Antimicrobial Resistance Profile of mcr-1 Positive Clinical Isolates of Escherichia coli in China From 2013 to 2016
文献类型：期刊论文
| 作者 | Wang, Xiaoxue1,2; Li, Baiyuan2; Ke, Bixia3; Zhao, Xuanyu1,2; Guo, Yunxue2; Wang, Weiquan1,2; Zhu, Honghui |
| 刊名 | FRONTIERS IN MICROBIOLOGY
 |
| 出版日期 | 2018 |
| 卷号 | 9页码:2514 |
| 关键词 | multidrug-resistant clinical isolates Estherichie coil mcr-1 plasmid |
| ISSN号 | 1664-302X |
| 英文摘要 | Multidrug-resistant (MDR) Escherichia coli poses a great challenge for public health in recent decades. Polymyxins have been reconsidered as a valuable therapeutic option for the treatment of infections caused by MDR E. coll. A plasmid-encoded colistin resistance gene mcr-1 encoding phosphoethanolamine transferase has been recently described in Enterobacteriaceae. In this study, a total of 123 E. coli isolates obtained from patients with diarrheal diseases in China were used for the genetic analysis of colistin resistance in clinical isolates. Antimicrobial resistance profile of polymyxin B (PB) and 11 commonly used antimicrobial agents were determined. Among the 123 E. coli isolates, 9 isolates (7.3%) were resistant to PB and PCR screening showed that seven (5.7%) isolates carried the mcr-1 gene. A hybrid sequencing analysis using singlemolecule, real-time (SMRT) sequencing and Illumina sequencing was then performed to resolve the genomes of the seven mcr-1 positive isolates. These seven isolates harbored multiple plasmids and are MDR, with six isolates carrying one mcr-1 positive plasmid and one isolate (14EC033) carrying two mcr-1 positive plasmids. These eight mcr-1 positive plasmids belonged to the IncX4, Inc12, and IncP1 types. In addition, the mcr-1 gene was the solo antibiotic resistance gene identified in the mcr-1 positive plasmids, while the rest of the antibiotic resistance genes were mostly clustered into one or two plasmids. Interestingly, one mcr-1 positive isolate (14EC047) was susceptible to PB, and we showed that the activity of MCR-1-mediated colistin resistance was not phenotypically expressed in 14EC047 host strain. Furthermore, three isolates exhibited resistance to PB but did not carry previously reported mcr-related genes. Multilocus sequence typing (MAST) showed that these mcr-1 positive E. coil isolates belonged to five different STs, and three isolates belonged to ST301 which carried multiple virulence factors related to diarrhea. Additionally, the mcr-1 positive isolates were all susceptible to imipenem (IMP), suggesting that IMP could be used to treat infection caused by mcr-1 positive E. coli isolates. Collectively, this study showed a high occurrence of mcr1 positive plasmids in patients with diarrheal diseases of Guangzhou in China and the abolishment of the MCR-1 mediated colistin resistance in one E. coli isolate. |
| 源URL | [http://ir.scsio.ac.cn/handle/344004/17622]  |
| 专题 | 南海海洋研究所_中科院海洋生物资源可持续利用重点实验室 |
| 作者单位 | 1.Ctr Dis Control & Prevent Guangdong Prov, Guangzhou, Guangdong, Peoples R China 2.Guangdong Microbial Culture Collect Ctr GDMCC, Guangdong Inst Microbiol,Guangdong Open Lab Appl, State Key Lab Appl Microbiol Southern China, Guangdong Prov Key Lab Microbial Culture Collect, Guangzhou, Guangdong, Peoples R China 3.Chinese Acad Sci, RNAM Ctr Marine Microbiol, South China Sea Inst Oceanol, CAS Key Lab Trop Marine Bioresources & Ecol,Gaung, Guangzhou, Guangdong, Peoples R China 4.Univ Chinese Acad Sci, Beijing, Peoples R China |
| 推荐引用方式 GB/T 7714 | Wang, Xiaoxue,Li, Baiyuan,Ke, Bixia,et al. Antimicrobial Resistance Profile of mcr-1 Positive Clinical Isolates of Escherichia coli in China From 2013 to 2016[J]. FRONTIERS IN MICROBIOLOGY,2018,9:2514. |
| APA | Wang, Xiaoxue.,Li, Baiyuan.,Ke, Bixia.,Zhao, Xuanyu.,Guo, Yunxue.,...&Zhu, Honghui.(2018).Antimicrobial Resistance Profile of mcr-1 Positive Clinical Isolates of Escherichia coli in China From 2013 to 2016.FRONTIERS IN MICROBIOLOGY,9,2514. |
| MLA | Wang, Xiaoxue,et al."Antimicrobial Resistance Profile of mcr-1 Positive Clinical Isolates of Escherichia coli in China From 2013 to 2016".FRONTIERS IN MICROBIOLOGY 9(2018):2514. |
入库方式： OAI收割
来源：南海海洋研究所
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