掠食性原生生物和掠食性细菌在细菌耐药性进化中的共同作用

IF 10.3 1区 农林科学 Q1 SOIL SCIENCE
Thi Bao-Anh Nguyen , Kenneth Dumack , Michael Bonkowski , Qing-Lin Chen , Tim Urich , Verena Groß , Ji-Zheng He , Hang-Wei Hu
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引用次数: 0

摘要

生物因素,特别是捕食者-猎物相互作用,是生态过程的关键驱动因素。然而,在复杂的自然土壤生态系统中,它们在推动抗生素耐药性演变中的作用仍然知之甚少,这是一个全球健康问题。掠夺性原生生物和掠夺性细菌是主要的细菌捕食者,然而,在多营养土壤生态系统中,它们的捕食对细菌抗生素耐药性丰富度和丰度的影响机制仍然知之甚少。在细菌的竞争对手真菌的控制下,我们评估了不同浓度的土壤掠食性原生生物对掠食性细菌和抗生素抗性基因(ARGs)的影响。我们的研究结果表明,高原生生物捕食压力显著增加了捕食性细菌链霉菌和黏液球菌的相对丰度。与掠食性细菌和产生抗生素的细菌的丰度上升一致,在高原生生物浓度下,土壤ARGs的相对丰度和多样性显著增加,而不考虑真菌的影响。许多编码关键耐药机制(抗生素失活和外排泵)的ARGs在复杂的群间相互作用中对掠夺性原生生物的反应中富集。此外,这些富集的ARGs与掠食性细菌和掠食性原生生物密切相关。在真菌存在的情况下,捕食原生生物对掠食性细菌和土壤ARGs的影响更为深远。我们的研究提供了新的证据,证明在自然土壤中,在复杂的多营养相互作用下,掠食性原生生物在形成掠食性细菌群落和驱动细菌抗生素耐药性方面的关键作用。这些发现为未来旨在减轻这一全球健康问题和揭示其他生态过程的研究铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Joint effects of predatory protists and predatory bacteria on driving the evolution of bacterial antibiotic resistance
Biological factors, especially predator-prey interactions, are crucial drivers of ecological processes. However, their roles in driving the evolution of antibiotic resistance, a global health concern, remain poorly understood in complex natural soil ecosystems. Predatory protists and predatory bacteria are primary bacterial predators, however, mechanisms underlying the influence of their predation on the richness and abundance of bacterial antibiotic resistance within a multitrophic soil ecosystem are still poorly known. Here, we assessed effects of soil predatory protists on predatory bacteria and antibiotic resistance genes (ARGs) across a gradient of protist concentrations under the control of bacteria's competitors – fungi. Our findings reveal that high-protist predation pressure significantly amplified the relative abundance of predatory bacteria Streptomycetales and Myxococcales between days 15 and 45 of the microcosm incubation. Aligning with a rising abundance of predatory bacteria and antibiotic-producing bacteria, the relative abundance and diversity of soil ARGs significantly increased under high protist concentrations, regardless of fungal effects. Many ARGs encoding key resistance mechanisms (antibiotic deactivation and efflux pumps) were enriched in response to predatory protists within complex inter-group interactions. Moreover, these enriched ARGs were strongly associated with both predatory bacteria and predatory protists. More profound effects of predatory protists on the predatory bacteria and soil ARGs were identified in the presence of fungi. Our study provides novel evidence about crucial effects of predatory protists on shaping the predatory bacterial community and driving bacterial antibiotic resistance under complex multitrophic interactions in a natural soil. These findings pave the way for future research aimed at mitigating this global health issue and uncovering other ecological processes.
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来源期刊
Soil Biology & Biochemistry
Soil Biology & Biochemistry 农林科学-土壤科学
CiteScore
16.90
自引率
9.30%
发文量
312
审稿时长
49 days
期刊介绍: Soil Biology & Biochemistry publishes original research articles of international significance focusing on biological processes in soil and their applications to soil and environmental quality. Major topics include the ecology and biochemical processes of soil organisms, their effects on the environment, and interactions with plants. The journal also welcomes state-of-the-art reviews and discussions on contemporary research in soil biology and biochemistry.
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