Evidence map›Paper›PMID 39528974›Full record

ArticleBMC infectious diseases2024

Coexistence of the blaZ gene and selected virulence determinants in multidrug-resistant Staphylococcus aureus: insights from three Nigerian tertiary hospitals.

Adetunji Misbau Kilani, Emmanuel Dayo Alabi, Oluwafemi Ezekiel Adeleke

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Article in BMC infectious diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Article
  2. Study on the Mechanism of Berberine Reversing MRSA Resistance to β-Lactam Antibiotics by Inhibiting blaZ Expression.International microbiology : the official journal of the Spanish Society for Microbiology · 2026
    Article
  3. Study on the Mechanism of Berberine Reversing MRSA Resistance to β-Lactam Antibiotics by Inhibiting blaZ Expression.International microbiology : the official journal of the Spanish Society for Microbiology · 2026
    Article
  4. Review
  5. Article
  6. Emergence of a methicillin-susceptibleFrontiers in cellular and infection microbiology · 2026
    Article
  7. Article
4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Adetunji Misbau KilaniDepartment of Microbiology, Federal University Dutsin-Ma, Dutsin-Ma, Katsina State, Nigeria.
Emmanuel Dayo AlabiDepartment of Microbiology, Federal University Dutsin-Ma, Dutsin-Ma, Katsina State, Nigeria. edayoalabi@gmail.com.ORCID https://orcid.org/0009-0003-0968-3143
Oluwafemi Ezekiel AdelekeDepartment of Pharmaceutical Microbiology, University of Ibadan, Ibadan, Oyo State, Nigeria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeInfections caused by β-lactamase-producing strains of Staphylococcus aureus have become increasingly difficult to treat due to the expression of multiple virulence factors. This has heightened concerns about managing S. aureus-related infections. This study was conducted to characterize the blaZ gene and selected virulence determinants in β-lactam resistant S. aureus from human sources in three Nigerian tertiary hospitals. MATERIALS AND

methodsThree hundred and sixty samples were collected for the study. S. aureus was isolated and characterized following standard microbiological protocols and nuc gene amplification. Antibiotic susceptibility and minimum inhibitory concentration tests were performed using the disk diffusion method and E-tests, respectively. Biofilm formation and β-lactamase production were assessed using Congo red agar and nitrocefin kits, while the blaZ gene was examined using conventional PCR. Capsular polysaccharide genotyping, accessory gene regulator (agr) detection, Panton-valentine leucocidin (PVL), and PVL proteins were performed using PCR and Western blotting.

resultsS. aureus was recovered from 145 samples, 50 (34.5%) of these isolates exhibited multidrug resistance, with MICs ranging from 0.125 to 1.00 µg/mL, and showed significant resistance to aminoglycosides, fluoroquinolones, and β-lactams. Of these, 31 strains produced β-lactamases, 30 of which carried the blaZ gene in combination with cap8 (80%) or cap5 (20%). Biofilm formation and PVL gene were observed in 85% of the 20 randomly selected blaZ-positive multidrug-resistant (MDR) strains. The agr2 allele was predominant, found in 70% of the selected MDR strains. No significant difference in the occurrence of the blaZ gene was found among the three clinical sources (p ≤ α0.05).

conclusionThe co-occurrence of the blaZ gene with PVL, capsular polysaccharide genes, and agr alleles is associated with biofilm formation, indicating a high risk of β-lactam-resistant S. aureus infections. Our findings highlight the need for continuous molecular surveillance to enhance infection management, treatment options, and patient outcomes in the study locality. A limitation of this study is the random selection of MDR isolates, which may affect the comprehensiveness of the analyses.

Indexed as

Anti-Bacterial AgentsBacterial Proteinsbeta-LactamasesBiofilmsDrug Resistance, Multiple, BacterialMicrobial Sensitivity TestsStaphylococcal InfectionsStaphylococcus aureusTertiary Care CentersVirulence FactorsAdolescentAdultAgedBacterial ToxinsChildExotoxinsAnti-Bacterial AgentsBacterial ProteinsBacterial Toxinsbeta-LactamasesExotoxinsLeukocidinsPanton-Valentine leukocidinVirulence FactorsBiofilmMultidrug-resistant Staphylococcus aureusPenicillinaseVirulence determinantsΒ-lactamase

Identifiers

PMID39528974
PMCPMC11552187

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.