Cargando…
Increasing frequency of OXA-48-producing Enterobacterales worldwide and activity of ceftazidime/avibactam, meropenem/vaborbactam and comparators against these isolates
OBJECTIVES: To investigate the increase in the rates of OXA-48-like-producing isolates during 3 years of global surveillance. METHODS: Among 55?>162 Enterobacterales isolates, 354 carbapenem-resistant isolates carried genes encoding OXA-48-like enzymes. Isolates were susceptibility tested for cef...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8598286/ https://www.ncbi.nlm.nih.gov/pubmed/34459890 http://dx.doi.org/10.1093/jac/dkab306 |
_version_ | 1784600789068546048 |
---|---|
author | Castanheira, Mariana Doyle, Timothy B Collingsworth, Timothy D Sader, Helio S Mendes, Rodrigo E |
author_facet | Castanheira, Mariana Doyle, Timothy B Collingsworth, Timothy D Sader, Helio S Mendes, Rodrigo E |
author_sort | Castanheira, Mariana |
collection | PubMed |
description | OBJECTIVES: To investigate the increase in the rates of OXA-48-like-producing isolates during 3 years of global surveillance. METHODS: Among 55?>162 Enterobacterales isolates, 354 carbapenem-resistant isolates carried genes encoding OXA-48-like enzymes. Isolates were susceptibility tested for ceftazidime/avibactam and comparators by broth microdilution methods. Analysis of β-lactam resistance mechanisms and MLST was performed in silico using WGS data. RESULTS: OXA-48-like-producing isolates increased from 0.5% (94/18 656) in 2016 to 0.9% (169/18?>808) in 2018. OXA-48 was the most common variant; isolates primarily were Klebsiella pneumoniae (318/354 isolates) from Europe and adjacent countries. MLST analysis revealed a diversity of STs, but K. pneumoniae belonging to ST395, ST23 and ST11 were observed most frequently. Thirty-nine isolates harboured MBLs and were resistant to most agents tested. The presence of bla(CTX-M-15) (258 isolates), OmpK35 nonsense mutations (232) and OmpK36 alterations (316) was common among OXA-48 producers. Ceftazidime, cefepime and aztreonam susceptibility rates, when applying CLSI breakpoints, were 12%–15% lower for isolates carrying ESBLs alone and with either or both OmpK35 stop codons and OmpK36 alterations. Meropenem and, remarkably, meropenem/vaborbactam were affected by specific OmpK36 alterations when a deleterious mutation also was observed in OmpK35. These mechanisms caused a decrease of 12%–42% in the susceptibility rates for meropenem and meropenem/vaborbactam. Ceftazidime/avibactam susceptibility rates were >98.9%, regardless of the presence of additional β-lactam resistance mechanisms. CONCLUSIONS: Guidelines for the treatment of infections caused by OXA-48-producing isolates are scarce and, as the dissemination of these isolates continues, studies are needed to help physicians understand treatment options for these infections. |
format | Online Article Text |
id | pubmed-8598286 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-85982862021-11-18 Increasing frequency of OXA-48-producing Enterobacterales worldwide and activity of ceftazidime/avibactam, meropenem/vaborbactam and comparators against these isolates Castanheira, Mariana Doyle, Timothy B Collingsworth, Timothy D Sader, Helio S Mendes, Rodrigo E J Antimicrob Chemother Original Research OBJECTIVES: To investigate the increase in the rates of OXA-48-like-producing isolates during 3 years of global surveillance. METHODS: Among 55?>162 Enterobacterales isolates, 354 carbapenem-resistant isolates carried genes encoding OXA-48-like enzymes. Isolates were susceptibility tested for ceftazidime/avibactam and comparators by broth microdilution methods. Analysis of β-lactam resistance mechanisms and MLST was performed in silico using WGS data. RESULTS: OXA-48-like-producing isolates increased from 0.5% (94/18 656) in 2016 to 0.9% (169/18?>808) in 2018. OXA-48 was the most common variant; isolates primarily were Klebsiella pneumoniae (318/354 isolates) from Europe and adjacent countries. MLST analysis revealed a diversity of STs, but K. pneumoniae belonging to ST395, ST23 and ST11 were observed most frequently. Thirty-nine isolates harboured MBLs and were resistant to most agents tested. The presence of bla(CTX-M-15) (258 isolates), OmpK35 nonsense mutations (232) and OmpK36 alterations (316) was common among OXA-48 producers. Ceftazidime, cefepime and aztreonam susceptibility rates, when applying CLSI breakpoints, were 12%–15% lower for isolates carrying ESBLs alone and with either or both OmpK35 stop codons and OmpK36 alterations. Meropenem and, remarkably, meropenem/vaborbactam were affected by specific OmpK36 alterations when a deleterious mutation also was observed in OmpK35. These mechanisms caused a decrease of 12%–42% in the susceptibility rates for meropenem and meropenem/vaborbactam. Ceftazidime/avibactam susceptibility rates were >98.9%, regardless of the presence of additional β-lactam resistance mechanisms. CONCLUSIONS: Guidelines for the treatment of infections caused by OXA-48-producing isolates are scarce and, as the dissemination of these isolates continues, studies are needed to help physicians understand treatment options for these infections. Oxford University Press 2021-08-30 /pmc/articles/PMC8598286/ /pubmed/34459890 http://dx.doi.org/10.1093/jac/dkab306 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Research Castanheira, Mariana Doyle, Timothy B Collingsworth, Timothy D Sader, Helio S Mendes, Rodrigo E Increasing frequency of OXA-48-producing Enterobacterales worldwide and activity of ceftazidime/avibactam, meropenem/vaborbactam and comparators against these isolates |
title | Increasing frequency of OXA-48-producing Enterobacterales worldwide and activity of ceftazidime/avibactam, meropenem/vaborbactam and comparators against these isolates |
title_full | Increasing frequency of OXA-48-producing Enterobacterales worldwide and activity of ceftazidime/avibactam, meropenem/vaborbactam and comparators against these isolates |
title_fullStr | Increasing frequency of OXA-48-producing Enterobacterales worldwide and activity of ceftazidime/avibactam, meropenem/vaborbactam and comparators against these isolates |
title_full_unstemmed | Increasing frequency of OXA-48-producing Enterobacterales worldwide and activity of ceftazidime/avibactam, meropenem/vaborbactam and comparators against these isolates |
title_short | Increasing frequency of OXA-48-producing Enterobacterales worldwide and activity of ceftazidime/avibactam, meropenem/vaborbactam and comparators against these isolates |
title_sort | increasing frequency of oxa-48-producing enterobacterales worldwide and activity of ceftazidime/avibactam, meropenem/vaborbactam and comparators against these isolates |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8598286/ https://www.ncbi.nlm.nih.gov/pubmed/34459890 http://dx.doi.org/10.1093/jac/dkab306 |
work_keys_str_mv | AT castanheiramariana increasingfrequencyofoxa48producingenterobacteralesworldwideandactivityofceftazidimeavibactammeropenemvaborbactamandcomparatorsagainsttheseisolates AT doyletimothyb increasingfrequencyofoxa48producingenterobacteralesworldwideandactivityofceftazidimeavibactammeropenemvaborbactamandcomparatorsagainsttheseisolates AT collingsworthtimothyd increasingfrequencyofoxa48producingenterobacteralesworldwideandactivityofceftazidimeavibactammeropenemvaborbactamandcomparatorsagainsttheseisolates AT saderhelios increasingfrequencyofoxa48producingenterobacteralesworldwideandactivityofceftazidimeavibactammeropenemvaborbactamandcomparatorsagainsttheseisolates AT mendesrodrigoe increasingfrequencyofoxa48producingenterobacteralesworldwideandactivityofceftazidimeavibactammeropenemvaborbactamandcomparatorsagainsttheseisolates |