Literature DB >> 29665444

NDM-1- and OXA-23-producing Acinetobacter baumannii isolated from intensive care unit patients in Tunisia.

Elaa Maamar1, Carla Andrea Alonso2, Sana Ferjani3, Ali Jendoubi4, Zaineb Hamzaoui3, Alia Jebri4, Mabrouka Saidani5, Salma Ghedira4, Carmen Torres2, Ilhem Boutiba-Ben Boubaker5.   

Abstract

Gastrointestinal colonisation by carbapenem-resistant Acinetobacter baumannii (CRAB) is a critical step before nosocomial infection. This study evaluated CRAB intestinal carriage in patients admitted to a Tunisian ICU and determined the antimicrobial resistance mechanisms involved. From December 2014 to February 2015, all 63 patients admitted to the ICU were screened for rectal CRAB colonisation upon admission and once weekly thereafter. ICU patients who acquired a CRAB nosocomial infection were also included. β-Lactamases and associated resistance genes were screened by PCR sequencing, and molecular typing was performed by PFGE and MLST. The CRAB faecal carriage rate at admission was 4.8% (3/63). The CRAB acquisition rate during ICU stay was analysed in 39 of the remaining 60 patients and the rate of acquired CRAB faecal carriage was 15.4% (6/39); 4 patients also showed an ICU-acquired CRAB infection (one patient was a faecal carrier and suffered infection). Overall, 13 CRAB isolates were collected from 12 patients, of which 11 isolates showed resistance to all antibiotics tested except colistin. blaOXA-23 and blaNDM-1 were detected in 11 and 2 isolates, respectively. All OXA-23-producing strains carried armA, tetB, sul1 and catB, and some of them carried aph(3')-VIa, blaTEM-1, aph(3')-Ia and ant(2'')-Ia. The blaNDM-1-positive isolates harboured aph(3')-VIa and catB. Three PFGE patterns and two STs were identified [ST195 (n = 11), ST1089 (n = 2, NDM-1-positive)]. Whether imported or acquired during ICU stay, CRAB colonisation is a major risk factor for the occurrence of serious nosocomial infection. Systematic screening of faecal carriage is mandatory to prevent their spread.
Copyright © 2018 Elsevier B.V. and International Society of Chemotherapy. All rights reserved.

Entities:  

Keywords:  Acinetobacter baumannii; Gastrointestinal colonisation; ICU; arbapenemase

Mesh:

Substances:

Year:  2018        PMID: 29665444     DOI: 10.1016/j.ijantimicag.2018.04.008

Source DB:  PubMed          Journal:  Int J Antimicrob Agents        ISSN: 0924-8579            Impact factor:   5.283


  4 in total

1.  Antimicrobial biopolymer formation from sodium alginate and algae extract using aminoglycosides.

Authors:  Lokender Kumar; John Brice; Linda Toberer; Judith Klein-Seetharaman; Daniel Knauss; Susanta K Sarkar
Journal:  PLoS One       Date:  2019-03-26       Impact factor: 3.240

Review 2.  Carbapenemase Producing Gram-Negative Bacteria in Tunisia: History of Thirteen Years of Challenge.

Authors:  Olfa Dziri; Raoudha Dziri; Allaaeddin Ali El Salabi; Chedly Chouchani
Journal:  Infect Drug Resist       Date:  2020-11-23       Impact factor: 4.003

3.  A high mortality rate associated with multidrug-resistant Acinetobacter baumannii ST79 and ST25 carrying OXA-23 in a Brazilian intensive care unit.

Authors:  Kesia Esther da Silva; Wirlaine Glauce Maciel; Julio Croda; Rodrigo Cayô; Ana Carolina Ramos; Romário Oliveira de Sales; Mariana Neri Lucas Kurihara; Nathalie Gaebler Vasconcelos; Ana Cristina Gales; Simone Simionatto
Journal:  PLoS One       Date:  2018-12-28       Impact factor: 3.240

4.  Rectal Colonization and Nosocomial Transmission of Carbapenem-Resistant Acinetobacter baumannii in an Intensive Care Unit, Southwest Nigeria.

Authors:  Erkison Ewomazino Odih; Emmanuel Oladayo Irek; Temitope O Obadare; Anderson O Oaikhena; Ayorinde O Afolayan; Anthony Underwood; Anthony T Adenekan; Veronica O Ogunleye; Silvia Argimon; Anders Dalsgaard; David M Aanensen; Iruka N Okeke; A Oladipo Aboderin
Journal:  Front Med (Lausanne)       Date:  2022-03-07
  4 in total

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