黑腹果蝇对病原体感染的实验性适应可改善交配对宿主感染后存活率的负面影响

IF 1.6 3区 生物学 Q2 ZOOLOGY
Zoology Pub Date : 2024-08-13 DOI:10.1016/j.zool.2024.126198
Aabeer Basu, Aparajita Singh, B.G. Ruchitha , Nagaraj Guru Prasad
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引用次数: 0

摘要

性活动(交配)会对各种昆虫的免疫功能产生负面影响。在黑腹果蝇雌虫中,交配会增加对病原体挑战的易感性,并促进宿主内病原体的扩散。这种效应取决于病原体和宿主基因型。我们测试了在实验中适应病原体感染的宿主中,交配引起的感染易感性增加的程度是更高还是更低。我们选择了感染细菌病原体粪肠球菌后存活率增加的黑腹蝇蛆重复种群。我们发现,与对照种群的雌性黑腹滨蝇相比,选育种群的雌性黑腹滨蝇在病原体感染后的存活率更高。无论是用于选择的病原体还是其他新型病原体(即宿主近期未遇到过的病原体)都是如此。此外,交配对感染后存活率的负面影响仅限于对照种群中的雌性。因此,我们已经证明,通过实验选择提高感染后存活率可以改善交配对宿主感染易感性的负面影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Experimental adaptation to pathogenic infection ameliorates negative effects of mating on host post-infection survival in Drosophila melanogaster

Sexual activity (mating) negatively affects immune function in various insect species across both sexes. In Drosophila melanogaster females, mating increases susceptibility to pathogenic challenges and encourages within-host pathogen proliferation. This effect is pathogen and host genotype dependent. We tested if mating-induced increased susceptibility to infections is more, or less, severe in hosts experimentally adapted to pathogenic infection. We selected replicate D. melanogaster populations for increased post-infection survival following infection with a bacterial pathogen, Enterococcus faecalis. We found that females from the selected populations were better at surviving a pathogenic infection compared to the females from the control populations. This was true in the case of both the pathogen used for selection and other novel pathogens (i.e., pathogens the hosts have not encountered in recent history). Additionally, the negative effect of mating on post-infection survival was limited to only the females from control populations. Therefore, we have demonstrated that experimental selection for increased post-infection survival ameliorates negative effects of mating on host susceptibility to infections.

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来源期刊
Zoology
Zoology 生物-动物学
CiteScore
3.90
自引率
0.00%
发文量
37
审稿时长
70 days
期刊介绍: Zoology is a journal devoted to experimental and comparative animal science. It presents a common forum for all scientists who take an explicitly organism oriented and integrative approach to the study of animal form, function, development and evolution. The journal invites papers that take a comparative or experimental approach to behavior and neurobiology, functional morphology, evolution and development, ecological physiology, and cell biology. Due to the increasing realization that animals exist only within a partnership with symbionts, Zoology encourages submissions of papers focused on the analysis of holobionts or metaorganisms as associations of the macroscopic host in synergistic interdependence with numerous microbial and eukaryotic species. The editors and the editorial board are committed to presenting science at its best. The editorial team is regularly adjusting editorial practice to the ever changing field of animal biology.
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