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Genomic surveillance of Acinetobacter baumannii in the Philippines, 2013–2014
OBJECTIVE: Acinetobacter baumannii is an opportunistic nosocomial pathogen that has increasingly become resistant to carbapenems worldwide. In the Philippines, rates of carbapenem resistance and multidrug resistance are above 50%. We undertook a genomic study of carbapenem-resistant A. baumannii in...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
World Health Organization
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8873916/ https://www.ncbi.nlm.nih.gov/pubmed/35251744 http://dx.doi.org/10.5365/wpsar.2021.12.4.863 |
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author | Chilam, Jeremiah Argimón, Silvia Limas, Marilyn T. Masim, Melissa L. Gayeta, June M. Lagrada, Marietta L. Olorosa, Agnettah M. Cohen, Victoria Hernandez, Lara T. Jeffrey, Benjamin Abudahab, Khalil Hufano, Charmian M. Sia, Sonia B. Holden, Matthew T.G. Stelling, John Aanensen, David M. Carlos, Celia C. |
author_facet | Chilam, Jeremiah Argimón, Silvia Limas, Marilyn T. Masim, Melissa L. Gayeta, June M. Lagrada, Marietta L. Olorosa, Agnettah M. Cohen, Victoria Hernandez, Lara T. Jeffrey, Benjamin Abudahab, Khalil Hufano, Charmian M. Sia, Sonia B. Holden, Matthew T.G. Stelling, John Aanensen, David M. Carlos, Celia C. |
author_sort | Chilam, Jeremiah |
collection | PubMed |
description | OBJECTIVE: Acinetobacter baumannii is an opportunistic nosocomial pathogen that has increasingly become resistant to carbapenems worldwide. In the Philippines, rates of carbapenem resistance and multidrug resistance are above 50%. We undertook a genomic study of carbapenem-resistant A. baumannii in the Philippines to characterize the population diversity and antimicrobial resistance mechanisms. METHODS: We sequenced the whole genomes of 117 A. baumannii isolates recovered by 16 hospitals in the Philippines between 2013 and 2014. From the genome sequences, we determined the multilocus sequence type, presence of acquired determinants of antimicrobial resistance and relatedness between isolates. We also compared the phenotypic and genotypic resistance results. RESULTS: Carbapenem resistance was mainly explained by acquisition of the class-D β-lactamase gene bla(OXA-23). The concordance between phenotypic and genotypic resistance to imipenem was 98.15%, and it was 94.97% overall for the seven antibiotics analysed. Twenty-two different sequence types were identified, including 7 novel types. The population was dominated by the high-risk international clone 2 (i.e. clonal complex 92), in particular by ST195 and ST208 and their single locus variants. Using whole-genome sequencing, we identified local clusters representing potentially undetected nosocomial outbreaks, as well as multihospital clusters that indicated interhospital dissemination. Comparison with global genomes suggested that the establishment of carbapenem-resistant international clone 2 in the Philippines is likely the result of clonal expansion and geographical dissemination, and at least partly explained by inadequate hospital infection control and prevention. DISCUSSION: This is the first extensive genomic study of carbapenem-resistant A. baumannii in the Philippines, and it underscores the importance of hospital infection control and prevention measures to contain high-risk clones. |
format | Online Article Text |
id | pubmed-8873916 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | World Health Organization |
record_format | MEDLINE/PubMed |
spelling | pubmed-88739162022-03-04 Genomic surveillance of Acinetobacter baumannii in the Philippines, 2013–2014 Chilam, Jeremiah Argimón, Silvia Limas, Marilyn T. Masim, Melissa L. Gayeta, June M. Lagrada, Marietta L. Olorosa, Agnettah M. Cohen, Victoria Hernandez, Lara T. Jeffrey, Benjamin Abudahab, Khalil Hufano, Charmian M. Sia, Sonia B. Holden, Matthew T.G. Stelling, John Aanensen, David M. Carlos, Celia C. Western Pac Surveill Response J Non Theme Issue OBJECTIVE: Acinetobacter baumannii is an opportunistic nosocomial pathogen that has increasingly become resistant to carbapenems worldwide. In the Philippines, rates of carbapenem resistance and multidrug resistance are above 50%. We undertook a genomic study of carbapenem-resistant A. baumannii in the Philippines to characterize the population diversity and antimicrobial resistance mechanisms. METHODS: We sequenced the whole genomes of 117 A. baumannii isolates recovered by 16 hospitals in the Philippines between 2013 and 2014. From the genome sequences, we determined the multilocus sequence type, presence of acquired determinants of antimicrobial resistance and relatedness between isolates. We also compared the phenotypic and genotypic resistance results. RESULTS: Carbapenem resistance was mainly explained by acquisition of the class-D β-lactamase gene bla(OXA-23). The concordance between phenotypic and genotypic resistance to imipenem was 98.15%, and it was 94.97% overall for the seven antibiotics analysed. Twenty-two different sequence types were identified, including 7 novel types. The population was dominated by the high-risk international clone 2 (i.e. clonal complex 92), in particular by ST195 and ST208 and their single locus variants. Using whole-genome sequencing, we identified local clusters representing potentially undetected nosocomial outbreaks, as well as multihospital clusters that indicated interhospital dissemination. Comparison with global genomes suggested that the establishment of carbapenem-resistant international clone 2 in the Philippines is likely the result of clonal expansion and geographical dissemination, and at least partly explained by inadequate hospital infection control and prevention. DISCUSSION: This is the first extensive genomic study of carbapenem-resistant A. baumannii in the Philippines, and it underscores the importance of hospital infection control and prevention measures to contain high-risk clones. World Health Organization 2021-10-27 /pmc/articles/PMC8873916/ /pubmed/35251744 http://dx.doi.org/10.5365/wpsar.2021.12.4.863 Text en (c) 2021 The authors; licensee World Health Organization. https://creativecommons.org/licenses/by/3.0/igo/This is an open access article distributed under the terms of the Creative Commons Attribution IGO License (http://creativecommons.org/licenses/by/3.0/igo/legalcode (https://creativecommons.org/licenses/by/3.0/igo/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. In any reproduction of this article there should not be any suggestion that WHO or this article endorse any specific organization or products. The use of the WHO logo is not permitted. This notice should be preserved along with the article's original URL. |
spellingShingle | Non Theme Issue Chilam, Jeremiah Argimón, Silvia Limas, Marilyn T. Masim, Melissa L. Gayeta, June M. Lagrada, Marietta L. Olorosa, Agnettah M. Cohen, Victoria Hernandez, Lara T. Jeffrey, Benjamin Abudahab, Khalil Hufano, Charmian M. Sia, Sonia B. Holden, Matthew T.G. Stelling, John Aanensen, David M. Carlos, Celia C. Genomic surveillance of Acinetobacter baumannii in the Philippines, 2013–2014 |
title | Genomic surveillance of Acinetobacter baumannii in the Philippines, 2013–2014 |
title_full | Genomic surveillance of Acinetobacter baumannii in the Philippines, 2013–2014 |
title_fullStr | Genomic surveillance of Acinetobacter baumannii in the Philippines, 2013–2014 |
title_full_unstemmed | Genomic surveillance of Acinetobacter baumannii in the Philippines, 2013–2014 |
title_short | Genomic surveillance of Acinetobacter baumannii in the Philippines, 2013–2014 |
title_sort | genomic surveillance of acinetobacter baumannii in the philippines, 2013–2014 |
topic | Non Theme Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8873916/ https://www.ncbi.nlm.nih.gov/pubmed/35251744 http://dx.doi.org/10.5365/wpsar.2021.12.4.863 |
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