The prevalent dynamic and genetic characterization of mcr-1 encoding multidrug resistant Escherichia coli strains recovered from poultry in Hebei, China

被引:1
|
作者
Wang, Qing [1 ,2 ,3 ,4 ]
Wang, Weiwei [2 ,3 ,4 ]
Zhu, Qiqi [2 ,3 ,4 ,5 ]
Shoaib, Muhammad [2 ,3 ,4 ]
Chengye, Wang
Zhu, Zhen
Wei, Xiaojuan
Bai, Yubin
Zhang, Jiyu [1 ]
机构
[1] Gansu Agr Univ, Coll Vet Med, 1 Yingmen Village, Lanzhou 730070, Gansu, Peoples R China
[2] Key Lab New Anim Drug Project Gansu Prov, Lanzhou, Gansu, Peoples R China
[3] Minist Agr, Key Lab Vet Pharmaceut Dev, Lanzhou, Gansu, Peoples R China
[4] Chinese Acad Agr Sci, Lanzhou Inst Husb & Pharmaceut Sci, Lanzhou, Gansu, Peoples R China
[5] Hebei Univ Engn, Coll Life Sci & Food Engn, Handan, Hebei, Peoples R China
关键词
Escherichia coli; Antimicrobial resistance; Colistin resistance; mcr-1; Poultry;
D O I
10.1016/j.jgar.2024.04.001
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: Colistin is known as the last resort antibiotic to treat the infections caused by multidrug resistant foodborne pathogens. The emergence and widespread dissemination of plasmid-mediated colistin resistance gene mcr-1 in the Escherichia coli ( E. coli ) incurs potential threat to public health. Here, we investigated the epidemiology, transmission dynamics, and genetic characterization of mcr-1 harbouring E. coli isolates from poultry originated in Hebei Province, China. Methods: A total of 297 faecal samples were collected from the two large poultry farms in Hebei Province, China. The samples were processed for E. coli identification by matrix-assisted laser desorption ionizationtime of flight mass spectrometry and 16S rDNA sequencing. Then, the mcr-1 gene harbouring E. coli strains were identified by polymerase chain reaction and subjected to antimicrobial susceptibility testing by broth microdilution assay. The genomic characterization of the isolates was done by whole genome sequencing using the various bioinformatics tools, and multi-locus sequence typing was done by sequence analysis of the seven housekeeping genes. The conjugation experiment was done to check the transferability of mcr-1 along with the plasmid stability testing. Results: A total of six mcr-1 E. coli isolates with minimum inhibitory concentration of 4 mu g/mL were identified from 297 samples (2.02%). The mcr-1 harbouring E. coli were identified as multidrug resistant and belonged to ST101 ( n = 4) and ST410 ( n = 2). The genetic environment of mcr-1 presented its position on IncHI2 plasmid in 4 isolates and p0111 in 2 isolates, which is a rarely reported plasmid type for mcr-1 . Moreover, both type of plasmids was transferable to recipient J53, and mcr-1 was flanked by 3 mobile elements ISApl1 , Tn3, and IS26 forming a novel backbone Tn3-IS26-mcr-1- pap2-ISApl1 on the p0111 plasmid. The phylogenetic analysis shared a common lineage with mcr-1 harbouring isolates from the environment, humans, and animals, which indicate its horizontal spread among the diverse sources, species, and hosts. Conclusion: This study recommends the one health approach for future surveillance across multiple sources and bacterial species to adopt relevant measures and reduce global resistance crises. (c) 2024 The Author(s). Published by Elsevier Ltd on behalf of International Society for Antimicrobial Chemotherapy. This is an open access article under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/ )
引用
收藏
页码:354 / 362
页数:9
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