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Molecular epidemiology of Klebsiella pneumoniae invasive infections over a decade at Kilifi County Hospital in Kenya
Multidrug resistant (MDR) Klebsiella pneumoniae is a common cause of nosocomial infections worldwide. Recent years have seen an explosion of resistance to extended-spectrum β-lactamases (ESBLs) and emergence of carbapenem resistance. Here, we examine 198 invasive K. pneumoniae isolates collected fro...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Urban & Fischer Verlag
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615107/ https://www.ncbi.nlm.nih.gov/pubmed/28789913 http://dx.doi.org/10.1016/j.ijmm.2017.07.006 |
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author | Henson, Sonal P. Boinett, Christine J. Ellington, Matthew J. Kagia, Ngure Mwarumba, Salim Nyongesa, Sammy Mturi, Neema Kariuki, Samuel Scott, J. Anthony G. Thomson, Nicholas R. Morpeth, Susan C. |
author_facet | Henson, Sonal P. Boinett, Christine J. Ellington, Matthew J. Kagia, Ngure Mwarumba, Salim Nyongesa, Sammy Mturi, Neema Kariuki, Samuel Scott, J. Anthony G. Thomson, Nicholas R. Morpeth, Susan C. |
author_sort | Henson, Sonal P. |
collection | PubMed |
description | Multidrug resistant (MDR) Klebsiella pneumoniae is a common cause of nosocomial infections worldwide. Recent years have seen an explosion of resistance to extended-spectrum β-lactamases (ESBLs) and emergence of carbapenem resistance. Here, we examine 198 invasive K. pneumoniae isolates collected from over a decade in Kilifi County Hospital (KCH) in Kenya. We observe a significant increase in MDR K. pneumoniae isolates, particularly to third generation cephalosporins conferred by ESBLs. Using whole-genome sequences, we describe the population structure and the distribution of antimicrobial resistance genes within it. More than half of the isolates examined in this study were ESBL-positive, encoding CTX-M-15, SHV-2, SHV-12 and SHV-27, and 79% were MDR conferring resistance to at least three antimicrobial classes. Although no isolates in our dataset were found to be resistant to carbapenems we did find a plasmid with the genetic architecture of a known New Delhi metallo-β-lactamase-1 (NDM)-carrying plasmid in 25 isolates. In the absence of carbapenem use in KCH and because of the instability of the NDM-1 gene in the plasmid, the NDM-1 gene has been lost in these isolates. Our data suggests that isolates that encode NDM-1 could be present in the population; should carbapenems be introduced as treatment in public hospitals in Kenya, resistance is likely to ensue rapidly. |
format | Online Article Text |
id | pubmed-5615107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Urban & Fischer Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-56151072017-10-05 Molecular epidemiology of Klebsiella pneumoniae invasive infections over a decade at Kilifi County Hospital in Kenya Henson, Sonal P. Boinett, Christine J. Ellington, Matthew J. Kagia, Ngure Mwarumba, Salim Nyongesa, Sammy Mturi, Neema Kariuki, Samuel Scott, J. Anthony G. Thomson, Nicholas R. Morpeth, Susan C. Int J Med Microbiol Article Multidrug resistant (MDR) Klebsiella pneumoniae is a common cause of nosocomial infections worldwide. Recent years have seen an explosion of resistance to extended-spectrum β-lactamases (ESBLs) and emergence of carbapenem resistance. Here, we examine 198 invasive K. pneumoniae isolates collected from over a decade in Kilifi County Hospital (KCH) in Kenya. We observe a significant increase in MDR K. pneumoniae isolates, particularly to third generation cephalosporins conferred by ESBLs. Using whole-genome sequences, we describe the population structure and the distribution of antimicrobial resistance genes within it. More than half of the isolates examined in this study were ESBL-positive, encoding CTX-M-15, SHV-2, SHV-12 and SHV-27, and 79% were MDR conferring resistance to at least three antimicrobial classes. Although no isolates in our dataset were found to be resistant to carbapenems we did find a plasmid with the genetic architecture of a known New Delhi metallo-β-lactamase-1 (NDM)-carrying plasmid in 25 isolates. In the absence of carbapenem use in KCH and because of the instability of the NDM-1 gene in the plasmid, the NDM-1 gene has been lost in these isolates. Our data suggests that isolates that encode NDM-1 could be present in the population; should carbapenems be introduced as treatment in public hospitals in Kenya, resistance is likely to ensue rapidly. Urban & Fischer Verlag 2017-10 /pmc/articles/PMC5615107/ /pubmed/28789913 http://dx.doi.org/10.1016/j.ijmm.2017.07.006 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Henson, Sonal P. Boinett, Christine J. Ellington, Matthew J. Kagia, Ngure Mwarumba, Salim Nyongesa, Sammy Mturi, Neema Kariuki, Samuel Scott, J. Anthony G. Thomson, Nicholas R. Morpeth, Susan C. Molecular epidemiology of Klebsiella pneumoniae invasive infections over a decade at Kilifi County Hospital in Kenya |
title | Molecular epidemiology of Klebsiella pneumoniae invasive infections over a decade at Kilifi County Hospital in Kenya |
title_full | Molecular epidemiology of Klebsiella pneumoniae invasive infections over a decade at Kilifi County Hospital in Kenya |
title_fullStr | Molecular epidemiology of Klebsiella pneumoniae invasive infections over a decade at Kilifi County Hospital in Kenya |
title_full_unstemmed | Molecular epidemiology of Klebsiella pneumoniae invasive infections over a decade at Kilifi County Hospital in Kenya |
title_short | Molecular epidemiology of Klebsiella pneumoniae invasive infections over a decade at Kilifi County Hospital in Kenya |
title_sort | molecular epidemiology of klebsiella pneumoniae invasive infections over a decade at kilifi county hospital in kenya |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615107/ https://www.ncbi.nlm.nih.gov/pubmed/28789913 http://dx.doi.org/10.1016/j.ijmm.2017.07.006 |
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