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Wolbachia-Host Interactions: Host Mating Patterns Affect Wolbachia Density Dynamics

  • Dong-Xiao Zhao,

    Affiliation Department of Entomology, Nanjing Agricultural University, Nanjing, Jiangsu, China

  • Xiang-Fei Zhang,

    Affiliation Department of Entomology, Nanjing Agricultural University, Nanjing, Jiangsu, China

  • Da-Song Chen,

    Affiliation Department of Entomology, Nanjing Agricultural University, Nanjing, Jiangsu, China

  • Yan-Kai Zhang,

    Affiliation Department of Entomology, Nanjing Agricultural University, Nanjing, Jiangsu, China

  • Xiao-Yue Hong

    xyhong@njau.edu.cn

    Affiliation Department of Entomology, Nanjing Agricultural University, Nanjing, Jiangsu, China

Wolbachia-Host Interactions: Host Mating Patterns Affect Wolbachia Density Dynamics

  • Dong-Xiao Zhao, 
  • Xiang-Fei Zhang, 
  • Da-Song Chen, 
  • Yan-Kai Zhang, 
  • Xiao-Yue Hong
PLOS
x

Abstract

Wolbachia are maternally inherited intracellular bacteria that infect a wide range of arthropods and cause an array of effects on host reproduction, fitness and mating behavior. Although our understanding of the Wolbachia-associated effects on hosts is rapidly expanding, our knowledge of the host factors that mediate Wolbachia dynamics is rudimentary. Here, we explore the interactions between Wolbachia and its host, the two-spotted spider mite Tetranychus urticae Koch. Our results indicate that Wolbachia induces strong cytoplasmic incompatibility (CI), increases host fecundity, but has no effects on the longevity of females and the mating competitiveness of males in T. urticae. Most importantly, host mating pattern was found to affect Wolbachia density dynamics during host aging. Mating of an uninfected mite of either sex with an infected mite attenuates the Wolbachia density in the infected mite. According to the results of Wolbachia localization, this finding may be associated with the tropism of Wolbachia for the reproductive tissue in adult spider mites. Our findings describe a new interaction between Wolbachia and their hosts.

Introduction

Endosymbiotic bacteria are very common in invertebrates [1]. The α-proteobacterium Wolbachia pipientis, one of the most common endosymbionts, infects an estimated 25–76% of all insect species, as well as many other arthropod and filarial nematode species [2], [3], [4]. Wolbachia have a remarkable variety of effects on host biology, including reproduction, fitness and mating behavior.

Vertically inherited by transovarial transmission, Wolbachia have evolved a number of different manipulations of host reproduction which impart a selective advantage for the bacteria [5], [6]. Within arthropods, these manipulations include feminization, male killing, parthenogenesis, and cytoplasmic incompatibility (CI), the inability of infected males to successfully fertilize eggs from uninfected females [7]. Cytological analyses suggest that Wolbachia target cell cycle regulatory proteins. CI results from delayed nuclear envelope breakdown of the male pronucleus [8]. CI has been described in most insect orders (Diptera, Coleoptera, Hymenoptera, Orthoptera, and Lepidoptera) [7], in mites [9], [10], [11], [12], and in the terrestrial isopod Porcellio dilatatus [13]. Although most molecular mechanisms employed by Wolbachia to manipulate the host cytoplasmic machinery and to ensure vertical transmission have not been discovered, intensive research in host-Wolbachia interactions and genomes of Wolbachia strains have provided important hints to reveal the molecular mechanism [14].

The interaction between Wolbachia and its hosts can evolve rapidly over time [15], leading to both positive and negative effects on host fitness, and even to the extreme case where Wolbachia become essential for host fertility. In some cases, such as in the parasitoid wasp Leptopilina heterotoma, Wolbachia can negatively affect fecundity, locomotor performance and longevity [16]. On the other hand, super Wolbachia infection (co-infection with two or more Wolbachia strains) has been reported to improve fecundity in Aedes albopictus, accelerating the rate of Wolbachia invasion in the host population [17]. Furthermore, oogenesis of the parasitic wasp Asobara tabida is dependent on Wolbachia [18].

One of the most interesting discoveries about Wolbachia infection is that infected Drosophila simulans males produce less sperm than their uninfected counterparts [19]. This led to the hypothesis that Wolbachia infection affects the mating behavior of males as a consequence of this physiological cost. Several reports have provided support for this hypothesis. Champion et al. examined the impact of Wolbachia on mating behavior in male Drosophila melanogaster and D. simulans, and showed that infected males mate at a higher rate than uninfected males in both species [20]. In addition, male D. simulans exhibited some preference for mating with females of the same infection status [21]. More importantly, Wolbachia promote speciation of Drosophila melanogaster by contributing to the level of mate discrimination between diverging D. melanogaster populations [22].

Although it is clear that Wolbachia affect the reproduction and behavior of hosts, do hosts also affect the dynamics of Wolbachia? We used the two-spotted spider mite –Wolbachia symbiosis to address this question. The two-spotted spider mite Tetranychus urticae Koch is a worldwide pest threatening many agricultural crops and fruit trees. We previously showed that Wolbachia was widely distributed in Chinese populations of T. urticae. All populations were found to be infected with Wolbachia, with the infection rate ranging from 2.5 to 85% [23]. Several studies have shown that Wolbachia can induce variable reproduction and fitness effects on the two-spotted spider mite T. urticae [9], [24], [25], [26]. Wolbachia can also affect oviposition and mating behavior of T. urticae [27]. In this study, we explored the Wolbachia-effects on the spider mite host by measuring the strength of CI, sex ratio, fecundity, survival and male mating competitiveness between infected and uninfected strains under laboratory conditions. In order to improve our understanding of interactions between Wolbachia and the two-spotted spider mite T. urticae, we also determined whether the mite influences Wolbachia dynamics by examining the relative density of Wolbachia in mites whose mates had different infection statuses. In addition, we studied Wolbachia spatial localization in the adults using fluorescence in situ hybridization (FISH).

Materials and Methods

Preparation of Spider Mite Lines

Ethics statement.

No specific permits were required for the described field studies. (a) No specific permissions were required for the collection because the spider mite is a pest on the soybean; (b) The location is not privately-owned in any way; (c) The field studies did not involve endangered or protected species.

The two-spotted spider mite T. urticae was collected from soybean [Glycine max (L.) Merr.] leaves in Hohhot, Inner Mongolia, northeast China in July 2010. Mites were reared on a leaf of the common bean (Phaseolus vulgaris L.) placed on a water-saturated sponge mat in Petri dishes (dia. 9) at 25±1°C, 60% r.h. and under L16-D8 conditions.

To evaluate the effects of Wolbachia on spider mites, 100% infected and 100% uninfected lines were prepared. Females from the teleiochrysalis stage were allowed to lay eggs without being crossed with males. The eggs were reared until adulthood (males). After the males reached sexual maturity, they were backcrossed with the mothers. Then, the female adults were transferred to new leaf discs and were allowed to lay eggs for 3–5 days. The females were checked for Wolbachia infection status by PCR amplification. The eggs were separately reared on new leaf discs depending on the infection status of the mother. The above process was continued for three to four generations until a 100% infected population was obtained. The eggs of the uninfected mothers were reared to establish the uninfected line.

DNA Extraction and Diagnostic PCR

DNA was extracted by homogenizing a single adult in a 25 µl mixture of sodium chloride-Tris-EDTA (STE) buffer (100 mM NaCl, 10 mM Tris-HCl, 1 mM EDTA, pH 8.0) and proteinase K (10 mg/ml, 2 µl) in a 1.5 ml Eppendorf tube. The mixture was incubated at 37°C for 30 min and later 95°C for 5 min. The samples were centrifuged briefly, and used immediately for the PCR reactions or stored at −20°C for later use.

A fragment of the gene encoding the Wolbachia surface protein wsp was amplified by PCR from samples using primers wsp81F and wsp691R [28]. We also amplified five Wolbachia housekeeping genes for multi-locus sequence typing (MLST) analysis to determine the number of Wolbachia strains in this spider mite population [29]. PCR reactions were run in 25 µl buffer using the TAKARA (Takara, Shuzo, Otsu, Japan) Taq kit: 16.3 µl H2O, 2.5 µl 10×buffer, 1.5 µl of 2.5 mM deoxyribonucleotide triphosephates (dNTPs), 1.5 µl of 25 mM MgCl2, 0.2 µl Taq polymerase (5 U/µl, Takara), 2 µl sample and 1 µl primers (10 mM each). Cycling conditions were 94°C for 2 min followed by 40 cycles of 94°C for 30 s, 52°C for 45 s and 72°C for 1 min and finally 72°C for 7 min. For samples failing to amplify Wolbachia genes, primers COI-forward and COI-reverse [30] were used to amplify mitochondria DNA as a positive control for template DNA quality.

Amplified fragments were purified using a Gel Extraction Mini kit (Watson, Shanghai, China). Then, the distinct single-band amplicons were cloned into pGEM T-Easy Vector (Promega, Madison, WI, USA) and the positive clones were screened and finally confirmed by direct sequencing.

Cross Experiments

In order to determine reproductive compatibility in intra-population crosses, four cross combinations were carried out: uninfected females were crossed with uninfected males, uninfected females were crossed with infected males, infected females were crossed with uninfected males, and infected females were crossed with infected males. Female teleiochrysalids, the last developmental stage before adult emergence, were placed with two males on the same leaf disk. We used 1-day-old virgin males produced as a cohort by groups of females isolated as teleiochrysalids. This procedure was designed to avoid the potential decrease of the Wolbachia effect due to male ageing or repeated consecutive mating. Males were discarded 2 days after the females’ eclosion, and mated females were allowed to oviposit for 5 days. Eggs on leaf discs were checked daily to determine the hatchability, sex ratio (% daughters) and mortality of offspring. The effects of infection on female fecundity were tested by comparing the number of eggs laid in the first 5 days by infected and uninfected females who were crossed with uninfected males (♀u×♂u and ♀w×♂u) to exclude any influence of differences in male fertility due to infection. To normalize the data, log transformation was used for the number of eggs laid per female, and arcsine square root transformation was used for egg hatchability, sex ratio and mortality. The transformed data which were normally distributed (Kolmogorov-Smirnov test) were analyzed with one-way analysis of variance (ANOVA), and the means were compared using Tukey-HSD test (SPSS 17.0).

Survival Assessment

Age-specific survival of infected and uninfected lines was measured. Survivorship in infected and uninfected strains was measured by placing a total of 25 virgin females and 25 virgin males of the same infection status on the same leaf. Three leaves were used for each Wolbachia infection status. Adult females were monitored at 24-h intervals, during which dead mites were removed and counted. The test was stopped when all the mites had died.

Survival curves for infected and uninfected females were compared using the Kaplan-Meier method [31] and log-rank test [32] (SPSS 17.0).

Male Mating Competitiveness

In order to compare the mating competitiveness of uninfected and infected males, cross experiments were designed according to the method of Calvitti M et al [33]. Three groups of crosses were carried out, including compatible cross (cross A, between uninfected males and females), incompatible cross (cross B, between uninfected females and infected males), and competition study (cross C, between uninfected females and both infected and uninfected males). The competition study was performed by keeping uninfected females and both infected and uninfected males (♀u×[♂ u+♂ w]) on the same leaf disk. Four replicates of each cross were performed. Female teleiochrysalids, the last developmental stage before adult emergence, were isolated to assure virginity. Newly emerged females and males were kept on the same leaf disk for 3 days to mate. Females were added after all of the males had been put on the leaf because of the males’ high escape frequency. After oviposition, all females were put on the leaf disks separately. The eggs that hatch successfully are laid by fertile females (mating with uninfected males). By contrast, the eggs that fail to hatch are laid by incompatible females (mating with infected males). In T. urticae, females may mate multiply but there is no evidence that they can select sperm once inseminated [34]. Therefore, mating competitiveness between infected and uninfected males can be assessed by comparing the number of compatible and incompatible females. If there were no difference in mating competitiveness between infected and uninfected males, the number of compatible females and incompatible females would be approximately equal.

Quantitative PCR

Quantitative PCR (Q-PCR) was performed using an ABI PRISM 7300 Sequence Detection System (Applied Biosystems) to estimate the density of Wolbachia in T. urticae. The 20 µl reaction mixture consisted of 10 µl 2×SYBRq Premix Ex Taq (Takara, Shuzo, Otsu, Japan), 0.4 µl 10 mM of each primer, 0.4 µl 50×ROX Reference Dye, 2 µl DNA template and 6.8 µl H2O in single wells of a 96-well plate (PE Applied Biosystems). The Q-PCR cycling conditions included 1 cycle (10 s 95°C) followed by 40 cycles (5 s 95°C, 31 s 60°C), and finally 1 cycle (15 s 95°C, 1 min 60°C, 15 s 95°C). Wolbachia wsp gene was quantified using the primer set QwspF (5′-GCA GCG TAT GTA AGC AAT CC-3′) and QwspR (5′-ATA ACG AGC ACC AGC ATA AAG-3′), which amplified a wsp fragment (137 bp). To estimate the Wolbachia densities, the host the β-actin gene was quantified using the primer set QactinF (5′-CCA TTG AAT CCA AAA GCT AAC CGT-3′) and QactinR (5′-CCA TCA CCA GAG TCG AGG ACA-3′) in the same samples, which amplified a β-actin fragment (149 bp). We used absolute quantitative PCR to determine wsp and β-actin copy numbers. Standard curves were plotted using a 10-fold dilution series consisting of 10−7 to 10−3 dilutions of the DNA standards prepared from plasmid DNA. The quality and concentration of all purified standard DNA were measured by OD absorbance at 260 nm. The copy numbers of each wsp and β-actin genes were calculated from the intensity of the fluorescence on the basis of the standard curves. Wolbachia density was expressed in terms of the number of wsp copies per β-actin copy. Wolbachia densities of mites which were virginal, mated to infected ones, and mated to uninfected ones were measured. In order to obtain mites of different mating patterns, newly emerged infected females and males were kept separately and divided into three groups. In the first group, they were kept alone to obtain virgin males and females. In the second group, they were kept with the infected mates for 24 hours. Similarly, in the third group, they were kept with the uninfected mates for 24 hours. All measurements of Wolbachia densities in females and males were taken from five ages (2 d, 4 d, 6 d, 8 d, and 10 d) of adults. We compared Wolbachia densities in mites of different mating patterns at each age, in order to examine the relationship between the host mating pattern and the density dynamics of Wolbachia. DNA of single mites was extracted using the above method. Three replicates were run and averaged for each DNA sample. Negative controls were included in all amplification reactions.

To compare Wolbachia densities in mites of different mating patterns, we analyzed data of each age with one-way analysis of variance (ANOVA) and means were compared using the Tukey-HSD test (SPSS17.0).

Fluorescence in situ Hybridization (FISH)

The fluorescence in situ hybridization (FISH) procedure generally followed the method of Yuval Gottlieb et al [35], with slight modifications. Adults were collected with a brush pen under a Nikon SMZ800 stereoscopic microscope (Nikon, Japan). After being washed in 50 µl of phosphate buffered saline (PBS: 8 g NaCl, 0.2 g KCl, and 1.44 g Na2HPO4 in 1 liter of distilled water, pH 7.2), specimens were put directly into Carnoy’s fixative (chloroform: ethanol: glacial acetic acid, 6∶3∶1) and fixed overnight. After fixation, the samples were decolorized in 6% H2O2 in ethanol for two hours. Hybridization was performed at 45°C in a dark moisture chamber. After a 30 min pre-incubation period in hybridization buffer (0.9 M NaCl/20 mM Tris·HCl/5 mM EDTA/0.1% SDS/10×Denhardt’s solution), probes were added and incubation was continued for 3 hr. Post-hybridization washes were performed 5 min with 2×SSC pH 7.0 at 45°C, 5 min with 1×SSC pH 7.0 and 5 min with 0.5×SSC pH 7.0 at 37°C, all with agitation. In the end, the adults were put on clean slides (cleaned with alcohol) and were mounted in Vectashield medium (Vector Laboratories). Specific oligonucleotide probes were designed by sequence alignment of Wolbachia 16 S rDNA. Two Wolbachia probes 5′ end labeled with rhodamine described by Heddi et al [36] were used to increase the signals: W1, 5′-AATCCGGCCGARCCGACCC-3′, and W2, 5′-CTTCTGTGAGTACCGTCATTATC-3′. Stained and mounted samples were viewed under a ZEISS LSM 700 confocal microscope (Carl Zeiss, Germany). Wolbachia appear as fluorescent red spots. Specificity of the detection was confirmed using the Wolbachia-free mites as a control.

Results

Multi-locus Sequence Typing (MLST) for Wolbachia Infecting T. urticae

We amplified the wsp gene and a set of housekeeping genes, including coxA, fbpA, gatB, ftsZ and hcpA, from Wolbachia infecting T. urticae. The sequences were submitted to the GenBank database (GenBank numbers: wsp: JX094384; coxA: JX094415; fbpA: JX094395; gatB: JX094426; ftsZ: JX094402; hcpA: JX094409). The MLST results show that there is only one strain of Wolbachia belonging to supergroup B in this spider mite population [28].

Strength of Cytoplasmic Incompatibility

Wolbachia showed a high level of CI in the T. urticae population. The number of aborted eggs was significantly different among the four crosses (Table 1). In the predicted incompatible cross (♀u×♂w), on average, 45.0% of all eggs hatched, compared to 93.5–97.3% in the other crosses. The sex ratio of the offspring from the incompatible cross was significantly lower than the sex ratios from the compatible crosses. In addition, the incompatible cross displayed a significantly higher mortality than the compatible crosses.

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Table 1. Results of crossing experiments between infected (w) and uninfected (u) mites.

https://doi.org/10.1371/journal.pone.0066373.t001

Effects of Wolbachia Infection on Host Fecundity and Longevity

We compared fecundity of crosses in which females were crossed with uninfected males to exclude any influence of differences in male fertility due to infection. Interestingly, infected females laid significantly more eggs than uninfected females (independent t-test, P<0.001) (Table 1). For infected females, mating with infected males even reduced the number of eggs laid (independent t-test, P<0.001) (Table 1). Survival curves indicated that there was no difference between the mean longevities of infected (15.32±3.27 days) and uninfected females (14.74±1.78 days) (Fig. 1).

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Figure 1. Comparison of Wolbachia effect on female longevity in T. urticae.

W, Wolbachia infected strains; U, uninfected strains. Survivor curves for individual hosts were compared using the Kaplan-Meier method and log-rank test.

https://doi.org/10.1371/journal.pone.0066373.g001

Male Mating Competitiveness

According to the results shown in Table 2, no significant differences in the number of compatible and incompatible females were found in cross C (♀u×[♂u+♂ w]) (X2 tests, P>0.05), indicating that infected and uninfected males had the same chance to mate with uninfected females. These results indicate that Wolbachia has no effects on male mating competitiveness in T. urticae.

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Table 2. Mating competitiveness of T. urticae based on the mean number of compatible females and incompatible females.

https://doi.org/10.1371/journal.pone.0066373.t002

Wolbachia Density

Wolbachia densities (as determined by wsp gene relative copy number) in females rose rapidly with age (Fig. 2A). In the virgin females, Wolbachia density rose from (1.20±0.06) to (3.65±0.14) step by step from the second day to the tenth day of the mite life span. In addition, Wolbachia density increased more rapidly in females mated with infected males (from (1.52±0.07) to (3.69±0.16)) than in females mated with uninfected males (from (1.60±0.10) to (3.04±0.13)). Specifically, from the second day to the tenth day (only except the sixth day), females mated with infected males contain more Wolbachia than the females mated with uninfected males. Wolbachia replicates most rapidly in virgin females, while it replicates most slowly in females that mated with uninfected males (Fig. 2B). In male adults of T. urticae, Wolbachia density increased in the younger ones but decreased in the older ones. Wolbachia density began to decrease earlier in virgin males than in males that had mated with infected and uninfected females, indicating that mating behavior had a negative effect on the density of Wolbachia. Interestingly, Wolbachia density in males that mated with uninfected females was comparatively lower than the densities in the other two groups of males (virgin males and males mated with infected females). It also increased very little during the lifespan of the mite. In contrast, mating with infected females was found to be beneficial for the maintenance of Wolbachia. During the first 8 days of the males’ life span, the density of Wolbachia increased most rapidly. However, the density decreased only slightly from the eighth day to the tenth day. As a result, on the tenth day of the life span, Wolbachia density in the males that had mated with infected females was significantly higher than it was in virgin males or males that had mated with uninfected females. Together, these results indicate that mating pattern of hosts affects the dynamics of Wolbachia density. Mating with uninfected mites attenuated Wolbachia in the infected mites.

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Figure 2. Dynamics of Wolbachia density during aging of female (A) and male (B) spider mite T. urticae expressed in terms of number of wsp copies per β-actin copy.

(a) virgin females (males); (b) females (males) mated with infected males (females); (c) females (males) mated with uninfected males (females). Each point is the average of three measurements of 12 samples. Bars indicate standard errors. NS, not significant; *P<0.05; **P<0.01; ***P<0.001.

https://doi.org/10.1371/journal.pone.0066373.g002

Wolbachia Localization

Wolbachia localization was carried out in more than 50 adults taken from six ages (2 d, 4 d, 6 d, 8 d, 10 d and 13 d). However, we found that there was no age effect on Wolbachia localization. Generally, Wolbachia are located in the ovaries in the female abdomen and the gnathosoma (Fig. 3A and B). In male mites, although the signal specific to Wolbachia can be detected throughout the body, there is higher intensity in testes and gnathosoma (Fig. 3C and D).

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Figure 3. FISH of T. urticae adults.

(A, B) Wolbachia (arrow) in a female abdomen and gnathosoma (combined Z sections). (C, D) Wolbachia (arrow) in male gnathosoma and abdomen (combined Z sections). Right panels, bright field and fluorescence; left panels, fluorescence only.

https://doi.org/10.1371/journal.pone.0066373.g003

In pregnant females, Wolbachia signals were observed only in the developing embryo and were hardly detectable in other parts of the female body (Figure 4A–D), indicating that Wolbachia is ovarially transferred from the mother to the offspring through the egg. Wolbachia was also localized in egg-laying females (Fig. 4A and B). Interestingly, in our FISH analysis, most Wolbachia were transferred into the egg. At this stage, Wolbachia were present only at low density and exhibited a weak signal intensity in ovaries and in the middle of the gnathosoma (Fig. 4C and D). No signals were observed in the control (Fig. 5).

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Figure 4. FISH of T. urticae females who were pregnant or were laying an egg.

(A, B) Wolbachia (arrow) concentrated in the developing embryo in the female abdomen (combined Z sections). (C, D) Wolbachia (arrow) were transovarially transferred from the mother to the offspring through the egg (combined Z sections). Right panels, bright field and fluorescence; left panels, fluorescence only.

https://doi.org/10.1371/journal.pone.0066373.g004

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Figure 5. FISH of an uninfected T. urticae adult as a negative control.

No Wolbachia specific signal was detected throughout the body. (A) fluorescence panel only (combined Z sections); (B) bright field and fluorescence panel (combined Z sections).

https://doi.org/10.1371/journal.pone.0066373.g005

Discussion

Wolbachia have attracted increasing attention over the past decade because an array of effects on their hosts may be used as a gene-driving system for genetic control of insect and other arthropod vectors and pests [37], [38], [39]. However, factors that can influence the densities of Wolbachia are rarely considered in laboratory studies, making the study of the interaction between Wolbachia and host unidirectional. In this study, we explored the relationships between Wolbachia and the spider mite T. urticae from a bidirectional perspective. We investigated the effects of Wolbachia on host reproduction, fitness, mating behavior (male mating competitiveness), as well as the effects of mating patterns on the density dynamics of Wolbachia during adult aging. Inbreeding effects on fitness traits differ between isofemale lines. As a result, it can be challenging to determine whether fitness differences are induced by Wolbachia or by the nuclear background [40]. In order to avoid inbreeding effects, each of the lines (infected line and uninfected line) used in this research was composed of more than 3 isofemale lines. We observed the fitness traits on different host backgrounds, and the effects were repeatable between infected and uninfected lines. Therefore, the fitness differences between infected and uninfected lines were induced by Wolbachia infection not by inbreeding effects.

Wolbachia infecting this spider mite population cause strong CI. CI is expressed as a significant reduction in egg hatchability and sex ratio (%females) in crosses between uninfected females and infected males. Interestingly, there is a strong reduction in the number of daughters in incompatible crosses, whereas male production was not significantly different in the compatible crosses. This pattern suggests that fertilized eggs, which would normally develop into females, have a higher mortality, and is concordant with the female mortality type of CI [9], [41], [42], [43]. However, this CI-inducing Wolbachia strain has no effect on the longevity of the female mites. In previous studies, Xie et al. reported both positive and negative effects of Wolbachia infection on longevity of T. urticae in China [26]. Similarly, both Wolbachia-associated benefits and costs in survival were found in Drosophila melanogaster [44], [45]. The different effects of Wolbachia on hosts have been attributed to several factors, including Wolbachia strain [46] and the nuclear background [47]. From an evolutionary perspective, bacteria and their hosts represent components of a dynamic interacting system that can evolve rapidly over time, which can explain the inconsistent effects of Wolbachia on host fitness detected in the above studies [15].

Several studies have investigated the relationship between Wolbachia and host mating behavior. Due to their effects on levels of pre- and postmating reproductive incompatibility, cytoplasmic-incompatible Wolbachia have been proposed to promote host speciation. The study by Koukou et al shows that the presence of Wolbachia (or another undetected bacterial associate) contribute to the level of pre-mating isolation between Drosophila melanogaster populations, which could be relevant to some speciation events [22]. In Drosophila paulistorum, there is a quantitative shift of Wolbachia densities from extremely low in native hosts to intermediate in interstrain hybrids, strongly suggesting that the causative agent of incipient D. paulistorum speciation is Wolbachia [48]. Furthermore, Wolbachia have strong effects on premating isolation between D. paulistorum semispecies in a titer-dependent manner. These results indicate that Wolbachia have the potential to trigger pre- and postmating isolation. In the present study, we found that different host mating patterns induced different Wolbachia density dynamics during host aging. However, no differences were observed between uninfected and infected males with respect to mating competitiveness. In order to reveal whether this cytoplasmic-incompatible Wolbachia plays a significant role in driving natural speciation of T. urticae, additional studies are needed to determine how the presence of Wolbachia alters mate behavior of T. urticae.

Our FISH results reveal that Wolbachia are more abundant in the reproductive tissues in both male and female T. urticae. Clark et al [49] proposed that Wolbachia infection in spermatocytes and then spermatids during sperm development is required for CI expression. Wolbachia induce high levels of CI only when spermatocytes or spermatids harbor this microbe. Wolbachia infection of somatic cyst cells, although sometimes present at high levels, does not result in significant CI expression. In addition, the study of Veneti et al revealed a strong positive correlation between CI expression levels and the percentage of infected sperm cysts [50]. On the basis of these theories, together with our FISH results and cross experiment results, we confer that the high level of CI expression in this T. urticae population results from the high percentage of infected sperm cysts and the presence of Wolbachia within the spermatocytes and spermatids of T. urticae. For Wolbachia to become fixed in a population, the bacterial cells must be transmitted to the next generation through the germline. It is important that Wolbachia were detected in the eggs in pregnant and egg-laying females, which suggests vertical transmission of Wolbachia. Until recently, it was unknown how Wolbachia enter the germline. Frydman et al answered this question by showing that Wolbachia accumulate in the somatic stem cell niche (SSCN) of Drosophila germarium, which is the site of egg chamber formation [51]. Further studies are needed to determine whether Wolbachia exhibits somatic stem cell niche tropism in T. urticae. Interestingly, Wolbachia densities are high in eggs present in pregnant mites. Meanwhile, the density measurement results indicate that Wolbachia density increases concomitantly with days after female emergence. These observations suggest that Wolbachia densities in females increase with increasing egg production. However, why would Wolbachia reside in the gnathosoma of mites? Why is Wolbachia signal less clear in pregnant females? More work remains to be performed to resolve these questions. To our knowledge, this is the first report to describe the localization of Wolbachia in spider mite adults.

Whereas our understanding of the Wolbachia-associated effects on hosts is rapidly expanding, our knowledge of the host factors that mediate Wolbachia dynamics is rudimentary. In this research, we reveal that host mating pattern affects Wolbachia density dynamics during host aging. Specifically, mating of an uninfected mite of either sex with an infected mite attenuates the Wolbachia density in the infected mite. This is the first empirical evidence indicating that host mating pattern affects Wolbachia density dynamics. During copulation, reproductive tissues probably experience high metabolic activity. In addition, we found a tropism of Wolbachia for the reproductive tissue in this spider mite population. Therefore, Wolbachia can be affected directly by host mating pattern. This is another phenotypic consequence of the tropism of Wolbachia for the hosts’ reproductive tissue. Recent reports have shown that Wolbachia in host reproductive tissues mediate the host cellular processes, such as mitotic activity and programmed cell death, which suggests that host cells and Wolbachia interact [51], [52], [53]. Our finding that Wolbachia density in males began to decline earlier than in females and the previous finding that Wolbachia replication is dependent on host cell replication [54] suggest that male host cells undergo earlier senescence and death than female host cells.

Our findings provide new avenues by which Wolbachia interacts with the host, indicating an urgent need to reveal the nature of the interaction between Wolbachia and their hosts.

Acknowledgments

We thank Prof. Ary A. Hoffmann of the Department of Genetics, Centre for Environmental Stress and Adapatation Research, University of Melbourne, Australia for his valuable comments and suggestions on the early version of the manuscript. We also thank Xiao-Feng Xue, Jing-Tao Sun, Si-Xia Yang and Hao-Sen Li of the Department of Entomology, Nanjing Agricultural University (NJAU) for help with the collection of Tetranychus urticae population. We are grateful to the undergraduate students Mei-Jing Lan and Xue-Fei Jiang of NJAU for their kind help with experiments.

Author Contributions

Performed the experiments: DXZ XFZ DSC. Analyzed the data: DXZ YKZ. Wrote the paper: XYH DXZ. Conceived the project: XYH. Designed the experiments: XYH DXZ.

References

  1. 1. Corsaro D, Venditti D, Padula M, Valassina M (1999) Intracellular life. Crit Rev Microbiol 25: 39–79.
  2. 2. Hilgenboecker K, Hammerstein P, Schlattmann P, Telschow A, Werren JH (2008) How many species are infected with Wolbachia? A statistical analysis of current data. Fems Microbiol Lett 281: 215–220.
  3. 3. Jeyaprakash A, Hoy MA (2000) Long PCR improves Wolbachia DNA amplification: wsp sequences found in 76% of sixty-three arthropod species. Insect Mol Biol 9: 393–405.
  4. 4. Zug R, Hammerstein P (2012) Still a host of hosts for Wolbachia: Analysis of recent data suggests that 40% of terrestrial arthropod species are infected. PLoS ONE 7 (6): e38544.
  5. 5. Werren JH (1997) Biology of Wolbachia. Annu Rev Entomol 42: 587–609.
  6. 6. Werren JH, Baldo L, Clark ME (2008) Wolbachia: master manipulators of invertebrate biology. Nature Rev Microbiol 6: 741–751.
  7. 7. Stouthamer R, Breeuwer JAJ, Hurst GDD (1999) Wolbachia pipientis: Microbial manipulator of arthropod reproduction. Annu Rev Microbiol 53: 71–102.
  8. 8. Tram U, Sullivan W (2002) Rote of delayed nuclear envelope breakdown and mitosis in Wolbachia-induced cytoplasmic incompatibility. Science 296: 1124–1126.
  9. 9. Breeuwer JAJ (1997) Wolbachia and cytoplasmic incompatibility in the spider mites Tetranychus urticae and T. turkestani. Heredity 461 (79): 41–47.
  10. 10. Lu MH, Zhang KJ, Hong XY (2012) Tripartite associations among bacteriophage WO, Wolbachia, and host affected by temperature and age in Tetranychus urticae. Exp Appl Acarol 58: 207–220.
  11. 11. Zhu LY, Zhang KJ, Zhang YK, Ge C, Gotoh T, et al. (2012) Wolbachia strengthens Cardinium-induced cytoplasmic incompatibility in the spider mite Tetranychus piercei McGregor. Curr Microbiol 65: 516–523.
  12. 12. Zhao DX, Chen DS, Ge C, Gotoh T, Hong XY (2013) Multiple infections with Cardinium and two strains of Wolbachia in the spider mite Tetranychus phaselus Ehara: revealing new forces driving the spread of Wolbachia. PLoS ONE 8 (1): e54964.
  13. 13. Rousset F, Bouchon D, Pintureau B, Juchault P, Solignac M (1992) Wolbachia endosymbionts responsible for various alterations of sexuality in arthropods. Proc R Soc Lond Ser B 250: 91–98.
  14. 14. Saridaki A, Bourtzis K (2010) Wolbachia: more than just a bug in insects genitals. Curr Opin Microbiol 13: 67–72.
  15. 15. Weeks AR, Turelli M, Harcombe WR, Tracy Reynolds K, Hoffmann AA (2007) From parasite to mutualist: rapid evolution of Wolbachia in natural populations of Drosophila. PLoS Biol 5: 997–1005.
  16. 16. 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: 493–500.
  17. 17. Dobson SL, Rattanadechakul W, Marsland EJ (2004) Fitness advantage and cytoplasmic incompatibility in Wolbachia single- and superinfected Aedes albopictus. Heredity 93: 135–142.
  18. 18. 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 USA 98: 6247–6252.
  19. 19. 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.
  20. 20. de Crespigny FEC, Pitt TD, Wedell N (2006) Increased male mating rate in Drosophila is associated with Wolbachia infection. J Evol Biol 19: 1964–1972.
  21. 21. de Crespigny FEC, Wedell N (2007) Mate preferences in Drosophila infected with Wolbachia? Behav Ecol Sociobiol 61: 1229–1235.
  22. 22. Koukou K, Pavlikaki H, Kilias G, Werren JH, Bourtzis K, et al. (2006) Influence of antibiotic treatment an Wolbachia curing on sexual isolation among Drosophila melanogaster cage populations. Evolution 60 (1): 87–96.
  23. 23. Xie L, Miao H, Hong XY (2006) The two-spotted spider mite Tetranychus urticae Koch and the carmine spider mite Tetranychus cinnabarinus (Boisduval) in China mixed in their Wolbachia phylogenetic tree. Zootaxa 1165: 33–46.
  24. 24. Perrot-Minnot MJ, Cheval B, Migeon A, Navajas M (2002) Contrasting effects of Wolbachia on cytoplasmic incompatibility and fecundity in the haplodiploid mite Tetranychus urticae. J Evol Biol 15: 808–817.
  25. 25. Vala F, Breeuwer JAJ, Sabelis MW (2000) Wolbachia-induced ‘hybrid breakdown’ in the two-spotted spider mite Tetranychus urticae Koch. Proc R Soc Lond Ser B 267: 1931–1937.
  26. 26. Xie RR, Chen XL, Hong XY (2011) Variable fitness and reproductive effects of Wolbachia infection in populations of the two-spotted spider mite Tetranychus urticae Koch in China. Appl Entomol Zool 46: 95–102.
  27. 27. Vala F, Breeuwer JAJ, Sabelis MW (2003) No variation for Wolbachia-induced hybrid breakdown in two populations of a spider mite. Exp Appl Acarol 29: 1–12.
  28. 28. Zhou W, Rousset F, O’Neil SL (1998) Phylogeny and PCR-based classification of Wolbachia strains using wsp gene sequences. Proc R Soc Lond Ser B 265: 509–515.
  29. 29. Baldo L, Hotopp J, Jolley K, Bordenstein SR, Biber S, et al. (2006) Multilocus sequence typingsystem for the endosymbiont Wolbachia pipientis. Appl Environ Microbiol 72: 7098–7110.
  30. 30. Navajas M, Gutierrez J, Lagnel J, Boursot J (1996) Mitochondrial cytochrome oxidase I in tetranychid mites: a comparison between molecular phylogeny and changes of morphological and life history traits. Bull Entomol Res 86: 407–417.
  31. 31. Kaplan EL, Meier P (1958) Non-parametric estimation from incomplete data. J Am Stat Assoc 53: 457–481.
  32. 32. Bland JM, Altman DG (2004) The log-rank test. Brit Med J 328: 1073.
  33. 33. Calvitti M, Moretti R, Porretta D, Bellini R, Urbanelli S (2009) Effects on male fitness of removing Wolbachia infections from the mosquito Aedes albopictus. Med Vet Entomol 23: 132–140.
  34. 34. Cone WW (1985) Mating and chemical communication. In: Spider Mites: Their Biology, Natural Enemies and Control. 243–247. Elsevier, Amsterdam.
  35. 35. Gottlieb Y, Ghanim M, Chiel E, Gerling D, Portnoy V, et al. (2006) Identification and Localization of a Rickettsia sp. in Bemisia tabaci (Homoptera: Aleyrodidae). Appl Environ Microbiol 72 (5): 3646–3652.
  36. 36. Heddi A, Grenier AM, Khatchadourian C, Charles H, Nardon P (1999) Four intracellular genomes direct weevil biology: Nuclear, mitochondrial, principal endosymbiont, and Wolbachia. Proc Natl Acad Sci USA 96: 6814–6819.
  37. 37. McMenima CJ, Lane RV, Cass BN, Fong AW, Sidhu M, et al. (2009) Stable introduction of a life-shortening Wolbachia infection into the mosquito Aedes aegypti. Science 323: 141–144.
  38. 38. Turley AP, Moreira LA, O’Neill SL, McGraw EA (2009) Wolbachia infection reduces blood-feeding success in the dengue fever mosquito, Aedes aegypti. PLoS Negl Trop Dis 3: e516.
  39. 39. Kambris Z, Cook PE, Phuc HK, Sinkins SP (2009) Immune activation by life-shortening Wolbachia and reduced filarial competence in mosquitoes. Science 326: 134–136.
  40. 40. Vala F, Breeuwer JAJ, Sabelis MW (2003) Sorting out the effects of Wolbachia, genotype and inbreeding on life-history traits of a spider mite. Exp Appl Acarol 29: 253–264.
  41. 41. Vavre F, Fleury F, Varaldi J, Fouillet P, Bouletreau M (2000) Evidence for female mortality in Wolbachia-mediated cytoplasmic incompatibility in haplodiploid insects: Epidemiologic and evolutionary consequences. Evolution 54: 191–200.
  42. 42. Bordenstein SR, Uy JJ, Werren JH (2003) Host genotype determines cytoplasmic incompatibility type in the haplodiploid genus Nasonia. Genetics 164: 223–233.
  43. 43. Mouton L, Henri H, Bouletreau M, Vavre F (2005) Multiple infections and diversity of cytoplasmic incompatibility in a haplodiploid species. Heredity 94: 187–192.
  44. 44. Min K-T, Benzer S (1997) Wolbachia, normally a symbiont of Drosophila, can be virulent, causing degeneration and early death. Proc Natl Acad Sci USA 94: 10792–10796.
  45. 45. Fry AJ, Palmer MR, Rand DM (2004) Variable fitness effects of Wolbachia infection in Drosophila melanogaster. Heredity 93: 379–389.
  46. 46. Ros VID, Breeuwer JAJ (2009) The effects of, and interactions between, Cardinium and Wolbachia in the doubly infected spider mite Bryobia sarothamni. Heredity 102: 413–422.
  47. 47. Carrington LB, Hoffmann AA, Weeks AR (2010) Monitoring long-term evolutionary changes following Wolbachia introduction into a novel host: the Wolbachia popcorn infection in Drosophila simulans. Proc R Soc Lond Ser B 277: 2059–2068.
  48. 48. Miller WJ, Ehrman L, Sceneider D (2010) Infectious speciation revisited: impact of symbiont-depletion on female fitness and mating behavior of Drosophila paulistorum. PLoS Pathog 6 (12): e1001214.
  49. 49. Clark ME, Veneti Z, Bourtzis K, Karr TL (2003) Wolbachia distribution and cytoplasmic incompatibility during sperm development: the cyst as the basic cellular unit of CI expression. Mech Develop 120: 185–198.
  50. 50. Veneti Z, Clark ME, Zabalou S, Karr TL, Savakis C, et al. (2003) Cytoplasmic incompatibility and sperm cyst infection in different Drosophila-Wolbachia associations. Genetics 164: 545–552.
  51. 51. Frydman HM, Li JM, Robson DN, Wieschaus E (2006) Somatic stem cell niche tropism in Wolbachia. Nature 441 (7092): 509–512.
  52. 52. Hosokawa T, Koga R, Kikuchi Y, Meng XY, Fukatsu T (2010) Wolbachia as a bacteriocyte-associated nutritional mutualist. Proc Natl Acad Sci USA 107 (2): 769–774.
  53. 53. Fast EM, Toomey ME, Panaram K, Desjardins D, Kolaczyk ED, et al. (2011) Wolbachia Enhance Drosophila stem cell proliferation and target the germline stem cell niche. Science 334: 990–992.
  54. 54. Ruang-areerate T, Kittayapong P, McGraw EA, Baimai V, O’Neill SL (2004) Wolbachia Replication and Host Cell Division in Aedes albopictus. Curr Microbiol 49: 10–12.