N J L M

 
Subscribe Via RSS
  • Home
  • About
    Salient Features Bibliographic Information Abstracting and Indexing Specialties Covered Publisher Journal Policy
  • Issues
    Current Issue Online Ahead of Print Archive Forthcoming issue
  • Editorial
    Editorial Statements Editorial-PeerReview Process Editorial Board Publication Ethics & Malpractice Join us
  • Authors
    Submit an Article Manuscript Instructions Manuscript Assistance Publication Charges Paid Services Early Online Publication Service
  • Reviewers
    Apply as Reviewer Reviewers Acknowledgment
  • Search
    Simple Search Advanced Search
  • Member
    Register Login
  • Contact
  • Subscription
Original article / research
Year : 2025 Month : April Volume : 14 Issue : 2 Page : MO01 - MO05 Full Version

Prevalence of Staphylococcus aureus Isolated from Clinical Samples that Exhibits Inducible Clindamycin Resistance: A Cross-sectional Study


Akansha Goyal, Akansha Arya, Kajal Rajput, Sapna Chauhan
1. Assistant Professor, Department of Microbiology, Muzaffarnagar Medical College, Muzaffarnagar, Uttar Pradesh, India. 2. Postgraduate Student, Department of Microbiology, Muzaffarnagar Medical College, Muzaffarnagar, Uttar Pradesh, India. 3. Postgraduate Student, Department of Microbiology, Muzaffarnagar Medical College, Muzaffarnagar, Uttar Pradesh, India. 4. Professor and Head, Department of Microbiology, Muzaffarnagar Medical College, Muzaffarnagar, Uttar Pradesh, India.
 
Correspondence Address :
Dr. Sapna Chauhan,
Professor and Head, Department of Microbiology, Muzaffarnagar Medical College, Opp. Begrajpur Industrial Area, Muzaffarnagar-251001, Uttar Pradesh, India.
E-mail: connect.akansha@gmail.com; drsapnachauhan@gmail.com
 
ABSTRACT
: Introduction: The resistance to Macrolide-Lincosamide-Streptogramin B (MLSB) in Staphylococcus aureus is often caused by erm genes, which can either be constitutive MLSB (cMLSB) or inducible MLSB (iMLSB). Clindamycin (CLI), a lincosamide, and erythromycin (ERY), a macrolide, both act by binding to the 50S ribosomal subunits of bacterial cells, inhibiting protein synthesis. Methylation of the ribosomal target site in iMLSB-resistant isolates displays resistance to ERY but allows susceptibility to CLI. iMLSB resistance emerges when a strong inducer of the methylase enzyme, such as ERY, is present. Identifying iMLSB resistance is crucial for effectively managing S. aureus.

Aim: To detect the prevalence of inducible CLI resistance in S. aureus isolates from various clinical samples and to determine the association between methicillin resistance and inducible CLI resistance in S. aureus isolates.

Materials and Methods: The study was a cross-sectional study conducted at Muzaffarnagar Medical College and Hospital, Muzaffarnagar, Uttar Pradesh, India over a period of six months, from January 2024 to June 2024. A total of 100 isolates of S. aureus obtained from various clinical samples were included. Simple random sampling was employed to ensure an unbiased selection of isolates. Only culture-confirmed S. aureus isolates were considered, while duplicate isolates and samples showing polymicrobial growth were excluded from the study. The sample population comprised individuals of varying ages and genders who sought treatment at the hospital during the study period due to symptoms indicating potential infections. The S. aureus isolates were initially identified using standard biochemical techniques and were then tested for susceptibility using the modified Kirby-Bauer disc diffusion method on Mueller-Hinton agar plates, following Clinical and Laboratory Standards Institute (CLSI) guidelines. The CLSI guidelines were also followed to test for inducible resistance to CLI using the ‘D test’ method. Data were entered and analysed using the Statistical Package for the Social Sciences (SPSS) software, version 24.0, with statistical significance considered at a p-value <0.05.

Results: Routine disc diffusion testing was employed to examine antibiotic susceptibility in 100 S. aureus strains, revealing that 44 (44%) displayed resistance to ERY. Out of the 100 strains, 22 (22%) showed iMLSB resistance, 27 (27%) were cMLSB-positive, and 15 (15%) had the Macrolide-Streptogramin B (MS) phenotype. In this study, it was discovered that 18 (82%) of the S. aureus isolates that were positive for the D test were Methicillin-Resistant S. aureus (MRSA), while 4 (18%) were sensitive to cefoxitin (MSSA).

Conclusion: This study revealed a substantial prevalence of inducible CLI resistance among S. aureus isolates, with a pronounced association in MRSA strains. The strong correlation between methicillin and iMLSB resistance underscores the critical need for routine D-test screening to guide precise antimicrobial therapy, mitigate treatment failures and support effective antimicrobial stewardship practices.
Keywords : D-test, Methylation, Methicillin resistant Staphylococcus aureus
DOI and Others : DOI: 10.7860/NJLM/2025/77170.2911 Date of Submission: Dec 06, 2024 Date of Peer Review: Feb 17, 2025 Date of Acceptance: Mar 26, 2025 Date of Publishing: Apr 01, 2025 AUTHOR DECLARATION: • Financial or Other Competing Interests: None • Was Ethics Committee Approval obtained for this study? Yes • Was informed consent obtained from the subjects involved in the study? Yes • For any images presented appropriate consent has been obtained from the subjects. NA PLAGIARISM CHECKING METHODS: • Plagiarism X-checker: Dec 06, 2024 • Manual Googling: Mar 22, 2025 • iThenticate Software: Mar 24, 2025 (15%) ETYMOLOGY: Author Origin EMENDATIONS: 7
 
TABLES AND FIGURES
 
  • In This Article

    • Abstract
    • Material and Methods
    • Results
    • Discussion
    • Conclusion
    • Acknowledgement
    • References
  • Article Utilities

    • Readers Comments
    • Article in PDF
    • Citation Manager
    • How to Cite
    • Article Statistics
    • Print this Article
    • Send to a Friend
  • Go To Issues

    • Current Issue
    • Past Issues
  • Search Articles

    • Simple Search
    • Advance Search
  • Authors Facilities

    • Extensive Author Support
    • Submit Manuscript
    • ONLINE First Facility
    • NJLM Pre Publishing
  • Quick Links

    • REVIEWER
    • ACCESS STATISTICS
  • Users

    • Register
    • Log in
  • Pages

    • About
    • Issues
    • Editorials
    • Authors
    • Reviewers
    • Search
    • Contacts
  • Issues Archives

  • Affiliated Websites

    • JCDR Prepublishing
    • Neonatal Database Home
    • JCDR Neonatal Database download center