Dopamine drives Drosophila sechellia adaptation to its toxic host

  1. Sofía Lavista-Llanos  Is a corresponding author
  2. Aleš Svatoš
  3. Marco Kai
  4. Thomas Riemensperger
  5. Serge Birman
  6. Marcus C Stensmyr
  7. Bill S Hansson
  1. Max Planck Institute for Chemical Ecology, Germany
  2. Neurobiology Unit, CNRS, ESPCI ParisTech, France

Abstract

Many insect species are host-obligate specialists. The evolutionary mechanism driving the adaptation of a species to a toxic host is, however, intriguing. We analyzed the tight association of Drosophila sechellia to its sole host, the fruit of Morinda citrifolia, which is toxic to other members of the melanogaster species group. Molecular polymorphisms in the dopamine regulatory protein Catsup cause infertility in D. sechellia due to maternal arrest of oogenesis. In its natural host, the fruit compensates for the impaired maternal dopamine metabolism with the precursor l-DOPA, resuming oogenesis and stimulating egg production. l-DOPA present in morinda additionally increases the size of D. sechellia eggs, what in turn enhances early fitness. We argue that the need of l-DOPA for successful reproduction has driven D. sechellia to become an M. citrifolia obligate specialist. This study illustrates how an insect's dopaminergic system can sustain ecological adaptations by modulating ontogenesis and development.

https://doi.org/10.7554/eLife.03785.001

eLife digest

Many insect species rely on another animal or plant species for their own reproduction. For example, a fruit fly called Drosophila sechellia—which is found in the Seychelles—will only feed and lay its eggs on the fruit of a species of tree called Morinda citrifolia. This pairing is particularly unusual because these fruits, commonly called morinda, are toxic to all other Drosophila species.

Female Drosophila sechellia flies produce fewer eggs than other Drosophila species, which makes it difficult to raise this species in the laboratory. However providing these flies with morinda fruit, or chemicals from this fruit, was known to increase the expression of many genes involved in egg production and stimulate the flies to lay more eggs. Nevertheless, the reasons why this species of fruit fly depends on the toxic morinda fruit were unclear.

Now Lavista-Llanos et al. have confirmed that feeding Drosophila sechellia flies a diet of morinda fruit—instead of a typical laboratory diet—causes these flies to produce six-times as many eggs. Furthermore, this morinda diet had effects that went beyond the previously reported stimulatory effects of acidic chemicals in the fruits triggering the flies to lay more eggs.

Egg production in flies is controlled by dopamine, and a lack of this hormone is known to reduce the size of other fruit flies' ovaries and the number of eggs that they produce. Lavista-Llanos et al. went on to feed female Drosophila sechellia flies the chemical building blocks that make up the dopamine hormone, and one such chemical (called l-DOPA) caused the flies to produce more eggs. This did not occur when the flies were fed dopamine itself.

Lavista-Llanos et al. discovered that Drosophila sechellia flies have very high levels of dopamine but much lower levels of l-DOPA than other Drosophila fly species; and revealed that this was because a gene called Catsup is mutated in Drosophila sechellia. When Lavista-Llanos et al. mutated the same gene in another Drosophila species, the mutant flies produced fewer eggs and abnormally accumulated an enzyme (which makes l-DOPA) inside their developing eggs—just like Drosophila sechellia.

The presence of l-DOPA in morinda fruit partly compensates for the reduced fertility of Drosophila sechellia and the other flies with mutations in the Catsup gene. Lavista-Llanos et al. discovered that removing or replacing l-DOPA in the morinda fruit caused the flies to produce fewer eggs. Furthermore, the l-DOPA present in morinda increases the size of Drosophila sechellia eggs, which in turn helps them to survive their toxic environment.

Lavista-Llanos et al. also discovered that feeding dopamine to vulnerable Drosophila species helps them to cope with the toxic effects of a morinda diet. One of the next challenges will be to uncover how chemicals from the morinda fruit affect the dopamine system of the flies. It is also unknown if the dopamine hormone also influences the strong attraction that Drosophila sechellia feels towards its only host, the morinda fruit.

https://doi.org/10.7554/eLife.03785.002

Introduction

Morinda citrifolia fruit (morinda) is the sole host of Drosophila sechellia (Tsacas and Baechli, 1981), a close relative of Drosophila melanogaster and endemic to the Seychelles archipelago (Louis and David, 1986). A peculiar aspect of the specialization is that morinda fruits are toxic to all other drosophilids (Legal et al., 1992). The toxicity stems from a high content of carboxylic acids (primarily octanoic and hexanoic acid) (Legal et al., 1994), to which D. sechellia appears to be resistant (Farine et al., 1996). The chemosensory system of D. sechellia is specialized in detecting and coding key volatiles produced by morinda (Dekker et al., 2006) while devoid of the repellence towards the acids (Matsuo et al., 2007). On the other hand, D. sechellia females exhibit a low reproductive potential, partly because of a low ovariole number and partly because of fairly low egg production (R'Kha et al., 1991; R'kha et al., 1997), making it difficult to raise D. sechellia under laboratory conditions. In turn, morinda stimulates egg production (R'kha et al., 1997), and D. sechellia clearly prefers to oviposit in medium containing morinda carboxylic acids (Amlou et al., 1998). On its host, D. sechellia increases expression of genes involved with oogenesis and fatty acid metabolism (Dworkin and Jones, 2009). Thus, we here examined the dependence of Drosophila sechellia on morinda, for optimal reproduction.

All animal embryos rely on maternally provided gene products for their initial development prior to zygotic genetic synthesis. Maternal effects can thus act as a form of cross-generational phenotypic plasticity, playing a role in an animal's adaptation to toxic environments. Embryonic survival in morinda is a maternally inherited trait and does not depend on the genotype of the embryo (R'Kha et al., 1991). We therefore considered if maternal effects sustained the evolutionary process that has driven the specialization of D. sechellia. Results enhance our understanding of the reproductive behaviour of Drosophila and suggest an ontogenetic mechanism of insect adaptation to a toxic host.

Results and discussion

We first examined the influence of chemicals found in morinda on the reproductive system of D. sechellia by testing the effect of diet on egg production. We raised two geographically different populations of D. sechellia on standard Drosophila cornmeal medium (standard diet), on morinda fruit (morinda diet), or on a non-host fruit (banana diet). For comparison, we also raised two strains of D. melanogaster (wild-type Berlin and Canton-S) on the same media (see ‘Materials and methods’). To score the rate of egg production, we transferred the flies to oviposition cages containing agar plates devoid of oviposition stimuli (i.e., yeast or morinda carboxylic acids). In agreement with previous reports, D. sechellia raised on standard diet produced few eggs compared to D. melanogaster wild-type Berlin and D. melanogaster Canton-S (Figure 1A and Figure 1—figure supplement 1), raised on the same media. The addition of morinda carboxylic acids to the standard diet did not increase egg production in D. sechellia (Figure 1B). D. sechellia raised on a non-host fruit (banana diet) showed a slight increase in the number of eggs laid (Figure 1B), but this number did not increase further with the addition of morinda carboxylic acids (Figure 1B). D. sechellia raised on morinda diet, however, showed a sixfold increase in egg production (Figure 1B and Figure 1—figure supplement 1). Morinda diet did not affect the number of eggs produced by D. melanogaster wild-type Berlin and slightly reduced those of D. melanogaster Canton-S (Figure 1C and Figure 1—figure supplement 1), as did the addition of morinda carboxylic acids to the standard diet (Figure 1C). Banana, however, tripled egg production in D. melanogaster wild-type Berlin (Figure 1C). This increase could be inhibited by the addition of morinda carboxylic acids to the banana (Figure 1C). These results demonstrate that the presence of a natural host modulates the reproductive capacity of Drosophila. In particular, morinda has a strong effect on D. sechellia egg production that goes beyond the reported stimulatory effect of the carboxylic acids on oviposition (Amlou et al., 1998).

Figure 1 with 3 supplements see all
Morinda increases egg production in D. sechellia.

(AC) Egg production (egg/female/day) (N > 20) (A) and its relative change (N > 5) (B and C) in D. sechellia (14021–0248.25, sec) and D. melanogaster wild-type Berlin (wtB) fed a standard diet (sd), or morinda diet (md), or banana diet (bd), or diets supplemented with morinda carboxylic acids (+OA:HA). (D) Confocal images showing the surface (top) or the interior (middle) of ovarioles stained with nucleic acid specific dyes (sytox orange (SO) and TOTO) of D. sechellia (14021–0248.25) fed a standard diet (sec-sd) or a morinda diet (sec-md). The follicle cells (f) surrounding the oocyte (o) or stretched over the nurse cells (n) (arrow) are indicated for early (<S8) or vitellogenic cysts (>S8). Scale bar 100 μm. (E) Rate of vitellogenesis (>S8/<S8, top graph) and number of cysts (total cysts, lower graph) (N > 8) in D. sechellia (14021–0248.25, sec) and D. melanogaster wild-type Berlin (wtB) fed a standard diet (sd), or a morinda diet (md), or a diet supplemented with morinda carboxylic acids (+OA:HA). Different letters denote significant differences (p < 0.01) using ANOVA followed by Tukey's test (BE); ****p < 0.00001 using Student's t test to compare species (A). Error bars represent s.e.m.

https://doi.org/10.7554/eLife.03785.003

To study the mechanism behind the dietary modulation of egg production, we next examined oocyte development. The germarium in each ovariole continuously produces oocyte-cysts, each composed of 15 nurse cells and one oocyte, surrounded by a layer of follicular cells (Figure 1D). Each oocyte-cyst follows 14 stereotypical consecutive stages of pre-vitellogenic (S1–S7) and vitellogenic (S8–S14) growth, each easily distinguishable by morphological criteria (Spradling et al., 1997). Mated D. melanogaster females typically exhibit multiple ovarioles carrying vitellogenic cysts (Spradling et al., 1997). Females of D. sechellia had cysts normally composed of 15 nurse cells and one oocyte, surrounded by follicular cells (Figure 1D). Kept on standard diet, mated D. sechellia held oocytes in early developmental stages (<S8) (Figure 1D) with few ovarioles, if any, carrying vitellogenic cyst (>S8), what resulted in a significantly lowered rate of vitellogenesis (calculated as >S8/<S8) in D. sechellia compared to D. melanogaster wild-type Berlin (Figure 1E). The low number of ovarioles in D. sechellia (R'kha et al., 1997) was reflected in the low number of total cysts compared to in D. melanogaster wild-type Berlin (Figure 1E). The halt in oocyte development explains the low production of eggs in D. sechellia raised on standard diet. D. sechellia fed on morinda diet showed a significantly increased vitellogenesis rate (Figure 1D,E). Adding the morinda carboxylic acids, however, had no effect on vitellogenesis in D. sechellia (Figure 1E). We thus conclude that D. sechellia requires components of the morinda fruit other than just the carboxylic acids to induce vitellogenesis and increase egg production.

Environmental and physiological stressors can cause egg chambers in the ovaries of Drosophila to be eliminated by apoptosis at oogenesis checkpoints in region-2/3 of the germarium or cyst stage S7/S8 (the mid-oogenesis checkpoint) (Drummond-Barbosa and Spradling, 2001; McCall, 2004). To analyze if apoptosis occurs in D. sechellia, we stained live ovaries with the vital dye acridine orange (Arama and Steller, 2006). Flies fed a standard diet showed massive apoptosis occurring at S7/S8 cysts, and to a lesser extent in region-2/3 of the germarium (Figure 1—figure supplement 2); suggesting that apoptosis could be the reason for the depressed oviposition on standard media. On the other hand, D. sechellia flies fed a morinda diet showed strikingly few apoptotic cysts (Figure 1—figure supplement 2), in line with the stimulatory effect of morinda in egg-production. Low food availability can trigger the mid-oogenesis checkpoint (Terashima and Bownes, 2004). Thus, we asked if the observed apoptosis in D. sechellia raised on standard diet was a consequence of starvation or aberrant feeding behaviour. In fact, D. sechellia adults raised on the standard diet showed slightly higher weights (Figure 1—figure supplement 3), and also consumed more food than did flies raised on morinda diet (Figure 1—figure supplement 3). Hence, we conclude that the halt in oogenesis observed in D. sechellia is not a consequence of starvation or aberrant feeding behaviour.

Oocyte-cyst progression is under tight maternal hormonal regulation: juvenile- and steroid hormones are mutually controlled by the biogenic amine dopamine (DA), ensuring normal oogenesis (Gruntenko and Rauschenbach, 2008). Interruption of DA during development in D. melanogaster results in small ovaries and poor egg production (Neckameyer, 1996), both of which are features that characterise adult D. sechellia (R'kha et al., 1997). Moreover, genes involved in DA differentiation were shown differentially expressed in D. sechellia compared to the generalists species D. melanogaster and the sister Drosophila simulans (Dworkin and Jones, 2009; Wurmser et al., 2011). Accordingly, we wondered if D. sechellia suffers from a DA deficiency. Therefore, we first tested if the addition of monoamines was sufficient to rescue egg production by feeding D. sechellia standard diet supplemented with amines and amine precursors. Indeed, supplementing the standard diet with the DA precursor 3,4-dihydroxyphenylalanine (l-DOPA) significantly increased the number of eggs produced by D. sechellia (Figure 2A), whereas the addition of DA itself had no effect (Figure 2A). Likewise, adding the monoamine octopamine (OA), or its precursor tyramine (TA), did not affect egg production (Figure 2A). l-DOPA supplementation did not change the total number of D. sechellia oocyte-cysts (p = 0.28103, one-way ANOVA). Instead, it drastically reduced apoptosis in the ovary (Figure 2B) increasing vitellogenesis significantly (Figure 2C), whereas DA, TA and OA had no such effect. These results show that the administration of the DA precursor l-DOPA is sufficient to stimulate oocyte progression and egg production in D. sechellia.

Figure 2 with 1 supplement see all
Morinda l-DOPA is required to stimulate egg production.

(A) Egg production (egg/female/day) (N > 6) (B) quantification of apoptosis (apoptotic cysts/ovary) (N > 6) and (C) rate of vitellogenesis (>S8/<S8) (N > 12) in D. sechellia (14021–0248.25) flies fed a non-supplemented (−) standard diet (sd) or a standard diet supplemented with L-3,4-dihydroxyphenylalanine (1 mg/ml, l-DOPA); dopamine (1 mg/ml, DA); tyramine (2 mg/ml, TA) or octopamine (2 mg/ml, OA); or a non- pretreated morinda diet (md) or a morinda diet pre-treated with catechol-O-methyltransferase (2.5 U per gram of fruit, md + COMT). Different letters denote significant differences (p < 0.01) using ANOVA followed by Tukey's test. Error bars represent s.e.m. (D) The total ion chromatogram (top trace) shows all compounds present in morinda extract, and the extracted ion chromatogram (lower trace) corresponds to the exact mass of sum formula of L-3,4-dihydroxyphenylalanine (l-DOPA) present in the fruit; as analysed by UHPLC-MS. (E) Egg production (eggs/female/day) (N > 3) in D. sechellia (14021–0248.25) flies fed a morinda diet (md) non-pre-treated (−), pre-treated with catechol-O-methyltransferase (2.5 U per gram of fruit, COMT) or α-methyl-DOPA (0.4 mM, mDp). Different letters denote significant differences (p < 0.01) using ANOVA followed by Tukey's test. Error bars represent s.e.m.

https://doi.org/10.7554/eLife.03785.007

The findings so far thus led us to speculate that morinda contains monoamines, which stimulate oogenesis in D. sechellia. Indeed, we detected 180.4 ± 3.5 ng l-DOPA (mean ± s.e.m; N = 3) per gram of fruit pulp (Figure 2D) in morinda extracts analysed by ultra-high-performance liquid chromatography coupled to mass spectrometry (UHPLC-MS). Notably, we did not detect DA, OA or TA in morinda. Unripe (150.99 ± 8 ng l-DOPA [mean ± s.e.m; N = 3] per gram of fruit) and overripe (147.47 ± 8 ng l-DOPA [mean ± s.e.m; N = 3] per gram of fruit) morinda fruits contained l-DOPA in equal amounts, what suggests that oxidisation, known to occur commonly in monoamines through atmospherical exposure, is prevented in morinda. The preservation of l-DOPA is likely due to the high carboxylic acid content—octanoic and hexanoic acids have been shown to inhibit diphenol oxidase activity (Guo et al., 2010)—and the ensuing low pH of the fruit (4.1 ± 0.1 [N = 7] and 3.6 ± 0.1 [N = 5] [mean ± s.e.m.], ripe and overripe morinda, respectively; for comparison, 5.7 ± 0.2 [mean ± s.e.m.], [N = 4], ripe banana; p = 0.0001; one-way ANOVA), known for its antioxidant properties. Banana is reported to contain up to 1 mg DA per gram of fresh weight (Kanazawa and Sakakibara, 2000). Notably, DA in banana is synthesized directly from TA (Deacon and Marsh, 1971) and not via synthesis of l-DOPA. Presumably, the absence of l-DOPA in banana renders this non-host fruit unable to stimulate egg production in D. sechellia (see Figure 1B).

Is the presence of l-DOPA in morinda then necessary for the stimulatory effect on egg production? To address this question, we depleted levels of l-DOPA in morinda by pre-incubating fruit pulp with catechol-O-methyltransferase (COMT, 2.5 U/g morinda), an enzyme that catabolises l-DOPA into an unusable product (Gordonsmith et al., 1982). Treatment with COMT suppressed the anti-apoptotic effects of morinda (Figure 2B) and hindered the fruit from stimulating vitellogenesis (Figure 2—figure supplement 1) and egg production in D. sechellia (Figure 2E), reducing the number of eggs to levels in a standard diet (compare Figure 2A and Figure 2E). Additionally, we added α-methyl-DOPA (mDp, 0.4 mM), a non-hydrolysable l-DOPA analogue and a competitive inhibitor of the enzyme dopa decarboxylase that converts l-DOPA into DA, separately to the fruit. The presence of mDp in morinda strongly reduced egg production (Figure 2E); feeding a corresponding mDp-supplemented diet to D. melanogaster wild-type Berlin did not have such an effect (not shown). Notably, mDp in the fruit did not hinder oogenesis; instead, eggs were retained in the ovaries (Figure 2—figure supplement 1). This halt in ovulation was completely reversed one day after flies were moved to fresh medium (Figure 2—figure supplement 1), and, remarkably, oviposition was significantly enhanced when morinda was offered as an oviposition substrate (Figure 2—figure supplement 1). We conclude that morinda contains l-DOPA and that its presence in the fruit pulp is both sufficient and necessary to stimulate egg production in D. sechellia.

Morinda, accordingly, provides D. sechellia with the DA precursor necessary for the progression of oogenesis. Although providing a critical chemical, the acidity of the fruit, which helps preserve l-DOPA by preventing oxidisation, creates a hostile environment for the eggs to develop in. How do flies ensure that the eggs survive in this toxic environment? An interesting observation provides one clue. Eggs of D. sechellia are characteristically large compared to those of sibling species D. melanogaster, D. simulans, Drosophila ananassae, Drosophila erecta, Drosophila mojavensis, Drosophila persimilis, Drosophila pseudoobscura, Drosophila virilis, Drosophila willistoni and Drosophila yakuba (Markow et al., 2009). In accordance, we observed D. sechellia eggs to be 45% larger in size compared to eggs of D. melanogaster wild-type Berlin (Figure 3A), in a standard diet condition. Upon being fed a morinda diet, eggs of D. sechellia increased in volume twofold compared to eggs of conspecifics fed standard medium (Figure 3A and Figure 3—figure supplement 1); the resulting eggs had an almost threefold larger volume than did D. melanogaster wild-type Berlin eggs in standard conditions (Figure 3A). This effect could be replicated by supplementing standard diet with l-DOPA or, notably, DA (Figure 3B). On the other hand, adding COMT or mDp to a morinda diet prevented the fruit from having any effect on the volume of eggs (Figure 3C). These results indicate that egg size is also under a dopaminergic control regime during egg development. The increased size may provide buffering capacity to the eggs, helping them to cope with the toxic environment of the host. Indeed, the hatching rate of eggs transferred onto a morinda-containing medium was significantly higher in the enlarged eggs of flies fed morinda than in the smaller eggs of individuals fed only standard medium (Figure 3D). The low number of ovarioles of D. sechellia (R'kha et al., 1997) thus seems to be a result of a trade-off between number and size (Figure 3—figure supplement 2), favouring the enlarged eggs of females fed morinda.

Figure 3 with 2 supplements see all
Morinda enhances early fitness.

(AC) Volume (mm3(10−3)) of D. melanogaster wild-type Berlin (wtB) and D. sechellia (14021–0248.25, sec) eggs produced by flies fed a standard diet (sd) or morinda diet (md) (N > 15) (A); D. sechellia (14021–0248.25) flies fed a non-supplemented (−) standard diet (sd), or supplemented with L-3,4-dihydroxyphenylalanine (1 mg/ml, l-DOPA) or dopamine (1 mg/ml, DA) (N > 23) (B); D. sechellia (14021–0248.25) flies fed a non-pre-treated (−) morinda diet (md), or pre-treated with catechol-O-methyltransferase (2.5 U per gram of fruit, COMT) or α-methyl-DOPA (0.4 mM, mDp) (N > 10) (C). (D) Egg hatching rate (N > 5) in D. sechellia (14021–0248.25) fed (feed) a standard diet (sd) or morinda diet (md), ovipositing (ovip.) in either media. Different letters denote significant differences (p < 0.01) using ANOVA followed by Tukey's test. Error bars represent s.e.m.

https://doi.org/10.7554/eLife.03785.009

Genetic changes in a single gene of the steroid hormone biosynthetic pathway made Drosophila pachea dependent on the uncommon sterols of its host plant, the toxic senita cactus (Lang et al., 2012). Likewise, the requirement of dietary l-DOPA suggests that its metabolism is impaired in D. sechellia. We next quantified l-DOPA in fly-tissue extracts by UHPLC-MS. D. sechellia—kept on standard diet—showed significantly lower levels of l-DOPA in whole flies, bodies and ovaries than did D. melanogaster wild-type Berlin (Figure 4A). However, in D. sechellia fed a morinda diet, l-DOPA levels were significantly increased compared to levels in conspecifics fed a standard diet, and surpassing those of D. melanogaster wild-type Berlin in standard diet (Figure 4B). In short, these results demonstrate that under laboratory conditions, l-DOPA is greatly reduced in D. sechellia, and that this l-DOPA deficiency can be remedied by a diet supplemented with morinda fruit.

Figure 4 with 5 supplements see all
Dopamine metabolism is impaired in D. sechellia.

(A) L-3,4-dihydroxyphenylalanine quantification (l-DOPA pg/fly) (N = 3) in whole fly, bodies and ovaries of female D. melanogaster wild-type Berlin (wtB) and D. sechellia (14021–0248.25, sec) fed a standard diet (sd). *p < 0.05 and **p < 0.002 using Student's t test. (B) Relative L-3,4-dihydroxyphenylalanine (% pg l-DOPA per mg body, % l-DOPA) (N = 3) in female D. melanogaster wild-type Berlin (wtB) and D. sechellia (14021–0248.25, sec) fed a standard diet (sd) or morinda diet (md). p = 0.0062 and p = 0.018 using Student's t test D. melanogaster vs D. sechellia fed, respectively, a standard diet or morinda diet. (C) Western blots of total protein whole-fly extracts for TH-PLE, CATSUP, and α-TUBULIN as a loading control, in D. melanogaster wild-type Berlin (wtB) and D. sechellia (14021–0248.25, sec) fed a standard diet (sd) or morinda diet (md). The numbers under TH-PLE and CATSUP protein lanes indicate the relative protein levels (normalised to α-TUBULIN). (D) Ratios of L-3,4-dihydroxyphenylalanine (l-DOPA/tyr) (N = 3) and dopamine (DA/tyr) (N = 3) to tyrosine substrate in female D. melanogaster wild-type Berlin (wtB) and D. sechellia (14021–0248.25, sec) fed a standard diet (sd). **p < 0.007 and ***p < 0.000007 using Student's t test. (E) Drosophila CATSUP protein structure scheme showing a signal peptide (grey box) and six trans-membrane domains (black boxes). Deletions (dash) and exchanges (grey or white) of amino acids in D. sechellia (14021–0248.25, sec) compared to in D. melanogaster wild-type Berlin (wtB) and in D. melanogaster DGRP-357 (DGRP-357) CATSUP are indicated. (FH) Dopamine (DA ng/fly) (N = 3) (F), relative rate of vitellogenesis (% >S8/<S8) (N > 10) (G), and egg-volume (% mm3(10−3)) (n > 10) (H) in D. sechellia (14021–0248.25, sec), D. melanogaster wild-type Berlin (wtB) and D. melanogaster DGRP-357 (DGRP-357) fed a standard diet (sd). (I) Egg production (egg/female/day) (N > 3) in D. melanogaster wild-type Berlin (wtB), heterozygote flies (Catsup1/CyO), D. melanogaster DGRP-357 (CatsupIn270Del/CatsupIn270Del), trans heterozygote flies (CatsupIn270Del/Catsup1) and D. sechellia (14021–0248.25, sec), fed a standard diet (sd). Different letters denote significant differences (p < 0.05) using ANOVA followed by Tukey's test (FI). Error bars represent s.e.m.

https://doi.org/10.7554/eLife.03785.012

The oxidation of the precursor amino acid tyrosine into l-DOPA is the first and rate-limiting step in the DA biosynthetic pathway (Levitt et al., 1965). This oxidation is catalysed by the enzyme tyrosine hydroxylase (TH), which is encoded by the pale (ple) locus in Drosophila (Neckameyer and White, 1993). The whole-fly expression of TH-PLE was increased in D. sechellia relative to in D. melanogaster wild-type Berlin (Figure 4C) and Canton-S (Figure 4—figure supplement 1), as revealed by Western blots. Thus, l-DOPA impairment in D. sechellia seems not to result from a low expression of its synthesizing enzyme. To assess if the activity of TH-PLE was altered in D. sechellia, we compared the ratios of product (l-DOPA and DA) to substrate (tyrosine) in whole-fly extracts. D. sechellia showed a 3.3-fold decrease in the l-DOPA/tyrosine ratio as compared to in D. melanogaster wild-type Berlin (Figure 4D) with a 1.4-fold increase in tyrosine content (Figure 4—figure supplement 2). However, in D. sechellia the DA/tyrosine ratio was increased 2.4 times with respect to in D. melanogaster wild-type Berlin (Figure 4D). DA itself was increased 4.8 times in D. sechellia (Figure 4F). In sum, we conclude that TH-PLE is active; in fact, DA levels are drastically enhanced in D. sechellia.

TH-PLE activity is negatively regulated via direct physical interactions with the protein Catecholamines up (Catsup) (Stathakis et al., 1999). Interestingly, Catsup loss-of-function mutations cause hyperactivation of TH-PLE and abnormally high levels of catecholamines (Stathakis et al., 1999), as well as infertility due to maternal arrest of oogenesis (Schupbach and Wieschaus, 1991; Stathakis et al., 1999). These phenotypes prompted us to investigate whether Catsup is impaired in D. sechellia. We cloned the ortholog of Catsup from D. sechellia, which revealed a 45 bp in-frame deletion of 15 amino acids in a predicted zinc-binding region of the protein (O'Donnell et al., 2002) and seven single amino acid exchanges (Figure 4E). Additionally, Western blots of whole-fly extracts revealed 2- to 3.7-fold decrease in CATSUP expression in D. sechellia compared to CATSUP expression in D. melanogaster wild-type Berlin (Figure 4C) and Canton-S (Figure 4—figure supplement 1). The reduced expression of D. sechellia CATSUP would explain the high DA levels in D. sechellia (see Figure 4F).

Is Catsup then responsible for the reproductive phenotypes in D. sechellia? An allele (In270Del) similar to D. sechellia Catsup has been described for a natural D. melanogaster population (DGRP-357) (Carbone et al., 2006) (Figure 4E). CatsupIn270Del has been associated with polymorphisms in the number of sensory bristles, starvation resistance and locomotor behavior (Carbone et al., 2006). As for D. sechellia, we found increased DA levels in adult D. melanogaster DGRP-357 compared to in D. melanogaster wild-type Berlin (Figure 4F). Reciprocally, D. sechellia showed an increased number of sensory bristles that were present in flies of three geographically different populations (Figure 4—figure supplement 3). To test if CatsupIn270Del was sufficient to generate egg phenotypes on par with those of D. sechellia, we next examined egg growth in D. melanogaster DGRP-357 females. Both D. sechellia traits—low levels of vitellogenesis (Figure 4G) and enlarged eggs (Figure 4H)—were present in D. melanogaster DGRP-357. Furthermore, D. melanogaster DGRP-357 produced fewer eggs than did D. melanogaster wild-type Berlin (Figure 4I), and the ovariole rate of egg production in D. melanogaster DGRP-357 females did not differ significantly from that of D. sechellia (p = 0.2104; Student's t test). To control for non-identified gene mutations present in D. melanogaster DGRP-357 that could contribute to lowering egg production, we generated heteroallelic flies carrying CatsupIn270Del in trans-heterozygosis with the null Catsup1 allele (Stathakis et al., 1999). CatsupIn270Del/Catsup1 females displayed significantly decreased egg production, below that of D. melanogaster wild-type Berlin and parental lines (Figure 4I), that could be rescued by feeding the flies a standard diet supplemented with l-DOPA (Figure 4—figure supplement 4). In sum, these results show that D. melanogaster flies carrying a D. sechellia Catsup-like allele mirror D. sechellia's low production of eggs.

The formation of TH-PLE functional protein begins during the maternal phase of egg development (Pendleton et al., 2007). Pharmacologically inhibiting TH-PLE arrests oocytes at S8 stage of development, which is prevented by the co-administration of l-DOPA (Pendleton et al., 1996). We thus asked if the diet requirement of morinda for D. sechellia oocyte progression results from a maternal impairment of the enzyme synthesizing l-DOPA. Ple mRNA has been shown expressed by in situ hybridization in nurse- and follicle cells (Neckameyer, 1996). We detected TH-PLE in the ooplasm of D. melanogaster wild-type Berlin developing oocytes (Figure 5A). Remarkably, D. sechellia oocytes showed big masses of TH-PLE abnormally accumulated in their ooplasm (Figure 5B), suggesting that the nurse-to-oocyte traffic of maternal Ple is hindered in this fly.

Figure 5 with 1 supplement see all
Expression of TH-PLE and CATSUP in Drosophila female reproductive system.

(AC) Confocal images showing striking accumulation (arrowhead) of TH-PLE (green, anti-TH) in D. sechellia (14021–0248.25) (B) and D. melanogaster DGRP-357 (C), compared to in D. melanogaster wild-type Berlin (wtB) (A) oocytes. (DF) Confocal images showing CATSUP (magenta, anti-SLC39A7) expressed in the nurse cells (arrow) of D. melanogaster wild-type Berlin (wtB) oocytes (D) and absent in the nurse cells of D. sechellia (14021–0248.25, sec) (E) and D. melanogaster DGRP-357 (DGRP-357) (F) oocytes. (GI) Confocal image showing CATSUP expressed in the nuclei (arrow) and the membrane (arrowhead) of D. melanogaster wild-type Berlin (wtB) spermatheca secretory cells (G), and absent from D. sechellia (14021–0248.25) (H) and D. melanogaster DGRP-357 (DGRP-357) (I). Scale bar 20 μm.

https://doi.org/10.7554/eLife.03785.018

Catsup encodes the Drosophila ortholog of the mammalian ZIP7/SLC39A7 zinc transporter and has recently been associated with trafficking of proteins during development (Groth et al., 2013). Flies carrying the I288T amino acid exchange shared in D. sechellia CATSUP and D. melanogaster DGRP-357 CATSUP (see Figure 4E) accumulate abnormal amounts of proteins in developing tissue (Groth et al., 2013). Notably, as for D. sechellia, we found big masses of TH-PLE abnormally accumulated in the ooplasm of D. melanogaster DGRP-357 oocytes (Figure 5C) strongly suggesting that CATSUP could regulate the nurse-to-oocyte traffic of maternal Ple in Drosophila. CATSUP was expressed in the perinuclear endoplasmic reticulum- and golgi-like cisternae of the nurse cells of S8 oocyte cysts (Figure 5D), what results a suitable intracellular distribution for a protein with traffic nurse-to-oocyte function. We found, additionally, CATSUP expressed in the spermathecal secretory cells (SSC) of the female reproductive tract (Figure 5G). As for whole flies extracts, D. sechellia and DGRP-357 showed diminished expression of CATSUP in the nurse cells (Figure 4E,F) and SSC (Figure 4H,I). A recent study showed that the SSC require a not-yet identified secretory pathway to control the ovulation and downstream movement of the eggs (Sun and Spradling, 2013). The ablation of the SSC causes ovoviviparity in D. melanogaster (Schnakenberg et al., 2011), a condition naturally occurring in D. sechellia (Markow et al., 2009). Remarkably, 81.8% of D. melanogaster DGRP-357 mated females had an egg in their uterus (against 22.7% of D. melanogaster wild-type Berlin; p < 0.0001, chi-squared test); many eggs showed an advanced embryonic development and even hatched inside the female reproductive tract (Figure 5—figure supplement 1).

Null ple alleles (Neckameyer and White, 1993) and conditional ple mutants at its restrictive temperature (Pendleton et al., 2007) are lethal at late embryonic stage. Zygotic ple expression starts at later stages of embryonic development (Lundell and Hirsh, 1994; Pendleton et al., 2007), with early stages depending on maternal TH-PLE. Maximal survival of D. sechellia egg (R'Kha et al., 1991) matches the proportion of eggs hatching in the term of 2.5 hr after oviposition (Markow et al., 2009)—that is: laid at ∼22 hr of embryonic development—what coincides with the peak of DA synthesis during embryogenesis (Wright, 1987). Thus, being ovoviviparous (Markow et al., 2009) may benefit D. sechellia embryos with dietary maternal l-DOPA and, additionally, provide the eggs with a protective cuticle (secreted at a late stage of embryonic development) highly resistant to environmental hazards. In fact, susceptible siblings embryos resist contact with morinda at late developmental stages (R'Kha et al., 1991). While no D. melanogaster (N = 345) eggs or D. sechellia sister species D. simulans (N = 58) and D. mauritiana (N = 226) eggs completely hatched in morinda pulp, 33% of D. melanogaster eggs produced by flies carrying CatsupIn270Del allele DGRP- (N = 271) hatched to larva 1 (Figure 5—figure supplement 1), some even reaching larva 2 and larva3. These results illustrate how a mutation that reduces female fertility can concomitantly contribute to increase fecundity in a novel niche.

How do D. sechellia adults cope with the toxic environment of morinda fruits to lay their eggs in the first place? In non-sechellia Drosophilids, morinda acids toxicity is mostly manifested as locomotion disorders followed by slowness in movement until complete immobilization and death (Legal et al., 1992). These behavioral phenotypes resemble the neurotoxic effects described in Drosophila upon exposure to fungal-derived organic volatiles of similar chemical structure to morinda carboxylic acids (Inamdar and Bennett, 2014), which have been portrayed as reducing DA in the flies (Inamdar et al., 2013). Thus, we asked if incrementing DA could aid the adult flies in overcoming the behavioral effects of morinda carboxylic acids. To test this, we fed adult D. melanogaster wild-type Berlin a synthetic diet supplemented with increasingly amounts of DA and tested their survival upon exposure to morinda carboxylic acids. After a few minutes of experiencing a natural concentration mix of octanoic and hexanoic acids, D. melanogaster wild-type Berlin flies fed a standard diet showed general restlessness and altered equilibrium with incorrect positioning of tarsi, followed by slowness in movement until complete immobilization. A 66% of females (Figure 6A) and 53% of males (Figure 6B) were completely immobilized after 120 min of exposure to the mix of acids. Dietary administration of DA declined the locomotion behavioral effects of morinda carboxylic acids in a dose-dependent manner (Figure 6A,B). D. melanogaster wild-type Berlin flies (females and males) treated with 100 mg/ml DA reached a survival degree not significantly different from that of D. sechellia (Figure 6C,D). These results suggest that the endogenously increased DA levels in D. sechellia (see Figure 4F) contribute to override the behavioral effects of morinda carboxylic acids. On the other hand, DGRP-357 flies—of intermediate DA levels (see Figure 4F)—showed D. melanogaster levels of resistance to morinda (41.2 ± 4.7 and 52.5 ± 2.8% survival in morinda, respectively in DGRP-357 [N = 6] and D. melanogaster wild-type Berlin [N = 4]; p = 0.09 using Student's t test), suggesting that further genes might contribute to elevate the levels of DA in D. sechellia. D. sechellia shows protein levels of TH-PLE, the rate limiting enzyme in DA production, higher than in the sister species D. simulans and D. mauritiana, and in wild type D. melanogaster (wild-type Berlin, CS) and DGRP-357 (see Figure 4E and Figure 4—figure supplement 1). Additionally, in a screen for genes that differ in expression between D. sechellia and four geographically distinct populations of its generalist sister species D. simulans, Wurmser et al. (2011) showed lower expression of the DA catabolic enzyme (Dopamine-N-acetyltransferase), what probably contributes to almost quintuplicate DA in D. sechellia (see Figure 4F). Thus, the enhancement of DA could have served as a founder event in the history of morinda becoming an obligate host for the specialist D. sechellia.

DA contributes to the behavioral resistance to morinda carboxylic acids.

(AB) Survival kinetic curves for D. melanogaster wild-type Berlin (wtB) (A) females (f, N > 3) and (B) males (m, N > 3) exposed to morinda carboxylic acids (OA:HA) and fed a standard diet supplemented with either no (−), or increasing doses of DA (5 mg/ml, 10 mg/ml and 100 mg/ml). *p < 0.02 and **p < 0.002 using Student's t test. (CD) Survival (%) (N > 3) of D. sechellia (14021–0248.25, sec) and D. melanogaster wild-type Berlin (wtB) (C) females (f) and (D) males (m), fed a non-supplemented (−) or DA (+DA, 100 mg/ml) supplemented standard diet upon 2 hr exposure to morinda carboxylic acids (OA:HA). Different letters denote significant differences (p < 0.01) using ANOVA followed by Tukey's test. Error bars represent s.e.m.

https://doi.org/10.7554/eLife.03785.020

Our results are compatible with an evolutionary scenario in which an original Catsup allele carrying a 45-bp deletion and six non-synonymous mutations was present in the ancestor of present-day D. sechellia (Figure 4—figure supplement 5), probably showing differentially low expression of CATSUP compared to D. melanogaster and the sister species D. simulans and D. mauritiana (see Figure 4E and Figure 4—figure supplement 1); what caused diminished egg production and concomitantly enhanced early survival in the fruit. A second event, further elevating DA (see Figure 4F), would have redeemed adult D. sechellia from the toxic effects of morinda acids allowing them to oviposit in ripe fruits, benefiting from morinda stimulating effect on egg production and from the lack of siblings competition, rendering D. sechellia dependent on morinda. This dependency would have, in turn, shaped the super specialization of the chemosensory system (Dekker et al., 2006; Matsuo et al., 2007; Dworkin and Jones, 2009) present in today's D. sechellia morinda obligate specialist.

Conclusions

The molecular traits underlying adaptations and endurance to new toxic-hosts remain unknown. We present a novel role for the Drosophila catecholamine regulatory protein Catsup in maternal secretory functions and suggest that the malfunction of CATSUP contributed to D. sechellia becoming an obligate specialist on its toxic host. We propose an evolutionary scenario in which an initial mutation in D. sechellia DA metabolism caused impaired female fertility and fecundity, but concomitantly provided eggs and adults with resistance to morinda toxic acids. Together with an early loss of repellence (Matsuo et al., 2007), this initial maternally inherited tolerance allowed individuals to develop in morinda and feed the DA precursor, particularly enriched in this fruit, which strongly increased adult female fertility. In turn, the lack of repellence (Matsuo et al., 2007), and instead the strong attraction to morinda volatiles (Dekker et al., 2006), combined with the beneficial morinda effect on ovulation and egg laying (Figure 2—figure supplement 1), shaped D. sechellia's preference to oviposit in its natural host (Amlou et al., 1998).

Materials and methods

Chemicals

All used chemicals were of commercial origin and used without further purification. UHPLC-MS- grade water and methanol were used for chromatography.

Fly stocks and rearing

Request a detailed protocol

D. sechellia (14021–0248.03, 14021–0248.07, 14021–0248.08, 14021–0248.25, 14021–0248.27, 14021–0248.28, 14021–0248.31) were obtained from the Drosophila Species Stock Center (DSSC, https://stockcenter.ucsd.edu). D. sechellia (14021–0248.25), D. simulans (14021–0251.004) and D. mauritiana (14021–0241.01) were kindly provided by the Division of Chemical Ecology, Swedish University of Agricultural Sciences. D. melanogaster line wild-type Berlin was kindly provided by Silke Sachse. D. melanogaster line Oregon-R was kindly provided by Rafael Cantera. D. melanogaster pforta was captured in the Weingut Kloster Pforta (Naumburg, Germany). D. melanogaster lines Canton-S (BL1), DGRP-357 (BL25184), DGRP-437 (25194), DGRP-304 (BL25177) and Catsup1/CyO (BL5138) were obtained at the Bloomington Stock Center at Indiana University (http://flystocks.bio.indiana.edu/). The CatsupIn270De/Catsup1 flies were selected as not carrying CyO from the F1 of a corresponding crossing of the parental lines DGRP-357 and Catsup1/CyO. Flies were reared in vials (50 mm diameter × 95 mm high) at 25°C, 70% RH in L:D 12:12 on standard cornmeal–yeast–agar medium (standard diet), supplemented as specified in the text, or on fresh morinda pulp (morinda diet) collected from fruits of M. citrifolia plants kept in our greenhouse, or on banana. We observed no differences in survival to morinda fruit in our D. sechellia experimental stock along the successive generations (5 days survival in ripe morinda: 70.7 ± 5.6% and 83.2 ± 3.6% for new and old females [N = 3], p = 0.147 using Student's t test to compare stocks, respectively; 83.3 ± 16.7 and 64.7 ± 18.2 for new and old males, [N = 3], p = 0.493 using Student's t test to compare stocks, receptively), discarding an artificial adaptation to morinda acids. On the other hand, morinda toxicity (Legal and Plawecki, 1995) hindered a permanent experimental stock of D. melanogaster in the fruit, for what flies were fed morinda for as long as the experiment lasted. Morinda carboxylic acids were added to the standard diet or agar plates as indicated in the text, using a range of natural concentrations (0.07% vol/V of 3:1 octanoic:hexanoic mix) (Legal et al., 1994).

Adult survival

Request a detailed protocol

Triplicates of 10–20 flies were placed in vials (25 mm diameter × 95 mm high) containing ripe morinda and maintained at 25°C, 70% RH in L:D 12:12. Live adults were flipped daily to new vials, recording female and male survival. Data is expressed as percentage of females and males alive.

Egg production and oviposition

Request a detailed protocol

Egg production was scored in groups of 10–20 females and males kept during 4 days in cages (37.5 mm diameter and 58 mm high) holding agar plates containing 5% sucrose and devoid of yeast at 25°C, 70% RH in L:D 12:12. Agar plates were changed daily and the total number of eggs was summed. Egg production is expressed as number of eggs per female per day, averaged over >5 independent experiments. Oviposition of the eggs retained by mated females fed a morinda diet supplemented with α-methyl-DOPA (0.4 mM, mDp) was scored in groups of 20 females transferred to non-supplemented standard diet or morinda diet as oviposition substrates. The number of laid eggs was averaged over three independent experiments and expressed as number of eggs per female per day.

Ovariole staining and immunofluorescence

Request a detailed protocol

Ovaries (N > 8) were dissected and fixed in 500 μl of 4% paraformaldehyde in PT (phosphate buffer saline [PBS], 0.1% Triton X-100 [Sigma, St. Louis, MO]) during 30 min at room temperature. After being rinsed three times during 10 min in 1 ml PT, ovaries were incubated in 500 μl PT + 0.5 μl TOTO-3 (1 mM, Invitrogen, Life Technologies GmbH, Germany) + 0.5 μl SYTOX Orange (5 mM, Invitrogen, Life Technologies GmbH, Germany) and protected from light, overnight (ON) at 4°C. Ovaries were rinsed three times during 10 min in 1 ml PT and mounted in Vectashield (Sigma, St. Louis, MO). Oocyte-cyst stages were visually determined by inspection of stained ovaries under fluorescent microscope. Alternatively, fixed ovaries were blocked in PBST (PT, 5% normal goat serum [Sigma, St. Louis, MO]), incubated 24 hr at 4°C with primary antibody anti-TH (1:100, mouse, ImmunoStar, Acris Antibodies, GmbH, Germany) or anti-SLC39A7 (1:1000, rabbit, Sigma, St. Louis, MO), diluted in PBST, further rinsed three times in 1 ml PT during 10 min at room temperature (RT) and incubated respectively with fluorescently conjugated secondary antibodies anti-mouse (AlexaFluor488, Invitrogen, Life Technologies GmbH, Germany) and anti-rabbit (AlexaFluor546, Invitrogen, Life Technologies GmbH, Germany), diluted 1:250 in PBST at RT, protected from light. Ovaries were rinsed three times in 1 ml PT during 10 min and mounted in Vectashield (Sigma, St. Louis, MO). Confocal images were obtained at 1-μm intervals over 20 μm Z-stack using a LSM510 Meta confocal microscope (Zeiss, Jena, Germany).

Apoptosis

Request a detailed protocol

Apoptosis in D. sechellia ovaries (N > 6) was visualized following the protocol by Arama and Steller (McCall, 2004). Briefly, live ovaries were dissected in PBS and incubated in a freshly prepared solution of 0.6 μg/ml acridine orange (Sigma, St. Louis, MO) for 5 min, at RT. Ovaries were rinsed briefly in PBS and mounted in a drop of Halocarbon 700 oil (Sigma, St. Louis, MO) and observed immediately. Confocal images were obtained at 1-μm intervals over 20 μm Z-stack using a LSM510 Meta confocal microscope (Zeiss, Jena, Germany).

Feeding assay

Request a detailed protocol

Feeding assay was performed as described previously (Riemensperger et al., 2011). 10 D. sechellia 5-day-old flies (five females and five males) were starved for 2 hr at 25°C and transferred to vials with cornmeal-yeast food (standard diet) or morinda fresh pulp (morinda diet), containing 10 mM sulforhodamine B (Sigma, St. Louis, MO). Flies were allowed to feed for 1 hr and were immediately frozen at −20°C for 2 hr. Females and males were processed separately. Heads were removed to prevent contamination with eye pigments, and the bodies were homogenized in 250 μl of PBS. Samples were micro-centrifuged at 17,000×g (Eppendorf Centrifuge 5415 R) for 7 min at 4°C, after which the supernatant was collected, mixed with 60 μl of chloroform and micro-centrifuged for 6 min. The optical density of the supernatant was determined at 570 nm (BioSpectrophotometer, Eppendorf). Results are the mean of three independent determinations in each food condition.

Amine and precursors quantification

Request a detailed protocol

Fresh morinda fruits (10 g) were homogenized in 15 ml 0.1 M perchloric acid, incubated during 5 min at RT and micro-centrifuged at 17,000×g (Eppendorf Centrifuge 5415 R) for 5 min at 4°C. The resulting supernatant was measured in a RS-3000-LTQ-Orbitrap XL instrument (Dionex and Thermo Fischer) (Docimo et al., 2012). l-3,4-dihydroxyphenylalanine (l-DOPA) values were estimated by calibration curve regression. Arithmetic mean and standard deviation were calculated over three independent samples and values expressed as nanogram of l-DOPA per gram of fruit. Other amines, DA, TA and OA, were not detected in morinda fruit under these conditions. Fly samples (5 whole flies, or 6 bodies or 10 ovaries) were processed in 50 μl of 0.1 M perchloric acid with 0.3 mM mDp as an internal standard, using ceramic beads (peqlab, Biotechnology GmbH) in TissueLyser LT (QIAGEN). Samples were micro-centrifuged twice at 17,000×g (Eppendorf Centrifuge 5415 R) for 5 min at 4°C and the supernatant measured as above. Tyrosine, l-DOPA and DA absolute values were calculated by calibration curve regression using XCMS/MZMatchR program (Tautenhahn et al., 2008). Arithmetic mean and standard deviation were calculated over three independent samples. For flies fed a standard diet, values were expressed as picogram of l-DOPA or DA per fly (fly weights showed no statistically significant difference [p = 0.85564545, D. melanogaster vs D. sechellia, Student's t test]). To compare flies fed different diets, values were expressed as picogram of l-DOPA per milligram of body tissue.

Fruit pH measurements

Request a detailed protocol

The fruit pulp of ripe or overripe morinda and banana was mashed lightly and the pH was measured with a glass electrode. Results are the mean of three independent determinations for each fruit.

Egg-hatching rate and size

Request a detailed protocol

D. sechellia 10–20 females and males fed a standard diet were placed in oviposition cages (37.5 mm diameter and 58 mm high) holding plates containing either a standard diet or fresh morinda pulp, at 25°C, 70% RH in L:D 12:12. In parallel, D. sechellia 10–20 females and males fed a diet of morinda were placed in oviposition cages (37.5 mm diameter and 58 mm high) holding plates containing fresh morinda pulp, at 25°C, 70% RH in L:D 12:12. Plates were changed every 0.5 hr to get pools of synchronized eggs and further incubated at 25°C. Hatching rate was expressed as the relative number of hatched eggs (larvae 1) to the total number of eggs produced. Egg size was measured within 1 hr of oviposition or on pre-fertilized eggs inside the ovary (there was not a statistically significant difference between these groups). For each species, the lengths (L) and widths (W) of 15–30 eggs were measured and their volumes were determined according to the formula (1/6)πW2L (Markow et al., 2009). Values were expressed as mm3 (10−3).

Western blots

Request a detailed protocol

For each species, 20 adult flies were homogenized in 200 μl lysis buffer (50 mM Tris–HCl pH 7.5, 0.1% [vol/V] Triton X-100, 100 mM NaCl, 1 mM DTT, 10% glycerol, 15 mM EDTA) freshly prepared with protease inhibitor cocktail (Roche) added immediately before use, using ceramic beads (peqlab, Biotechnology GmbH, Germany) in TissueLyser LT (QIAGEN GmbH, Germany). Whole protein extracts of one same experiment were separated in parallel by 10% SDS-PAGE plus electronic transfer to PVDF membranes (BioRad, Germany). After being blocked in 5% non-fat milk in TBS-tween (TBS, 0.05% Tween-20 [Sigma, St. Louis, MO]) for 2 hr, at RT, membranes were incubated with 1:1000 dilutions of primary antibodies (anti-TH [mouse, ImmunoStar, Acris Antibodies, GmbH, Germany], or anti-SLC39A7 [rabbit, Sigma, St. Louis, MO] or anti-α-tubulin [mouse, Sigma, St. Louis, MO]) diluted in 2.5% non-fat milk in TBS tween ON at 4°C. Membranes were further washed in TBS-tween at RT and re-blocked in 10% non-fat milk TBS-tween for 10 min at RT before being incubated with 1:10000 dilution of corresponding secondary HRP-conjugated anti-mouse or anti-rabbit (BioRad, Germany). Proteins were detected using an enhanced chemiluminescence detection kit (Thermo scientific pierce, Germany). The densitometry of bands was performed using ImageJ package (http://imagej.nih.gov/ij/). Relative densities of TH-PLE and CATSUP were scaled using the relative densities of the loading-controls (α-Tubulin).

Gene cloning and sequencing

Request a detailed protocol

For each species, we prepared total RNA (Trizol, Invitrogen, Life Technologies GmbH, Germany) and synthesized cDNA (SuperScript III First-Strand Synthesis System, Invitrogen, Life Technologies GmbH, Germany) that was used to amplify Catsup transcript by PCR (Advantage HD Polymerase, Clontech) with specific primers (forward 5′-ATGGCCAAACAAGTGGCTGA-3′ and reverse 5′-TTACTCGAACTTGGCGATAAC-3′). Each PCR product was cloned in pCRII vector (Invitrogen, Life Technologies GmbH, Germany) and at least 10 colonies were picked for plasmid DNA purification and sequencing. These sequences were aligned using MegAlign (DNASTAR) and a consensus sequence was obtained for each species. The sequence of CatsupIn270Del was obtained from the Drosophila Polymorphism Database (DPDB) (Casillas et al., 2005).

Sternopleural bristle quantification

Request a detailed protocol

Total (macro and micro) bristles of each sternopleural plaque were counted in females of D. melanogaster wild-type Berlin (N = 34), D. melanogaster Canton-S (N = 54), D. melanogaster DGRP-357 (N = 61), DGRP-437 (N = 18), DGRP-304 (N = 16)—three independent lines carrying CatsupIn270Del allele—and D. sechellia lines 14021–0248.08 (N = 98), 14021–0248.25 (N = 74), 14021–0248.27 (N = 25), 14021–0248.28 (N = 56) and 14021–0248.31 (N = 50). Data is expressed as frequency histograms and a bar-graph showing the mode of each population.

Behavioural assay

Request a detailed protocol

5-day-old flies were fed a standard diet either not- or supplemented with increasingly amounts of DA (5 mg/ml, 10 mg/ml and 100 mg/ml) during 16 hr prior to their behavioural assessment, at 25°C, 70% RH in L:D 12:12. The locomotion behaviour was scored in groups of 30 females and 30 males kept in cages (37.5 mm diameter and 58 mm high) holding agar plates containing 5% sucrose and a mix of 0.07% vol/V 3:1 octanoic:hexanoic acids. M. citrifolia fruits contain highly volatile compounds that confer toxicity (Legal et al., 1994), with the two most abundant being octanoic acid (58%) and hexanoic acid (19.24%) (Farine et al., 1996). Octanoic acid is the most toxic compound in the ripe fruit (Legal et al., 1994), which D. sechellia has been able to overcome by the development of both larval and adult tolerance mechanisms (R'Kha et al., 1991; Legal et al., 1992; Amlou et al., 1997, 1998; Jones, 1998, 2001, 2005). Given these observations, the ratio provided on par. A drop of fresh yeast was added to the plates forcing the attracted flies to enter in contact to the acids. Flies were carefully observed under a stereoscope and the number of immobilized flies was recorded every 5 min independently for females and males. Results are the mean of three to five independent determinations in each food condition.

References

    1. Jones CD
    (1998)
    The genetic basis of Drosophila sechellia's resistance to a host plant toxin
    Genetics 149:1899–1908.
    1. Legal L
    2. Plawecki M
    (1995)
    Comparative sensitivity of various insects to toxic compounds from Morinda citrifolia
    Entomol Probl. 26:155–159.
    1. Levitt M
    2. Spector S
    3. Sjoerdsma A
    4. Udenfriend S
    (1965)
    Elucidation of the rate-limiting step in norepinephrine biosynthesis in the perfused guinea-pig heart
    The Journal of Pharmacology and Experimental Therapeutics 148:1–8.
    1. Louis J
    2. David J
    (1986)
    Ecological specialization in the Drosophila melanogaster species subgroup - a case study of D. sechellia
    Acta Oecologica-Oecologica Generalis 7:215–229.
  1. Book
    1. O'Donnell JM
    2. Stathakis DG
    3. Burton DY
    4. Chen Z
    (2002)
    Catecholamines-up, a negative regulator of tyrosine hydroxylase and GTP Cyclohydrolase I in Drosophila Melanogaster
    In: Milstein GKS, Levine R, Shane B, editors. Chemistry and biology of pteridines and folates. Boston: Kluwer Academic. pp. 211–215.
    1. Schupbach T
    2. Wieschaus E
    (1991)
    Female sterile mutations on the second chromosome of Drosophila melanogaster. II. Mutations blocking oogenesis or altering egg morphology
    Genetics 129:1119–1136.
    1. Stathakis DG
    2. Burton DY
    3. McIvor WE
    4. Krishnakumar S
    5. Wright TR
    6. O'Donnell JM
    (1999)
    The catecholamines up (Catsup) protein of Drosophila melanogaster functions as a negative regulator of tyrosine hydroxylase activity
    Genetics 153:361–382.
    1. Tsacas LGB
    2. Baechli G
    (1981)
    Drosophila sechellia. n. sp., huitième espèce du sous-groupe melanogaster des iles Séchelles (Diptera, Drosophilidae)
    Revue Francaise d’Entomologie 3:146–150.
    1. Wright TR
    (1987)
    The genetics of biogenic amine metabolism, sclerotization, and melanization in Drosophila melanogaster
    Advances in Genetics 24:127–222.

Article and author information

Author details

  1. Sofía Lavista-Llanos

    Max Planck Institute for Chemical Ecology, Jena, Germany
    Contribution
    SL-L, Conception and design, Acquisition of data, Analysis and interpretation of data, Drafting or revising the article
    For correspondence
    slavista-llanos@ice.mpg.de
    Competing interests
    No competing interests declared.
  2. Aleš Svatoš

    Max Planck Institute for Chemical Ecology, Jena, Germany
    Contribution
    AS, Acquisition of data, Analysis and interpretation of data
    Competing interests
    No competing interests declared.
  3. Marco Kai

    Max Planck Institute for Chemical Ecology, Jena, Germany
    Present address
    Institute for Biological Science, Department of Biochemistry, University of Rostock, Rostock, Germany
    Contribution
    MK, Acquisition of data, Analysis and interpretation of data
    Competing interests
    No competing interests declared.
  4. Thomas Riemensperger

    Genetics and Physiopathology of Neurotransmission, Neurobiology Unit, CNRS, ESPCI ParisTech, Paris, France
    Present address
    Molecular Neurobiology of Behaviour, Johann Friedrich Blumenbach Institute, Georg August University of Goettingen, Goettingen, Germany
    Contribution
    TR, Acquisition of data, Analysis and interpretation of data
    Competing interests
    No competing interests declared.
  5. Serge Birman

    Genetics and Physiopathology of Neurotransmission, Neurobiology Unit, CNRS, ESPCI ParisTech, Paris, France
    Contribution
    SB, Conception and design, Drafting or revising the article
    Competing interests
    No competing interests declared.
  6. Marcus C Stensmyr

    Max Planck Institute for Chemical Ecology, Jena, Germany
    Present address
    Department of Biology, Lund University, Lund, Sweden
    Contribution
    MCS, Conception and design, Drafting or revising the article
    Competing interests
    No competing interests declared.
  7. Bill S Hansson

    Max Planck Institute for Chemical Ecology, Jena, Germany
    Contribution
    BSH, Conception and design, Drafting or revising the article
    Competing interests
    BSH: Vice president of the Max Planck Society, one of the three founding funders of eLife, and a member of eLife's Board of Directors.

Funding

Max-Planck-Gesellschaft

  • Sofía Lavista-Llanos
  • Aleš Svatoš
  • Marco Kai
  • Marcus C Stensmyr
  • Bill S Hansson

Centre National de la Recherche Scientifique (ESPCI ParisTech)

  • Thomas Riemensperger
  • Serge Birman

Fondation de France

  • Thomas Riemensperger
  • Serge Birman

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

Acknowledgements

We wish to thank Regina Stieber, Sandra Scholz and Céline Callens for expert technical support; and Emily Wheeler, Boston, for editorial assistance. Stocks obtained from the Bloomington Drosophila Stock Center (NIH P40OD018537) were used in this study. This work was supported by the Max Planck Society (SL-LL, AS, MK, MCS and BSH) and by grants from the ESPCI ParisTech and the Fondation de France to SB (TR and SB).

Version history

  1. Received: June 25, 2014
  2. Accepted: November 1, 2014
  3. Version of Record published: December 9, 2014 (version 1)

Copyright

© 2014, Lavista-Llanos 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.

Metrics

  • 3,894
    Page views
  • 454
    Downloads
  • 38
    Citations

Article citation count generated by polling the highest count across the following sources: Scopus, Crossref, PubMed Central.

Download links

A two-part list of links to download the article, or parts of the article, in various formats.

Downloads (link to download the article as PDF)

Open citations (links to open the citations from this article in various online reference manager services)

Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)

  1. Sofía Lavista-Llanos
  2. Aleš Svatoš
  3. Marco Kai
  4. Thomas Riemensperger
  5. Serge Birman
  6. Marcus C Stensmyr
  7. Bill S Hansson
(2014)
Dopamine drives Drosophila sechellia adaptation to its toxic host
eLife 3:e03785.
https://doi.org/10.7554/eLife.03785

Share this article

https://doi.org/10.7554/eLife.03785

Further reading

    1. Ecology
    Yongzhi Yan, Scott Jarvie, Qing Zhang
    Research Article

    Habitat loss and fragmentation per se have been shown to be a major threat to global biodiversity and ecosystem function. However, little is known about how habitat loss and fragmentation per se alters the relationship between biodiversity and ecosystem function (BEF relationship) in the natural landscape context. Based on 130 landscapes identified by a stratified random sampling in the agro-pastoral ecotone of northern China, we investigated the effects of landscape context (habitat loss and fragmentation per se) on plant richness, above-ground biomass, and the relationship between them in grassland communities using a structural equation model. We found that habitat loss directly decreased plant richness and hence decreased above-ground biomass, while fragmentation per se directly increased plant richness and hence increased above-ground biomass. Fragmentation per se also directly decreased soil water content and hence decreased above-ground biomass. Meanwhile, habitat loss decreased the magnitude of the positive relationship between plant richness and above-ground biomass by reducing the percentage of grassland specialists in the community, while fragmentation per se had no significant modulating effect on this relationship. These results demonstrate that habitat loss and fragmentation per se have inconsistent effects on BEF, with the BEF relationship being modulated by landscape context. Our findings emphasise that habitat loss rather than fragmentation per se can weaken the positive BEF relationship by decreasing the degree of habitat specialisation of the community.

    1. Ecology
    Anna L Erdei, Aneth B David ... Teun Dekker
    Research Article

    Over two decades ago, an intercropping strategy was developed that received critical acclaim for synergizing food security with ecosystem resilience in smallholder farming. The push-pull strategy reportedly suppresses lepidopteran pests in maize through a combination of a repellent intercrop (push), commonly Desmodium spp., and an attractive, border crop (pull). Key in the system is the intercrop's constitutive release of volatile terpenoids that repel herbivores. However, the earlier described volatiles were not detectable in the headspace of Desmodium, and only minimally upon herbivory. This was independent of soil type, microbiome composition, and whether collections were made in the laboratory or in the field. Further, in oviposition choice tests in a wind tunnel, maize with or without an odor background of Desmodium was equally attractive for the invasive pest Spodoptera frugiperda. In search of an alternative mechanism, we found that neonate larvae strongly preferred Desmodium over maize. However, their development stagnated and no larva survived. In addition, older larvae were frequently seen impaled and immobilized by the dense network of silica-fortified, non-glandular trichomes. Thus, our data suggest that Desmodium may act through intercepting and decimating dispersing larval offspring rather than adult deterrence. As a hallmark of sustainable pest control, maize-Desmodium push-pull intercropping has inspired countless efforts to emulate stimulo-deterrent diversion in other cropping systems. However, detailed knowledge of the actual mechanisms is required to rationally improve the strategy, and translate the concept to other cropping systems.