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Original Research Article | OPEN ACCESS

Molecular characterization of selected nasal isolates of methicillin-resistant Staphylococcus aureus (MRSA) from healthy students of a tertiary institution

Clement Oliseloke Anie1, Emmanuel Chinedum Ibezim2, Charles Okechukwu Esimone3, Matthew Ikhuoria Arhewoh4

1Department of Pharmaceutical Microbiology, Faculty of Pharmacy, Delta State University, Abraka, Delta State, Nigeria; 2Department of Pharmaceutical Microbiology, Faculty of Pharmacy, University of Nigeria, Nsukka, Nigeria; 3Department of Pharmaceutical Microbiology and Biotechnology, Faculty of Pharmacy, Nnamdi Azikiwe University, Awka, Nigeria; 4Department of Pharmaceutics and Pharmaceutical Technology, Faculty of Pharmacy, University of Benin, Benin City, Nigeria.

For correspondence:-  Matthew Arhewoh   Email: arhewoh@uniben.edu   Tel:+2348055306846

Accepted: 26 March 2022        Published: 30 April 2022

Citation: Anie CO, Ibezim EC, Esimone CO, Arhewoh MI. Molecular characterization of selected nasal isolates of methicillin-resistant Staphylococcus aureus (MRSA) from healthy students of a tertiary institution. Trop J Pharm Res 2022; 21(4):825-831 doi: 10.4314/tjpr.v21i4.20

© 2022 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To investigate the incidence of methicillin-resistant Staphylococcus aureus (MRSA) and carry out molecular characterization in selected nasal isolates from healthy students in Abraka, Nigeria.
Methods: Three hundred (300) samples were obtained from apparently healthy 150 female and 150 male students and were cultured in suitable media for identification. The MRSA were detected by means of oxacillin antibiotic sensitivity disk. Antibiotics susceptibility pattern of MRSA isolates was carried out in accordance with the guidelines of Clinical Laboratory Standard Institute. Tests were carried out to determine the presence of penicillin binding protein2a (PBP2a). Molecular characterization of twenty (20) MRSA representatives was done to establish the existence of the mecA genes among the isolates.
Results: The incidence of MRSA colonization amongst apparently healthy students in the community was 68 (22.7 %). The sensitivity pattern was: amoxicillin, 40 (58.8 %); amoxicillin/clavulanate, 15 (22.1 %); chloramphenicol, 15 (22.1 %); ciprofloxacin, 19 (27.9 %); co-trimoxazole, 9 (13.2 %); gentamicin, 9 (13.2 %); ofloxacin, 8 (11.1 %); and streptomycin, 30 (44.1 %). All the twenty (20) isolates subjected to molecular characterization possessed penicillin binding protein2a (PBP2a) while only one possessed the mecA gene.
Conclusion: The MRSA is present among healthy individuals in Abraka, Delta State. It is also possible not to detect the existence of the mecA gene even when penicillin binding protein2a is present. Since most of the MRSA isolates are multi-drug resistant, there is a tendency for clinical antibiotic therapy failure in this area.

Keywords: Abraka, Resistance, Staphylococcus aureus, Antibiotic therapy failurre, MRSA, MecA

Impact Factor
Thompson Reuters (ISI): 0.523 (2021)
H-5 index (Google Scholar): 39 (2021)

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