Loading…

Emergence and Persistence of High-Risk Clones Among MDR and XDR A. baumannii at a Brazilian Teaching Hospital

Dissemination of carbapenem-resistant is currently one of the priority themes discussed around the world, including in Brazil, where this pathogen is considered endemic. A total of 107 carbapenem-resistant (CRAB) isolates were collected from patients with bacteraemia attended at a teaching hospital...

Full description

Saved in:
Bibliographic Details
Published in:Frontiers in microbiology 2019-01, Vol.9, p.2898-2898
Main Authors: Tavares, Laís Calissi Brisolla, de Vasconcellos, Francielli Mahnic, de Sousa, William Vaz, Rocchetti, Taisa Trevizani, Mondelli, Alessandro Lia, Ferreira, Adriano Martison, Montelli, Augusto Cezar, Sadatsune, Terue, Tiba-Casas, Monique Ribeiro, Camargo, Carlos Henrique
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Dissemination of carbapenem-resistant is currently one of the priority themes discussed around the world, including in Brazil, where this pathogen is considered endemic. A total of 107 carbapenem-resistant (CRAB) isolates were collected from patients with bacteraemia attended at a teaching hospital in Brazil from 2008 to 2014. From these samples, 104 (97.2%) carried , all of them associated with IS The (1.9%) and (0.9%) genes were also detected in low frequencies. All isolates were susceptible to minocycline, and 38.3% of isolates presented intermediate susceptibility to tigecycline (MIC = 4 μg/ml). Molecular typing assessed by multi-locus sequence typing demonstrated that the strains were mainly associated with clonal complexes CC79 (47.4%), followed by CC1 (16.9%), and CC317 (18.6%), belonging to different pulsotypes and in different prevalences over the years. Changes in the clones' prevalence reinforce the need of identifying and controlling CRAB in hospital settings to preserve the already scarce therapeutic options available.
ISSN:1664-302X
1664-302X
DOI:10.3389/fmicb.2018.02898