4.7 Article

Carbapenem-Resistant Acinetobacter baumannii in US Hospitals: Diversification of Circulating Lineages and Antimicrobial Resistance

Journal

MBIO
Volume 13, Issue 2, Pages -

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/mbio.02759-21

Keywords

Acinetobacter baumannii; carbapenem resistance; clinical epidemiology; molecular epidemiology

Categories

Funding

  1. National Institute of Allergy and Infectious Diseases of the National Institutes of Health [R21AI135522, UM1AI104681]
  2. Physician Scientist Incubator Program at the University of Pittsburgh - Burrows Wellcome Fund
  3. National Institutes of Health [R01AI072219, U01AI124302, R00EY02822, R01AI104895, R21AI151362, T32GM086330]
  4. PA CURES grant [4100085725]
  5. BD Diagnostics
  6. Hologic
  7. NIH/NIAID [R01-AI148342-01, R01AI134637, K24-AI121296, P01-AI152999-01]
  8. DiaSorin
  9. Lifescale

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Carbapenem-resistant Acinetobacter baumannii (CRAb) is a significant threat to public health, particularly for hospitalized patients. The Study Network of Acinetobacter as a Carbapenem-Resistant Pathogen (SNAP) conducted whole-genome sequencing (WGS) analysis of 120 CRAb patients from four U.S. centers, revealing the dominance of the ST2(Pas) lineage within clonal complex 2 (CC2), as well as the emergence of sublineages with different antibiotic resistance phenotypes. The study emphasizes the need for real-time surveillance and molecular epidemiology to understand CRAb dissemination and clinical impact.
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. IMPORTANCE Carbapenem-resistant Acinetobacter baumannii (CRAb) constitutes a major threat to public health. To elucidate the molecular and clinical epidemiology of CRAb in the United States, clinical CRAb isolates were collected along with data on patient characteristics and outcomes, and bacterial isolates underwent whole-genome sequencing and antibiotic susceptibility phenotyping. Key findings included emergence of new sublineages within the globally predominant clonal complex 2 (CC2), increased colistin and cefiderocol resistance within one of the CC2 sublineages, and emergence of ST499(Pas) as the dominant non-CC2 CRAb lineage in U.S. hospitals. Carbapenem-resistant Acinetobacter baumannii (CRAb) constitutes a major threat to public health. To elucidate the molecular and clinical epidemiology of CRAb in the United States, clinical CRAb isolates were collected along with data on patient characteristics and outcomes, and bacterial isolates underwent whole-genome sequencing and antibiotic susceptibility phenotyping.

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