The dynamics of microbiome and virome in migratory birds of southwest China.

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Qingqing Luo, Hongyan Gao, Yujia Xiang, Jian Li, Lin Dong, Xingran Wang, Fangqing Liu, Yuhong Guo, Chao Shen, Qiang Ding, Chengfeng Qin, Guanxiang Liang, Longying Wen
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Abstract

Migratory birds carry pathogens, posing a significant threat to environmental and human health. We documented the metatranscriptome and RNA virome of 896 stool samples from migratory birds and environmental samples over four consecutive years in southwest China. Our analysis identified Catellicoccus marimammalium as the predominant bacterium in the gut of black-headed gulls, with an average relative abundance of 79.3%. Strain-level analysis of C. marimammalium revealed a dominant population with some longitudinal diversity over the four years. Additionally, the gut of black-headed gulls was found to harbor numerous viruses, including a novel hepatovirus. Lysates of cells of C. marimammalium but not other bacteria derived from black-headed gulls could inhibit the replication of human hepatovirus, suggesting a potential regulatory role for gut commensal bacteria in modulating viral carriage. These findings enhance our understanding of the microbiome and RNA virome diversity in migratory birds and provide insights into the modulation of asymptomatic infections.

西南地区候鸟微生物群和病毒群动态。
候鸟携带病原体,对环境和人类健康构成重大威胁。我们记录了中国西南地区896份候鸟粪便样本和环境样本的亚转录组和RNA病毒组。通过分析发现,黑头鸥肠道中的优势菌为海洋哺乳Catellicoccus marim哺乳菌,平均相对丰度为79.3%。种群水平分析表明,4年间海带海带海带具有一定的纵向多样性,为优势种群。此外,黑头鸥的肠道被发现含有许多病毒,包括一种新的肝病毒。来源于黑头鸥的C. marimamalium细胞的裂解物能够抑制人肝病毒的复制,而其他来源于黑头鸥的细菌则不能,这表明肠道共生菌在调节病毒携带方面具有潜在的调节作用。这些发现增强了我们对候鸟微生物组和RNA病毒组多样性的理解,并为无症状感染的调节提供了见解。
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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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