Overexpression of blaOXA-58 Gene Driven by ISAba3 Is Associated with Imipenem Resistance in a Clinical Acinetobacter baumannii Isolate from Vietnam

Author:

Nguyen Anh T.123ORCID,Pham Son C.4,Ly Anh K.4,Nguyen Chau V. V.5,Vu Thanh T.36,Ha Tuan M.36ORCID

Affiliation:

1. Research Center for Genetics and Reproductive Health, School of Medicine, Ho Chi Minh City, Vietnam

2. Vietnam National University, Ho Chi Minh City, Vietnam

3. Molecular Biomedical Center, University Medical Center-Campus 2, Ho Chi Minh City, Vietnam

4. Department of Genetics, Faculty of Biology, University of Science, Vietnam National University, Ho Chi Minh City, Vietnam

5. The Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam

6. University Medical Center-Campus 2, Ho Chi Minh City, Vietnam

Abstract

The aim of this study was to investigate genetic structures and expression of blaOXA-58 gene in five Acinetobacter baumannii clinical isolates recovered from two hospitals in southern Vietnam during 2012-2014. A. baumannii isolates were identified by automated microbiology systems and confirmed by PCR. All isolates were characterized as multidrug resistant by antimicrobial testing using the disk diffusion method. Four imipenem susceptible and one nonsusceptible isolates (MIC>32μg·ml-1) were identified by E-test. PCR amplification of blaOXA-58 gene upstream and downstream sequences revealed the presence of ISAba3 at both locations in one multidrug-resistant isolate. Semiquantitation of blaOXA-51 and blaOXA-58 gene expression was performed by the 2-ΔΔCt method. The blaOXA-51 gene expression of five isolates showed little difference, but the isolate bearing ISAba3-blaOXA-58-ISAba3 exhibited significantly higher blaOXA-58 mRNA level. Higher β-lactamases activity in periplasmic than cytoplasmic fraction was found in most isolates. The isolate overexpressing blaOXA-58 gene possessed very high periplasmic enzyme activity. In conclusion, the A. baumannii isolate bearing ISAba3-blaOXA-58 gene exhibited high resistance to imipenem, corresponding to an overexpression of blaOXA-58 gene and very high periplasmic β-lactamase activity.

Funder

Vietnam National University Ho Chi Minh City

Publisher

Hindawi Limited

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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