Wolbachia bacteria inhabit the cells of about half of all arthropod species, an unparalleled success stemming in large part from selfish invasive strategies. Cytoplasmic incompatibility (CI), whereby the symbiont makes itself essential to embryo viability, is the most common of these and constitutes a promising weapon against vector-borne diseases. After decades of theoretical and experimental struggle, major recent advances have been made toward a molecular understanding of this phenomenon. As pieces of the puzzle come together, from yeast and Drosophila fly transgenesis to CI diversity patterns in natural mosquito populations, it becomes clearer than ever that the CI induction and rescue stem from atoxin-antidote (TA) system. Further, the tight association of the CI genes with prophages provides clues to the possible evolutionary origin of this phenomenon and the levels of selection at play.
The endocellular bacterium Wolbachia manipulates the reproduction of its arthropod hosts for its own benefit by various means, the most widespread being cytoplasmic incompatibility (CI). To date, the molecular mechanism involved in CI has not been elucidated. We examine here three different CI models described in previous literature, namely, the "lock-and-key", "titration-restitution" and "slow-motion" models. We confront them with the full range of CI patterns discovered so far, including the most complex ones such as multiple infections, asymmetrical and partial compatibility relationships and the existence of Wolbachia variants that can rescue the host from CI but not induce it. We conclude that the lock-and-key model is the most parsimonious of the models and fits the observations best. The two other models cannot be categorically invalidated, but they encounter some difficulties that make additional hypotheses necessary.
Although hyperparasitism frequently occur in parasitic insects, many aspects of this strategy remain unknown. We investigated possible fitness costs of hyperparasitism as influenced by host size. Our study was conducted with the facultative hyperparasitoid Pachycrepoideus dubius Ashmead (Hymenoptera: Pteromalidae), which parasitizes host species differing greatly in size. We compared some fitness traits (level of successful parasitism, development time, sex ratio and offspring size) of P. dubius developing on large secondary/primary (Delia radicum L. (Diptera: Anthomyiidae)/Trybliographa rapae Westwood (Hymenoptera: Figitidae)) or small secondary/primary host species (Drosophila melanogaster L./Asobara tabida Nees (Hymenoptera: Braconidae)). In no‐choice and choice experiments, P. dubius was able to develop on different stages of T. rapae (L2 (endophagous), L4 (ectophagous), and pupae) but that it preferred to parasitize unparasitized D. radicum pupae over pupae parasitized by T. rapae. Furthermore, in P. dubius, hyperparasitism was associated with fitness costs (lower level of successful parasitism, smaller adult size) and these costs were greater on the smallest host complex. We hypothesize that the size of D. melanogaster pupae parasitized by A. tabida may be close to the suboptimal host size for P. dubius beneath which the costs of hyperparasitism make this strategy nonadaptive. Hyperparasitism in terms of trade‐offs between host quality and abundance of competitors is discussed.
Wolbachia are maternally‐transmitted endocellular bacteria infecting several arthropod species. In order to study the possibility of Wolbachia segregation in a naturally bi‐infected host, isofemale lines from a bi‐infected Drosophila simulans (Sturtevant) strain from Nouméa (New Caledonia) were backcrossed using uninfected males carrying the same nuclear background. Uninfected males were used to avoid the cytoplasmic incompatibility syndrome (CI) associated with the presence of Wolbachia in males. Each line was established using a female infected simultaneously by the two different Wolbachia variants wHa and wNo. The backcross led to some individuals carrying only one type of infection being recovered among the progeny of the bi‐infected foundress females. Rarely, uninfected individuals were also recovered. Isolated for the first time in its natural host, wNo exhibited a significantly weaker CI phenotype than the isolated wHa variant. Infection fate when backcross conditions were relaxed varied depending on rearing conditions of the host. Under favourable conditions, the infection was generally maintained, while it was frequently lost under unfavourable conditions. This result probably reflects the direct fitness dependence of the symbiont on its host.
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