Distribution of MecA and Erm Genes among Methicillin-resistant Staphylococcus Aureus with Inducible Resistance to Clindamycin.


Journal

Journal of Nepal Health Research Council
ISSN: 1999-6217
Titre abrégé: J Nepal Health Res Counc
Pays: Nepal
ID NLM: 101292936

Informations de publication

Date de publication:
08 Sep 2023
Historique:
received: 01 07 2022
accepted: 08 09 2023
medline: 25 9 2023
pubmed: 24 9 2023
entrez: 24 9 2023
Statut: epublish

Résumé

The emergence of Methicillin-resistant Staphylococcus aureus and its ability to confer cross-resistance to macrolide-lincosamide-streptogramin B has complicated the treatment against it. Gene-based studies among phenotypic methicillin-resistant isolates with inducible resistance to clindamycin are less available in Nepal. This work was undertaken to detect the mecA and erm genes among such phenotypes isolated from clinical samples. S. aureus isolated from different clinical samples was identified by standard microbiological procedures (Gram-staining, colony morphology, and different biochemical tests). Methicillin-resistant and inducible resistant to clindamycin phenotypes were detected by using cefoxitin disc (30 µg) and a double disk diffusion test according to the Clinical and Laboratory Standards Institute guidelines and mecA and erm genes were detected by polymerase chain reaction. Among 120 S. aureus isolates, 51.67% (n=62) were MRSA, and the prevalence of inducibly-resistant, constitutively-resistant and Macrolide-Streptogramin phenotypes were 15.83% (n=19), 28.33% (n=34) and 15.83% (n=19) respectively. While 35.84% (n=43) of isolates showed sensitivity to both antibiotics, erythromycin and clindamycin. Out of 14 inducibly-resistant phenotypes, 57.14% (n=8) were found carrying ermC and 28.57% (n=4) phenotypes contained both ermA and ermC. All phenotypes were positive for the mecA gene. Macrolides-Lincosamide-Streptogramin B resistance was predominant among methicillin-resistant S. aureus. While all isolates with inducible clindamycin resistance harbored mecA gene, most of them also harbored ermC gene. The higher prevalence of inducible-resistant to clindamycin indicated the need for rational use of antimicrobial agents.

Sections du résumé

BACKGROUND BACKGROUND
The emergence of Methicillin-resistant Staphylococcus aureus and its ability to confer cross-resistance to macrolide-lincosamide-streptogramin B has complicated the treatment against it. Gene-based studies among phenotypic methicillin-resistant isolates with inducible resistance to clindamycin are less available in Nepal. This work was undertaken to detect the mecA and erm genes among such phenotypes isolated from clinical samples.
METHODS METHODS
S. aureus isolated from different clinical samples was identified by standard microbiological procedures (Gram-staining, colony morphology, and different biochemical tests). Methicillin-resistant and inducible resistant to clindamycin phenotypes were detected by using cefoxitin disc (30 µg) and a double disk diffusion test according to the Clinical and Laboratory Standards Institute guidelines and mecA and erm genes were detected by polymerase chain reaction.
RESULTS RESULTS
Among 120 S. aureus isolates, 51.67% (n=62) were MRSA, and the prevalence of inducibly-resistant, constitutively-resistant and Macrolide-Streptogramin phenotypes were 15.83% (n=19), 28.33% (n=34) and 15.83% (n=19) respectively. While 35.84% (n=43) of isolates showed sensitivity to both antibiotics, erythromycin and clindamycin. Out of 14 inducibly-resistant phenotypes, 57.14% (n=8) were found carrying ermC and 28.57% (n=4) phenotypes contained both ermA and ermC. All phenotypes were positive for the mecA gene.
CONCLUSIONS CONCLUSIONS
Macrolides-Lincosamide-Streptogramin B resistance was predominant among methicillin-resistant S. aureus. While all isolates with inducible clindamycin resistance harbored mecA gene, most of them also harbored ermC gene. The higher prevalence of inducible-resistant to clindamycin indicated the need for rational use of antimicrobial agents.

Identifiants

pubmed: 37742145
doi: 10.33314/jnhrc.v21i1.4337
doi:

Substances chimiques

Clindamycin 3U02EL437C
Streptogramin B 3131-03-1
Anti-Bacterial Agents 0
Lincosamides 0
Macrolides 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

29-33

Auteurs

Dudha Raj Malla Thakuri (DR)

Department of Microbiology, National College,Tribhuvan University, Kathmandu, Nepal.

Anil Pokhrel (A)

Central Department of Microbiology, Tribhuvan University, Kathmandu, Nepal.

Ritu Amatya (R)

Department of Microbiology, OM hospital and Research Centre, Kathmandu, Nepal.

Narayan Sharma Bashyal (N)

Central Department of Microbiology, Tribhuvan University, Kathmandu, Nepal.

Mary Neupane (M)

Department of Microbiology, National College,Tribhuvan University.

Sudeep Kc (S)

Central Department of Microbiology, Tribhuvan University, Kathmandu, Nepal.

Dev Raj Joshi (DR)

Central Department of Microbiology, Tribhuvan University, Kathmandu, Nepal.

Santosh Khanal (S)

Department of Microbiology, National College,Tribhuvan University, Kathmandu, Nepal.

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Classifications MeSH