# Molecular Characterization of Cefoxitin-Resistant Coagulase-Negative Staphylococci From Frequently Touched Surfaces of Hospital and Urban-Built Environments of Central India

**Authors:** Anushri Keshri, Dilip Govardhan Gore, Indu Singh, Divakar Sharma, Varaprasad Kolla

PMC · DOI: 10.1155/cjid/5766823 · The Canadian Journal of Infectious Diseases & Medical Microbiology = Journal Canadien des Maladies Infectieuses et de la Microbiologie Médicale · 2025-02-05

## TL;DR

This study identifies antibiotic-resistant staphylococci on hospital and urban surfaces in India, highlighting the need for surveillance to control infections.

## Contribution

The study provides molecular characterization of cefoxitin-resistant CoNS isolates and identifies genetic polymorphisms in the mecA gene.

## Key findings

- 19 cefoxitin-resistant CoNS isolates were identified from 200 samples.
- Only 47.36% of mecA-positive isolates showed resistance to vancomycin.
- SNP analysis revealed 80 polymorphic sites in the mecA gene sequences.

## Abstract

Coagulase-negative staphylococci (CoNS) are the major pathogen (hospital as well as environmental) and their emerging multidrug-resistant (MDR) strains complicate the treatment process. In this study, we investigated the prevalence and antibiotic resistance of CoNS on frequently touched surfaces in hospital and urban built environments (UBEs) in Vidarbha, Maharashtra, India. A total of 200 isolates screened for Staphylococcus species and 55 methicillin-resistant staphylococci isolates were identified, and among them, 19 were classified as cefoxitin-resistant CoNS. These 19 cefoxitin-resistant CoNS isolates were tested for the presence of the mecA gene by conventional PCR and only nine (47.36%) were found to be mecA-positive. mecA-positive strains were tested to check MIC for various antibiotics and three marker gene characteristics, namely, ß-lactamase, cefoxitin screen, and inducible clindamycin resistance via the VITEK 2 system. These strains were 100% resistant to benzylpenicillin and oxacillin, and approximately 50% were resistant to vancomycin. Amplified mecA gene fragments were sequenced, and SNP analysis was performed alongside a standard sequence from Staphylococcus aureus (Acc no. NG_047938.1). In total, among the 466 nucleotides, 386 sequences were found to be invariable, and 80 polymorphic variables were identified (46 singleton variable sites and 34 parsimony information sites). The spread of antibiotic resistance is very common in both UBEs and hospital environments; thus, our study concluded that a surveillance program is recommended for the Vidarbha region for the assessment of co-occurring CoNS and better infection control of the environment for future reduction in contact infection.

## Linked entities

- **Genes:** mecA (adaptor protein controlling oligomerization of the AAA+ protein ClpC) [NCBI Gene 936406]
- **Chemicals:** cefoxitin (PubChem CID 441199), benzylpenicillin (PubChem CID 5904), oxacillin (PubChem CID 6196), vancomycin (PubChem CID 14969)
- **Species:** Staphylococcus (taxon 1279)

## Full-text entities

- **Diseases:** CoNS (MESH:D064726), contact infection (MESH:D007239)
- **Chemicals:** oxacillin (MESH:D010068), methicillin (MESH:D008712), vancomycin (MESH:D014640), Cefoxitin (MESH:D002440), clindamycin (MESH:D002981), benzylpenicillin (MESH:D010400)
- **Species:** Staphylococcus aureus (species) [taxon 1280]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11824842/full.md

## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC11824842/full.md

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Source: https://tomesphere.com/paper/PMC11824842