解密根瘤菌圈中微生物的适应性:洞察生态位偏好、功能特征和跨群落共存。

IF 3.3 3区 生物学 Q2 ECOLOGY
Yansu Wang, Quan Zou
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引用次数: 0

摘要

根圈微生物群落是植物生长和生命力的关键因素,其适应性分化策略受到越来越多的关注,但人们对其了解甚少。在这项研究中,我们从不同生态系统的根圈和大体积土壤中获取了细菌和真菌扩增子序列,以研究微生物适应根圈环境的潜在机制。我们的研究重点包括三个方面:生态位偏好、功能特征和跨领域共存模式。我们的发现揭示了生态位相似性与核苷酸距离之间的相关性,表明生态位适应可以解释一些密切相关的扩增子序列变体(ASV)之间的核苷酸变异。此外,生物大分子代谢和丰富细菌之间的交流在根瘤菌层条件下有所增加,这表明细菌功能在新生境的适应性方面是由性状介导的。此外,我们对跨领域网络的分析表明,真菌是促进细菌之间联系的中介,这表明微生物可以改变它们的合作关系以适应环境。总之,通过基因、功能和共生模式的差异,根瘤微生物群落适应性的证据阐明了根瘤微生物群落通过生态位转移而获得的遗传和功能灵活性的适应性益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Deciphering Microbial Adaptation in the Rhizosphere: Insights into Niche Preference, Functional Profiles, and Cross-Kingdom Co-occurrences.

Deciphering Microbial Adaptation in the Rhizosphere: Insights into Niche Preference, Functional Profiles, and Cross-Kingdom Co-occurrences.

Rhizosphere microbial communities are to be as critical factors for plant growth and vitality, and their adaptive differentiation strategies have received increasing amounts of attention but are poorly understood. In this study, we obtained bacterial and fungal amplicon sequences from the rhizosphere and bulk soils of various ecosystems to investigate the potential mechanisms of microbial adaptation to the rhizosphere environment. Our focus encompasses three aspects: niche preference, functional profiles, and cross-kingdom co-occurrence patterns. Our findings revealed a correlation between niche similarity and nucleotide distance, suggesting that niche adaptation explains nucleotide variation among some closely related amplicon sequence variants (ASVs). Furthermore, biological macromolecule metabolism and communication among abundant bacteria increase in the rhizosphere conditions, suggesting that bacterial function is trait-mediated in terms of fitness in new habitats. Additionally, our analysis of cross-kingdom networks revealed that fungi act as intermediaries that facilitate connections between bacteria, indicating that microbes can modify their cooperative relationships to adapt. Overall, the evidence for rhizosphere microbial community adaptation, via differences in gene and functional and co-occurrence patterns, elucidates the adaptive benefits of genetic and functional flexibility of the rhizosphere microbiota through niche shifts.

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来源期刊
Microbial Ecology
Microbial Ecology 生物-海洋与淡水生物学
CiteScore
6.90
自引率
2.80%
发文量
212
审稿时长
3-8 weeks
期刊介绍: The journal Microbial Ecology was founded more than 50 years ago by Dr. Ralph Mitchell, Gordon McKay Professor of Applied Biology at Harvard University in Cambridge, MA. The journal has evolved to become a premier location for the presentation of manuscripts that represent advances in the field of microbial ecology. The journal has become a dedicated international forum for the presentation of high-quality scientific investigations of how microorganisms interact with their environment, with each other and with their hosts. Microbial Ecology offers articles of original research in full paper and note formats, as well as brief reviews and topical position papers.
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