Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Wolbachia Mediate Variation of Host Immunocompetence

  • Christine Braquart-Varnier ,

    Contributed equally to this work with: Christine Braquart-Varnier, Marion Lachat

    Affiliation Université de Poitiers, Laboratoire Ecologie, Evolution, Symbiose, UMR CNRS 6556, 40 avenue du recteur Pineau, Poitiers, France

  • Marion Lachat ,

    Contributed equally to this work with: Christine Braquart-Varnier, Marion Lachat

    Affiliation Université de Poitiers, Laboratoire Ecologie, Evolution, Symbiose, UMR CNRS 6556, 40 avenue du recteur Pineau, Poitiers, France

  • Juline Herbinière,

    Affiliation Université de Poitiers, Laboratoire Ecologie, Evolution, Symbiose, UMR CNRS 6556, 40 avenue du recteur Pineau, Poitiers, France

  • Monique Johnson,

    Affiliation Université de Poitiers, Laboratoire Ecologie, Evolution, Symbiose, UMR CNRS 6556, 40 avenue du recteur Pineau, Poitiers, France

  • Yves Caubet,

    Affiliation Université de Poitiers, Laboratoire Ecologie, Evolution, Symbiose, UMR CNRS 6556, 40 avenue du recteur Pineau, Poitiers, France

  • Didier Bouchon,

    Affiliation Université de Poitiers, Laboratoire Ecologie, Evolution, Symbiose, UMR CNRS 6556, 40 avenue du recteur Pineau, Poitiers, France

  • Mathieu Sicard

    mathieu.sicard@univ-poitiers.fr

    Affiliation Université de Poitiers, Laboratoire Ecologie, Evolution, Symbiose, UMR CNRS 6556, 40 avenue du recteur Pineau, Poitiers, France

Wolbachia Mediate Variation of Host Immunocompetence

  • Christine Braquart-Varnier, 
  • Marion Lachat, 
  • Juline Herbinière, 
  • Monique Johnson, 
  • Yves Caubet, 
  • Didier Bouchon, 
  • Mathieu Sicard
PLOS
x

Abstract

Background

After decades during which endosymbionts were considered as silent in their hosts, in particular concerning the immune system, recent studies have revealed the contrary. In the present paper, we addressed the effect of Wolbachia, the most prevalent endosymbiont in arthropods, on host immunocompetence. To this end, we chose the A. vulgare-Wolbachia symbiosis as a model system because it leads to compare consequences of two Wolbachia strains (wVulC and wVulM) on hosts from the same population. Moreover, A. vulgare is the only host-species in which Wolbachia have been directly observed within haemocytes which are responsible for both humoral and cellular immune responses.

Methodology/Principal Findings

We sampled gravid females from the same population that were either asymbiotic, infected with wVulC, or infected with wVulM. The offspring from these females were tested and it was revealed that individuals harbouring wVulC exhibited: (i) lower haemocyte densities, (ii) more intense septicaemia in their haemolymph and (iii) a reduced lifespan as compared to individuals habouring wVulM or asymbiotic ones. Therefore, individuals in this population of A. vulgare appeared to suffer more from wVulC than from wVulM. Symbiotic titer and location in the haemocytes did not differ for the two Wolbachia strains showing that these two parameters were not responsible for differences observed in their extended phenotypes in A. vulgare.

Conclusion/Significance

The two Wolbachia strains infecting A. vulgare in the same population induced variation in immunocompetence and survival of their hosts. Such variation should highly influence the dynamics of this host-symbiont system. We propose in accordance with previous population genetic works, that wVulM is a local strain that has attenuated its virulence through a long term adaptation process towards local A. vulgare genotypes whereas wVulC, which is a widespread and invasive strain, is not locally adapted.

Introduction

Investigations on the consequences of endosymbionts on their host's fitness have revealed that some of them exhibit variable effects, blurring the distinction between mutualism and parasitism. It is now admitted that symbionts are deeply involved in the evolutionary process of their hosts and that variations in symbiont genotypes may trigger more important differences in host life history traits than variations of the host genotypes themselves [1]. Thus, the entity that undergoes selection is clearly the extended phenotype of symbionts in their host. Within such a conceptual framework, the studies that focus on an understanding of host population dynamics need to consider symbiosis as a central parameter. Of the endosymbionts known to exhibit various effects on their host fitness, Wolbachia are the most prevalent in arthropods. The diversity of the interactions between Wolbachia and their hosts is mainly illustrated by the various strategies these endosymbionts exhibit in order to secure their vertical transmission. Hence, in some host species Wolbachia decrease the fitness of uninfected individuals (i.e. cytoplasmic incompatibility) while in others they increase female ratio in populations (i.e. parthenogenesis, male-killing and feminization) [2], [3]. As the transmission of Wolbachia is vertical, their fitness is directly linked to the fitness of their hosts. Therefore, such situations could be seen as favourable to evolve towards obligate symbiosis and therefore mutualism. However, such obligate Wolbachia symbioses have only been described in filarial nematodes and in the parasitic wasp Asobara tabida [4], [5]. In both models, aposymbiotic females failed to produce mature oocytes showing that Wolbachia are obligate for reproduction [4], [5]. Other studies have shown that Wolbachia may be mutualists by improving development, survival and reproduction of their hosts [6][10]. However, these effects can vary over time or with respect to host genotypes and cause continuous evolutionary changes [7], [10].

Despite these few examples of dependency or mutualism between Wolbachia and their hosts, Wolbachia are mostly described as facultative endosymbionts that negatively influence their hosts' life history traits, including body size [11], fecundity [11][13], survival [13][15], larval competitiveness [16], male fertility and sperm cyst production [17] and mating choice [18]. Recently, Fytrou et al. (2006) [19] hypothesized that Wolbachia may also immunodepress their hosts. Indeed, they observed that Drosophila infected by Wolbachia showed less encapsulation of parasitic wasp eggs than cured ones. The capacity of Wolbachia to interact with the arthropod immune system has also been recently suggested by (i) the discovery of an intracellular sensor of Gram (-) bacteria in Drosophila and (ii) the observed modifications of the immune response in Drosophila melanogaster and Aedes albopictus cell lineages due to the presence of Wolbachia [20][22]. Moreover, molecular evolution studies within Wolbachia-infecting insects have revealed that the Wolbachia outer membrane protein wsp, which has been shown to play a role in filarial nematode infection success [23], is under strong positive selection thus suggesting that invertebrate immune response may be an important selection factor for Wolbachia [24]. In invertebrates, immune cells (i.e. haemocytes) are essential effectors of immunity [20]. They are responsible for both cellular (encapsulation, phagocytosis etc.) and humoral (antimicrobial peptides, phenoloxydase cascade etc.) responses. Wolbachia have been observed within host haemocytes in only one species: the terrestrial isopod Armadillidium vulgare [25]. In light of this observation and also due to the even more central role of haemocytes in crustacean immune systems [26], the A. vulgare-Wolbachia association appears to be a very pertinent biological model to study the influence of symbiosis on host immunocompetence. In addition, A. vulgare is of particular interest because individuals from the same population are mono-infected (to date, no naturally co-infected individuals have been observed) by one of three different strains of Wolbachia (wVulM, wVulC and wVulP) [27], [28]. wVulP, which has only been identified recently and which is less prevalent than the others, seems to be the result of a recombination event between wVulM and wVulC suggesting that co-infections do occur but are unstable. This would explain why co-infected individuals are never observed in sampled populations [28]. Both wVulC or wVulM are feminizing strains since offspring from sampled A. vulgare females are highly female-biased [27]. A. vulgare lineages infected with wVulC or wVulM are maintained in laboratory for decades showing that the symbiotic transmission and feminizing phenotypes of these two Wolbachia strains persist through generations (Bouchon et al., unpublished data). However, despite these similarities, population genetic studies suggest that wVul strains exhibit different strategies [27], [29]. wVulC would be the most invading strain able to replace previous Wolbachia strains including wVulM [27], [29], whereas wVulM would be the resident strain, more locally adapted to host genotypes. As immunocompetence is obviously a primordial parameter in host dynamics, it is thus of great interest to compare the effect of these two Wolbachia strains on host immune capacities.

In the present study, a comparison was made of the extended phenotype of wVulC and wVulM in A. vulgare. To this end, we evaluated in A. vulgare individuals infected by wVulC or wVulM: (i) the titer of Wolbachia in ovaries by qPCR (ii) the presence of Wolbachia in haemocytes by electronic microscopy, (iii) the density of haemocytes, (iv) the intensity of natural septicaemia (i.e. number of CFU obtained from haemolymph) (v) their survival over a 7 month period. These results were used to detect differences in immunocompetence and survival of A. vulgare as a function of Wolbachia genotype.

Materials and Methods

A. vulgare lineages

Gravid females (F0) of A. vulgare were sampled in the natural park of Chizé (Western France 46°08′05″N-0°24′21″W) and brought back to the laboratory. The infection status of each gravid female (infected with Wolbachia wVulC or wVulM or asymbiotic i.e. noninfected by Wolbachia) was determined as described below. To avoid any maternal effect in further experiments at least three gravid females (F0) for each infection status were used to start lineages. Their offspring (F1) were born and reared in the laboratory. For each infection status, one hundred virgin females from the F1 generation were kept and placed individually with one male (F1) in individual boxes. Over a 7 month period, the survival of these F1 females was monitored every three days and their progenies (F2) were collected. The virgin F2 females grew during two years before immunocompetence experiments. In order to simplify the reading of the paper, virgin asymbiotic females were called A females, virgin females infected with wVulC were called C females, virgin females infected with wVuM were called M females. All of these lineages were grown at 20°C on moistened potting mix derived from peat from sphagnum moss (pH = 6.4 and conductivity = 50.0 mS/m) with dead leaves and carrot slices as a food source.

Additionally, a lineage of females experimentally infected by wVulC (herein called injC females) was created. For this, the ovaries of 10 C females (F0) were collected and crushed into 1ml of Ringer solution. The resulting suspension was filtered through a 1.2 µm pore membrane, and 1 µl of filtrate injected into non gravid A females (F0) using a thin glass needle (Bouchon et al., 1998). F0 injC females were then crossed with asymbiotic males for two generations in order to produce two year old F2 virgin injC females.

F2 females (A, C, M) were used to assess: Wolbachia titer, haemocytes density and intensity of natural septicaemia. Due to a small number of individuals, injC females (F2) were only used to highlight the assessment of the effect of wVulC on haemocyte density.

Infection status and Wolbachia titer

The infection status of each A. vulgare female used in experiments was determined by a PCR-RFLP assay. Individuals were dissected and total DNA extracted from the ovary as previously described [30]. PCR amplifications were then performed to test for presence/absence of Wolbachia using specific primer sets for the wsp gene [31] and conditions as previously described [27]. In order to discriminate each Wolbachia strain, a PCR-RFLP test was performed based on the analysis of wVulC and wVulM wsp sequences (wVulM: AJ419984 and wVulC: AJ419987). Two restriction enzymes were used: BsrI, which cuts wsp amplicons in wVulC but not in wVulM, and MFeI, which cuts wsp amplicons in wVulM but not in wVulC.

Comparative analysis of the titer of Wolbachia in ovaries between C females and M females was performed using qPCR of the wsp gene. Total DNA from the ovaries of 20 females of each infection status were individually extracted [30]. To prepare the standard, 7 µl of purified wsp gene PCR product were directly ligated into a pGEM-T-easy vector (Promega) and one site was cut with Ncol enzyme at 37°C overnight to linearize the plasmid. Plasmid concentration was subsequently determined using a spectrophotometer and the number of wsp copies calculated. For each DNA sample, the qPCR was carried out under the following conditions: 2 µl of 10× Light Cycler Mix (Roche™), 0.2 µl of 20 µM of wsp primers, 1.6 µl of 25mM MgCl2. The thermal cycling used an initial denaturation period of 8 min at 95°C, followed by 45 cycles of denaturing temperature at 95°C for 15 sec., the annealing temperature for the reaction was 57°C for 14 sec. and 72°C for 28°C and a final extension step at 72°C for 28 sec.

Haemolymph sampling

Haemolymph was sampled in the same way for all following experiments: cuticles were disinfected by immersing individuals for 30 sec. in a 10% sodium hypochlorite solution followed by a 30 sec. immersion in distilled water. The cuticle was then pierced dorsally between the sixth and seventh abdominal segments using a fine needle and 10 µl haemolymph were collected with a micropipette.

Wolbachia in haemocytes

The haemolymph from 20 females of each infection status (A females, C females and M females) was individually sampled and half diluted in an anticoagulant solution [Modified Alsever's solution MAS 27 mM sodium citrate: 336 mM NaCl, 115 mM glucose, 9 mM EDTA, pH 7; [32]]. Haemocytes were separated from plasma by centrifugation (400× g, 10 min, 4°C) and washed with the same buffer. Haemocytes were fixed (9% glutaraldehyde, 0.3M sodium cacodylate, 3% NaCl, v/v/v) for 45 min at 4°C and then centrifuged (400× g, 10 min, 4°C). Cells were washed (0.3M sodium cacodylate, 3% NaCl, 0.8M sucrose, v/v/v) for 15 min at 4°C then centrifuged (400× g, 10 min, 4°C). Haemocytes were included in a 2% agar gel (37°C) and 1mm3 plugs were cut and placed in wash buffer for 2h at 4°C following which they were post fixed into 4% OsO4, 0.3M sodium cacodylate, 5.5% NaCl for 45 min. Haemocytes were subsequently dehydrated through a graded series of acetone solutions, infiltrated, and embedded in resin (Spurr, Polyscience Inc.). Thick sections (0.5 µm) were stained with 1% toluidin blue. Thin sections (90nm) were contrasted by incubation in 1% uranyl acetate in 50% ethanol for 1 min, and then stained with lead citrate. Sections were observed using a transmission electronic microscope (JEOL 100C).

Haemocyte density in haemolymph

The haemolymph (10 µl) of 35 females of each infection status (A females, C females, M females and injC females) was individually sampled and added to 10 µl of MAS and 60 µl of 0.4% Trypan blue to discriminate dead haemocytes from living ones. The actual number of living haemocytes in each sample was evaluated using a Thoma counting chamber.

Natural septicaemia assessment

The haemolymph (10 µl) of 60 females of each infection status (A females, C females and M females) was individually sampled and added to 290 µl of LB medium. An aliquot of 100 µl of this suspension was streaked onto one plate of each of the three different solid agar media used: (i) a non selective chocolate medium (Biomérieux) on which most bacteria, even fastidious ones, can grow, (ii) the Columbia Nalidixic Acid Agar (CNA) (Biomérieux) in order to preferentially select Gram (+) bacteria and (iii) the Mueller-Hinton Agar (MHA) (Biomérieux) (35g/l) with 10% sheep's blood and 10 µl/l vancomycin in order to preferentially select Gram (−) bacteria. After 3 days at 28°C, the number of colony forming units (CFUs) on each plate was determined.

Statistical analyses

All statistical analyses were performed using JUMP software (JMP, 2001, ver.4.03; SAS Institute, Cary, NC, USA). Survival estimates were assessed by a Kaplan-Meier analysis followed by a univariate Survival Analysis using a Wilcoxon test. As haemocyte density and natural septicaemia data showed homoscedasticity of variance (Levene test p>0.05), difference in mean responses was tested by an ANOVA followed by PLSD Fisher post-hoc test.

Results

Infection status and Wolbachia titer

All C, injC and M females used in this experiment were controlled positive for Wolbachia. The two strains of Wolbachia exhibited a similar titer (∼7,640×106 bacteria per µg total DNA) in the host (ANOVA, F1,35 = 1.92, p = 0.17). However, wVulM tended to show higher titer than wVulC (Fig. 1).

thumbnail
Figure 1. Titer of each Wolbachia strains in A. vulgare ovaries.

Comparative analysis of the titer of Wolbachia in ovaries between C females and M females was performed using qPCR of the wsp gene. The two strains of Wolbachia exhibited a similar titer (∼7,640×106 bacteria per µg total DNA; ANOVA, F1,35 = 1.92, p = 0.17).

http://dx.doi.org/10.1371/journal.pone.0003286.g001

Presence of Wolbachia in haemocytes

Wolbachia cells were observed by transmission electronic microscopy in haemocytes of all C and M females tested. In haemocytes, Wolbachia were included in a vacuole and did not seem to be undergoing any type of degradation process suggesting that they may survive and perhaps even multiply within such cells (Fig. 2).

thumbnail
Figure 2. Haemocyte from an A. vulgare female infected with wVulC observed by transmission electronic microscopy.

Haemocytes were included in agar gel and cut. Thick sections (0.5 µm) were stained and observed using a transmission electronic microscope.Wolbachia (notated w on the photography) cells were observed by transmission electronic microscopy in haemocytes of all C and M females tested.

http://dx.doi.org/10.1371/journal.pone.0003286.g002

Effect of Wolbachia on host survival

Comparison of survival plots between A females, C females and M females revealed significant differences (Wilcoxon test, χ2 = 10.87 df = 2 p = 0.004). C Females survived significantly less (19% mortality, mean time before death = 177.4±4.4 days) than A females (6% mortality, mean time before death = 189.1±2.7 days) (Wilcoxon test, χ2 = 9.39 df = 1 p = 0.002) whereas survival of M females (11% mortality, mean time before death = 177.8±2.1 days) was not significantly different from that of A females (Wilcoxon test, χ2 = 1.56 df = 1 p = 0.212) (Fig. 3). Finally, C females survived significantly less than M females (Wilcoxon test, χ2 = 4.05 df = 1 p = 0.044).

thumbnail
Figure 3. Effect of Wolbachia on host survival.

Comparison of survival plots between A females, C females and M females during 7 months revealed that C females survived significantly less than A females and M females.

http://dx.doi.org/10.1371/journal.pone.0003286.g003

Effect of Wolbachia on haemocyte density

Global comparison of haemocyte densities in A females, C females, M females and injC females exhibited significant heterogeneity (ANOVA, F3,141 = 18.91, p<0.0001) (Fig. 3). Statistical analysis revealed that A females exhibited significantly higher haemocyte densities (mean: 29,731 haemocytes per µl) than (i) C females (mean: 11,760 haemocytes per µl) (Fisher's PLSD test: p<0.0001), (ii) M females (mean: 22,805 haemocytes per µl) (Fisher's PLSD test: p = 0.0232) and injC females (mean: 15,722 haemocytes per µl) (Fisher's PLSD test: p<0.0001). However, M females exhibited higher haemocyte densities than either C females (Fisher's PLSD test: p<0.0001) or injC females (Fisher's PLSD test: p<0.009) (Fig. 4). C females and injC females showed similar haemocyte densities (Fisher's PLSD test: p = 0.104).

thumbnail
Figure 4. Effect of Wolbachia on haemocyte density.

Global comparison of haemocyte densities in haemolymph of A. vulgare females infected or not by Wolbachia revealed that A females exhibited significantly higher haemocyte densities than C females, M females and injC females.

http://dx.doi.org/10.1371/journal.pone.0003286.g004

Effect of Wolbachia on natural septicaemia

On CNA [selective medium for Gram (+) bacteria], the mean number of CFUs obtained for haemolymph samples from (i) A females, (ii) C females and (iii) M females showed heterogeneity (ANOVA, F2,174 = 3.961, p = 0.0208). The mean CFUs was significantly higher in the haemolymph from C females (mean: 81 bacteria/µl) than in A females (mean: 18 bacteria/µl) (Fisher's PLSD test: p = 0.0133) or M females (mean: 21 bacteria/µl) (Fisher's PLSD test: p = 0.0179). Differences between mean CFUs on MHA [selective medium for Gram (-) bacteria)] and chocolate medium (“non-selective” medium) were not significant (ANOVA, F2,174 = 0.769, p = 0.4650 and F2,174 = 2.850, p = 0.0606, respectively) (Fig. 5). However, in all media, C females tend to harbour more bacteria in their haemolymph than other females (Fig. 4).

thumbnail
Figure 5. Effect of Wolbachia on CFUs obtained from haemolymph samples.

Haemolymph samples from A. vulgare females infected or not by Wolbachia were streaked onto several agar media (CNA, MHA and Chocolate). On CNA [selective medium for Gram (+) bacteria], the mean number of CFUs obtained for haemolymph samples from C females was significantly higher than in A females or M females.

http://dx.doi.org/10.1371/journal.pone.0003286.g005

Discussion

Infection dynamics of vertically transmitted endosymbiotic bacteria is highly dependant on their host's reproductive success. However, symbionts such as Wolbachia often lead to physiological alterations which can negatively impact host fitness. Among potentially important effects, the impact on immunocompetence seems of particular interest in light of its fundamental role on host fitness. Two arthropod bacterial endosymbionts (Serratia symbiotica and Hamiltonella defensa) have been demonstrated to increase pea aphid resistance towards parasitoids showing that some vertically transmitted symbionts are able to improve immunocompetence [1], [33]. For Wolbachia, which are the most frequent endosymbiotic bacteria in arthropods, two recent studies suggest that they may interact with the host immune system and thus modify the host's ability to overcome infection by other parasites [19], [22]. In the present study, we showed that reduction of haemocyte density in A. vulgare was due to Wolbachia and not to difference in host genotypes. Such reduction is an indication of immunodepression as haemocyte load is a determinant factor in the ability of crustaceans to mount an efficient immune response against parasites [26]. However, differences in the effects of the two Wolbachia strains on A. vulgare were observed: C females had less haemocytes but also more intense septicaemia than M females. These results highly suggest that haemocyte density and intensity of septicaemia are linked and that, in A. vulgare, wVulC is a more important immunodepressing biotic factor than wVulM.

Three non exclusive hypotheses can be proposed to explain how wVulC triggers a decrease in haemocyte density. A first hypothesis involves a direct negative effect of Wolbachia on haemocytes survival via toxins. Such /Wolbachia/-toxins could for example interfere with apoptosis in haemocytes as previously described for other cell types [34], [35]. A second hypothesis is that the decrease in haemocyte density is due to the impact of Wolbachia load in haemocytes whereby high symbiotic densities in a cell would lead to its destruction as previously described in other tissues for wPop [36]. This hypothesis is further supported by previous studies in which wVulC has been shown to generate effects comparable to those of wPop when injected into foreign recipient hosts [3], [37]. However, haemocytes observed here by transmission electronic microscopy mainly exhibited low bacterial loads. A third hypothesis would be that the global physiological cost of Wolbachia on their hosts leads to a decrease in their immunocompetence due to a drop in haemocyte production and a reduced capacity to cure bacteria from the haemolymph.

Our data revealed that the differences in immunocompetence and survival, in the population of A. vulgare we studied, are due to Wolbachia strains they harbour. The strain wVulC was the most immunodepressing and also reduced host lifespan the most, suggesting that these two life history traits may be linked and showing that wVulC is clearly more virulent than wVulM. This difference in virulence between wVulC and wVulM seems not due to different titer or location in haemocytes between these two Wolbachia strains but can be interpreted in the light of population genetic works conducted on the same populations [27], [29]. Such studies showed that the wVulC strain was widely distributed and associated with all A. vulgare mitochondrial lineages while wVulM was restricted to particular host mitochondrial lineages. In the area where gravid females (i.e. F0) were sampled, the mitochondrial lineages associated with wVulM are very frequent [27], [29]. Taking into account these data, Cordaux et al. (2004) proposed a scenario in which wVulM is a locally adapted strain (i.e. resident) while wVulC is invasive and widely distributed all over the world. Such a scenario, associated with expected evolutionary trends, would suggest that local adaptation occurred between wVulM and local host genotypes leading to the observed attenuation of its virulence compared to wVulC.

Even if virulence seems to decrease during local adaptation processes, we have demonstrated here that Wolbachia symbiosis is costly and can lead to a reduced lifespan for A. vulgare. It is hard to understand selective forces which would promote and maintain such genomic conflicts between symbionts and their hosts in the context of vertically transmitted symbioses. This discrepancy can be seen as the consequence of various strategies adopted by symbionts in order to invade host populations. While symbionts such as those in the pea aphid may spread by increasing their host's immunocompetence [1], [33], Wolbachia rely on manipulating host reproduction which can generate indirect costs. Such costs would tend to keep the prevalence of Wolbachia at lower levels than those predicted by feminizing effects alone and could help explain the low frequency of symbiotic females observed in natural populations of A. vulgare [29].

Acknowledgments

We thank Maryline Raimond for technical support.

Author Contributions

Conceived and designed the experiments: CBV ML YC DB SS. Performed the experiments: CBV ML JH MJ SS. Analyzed the data: CBV ML MJ SS. Contributed reagents/materials/analysis tools: CBV JH. Wrote the paper: CBV ML MJ DB SS.

References

  1. 1. Oliver KM, Moran NA, Hunter MS (2005) Variation in resistance to parasitism in aphids is due to symbionts not host genotype. Proc Natl Acad Sci U S A 102: 12795–12800.
  2. 2. Werren JH (1997) Biology of Wolbachia. Annu Rev Entomol 42: 587–609.
  3. 3. Bouchon D, Rigaud T, Juchault P (1998) Evidence for widespread Wolbachia infection in isopod crustaceans: molecular identification and host feminization. Proc Biol Sci 265: 1081–1090.
  4. 4. Hoerauf A, Nissen-Pahle K, Schmetz C, Henkle-Duhrsen K, Blaxter ML, et al. (1999) Tetracycline therapy targets intracellular bacteria in the filarial nematode Litomosoides sigmodontis and results in filarial infertility. J Clin Invest 103: 11–18.
  5. 5. Dedeine F, Vavre F, Fleury F, Loppin B, Hochberg ME, et al. (2001) Removing symbiotic Wolbachia bacteria specifically inhibits oogenesis in a parasitic wasp. Proc Natl Acad Sci U S A 98: 6247–6252.
  6. 6. De Barro PJ, Hart PJ (2001) Antibiotic curing of parthenogenesis in Eretmocerus mundus (Australian parthenogenic form). Entomol Exp Appl 99: 225–230.
  7. 7. Dean MD (2006) A Wolbachia-associated fitness benefit depends on genetic background in Drosophila simulans. Proc Biol Sci 273: 1415–1420.
  8. 8. Dobson SL, Marsland EJ, Rattanadechakul W (2002) Mutualistic Wolbachia infection in Aedes albopictus: accelerating cytoplasmic drive. Genetics 160: 1087–1094.
  9. 9. Dong P, Wang JJ, Hu F, Jia FX (2007) Influence of wolbachia infection on the fitness of the stored-product pest Liposcelis tricolor (Psocoptera: Liposcelididae). J Econ Entomol 100: 1476–1481.
  10. 10. Weeks AR, Turelli M, Harcombe WR, Reynolds KT, Hoffmann AA (2007) From parasite to mutualist: rapid evolution of Wolbachia in natural populations of Drosophila. PLoS Biol 5: e114.
  11. 11. Hoffmann AA, Turelli M (1988) Unidirectional Incompatibility in Drosophila Simulans: Inheritance, Geographic Variation and Fitness Effects. Genetics 119: 435–444.
  12. 12. Hoffmann AA, Turelli M, Harshman LG (1990) Factors affecting the distribution of cytoplasmic incompatibility in Drosophila simulans. Genetics 126: 933–948.
  13. 13. Fleury F, Vavre F, Ris N, Fouillet P, Bouletreau M (2000) Physiological cost induced by the maternally-transmitted endosymbiont Wolbachia in the Drosophila parasitoid Leptopilina heterotoma. Parasitology 121 Pt 5: 493–500.
  14. 14. Tagami Y, Miura K, Stouthamer R (2001) How does infection with parthenogenesis-inducing Wolbachia reduce the fitness of Trichogramma? J Invertebr Pathol 78: 267–271.
  15. 15. Fry AJ, Palmer MR, Rand DM (2004) Variable fitness effects of Wolbachia infection in Drosophila melanogaster. Heredity 93: 379–389.
  16. 16. Huigens ME, Hohmann CL, Luck RF, Gort G, Stouthamer R (2004) Reduced competitive ability due to Wolbachia infection in the parasitoid wasp Trichogramma kaykai. Entomol Exp Appl 110: 115–123.
  17. 17. Snook RR, Cleland SY, Wolfner MF, Karr TL (2000) Offsetting effects of Wolbachia infection and heat shock on sperm production in Drosophila simulans: analyses of fecundity, fertility and accessory gland proteins. Genetics 155: 167–178.
  18. 18. Rigaud T, Moreau M (2004) A cost of Wolbachia-induced sex reversal and female-biased sex ratios: decrease in female fertility after sperm depletion in a terrestrial isopod. Proc Biol Sci 271: 1941–1946.
  19. 19. Fytrou A, Schofield PG, Kraaijeveld AR, Hubbard SF (2006) Wolbachia infection suppresses both host defence and parasitoid counter-defence. Proc Biol Sci 273: 791–796.
  20. 20. Lemaitre B, Hoffmann J (2007) The host defense of Drosophila melanogaster. Annu Rev Immunol 25: 697–743.
  21. 21. Brennan LJ, Keddie BA, Braig HR, Harris HL (2008) The endosymbiont Wolbachia pipientis induces the expression of host antioxidant proteins in an Aedes albopictus cell line. PLoS ONE 3: e2083.
  22. 22. Xi Z, Gavotte L, Xie Y, Dobson SL (2008) Genome-wide analysis of the interaction between the endosymbiotic bacterium Wolbachia and its Drosophila host. BMC Genomics 9: 1.
  23. 23. Bazzocchi C, Comazzi S, Santoni R, Bandi C, Genchi C, et al. (2007) Wolbachia surface protein (WSP) inhibits apoptosis in human neutrophils. Parasite Immunol 29: 73–79.
  24. 24. Jiggins FM, Hurst GD, Yang Z (2002) Host-symbiont conflicts: positive selection on an outer membrane protein of parasitic but not mutualistic Rickettsiaceae. Mol Biol Evol 19: 1341–1349.
  25. 25. Rigaud T, Souty Grosset C, Raimond R, Mocquard JP, Juchault P (1991) Feminizing endocytobiosis in the terrestrial crustacean Armadillidium vulgare Latr. (Isopoda): Recent acquisitions. Endocytobiosis & Cell Res 7: 259–273.
  26. 26. Jiravanichpaisal P, Lee BL, Soderhall K (2006) Cell-mediated immunity in arthropods: hematopoiesis, coagulation, melanization and opsonization. Immunobiology 211: 213–236.
  27. 27. Cordaux R, Michel-Salzat A, Frelon-Raimond M, Rigaud T, Bouchon D (2004) Evidence for a new feminizing Wolbachia strain in the isopod Armadillidium vulgare: evolutionary implications. Heredity 93: 78–84.
  28. 28. Verne S, Johnson M, Bouchon D, Grandjean F (2007) Evidence for recombination between feminizing Wolbachia in the isopod genus Armadillidium. Gene 397: 58–66.
  29. 29. Rigaud T, Bouchon D, Souty-Grosset C, Raimond R (1999) Mitochondrial DNA polymorphism, sex ratio distorters and population genetics in the isopod Armadillidium vulgare. Genetics 152: 1669–1677.
  30. 30. Kocher TD, Thomas WK, Meyer A, Edwards SV, Paabo S, et al. (1989) Dynamics of mitochondrial DNA evolution in animals: amplification and sequencing with conserved primers. Proc Natl Acad Sci U S A 86: 6196–6200.
  31. 31. Zhou W, Rousset F, O'Neil S (1998) Phylogeny and PCR-based classification of Wolbachia strains using wsp gene sequences. Proc Biol Sci 265: 509–515.
  32. 32. Herbiniere J, Braquart-Varnier C, Greve P, Strub JM, Frere J, et al. (2005) Armadillidin: a novel glycine-rich antibacterial peptide directed against gram-positive bacteria in the woodlouse Armadillidium vulgare (Terrestrial Isopod, Crustacean). Dev Comp Immunol 29: 489–499.
  33. 33. Oliver KM, Campos J, Moran NA, Hunter MS (2008) Population dynamics of defensive symbionts in aphids. Proc Biol Sci 275: 293–299.
  34. 34. Pannebakker BA, Loppin B, Elemans CP, Humblot L, Vavre F (2007) Parasitic inhibition of cell death facilitates symbiosis. Proc Natl Acad Sci U S A 104: 213–215.
  35. 35. Siozios S, Sapountzis P, Ioannidis P, Bourtzis K (2008) Wolbachia symbiosis and insect immune response. Insect Science 15: 89–100.
  36. 36. Min KT, Benzer S (1997) Wolbachia, normally a symbiont of Drosophila, can be virulent, causing degeneration and early death. Proc Natl Acad Sci U S A 94: 10792–10796.
  37. 37. Juchault P, Legrand JJ, Martin G (1974) Action interspécifique du facteur épigénétique féminisant responsable de la théygénie et de l'intersexualité du Crustacé Armadillidium vulgare (Isopode Oniscoïde). Annales d'Embryologie et de Morphogenèse 7: 265–276.