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中国水中源性环境细菌和弗氏柠檬酸杆菌临床分离株中 qnr 和 aac(6')-Ib-cr 基因的高流行率。

High prevalence of qnr and aac(6')-Ib-cr genes in both water-borne environmental bacteria and clinical isolates of Citrobacter freundii in China.

机构信息

Second affiliated hospital of Zhejiang University, Zhejiang University, 88 JieFang Rd, Hangzhou 310009, China.

出版信息

Microbes Environ. 2012;27(2):158-63. doi: 10.1264/jsme2.me11308.

Abstract

We investigated the prevalence of qnr and aac(6')-Ib-cr genes in water-borne environmental bacteria and in clinical isolates of Enterobacteriaceae, as well as the subtypes of qnr. Environmental bacteria were isolated from surface water samples obtained from 10 different locations in Hangzhou City, and clinical isolates of Citrobacter freundii were isolated from several hospitals in four cities in China. qnrA, qnrB, qnrS, and aac(6')-Ib-cr genes were screened using PCR, and the genotypes were analyzed by DNA sequencing. Ten of the 78 Gram-negative bacilli isolated from water samples were C. freundii and 80% of these isolates carried the qnrB gene. qnrS1 and aac(6')-Ib-cr genes were detected in two Escherichia coli isolates and qnrS2 was detected in one species, Aeromonas punctata. The qnr and aac(6')-Ib-cr genes were present in 75 (72.8%) and 12 (11.6%) of 103 clinical isolates of C. freundii, respectively. Of the clinical C. freundii isolates with the qnr gene, 65 isolates (63.1%) carried qnrB, but only three (2.9%) and one (1.0%) carried qnrA1 and qnrS2, respectively, while five isolates carried both qnrA1 and qnrB, and one isolate carried both qnrS1 and qnrB. The qnrB9 gene was the dominant qnrB subtype, followed by qnrB8 and qnrB6. Southern hybridization studies indicated that the qnr genes are located on different plasmids. Plasmids isolated from both environmental and clinical C. freundii isolates appeared to be homogenous.

摘要

我们调查了水中环境细菌和肠杆菌科临床分离株中 qnr 和 aac(6')-Ib-cr 基因的流行情况,以及 qnr 的亚型。从杭州市 10 个不同地点的地表水样本中分离出环境细菌,从中国四个城市的几家医院分离出弗氏柠檬酸杆菌的临床分离株。使用 PCR 筛选 qnrA、qnrB、qnrS 和 aac(6')-Ib-cr 基因,并通过 DNA 测序分析基因型。从水样中分离出的 78 株革兰氏阴性杆菌中有 10 株为弗氏柠檬酸杆菌,其中 80%的分离株携带 qnrB 基因。在两株大肠杆菌分离株中检测到 qnrS1 和 aac(6')-Ib-cr 基因,在一株气单胞菌中检测到 qnrS2 基因。在 103 株弗氏柠檬酸杆菌临床分离株中,分别有 75 株(72.8%)和 12 株(11.6%)携带 qnr 和 aac(6')-Ib-cr 基因。在携带 qnr 基因的临床弗氏柠檬酸杆菌分离株中,有 65 株(63.1%)携带 qnrB,但仅 3 株(2.9%)和 1 株(1.0%)携带 qnrA1 和 qnrS2,而 5 株携带 qnrA1 和 qnrB,1 株携带 qnrS1 和 qnrB。qnrB9 是主要的 qnrB 亚型,其次是 qnrB8 和 qnrB6。Southern 杂交研究表明,qnr 基因位于不同的质粒上。从环境和临床弗氏柠檬酸杆菌分离株中分离出的质粒似乎是同质的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d40/4036021/ce9dfbbebe75/27_158f1.jpg

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