宿主转录组学揭示了共同感染期间防御-繁殖权衡的减少。

IF 3.9 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Ian Will, Emily J Stevens, Kayla C King, Kieran A Bates
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引用次数: 0

摘要

在感染期间,宿主可能将资源从繁殖转移到免疫防御。目前尚不清楚在保护性共感染期间,这些代价高昂的权衡可以在多大程度上得到缓解,即寄生虫之间的拮抗作用可以降低疾病的严重程度。我们使用转录组学来评估宿主基因表达反映保护效果的程度,以及减少或增加免疫投资是否会对生殖造成影响。与自然感染的“保护性寄生虫”白杆菌相比,白杆菌细菌的毒性感染在线虫宿主中引起了更大的权衡。我们进一步发现,共感染减弱了宿主对促免疫权衡的投资,而没有显著改变宿主基因的参与。然后,我们试图了解这种减弱的宿主反应是否与寄生虫间竞争的可能机制一致。我们对两种寄生虫的染色体长度基因组组装表明,保护性共感染可能通过对公共物品的竞争而起作用,例如铁载体介导的金属离子(如铁)的摄取或宿主角质层的定植。最后,我们表明,共同感染的寄生虫之间的竞争可以补充内源性宿主防御,并减轻对抗有害感染的生殖成本。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Host Transcriptomics Reveal Reduction in Defence-Reproduction Trade-Offs During Coinfection.

During infection, hosts may shift resources away from reproduction towards immune defence. It is unclear to what degree these costly trade-offs can be alleviated during protective coinfections, whereby antagonism between parasites reduces disease severity. We used transcriptomics to assess the extent to which host gene expression reflected the effect of protection and whether reducing or increasing investment in immunity carried costs to reproduction. Virulent infections by Leucobacter musarum bacteria elicited greater trade-offs in nematode hosts compared to the naturally coinfecting 'protective parasite' Leucobacter celer. We further found that coinfection attenuated host investment in pro-immune trade-offs, without significantly changing which host genes were involved. We then sought to understand if this attenuated host response would be consistent with possible mechanisms of inter-parasite competition. Our chromosome length genome assemblies for both parasite species revealed that protective coinfection may operate by competition for public goods, such as siderophore-mediated uptake of metal ions (e.g., iron) or colonisation of the host cuticle. Ultimately, we show that competition between coinfecting parasites can complement endogenous host defences and ease the reproductive costs of fighting harmful infection.

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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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