Ye Yixin H, Seleznev Andrei, Flores Heather A, Woolfit Megan, McGraw Elizabeth A
School of Biological Sciences, Monash University, Clayton, VIC 3800, Australia.
Peter MacCallum Cancer Centre, St Andrews Place, East Melbourne, VIC 8006, Australia.
J Invertebr Pathol. 2017 Feb;143:18-25. doi: 10.1016/j.jip.2016.11.011. Epub 2016 Nov 18.
Animals experience near constant infection with microorganisms. A significant proportion of these microbiota reside in the alimentary tract. There is a growing appreciation for the roles gut microbiota play in host biology. The gut microbiota of insects, for example, have been shown to help the host overcome pathogen infection either through direct competition or indirectly by stimulating host immunity. These defenses may also be supplemented by coinfecting maternally inherited microbes such as Wolbachia. The presence of Wolbachia in a host can delay and/or reduce death caused by RNA viruses. Whether the gut microbiota of the host interacts with Wolbachia, or vice versa, the precise role of Wolbachia in antiviral protection is not known. In this study, we used 16S rDNA sequencing to characterise changes in gut microbiota composition in Drosophila melanogaster associated with Wolbachia infection and antibiotic treatment. We subsequently tested whether changes in gut composition via antibiotic treatment altered Wolbachia-mediated antiviral properties. We found that both antibiotics and Wolbachia significantly reduced the biodiversity of the gut microbiota without changing the total microbial load. We also showed that changing the gut microbiota composition with antibiotic treatment enhanced Wolbachia density but did not confer greater antiviral protection against Drosophila C virus to the host. We concluded there are significant interactions between Wolbachia and gut microbiota, but changing gut microbiota composition is not likely to be a means through which Wolbachia conveys antiviral protection to its host.
动物几乎经常受到微生物感染。这些微生物群中有很大一部分存在于消化道中。人们越来越认识到肠道微生物群在宿主生物学中所起的作用。例如,已证明昆虫的肠道微生物群可通过直接竞争或通过刺激宿主免疫间接帮助宿主克服病原体感染。这些防御也可能由同时感染的母体遗传微生物(如沃尔巴克氏体)补充。宿主中存在沃尔巴克氏体可延迟和/或减少由RNA病毒引起的死亡。宿主的肠道微生物群是否与沃尔巴克氏体相互作用,反之亦然,沃尔巴克氏体在抗病毒保护中的具体作用尚不清楚。在本研究中,我们使用16S rDNA测序来表征与沃尔巴克氏体感染和抗生素治疗相关的黑腹果蝇肠道微生物群组成的变化。我们随后测试了通过抗生素治疗改变肠道组成是否会改变沃尔巴克氏体介导的抗病毒特性。我们发现抗生素和沃尔巴克氏体均显著降低了肠道微生物群的生物多样性,而未改变总微生物负荷。我们还表明,用抗生素治疗改变肠道微生物群组成可提高沃尔巴克氏体密度,但并未赋予宿主对果蝇C病毒更强的抗病毒保护。我们得出结论,沃尔巴克氏体与肠道微生物群之间存在显著相互作用,但改变肠道微生物群组成不太可能是沃尔巴克氏体向其宿主传递抗病毒保护的一种方式。