Evidence map›Paper›PMID 39382498›Full record

ArticleThe Indian journal of medical research2024

Presence of multiple van genes among glycopeptide non-susceptible Staphylococcus aureus exhibiting in vitro MIC creep phenomenon: A study from north-east India.

Monalisha Hazarika, Kathakali Nath, Deepshikha Bhowmik, K Melson Singha, Debadatta Dhar, Amitabha Bhattacharjee

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Article in The Indian journal of medical research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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6 authors.

Monalisha HazarikaDepartment of Microbiology, Assam University, Assam, India.
Kathakali NathDepartment of Microbiology, Assam University, Assam, India.
Deepshikha BhowmikDepartment of Microbiology, Assam University, Assam, India.
K Melson SinghaDepartment of Microbiology, Silchar Medical College and Hospital, Assam, India.
Debadatta DharDepartment of Microbiology, Silchar Medical College and Hospital, Assam, India.
Amitabha BhattacharjeeDepartment of Microbiology, Assam University, Assam, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background & objectives The global prevalence of vancomycin-resistant Staphylococcus aureus (VRSA) has increased two fold since 2010, accounting for 2.4 per cent of S. aureus infections. The emerging hVISA isolates and their increasing trends pose a serious therapeutic challenge. The present study investigated in vitro vancomycin and teicoplanin minimum inhibitory concentration (MIC) creep in S. aureus and assessed their revertants. Methods A total of 845 isolates were collected for this study, and 246 were confirmed as S. aureus. Molecular characterization of vancomycin resistance was carried out by PCR assay targeting genes types viz: vanA, vanB, vanC, vanC2/C3, vanD, vanE, and vanG. MIC was determined for vancomycin and teicoplanin by agar dilution method. MIC creep and revertant analysis were done by broth dilution method in the presence and absence of antibiotics. Results PCR assay confirmed 12 isolates were harboured vanA, followed by vanD (n=8) and vanB (n=7). The study showed 69 isolates were screened positive for glycopeptide non-susceptibility. While analyzing vancomycin MIC creep, four isolates showed a significant increase in MIC, whereas no creep phenomenon was observed for the rest. In the case of teicoplanin, seven isolates showed the MIC creep phenomenon. Revertant analysis of all the isolates that showed MIC creep phenomenon for vancomycin and teicoplanin reverted to their original MIC when the antibiotic pressure was withdrawn. Interpretation & conclusions In the present study setting, glycopeptide non-susceptibility was found in eight per cent of the isolates, and the present study found the occurrence of multiple van genes from isolates calculated from a single study center will impose a serious challenge in infection control and antibiotic policy. This study also underscores that heterogenic resistant isolates, upon exposure to vancomycin and teicoplanin at a minimum level, exhibited an increase in MIC, which will impact individuals receiving glycopeptide therapy.

Indexed as

Bacterial ProteinsMicrobial Sensitivity TestsStaphylococcal InfectionsTeicoplaninVancomycinAnti-Bacterial AgentsCarbon-Oxygen LigasesGlycopeptidesHumansIndiaStaphylococcus aureusVancomycin ResistanceVancomycin-Resistant Staphylococcus aureusAnti-Bacterial AgentsBacterial ProteinsCarbon-Oxygen LigasesGlycopeptidesTeicoplaninVancomycinMIC creepteicoplaninvancomycinVancomycin-resistant Staphylococcus aureus (VRSA)van gene

Identifiers

PMID39382498
PMCPMC11463864

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