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631. Laboratory Surveillance of Carbapenem-Resistant Enterobacteriaceae in an Endemic Country, Greece, 2015–2018
BACKGROUND: Greece is facing an endemic situation with carbapenem-resistant pathogens in the hospital sector. The Central Public Health Laboratory (CPHL) is the main laboratory for the surveillance of the carbapenem resistance mechanisms, accepting resistant isolates from hospitals on a voluntary ba...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6811253/ http://dx.doi.org/10.1093/ofid/ofz360.699 |
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author | Tryfinopoulou, Kyriaki Giakkoupi, Panagiota Pappa, Olga Karadimas, Kleon Tsiodras, Sotirios Vatopoulos, Alkiviadis |
author_facet | Tryfinopoulou, Kyriaki Giakkoupi, Panagiota Pappa, Olga Karadimas, Kleon Tsiodras, Sotirios Vatopoulos, Alkiviadis |
author_sort | Tryfinopoulou, Kyriaki |
collection | PubMed |
description | BACKGROUND: Greece is facing an endemic situation with carbapenem-resistant pathogens in the hospital sector. The Central Public Health Laboratory (CPHL) is the main laboratory for the surveillance of the carbapenem resistance mechanisms, accepting resistant isolates from hospitals on a voluntary basis. The aim of the present study is to evaluate the epidemiology of carbapenem-resistant Enterobacteriaceae (CRE) isolated in Greek hospitals the period 2014–2018 and their susceptibility to other antibiotic classes. METHODS: A total of 843 CRE isolates (741 Klebsiella spp., 47 Enterobacter spp., 35 Escherichia coli, and 20 others) have been submitted from 36 hospitals throughout the country (Figure 1) to the CPHL. They originated from different clinical specimens (295 urine, 157 blood, and 107 other) or surveillance cultures (185 rectal and 23 pharyngeal swabs) or unknown (n = 76). Carbapenemase genes were detected by PCR targeting bla(KPC), bla(NDM), bla(VIM), and bla (OXA-48). Resistance to aminoglycosides and fluoroquinolones was tested with the disk diffusion method according to EUCAST guidelines. RESULTS: The isolates were found positive for several carbapenemase genes (Table 1). Overall, KPC-2 (36%) was the predominant carbapenemase, followed by the metalloenzymes NDM (28%) and VIM (18%) while OXA-48 ranked fourth (7%). KPC enzyme was predominant among Klebsiella spp isolates followed by NDM, whereas among Enterobacter, E.coli, and other species, the VIM metalloenzyme predominated. Simultaneous detection of two carbapenemase genes was found in 30 (4%) isolates: 14 bla(KPC)/bla(VIM), 4 bla(KPC)/bla(NDM), 1 bla(KPC)/bla(OXA-48), 5 bla(NDM)/bla(VIM), 5 bla(NDM)/bla(OXA-48), and 1 bla(VIM)/bla(OXA-48). In 63 isolates (7%), the carbapenem resistance was attributed to other mechanisms, mainly production of ESBL or AmpC plus porin loss. In total, 590 (70%) CRE isolates exhibited a multidrug-resistant phenotype being simultaneously resistant to aminoglycosides and fluoroquinolones. CONCLUSION: The CRE isolates’ diversity, regarding bacterial species, carbapenemase types and combinations and their temporal and spatial distribution mandate a more structured, continuous laboratory surveillance to monitor the ongoing carbapenem and multidrug resistance evolution and inform infection control and public health actions. [Image: see text] [Image: see text] DISCLOSURES: All authors: No reported disclosures |
format | Online Article Text |
id | pubmed-6811253 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-68112532019-10-29 631. Laboratory Surveillance of Carbapenem-Resistant Enterobacteriaceae in an Endemic Country, Greece, 2015–2018 Tryfinopoulou, Kyriaki Giakkoupi, Panagiota Pappa, Olga Karadimas, Kleon Tsiodras, Sotirios Vatopoulos, Alkiviadis Open Forum Infect Dis Abstracts BACKGROUND: Greece is facing an endemic situation with carbapenem-resistant pathogens in the hospital sector. The Central Public Health Laboratory (CPHL) is the main laboratory for the surveillance of the carbapenem resistance mechanisms, accepting resistant isolates from hospitals on a voluntary basis. The aim of the present study is to evaluate the epidemiology of carbapenem-resistant Enterobacteriaceae (CRE) isolated in Greek hospitals the period 2014–2018 and their susceptibility to other antibiotic classes. METHODS: A total of 843 CRE isolates (741 Klebsiella spp., 47 Enterobacter spp., 35 Escherichia coli, and 20 others) have been submitted from 36 hospitals throughout the country (Figure 1) to the CPHL. They originated from different clinical specimens (295 urine, 157 blood, and 107 other) or surveillance cultures (185 rectal and 23 pharyngeal swabs) or unknown (n = 76). Carbapenemase genes were detected by PCR targeting bla(KPC), bla(NDM), bla(VIM), and bla (OXA-48). Resistance to aminoglycosides and fluoroquinolones was tested with the disk diffusion method according to EUCAST guidelines. RESULTS: The isolates were found positive for several carbapenemase genes (Table 1). Overall, KPC-2 (36%) was the predominant carbapenemase, followed by the metalloenzymes NDM (28%) and VIM (18%) while OXA-48 ranked fourth (7%). KPC enzyme was predominant among Klebsiella spp isolates followed by NDM, whereas among Enterobacter, E.coli, and other species, the VIM metalloenzyme predominated. Simultaneous detection of two carbapenemase genes was found in 30 (4%) isolates: 14 bla(KPC)/bla(VIM), 4 bla(KPC)/bla(NDM), 1 bla(KPC)/bla(OXA-48), 5 bla(NDM)/bla(VIM), 5 bla(NDM)/bla(OXA-48), and 1 bla(VIM)/bla(OXA-48). In 63 isolates (7%), the carbapenem resistance was attributed to other mechanisms, mainly production of ESBL or AmpC plus porin loss. In total, 590 (70%) CRE isolates exhibited a multidrug-resistant phenotype being simultaneously resistant to aminoglycosides and fluoroquinolones. CONCLUSION: The CRE isolates’ diversity, regarding bacterial species, carbapenemase types and combinations and their temporal and spatial distribution mandate a more structured, continuous laboratory surveillance to monitor the ongoing carbapenem and multidrug resistance evolution and inform infection control and public health actions. [Image: see text] [Image: see text] DISCLOSURES: All authors: No reported disclosures Oxford University Press 2019-10-23 /pmc/articles/PMC6811253/ http://dx.doi.org/10.1093/ofid/ofz360.699 Text en © The Author(s) 2019. 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 Tryfinopoulou, Kyriaki Giakkoupi, Panagiota Pappa, Olga Karadimas, Kleon Tsiodras, Sotirios Vatopoulos, Alkiviadis 631. Laboratory Surveillance of Carbapenem-Resistant Enterobacteriaceae in an Endemic Country, Greece, 2015–2018 |
title | 631. Laboratory Surveillance of Carbapenem-Resistant Enterobacteriaceae in an Endemic Country, Greece, 2015–2018 |
title_full | 631. Laboratory Surveillance of Carbapenem-Resistant Enterobacteriaceae in an Endemic Country, Greece, 2015–2018 |
title_fullStr | 631. Laboratory Surveillance of Carbapenem-Resistant Enterobacteriaceae in an Endemic Country, Greece, 2015–2018 |
title_full_unstemmed | 631. Laboratory Surveillance of Carbapenem-Resistant Enterobacteriaceae in an Endemic Country, Greece, 2015–2018 |
title_short | 631. Laboratory Surveillance of Carbapenem-Resistant Enterobacteriaceae in an Endemic Country, Greece, 2015–2018 |
title_sort | 631. laboratory surveillance of carbapenem-resistant enterobacteriaceae in an endemic country, greece, 2015–2018 |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6811253/ http://dx.doi.org/10.1093/ofid/ofz360.699 |
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