Plasmid-mediated mcr-1 colistin resistance in Escherichia coli and Klebsiella spp. clinical isolates from the Western Cape region of South Africa
Abstract Background Colistin is a last resort antibiotic for the treatment of carbapenem-resistant Gram negative infections. Until recently, mechanisms of colistin resistance were limited to chromosomal mutations which confer a high fitness cost and cannot be transferred between organisms. However,...
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BMC
2017-08-01
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Series: | Antimicrobial Resistance and Infection Control |
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Online Access: | http://link.springer.com/article/10.1186/s13756-017-0234-8 |
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author | Mae Newton-Foot Yolandi Snyman Motlatji Reratilwe Bonnie Maloba Andrew Christopher Whitelaw |
author_facet | Mae Newton-Foot Yolandi Snyman Motlatji Reratilwe Bonnie Maloba Andrew Christopher Whitelaw |
author_sort | Mae Newton-Foot |
collection | DOAJ |
description | Abstract Background Colistin is a last resort antibiotic for the treatment of carbapenem-resistant Gram negative infections. Until recently, mechanisms of colistin resistance were limited to chromosomal mutations which confer a high fitness cost and cannot be transferred between organisms. However, a novel plasmid-mediated colistin resistance mechanism, encoded by the mcr-1 gene, has been identified, and has since been detected worldwide. The mcr-1 colistin resistance mechanism is a major threat due to its lack of fitness cost and ability to be transferred between strains and species. Surveillance of colistin resistance mechanisms is critical to monitor the development and spread of resistance.This study aimed to determine the prevalence of the plasmid-mediated colistin resistance gene, mcr-1, in colistin-resistant E. coli and Klebsiella spp. isolates in the Western Cape of South Africa; and whether colistin resistance is spread through clonal expansion or by acquisition of resistance by diverse strains. Methods Colistin resistant E. coli and Klebsiella spp. isolates were collected from the NHLS microbiology laboratory at Tygerberg Hospital. Species identification and antibiotic susceptibility testing was done using the API® 20 E system and the Vitek® 2 Advanced Expert System™. PCR was used to detect the plasmid-mediated mcr-1 colistin resistance gene and REP-PCR was used for strain typing of the isolates. Results Nineteen colistin resistant isolates, including 12 E. coli, six K. pneumoniae and one K. oxytoca isolate, were detected over 7 months from eight different hospitals in the Western Cape region. The mcr-1 gene was detected in 83% of isolates which were shown to be predominantly unrelated strains. Conclusions The plasmid-mediated mcr-1 colistin resistance gene is responsible for the majority of colistin resistance in clinical isolates of E. coli and Klebsiella spp. from the Western Cape of South Africa. Colistin resistance is not clonally disseminated; the mcr-1 gene has been acquired by several unrelated strains of E. coli and K. pneumoniae. Acquisition of mcr-1 by cephalosporin- and carbapenem-resistant Gram negative bacteria may result in untreatable infections and increased mortality. Measures need to be implemented to control the use of colistin in health care facilities and in agriculture to retain its antimicrobial efficacy. |
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institution | Directory Open Access Journal |
issn | 2047-2994 |
language | English |
last_indexed | 2024-12-11T03:05:32Z |
publishDate | 2017-08-01 |
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spelling | doaj.art-b21ba7438e834099963232d9703eec7b2022-12-22T01:22:58ZengBMCAntimicrobial Resistance and Infection Control2047-29942017-08-01611710.1186/s13756-017-0234-8Plasmid-mediated mcr-1 colistin resistance in Escherichia coli and Klebsiella spp. clinical isolates from the Western Cape region of South AfricaMae Newton-Foot0Yolandi Snyman1Motlatji Reratilwe Bonnie Maloba2Andrew Christopher Whitelaw3Division of Medical Microbiology, Faculty of Medicine and Health Sciences, Stellenbosch UniversityDivision of Medical Microbiology, Faculty of Medicine and Health Sciences, Stellenbosch UniversityDivision of Medical Microbiology, Faculty of Medicine and Health Sciences, Stellenbosch UniversityDivision of Medical Microbiology, Faculty of Medicine and Health Sciences, Stellenbosch UniversityAbstract Background Colistin is a last resort antibiotic for the treatment of carbapenem-resistant Gram negative infections. Until recently, mechanisms of colistin resistance were limited to chromosomal mutations which confer a high fitness cost and cannot be transferred between organisms. However, a novel plasmid-mediated colistin resistance mechanism, encoded by the mcr-1 gene, has been identified, and has since been detected worldwide. The mcr-1 colistin resistance mechanism is a major threat due to its lack of fitness cost and ability to be transferred between strains and species. Surveillance of colistin resistance mechanisms is critical to monitor the development and spread of resistance.This study aimed to determine the prevalence of the plasmid-mediated colistin resistance gene, mcr-1, in colistin-resistant E. coli and Klebsiella spp. isolates in the Western Cape of South Africa; and whether colistin resistance is spread through clonal expansion or by acquisition of resistance by diverse strains. Methods Colistin resistant E. coli and Klebsiella spp. isolates were collected from the NHLS microbiology laboratory at Tygerberg Hospital. Species identification and antibiotic susceptibility testing was done using the API® 20 E system and the Vitek® 2 Advanced Expert System™. PCR was used to detect the plasmid-mediated mcr-1 colistin resistance gene and REP-PCR was used for strain typing of the isolates. Results Nineteen colistin resistant isolates, including 12 E. coli, six K. pneumoniae and one K. oxytoca isolate, were detected over 7 months from eight different hospitals in the Western Cape region. The mcr-1 gene was detected in 83% of isolates which were shown to be predominantly unrelated strains. Conclusions The plasmid-mediated mcr-1 colistin resistance gene is responsible for the majority of colistin resistance in clinical isolates of E. coli and Klebsiella spp. from the Western Cape of South Africa. Colistin resistance is not clonally disseminated; the mcr-1 gene has been acquired by several unrelated strains of E. coli and K. pneumoniae. Acquisition of mcr-1 by cephalosporin- and carbapenem-resistant Gram negative bacteria may result in untreatable infections and increased mortality. Measures need to be implemented to control the use of colistin in health care facilities and in agriculture to retain its antimicrobial efficacy.http://link.springer.com/article/10.1186/s13756-017-0234-8Colistin resistancemcr-1plasmid-mediated resistanceE. coliKlebsiella sppSouth Africa |
spellingShingle | Mae Newton-Foot Yolandi Snyman Motlatji Reratilwe Bonnie Maloba Andrew Christopher Whitelaw Plasmid-mediated mcr-1 colistin resistance in Escherichia coli and Klebsiella spp. clinical isolates from the Western Cape region of South Africa Antimicrobial Resistance and Infection Control Colistin resistance mcr-1 plasmid-mediated resistance E. coli Klebsiella spp South Africa |
title | Plasmid-mediated mcr-1 colistin resistance in Escherichia coli and Klebsiella spp. clinical isolates from the Western Cape region of South Africa |
title_full | Plasmid-mediated mcr-1 colistin resistance in Escherichia coli and Klebsiella spp. clinical isolates from the Western Cape region of South Africa |
title_fullStr | Plasmid-mediated mcr-1 colistin resistance in Escherichia coli and Klebsiella spp. clinical isolates from the Western Cape region of South Africa |
title_full_unstemmed | Plasmid-mediated mcr-1 colistin resistance in Escherichia coli and Klebsiella spp. clinical isolates from the Western Cape region of South Africa |
title_short | Plasmid-mediated mcr-1 colistin resistance in Escherichia coli and Klebsiella spp. clinical isolates from the Western Cape region of South Africa |
title_sort | plasmid mediated mcr 1 colistin resistance in escherichia coli and klebsiella spp clinical isolates from the western cape region of south africa |
topic | Colistin resistance mcr-1 plasmid-mediated resistance E. coli Klebsiella spp South Africa |
url | http://link.springer.com/article/10.1186/s13756-017-0234-8 |
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