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Carbapenem-Resistant Acinetobacter baumannii in U.S. Hospitals: Diversification of Circulating Lineages and Antimicrobial Resistance

Carbapenem-resistant Acinetobacter baumannii (CRAb) is a major cause of health care-associated infections. CRAb is typically multidrug resistant, and infection is difficult to treat. Despite the urgent threat that CRAb poses, few systematic studies of CRAb clinical and molecular epidemiology have be...

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Autores principales: Iovleva, Alina, Mustapha, Mustapha M., Griffith, Marissa P., Komarow, Lauren, Luterbach, Courtney, Evans, Daniel R., Cober, Eric, Richter, Sandra S., Rydell, Kirsten, Arias, Cesar A., Jacob, Jesse T., Salata, Robert A., Satlin, Michael J., Wong, Darren, Bonomo, Robert A., van Duin, David, Cooper, Vaughn S., Van Tyne, Daria, Doi, Yohei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9040734/
https://www.ncbi.nlm.nih.gov/pubmed/35311529
http://dx.doi.org/10.1128/mbio.02759-21
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author Iovleva, Alina
Mustapha, Mustapha M.
Griffith, Marissa P.
Komarow, Lauren
Luterbach, Courtney
Evans, Daniel R.
Cober, Eric
Richter, Sandra S.
Rydell, Kirsten
Arias, Cesar A.
Jacob, Jesse T.
Salata, Robert A.
Satlin, Michael J.
Wong, Darren
Bonomo, Robert A.
van Duin, David
Cooper, Vaughn S.
Van Tyne, Daria
Doi, Yohei
author_facet Iovleva, Alina
Mustapha, Mustapha M.
Griffith, Marissa P.
Komarow, Lauren
Luterbach, Courtney
Evans, Daniel R.
Cober, Eric
Richter, Sandra S.
Rydell, Kirsten
Arias, Cesar A.
Jacob, Jesse T.
Salata, Robert A.
Satlin, Michael J.
Wong, Darren
Bonomo, Robert A.
van Duin, David
Cooper, Vaughn S.
Van Tyne, Daria
Doi, Yohei
author_sort Iovleva, Alina
collection PubMed
description Carbapenem-resistant Acinetobacter baumannii (CRAb) is a major cause of health care-associated infections. CRAb is typically multidrug resistant, and infection is difficult to treat. Despite the urgent threat that CRAb poses, few systematic studies of CRAb clinical and molecular epidemiology have been conducted. The Study Network of Acinetobacter as a Carbapenem-Resistant Pathogen (SNAP) is designed to investigate the clinical characteristics and contemporary population structure of CRAb circulating in U.S. hospital systems using whole-genome sequencing (WGS). Analysis of the initial 120 SNAP patients from four U.S. centers revealed that CRAb remains a significant threat to hospitalized patients, affecting the most vulnerable patients and resulting in 24% all-cause 30-day mortality. The majority of currently circulating isolates belonged to ST2(Pas), a part of clonal complex 2 (CC2), which is the dominant drug-resistant lineage in the United States and Europe. We identified three distinct sublineages within CC2, which differed in their antibiotic resistance phenotypes and geographic distribution. Most concerning, colistin resistance (38%) and cefiderocol resistance (10%) were common within CC2 sublineage C (CC2C), where the majority of isolates belonged to ST2(Pas)/ST281(Ox). Additionally, we identified ST499(Pas) as the most common non-CC2 lineage in our study. Our findings suggest a shift within the CRAb population in the United States during the past 10 years and emphasize the importance of real-time surveillance and molecular epidemiology in studying CRAb dissemination and clinical impact.
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spelling pubmed-90407342022-04-27 Carbapenem-Resistant Acinetobacter baumannii in U.S. Hospitals: Diversification of Circulating Lineages and Antimicrobial Resistance Iovleva, Alina Mustapha, Mustapha M. Griffith, Marissa P. Komarow, Lauren Luterbach, Courtney Evans, Daniel R. Cober, Eric Richter, Sandra S. Rydell, Kirsten Arias, Cesar A. Jacob, Jesse T. Salata, Robert A. Satlin, Michael J. Wong, Darren Bonomo, Robert A. van Duin, David Cooper, Vaughn S. Van Tyne, Daria Doi, Yohei mBio Research Article Carbapenem-resistant Acinetobacter baumannii (CRAb) is a major cause of health care-associated infections. CRAb is typically multidrug resistant, and infection is difficult to treat. Despite the urgent threat that CRAb poses, few systematic studies of CRAb clinical and molecular epidemiology have been conducted. The Study Network of Acinetobacter as a Carbapenem-Resistant Pathogen (SNAP) is designed to investigate the clinical characteristics and contemporary population structure of CRAb circulating in U.S. hospital systems using whole-genome sequencing (WGS). Analysis of the initial 120 SNAP patients from four U.S. centers revealed that CRAb remains a significant threat to hospitalized patients, affecting the most vulnerable patients and resulting in 24% all-cause 30-day mortality. The majority of currently circulating isolates belonged to ST2(Pas), a part of clonal complex 2 (CC2), which is the dominant drug-resistant lineage in the United States and Europe. We identified three distinct sublineages within CC2, which differed in their antibiotic resistance phenotypes and geographic distribution. Most concerning, colistin resistance (38%) and cefiderocol resistance (10%) were common within CC2 sublineage C (CC2C), where the majority of isolates belonged to ST2(Pas)/ST281(Ox). Additionally, we identified ST499(Pas) as the most common non-CC2 lineage in our study. Our findings suggest a shift within the CRAb population in the United States during the past 10 years and emphasize the importance of real-time surveillance and molecular epidemiology in studying CRAb dissemination and clinical impact. American Society for Microbiology 2022-03-21 /pmc/articles/PMC9040734/ /pubmed/35311529 http://dx.doi.org/10.1128/mbio.02759-21 Text en Copyright © 2022 Iovleva et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Iovleva, Alina
Mustapha, Mustapha M.
Griffith, Marissa P.
Komarow, Lauren
Luterbach, Courtney
Evans, Daniel R.
Cober, Eric
Richter, Sandra S.
Rydell, Kirsten
Arias, Cesar A.
Jacob, Jesse T.
Salata, Robert A.
Satlin, Michael J.
Wong, Darren
Bonomo, Robert A.
van Duin, David
Cooper, Vaughn S.
Van Tyne, Daria
Doi, Yohei
Carbapenem-Resistant Acinetobacter baumannii in U.S. Hospitals: Diversification of Circulating Lineages and Antimicrobial Resistance
title Carbapenem-Resistant Acinetobacter baumannii in U.S. Hospitals: Diversification of Circulating Lineages and Antimicrobial Resistance
title_full Carbapenem-Resistant Acinetobacter baumannii in U.S. Hospitals: Diversification of Circulating Lineages and Antimicrobial Resistance
title_fullStr Carbapenem-Resistant Acinetobacter baumannii in U.S. Hospitals: Diversification of Circulating Lineages and Antimicrobial Resistance
title_full_unstemmed Carbapenem-Resistant Acinetobacter baumannii in U.S. Hospitals: Diversification of Circulating Lineages and Antimicrobial Resistance
title_short Carbapenem-Resistant Acinetobacter baumannii in U.S. Hospitals: Diversification of Circulating Lineages and Antimicrobial Resistance
title_sort carbapenem-resistant acinetobacter baumannii in u.s. hospitals: diversification of circulating lineages and antimicrobial resistance
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9040734/
https://www.ncbi.nlm.nih.gov/pubmed/35311529
http://dx.doi.org/10.1128/mbio.02759-21
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