Abstract

BackgroundTheory predicts that dependency within host-endosymbiont interactions results in endosymbiont genome size reduction. Unexpectedly, the largest Wolbachia genome was found in the obligate, parthenogenesis-associated wFol. In this study, we investigate possible processes underlying this genome expansion by comparing a re-annotated wFol genome to other Wolbachia genomes. In addition, we also search for candidate genes related to parthenogenesis induction (PI).ResultsWithin wFol, we found five phage WO regions representing 25.4% of the complete genome, few pseudogenized genes, and an expansion of DNA-repair genes in comparison to other Wolbachia. These signs of genome conservation were mirrored in the wFol host, the springtail F. candida, which also had an expanded DNA-repair gene family and many horizontally transferred genes. Across all Wolbachia genomes, there was a strong correlation between gene numbers of Wolbachia strains and their hosts. In order to identify genes with a potential link to PI, we assembled the genome of an additional PI strain, wLcla. Comparisons between four PI Wolbachia, including wFol and wLcla, and fourteen non-PI Wolbachia yielded a small set of potential candidate genes for further investigation.ConclusionsThe strong similarities in genome content of wFol and its host, as well as the correlation between host and Wolbachia gene numbers suggest that there may be some form of convergent evolution between endosymbiont and host genomes. If such convergent evolution would be strong enough to overcome the evolutionary forces causing genome reduction, it would enable expanded genomes within long-term obligate endosymbionts.

Highlights

  • Theory predicts that dependency within host-endosymbiont interactions results in endosymbiont genome size reduction

  • WTpre is in one scaffold that contains a total gap length of 16,680 bp and wLcla is in 46 pieces, we still miss information for both of these genomes

  • Large regions of phage origin (RPO) with ample repair genes and accumulation of repetitive and transposable elements make up most of the expansion of the wFol genome. This genomic signature of gene conservation was mirrored in the F. candida host genome

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Summary

Introduction

Theory predicts that dependency within host-endosymbiont interactions results in endosymbiont genome size reduction. There are ample examples of obligate endosymbionts, e.g. Buchnera in aphids [6, 7], Wigglesworthia in the tsetseflies [8], and Wolbachia in parasitic filarial nematodes [9, 10]. In these cases neither host nor endosymbiont are viable without the other, and these associations are usually characterised by a long evolutionary history, nutritional or developmental dependency, and vertical transmission of the symbiont [11]. Different genetic mechanisms have been implied as the driving forces

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