Figures
Abstract
Wolbachia bacteria are common endosymbionts of insects, and some strains are known to protect their hosts against RNA viruses and other parasites. This has led to the suggestion that releasing Wolbachia-infected mosquitoes could prevent the transmission of arboviruses and other human parasites. We have identified Wolbachia in Kenyan populations of the yellow fever vector Aedes bromeliae and its relative Aedes metallicus, and in Mansonia uniformis and Mansonia africana, which are vectors of lymphatic filariasis. These Wolbachia strains cluster together on the bacterial phylogeny, and belong to bacterial clades that have recombined with other unrelated strains. These new Wolbachia strains may be affecting disease transmission rates of infected mosquito species, and could be transferred into other mosquito vectors as part of control programs.
Citation: Osei-Poku J, Han C, Mbogo CM, Jiggins FM (2012) Identification of Wolbachia Strains in Mosquito Disease Vectors. PLoS ONE 7(11): e49922. https://doi.org/10.1371/journal.pone.0049922
Editor: Richard Cordaux, University of Poitiers, France
Received: August 17, 2012; Accepted: October 15, 2012; Published: November 21, 2012
Copyright: © 2012 Osei-Poku et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was funded by Wellcome Trust project grant WT094664. FMJ is supported by a Royal Society Research Fellowship and JOP by a Darwin Trust of Edinburgh studentship. Travel grants for this work were provided by the Genetics Society Heredity Fieldwork Grant, the Royal Entomological Society ORF and Clare College (Cambridge) Chibnall Travel Grant. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Wolbachia are common intracellular bacteria that are estimated to infect 40% of insect species [1]. They are typically vertically transmitted from infected females to their offspring, and are best known for manipulating host reproduction in ways that enhance their own transmission to future host generations. The commonest manipulations involve either distorting the offspring sex ratio of infected females towards daughters [2]–[4] or inducing cytoplasmic incompatibility [5], [6]. These manipulations allow the bacteria to rapidly spread through insect populations, often to the point where virtually all individuals are infected [7].
Some Wolbachia strains also protect infected insects against RNA viruses, and have the potential to prevent the transmission of human pathogens by insect vectors [8]–[10]. This effect was first reported in Drosophila, where Wolbachia-infected insects had increased survival and/or lower viral titres when infected with a range of positive-sense RNA viruses [8], [10], [11]. Subsequently, it was found that when D. melanogaster Wolbachia strains were transinfected into Ae. aegypti or Ae. albopictus, the mosquitoes had increased resistance to dengue and chikungunya viruses [9], [12], [13]. Furthermore, the bacteria also induced cytoplasmic incompatibility in their new hosts, so they have the potential to spread through wild and naïve mosquito populations [12]–[14]. Therefore, releasing Wolbachia-infected mosquitoes may provide a way to interrupt the transmission cycle of these viruses.
The effects of Wolbachia on metazoan parasites of public health importance have also been investigated. A virulent strain of Wolbachia, wMelPop, which over-replicates in somatic tissues and reduces the lifespan of infected hosts [15], [16], caused an upregulation of immune genes responsive to filarial worm infections when transinfected into Ae. aegypti [17]. wMelPop also reduced the intensity of the avian malaria parasite, Plasmodium gallinaceum, in Ae. aegypti [9] and the rodent parasite, P. berghei, in Anopheles gambiae [18].
While the ability of Wolbachia to spread rapidly through populations and impair the development of pathogens makes it an excellent candidate for reducing disease transmission by vector species, the choice of Wolbachia strain for such interventions needs to be carefully considered. For example, while wMelPop can prevent the normal replication of viruses and development of metazoans, it also shortens the life of infected mosquitoes and this high fitness cost may prevent it from stably establishing in mosquito populations [16], [18]. Furthermore, Wolbachia strains vary considerably in both the level of viral protection that they provide to their hosts [11] and the strength of cytoplasmic incompatibility that they induce [19], [20]. These, in turn, affect the ability of the bacteria to spread through populations and prevent disease transmission. For these reasons it is prudent to consider a range of strains before beginning any control programs.
Identifying naturally-occurring Wolbachia strains in mosquitoes is useful for two reasons. First, it is technically easier to transfer Wolbachia between closely related species [21], so strains which naturally occur in mosquitoes are well-suited for transinfection into related vector species. Second, the dynamics of Wolbachia strains that are introduced into an insect population may be altered by Wolbachia strains that already exist in that population due to cytoplasmic incompatibility among strains [22]. It is therefore important to critically assess the incidence of Wolbachia in natural populations of mosquitoes in order to better understand how introducing novel Wolbachia strains may alter a wild population that already harbours the bacteria. Naturally-occurring Wolbachia have been identified in a range of species of mosquitoes [23]–[25], many of which are not vectors of human disease. Here, we continue these efforts and examine Wolbachia infections in nine different species mosquitoes collected from Kenya and use multi-locus sequence typing (MLST) [26] to investigate relationships and patterns of genetic exchange among strains.
Methods
Mosquito Samples and Wolbachia Infection
We used DNA extractions from the guts of adult female mosquitoes collected from towns and villages along the Kenyan coast that have been described elsewhere [27]. Anopheles and Mansonia mosquitoes were collected from rural Mbogolo in the Malindi district and, Aedes and Culex from towns in the Kilifi district. The analysis was repeated on the heads and thoraces of a subset of these samples, but this did not lead to the discovery of any new infections, so the results are not reported. To detect Wolbachia, the gene encoding the surface protein of Wolbachia, wsp, was amplified with the primers wsp81F and wsp 691R [28]. PCR was performed with BIOTAQ polymerase (Bioline, UK) with each reaction at a final volume of 20 µl (2 µl of 10X PCR buffer, 1 µl of 50 mM MgCl2, 2 µl of 2 mM dNTP mix (Invitrogen), 0.2 µl each of 20 µM forward and reverse primers, 1 U Taq polymerase, 1 µL DNA sample and deionized water to the final voulme). The thermal cycling protocol was an initial denaturation at 95°C for 5 mins; 30 cycles of denaturation at 95°C for 30 s, annealing at 55°C for 20 s and extension at 72°C for 20 s; final extension at 72°C for 10 mins and held at 4°C. To check the DNA extraction had been successful, the insect ribosomal internal transcribed spacer region-1 (ITS1) and mtDNA cytochrome oxidase I (COI) were amplified for each sample using BD1 and 4S primers [29] and universal COI primers [30] respectively, in separate reactions.
wsp and ITS1 Sequencing
For each mosquito species that was infected with Wolbachia, a maximum of 4 positive samples were selected for sequencing both wsp and ITS1. Unincorporated primers and dNTPs were digested with exonuclease I (ExoI) (NEB) and shrimp alkaline phosphatase (USB Corporation). Cleaned products were sequenced with the forward and reverse primers for each amplicon using ABI PRISM BigDye Terminator kit (Perkin-Elmer Corporation, U.S.A). Sequencing was done at the Source Bioscience Center, UK. Sequences were trimmed and assembled using Sequencher v4.5 [31]. Chromatograms were inspected for single and double peaks.
Multi Locus Sequence Typing (MLST)
For typing the Wolbachia strains detected in our infected samples, we used the multi-locus typing as described [26]. The protocol suggests the amplification of 5 single copy genes that are widely distributed within the wMel genome – gatB, coxA, hcpA, ftsZ and fbpA. We selected two individuals from each of the mosquito species that were infected with Wolbachia, except for Ae. metallicus which had only one infected individual. We used a nested PCR to amplify hcpA for M. uniformis samples as these failed to amplify with the hcpA standard primers F1/R1. Firstly, hcpA F3/R3 primer set was used in a reaction with Promega GoTaq Hot Start Polymerase. Then, 1 µl of the F3/R3 reaction was used in the next round of PCR using the hcpA F1/R1 primers as already described. The PCR resulted in multiple bands for M. uniformis. The correct band size was excised and purified with Qiagen Gel extraction kit. All amplicons were cleaned and prepared for sequencing as previously described.
Forward and reverse sequences from each PCR product were aligned and visually inspected in Sequencher v4.5 [31]. Consensus sequences obtained from each individual for each gene were aligned and compared and, all sequence differences between Wolbachia strains were checked to confirm they had unambiguous peaks. As bacteria from each mosquito species had the same sequences, a consensus sequence for each gene per mosquito host species was obtained (except fbpA gene which was sequenced for one of the two M. uniformis samples). All consensus sequences were trimmed to the appropriate length for database query. We performed a BLAST search of each sequence in the Wolbachia MLST database (http://pubmlst.org/wolbachia) [32]. Where a sequence had an exact match in the database, it was assigned the designated allele number. We submitted 6 new alleles to the database for allele number assignment which includes all the genes for the Aedes sp. and hcpA for M. africana. The complete MLST profiles were submitted to the Wolbachia MLST database and have been assigned ID numbers 496–501 (http://pubmlst.org/wolbachia).
Phylogeny
To account for the effects of recombination on the phylogeny, we analysed the dataset with ClonalFrame v1.2 [33]. Unlike other phylogeny analysis software, ClonalFrame estimates clonal relationships while taking into account recombination as a mode of substitution within genes. This approach also estimates the contribution made by recombination to total substitutions [33]. The complete dataset included Wolbachia MLST sequences from 113 host strains obtained from MLST database (http://pubmlst.org/wolbachia), and our 5 sample species. We also performed a whole-genome shotgun (wgs) BLAST search of the wAlbB genome [34] for the MLST gene sequences of the Wolbachia B strain of Ae. albopictus. For the data downloaded from http://pubmlst.org/wolbachia, only host strains with complete information – details on the host genus and allele numbers for all 5 MLST genes – were included. If there were multiple MLST profiles from a single host that had identical sequences, only one of these was included.
All 5 gene sequences for the 119 sample set were aligned independently using Mauve v2.3.1 [35], which produces the appropriate file format for running ClonalFrame [33]. To check the analysis was converging, we performed 9 independent runs of our dataset in ClonalFrame v1.2 [33] with 100,000 MCMC iterations after 100,000 burn-in iterations. The number of iterations performed between recording parameters in the posterior sample was set at 100. Default settings were used for all other parameters. For the first 8 runs we used a uniformly chosen coalescent tree as the initial tree. As a UPGMA gives a good representation of tree topology [33], we performed the ninth run with parameters as previously mentioned, but starting with a UPGMA tree.
The output generated with the UPGMA starting tree was compared with the other 8 ClonalFrame outputs using the tree comparison tool in ClonalFrame [33]. This tool compares nodes of an uploaded tree to other tree outputs and plots the nodes according to similarity in observed nodes. The UPGMA tree showed good convergence with the other outputs (Figure S1). Good convergence of the various parameter estimates was demonstrated by the Gelman and Rubin test [36] implemented in ClonalFrame [33]. The UPGMA starting tree output was, therefore, used in further analyses. The posterior sample of trees was exported into MEGA 5.05 [37] and a consensus tree with branch support values was drawn at 50% majority rule. The resulting tree was visualized and rooted in FigTree v1.3.1 [38].
Where recombination was detected in our sequences by ClonalFrame, we attempted to identify the source of the ‘imported’ sequence. We used the criteria used by [39] to detect sources of imports in the mosquito clades. We checked the MLST database for sequences with two or fewer nucleotide differences from the gene being investigated (by first finding sequences that clustered together on a neighbour joining tree and then manually inspecting these sequences). If this sequence came from a bacterium that did not cluster with our sample on the MLST tree, then we classed it as a potential source of the sequence ‘imported’ by recombination [39].
Results
Wolbachia Infections
We investigated the presence of Wolbachia in mosquito guts of nine mosquito species. Due to variation in Wolbachia tissue tropism, some strains may go undetected. Nevertheless, it can provide a minimum estimate of the prevalence of Wolbachia. Five of the species sampled were infected (Table 1). Consistent with previous studies, none of the Anopheles species or Aedes aegypti were infected with Wolbachia [24], [25], while Culex quinquefasciatus and Mansonia uniformis were infected [24]. However, this is the first report of Wolbachia in Aedes bromeliae, Aedes metallicus and Mansonia africana. In Ae. bromeliae, 75% of individuals were infected, while in the closely related Ae. metallicus, one of the two samples was infected. Differences in the length and sequence of the mosquito internal transcribed spacer region-1 (ITS1) confirmed that the infected Ae. metallicus individual was of a distinct species to Ae. bromeliae. For each mosquito species, there were no nucleotide polymorphisms in the wsp sequences and the chromatograms showed clear single peaks, suggesting that a single strain was infecting these mosquitoes.
Phylogeny
We used the MLST gene sequences to reconstruct the Wolbachia phylogeny, and controlled for the confounding effects of recombination on tree reconstruction using ClonalFrame (Figure 1). The phylogeny grouped strains into supergroups A, B, F and D (Figure 1; supergroup D was used as the outgroup to root the tree) [40]–[43]. The Wolbachia strains we identified infecting the Culicini and Mansoniini tribes of mosquitoes belonged to supergroup B while those in the Aedini tribe were in supergroup A (Figure 1). Wolbachia strains in Ae. bromeliae and Ae. metallicus formed a monophyletic group, whose relationship with the strain from Ae. albopictus Wolbachia strain A (Figure 1; Aedes_albopictus_12_A) is poorly resolved. The three strains that infect Culex quinquefasciatus, Mansonia uniformis and Mansonia africana clustered together with three strains found in the Lepitoptera (Figure 1). There are numerous other strains from this clade in the MLST database, many of which infect Lepidoptera, and if these are included in the tree the relationships within the clade are poorly resolved (data not shown).
Tip labels include 115 host strains from PubMLST (http://pubmlst/wolbachia) and 5 mosquito host species from this study. Black arrows indicate positions of mosquito Wolbachia strains. The branch labels are posterior probabilities (only support values above 90% are shown). Blue circles are the nodes leading to Wolbachia strains in mosquitoes that are analysed in Figure 2. Branch lengths are proportional to divergence time in coalescent units. The tree was constructed using the Bayesian ClonalFrame software.
Recombination Events
Across the entire tree of 119 strains, we estimated that recombination involves a mean tract length of 127 bp being exchanged between strains (95% credibility interval: 98–164 bp). We estimated that recombination (r) and mutation (m) had a similar probability of introducing substitutions into the genome of Wolbachia (mean r/m = 1.36; 95% credibility interval: 1.01–1.79). Although both events may have equal chances of producing nucleotide substitutions, the rate at which each occurs could be different. Defined by ρ/θ (recombinational to mutational rate), point mutations were estimated to happen roughly four times more frequently than recombination (ρ/θ = 0.27, 95% credibility interval: 0.19–0.37).
We were specifically interested in recombination that involved Wolbachia strains related to those infecting mosquitoes. We inspected the substitutions that had occurred on individual branches leading to various nodes in the mosquito clades (shown by blue circles in Figure 1). There were several lineages where there was a high probability of recombination (posterior probability of import >0.95; Figure 2). On the branch that leads to the mosquito Wolbachia clade in supergroup B (Figure 2; node A), about a third of the length of the fbpA gene was imported. In the Aedes albopictus Wolbachia strain B (wAlbB) the full length of the coxA gene was imported (Figure 2; node B), differentiating this strain from those of the other mosquito species in this supergroup. Similarly, the entire coxA gene was imported on the lineage leading to the strains infecting Mansonia uniformis and Culex quinquefasciatus (Figure 2; node D). There was also evidence of three smaller recombination events in the mosquito clades (Figure 2; nodes C, E and F).
The nodes A–F are shown by blue circles in Figure 1. The red line is åthe posterior probability that the sequence was imported by recombination. Positions marked ‘x’ are nucleotide substitutions in the genes; intensity of ‘x’ markings are proportional to posterior probability of substitution with darker marks indicating higher probability.
Since the coxA gene has a high probability of the entire gene having been exchanged by recombination (Figure 2; nodes B and D), we investigated the possible sources of these imported sequences. To do this, we reconstructed a neighbour-joining tree using all published sequences of coxA, and looked for taxa which had very similar sequences (two or fewer differences) to the sequences from the Wolbachia strains that showed evidence of recombination but appeared elsewhere on the MLST tree. The source of coxA into Ae. albopictus wAlbB was not detected in the database. The source of the coxA sequence into the lineage on node D (Figure 2) appears to be host strains 355, 502, 439 and 492 in the MLST database (data not shown). Unfortunately, the names of the arthropod species that these strains infect have not been published.
Discussion
Wolbachia is an important component of the antiviral defences of insects [8], [10], [11], which has the potential to prevent mosquitoes from transmitting viruses like dengue and chikungunya [9], [13]. Furthermore, some strains of Wolbachia also affect metazoan parasites like Plasmodium [9], hence they may also play a role in affecting the transmission of these parasites [17], [18]. Here, we make the first report of Wolbachia infections in Ae. bromeliae, a vector of yellow fever virus [44], and M. africana, a vector of the filarial nematode Wuchereria bancrofti [45] – a major cause of lymphatic filariasis. Furthermore, we extend the known range of Wolbachia in M. uniformis from Southeast Asia [24] to Africa, where this species is a competent vector of Wuchereria bancrofti [45].
The Wolbachia strains we have identified may have implications for both the natural transmission rate of human disease, and the attempts to manipulate transmission rates through the release of Wolbachia-infected mosquitoes. As virus protection appears to be a common trait among Wolbachia strains in arboviral hosts [8], [10], [11], it is possible that these strains we have detected in the yellow fever vector Ae. bromeliae may reduce arboviral transmission rates in the wild. This has the potential to be significantly important since 75% of individuals were infected. These strains also have the potential to be transinfected into key vector species such as Ae. aegypti. This is likely to be far easier than transfers of strains from distantly related species like Drosophila, as transinfection is known to have higher success rates between more closely related species of insects [21], [46]. Finally, these resident Wolbachia strains might interfere with attempts to introduce novel strains into the population as part of control programs.
Wolbachia bacteria were first reported in C. pipiens [47] and since then many more strains have been reported in other mosquito genera [24], [25], [48], [49]. Our sample size was not as large and diverse as previous work have shown [24], [49] but, the presence of Wolbachia in the genera Aedes, Culex and Mansonia is confirmed, and the prevalence of infections in the three genera of mosquitoes was comparable to other studies [24]. The failure to detect Wolbachia in the three species of Anopheles in our study confirms the absence of Wolbachia in this group of mosquitoes [24], [49]. It was speculated that this may be due to the inability of Anophelines to support Wolbachia physiologically [24]. Recently, transinfection of Wolbachia into Anopheles has shown stable infections in somatic cells with striking effects on immune gene regulation in response to Plasmodium falciparum but, no infections in the ovaries was observed [50], [51].
With the confounding effects of recombination accounted for, we have provided analyses of the Wolbachia phylogeny. The Wolbachia strains in mosquitoes were clearly categorized into supergroups A and B, with at least two mosquito-infecting clades. The tendency of the mosquito-infecting strains to cluster together could be explained by an ancestral species being infected and then co-speciating with Wolbachia, or by horizontal transmission between mosquitoes. Horizontal transfer seems more probable, as it is known from other taxa that horizontal transmission most commonly occurs between the closest related host species [52].
Supporting Information
Figure S1.
ClonalFrame ‘tree comparison’ tool output of UPGMA starting tree with the 8 coalescent tree models. Shaded circles are proportional to the support on the nodes during the tree comparison. Black circles represent nodes that are present in the UPGMA starting trees and all the other trees, white nodes are nodes found on the UPGMA starting tree but not in the combined comparison with the other tree outputs.
https://doi.org/10.1371/journal.pone.0049922.s001
(PDF)
Acknowledgments
We are most grateful to the Staff of the Vector Biology Group, KEMRI (Kilifi) for their support and advice during the collection of mosquitoes.
Author Contributions
Conceived and designed the experiments: JOP FMJ. Performed the experiments: JOP CH. Analyzed the data: JOP CH FMJ. Contributed reagents/materials/analysis tools: FMJ. Wrote the paper: JOP FMJ. Logistics and field advice: CMM.
References
- 1. 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: e38544.
- 2. Hurst GDD, Jiggins FM, von der Schulenburg JHG, Bertrand D, West SA, et al. (1999) Male-killing Wolbachia in two species of insect. Proc R Soc Lond B Biol Sci 266: 735–740.
- 3. 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 B Biol Sci 250: 91–98.
- 4. Stouthamer R, Breeuwert JA, Luck RF, Werren JH (1993) Molecular identification of microorganisms associated with parthenogenesis. Nature 361: 66–68.
- 5. O’Neill SL, Karr TL (1990) Bidirectional incompatibility between conspecific populations of Drosophila simulans. Nature 348: 178–180.
- 6. Clancy DJ, Hoffmann AA (1996) Cytoplasmic incompatibility in Drosophila simulans: evolving complexity. Trends Ecol Evol 11: 145–146.
- 7. Turelli M, Hoffmann AA (1991) Rapid spread of an inherited incompatibility factor in California Drosophila. Nature 353: 440–442.
- 8. Hedges LM, Brownlie JC, ONeill SL, Johnson KN (2008) Wolbachia and virus protection in insects. Science 322: 702.
- 9. Moreira L, Iturbe-Ormaetxe I, Jeffery JA, Lu G, Pyke AT, et al. (2009) A Wolbachia symbiont in Aedes aegypti limits infection with dengue, Chikungunya, and Plasmodium. Cell 139: 1268–1278.
- 10. Teixeira L, Ferreira A, Ashburner M (2008) The bacterial symbiont Wolbachia induces resistance to RNA viral infections in Drosophila melanogaster. PLoS Biology 6: e2.
- 11. Osborne SE, Leong YS, O’Neill SL, Johnson KN (2009) Variation in antiviral protection mediated by different Wolbachia strains in Drosophila simulans. PLoS Pathogens 5: e1000656.
- 12. Blagrove MSC, Arias-Goeta C, Failloux AB, Sinkins SP (2012) Wolbachia strain wMel induces cytoplasmic incompatibility and blocks dengue transmission in Aedes albopictus. PNAS 109: 255–260.
- 13. Walker T, Johnson PH, Moreira LA, Iturbe-Ormaetxe I, Frentiu FD, et al. (2011) The wMel Wolbachia strain blocks dengue and invades caged Aedes aegypti populations. Nature 476: 450–453.
- 14. Hoffmann AA, Montgomery BL, Popovici J, Iturbe-Ormaetxe I, Johnson PH, et al. (2011) Successful establishment of Wolbachia in Aedes populations to suppress dengue transmission. Nature 476: 454–457.
- 15. Min KT, Benzer S (1997) Wolbachia, normally a symbiont of Drosophila, can be virulent, causing degeneration and early death. PNAS 94: 10792–10796.
- 16. McMeniman CJ, Lane RV, Cass BN, Fong AWC, Sidhu M, et al. (2009) Stable introduction of a life-shortening Wolbachia infection into the mosquito Aedes aegypti. Science 323: 141–144.
- 17. 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.
- 18. Kambris Z, Blagborough AM, Pinto SB, Blagrove MSC, Godfray HCJ, et al. (2010) Wolbachia stimulates immune gene expression and inhibits Plasmodium development in Anopheles gambiae. PLoS Pathogens 6: e1001143.
- 19. Reynolds KT, Hoffmann AA (2002) Male age, host effects and the weak expression or non-expression of cytoplasmic incompatibility in Drosophila strains infected by maternally transmitted Wolbachia. Genet Res 80: 79–87.
- 20. Sinkins SP, Walker T, Lynd AR, Steven AR, Makepeace BL (2005) Wolbachia variability and host effects on crossing type in Culex mosquitoes. Nature 436: 257–260.
- 21. Russell JA, Goldman-Huertas B, Moreau CS, Baldo L, Stahlhut JK, et al. (2009) Specialization and geographic isolation among Wolbachia symbionts from ants and lycaenid butterflies. Evolution 63: 624–640.
- 22.
Hoffmann AA, Turelli M (1997) Cytoplasmic incompatibility in insects. In: O’Neill SL, Hoffman A., Werren JH, editors. Influential passengers: inherited microorganisms and arthropod reproduction. UK: Oxford University Press, Oxford. 42–80.
- 23. Kittayapong P, Baimai V, ONeill SL (2002) Field prevalence of Wolbachia in the mosquito vector Aedes albopictus. Am J Trop Med Hyg 66: 108–111.
- 24. Kittayapong P, Baisley KJ, Baimai V, ONeill SL (2000) Distribution and diversity of Wolbachia infections in Southeast Asian mosquitoes (Diptera: Culicidae). J Med Entomol 37: 340–345.
- 25. Rasgon JL, Scott TW (2004) An initial survey for Wolbachia (Rickettsiales: Rickettsiaceae) infections in selected California mosquitoes (Diptera: Culicidae). J Med Entomol 41: 255–257.
- 26. Baldo L, Dunning Hotopp JC, Jolley KA, Bordenstein SR, Biber SA, et al. (2006) Multilocus sequence typing system for the endosymbiont Wolbachia pipientis. Appl Environ Microbiol 72: 7098–7110.
- 27. Osei-Poku J, Mbogo CM, Palmer WJ, Jiggins FM (2012) Deep sequencing reveals extensive variation in the gut microbiota of wild mosquitoes from Kenya. Mol Ecol 21: 5138–5150.
- 28. Braig HR, Zhou WG, Dobson SL, ONeill SL (1998) Cloning and characterization of a gene encoding the major surface protein of the bacterial endosymbiont Wolbachia pipientis. J Bacteriol 180: 2373–2378.
- 29. von der Schulenburg JH, Habig M, Sloggett JJ, Webberley KM, Bertrand D, et al. (2001) Incidence of male-killing Rickettsia spp. (alpha-proteobacteria) in the ten-spot ladybird beetle Adalia decempunctata L. (Coleoptera: Coccinellidae). Appl Environ Microbiol 67: 270–277.
- 30. Folmer O, Black M, Hoeh W, Lutz R, Vrijenhoek R (1994) DNA primers for amplification of mitochondrial cytochrome c oxidase subunit I from diverse metazoan invertebrates. Mol Mar Biol Biotechnol 3: 294–299.
- 31.
Sequencher® version 4.5 sequence analysis software. Gene Codes Corporation, Ann Arbor, MI USA. Available: http://www.genecodes.com.
- 32.
Jolley KA, Chan MS, Maiden MCJ (2004) mlstdbNet-Distributed multi-locus sequence typing (MLST) databases. BMC Bioinformatics. Available: http://pubmlst.org/wolbachia.
- 33. Didelot X, Falush D (2007) Inference of bacterial microevolution using multilocus sequence data. Genetics 175: 1251–1266.
- 34. Mavingui P, Valiente Moro C, Tran-Van V, Wisniewski-Dyé F, Raquin V, et al. (2012) Whole-genome sequence of Wolbachia strain wAlbB, an endosymbiont of tiger mosquito vector Aedes albopictus.. J Bacteriol 194: 1840.
- 35. Darling AE, Mau B, Blatter FR, Perna NT (2004) Mauve: multiple alignment of conserved genomic sequence with rearrangements. Genome Res 14: 1394–1403.
- 36. Gelman A, Rubin DB (1992) Inference from iterative simulation using multiple sequences. Stat Sci 7: 457–511.
- 37. Tamura K, Peterson D, Peterson N, Stecher G, Nei M, et al. (2011) MEGA5: Molecular Evoltionary Genetics Analysis using Maximum Likelihood, Evolutionary Distance, and Maximum Parsimony Methods. Mol Biol Evol 28: 2731–2739.
- 38.
Rambaut A (2006) FigTree v1.3.1 Available: http://tree.bio.ed.ac.uk/software/figtree.
- 39. Didelot X, Barker M, Falush D, Priest FG (2009) Evolution of pathogenicity in the Bacillus cereus group. Syst Appl Microbiol 32: 81–90.
- 40. Bandi C, Anderson TJC, Genchi C, Blaxter M (1998) Phylogeny of Wolbachia in filarial nematodes. Proc R Soc Lond B Biol Sci 265: 2407–2413.
- 41. Casiraghi M, Bordenstein SR, Baldo L, Lo N, Beninati T, et al. (2005) Phylogeny of Wolbachia pipientis based on gltA, groEL and ftsZ gene sequences: clustering of arthropod and nematode symbionts in the F supergroup, and evidence for further diversity in the Wolbachia tree. Microbiology 151: 4015–4022.
- 42. Lo N, Casiraghi M, Salati E, Bazzocchi C, Bandi C (2002) How many Wolbachia supergroups exist? Mol Biol Evol 19: 341–346.
- 43. Werren JH, Zhang W, Guo LR (1995) Evolution and phylogeny of Wolbachia: reproductive parasites of arthropods. Proc R Soc Lond B Biol Sci 261: 55–63.
- 44. Huang Y-M (1986) Aedes (Stegomyia) bromeliae: The Yellow fever (Diptera: Culicidae) vector in East Africa. J Med Entomol 23: 196–200.
- 45. Ughasi J, Bekhard HE, Coulibaly M, Adabie-Gomez D, Gyapong J, et al. (2012) Mansonia africana and Mansonia uniformis are vectors in the transmission of Wuchereria bancrofti lymphatic filariasis in Ghana. Parasit Vectors 5: 89.
- 46. Bian G, Xu Y, Lu P, Xie Y, Xi Z (2010) The endosymbiotic bacterium Wolbachia induces resistance to dengue virus in Aedes aegypti. PLoS Pathog 6: e1000833.
- 47. Hertig M, Wolbach SB (1924) Studies on Rickettsia-like micro-organisms in insects. J Med Res 44: 329–374.
- 48. Trpis M, Perrone JB, Reissig M, Parker KL (1981) Control of cytoplasmic incompatibility in the Aedes scutellaris complex: Incompatible crosses become compatible by treatment of larvae with heat or antibiotics. J Hered 72: 313–317.
- 49. Ricci I, Cancrini G, Gabrielli S, Damelio S, Favia G (2002) Searching for Wolbachia (Rickettsiales: Rickettsiaceae) in mosquitoes (Diptera: Culicidae): large polymerase chain reaction survey and new identifications. J Med Entomol 39: 562–567.
- 50. Hughes GL, Koga R, Xue P, Fukatsu T, Rasgon JL (2011) Wolbachia infections are virulent and inhibit the human malaria parasite Plasmodium falciparum in Anopheles gambiae. PLoS Pathog 7: e1002043.
- 51. Hughes GL, Ren X, Ramirez JL, Sakamoto JM, Bailey JA, et al. (2011) Wolbachia infections in Anopheles gambiae cells: transcriptomic characterization of a novel host-symbiont interaction. PLoS Pathog 7: e1001296.
- 52. Jiggins FM, Bentley JK, Majerus MEN, Hurst GDD (2002) Recent changes in phenotype and patterns of host specialization in Wolbachia bacteria. Mol Ecol 11: 1275–1283.