Gene horizontal transfers and functional diversity negatively correlated with bacterial taxonomic diversity along a nitrogen gradient.

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY npj Biofilms and Microbiomes Pub Date : 2024-11-16 DOI:10.1038/s41522-024-00588-4
Jian-Xia Yang, Yang Peng, Qing-Yi Yu, Jun-Jie Yang, Yun-Hai Zhang, Hai-Yang Zhang, Catharine Allyssa Adams, Claire Elizabeth Willing, Cong Wang, Qiu-Shi Li, Xing-Guo Han, Cheng Gao
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Abstract

Horizontal gene transfer (HGT) mediated diversification is a critical force driving evolutionary and ecological processes. However, how HGT might relate to anthropogenic activity such as nitrogen addition, and its subsequent effect on functional diversity and cooccurrence networks remain unknown. Here we approach this knowledge gap by blending bacterial 16S rRNA gene amplicon and shotgun metagenomes from a platform of cessation of nitrogen additions and continuous nitrogen additions. We found that bacterial HGT events, functional genes, and virus diversities increased whereas bacterial taxonomic diversity decreased by nitrogen additions, resulting in a counterintuitive strong negative association between bacterial taxonomic and functional diversities. Nitrogen additions, especially the ceased one, complexified the cooccurrence network by increasing the contribution of vitamin B12 auxotrophic Acidobacteria, indicating cross-feeding. These findings advance our perceptions of the causes and consequences of the diversification process in community ecology.

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沿氮梯度的基因水平转移和功能多样性与细菌分类多样性呈负相关。
水平基因转移(HGT)介导的多样化是推动进化和生态过程的关键力量。然而,HGT 与氮添加等人为活动的关系及其对功能多样性和共生网络的影响仍然未知。在这里,我们通过混合细菌 16S rRNA 基因扩增片段和来自停止加氮和持续加氮平台的散弹枪元基因组来填补这一知识空白。我们发现,细菌的 HGT 事件、功能基因和病毒多样性随着氮添加量的增加而增加,而细菌分类多样性则随着氮添加量的增加而减少,从而导致细菌分类多样性和功能多样性之间出现了一种反直觉的强烈负相关。氮添加(尤其是停止添加)增加了维生素 B12 辅助型酸杆菌的贡献,从而使共生网络复杂化,这表明存在交叉觅食现象。这些发现推进了我们对群落生态学中多样化过程的原因和后果的认识。
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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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