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      Colistin resistance and plasmid-mediated mcr genes in Escherichia coli and Salmonella isolated from pigs, pig carcass and pork in Thailand, Lao PDR and Cambodia border provinces

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          Abstract

          Background

          Colistin and carbapenem-resistant bacteria have emerged and become a serious public health concern, but their epidemiological data is still limited.

          Objectives

          This study examined colistin and carbapenem resistance in Escherichia coli and Salmonella from pigs, pig carcasses, and pork in Thailand, Lao PDR, and Cambodia border provinces.

          Methods

          The phenotypic and genotypic resistance to colistin and meropenem was determined in E. coli and Salmonella obtained from pigs, pig carcasses, and pork (n = 1,619). A conjugative experiment was performed in all isolates carrying the mcr gene (s) (n = 68). The plasmid replicon type was determined in the isolates carrying a conjugative plasmid with mcr by PCR-based replicon typing (n = 7). The genetic relatedness of mcr-positive Salmonella (n = 11) was investigated by multi-locus sequence typing.

          Results

          Colistin resistance was more common in E. coli (8%) than Salmonella (1%). The highest resistance rate was found in E. coli (17.8%) and Salmonella (1.7%) from Cambodia. Colistin-resistance genes, mcr-1, mcr-3, and mcr-5, were identified, of which mcr-1 and mcr-3 were predominant in E. coli (5.8%) and Salmonella (1.7%), respectively. The mcr-5 gene was observed in E. coli from pork in Cambodia. Two colistin-susceptible pig isolates from Thailand carried both mcr-1 and mcr-3. Seven E. coli and Salmonella isolates contained mcr-1 or mcr-3 associated with the IncF and IncI plasmids. The mcr-positive Salmonella from Thailand and Cambodia were categorized into two clusters with 94%–97% similarity. None of these clusters was meropenem resistant.

          Conclusions

          Colistin-resistant E. coli and Salmonella were distributed in pigs, pig carcasses, and pork in the border areas. Undivided-One Health collaboration is needed to address the issue.

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          Most cited references43

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          MEGA X: Molecular Evolutionary Genetics Analysis across Computing Platforms.

          The Molecular Evolutionary Genetics Analysis (Mega) software implements many analytical methods and tools for phylogenomics and phylomedicine. Here, we report a transformation of Mega to enable cross-platform use on Microsoft Windows and Linux operating systems. Mega X does not require virtualization or emulation software and provides a uniform user experience across platforms. Mega X has additionally been upgraded to use multiple computing cores for many molecular evolutionary analyses. Mega X is available in two interfaces (graphical and command line) and can be downloaded from www.megasoftware.net free of charge.
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            Emergence of plasmid-mediated colistin resistance mechanism MCR-1 in animals and human beings in China: a microbiological and molecular biological study.

            Until now, polymyxin resistance has involved chromosomal mutations but has never been reported via horizontal gene transfer. During a routine surveillance project on antimicrobial resistance in commensal Escherichia coli from food animals in China, a major increase of colistin resistance was observed. When an E coli strain, SHP45, possessing colistin resistance that could be transferred to another strain, was isolated from a pig, we conducted further analysis of possible plasmid-mediated polymyxin resistance. Herein, we report the emergence of the first plasmid-mediated polymyxin resistance mechanism, MCR-1, in Enterobacteriaceae.
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              Multiplex PCR for detection of acquired carbapenemase genes.

              A rapid and reliable PCR-based technique was developed for detection of genes encoding carbapenemases belonging to different classes. Primers were designed to amplify the following 11 genes: bla(IMP), bla(VIM), bla(NDM), bla(SPM), bla(AIM), bla(DIM), bla(GIM), bla(SIM)bla(KPC), bla(BIC), and bla(OXA-48). Three different multiplex reaction mixtures were defined and evaluated for the detection of all these 11 genes. Using optimized conditions, each reaction mixture allowed to identify the respective genes, with PCR giving distinct amplicon sizes corresponding to the different genes for each mixture. We reported here a rapid and reliable technique for screening all clinically relevant carbapenemase genes. Copyright © 2011 Elsevier Inc. All rights reserved.
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                Author and article information

                Journal
                J Vet Sci
                J Vet Sci
                JVS
                Journal of Veterinary Science
                The Korean Society of Veterinary Science
                1229-845X
                1976-555X
                September 2021
                03 August 2021
                : 22
                : 5
                : e68
                Affiliations
                [1 ]Research Unit in Microbial Food Safety and Antimicrobial Resistance, Department of Veterinary Public Health, Faculty of Veterinary Science, Chulalongkorn University, Bangkok 10330, Thailand.
                [2 ]Department of Microbiology and Immunology, College of Veterinary Medicine, Cornell University, Ithaca, NY 14850, United States.
                [3 ]Department of Farm Resources and Production Medicine, Faculty of Veterinary Medicine Kasetsart University, Kamphangsaen Nakornpathom 73140, Thailand.
                [4 ]Department of Veterinary Public Health, Faculty of Veterinary Medicine, Khon Kaen University, Khon Kaen 40002, Thailand.
                Author notes
                Corresponding author: Rungtip Chuanchuen. Faculty of Veterinary Science, Chulalongkorn University, Pathumwan, Bangkok 10330, Thailand. chuanchuen.r@ 123456gmail.com
                Author information
                https://orcid.org/0000-0002-0335-6761
                https://orcid.org/0000-0002-0486-5621
                https://orcid.org/0000-0003-3346-6299
                https://orcid.org/0000-0003-3445-4206
                https://orcid.org/0000-0002-1701-907X
                https://orcid.org/0000-0003-1242-7493
                https://orcid.org/0000-0002-1710-7424
                https://orcid.org/0000-0002-9714-9199
                Article
                10.4142/jvs.2021.22.e68
                8460466
                34423604
                31e4529c-6b8f-4c73-ae68-278f398b8944
                © 2021 The Korean Society of Veterinary Science

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( https://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 10 April 2021
                : 20 June 2021
                : 05 July 2021
                Funding
                Funded by: Thailand Research Fund, CrossRef https://doi.org/10.13039/501100004396;
                Award ID: BRG6080014
                Funded by: Chulalongkorn University, CrossRef https://doi.org/10.13039/501100002873;
                Funded by: 90th anniversary-Ratchadaphiseksomphot Endowment Fund
                Categories
                Original Article
                Microbiology

                Veterinary medicine
                drug resistance,swine,thailand,laos,cambodia
                Veterinary medicine
                drug resistance, swine, thailand, laos, cambodia

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