Title
Epidemiology and molecular characterization of multidrug-resistant escherichia coli isolates harboring bla<inf>CTX-M</inf> group 1 extended-spectrum β-lactamases causing bacteremia and urinary tract infection in manhiça, mozambique
Date Issued
03 July 2018
Access level
open access
Resource Type
journal article
Author(s)
Guiral E.
Vubil D.
Marí-Almirall M.
Sigaúque B.
Soto S.M.
Alonso P.L.
Vila J.
Mandomando I.
Hospital Clínico de la universidad de Barcelona
Hospital Clínico de la universidad de Barcelona
Publisher(s)
Dove Medical Press Ltd.
Abstract
Background: The emergence and spread of extended-spectrum β-lactamases (ESBLs), especially CTX-M, is an important public health problem with serious implications for low-income countries where second-line treatment is often unavailable. Knowledge of the local prevalence of ESBL is critical to define appropriate empirical therapeutic strategies for multidrug-resistant (MDR) organisms. This study aimed to assess and characterize the presence of ESBL and especially CTX-M-producing Escherichia coli MDR isolates from patients with urinary tract infections (UTIs) and bacteremia in a rural hospital in Mozambique. Materials and methods: One hundred and fifty-one E. coli isolates from bacteremia and UTI in children were screened for CTX-M, TEM, SHV and OXA β-lactamases by polymerase chain reaction and sequencing. Isolates carrying CTX-M group 1 β-lactamases were further studied. The resistance to other antibiotic families was determined by phenotypic and genotypic methods, the location of the blaCTX-M gene and the epidemiology of the isolates were studied, and extensive plasmid characterization was performed. Results: Approximately 11% (17/151) of E. coli isolates causing bacteremia and UTI were ESBL producers. CTX-M-15 was the most frequently detected ESBL, accounting for 75% of the total isolates characterized. The blaCTX-M gene is located in different plasmids belonging to different incompatibility groups and can be found in non-epidemiologically related isolates, indicating the high capacity of this resistance determinant to spread widely. Conclusion: Our data suggest the presence of a co-selection of third-generation cephalosporinresistant determinants in the study area despite limited access to these antibiotics. This highlights the importance of continuous surveillance of antimicrobial resistance of both genetic elements of resistance and resistant isolates in order to monitor the emergence and trends of ESBL-producing isolates to promote adequate therapeutic strategies for the management of MDR bacterial infections.
Start page
927
End page
936
Volume
11
Language
English
OCDE Knowledge area
Virología Epidemiología
Scopus EID
2-s2.0-85049634608
Source
Infection and Drug Resistance
ISSN of the container
11786973
Sponsor(s)
The authors thank all the clinical and laboratory staff from the CISM for their contribution in different stages of the study, specifically for Dinis Jantilal, Oscar Fraile, Tacilta Nhampossa, and Pedro Aide. Special thanks to the bacteriology laboratory technicians for their excellent support in performing antimicrobial susceptibility testing and ESBL phenotyping. The authors are also grateful to Alessandra Carattoli for providing the control strains for the PBRT and to Donna Pringle for language correction. This study received funding from Planes Nacionales de I+D+i 2008–2011/2013–2016 and the Instituto de Salud Carlos III, Subdirección General de Redes y Centros de Investigación Cooperativa, Ministerio de Economía y Competitividad, Spanish Network for Research in Infectious Diseases (REIPI RD12/0015/0013 and REIPI RD16/0016/0010) and was co-financed by European Development Regional Fund “A way to achieve Europe” and operative program Intelligent Growth 2014–2020. The CISM received core funding from the Agencia Española de Cooperación Internacional y Desarrollo (AECID). This work was also supported by grant 2009 SGR 1256 from the Agència de Gestió d’Ajuts Universitaris i de Recerca of the Generalitat de Catalunya. JR had a fellowship from program I3 of the Instituto de Salud Carlos III (ISCIII) (grant number: CES11/012). ISGlobal is a member of the Centres de Recerca de Catalunya (CERCA) Programme, Generalitat de Catalunya. This study received funding from Planes Nacionales de I+D+i 2008–2011/2013–2016 and the Instituto de Salud Carlos III, Subdirección General de Redes y Centros de Inves-tigación Cooperativa, Ministerio de Economía y Competi-tividad, Spanish Network for Research in Infectious Diseases (REIPI RD12/0015/0013 and REIPI RD16/0016/0010) and was co-financed by European Development Regional Fund “A way to achieve Europe” and operative program Intelligent Growth 2014–2020. The CISM received core funding from the Agencia Española de Cooperación Internacional y Desar - rollo (AECID). This work was also supported by grant 2009 SGR 1256 from the Agència de Gestió d’Ajuts Universitaris i de Recerca of the Generalitat de Catalunya. JR had a fellowship from program I3 of the Instituto de Salud Carlos III (ISCIII) (grant number: CES11/012).
Sources of information: Directorio de Producción Científica Scopus