Multidrug resistance plasmids underlie clonal expansions and international spread of Salmonella enterica serotype 1,4,[5],12:i:- ST34 in Southeast Asia

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作者
Hao Chung The
Phuong Pham
Tuyen Ha Thanh
Linh Vo Kim Phuong
Nguyen Phuong Yen
Son-Nam H. Le
Duong Vu Thuy
Tran Thi Hong Chau
Hoang Le Phuc
Nguyen Minh Ngoc
Lu Lan Vi
Alison E. Mather
Guy E. Thwaites
Nicholas R. Thomson
Stephen Baker
Duy Thanh Pham
机构
[1] Oxford University Clinical Research Unit,School of Biotechnology
[2] International University,Centre for Tropical Medicine and Global Health, Nuffield Department of Clinical Medicine
[3] Vietnam National University,Department of Medicine, Cambridge Institute of Therapeutic Immunology and Infectious Diseases (CITIID)
[4] Children’s Hospital No. 1,undefined
[5] Children’s Hospital No. 2,undefined
[6] The Hospital for Tropical Diseases,undefined
[7] Quadram Institute Bioscience,undefined
[8] Norwich Research Park,undefined
[9] University of East Anglia,undefined
[10] University of Oxford,undefined
[11] London School of Hygiene and Tropical Medicine,undefined
[12] The Wellcome Sanger Institute,undefined
[13] University of Cambridge,undefined
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Salmonella enterica serotype 1,4,[5],12:i:- (Typhimurium monophasic variant) of sequence type (ST) 34 has emerged as the predominant pandemic genotype in recent decades. Despite increasing reports of resistance to antimicrobials in Southeast Asia, Salmonella ST34 population structure and evolution remained understudied in the region. Here we performed detailed genomic investigations on 454 ST34 genomes collected from Vietnam and diverse geographical sources to elucidate the pathogen’s epidemiology, evolution and antimicrobial resistance. We showed that ST34 has been introduced into Vietnam in at least nine occasions since 2000, forming five co-circulating major clones responsible for paediatric diarrhoea and bloodstream infection. Most expansion events were associated with acquisitions of large multidrug resistance plasmids of IncHI2 or IncA/C2. Particularly, the self-conjugative IncA/C2 pST34VN2 (co-transferring blaCTX-M-55, mcr-3.1, and qnrS1) underlies local expansion and intercontinental spread in two separate ST34 clones. At the global scale, Southeast Asia was identified as a potential hub for the emergence and dissemination of multidrug resistant Salmonella ST34, and mutation analysis suggests of selection in antimicrobial responses and key virulence factors.
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