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Molecular Characterization of Carbapenem/Colistin-Resistant Acinetobacter baumannii Clinical Isolates from Egypt by Whole-Genome Sequencing

PURPOSE: The rise of carbapenem-resistant A. baumannii (CRAB) is considered a public health problem limiting the treatment options. Our current work studied the emergence and mechanisms of colistin-resistance among CRAB isolates in Egypt. MATERIALS AND METHODS: Seventeen clinically recovered A. baum...

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Detalles Bibliográficos
Autores principales: Fam, Nevine S, Gamal, Doaa, Mohamed, Sara H, Wasfy, Reham M, Soliman, May S, El-Kholy, Amani A, Higgins, Paul G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7751577/
https://www.ncbi.nlm.nih.gov/pubmed/33364795
http://dx.doi.org/10.2147/IDR.S288865
Descripción
Sumario:PURPOSE: The rise of carbapenem-resistant A. baumannii (CRAB) is considered a public health problem limiting the treatment options. Our current work studied the emergence and mechanisms of colistin-resistance among CRAB isolates in Egypt. MATERIALS AND METHODS: Seventeen clinically recovered A. baumannii were identified and screened for their antimicrobial susceptibilities using VITEK-2 system. Colistin susceptibility was evaluated using broth microdilution, and characterization of carbapenem/colistin resistance determinants was performed using whole-genome sequencing (Illumina MiSeq). RESULTS: About 52.9% (9/17) were colistin-resistant. PCR results revealed that all isolates carried bla(OXA-51-like genes), bla(OXA-23-like) was detected in 82.3% (14/17) and bla(NDM) in 23.5% (4/17). Two isolates harboured bla(GES-35) and bla(OXA-23). Furthermore, genome analysis of seven isolates revealed six belonged to international clone 2 (IC2) while the remaining isolate was a singleton (ST158), representing a clone circulating in Mediterranean/Middle Eastern countries. CONCLUSION: The emergence and high incidence of colistin-resistance among CRAB clinical isolates in Egypt are alarming because it further limits therapy options and requires prudent antimicrobial stewardship and stringent infection control measures. Whole-genome sequence analyses suggest that the resistance to colistin was associated with multiple mutations in the pmrCAB genes. The high incidence of the high-risk lineage IC2 harbouring bla(OXA-23-like) as well as bla(NDM) is also of concern.