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Intestinal co-colonization with different carbapenemase-producing Enterobacterales isolates is not a rare event in an OXA-48 endemic area

BACKGROUND: The current spread of carbapenemase-producing Enterobacterales (CPE) is a great concern. METHODS: We recovered 198 CPE from 162 patients admitted in our Hospital (March 2014-March 2016) during the R-GNOSIS European Project. Microbiological features and plasmid characteristics of CPE reco...

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Autores principales: Hernández-García, Marta, Pérez-Viso, Blanca, Navarro-San Francisco, Carolina, Baquero, Fernando, Morosini, María Isabel, Ruiz-Garbajosa, Patricia, Cantón, Rafael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6833436/
https://www.ncbi.nlm.nih.gov/pubmed/31709416
http://dx.doi.org/10.1016/j.eclinm.2019.09.005
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author Hernández-García, Marta
Pérez-Viso, Blanca
Navarro-San Francisco, Carolina
Baquero, Fernando
Morosini, María Isabel
Ruiz-Garbajosa, Patricia
Cantón, Rafael
author_facet Hernández-García, Marta
Pérez-Viso, Blanca
Navarro-San Francisco, Carolina
Baquero, Fernando
Morosini, María Isabel
Ruiz-Garbajosa, Patricia
Cantón, Rafael
author_sort Hernández-García, Marta
collection PubMed
description BACKGROUND: The current spread of carbapenemase-producing Enterobacterales (CPE) is a great concern. METHODS: We recovered 198 CPE from 162 patients admitted in our Hospital (March 2014-March 2016) during the R-GNOSIS European Project. Microbiological features and plasmid characteristics of CPE recovered from patients co-colonized with multiple CPE were studied. FINDINGS: Thirty patients (18.5%; CI 95%= 12.5%–24.5%) presented co-colonization with multiple CPE producing the same (CPE-SC) (15.4%) or a different carbapenemase (CPE-DC) (4.3%). OXA-48 (83.3%) was the most frequent carbapenemase, followed by VIM-1 (26.7%), NDM-1 (10%) and KPC-3 (3.3%). CPE-DC-patients had longer admissions [63 days (20–107)] than the other patients. Moreover, hospital stay until CPE detection was lower [9 days (5–14)] (p = 0.0052) in CPE-SC-patients than in those with a single colonization; 56% showed co-colonization in the first positive sample, although most of them had previous admissions and had received multiple antibiotic treatments. CPE were more frequently recovered in clinical samples from co-colonized [CPE-DC (28.6%), CPE-SC (24%)] patients than from patients with a single CPE (15.2%). Among CPE-SC—OXA-48 [80% (p = 0.11)], K. pneumoniae [88% (p = 0.006)] and E. coli [84% (p < 0.001)] were the most frequent species. In 60% of patients, K. pneumoniae and E. coli species were simultaneously recovered, frequently after a single OXA-48-K. pneumoniae colonization. High-risk clones (ST11, ST15, ST307) were detected in OXA-48-K. pneumoniae but a higher clonal diversity was found among E. coli. A frequent in-vivo cross-species plasmid transmission was shown, due to a dominant plasmid (IncL-pOXA-48), but also involving related or unrelated bla(VIM-1)-, bla(NDM-1)- and bla(KPC-3)-encoding plasmids. INTERPRETATION: CPE co-colonization status should be monitored during epidemiological surveillance cultures, as these patients might be at a higher risk for infection. FUNDING: European Commission Framework Programme 7 and Instituto de Salud Carlos III, Spain
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spelling pubmed-68334362019-11-08 Intestinal co-colonization with different carbapenemase-producing Enterobacterales isolates is not a rare event in an OXA-48 endemic area Hernández-García, Marta Pérez-Viso, Blanca Navarro-San Francisco, Carolina Baquero, Fernando Morosini, María Isabel Ruiz-Garbajosa, Patricia Cantón, Rafael EClinicalMedicine Research Paper BACKGROUND: The current spread of carbapenemase-producing Enterobacterales (CPE) is a great concern. METHODS: We recovered 198 CPE from 162 patients admitted in our Hospital (March 2014-March 2016) during the R-GNOSIS European Project. Microbiological features and plasmid characteristics of CPE recovered from patients co-colonized with multiple CPE were studied. FINDINGS: Thirty patients (18.5%; CI 95%= 12.5%–24.5%) presented co-colonization with multiple CPE producing the same (CPE-SC) (15.4%) or a different carbapenemase (CPE-DC) (4.3%). OXA-48 (83.3%) was the most frequent carbapenemase, followed by VIM-1 (26.7%), NDM-1 (10%) and KPC-3 (3.3%). CPE-DC-patients had longer admissions [63 days (20–107)] than the other patients. Moreover, hospital stay until CPE detection was lower [9 days (5–14)] (p = 0.0052) in CPE-SC-patients than in those with a single colonization; 56% showed co-colonization in the first positive sample, although most of them had previous admissions and had received multiple antibiotic treatments. CPE were more frequently recovered in clinical samples from co-colonized [CPE-DC (28.6%), CPE-SC (24%)] patients than from patients with a single CPE (15.2%). Among CPE-SC—OXA-48 [80% (p = 0.11)], K. pneumoniae [88% (p = 0.006)] and E. coli [84% (p < 0.001)] were the most frequent species. In 60% of patients, K. pneumoniae and E. coli species were simultaneously recovered, frequently after a single OXA-48-K. pneumoniae colonization. High-risk clones (ST11, ST15, ST307) were detected in OXA-48-K. pneumoniae but a higher clonal diversity was found among E. coli. A frequent in-vivo cross-species plasmid transmission was shown, due to a dominant plasmid (IncL-pOXA-48), but also involving related or unrelated bla(VIM-1)-, bla(NDM-1)- and bla(KPC-3)-encoding plasmids. INTERPRETATION: CPE co-colonization status should be monitored during epidemiological surveillance cultures, as these patients might be at a higher risk for infection. FUNDING: European Commission Framework Programme 7 and Instituto de Salud Carlos III, Spain Elsevier 2019-10-17 /pmc/articles/PMC6833436/ /pubmed/31709416 http://dx.doi.org/10.1016/j.eclinm.2019.09.005 Text en © 2019 Published by Elsevier Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Paper
Hernández-García, Marta
Pérez-Viso, Blanca
Navarro-San Francisco, Carolina
Baquero, Fernando
Morosini, María Isabel
Ruiz-Garbajosa, Patricia
Cantón, Rafael
Intestinal co-colonization with different carbapenemase-producing Enterobacterales isolates is not a rare event in an OXA-48 endemic area
title Intestinal co-colonization with different carbapenemase-producing Enterobacterales isolates is not a rare event in an OXA-48 endemic area
title_full Intestinal co-colonization with different carbapenemase-producing Enterobacterales isolates is not a rare event in an OXA-48 endemic area
title_fullStr Intestinal co-colonization with different carbapenemase-producing Enterobacterales isolates is not a rare event in an OXA-48 endemic area
title_full_unstemmed Intestinal co-colonization with different carbapenemase-producing Enterobacterales isolates is not a rare event in an OXA-48 endemic area
title_short Intestinal co-colonization with different carbapenemase-producing Enterobacterales isolates is not a rare event in an OXA-48 endemic area
title_sort intestinal co-colonization with different carbapenemase-producing enterobacterales isolates is not a rare event in an oxa-48 endemic area
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6833436/
https://www.ncbi.nlm.nih.gov/pubmed/31709416
http://dx.doi.org/10.1016/j.eclinm.2019.09.005
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