'Re-Wilding' an Animal Model With Microbiota Shifts Immunity and Stress Gene Expression During Infection.

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Ian Will, Emily J Stevens, Thomas Belcher, Kayla C King
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引用次数: 0

Abstract

The frequency of emerging disease is growing with ongoing human activity facilitating new host-pathogen interactions. Novel infection outcomes can also be shaped by the host microbiota. Caenorhabditis elegans nematodes experimentally colonised by a wild microbiota community and infected by the widespread animal pathogen, Staphylococcus aureus, have been shown to suffer higher mortality than those infected by the pathogen alone. Understanding the host responses to such microbiota-pathogen ecological interactions is key to pinpointing the mechanism underlying severe infection outcomes. We conducted transcriptomic analyses of C. elegans colonised by its native microbiota, S. aureus and both in combination. Correlations between altered collagen gene expression and heightened mortality in co-colonised hosts suggest the microbiota modified host resistance to infection. Furthermore, microbiota colonised hosts showed increased expression of immunity genes and variable expression of stress response genes during infection. Changes in host immunity and stress response could encompass both causes and effects of severe infection outcomes. 'Re-wilding' this model nematode host with its native microbiota indicated that typically commensal microbes can mediate molecular changes in the host that are costly when challenged by a novel emerging pathogen.

用微生物群 "野化 "动物模型,改变感染期间的免疫和应激基因表达。
随着人类活动不断促进新的宿主与病原体之间的相互作用,新发疾病的频率也在不断增加。新的感染结果也可能受宿主微生物群的影响。实验证明,被野生微生物群落定殖并被广泛传播的动物病原体金黄色葡萄球菌感染的秀丽隐杆线虫的死亡率高于仅被病原体感染的线虫。了解宿主对这种微生物群-病原体生态交互作用的反应是确定严重感染结果机制的关键。我们对被本地微生物群、金黄色葡萄球菌定殖的秀丽隐杆线虫进行了转录组分析。共同定植宿主的胶原蛋白基因表达改变与死亡率升高之间的相关性表明,微生物群改变了宿主对感染的抵抗力。此外,微生物群定植的宿主在感染期间表现出免疫基因表达的增加和应激反应基因表达的变化。宿主免疫力和应激反应的变化可能是造成严重感染结果的原因和影响。用本地微生物群 "野化 "这种线虫模式宿主表明,典型的共生微生物可以介导宿主的分子变化,而当宿主受到新出现的病原体挑战时,这种变化是代价高昂的。
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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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