NARA Discovery
Article Details
← Back to Search Results
Journal Article

Molecular detection of mecA gene from methicillin-resistant Staphylococcus aureus isolated from clinical and environmental samples and its potential inhibition by phytochemicals using in vitro and in silico approach

Mohammed M. Mohammed; Mustafa Alhaji Isa; Mustapha B. Abubakar; Abubakar Sadiq Baba Dikwa; Abidemi Paul Kappo
In Silico Pharmacology · Vol. 13, Issue 1 · 2025

Abstract

The increasing prevalence of Methicillin-resistant Staphylococcus aureus (MRSA) has posed significant challenges in clinical and environmental settings. MRSA's resistance is attributed to the mecA gene, which encodes the penicillin-binding protein 2a (PBP2a), conferring resistance to β-lactam antibiotics. This study aimed to molecularly detect the mecA gene in MRSA isolates from clinical and environmental samples and identify potential inhibitors of PBP2a using in vitro and in silico approaches. A total of 180 samples were collected, isolating 64 Staphylococcus aureus strains, of which 10 (37%) were confirmed as MRSA. Molecular detection confirmed the presence of the mecA gene in these isolates. Phytochemical analysis of Acacia nilotica and Mangifera indica extracts revealed bioactive compounds with antimicrobial properties. In vitro antimicrobial testing showed the plant extracts demonstrated significant inhibitory effects against MRSA, with minimum inhibitory concentrations (MIC) ranging from 0 to 6.20 mg/mL. Molecular docking and molecular dynamics simulation analyses identified three compounds (CID_628694, CID_546930, and CID_620007) with strong binding affinities and stable interactions with PBP2a, suggesting their potential as novel inhibitors. These findings highlight the therapeutic potential of phytochemicals in combating MRSA and provide a basis for future experimental validations.

Bibliographic Information

JournalIn Silico Pharmacology
PublisherSpringer
Publication Date2025-02-10
Publication Year2025
Volume13
Issue1
Document TypeJournal Article
eISSN2193-9616
DOI10.1007/s40203-024-00297-y

Access Information

NARA Access Coverage2013-01-01~Current
Journal Homepagehttps://www.springer.com/journal/40203
Publisher PageOpen Publisher Page
Full-text access depends on NARA's subscribed coverage and institutional access.