Cargando…

Molecular Dissection of an Outbreak of Carbapenem-Resistant Enterobacteriaceae Reveals Intergenus KPC Carbapenemase Transmission through a Promiscuous Plasmid

Carbapenem-resistant Enterobacteriaceae (CRE) have emerged as major causes of health care-associated infections worldwide. This diverse collection of organisms with various resistance mechanisms is associated with increased lengths of hospitalization, costs of care, morbidity, and mortality. The glo...

Descripción completa

Detalles Bibliográficos
Autores principales: Mathers, Amy J., Cox, Heather L., Kitchel, Brandon, Bonatti, Hugo, Brassinga, Ann Karen C., Carroll, Joanne, Scheld, W. Michael, Hazen, Kevin C., Sifri, Costi D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Microbiology 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3202755/
https://www.ncbi.nlm.nih.gov/pubmed/22045989
http://dx.doi.org/10.1128/mBio.00204-11
_version_ 1782215028243431424
author Mathers, Amy J.
Cox, Heather L.
Kitchel, Brandon
Bonatti, Hugo
Brassinga, Ann Karen C.
Carroll, Joanne
Scheld, W. Michael
Hazen, Kevin C.
Sifri, Costi D.
author_facet Mathers, Amy J.
Cox, Heather L.
Kitchel, Brandon
Bonatti, Hugo
Brassinga, Ann Karen C.
Carroll, Joanne
Scheld, W. Michael
Hazen, Kevin C.
Sifri, Costi D.
author_sort Mathers, Amy J.
collection PubMed
description Carbapenem-resistant Enterobacteriaceae (CRE) have emerged as major causes of health care-associated infections worldwide. This diverse collection of organisms with various resistance mechanisms is associated with increased lengths of hospitalization, costs of care, morbidity, and mortality. The global spread of CRE has largely been attributed to dissemination of a dominant strain of Klebsiella pneumoniae producing a serine β-lactamase, termed K. pneumoniae carbapenemase (KPC). Here we report an outbreak of KPC-producing CRE infections in which the degree of horizontal transmission between strains and species of a promiscuous plasmid is unprecedented. Sixteen isolates, comprising 11 unique strains, 6 species, and 4 genera of bacteria, were obtained from 14 patients over the first 8 months of the outbreak. Of the 11 unique strains, 9 harbored the same highly promiscuous plasmid carrying the KPC gene bla(KPC). The remaining strains harbored distinct bla(KPC) plasmids, one of which was carried in a strain of Klebsiella oxytoca coisolated from the index patient and the other generated from transposition of the bla(KPC) element Tn4401. All isolates could be genetically traced to the index patient. Molecular epidemiological investigation of the outbreak was aided by the adaptation of nested arbitrary PCR (ARB-PCR) for rapid plasmid identification. This detailed molecular genetic analysis, combined with traditional epidemiological investigation, provides insights into the highly fluid dynamics of drug resistance transmission during the outbreak.
format Online
Article
Text
id pubmed-3202755
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher American Society of Microbiology
record_format MEDLINE/PubMed
spelling pubmed-32027552011-11-04 Molecular Dissection of an Outbreak of Carbapenem-Resistant Enterobacteriaceae Reveals Intergenus KPC Carbapenemase Transmission through a Promiscuous Plasmid Mathers, Amy J. Cox, Heather L. Kitchel, Brandon Bonatti, Hugo Brassinga, Ann Karen C. Carroll, Joanne Scheld, W. Michael Hazen, Kevin C. Sifri, Costi D. mBio Research Article Carbapenem-resistant Enterobacteriaceae (CRE) have emerged as major causes of health care-associated infections worldwide. This diverse collection of organisms with various resistance mechanisms is associated with increased lengths of hospitalization, costs of care, morbidity, and mortality. The global spread of CRE has largely been attributed to dissemination of a dominant strain of Klebsiella pneumoniae producing a serine β-lactamase, termed K. pneumoniae carbapenemase (KPC). Here we report an outbreak of KPC-producing CRE infections in which the degree of horizontal transmission between strains and species of a promiscuous plasmid is unprecedented. Sixteen isolates, comprising 11 unique strains, 6 species, and 4 genera of bacteria, were obtained from 14 patients over the first 8 months of the outbreak. Of the 11 unique strains, 9 harbored the same highly promiscuous plasmid carrying the KPC gene bla(KPC). The remaining strains harbored distinct bla(KPC) plasmids, one of which was carried in a strain of Klebsiella oxytoca coisolated from the index patient and the other generated from transposition of the bla(KPC) element Tn4401. All isolates could be genetically traced to the index patient. Molecular epidemiological investigation of the outbreak was aided by the adaptation of nested arbitrary PCR (ARB-PCR) for rapid plasmid identification. This detailed molecular genetic analysis, combined with traditional epidemiological investigation, provides insights into the highly fluid dynamics of drug resistance transmission during the outbreak. American Society of Microbiology 2011-11-01 /pmc/articles/PMC3202755/ /pubmed/22045989 http://dx.doi.org/10.1128/mBio.00204-11 Text en Copyright © 2011 Mathers et al. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported License (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Mathers, Amy J.
Cox, Heather L.
Kitchel, Brandon
Bonatti, Hugo
Brassinga, Ann Karen C.
Carroll, Joanne
Scheld, W. Michael
Hazen, Kevin C.
Sifri, Costi D.
Molecular Dissection of an Outbreak of Carbapenem-Resistant Enterobacteriaceae Reveals Intergenus KPC Carbapenemase Transmission through a Promiscuous Plasmid
title Molecular Dissection of an Outbreak of Carbapenem-Resistant Enterobacteriaceae Reveals Intergenus KPC Carbapenemase Transmission through a Promiscuous Plasmid
title_full Molecular Dissection of an Outbreak of Carbapenem-Resistant Enterobacteriaceae Reveals Intergenus KPC Carbapenemase Transmission through a Promiscuous Plasmid
title_fullStr Molecular Dissection of an Outbreak of Carbapenem-Resistant Enterobacteriaceae Reveals Intergenus KPC Carbapenemase Transmission through a Promiscuous Plasmid
title_full_unstemmed Molecular Dissection of an Outbreak of Carbapenem-Resistant Enterobacteriaceae Reveals Intergenus KPC Carbapenemase Transmission through a Promiscuous Plasmid
title_short Molecular Dissection of an Outbreak of Carbapenem-Resistant Enterobacteriaceae Reveals Intergenus KPC Carbapenemase Transmission through a Promiscuous Plasmid
title_sort molecular dissection of an outbreak of carbapenem-resistant enterobacteriaceae reveals intergenus kpc carbapenemase transmission through a promiscuous plasmid
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3202755/
https://www.ncbi.nlm.nih.gov/pubmed/22045989
http://dx.doi.org/10.1128/mBio.00204-11
work_keys_str_mv AT mathersamyj moleculardissectionofanoutbreakofcarbapenemresistantenterobacteriaceaerevealsintergenuskpccarbapenemasetransmissionthroughapromiscuousplasmid
AT coxheatherl moleculardissectionofanoutbreakofcarbapenemresistantenterobacteriaceaerevealsintergenuskpccarbapenemasetransmissionthroughapromiscuousplasmid
AT kitchelbrandon moleculardissectionofanoutbreakofcarbapenemresistantenterobacteriaceaerevealsintergenuskpccarbapenemasetransmissionthroughapromiscuousplasmid
AT bonattihugo moleculardissectionofanoutbreakofcarbapenemresistantenterobacteriaceaerevealsintergenuskpccarbapenemasetransmissionthroughapromiscuousplasmid
AT brassingaannkarenc moleculardissectionofanoutbreakofcarbapenemresistantenterobacteriaceaerevealsintergenuskpccarbapenemasetransmissionthroughapromiscuousplasmid
AT carrolljoanne moleculardissectionofanoutbreakofcarbapenemresistantenterobacteriaceaerevealsintergenuskpccarbapenemasetransmissionthroughapromiscuousplasmid
AT scheldwmichael moleculardissectionofanoutbreakofcarbapenemresistantenterobacteriaceaerevealsintergenuskpccarbapenemasetransmissionthroughapromiscuousplasmid
AT hazenkevinc moleculardissectionofanoutbreakofcarbapenemresistantenterobacteriaceaerevealsintergenuskpccarbapenemasetransmissionthroughapromiscuousplasmid
AT sifricostid moleculardissectionofanoutbreakofcarbapenemresistantenterobacteriaceaerevealsintergenuskpccarbapenemasetransmissionthroughapromiscuousplasmid