Zhou Hong-Wei, Zhang Ting, Ma Ji-Hua, Fang Ying, Wang Han-Yu, Huang Zi-Xian, Wang Yang, Wu Congming, Chen Gong-Xiang
Second Affiliated Hospital of Zhejiang University, School of Medicine, Zhejiang University, Hangzhou, China.
The First Affiliated Hospital of Zhejiang University, School of Medicine, Zhejiang University, Hangzhou, China.
Antimicrob Agents Chemother. 2017 Jul 25;61(8). doi: 10.1128/AAC.00017-17. Print 2017 Aug.
The aim of this study was to investigate the prevalence of the polymyxin resistance gene in from environmental water sources in Hangzhou, China. Colistin-resistant bacteria were isolated from environmental water samples using an enrichment broth culture method, were screened for , and then were analyzed for the location and transferability of Isolates positive for were further examined to determine their susceptibility profiles and were screened for the presence of additional resistance genes. Twenty-three -positive isolates (16 , two , two , two , and one ) were isolated from 7/9 sampling locations; of those, eight -positive isolates also contained β-lactamase-resistance genes, eight contained , and 10 contained No -positive isolates were identified. The majority of isolates demonstrated a low to moderate level of colistin resistance. Transconjugation was successfully conducted from 14 of the 23 -positive isolates, and was identified on plasmids ranging from 60 to 220 kb in these isolates. Conjugation and hybridization experiments revealed that was chromosome-borne in only three isolates. Pulsed-field gel electrophoresis showed that the majority of isolates belonged to different clonal lineages. Multilocus sequence typing analysis revealed that sequence type 10 (ST10) was the most prevalent, followed by ST181 and ST206. This study demonstrates the utility of enrichment broth culture for identifying environmental -positive isolates. Furthermore, it highlights the importance of responsible agriculture and clinical use of polymyxins to prevent further widespread dissemination of polymyxin-resistant pathogens.
本研究旨在调查中国杭州环境水源中多粘菌素耐药基因的流行情况。采用富集肉汤培养法从环境水样中分离出耐黏菌素细菌,对其进行筛选,然后分析其位置和可转移性。对筛选呈阳性的分离株进一步检测以确定其药敏谱,并筛查是否存在其他耐药基因。从7/9个采样点分离出23株筛选呈阳性的分离株(16株肺炎克雷伯菌、2株大肠埃希菌、2株鲍曼不动杆菌、2株阴沟肠杆菌和1株产气肠杆菌);其中,8株筛选呈阳性的分离株还含有β-内酰胺酶耐药基因,8株含有mcr-1,10株含有mcr-2。未鉴定出mcr-3呈阳性的分离株。大多数分离株表现出低至中度的黏菌素耐药水平。23株筛选呈阳性的分离株中有14株成功进行了接合转移试验,在这些分离株中,mcr基因存在于大小为60至220 kb的质粒上。接合和杂交实验表明,仅3株分离株中的mcr基因位于染色体上。脉冲场凝胶电泳显示,大多数mcr分离株属于不同的克隆谱系。多位点序列分型分析表明,序列型10(ST10)最为常见,其次是ST181和ST206。本研究证明了富集肉汤培养法在鉴定环境中筛选呈阳性的分离株方面的实用性。此外,它强调了合理使用多粘菌素进行农业生产和临床应用以防止多粘菌素耐药病原体进一步广泛传播的重要性。