暴露于亚致死抗生素污染的质球微生物群的细菌动态。

IF 13.8 1区 生物学 Q1 MICROBIOLOGY Microbiome Pub Date : 2024-05-24 DOI:10.1186/s40168-024-01803-2
Brune Joannard, Concepcion Sanchez-Cid
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引用次数: 0

摘要

背景:抗生素和微塑料是两种主要的水生污染物,它们与环境中抗生素耐药性的选择有关,并被认为对人类健康构成风险。然而,人们对这些污染物在环境浓度下的相互作用以及质界微生物群落对亚致死抗生素污染的反应知之甚少。在此,我们采用多种方法(下一代测序和 qPCR)、测序目标(16S rRNA 基因、临床前和临床 1 类整合素盒和元基因组)、技术(短读和长读测序)和组装方法(非组装读数、基因组组装、噬菌体和质粒组装),从群落、抗性组和动员组水平描述了地表水细菌的这种反应所依据的细菌动力学:我们的研究结果表明,与地表水群落相比,塑球微生物群落对抗生素的反应发生了变化,并描述了对抗生素和微塑料污染做出不同反应的细菌亚群。质球对抗生素的耐受性增强,并选择了不同的抗生素耐药细菌(ARB)和抗生素耐药基因(ARGs)。从抗生素暴露的质球中提取的几个元基因组组装基因组(MAGs)含有ARGs、毒力因子和参与质粒共轭的基因。其中包括 Comamonas、Chryseobacterium、机会性病原体 Stenotrophomonas maltophilia,以及属于 Achromobacter 等与人类感染有关的菌属的其他 MAGs。在暴露于环丙沙星的情况下,淡水微生物群落和质体中与整合素相关的环丙沙星抗性基因 aac(6')-Ib-cr 的丰度都有所增加。关于抗生素移动组,虽然在污染样本中没有观察到 1 类整合子和质粒中 ARG 负荷的显著变化,但我们发现了三个含有 ARG 的病毒 contig,它们作为原生体整合到了 MAG 中:本研究说明了质粒的选择性如何在亚致死选择压力下影响细菌对抗生素的反应。这里发现的微生物变化有助于确定质膜的选择性作用及其对环境抗生素耐药性的维持以及其他人为污染物的影响。这项研究强调了利用综合压力的复杂情景来评估水生污染物对环境微生物群落影响的必要性。视频摘要。
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Bacterial dynamics of the plastisphere microbiome exposed to sub-lethal antibiotic pollution.

Background: Antibiotics and microplastics are two major aquatic pollutants that have been associated to antibiotic resistance selection in the environment and are considered a risk to human health. However, little is known about the interaction of these pollutants at environmental concentrations and the response of the microbial communities in the plastisphere to sub-lethal antibiotic pollution. Here, we describe the bacterial dynamics underlying this response in surface water bacteria at the community, resistome and mobilome level using a combination of methods (next-generation sequencing and qPCR), sequencing targets (16S rRNA gene, pre-clinical and clinical class 1 integron cassettes and metagenomes), technologies (short and long read sequencing), and assembly approaches (non-assembled reads, genome assembly, bacteriophage and plasmid assembly).

Results: Our results show a shift in the microbial community response to antibiotics in the plastisphere microbiome compared to surface water communities and describe the bacterial subpopulations that respond differently to antibiotic and microplastic pollution. The plastisphere showed an increased tolerance to antibiotics and selected different antibiotic resistance bacteria (ARB) and antibiotic resistance genes (ARGs). Several metagenome assembled genomes (MAGs) derived from the antibiotic-exposed plastisphere contained ARGs, virulence factors, and genes involved in plasmid conjugation. These include Comamonas, Chryseobacterium, the opportunistic pathogen Stenotrophomonas maltophilia, and other MAGs belonging to genera that have been associated to human infections, such as Achromobacter. The abundance of the integron-associated ciprofloxacin resistance gene aac(6')-Ib-cr increased under ciprofloxacin exposure in both freshwater microbial communities and in the plastisphere. Regarding the antibiotic mobilome, although no significant changes in ARG load in class 1 integrons and plasmids were observed in polluted samples, we identified three ARG-containing viral contigs that were integrated into MAGs as prophages.

Conclusions: This study illustrates how the selective nature of the plastisphere influences bacterial response to antibiotics at sub-lethal selective pressure. The microbial changes identified here help define the selective role of the plastisphere and its impact on the maintenance of environmental antibiotic resistance in combination with other anthropogenic pollutants. This research highlights the need to evaluate the impact of aquatic pollutants in environmental microbial communities using complex scenarios with combined stresses. Video Abstract.

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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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