Official Journal Health Science of Prince of Songkla University

  • Home
  • Search
  • Current
  • Archives
  • Announcements
  • Guide for Authors
  • Publication Ethics
  • Editorial Board
  • Submit
  • About
  • Contact
  • Online-first Articles
  • EVENTS
  • Review Process
Home > Online-first > Alam

Detection of Heterogeneous Vancomycin Intermediate Resistance in Methicillin- Resistant Staphylococcus Aureus Clinical Isolates

Shane Alam, Umar Farooq

Abstract

Objective: To detect methicillin-resistant Staphylococcus aureus (MRSA) using the cefoxitin disk diffusion method. The study also determined the minimum inhibitory concentration (MIC) of vancomycin through the broth microdilution (BMD) method and categorized it into vancomycin sensitive-MRSA (VS-MRSA), vancomycin intermediate-MRSA (VI-MRSA), and vancomycin resistance-MRSA (VR-MRSA). All the VS-MRSA strains were screened for heterogeneous vancomycin intermediate-MRSA (hV-MRSA).
Material and Methods: In this cross-sectional study, 210 MRSA strains were isolated from the different types of clinical specimens. Vancomycin susceptibility in MRSA isolates was investigated by determining the MIC using the BMD method. We used brain heart infusion screen agar with 4 µg/ml of vancomycin (BHIV4) to screen VS-MRSA strains for hV-MRSA and performed the modified population analysis profile area under the curve (PAP-AUC) method to confirm hV-MRSA.
Results: On the basis of MIC determination of vancomycin, out of the 210 MRSA strains, we found 202 VS-MRSA, 7 VI-MRSA, and 1 VR-MRSA. BHIV4 applied and screened 202 VS-MRSA isolates, and these were confirmed with the PAP-AUC method, which revealed 34 hV-MRSA.
Conclusion: All MRSA strains identified from the different clinical samples had a prevalence of hV-MRSA, 16.83%. Most of the hV-MRSA detected from the VS-MRSA strains showing the MIC of vancomycin on the borderline (2 µg/ml) indicate that the hV-MRSA is a prior stage of development of VI-MRSA.

 Keywords

Heterogeneous vancomycin-intermediate Staphylococcus aureus; Methicillin-resistant Staphylococcus aureus; Vancomycin-intermediate Staphylococcus aureus; Vancomycin-resistant Staphylococcus aureus; Vancomycin- susceptible Staphylococcus aureus

 Full Text:

PDF

References

Sreejisha M, Mulki SS, Shenoy S, Dhanashree B, Chakrapani M, Bhat G. Heterogeneous vancomycin intermediate Staphylococcus aureus infections in diabetic and non-diabetic patients–A hospital-based comparative study. Infect Drug Resist 2023;16:9.

Liu A, Garrett S, Hong W, Zhang J. Staphylococcus aureus infections and human intestinal microbiota. Pathog 2024;13:276.

Conly JM, Johnston BL. The emergence of methicillin-resistant Staphylococcus aureus as a community-acquired pathogen in Canada. Can J Infect Dis 2003;14:249.

Lohan K, Sangwan J, Mane P, Lathwal S. Prevalence pattern of MRSA from a rural medical college of North India: a cause of concern. J Family Med Prim Care 2021;10:752-7.

Liang J, Hu Y, Fu M, Li N, Wang F, Yu X, et al. Resistance and molecular characteristics of methicillin-resistant Staphylococcus aureus and heterogeneous vancomycin-intermediate Staphylococcus aureus. Infect Drug Resist 2023;31:379-88.

Hiramatsu K, Kayayama Y, Matsuo M, Aiba Y, Saito M, Hishinuma T, et al. Vancomycin-intermediate resistance in Staphylococcus aureus. J Glob Antimicrob Resist 2014;2:213-24.

CLSI. Performance standards for antimicrobial susceptibility testing: 34th informational supplement M100, antimicrobial testing standards M02, M07, and M11. Wayne (PA): Clinical and Laboratory Standards Institute; 2024.

Pardo L, Mota MI, Parnizari A, Varela A, Algorta G, Varela G. Detection of vancomycin resistance among methicillin-resistant Staphylococcus aureus strains recovered from children with invasive diseases in a reference pediatric hospital. Antibiotics 2024;13:298.

National Centre for Disease Control (India). Standard operating procedure for antimicrobial resistance surveillance: National AMR Surveillance Network (NARS-Net) [monograph on the Internet]. New Delhi: National Programme on Antimicrobial Resistance Containment, National Centre for Disease Control; 2023. Avaliable from: chrome-extension://efaidnbmnnnibpcajpcglclefindmkaj/https://ncdc.mohfw.gov.in/wp-content/uploads/2024/03/58495493521681880873.pdf

Satola SW, Farley MM, Anderson KF, Patel JB. Comparison of detection methods for heteroresistant vancomycin-intermediate Staphylococcus aureus, with the population analysis profile method as the reference method. J Clin Microbiol 2011;49:177-83.

Wootton M, Howe RA, Hillman R, Walsh TR, Bennett PM, MacGowan AP. A modified population analysis profile (PAP) method to detect hetero-resistance to vancomycin in Staphylococcus aureus in a UK hospital. J Antimicrob Chemother 2001;47:399-403.

Tawfeek CE, Khattab S, Elmaraghy N, Heiba AA, Nageeb WM. Reduced vancomycin susceptibility in Staphylococcus aureus clinical isolates: a spectrum of less investigated uncertainties. BMC Infect Dis 2024;24:1-10.

Havaei SA, Azimian A, Fazeli H, Naderi M, Ghazvini K, Samiee SM, et al. Genetic characterization of methicillin resistant and sensitive, vancomycin intermediate Staphylococcus aureus strains isolated from different Iranian Hospitals. Int Sch Res Notices 2012;2012:215275.

Khara RR, Lakhani SJ, Vasava S, Shah K, Panjwani D. Methicillin resistant Staphylococcus aureus (MRSA) and vancomycin resistant Staphylococcus aureus (VRSA) from a rural based tertiary care and teaching hospital in Vadodara district, Gujarat. IAIM 2016;3:187-95.

Raina D, Sakeena IC, Roy R. Detection of vancomycin susceptibility among methicillin resistant Staphylococcus aureus in a tertiary care hospital. Blood 2023;2:6-9.

Kaur K, Gill AK, Kaur M. Methicillin resistance, vancomycin intermediate and vancomycin resistance Staphylococcus aureus prevalence in a tertiary care hospital of Punjab, India. Blood 2019;21:12-9.

Mandal M, Dey S, Kumar D, Biswas PP, Nandan K, Sen A. Determination of vancomycin and linezolid resistance in Staphylococcus aureus isolated from Katihar district of Bihar, India. J Evol Med Dent Sci 2017;6:1244-7.

Sapkota J, Sharma M, Jha B, Bhatt CP. Prevalence of Staphylococcus aureus isolated from clinical samples in a tertiary care hospital: a descriptive cross-sectional study. J Nepal Med Assoc 2019;57:398.

Bhatt MP, Bhalla GS, Tandel K, Jindamwar P, Chaudhari CN, Grover N, et al. Antimicrobial susceptibility profile of methicillin-resistant Staphylococcus aureus at a tertiary care centre. Arch Clin Microbiol 2015;6:1-5.

Amberpet R, Sistla S, Sugumar M, Nagasundaram N, Manoharan M, Parija SC. Detection of heterogeneous vancomycin-intermediate Staphylococcus aureus: a preliminary report from south India. Indian J Med Res 2019;150:194-8.

Singh A, Prasad KN, Misra R, Rahman M, Singh SK, Rai RP, et al. Increasing trend of heterogeneous vancomycin intermediate Staphylococcus aureus in a tertiary care center of Northern India. Microb Drug Resist 2015;21:545-50.

Chaudhari CN, Tandel K, Grover N, Sen S, Bhatt MP, Sahni AK, et al. Heterogeneous vancomycin-intermediate among methicillin resistant Staphylococcus aureus. Med J Armed Forces India 2015;71:15-8.

Campanile F, Borbone S, Perez M, Bongiorno D, Cafiso V, Bertuccio T, et al. Heteroresistance to glycopeptides in Italian meticillin-resistant Staphylococcus aureus (MRSA) isolates. Int J antimicrob agents 2010;36:415-9.

Howden BP, Ward PB, Charles PG, Korman TM, Fuller A, Du Cros P, et al. Treatment outcomes for serious infections caused by methicillin-resistant Staphylococcus aureus with reduced vancomycin susceptibility. Clin Infect Dis 2004;38:521-8.

Huang SH, Chen YC, Chuang YC, Chiu SK, Fung CP, Lu PL, et al. Prevalence of vancomycin-intermediate Staphylococcus aureus (VISA) and heterogeneous VISA among methicillin-resistant S. aureus with high vancomycin minimal inhibitory concentrations in Taiwan: a multicenter surveillance study, 2012–2013. J Microbiol Immunol Infect 2016;49:701-7.

Song KH, Kim M, Kim CJ, Cho JE, Choi YJ, Park JS, et al. Impact of vancomycin MIC on treatment outcomes in invasive Staphylococcus aureus infections. Antimicrob Agents Chemother 2017;61:e01845-16.

Kejela T, Dekosa F. High prevalence of MRSA and VRSA among inpatients of Mettu Karl referral hospital, southwest Ethiopia. Trop Med Int Health 2022;27:735-41.

DOI: http://dx.doi.org/10.31584/jhsmr.20251263

Refbacks

  • There are currently no refbacks.
Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

SUBMIT A PAPER

JHSMR accepts online submission through

AHR-iCON 2025

Journal Metrics


2020
Acceptance rate: 52%
2021
Acceptance rate: 27.8%
2022 (March)
Acceptance rate: 15.6%
2023 (June)
Acceptance rate: 23.6%
2024 (June)
Acceptance rate: 19%


Submission to final decision
74 days

Acceptance to publication
40 days

0.6
2024CiteScore
 
 
31st percentile
Powered by Scopus
About The Authors

Shane Alam
Research Scholar, Department of Microbiology, Teerthanker Mahaveer Medical College and Research Centre, Teerthanker Mahaveer University, Moradabad (U.P.) 244001,
India

Umar Farooq
Professor and Head, Department of Microbiology, Teerthanker Mahaveer Medical College and Research Centre, Teerthanker Mahaveer University, Moradabad (U.P.) 244001,
India

Article Tools
Abstract
Print this article
Indexing metadata
How to cite item
Email this article (Login required)
Email the author (Login required)

Supported by

 

JHSMR now Indexed in



Scopus logo.svg






Image result for crossref





PSUMJ Homepage

Keywords COVID-19 SARS-CoV-2 Thailand Vietnam children computed tomography cross-cultural adaptation depression diabetes diabetes mellitus elderly hypertension knowledge mental health mortality prevalence quality of life reliability risk factors treatment validity
Journal Content

Browse
  • By Issue
  • By Author
  • By Title
Font Size

Open Journal Systems