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2560. Multispecies Outbreak of KPC-2 Producing Enterobacteriaceae in a Chilean Pediatric Hospital

BACKGROUND: Carbapenem-resistant Enterobacteriaceae (CRE) are a critical global health problem. We detected a surge of CRE cases in a pediatric hospital in Chile, a country with a low endemicity of KPC-producing organisms. Herein, we describe the molecular epidemiology of this outbreak. METHODS: CRE...

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Autores principales: Rojas, Laura J, Marshall, Steven H, Rivas, Lina M, Spencer, Maria, Rutter, Joseph, Jacobs, Michael R, Perez, Federico, Coria, Paulina, Valdivieso, Francisca, Bralic, Rafael Araos, Munita, Jose M, Bonomo, Robert A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6252654/
http://dx.doi.org/10.1093/ofid/ofy209.168
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author Rojas, Laura J
Marshall, Steven H
Rivas, Lina M
Spencer, Maria
Rutter, Joseph
Jacobs, Michael R
Perez, Federico
Coria, Paulina
Valdivieso, Francisca
Bralic, Rafael Araos
Munita, Jose M
Bonomo, Robert A
author_facet Rojas, Laura J
Marshall, Steven H
Rivas, Lina M
Spencer, Maria
Rutter, Joseph
Jacobs, Michael R
Perez, Federico
Coria, Paulina
Valdivieso, Francisca
Bralic, Rafael Araos
Munita, Jose M
Bonomo, Robert A
author_sort Rojas, Laura J
collection PubMed
description BACKGROUND: Carbapenem-resistant Enterobacteriaceae (CRE) are a critical global health problem. We detected a surge of CRE cases in a pediatric hospital in Chile, a country with a low endemicity of KPC-producing organisms. Herein, we describe the molecular epidemiology of this outbreak. METHODS: CRE isolates from clinical specimens and surveillance rectal swabs (obtained using chromID CARBA SMART agar, BioMerieux) of pediatric patients were collected from July 2015 to January 2017. Species identity was confirmed by MALDI-TOF. Carbapenemase genes (bla(KPC), bla(NDM), bla(VIM), bla(IMP), and bla(OXA-48-like)) were detected by multiplex PCR, followed by amplification and sequencing of the bla(KPC) allele. Conjugation experiments were conducted with representative species as donors and sodium azide-resistant E. coli J53 as recipient. PCR-based plasmid typing (PBRT Diatheva kit) was then performed on donors and recipients. For K. pneumoniae, genetic relatedness was investigated by PFGE, multilocus sequence typing and wzi typing. RESULTS: Sixty-one CRE clinical and surveillance isolates were obtained from 49 patients aged 17 days to 16 years. bla(KPC-2) was present in 57/62 isolates; no other carbapenemases were found. For 11 patients, multiple cultures were obtained; 4/11 had more than one KPC-harboring species. KPC-harboring isolates displayed ertapenem MICs ranging from 1 to >8 mg/L. Preliminary analyses suggest that bla(KPC-2) is contained within a nonclassical Tn4401 structure (lacking the upstream promoter). Mating experiments indicate that bla(KPC-2) is carried by a conjugative IncN backbone plasmid. Interestingly, K. pneumoniae isolates were nonclonal by PFGE and belonged to multiple STs unrelated to CG258 (ST34, ST36, among others) and different wzi types (37, 154, among others). [Image: see text] CONCLUSION: We report a multispecies outbreak of KPC-2 producing CRE in children mainly driven by horizontal dissemination of a promiscuous IncN plasmid. The nonclonal, multispecies nature of this outbreak provides insights into the complex dynamics of KPC dissemination in countries like Chile, where the clonal spread of highly successful clones like CG258 is not the predominant dissemination vehicle, and instead HGT-related spread could be playing a more important role. DISCLOSURES: All authors: No reported disclosures.
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spelling pubmed-62526542018-11-28 2560. Multispecies Outbreak of KPC-2 Producing Enterobacteriaceae in a Chilean Pediatric Hospital Rojas, Laura J Marshall, Steven H Rivas, Lina M Spencer, Maria Rutter, Joseph Jacobs, Michael R Perez, Federico Coria, Paulina Valdivieso, Francisca Bralic, Rafael Araos Munita, Jose M Bonomo, Robert A Open Forum Infect Dis Abstracts BACKGROUND: Carbapenem-resistant Enterobacteriaceae (CRE) are a critical global health problem. We detected a surge of CRE cases in a pediatric hospital in Chile, a country with a low endemicity of KPC-producing organisms. Herein, we describe the molecular epidemiology of this outbreak. METHODS: CRE isolates from clinical specimens and surveillance rectal swabs (obtained using chromID CARBA SMART agar, BioMerieux) of pediatric patients were collected from July 2015 to January 2017. Species identity was confirmed by MALDI-TOF. Carbapenemase genes (bla(KPC), bla(NDM), bla(VIM), bla(IMP), and bla(OXA-48-like)) were detected by multiplex PCR, followed by amplification and sequencing of the bla(KPC) allele. Conjugation experiments were conducted with representative species as donors and sodium azide-resistant E. coli J53 as recipient. PCR-based plasmid typing (PBRT Diatheva kit) was then performed on donors and recipients. For K. pneumoniae, genetic relatedness was investigated by PFGE, multilocus sequence typing and wzi typing. RESULTS: Sixty-one CRE clinical and surveillance isolates were obtained from 49 patients aged 17 days to 16 years. bla(KPC-2) was present in 57/62 isolates; no other carbapenemases were found. For 11 patients, multiple cultures were obtained; 4/11 had more than one KPC-harboring species. KPC-harboring isolates displayed ertapenem MICs ranging from 1 to >8 mg/L. Preliminary analyses suggest that bla(KPC-2) is contained within a nonclassical Tn4401 structure (lacking the upstream promoter). Mating experiments indicate that bla(KPC-2) is carried by a conjugative IncN backbone plasmid. Interestingly, K. pneumoniae isolates were nonclonal by PFGE and belonged to multiple STs unrelated to CG258 (ST34, ST36, among others) and different wzi types (37, 154, among others). [Image: see text] CONCLUSION: We report a multispecies outbreak of KPC-2 producing CRE in children mainly driven by horizontal dissemination of a promiscuous IncN plasmid. The nonclonal, multispecies nature of this outbreak provides insights into the complex dynamics of KPC dissemination in countries like Chile, where the clonal spread of highly successful clones like CG258 is not the predominant dissemination vehicle, and instead HGT-related spread could be playing a more important role. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2018-11-26 /pmc/articles/PMC6252654/ http://dx.doi.org/10.1093/ofid/ofy209.168 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Rojas, Laura J
Marshall, Steven H
Rivas, Lina M
Spencer, Maria
Rutter, Joseph
Jacobs, Michael R
Perez, Federico
Coria, Paulina
Valdivieso, Francisca
Bralic, Rafael Araos
Munita, Jose M
Bonomo, Robert A
2560. Multispecies Outbreak of KPC-2 Producing Enterobacteriaceae in a Chilean Pediatric Hospital
title 2560. Multispecies Outbreak of KPC-2 Producing Enterobacteriaceae in a Chilean Pediatric Hospital
title_full 2560. Multispecies Outbreak of KPC-2 Producing Enterobacteriaceae in a Chilean Pediatric Hospital
title_fullStr 2560. Multispecies Outbreak of KPC-2 Producing Enterobacteriaceae in a Chilean Pediatric Hospital
title_full_unstemmed 2560. Multispecies Outbreak of KPC-2 Producing Enterobacteriaceae in a Chilean Pediatric Hospital
title_short 2560. Multispecies Outbreak of KPC-2 Producing Enterobacteriaceae in a Chilean Pediatric Hospital
title_sort 2560. multispecies outbreak of kpc-2 producing enterobacteriaceae in a chilean pediatric hospital
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6252654/
http://dx.doi.org/10.1093/ofid/ofy209.168
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