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疾病相关人体肠道微生物组中的耐药组扩张。

Resistome expansion in disease-associated human gut microbiomes.

机构信息

Host-Microbe Interactomics Group, Animal Sciences Department, Wageningen University & Research, Wageningen, The Netherlands.

出版信息

Microbiome. 2023 Jul 29;11(1):166. doi: 10.1186/s40168-023-01610-1.

Abstract

BACKGROUND

The resistome, the collection of antibiotic resistance genes (ARGs) in a microbiome, is increasingly recognised as relevant to the development of clinically relevant antibiotic resistance. Many metagenomic studies have reported resistome differences between groups, often in connection with disease and/or antibiotic treatment. However, the consistency of resistome associations with antibiotic- and non-antibiotic-treated diseases has not been established. In this study, we re-analysed human gut microbiome data from 26 case-control studies to assess the link between disease and the resistome.

RESULTS

The human gut resistome is highly variable between individuals both within and between studies, but may also vary significantly between case and control groups even in the absence of large taxonomic differences. We found that for diseases commonly treated with antibiotics, namely cystic fibrosis and diarrhoea, patient microbiomes had significantly elevated ARG abundances compared to controls. Disease-associated resistome expansion was found even when ARG abundance was high in controls, suggesting ongoing and additive ARG acquisition in disease-associated strains. We also found a trend for increased ARG abundance in cases from some studies on diseases that are not treated with antibiotics, such as colorectal cancer.

CONCLUSIONS

Diseases commonly treated with antibiotics are associated with expanded gut resistomes, suggesting that historical exposure to antibiotics has exerted considerable selective pressure for ARG acquisition in disease-associated strains. Video Abstract.

摘要

背景

抗药基因组,即微生物组中抗生素抗性基因(ARGs)的集合,越来越被认为与临床相关的抗生素抗性的发展有关。许多宏基因组研究报告了不同群体之间的抗药基因组差异,这些差异通常与疾病和/或抗生素治疗有关。然而,抗生素和非抗生素治疗疾病与抗药基因组之间的关联的一致性尚未得到证实。在这项研究中,我们重新分析了来自 26 项病例对照研究的人类肠道微生物组数据,以评估疾病与抗药基因组之间的联系。

结果

人类肠道抗药基因组在个体内和个体间的个体内和个体间都有很高的变异性,但即使在没有大的分类差异的情况下,病例组和对照组之间也可能存在显著差异。我们发现,对于常见的抗生素治疗疾病,即囊性纤维化和腹泻,患者的微生物组中 ARG 的丰度明显高于对照组。即使在对照组中 ARG 丰度较高的情况下,也发现了与疾病相关的抗药基因组扩张,这表明与疾病相关的菌株中持续存在并不断积累 ARG。我们还发现,一些未用抗生素治疗的疾病(如结直肠癌)的研究中,病例组的 ARG 丰度也有增加的趋势。

结论

常见的抗生素治疗疾病与肠道抗药基因组的扩张有关,这表明抗生素的历史暴露对与疾病相关的菌株中 ARG 的获得施加了相当大的选择压力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb47/10386251/5444f52837f8/40168_2023_1610_Fig1_HTML.jpg

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