out with cells grown in type 21C minimal media (MM, Supplementary file 2; Gerhardt, 1981) supplemented with 10 mM sodium succinate or 5 mM 3-chlorobenzoate (3-CBA). Antibiotics were used at the following concentrations: ampicillin (Ap), 100 µg ml–1 for E. coli and 500 µg ml–1 for P. putida; gentamicin (Gm), 10 µg ml–1 for E. coli, 20 µg ml–1 for P. putida; kanamycin (Kn), 50 µg ml–1; tetracycline (Tc), 12 µg ml–1 for E. coli, 100 µg ml–1 or 12.5 µg ml–1 for P. putida grown in LB or MM, respectively. Genes were induced from Ptac by supplementing cultures with 0.05 mM isopropyl β-D-1-thiogalactopyranoside (IPTG; or else at the indicated concentrations).

Table 1
Strains and plasmids used in this study.
Strains or plasmidsRelevant genotype or phenotypeReferences
E. coli
DH5αλpirendA1 hsdR17 glnV44 (=supE44) thi-1 recA1 gyrA96 relA1 φ80dlacΔ(lacZ)M15 Δ(lacZYA-argF)U169 zdg-232::Tn10 uidA::pir+Platt et al., 2000
P. putida UWC1plasmid-free derivative ofP. putida KT2440 (Rif)McClure et al., 1989
UWCGCSingle copy integration of lacI-less Ptac promoter controlling echerry expression (Gm)Miyazaki and van der Meer, 2011b
ICEclcICEclc copy integrated into tRNAgly-5 (3-CBA)Miyazaki and van der Meer, 2011b
ICEclc ∆tciRtciR (orf17162) derivative mutant of ICEclc (3-CBA)Pradervand et al., 2014
ICEclc ∆bisRbisR (orf101284) derivative mutant of ICEclc (3-CBA)This work
ICEclc ∆bisDbisD (orf98147) derivative mutant of ICEclc (3-CBA)This work
miniTn7::PinR-egfpSingle copy chromosomal integration of PinR promoter fused to egfp (Gm)This work
miniTn7::PalpA-egfpSingle copy chromosomal integration of PalpA promoter fused to egfp (Gm)This work
miniTn5:: PbisR-egfpSingle copy chromosomal integration of PbisR promoter fused to egfp (Kn)This work
miniTn5:: Pint-echerry/PinR egfp (C)Single copy chromosomal integration of a dual reporter Pint and PinR promoter fused to echerry and egfp, respectively (Kn)Minoia et al., 2008
miniTn7::Ptac-bisR (A)Single copy chromosomal integration of Ptac promoter fused to bisR (Gm)This work
miniTn7::Ptac-echerrySingle copy chromosomal integration of Ptac promoter fused to echerry (Gm)This work
Plasmids
pME6032pVS1-p15A shuttle vector carrying the lacIq-Ptac expression system (Tc)Heeb et al., 2000
pMEtciRpME6032 derivative allowing IPTG-controlled expression of tciR (Tc)This work
pMEbisRpME6032 derivative allowing IPTG-controlled expression of bisR (Tc)This work
pMEbisCpME6032 derivative allowing IPTG-controlled expression of bisC (Tc)This work
pMEbisDpME6032 derivative allowing IPTG-controlled expression of bisD (Tc)Reinhard et al., 2013
pMEbisDCpME6032 derivative allowing IPTG-controlled expression of bisCD (Tc)This work
pMEparApME6032 derivative allowing IPTG-controlled expression of parA (Tc)Reinhard et al., 2013
pMEparA-shi-bisDpME6032 derivative allowing IPTG-controlled expression ofparA, shi and bisD (Tc)Reinhard et al., 2013
pMEbisC96pME6032 derivative allowing IPTG-controlled expression of bisC and 96323 (Tc)This work
pMEalpApME6032 derivative allowing IPTG-controlled expression of alpA (Tc)This work
pMEinrRpME6032 derivative allowing IPTG-controlled expression of inrR (Tc)This work
pMEregpME6032 derivative allowing IPTG-controlled expression of the alpA-inrR loci (Tc)This work
pMEreg∆alpApME6032 derivative allowing IPTG-controlled expression of the parA-inrR loci (Tc)This work
pMEreg∆alpA∆PpMEreg∆alpA derivative lacking 3’ half of 96323, 95213 and inrR (Tc)This work
pMEreg∆alpA∆ApMEreg∆alpA derivative lacking the bisC, 96323, 95213 and inrR (Tc)This work
pMEreg∆PpMEreg derivative lacking 3’ half of 96323, 95213 and inrR (Tc)This work
pMEreg∆ApMEreg derivative lacking the bisC, 96323, 95213 and inrR (Tc)This work
pMEbglacIq-Ptac-less pME6032 derivative carrying the PalpA-inrR loci (Tc)This work
pMEbg_short (comp B)pMEbg derivative lacking 96323, 95213 and inrR (Tc)This work
pUX-BF13helper plasmid for integration of Tn7 (Ap)Heeb et al., 2000

  1. 3-chlorobenzoate (3-CBA); Ampicillin (Ap); gentamycin (Gm); kanamycin (Kn); rifampicin (Rf); tetracycline (Tc).

    (A), (B) and (C) refer to components of the reconstituted bistability generator.

  2. For strain numbers, see Supplementary file 1.

Molecular biology methods

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Plasmid DNA was purified using the Nucleospin Plasmid kit (Macherey-Nagel) according to manufacturer’s instructions. All enzymes used in this study were purchased from New England Biolabs. PCR reactions were carried out with primers described in Supplementary file 3. PCR products were purified using Nucleospin Gel and PCR Clean-up kits (Macherey-Nagel) according to manufacturer’s instructions. E. coli and P. putida were transformed by electroporation as described by Dower et al., 1988. in a Bio-Rad GenePulser Xcell apparatus set at 25 µF, 200 V and 2.5 kV for E. coli and 2.2 kV for P. putida using 2 mm gap electroporation cuvettes (Cellprojects). All constructs were verified by DNA sequencing (Eurofins).

Cloning of regulatory pathway elements

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Different ICEclc gene configurations were cloned in P. putida with or without ICEclc, and further with different promoter-reporter fusions, using the broad host-range vector pME6032, allowing IPTG-controlled expression from the LacIq-Ptac promoter (Koch et al., 2001; Table 1). Genes tciR, bisR, bisC, bisDC, bisC+96323, alpA and inrR were amplified using primer pairs as specified in Supplementary file 3, with genomic DNA of P. putida UWC1-ICEclc as template. Amplicons were digested by EcoRI and cloned into EcoRI-digested pME6032 using T4 DNA ligase, producing after transformation the plasmids listed in Table 1. The 6.4 kb ICEclc left-end fragment encompassing parA-inrR was recovered from pTCB177 (Sentchilo et al., 2003) and cloned into pME6032 (producing pMEreg∆alpA, Supplementary file 1). An alpA-parA-shi-bisD’ fragment was amplified by PCR (Supplementary file 2) and cloned into pME6032 using EcoRI restriction sites (Supplementary file 1). The resulting plasmid was digested with SalI and the 4.8 kb fragment containing the Ptac promoter, alpA-parA-shi-bisD’ was recovered and used to replace the parA-shi-parB part of pMEreg∆alpA. This generated a cloned fragment encompassing alpA all the way to inrR (pMEreg, Supplementary file 1). Further 3’ deletions removing orf96323-inrR or bisC-inrR were generated by PstI and AfeI digestion and religation (Supplementary file 1). A DNA fragment containing PalpA, alpA, parA, shi and the 5’ part of bisD was synthesized (ThermoFisher Scientific), and ligated by Quick-Fusion cloning (Bimake) into pMEreg∆alpA digested with PmlI and BamHI to remove the part containing lacIq, Ptac, parA, shi and bisD. This plasmid was then digested by PstI to remove orf96323-inrR and religated (Supplementary file 1).

Deletions of bisR or bisD in ICEclc were constructed using the two-step seamless chromosomal gene inactivation technique as described elsewhere (Martínez-García and de Lorenzo, 2011).

Reporter gene constructs

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Activation of key ICEclc promoters was determined in strains with a single-copy chromosomal insertions to promoterless egfp or echerry genes, for most cases delivered by a suicide miniTn7 system at a fixed unique position (Table 1). In other cases, particularly in combination with other single-copy inserted gene fragments, we used miniTn5 random delivery. The promoter regions upstream of bisR or alpA were amplified in the PCR (Supplementary file 3) and cloned into the promoterless egfp reporter miniTn5 delivery plasmid pBAM1 (Martínez-García et al., 2011) or into a pUC18-derived miniTn7 delivery plasmid (Choi et al., 2005). The PinR-egfp insert was recovered from the miniTn5-based reporter system (Minoia et al., 2008) using HindIII and KpnI, and subsequently cloned into pUC18miniTn7 digested by the same enzymes. The dual miniTn5::PinR-egfp/Pint-echerry reporter has been described previously (Minoia et al., 2008). A miniTn7::Ptac-echerry reporter was reconstructed from pZS2FUNR (Minoia et al., 2008) and the general miniTn7:Ptac suicide delivery vector (Choi et al., 2005; Supplementary file 2). All reporter constructs were integrated in single copy into the chromosomal attBTn7 site of P. putida by using pUX-BF13 for miniTn7, or randomly for miniTn5-based constructs (Martínez-García et al., 2011; Koch et al., 2001), in which case three independent clones were recovered, stored and analysed. The intactness of the inserted reporter constructs was verified by PCR amplification and sequencing.

ICEclc transfer assays

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ICEclc transfer was tested with 24-h-succinate-grown donor and recipient cultures. Cells were harvested by centrifugation of 1 ml (donor) and 2 ml culture (recipient, Gm-resistant P. putida UWCGC) for 3 min at 1200 × g, washed in 1 ml of MM without carbon substrate, centrifuged again and finally resuspended in 20 µl of MM. Donor or recipient alone, and a donor-recipient mixture were deposited on 0.2–µm cellulose acetate filters (Sartorius) placed on MM succinate agar plates, and incubated at 30°C for 48 hr. The cells were recovered from the filters in 1 ml of MM and serially diluted before plating. Donors, recipients and exconjugants were selected on MM agar plates containing appropriate antibiotics and/or carbon source (3-CBA). Transfer frequencies are reported as the mean of the exconjugant colony forming units compared to that of the donor in the same assay.

Molecular phylogenetic analysis

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BisDC phylogeny was inferred from 148 aligned homolog amino acid sequences by using the Maximum Likelihood method based on the Tamura-Nei model (Tamura and Nei, 1993), eliminating positions with less than 95% site coverage. The final dataset was aligned using MEGA7 (Kumar et al., 2016) and contained a total of 2091 positions. Initial tree(s) for the heuristic search were obtained automatically by applying Neighbour-Joining and BioNJ algorithms to a matrix of pairwise distances estimated using the Maximum Composite Likelihood (MCL) approach, and then selecting the topology with superior log likelihood value.

Fluorescent reporter assays

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For quantification of eGFP and eCherry fluorescence in single cells, P. putida strains were cultured overnight at 30°C in LB medium. The overnight culture was diluted 200 fold in 8 ml of MM supplemented with succinate (10 mM) and appropriate antibiotic(s), and grown at 30°C and 180 rpm to stationary phase. 150 µl of culture were then sampled, vortexed for 30 s at max speed, after which drops of 5 µl were deposited on a regular microscope glass slide (VWR) coated with a thin film of 1% agarose in MM. Cells were covered with a 24 × 50 mm cover slip (Menzel-Gläser) and imaged immediately with a Zeiss Axioplan II microscope equipped with an EC Plan-Neofluar 100×/1.3 oil objective lens (Carl Zeiss), and a SOLA SE light engine (Lumencor). A SPOT Xplorer slow-can charge coupled device camera (1.4 Megapixels monochrome w/o IR; Diagnostic Instruments) fixed on the microscope was used to capture images. Up to ten images at different positions were acquired using Visiview software (Visitron systems GMbH), with exposures set to 40 ms (phase contrast, PhC) and 500 ms (eGFP and eCherry). Cells were automatically segmented on image sets using procedures described previously (Delavat et al., 2016), from which their fluorescence (eGFP or eCherry) was quantified. Subpopulations of tc cells were quantified using quantile-quantile-plotting as described previously (Reinhard and van der Meer, 2013). Fluorescent images for display were scaled to the same brightness in ImageJ (Schneider et al., 2012) as indicated, saved as 8-bit gray tiff-files and cropped to the display area in Adobe Photoshop (Adobe, 2020).

Statistical analysis

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Fluorescent reporter intensities were compared among biological triplicates. In case of mini-Tn5 insertions, this involved three clones with potentially different insertion sites, each measured individually. For mini-Tn7 inserted reporter constructs, we measured three biological replicates of a unique clone. Expression differences between mutants and a strain with the same genetic background but carrying the empty pME6032 plasmid were tested on triplicate means of individual median or 75th percentile values in a one-sided t-test (the hypothesis being that the mutant expression is higher than the control). Comparison of 75th percentiles rather than median or mean is justified when populations are extremely skewed, as we previously demonstrated (Reinhard and van der Meer, 2013). Coherent simultaneous data series were tested for significance of reporter expression or transfer frequency differences in ANOVA, followed by a post-hoc Tukey test. Quantile-quantile plots were produced in MatLab (v 2016a), violin -boxplots by using ggplot2 in R.

Mathematical model of ICEclc activation

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ICEclc activation was simulated as a series of stochastic events in different network configurations (as schematically depicted in Figure 6A, Supplementary file 4). TciR, BisR, BisDC and protein output levels were then simulated using the Gillespie algorithm (Gillespie, 1977; Gillespie, 1976), implemented in Julia using its DifferentialEquations.jl package (Rackauckas and Nie, 2017). 10,000 individual simulations (each simulation corresponding to a single ‘cell’) were conducted per network configuration during 100 time steps, during or after which the remaining protein levels were counted and summarized. The code for the mathematical implementation is provided in the Source code 1.

Data availability

All data generated or analysed during this study are included in the manuscript and supporting files. Source data files have been provided.

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Article and author information

Author details

  1. Nicolas Carraro

    Department of Fundamental Microbiology, University of Lausanne, Lausanne, Switzerland
    Contribution
    Conceptualization, Data curation, Formal analysis, Validation, Investigation, Methodology, Writing - original draft, Writing - review and editing
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0001-6364-547X

  2. Xavier Richard

    1. Department of Fundamental Microbiology, University of Lausanne, Lausanne, Switzerland
    2. Department of Mathematics, University of Fribourg, Fribourg, Switzerland
    Contribution
    Software, Validation, Visualization, Methodology, Writing - review and editing
    Competing interests
    No competing interests declared

  3. Sandra Sulser

    Department of Fundamental Microbiology, University of Lausanne, Lausanne, Switzerland
    Contribution
    Conceptualization, Investigation, Methodology, Writing - review and editing
    Competing interests
    No competing interests declared

  4. François Delavat

    1. Department of Fundamental Microbiology, University of Lausanne, Lausanne, Switzerland
    2. UMR CNRS 6286 UFIP, University of Nantes, Nantes, France
    Contribution
    Data curation, Investigation, Methodology, Writing - review and editing
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-5985-4583

  5. Christian Mazza

    Department of Mathematics, University of Fribourg, Fribourg, Switzerland
    Contribution
    Conceptualization, Software, Formal analysis, Supervision, Funding acquisition, Writing - review and editing
    Competing interests
    No competing interests declared

  6. Jan Roelof van der Meer

    Department of Fundamental Microbiology, University of Lausanne, Lausanne, Switzerland
    Contribution
    Conceptualization, Data curation, Formal analysis, Supervision, Funding acquisition, Validation, Investigation, Visualization, Methodology, Writing - original draft, Project administration, Writing - review and editing
    For correspondence
    JanRoelof.VanDerMeer@unil.ch
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-1485-3082

Funding

Swiss National Science Foundation (31003A_175638)

  • Jan Roelof van der Meer

SystemsX.ch (Interdisciplinary Grant)

  • Christian Mazza

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Acknowledgements

The authors thank Fabrice Merz and Noëmie Matthey for their help in technical parts of this study. We thank Aleksandar Vjestica, Roxane Moritz and Andrea Daveri for critical reading. The work was supported by Swiss National Science Foundation grant to JvdM 31003A_175638 and by a SystemsX.ch Interdisciplinary grant to CM and JvdM.

The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Version history

  1. Received: April 15, 2020
  2. Accepted: July 24, 2020
  3. Accepted Manuscript published: July 28, 2020 (version 1)
  4. Version of Record published: August 12, 2020 (version 2)

Copyright

© 2020, Carraro et al.

This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

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  1. Nicolas Carraro
  2. Xavier Richard
  3. Sandra Sulser
  4. François Delavat
  5. Christian Mazza
  6. Jan Roelof van der Meer
(2020)
An analog to digital converter controls bistable transfer competence development of a widespread bacterial integrative and conjugative element
eLife 9:e57915.
https://doi.org/10.7554/eLife.57915

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