Prophage regulation of Shewanella fidelis 3313 motility and biofilm formation with implications for gut colonization dynamics in Ciona robusta
- Department of Pediatrics, Morsani College of Medicine, University of South Florida, United States
- College of Marine Science, University of South Florida, United States
- Biomedical Sciences Program, University of South Florida, United States
- Department of Cell Biology, Microbiology, and Molecular Biology, University of South Florida, United States
- Stazione Zoologica Anton Dohrn, Italy
- BioTechnology Institute, University of Minnesota, United States
- Plant and Microbial Biology, University of Minnesota, United States
Figures
Figure 1
General prophage deletion scheme.
(a) Location of upstream, downstream, and flanking primers used in the deletion of SfPat, primer orientation shown with respect to the prophage. (b) Deletion of SfPat from S. fidelis 3313 identified after assembling Illumina (short-read) sequenced genomes and mapping onto the improved (short and long-read, PacBio, sequencing) WT genome. The figure illustrates SfPat deletion as revealed by subsequent Illumina sequencing. The solid gray areas on the SfPat genome indicate regions that share identity with the WT.
Figure 2 with 1 supplement
Effects of prophages on biofilm and swimming in S. fidelis 3313.
(a) Influence of prophages on in vitro biofilm formation over 24 hours quantified with crystal violet assay (n=3), (b) role of prophages in swimming quantified as the diameter of spread on soft agar after 24 hours (n=6), and (c) fold-change of pdeB (with Rho as internal control) from 24 hour biofilm (in vitro) (n=4) and 24 hour in vivo (n=4). *p-value<0.05, **p-value<0.01; ns = not significant.
Figure 2—figure supplement 1
qPCR showing relative fold change gene expression with Rho as an endogenous control.
(a) Cyclic-di-GMP regulators expression in WT and ΔSfPat in vitro after 24 hours of exposure (n=4), (b) Cyclic-di-GMP regulators expression in WT and ΔSfPat in vivo of Ciona MS4 after 24 hours of exposure (n=4). ns = not significant.
Figure 3 with 2 supplements
The influence of SfPat prophage on gut colonization in Ciona.
(a) Results of six biological replicates (n=6, each replicate being a pool of ten juvenile tunicates) of the experimental exposure of Ciona MS4 juveniles to either WT or ΔSfPat strains for 1 hour and 24 hours; retention quantification displayed as a Beeswarm plot of colony-forming units (CFUs). There is significant retention observed in WT after 24 hours. The MS4 juveniles reveal differential colonization of WT and ΔSfPat after 1 hour of exposure (b–e), where WT strain is stained with BacLight Red and ΔSfpat is stained with BacLight Green reveal (b) WT is seen localized in the lower esophagus to anterior stomach, while the ΔSfPat deletion strain localized to the hindgut, while (c) the WT is seen localized mostly as a fecal pellet in the center of the stomach, while ΔSfPat prefers to localize to the stomach wall. (d) The WT strain is retained in the pyloric cecum. (e) Summary schematic of asymmetric bilateral views of MS4 animals; top of image is anterior and stomach is posterior. The ventral side is the ‘En’ side, and the dorsal side is the opposite side. The findings can be summarized as such: WT is retained in E and S, in PC, and also in the HG, while the ΔSfPat is retained in the stomach folds, MG, and portions of the HG. Some overlap in signal is noted with yellow coloring. En = endostyle, E = esophagus, S = stomach, MG = mid gut, HG = hind gut, PC = pyloric cecum.
Figure 3—figure supplement 1
BacLight-stained WT localization in Ciona MS4 after 1-hour exposure.
WT stained with BacLight Red exposed to Ciona MS4 for 1 hour. (a) WT found in esophagus (E), stomach (S), and fecal pellet (FP). (b) WT also found to occupy the hind gut (HG). (c) WT is retained in the center of the stomach but not the stomach walls.
Figure 3—figure supplement 2
BacLight-stained ΔSfPat localization in Ciona MS4 after 1-hour exposure.
ΔSfPat localization in Ciona MS4 after 1-hour exposure. (a) Stained with BacLight Red, ΔSfPat is found adhered to the stomach (S) and mid gut (MG). (b) Stained with BacLight Green, ΔSfPat is found in the mid gut and hind gut (HG). (c) ΔSfPat is more localized in the stomach fold than the center of the stomach, with presence in the mid gut.
Figure 4
The influence of prophages on host gene expression.
(a) VCBP-C gene expression in MS4 juveniles after 1 hour of exposure to S. fidelis 3313 strains (n=4). (b) Survey of additional innate immune gene expression in MS4 juveniles after 24-hour exposure to WT or ΔSfPat mutant strains (n=3). Actin is the internal control. *p-value<0.05, **p-value<0.01, ns = not significant.
Figure 5 with 1 supplement
Lysogen gene expression in response to host immune effector binding.
Gene expression of SfPat structural protein P5, recA and lexA of WT strain grown as a 24-hour biofilm while exposed to 50 μg/ml VCBP-C. Rho is the internal control (n=4). *p-value<0.05, ns = not significant.
Figure 5—figure supplement 1
RefFinder identifying Rho as the stable endogenous control.
Rho is the most stable gene across strains when tested in vitro (n=3).
Author response image 1
WT S.
fidelis 3313 was exposed in vitro to 50 µg/ml VCBP-C in stationary cultures. Biofilms were observed for 24hrs. At 12 hrs, the presence of VCBP-C increased the amount of biofilms, whereas reduced biofilms were observed at 4 and 24hrs. Our findings (manuscript Fig 2a) reveal that SfPat contributes to biofilm formation, exposure to SfPat deletion mutants increases host VCBP-C expression (manuscript Fig. 4a), and VCBP-C binding to WT S. fidelis 3313 reduces the expression of SfPat P5 capsid protein (manuscript Fig. 5). These findings suggest that in vivo exposure/ colonization assays benefit from detailed time-course observations to be further explored in follow-up, future experiments.
Tables
Table 1
All S. fidelis 3313 strains are submitted under the BioProject PRJNA 90327 on NCBI, accession: SAMN31793880 ID:31793880.
| Organisms | Phenotype | NCBI RefSeq assembly |
|---|---|---|
| JG4066 | WT | GCF_033441085.1 |
| JG3862 | ΔSfPat | GCF_033441065.1 |
Table 2
Primer sequences on S. flidelis 3313 used for generating ΔSfPat deletion suicide vector and for deletion verification.
| Primer ID | Sequence (5’–3’) |
|---|---|
| EDK77 | AAATGGATCCCGATCAGCCTGCTAGTTTATT |
| EDK78 | ACGGAATAGGTTGAATGCGACTCAGGC |
| EDK79 | TCGCATTCAACCTATTCCGTCATGTTTAGCC |
| EDK80 | ACATGAGCTCGATGCAGATAAAGAGCCGTAAA |
| EDK81 | GTTTATTTTGTGGCAATCGCA |
| EDK82 | GGTAGCAGTGCTTAAACGAT |
Table 3
Plasmids and strains used in the study.
| Plasmids/ strains | Genotype | Source/reference |
|---|---|---|
| E. coli UQ950 | E. coli DH5αλ(pir) host for cloning; FΔ(argFac)169Φ80dlacZ58(ΔM15) glnV44(AS)rfbD1 gyrA96(NalR) recA1endA1spoT1 thi1 hsdR17 deoR Λ pir+ | Saltikov and Newman, 2003 |
| pSMV3−Δ SfPat | pSMV3 with 778 bp upstream and 779 bp downstream of flanking regions of SfPat | This study |
Table 4
Ciona genes targeted and the necessary reverse transcription-qPCR primers.
| Gene | Function | GenBank accession no. | Primer (5’–3’) | Reference |
|---|---|---|---|---|
| VCBP-C-Fwd | Secreted immune effector in the gut | HQ324151 | AGACCAACGCCAACACAGTA | Liberti et al., 2018 |
| VCBP-C-Rev | CCCCATACATTGCAGCATTTC | |||
| Actin–Fwd | Cytoskeletal actin | AJ297725 | CCCAAATCATGTTCGAAACC | Liberti et al., 2018 |
| Actin-Rev | Reference gene | ACACCATCACCACTGTCGAA | ||
| IL17-1-Fwd | Interleukin 17 | NM_001129875.1 | AGGTTAAGAATCCCTATGGTGC | Liberti et al., 2023 |
| IL17-1-Rev | Effector cytokine | CAAAGGCACAGACGCAAAGG | ||
| IL17-1R-Fwd | Interleukin 17 receptor | NM_001245045 | TGTTGGCATGAGTGTTCGGT | |
| IL17-1R-Rev | AGTTGGTTCTGCCCCAAAGT | |||
| NFκ-B-Fwd | Immune regulatory | NM_001078304 | TGTCGCTTGTCGTCATGGAA | Liberti et al., 2023 |
| NFκ-B-Rev | Transcription factor | AACACCCAAGACCGTCGAAA | ||
| TNFα-Fwd | Tumor necrosis factor | NM_001128107 | TTCAGAAAGATTGGACGACGA | Liberti et al., 2023 |
| TNFα-Rev | Inflammatory effector | TCGTTTAGAAATGCTGCTGTGG | ||
| C3A-R-Fwd | Complement C3 | NM_001078552 | TTGTAAGCTGGCACAAGGTGT | This study |
| C3A-R-Rev | Inflammatory mediator | GACCGTAGTCTGGTAGAGGTC | ||
| MBL-Fwd | Mannose binding lectin | NM_001167707.2 | TTATTGATGGGAAAGTTTGGT | This study |
| MBL-Rev | TAACATCTCTGTTCTTGGGTC |
Table 5
S. fidelis 3313 genes targeted and the necessary reverse transcription-qPCR primers.
| Gene | Function | Genbank accession no. | Primer (5’–3’) | Reference |
|---|---|---|---|---|
| pleD-Fwd | Regulates production of cyclic di-GMP | NZ_KI912459.1 | CTCTTCACCGCCACTTCTT | This study |
| pleD-Rev | GGTGTGGTCTCTTATGCCTATC | |||
| Chitinase-Fwd | Chitin utilization gene | NF027718.3 | CAGTGTAGCTAAGTCGTCATC | This study |
| Chitinase-Rev | CGCCAACCAGTGCTTTATTG | |||
| pilZ-Fwd | Type IV Pilus control protein | NZ_JADX01000014.1 | TGGCAAGGTCGTTTGGATTA | This study |
| pilZ-Rev | AGGCAAGCTCACTGGAAAG | |||
| pdeB-Fwd | Phosphodiesterase | NF012772.3 | GCATCAGGGCTCTTACCAATAG | This study |
| pdeB-Rev | GAGGCGGTGATCCTTACAGATA | |||
| RecA-Fwd | Bacterial recombinase/bacterial reference gene | NZ_KI912459.1 | CGTAGTGGTGCGGTAGATGT | This study |
| RecA-Rev | CGCATTGCTTGGCTCATCAT | |||
| LexA-fwd | Regulator of recombinase | NZ_JADX01000011.1 | TGACCCAGCTATGTTCCGCC | This study |
| LexA-Rev | GCTCAACCTTGTGTACGGCG | |||
| Rho-Fwd | Bacterial reference gene | NZ_JADX01000026.1 | CACGTACAAGTTGCCGAAATG | This study |
| Rho-Rev | CAAGACGGGTGATAGAGTCAAG | |||
| gyrB-Fwd | Bacterial reference gene | AM229309.2 | TCACGAGCATCATCACCCGT | This study |
| gyrB-Rev | GGCTTCCGTGGTGCGTTAAC |
Additional files
-
Supplementary file 1
RAST annotations of the prophage SfPat.
- https://cdn.elifesciences.org/articles/103107/elife-103107-supp1-v1.xlsx
-
MDAR checklist
- https://cdn.elifesciences.org/articles/103107/elife-103107-mdarchecklist1-v1.docx
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Prophage regulation of Shewanella fidelis 3313 motility and biofilm formation with implications for gut colonization dynamics in Ciona robusta
eLife 14:RP103107.
https://doi.org/10.7554/eLife.103107.3
