Growth of microbes in competitive lifestyles promotes increased ARGs in soil microbiota: insights based on genetic traits.

IF 13.8 1区 生物学 Q1 MICROBIOLOGY
Zishu Liu, Xiangwu Yao, Chengyi Chen, Yuxiang Zhao, Chifei Dong, Lingtao Sun, Junxian Zhao, Baofeng Zhang, Zhendi Yu, Dongqing Cheng, Lizhong Zhu, Baolan Hu
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引用次数: 0

Abstract

Background: The widespread selective pressure of antibiotics in the environment has led to the propagation of antibiotic resistance genes (ARGs). However, the mechanisms by which microbes balance population growth with the enrichment of ARGs remain poorly understood. To address this, we employed microcosm cultivation at different antibiotic (i.e., Oxytetracycline, OTC) stresses across the concentrations from the environmental to the clinical. Paired with shot-gun metagenomics analysis and quantification of bacterial growth, trait-based assessment of soil microbiota was applied to reveal the association between key ARG subtypes, representative bacterial taxa, and functional-gene features that drive the growth of ARGs.

Results: Our results illuminate that resistome variation is closely associated with bacterial growth. A non-monotonic change in ARG abundance and richness was observed over a concentration gradient from none to 10 mg/l. Soil microbiota exposed to intermediate OTC concentrations (i.e., 0.1 and 0.5 mg/l) showed greater increases in the total abundance of ARGs. Community compositionally, the growth of representative taxa, i.e., Pseudomonadaceae was considered to boost the increase of ARGs. It has chromosomally carried kinds of multidrug resistance genes such as mexAB-oprM and mexCD-oprJ could mediate the intrinsic resistance to OTC. Streptomycetaceae has shown a better adaptive ability than other microbes at the clinical OTC concentrations. However, it contributed less to the ARGs growth as it represents a stress-tolerant lifestyle that grows slowly and carries fewer ARGs. In terms of community genetic features, the community aggregated traits analysis further indicates the enhancement in traits of resource acquisition and growth yield is driving the increase of ARGs abundance. Moreover, optimizations in energy production and conversion, alongside a streamlining of bypass metabolic pathways, further boost the growth of ARGs in sub-inhibitory antibiotic conditions.

Conclusion: The results of this study suggest that microbes with competitive lifestyles are selected under the stress of environmental sub-inhibitory concentrations of antibiotics and nutrient scarcity. They possess greater substrate utilization capacity and carry more ARGs, due to this they were faster growing and leading to a greater increase in the abundance of ARGs. This study has expanded the application of trait-based assessments in understanding the ecology of ARGs propagation. And the finding illustrated changes in soil resistome are accompanied by the lifestyle switching of the microbiome, which theoretically supports the ARGs control approach based on the principle of species competitive exclusion. Video Abstract.

微生物在竞争性生活方式中的生长促进了土壤微生物群中ARGs的增加:基于遗传性状的见解。
背景:抗生素在环境中的广泛选择压力导致抗生素耐药基因(ARGs)的繁殖。然而,微生物平衡种群增长与ARGs富集的机制仍然知之甚少。为了解决这个问题,我们在不同的抗生素(即土霉素,OTC)压力下进行了微观培养,从环境浓度到临床浓度。结合微基因组学分析和细菌生长定量分析,采用基于性状的土壤微生物群评估来揭示关键ARG亚型、代表性细菌分类群和驱动ARG生长的功能基因特征之间的关联。结果:我们的研究结果表明,抵抗组变异与细菌生长密切相关。在浓度梯度从0到10 mg/l范围内,ARG丰度和丰富度呈非单调变化。暴露于中等OTC浓度(即0.1和0.5 mg/l)的土壤微生物群显示出更大的ARGs总丰度增加。群落组成上,假单胞菌科(Pseudomonadaceae)等代表性类群的生长促进了ARGs的增加。染色体携带的多药耐药基因如mexAB-oprM和mexd - oprj可介导OTC的内在耐药。链霉菌科在临床OTC浓度下表现出比其他微生物更好的适应能力。然而,它对arg的增长贡献较小,因为它代表了一种生长缓慢且携带较少arg的耐压生活方式。群落遗传特征方面,群落聚集性状分析进一步表明,资源获取性状和生长产量性状的提高是ARGs丰度增加的驱动因素。此外,能量产生和转化的优化,以及旁路代谢途径的简化,进一步促进了亚抑制性抗生素条件下ARGs的生长。结论:本研究结果表明,在抗生素亚抑制浓度和营养物质匮乏的环境压力下,具有竞争性生活方式的微生物被选择。它们具有更大的底物利用能力,携带更多的arg,因此它们生长更快,导致arg丰度增加更大。本研究拓展了性状评价在认识ARGs繁殖生态学中的应用。研究结果表明,土壤抗性组的变化伴随着微生物组生活方式的改变,这在理论上支持了基于物种竞争排斥原理的ARGs控制方法。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.
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