肠道微生物群的早期破坏对两种宿主的寄生虫抵抗力具有相反的影响

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Ashley C Love, Mia L Nahom, Jessica Gutierrez, Lauren Albert, Sarah A Knutie
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引用次数: 0

摘要

肠道微生物群调节宿主健康的多个方面,包括新陈代谢和免疫系统的发育。然而,对于肠道微生物群如何影响野生生物宿主对寄生虫的反应,尤其是宿主与微生物群之间的相互作用是否会导致宿主物种之间寄生虫的差异,我们仍然知之甚少。本研究的目的是确定肠道微生物群在影响鸟类对巢穴寄生虫的反应中的作用,并调查这种关系在宿主物种之间是否存在差异。东部蓝鸟(Sialia sialis)和树燕(Tachycineta bicolor)都被吹蝇(Protocalliphora sialia)寄生,吹蝇幼虫以雏鸟的血液为食。我们通过实验操纵了蓝鸟和树燕雏鸟的肠道微生物群,给雏鸟口服抗生素或以无菌水作为对照。然后,我们对雏鸟的生理机能(血红蛋白、葡萄糖、寄生虫特异性 IgY 抗体水平)、身体形态测量、羽化前的存活率以及吹蝇的数量和大小进行了量化。实验性破坏雏鸟肠道微生物群会增加寄生虫在树燕体内的数量,但会降低寄生虫在蓝鸟体内的数量,这表明破坏微生物群对不同宿主物种的抵抗力有相反的影响。此外,实验性处理延缓了寄生虫的发育,并对两种宿主的雏鸟身体形态和生理产生了不同的影响。这些结果表明,肠道微生物群会导致宿主对吹蝇的抵抗力差异,并影响宿主与寄生虫之间的相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Early-Life Disruption of Gut Microbiota Has Opposing Effects on Parasite Resistance in Two Host Species.

Gut microbiota regulate multiple aspects of host health, including metabolism and the development of the immune system. However, we still know relatively little about how the gut microbiota influences host responses to parasitism in wild organisms, particularly whether host-microbiota interactions contribute to variation in parasitism across host species. The goal of this study was to determine the role of gut microbiota in shaping how birds respond to nest parasites and investigate whether this relationship varies between host species. Both eastern bluebirds (Sialia sialis) and tree swallows (Tachycineta bicolor) are parasitized by blow flies (Protocalliphora sialia), for which larval flies feed on nestlings' blood. We experimentally manipulated the gut microbiota of nestling bluebirds and tree swallows by dosing nestlings with an oral antibiotic or sterile water as a control. We then quantified nestling physiology (haemoglobin, glucose, parasite-specific IgY antibody levels), body morphometrics, and survival until fledging, as well as blow fly abundance and size. An experimental disruption of nestling gut microbiota increased parasite abundance in tree swallows, but decreased parasite abundance in bluebirds, which suggests that the disruption has opposing effects on resistance across host species. Furthermore, experimental treatment delayed parasite development and had variable effects on nestling body morphometrics and physiology across the two host species. Together, these results suggest that gut microbiota contribute to host differences in resistance to blow flies and can influence host-parasite interactions.

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来源期刊
Molecular Ecology
Molecular Ecology 生物-进化生物学
CiteScore
8.40
自引率
10.20%
发文量
472
审稿时长
1 months
期刊介绍: Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include: * population structure and phylogeography * reproductive strategies * relatedness and kin selection * sex allocation * population genetic theory * analytical methods development * conservation genetics * speciation genetics * microbial biodiversity * evolutionary dynamics of QTLs * ecological interactions * molecular adaptation and environmental genomics * impact of genetically modified organisms
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