Air pollution modifies colonisation factors in beneficial symbiont Snodgrassella and disrupts the bumblebee gut microbiome.

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY npj Biofilms and Microbiomes Pub Date : 2025-01-02 DOI:10.1038/s41522-024-00632-3
Hannah R Sampson, Natalie Allcock, Eamonn B Mallon, Julian M Ketley, Julie A Morrissey
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Abstract

Particulate air pollutants, a major air pollution component, are detrimental to human health and a significant risk to wildlife and ecosystems globally. Here we report the effects of particulate pollutant black carbon on the beneficial gut microbiome of important global insect pollinator, the buff-tailed bumblebee (Bombus terrestris). Our data shows that exposure to black carbon particulates alters biofilm structure, gene expression and initial adhesion of beneficial bee gut coloniser, Snodgrassella alvi. Exposure of adult Bombus terrestris to non-toxic black carbon particulates significantly increased viable bacteria on MRS agar and 16S absolute abundance of beneficial bacteria Bombilactobacillus in Post-treated bumblebees compared to Pre-treated, demonstrating disruption of the bumblebee gut microbiome. These findings show that black carbon exposure has direct, measurable effects on bees' beneficial commensal bacteria and microbiome. Together these data highlight that black carbon, a single type of particulate pollution, is an underexplored risk to insect pollinator health.

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空气污染改变了有益共生体雪草的定植因子,破坏了大黄蜂的肠道微生物群。
颗粒物空气污染物是空气污染的一个主要组成部分,对人类健康有害,并对全球野生动物和生态系统构成重大风险。在这里,我们报告了颗粒污染物黑碳对全球重要昆虫传粉者黄尾大黄蜂有益肠道微生物群的影响。我们的数据表明,暴露于黑碳颗粒会改变有益的蜜蜂肠道殖民者斯诺德·格拉·阿尔维的生物膜结构、基因表达和初始粘附。与预处理相比,将成虫暴露于无毒黑碳颗粒中显著增加了MRS琼脂上的活菌和处理后的大黄蜂中有益细菌Bombilactobacillus的16S绝对丰度,证明了大黄蜂肠道微生物群的破坏。这些发现表明,黑碳暴露对蜜蜂有益的共生细菌和微生物群有直接的、可测量的影响。总之,这些数据突出表明,黑碳是一种单一类型的颗粒污染,对传粉昆虫的健康构成了未被充分探索的风险。
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来源期刊
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
期刊介绍: npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.
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