Bacteria of the genus Wolbachia are masters in the art of sex-determination manipulation. By exploiting the haplodiploid system of sex determination (in which haploid eggs develop into males and diploid eggs develop into females) in certain Hymenoptera, Wolbachia are able to convert unfertilized eggs, which would normally develop as males, into females. As a consequence, a sexually reproducing wasp population might, on infection with Wolbachia, become parthenogenetic. Furthermore, it is a well-established fact that the life style of many parasitoid wasp species favours a female-biased sex ratio. Therefore, one would expect in Trichogramma kaykai, a minute wasp that parasitizes the eggs of a lycaenid butterfly and which has a typical sex ratio consisting of 22–29% males, that infection with Wolbachia would mean just one thing: switch to parthenogenesis. Alas, this is not the case, with Wolbachia infection levels being stably maintained in frequencies of between 5% and 25%. In a recent paper, Stouthamer et al. 1xSelfish element maintains sex in natural populations of a parasitoid wasp. Stouthamer, R. et al. Proc. R. Soc. London B Biol. Sci. 2001; 268: 617–622Crossref | Scopus (53)See all References1 exploited this system for some elegant experimental and theoretical work.Three hypotheses could explain such infection levels; inefficient transmission of Wolbachia; presence of a suppressor gene that either kills Wolbachia or balances its sex-ratio-distorting effect; or another non-Mendelian balancing factor acting in the opposite direction from Wolbachia (i.e. favouring a male-biased sex ratio). Plotting Wolbachia transmission frequencies versus a range of infection costs is enough to show that, for the range of infection frequencies observed in field populations of T. kaykai, the two possible outcomes are either the fixation or loss of the Wolbachia infection (rather than a maintenance of a stable equilibrium of about 5–25%). Adding to this, the recent demonstration (by the same research group) that Wolbachia might be horizontally transmitted at an appreciable frequency (37%) and inefficient transmission of Wolbachia as the sole explanation for the low levels of infection becomes unlikely.Alternatively, low infection levels of Wolbachia could be explained by the presence of suppressor genes that could either kill the bacteria or eliminate their effect on the host. Modelling carried out by Stouthamer et al., which takes into account the peculiarities of the T. kaykai system, shows that the presence of a suppressor gene would be a plausible theoretical outcome; however, detailed crossing protocols failed to demonstrate its presence.A third scenario invokes the presence of a sex-ratio factor acting in the opposite direction from Wolbachia, favouring male production. Such elements are collectively called paternal sex ratio (PSR) factors and have been identified in previous studies on parasitic wasps. PSRs are paternally transmitted and eggs fertilized with sperm from PSR-bearing males become male instead of female (exactly the opposite effect of that of Wolbachia). By crossing experiments and chromosome karyotypes, Stouthamer et al. present compelling evidence for the major effect of a PSR factor keeping Wolbachia infection levels low.This study is an elegant example of the occurrence of genomic conflict in a natural population. As our knowledge of the characterization and capabilities of these amazing reproductive parasites increases, ever more exciting cases of genomic parasitism will appear.
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