High prevalence of OXA-143 and alteration of outer membrane proteins in carbapenem-resistant Acinetobacter spp. isolates in Brazil


Autoria(s): Mostachio, Anna Karina; Levin, Anna Sara; Rizek, Camila; Rossi, Flavia; Zerbini, Jessika; Costa, Silvia Figueiredo
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

31/10/2013

31/10/2013

02/08/2013

Resumo

Carbapenem resistance amongst Acinetobacter spp. has been increasing in the last decade. This study evaluated the outer membrane protein (OMP) profile and production of carbapenemases in 50 carbapenem-resistant Acinetobacter spp. isolates from bloodstream infections. Isolates were identified by API20NE. Minimum inhibitory concentrations (MICs) for carbapenems were determined by broth microdilution. Carbapenemases were studied by phenotypic tests, detection of their encoding gene by polymerase chain reaction (PCR) amplification, and imipenem hydrolysis. Nucleotide sequencing confirming the enzyme gene type was performed using MegaBACE 1000. The presence of OMPs was studied by sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) and PCR. Molecular typing was performed using pulsed-field gel electrophoresis (PFGE). All isolates were resistant to carbapenems. Moreover, 98% of the isolates were positive for the gene encoding the enzyme OXA-51-like, 18% were positive for OXA-23-like (only one isolate did not show the presence of the insertion sequence ISAba1 adjacent to this gene) and 76% were positive for OXA-143 enzyme. Five isolates (10%) showed the presence of the IMP-1 gene. Imipenem hydrolysing activity was detected in only three strains containing carbapenemase genes, comprising two isolates containing the bla(IMP) gene and one containing the bla(OXA-51/OXA-23-like) gene. The OMP of 43 kDa was altered in 17 of 25 strains studied, and this alteration was associated with a high meropenem MIC (256 mu g/mL) in 5 of 7 strains without 43 kDa OMP. On the other hand, decreased OMP 33-36 kDa was found in five strains. The high prevalence of OXA-143 and alteration of OMPs might have been associated with a high level of carbapenem resistance. (C) 2012 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.

FAPESP (Fundacao de Amaparo a Pesquisa do estado de Sao Paulo, Brazil)

FAPESP (Fundacao de Amaparo a Pesquisa do estado de Sao Paulo, Brazil)

CNPq (Conselho Nacional de Desenvolvimento Cientifico e Tecnologico)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Identificador

INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, AMSTERDAM, v. 39, n. 5, supl. 1, Part 2, pp. 396-401, MAY, 2012

0924-8579

http://www.producao.usp.br/handle/BDPI/37118

10.1016/j.ijantimicag.2012.01.021

http://dx.doi.org/10.1016/j.ijantimicag.2012.01.021

Idioma(s)

eng

Publicador

ELSEVIER SCIENCE BV

AMSTERDAM

Relação

INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS

Direitos

closedAccess

Copyright ELSEVIER SCIENCE BV

Palavras-Chave #CARBAPENEM RESISTANCE #ACINETOBACTER #OXA-143 #OUTER MEMBRANE PROTEIN #BETA-LACTAMASES #IMIPENEM RESISTANCE #LATIN-AMERICA #EFFLUX PUMP #BAUMANNII #OUTBREAK #STRAIN #SUSCEPTIBILITY #DIVERSITY #SPREAD #INFECTIOUS DISEASES #MICROBIOLOGY #PHARMACOLOGY & PHARMACY
Tipo

article

original article

publishedVersion