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在一项宏基因组分析中,健康韩国人群的粪便中携带 bla、bla 和质粒介导的喹诺酮耐药基因。

High fecal carriage of bla, bla, and plasmid-mediated quinolone resistance genes among healthy Korean people in a metagenomic analysis.

机构信息

Division of Infectious Disease, Department of Internal Medicine, College of Medicine, Hanyang University, 222 Wangsimni-ro, Seongdong-gu, Seoul, 04763, Republic of Korea.

Department of Family Medicine, College of Medicine, Hanyang University, Seoul, 04763, Republic of Korea.

出版信息

Sci Rep. 2021 Mar 12;11(1):5874. doi: 10.1038/s41598-021-84974-4.

Abstract

To characterize the carriage of antibiotic resistance genes (ARGs) in the gut microbiome of healthy individuals. Fecal carriage of ARGs was investigated in 61 healthy individuals aged 30 to 59 years through whole metagenome sequencing of the gut microbiome and a targeted metagenomic approach. The number of ARGs in the gut microbiome was counted and normalized per million predicted genes (GPM). In the Korean population, the resistome ranged from 49.7 to 292.5 GPM (median 89.7). Based on the abundance of ARGs, the subjects were categorised into high (> 120 GPM), middle (60‒120 GPM), and low (< 60 GPM) ARG groups. Individuals in the high ARG group tended to visit hospitals more often (P = 0.065), particularly for upper respiratory tract infections (P = 0.066), and carried more bla (P = 0.008). The targeted metagenome approach for bla and plasmid-mediated quinolone resistance (PMQR) genes revealed a high fecal carriage rate; 23% or 13.1% of the subjects carried bla or bla, respectively. Regarding PMQR genes, 59% of the subjects carried PMQR, and 83% of them harboured 2‒4 PMQR genes (qnrB 44.3%, qnrS 47.5% etc.). The presence of bla correlated with ARG abundance in the gut resistome, whereas PMQR genes were irrelevant to other ARGs (P = 0.176). Fecal carriage of bla and PMQR genes was broad and multiplexed among healthy individuals.

摘要

目的

描述健康个体肠道微生物组中携带抗生素耐药基因(ARGs)的特征。

方法

通过对 61 名 30 至 59 岁健康个体的肠道微生物组进行全宏基因组测序和靶向宏基因组学分析,研究了 ARGs 在粪便中的携带情况。计算肠道微生物组中 ARGs 的数量,并按每百万个预测基因(GPM)进行标准化。在韩国人群中,耐药组的范围为 49.7 至 292.5 GPM(中位数 89.7)。根据 ARGs 的丰度,将受试者分为高(>120 GPM)、中(60-120 GPM)和低(<60 GPM)ARG 组。ARG 组较高的个体更倾向于经常去医院就诊(P=0.065),特别是上呼吸道感染(P=0.066),携带更多 bla(P=0.008)。针对 bla 和质粒介导的喹诺酮类耐药(PMQR)基因的靶向宏基因组学方法显示粪便携带率较高;分别有 23%或 13.1%的受试者携带 bla 或 bla。关于 PMQR 基因,59%的受试者携带 PMQR,其中 83%携带 2-4 种 PMQR 基因(qnrB 44.3%,qnrS 47.5%等)。bla 的存在与肠道耐药组中 ARG 的丰度相关,而 PMQR 基因与其他 ARGs 无关(P=0.176)。bla 和 PMQR 基因在健康个体中的粪便携带广泛且呈多重耐药。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b2b/7955109/53b0b9d1f2b4/41598_2021_84974_Fig1_HTML.jpg

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Transferable Mechanisms of Quinolone Resistance from 1998 Onward.1998 年以来喹诺酮类耐药的可转移机制。
Clin Microbiol Rev. 2019 Aug 14;32(4). doi: 10.1128/CMR.00007-19. Print 2019 Sep 18.

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