Alexandra A. Grossi , Min Zhang , Fasheng Zou , Daniel R. Gustafsson
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引用次数: 0
Abstract
Endosymbiotic bacteria of insects can facilitate host expansion into novel niches by providing their host with a fitness benefit such as vitamins or amino acids that are otherwise lacking in their hosts' diet. This close association can lead to cospeciation between insects and their symbionts; however, the symbionts’ small genome size leaves it susceptible to genome derogation which can result in symbiont replacement. Here, we screen chewing lice infesting shorebirds and terns to see what endosymbiotic bacteria are present, and build a summary phylogeny that includes louse endosymbiont sequences from this study as well as those from other louse genera, insects and bacteria strains from GenBank. We found a Sodalis-allied endosymbiont in Carduiceps, Lunaceps, Quadraceps, and Saemundssonia, as well as symbionts belonging to the family Enterobacteriaceae in Lunaceps, and Quadraceps. No louse species were host to both endosymbionts; however, the birds Kentish Plover (Charadrius alexandrinus) and Greater Crested Tern (Thalasseus bergii) were host to two genera of lice, each of which was infested with a different group of endosymbionts. In the summary phylogeny the endosymbionts from shorebirds, and tern lice did not form a monophyletic group, and therefore likely acquired their bacterial endosymbionts multiple times.
期刊介绍:
Avian Research is an open access, peer-reviewed journal publishing high quality research and review articles on all aspects of ornithology from all over the world. It aims to report the latest and most significant progress in ornithology and to encourage exchange of ideas among international ornithologists. As an open access journal, Avian Research provides a unique opportunity to publish high quality contents that will be internationally accessible to any reader at no cost.