Abstract

Many species of arthropods carry maternally inherited bacterial endosymbionts that can influence host sexual reproduction to benefit the bacterium. The most well-known of such reproductive parasites is Wolbachia pipientis. Wolbachia are obligate intracellular α-proteobacteria found in nearly half of all arthropod species. This success has been attributed in part to their ability to manipulate host reproduction to favor infected females. Cytoplasmic incompatibility (CI), a phenomenon wherein Wolbachia infection renders males sterile when they mate with uninfected females, but not infected females (the rescue mating), appears to be the most common. CI provides a reproductive advantage to infected females in the presence of a threshold level of infected males. The molecular mechanisms of CI and other reproductive manipulations, such as male killing, parthenogenesis, and feminization, have remained mysterious for many decades. It had been proposed by Werren more than two decades ago that CI is caused by a Wolbachia-mediated sperm modification and that rescue is achieved by a Wolbachia-encoded rescue factor in the infected egg. In the past few years, new research has highlighted a set of syntenic Wolbachia gene pairs encoding CI-inducing factors (Cifs) as the key players for the induction of CI and its rescue. Within each Cif pair, the protein encoded by the upstream gene is denoted A and the downstream gene B. To date, two types of Cifs have been characterized based on the enzymatic activity identified in the B protein of each protein pair; one type encodes a deubiquitylase (thus named CI-inducing deubiquitylase or cid), and a second type encodes a nuclease (named CI-inducing nuclease or cin). The CidA and CinA proteins bind tightly and specifically to their respective CidB and CinB partners. In transgenic Drosophila melanogaster, the expression of either the Cid or Cin protein pair in the male germline induces CI and the expression of the cognate A protein in females is sufficient for rescue. With the identity of the Wolbachia CI induction and rescue factors now known, research in the field has turned to directed studies on the molecular mechanisms of CI, which we review here.

Highlights

  • The prevalence of maternally inherited bacterial endosymbionts among invertebrate animals is widely recognized

  • With the identity of the Wolbachia Cytoplasmic incompatibility (CI) induction and rescue factors known, research in the field has turned to directed studies on the molecular mechanisms of CI, which we review here

  • Since Wolbachia are inherited by transmission through the female germline, the reproductive advantage Wolbachia provides to an infected female host enhances its own ability to propagate in an insect population [5,6]

Read more

Summary

Introduction

The prevalence of maternally inherited bacterial endosymbionts among invertebrate animals is widely recognized. While this work did not prove a role for CidA in CI, and the predicted CidB protein from the same operon was not detected in infected sperm, one or more intact cidA–cidB-related syntenic gene pairs were observed in the genomes of several other Wolbachia strains that cause CI in insects but not in those from filarial nematodes that do not. The relevance of the cin-type operons to CI caused by Wolbachia strains, such as wNo and wYak, on the other hand, was emphasized in recent genomic analyses of these strains, which infect various Drosophila species [44,45] These studies together establish a strong genetic foundation supporting the essential role of the cif genes in Wolbachia-induced CI. WO prophages may reflect how the EAM genes, including those responsible for CI, were acquired by different Wolbachia strains; active WO phage particles can be generated from these prophages, a potential means of horizontal gene transfer and possibly even vertical transmission [47]

Sequence Motifs and Biochemical Activities of the Cif Proteins
Models of CI Induction and Rescue
Hypothetical molecularmechanism mechanismofofCI
Future Prospects
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call