From grasslands to genes: exploring the major microbial drivers of antibiotic-resistance in microhabitats under persistent overgrazing.

IF 13.8 1区 生物学 Q1 MICROBIOLOGY Microbiome Pub Date : 2024-11-22 DOI:10.1186/s40168-024-01965-z
Jian Li, Quanhui Ma, Mingkang Jin, Lijie Huang, Dafeng Hui, Jordi Sardans, Josep Peñuelas, Patrick O'Connor, Yu Zhu, Xiaoru Yang, Ling Wang, Yong-Guan Zhu
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Abstract

Background: The extensive use of antibiotics in the global livestock industry in recent decades has accelerated the accumulation and dissemination of antibiotic-resistance genes (ARGs) within terrestrial ecosystems. This occurs due to the limited absorption of most antibiotics, leading to their release into the environment through feces and urine. This poses a significant threat to both the environment and human health. However, the response of antibiotic-resistant microorganisms and their ARGs in grasslands to prolonged grazing, as well as the primary microbial taxa driving the ARG distribution, remain poorly understood, especially within various microhabitats. In this study, we characterized ARGs in the phyllosphere, litter, and soil after decades of livestock grazing in a meadow steppe. We particularly focused on identifying the major members of the microbial community influencing ARGs and the distinction between microbial generalists and specialists.

Results: Our findings indicate that a core set of ARGs accounted for 90% of the abundance in this plant-soil ecosystem. While the soil exhibited the highest ARG abundance, the phyllosphere, and litter displayed higher ARG diversity and diverse distribution patterns after overgrazing. Grazing increased ARG abundance by elevating the proportion of core ARGs and suppressing stochastic ARGs in the phyllosphere and litter, while it had little effect on the ARGs in the soil. Additionally, microbial generalist abundance increased, but specialist abundance decreased in the phyllosphere and litter, with no effect in the soil, under grazed conditions. Ultimately, microbial microhabitats and grazing influenced ARG community characteristics through direct (i.e., feces and other exogenous ARG input) and indirect (i.e., trampling and selective feeding) effects on nutrient availability, microbial community composition, and mobile genetic elements. The generalist community, with its broad ecological niches and phylogenetic composition, made the most significant contribution to the ARG characteristics.

Conclusions: This study underscores the impact of environmental disturbances on the distributional patterns of ARGs in ecosystems, mediated by the regulation of microbial generalized species. These insights enhance our understanding of microbial control over ARGs and facilitate predictions regarding the dynamics and risk of ARGs in diverse ecological niches subjected to anthropogenic disturbances. Video Abstract.

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从草原到基因:探索持续过度放牧下微生境中抗生素耐药性的主要微生物驱动因素。
背景:近几十年来,全球畜牧业广泛使用抗生素,加速了抗生素耐药性基因(ARGs)在陆地生态系统中的积累和传播。这是因为大多数抗生素的吸收能力有限,导致抗生素通过粪便和尿液释放到环境中。这对环境和人类健康都构成了重大威胁。然而,人们对草地中抗生素微生物及其ARG对长期放牧的反应以及驱动ARG分布的主要微生物类群仍然知之甚少,尤其是在各种微生境中。在这项研究中,我们描述了草甸草原经过数十年牲畜放牧后植物圈、枯落物和土壤中 ARG 的特征。我们特别关注确定影响ARGs的微生物群落的主要成员,以及微生物通才和专才之间的区别:结果:我们的研究结果表明,在这个植物-土壤生态系统中,一组核心 ARGs 占到丰度的 90%。虽然土壤中的ARG丰度最高,但过度放牧后,植被层和枯落物中的ARG多样性更高,分布模式也更多样。放牧提高了ARG的丰度,增加了核心ARG的比例,抑制了植被层和枯落物中的随机ARG,而对土壤中的ARG几乎没有影响。此外,在放牧条件下,植被层和枯落物中的微生物通性丰度增加,但专性丰度降低,而土壤中则没有影响。最终,微生物微生境和放牧通过直接(即粪便和其他外源 ARG 输入)和间接(即践踏和选择性取食)影响养分供应、微生物群落组成和移动遗传元素,从而影响 ARG 群落特征。普通群落具有广泛的生态位和系统发育组成,对ARG特征的贡献最大:这项研究强调了环境干扰对生态系统中 ARGs 分布模式的影响,这种影响是通过微生物广义物种的调控来实现的。这些见解加深了我们对微生物控制ARGs的理解,有助于预测ARGs在受到人为干扰的不同生态位中的动态和风险。视频摘要。
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来源期刊
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
期刊介绍: Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.
期刊最新文献
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