TO STUDY THE PREVALENCE OF MRSA AND ITS ANTIMICROBIAL SUSCEPTIBILITY PATTERN AMONG STAPHYLOCOCCUS AUREUS ISOLATED FROM VARIOUS CLINICAL SAMPLES

Main Article Content

Dr. Raees Ahmed
Dr. Anita E.Chand
Dr. Nashra Afaq

Keywords

MRSA, Disc Diffusion, CLSI, Prevalence, AST

Abstract

Introduction: Methicillin-resistant Staphylococcus aureus (MRSA) is a common nosocomial infection that causes severe morbidity and mortality. MRSA (methicillin-resistant S. aureus) is now endemic in India. In India, the prevalence of Methicillin-Resistant Staphylococcus aureus (MRSA) ranges between 30 to 70%, resulting in high mortality, increased economic burden, and treatment failure in tertiary care facilities. Rapid and consistent MRSA detection is crucial for infection control and preventing unnecessary antibiotic use.


Aim and Objective:This study aimed to find out the prevalence of MRSA and to assess antibiotic activity against methicillin-resistant Staphylococcus aureus in vitro.


Material and Methods: This was a Cross-sectional observational study carried out in the Department of Microbiology at Government Medical College, Kota, Rajasthanfor a period of three years, starting from September 7, 2019, to September 6, 2022. A total of 384 Staphylococcus aureus isolated from different clinical samples were analyzed.  MRSA isolates were screened and confirmed using standard methods recommended by the Clinical and Laboratory Standards Institute (CLSI). Methicillin resistance, in Staphylococcus aureus strains, was evaluated using cefoxitin. The Kirby-Bauer disc diffusion technique was used to assess the antibiotic susceptibility pattern of all MRSA strains. Antimicrobial susceptibility testing was performed using the Kirby-Bauer disk diffusion method according to the CLSI guidelines 2019.


Results:In the present study a total of 384 Staphylococcus aureus isolates were obtained from various clinical samples. The prevalence of MRSA was observed to be 48.1%. Among 384 S. aureus isolates, 70 (18.23%) belonged to (21-30) age group followed by 67 (17.45%)  and least was observed in the age group 15 (3.91%) from (0-10) age group. The ratio of males was more compared to the females 195 (50.7%), 189 (49%) respectively in case of S.aureus and for MRSA Male was observed to be 98 (52%), female 87 (47.2%) respectively. The maximum number of isolates were observed forpus followed by urine and least for pleural fluid.  It was also noted that Vancomycin was found to be the most sensitive with the sensitivity of 97.3%, followed by Linezolid 96.2% and then Teicoplanin 89.73 % was found to be the most effective drug of choice.


Conclusion: The prevalence of MRSA varies according to geographical region, hospital type, examined population, and detection technique. Effective antimicrobial activity as well as cost effectiveness should be considered in drugs prescribed for MRSA infections. Given the clinical implications of MRSA infection and its rapid transmission potential, MRSA strains must be evaluated on a frequent basis.

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References

1. Choo EJ. Community-associated methicillin-resistant staphylococcus aureus in nosocomial infections. Infect Chemother 2017;49:158–9. 10.
2. World Health Organization. Fact sheet antimicrobial resistance. 2018. Available: https://www.who.int/news-room/fact-sheets/detail/antimicrobial-resistance
3. O’Riordan W, McManus A, Teras J, et al.. A comparison of the efficacy and safety of intravenous followed by oral delafloxacin with vancomycin plus aztreonam for the treatment of acute bacterial skin and skin structure infections: A phase 3, multinational, double-blind, randomized study. Clin Infect Dis 2018;67:657–66.
4. Turner NA, Sharma-Kuinkel BK, Maskarinec SA, et al.. Methicillin-resistant staphylococcus aureus: an overview of basic and clinical research. Nat Rev Microbiol 2019;17:203–18.
5. Qiao Y, Liu X, Li B, et al.. Treatment of MRSA-infected osteomyelitis using bacterial capturing, magnetically targeted composites with microwave-assisted bacterial killing. Nat Commun 2020; 11:1–13.
6. Tiwari HK, Sapkota D, Sen MR. High prevalence of multidrug-resistant MRSA in a tertiary care hospital of northern india. Infect Drug Resist .2008;1:57–61.
7. Dadashi M, Nasiri MJ, Fallah F, et al.. Methicillin-resistant staphylococcus aureus (MRSA) in iran: a systematic review and meta-analysis. J Glob Antimicrob Resist 2018;12:96–103.
8. Álvarez A, Fernández L, Gutiérrez D, et al.. Methicillin-resistant staphylococcus aureus in hospitals: latest trends and treatments based on bacteriophages. J Clin Microbiol 2019;57:e01006-19.
9. Garoy EY, Gebreab YB, Achila OO, et al.. Methicillin-Resistant Staphylococcus aureus (MRSA): prevalence and antimicrobial sensitivity pattern among patients-a multicenter study in asmara, eritrea. Can J Infect Dis Med Microbiol 2019;2019:8321834.
10. Lee J, Austin JM, Kim J, Miralles PD, Kaafarani HMA, Pronovost PJ, Ghimire V, Berenholtz SM, Donelan K, Martinez E. Developing and Testing a Chart Abstraction Tool for ICU Quality Measurement. Am J Med Qual. 2019;34(4):324-330.
11. Sabbagh P, Riahi SM, Gamble HR, Rostami A. The global and regional prevalence, burden, and risk factors for methicillin-resistant Staphylococcus aureus colonization in HIV-infected people: A systematic review and meta-analysis. Am J Infect Control. 2019;47(3):323-333
12. Abdul H. Siddiqui et al. Methicillin-Resistant Staphylococcus aureus. StatPearls [Internet]. 2023
13. Abao Xing et al. The Prevalence, Epidemiological, and Molecular Characterization of Methicillin-Resistant Staphylococcus aureus (MRSA) in Macau (2017–2022). Microorganisms 2024; 12(1), 148.
14. Hasmukharay, K.; Ngoi, S.T.; Saedon, N.I.; Tan, K.M.; Khor, H.M.; Chin, A.V.; Tan, M.P.; Kamarulzaman, A.; Idris, N.B.; Niek, W.K. Evaluation of methicillin-resistant Staphylococcus aureus (MRSA) bacteremia: Epidemiology, clinical characteristics, and outcomes in the older patients in a tertiary teaching hospital in Malaysia. BMC Infect. Dis. 2023; 23, 241.
15. Clinical and Laboratory Standards Institute. Performance standards for antimicrobial susceptibility testing, 29th informational supplement (M100-S22). Wayne Pa: Clinical and Laboratory Standards Institute; 2019 Jan.
16. Assadullah S, Kakru DK, Thoker MA, Bhat FA, 6. Hussain N, Shah A. Emergence of low level vancomycin resistance in MRSA. Indian J Med Microbiol.2003; 21: 196-198.
17. Sonavane, A, Mathur, M. Screening for vancomycin 7. intermediate - resistant Staphylococcus aureus among clinical isolates of MRSA. Indian J Med Microbiol.2007; 25: 79-80.
18. Mehdinejad M, Sheikh AF, Jolodar A. Study of .methicillin resistance in Staphylococcus aureus and species of coagulase negative Staphylococci isolated from various clinical specimens. Pak J Med Sci.2008; 24: 719-24.
19. Idree. s F, Jabeen K, Khan MS and Zafar A. Antimicrobial resistance profile of methicillin resistant staphylococcal aureus from skin and soft tissue isolates. J Pak Med Assoc .2009; 59: 266-269.
20. Gadepalli R, Dhawan B, Kapil A, Sreenivas V, Jais M,Gaind R, et al. Clinical and molecular characteristics ofnosocomial methicillin-resistant Staphylococcus aureus skin and soft tissue isolates from three Indian hospitals. JHosp Infect. 2009; 73:253–63.
21. Gopalakrishnan R, Sureshkumar D. Changing trends in antimicrobial susceptibility and hospital acquired infections over an 8 year period in a tertiary care hospital in relation to introduction of an infection control programme. J Assoc Physicians India. 2010;58:25–31.
22. Vikas Manchanda et al. Methicillin resistant Staphylococcus aureus (MRSA) in India: Prevalence & susceptibility pattern. Indian J Med Res. 2013 ; 137(2): 363–369.
23. Maj Puneet Bhatt, Gurpreet Singh Bhalla, Kundan Tandel, Prashant Jindamwar, CN Chaudhari, Naveen Grover Ajay Kumar Sahni. Antimicrobial Susceptibility Profile of Methicillin-resistant Staphylococcus aureus at a Tertiary Care centre. Archives of clinicalmicrobiology. 2015; 6 : 3:6.
24. Kaur K, Gill AK, Kaur M. Methicillin resistance, vancomycin intermediate and vancomycin resistance Staphylococcus aureus prevalence in a tertiary care hospital of Punjab, India. National Journal of Laboratory Medicine, 2019; l-8(3): MO01-MO03.
25. Goyal A, Diwakar ML, Bhooshan S, Goyal S, Agrawal A. Prevalence and antimicrobial susceptibility pattern of methicillin-resistant Staphylococcus aureus [MRSA] isolates at a tertiary care hospital in Agra, North India – A systemic annual review. IOSR Journal of Dental and Medical Sciences (IOSR-JDMS). 2013; 11(6):80-4.
26. Mandal M, Dey S, Kumar D, Biswas PP, Nandan K and Sen A. Determination of vancomycin and linezolid resistance in staphylococcus aureus isolated from Katihar district of Bihar, India. J. Evolution Med. Dent. Sci. 2017 ;6(16):1244-1247.
27. Sarrafzadeh F, Mirzabiegi Z, Torabi-Nami M. Vancomycin-resistant Staphylococcus aureus isolates among hospitalized patients; a tertiary medical care center experience from Southern Iran. Cogent Medicine. 2016; 3(1):1163768.
28. Adhikari A, Kshetri B, Sharma KN, Khanal S, Panta OP, Sharma S et al. Prevalence of methicillin-resistant Staphylococcus aureus isolated from clinical samples at Narayani Samudayik Hospital, Chitwan, Nepal. TUJM. 2020; 7(1):37-42.
29. Joshi S, Ray P, Manchanda V, Bajaj J, Chitnis DS, Gautam V et al. Methicillin resistant Staphylococcus aureus (MRSA) in India: Prevalence & susceptibility pattern.Indian J Med Res. 2013; 137:363-9.
30. Maharjan M, Sah AK, Pyakurel S, Thapa S, Maharjan S, Adhikari N et al. Molecular confirmation of vancomycin-resistant Staphylococcus aureus with vanA Gene from a hospital in Kathmandu. International Journal of Microbiology, 2021; Article ID 3847347.
31. Kaleem F, Usman J, Sattar A, Amanat ST, Hassan A, Omair M et al. Current status of vancomycin susceptibility against methicillin resistant Staphylococcus aureus (MRSA) strains: A study at two tertiary care hospitals of Pakistan. African Journal of Microbiology Research. 2012; 6:6243-6.
32. Shilpa Arora. Prevalence of Methicillin-resistant Staphylococcus Aureus (MRSA) in a Tertiary Care Hospital in Northern India. J Lab Physicians. 2010 Jul-Dec; 2(2): 78–81.
33. Kandel SN, Adhikari N, Dhungel B. Characteristics of Staphylococcus aureus isolated from clinical specimens in a tertiary care hospital, Kathmandu, Nepal. Microbiology Insights, 2020; 13: Article ID 1178636120972695.
34. Nepal N, Mahara P, Subedi S, Rijal KR, Ghimire P, Banjara MR et al. Genotypically confirmed vancomycin-resistant Staphylococcus aureus with van B gene among clinical isolates in Kathmandu. Microbiology Insights. 2023; 16:1-9.
35. Osman MW, Osman MM, Mohamed NA, Osman SM, Magzoub M, El-Sanousi SM. Investigation on vancomycin resistance (VRSA) among methicillin resistant S. aureus (MRSA) in Khartoum State, Sudan. American Journal of Microbiological Research. 2016; 4(2):56-60.
36. Arora S, Devi P, Arora U, Devi B. Prevalence of methicillin resistanceStaphylococcus Aureus (MRSA) in a tertiary care hospital in Northern India. India J LabPhysician. 2010; 2(2):78-81.
37. Jayshree, Singh VK, Kumar A, Yadav SK. Prevalence of methicillin resistantstaphylococcus aureus (MRSA) at tertiary care hospital of Mathura, India. Progressiveresearch – an International Journal in Agriculture and Technology. 2016; 11(Special-
38. Thati VB, Shivannavar CT, Gaddad SM. Vancomycin resistance among methicillin resistant Staphylococcus aureus isolated from Intensive care unit of tertiary care hospital in Hyderabad. Indian J Med Res. 2011 ; 134(5):704-8.
39. Rana Khara R, 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(7): 187-95.
40. Lama U, Shah D, Shrestha UT. Vancomycin resistant Staphylococcus aureus reported from tertiary care hospital in Nepal. TUJM. 2017; 4(1):63-72.
41. Mohanty S, Behera B, Sahu S, Praharaj AK. Recent pattern of antibiotic resistance in Staphylococcus aureus clinical isolates in Eastern India and the emergence of reduced susceptibility to vancomycin. J Lab Physicians, 2019; 11:340-5.
42. Lama U, Shah D, Shrestha UT. Vancomycin resistant Staphylococcus aureus reported from tertiary care hospital in Nepal. TUJM, 2017; 4(1):63-72.
43. Ghosh S, Banerjee M. Methicillin resistance & inducible clindamycin resistance in Staphylococcus aureus. Indian J Med Res, 2016; 143: 362-4.
44. Rana KR, 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 July;3(7):187-195.
45. Kumari J, M S Shalini, M Chakrapani, K Vidyalakshmi and K B Gopalkrishna. Comparision of Etest and Agar dilution for determining minimum inhibitory concentration of vancomycin to healthcare-associated methicillin-resistant staphylococcus aureus. Asian J Pharm Clin Res, 31 March 2016; 9(4):1-3.
46. Osman MW, Osman MM, Mohamed NA, Osman SM, Magzoub M, El-Sanousi SM. Investigation on vancomycin resistance (VRSA) among methicillin resistant S. aureus (MRSA) in Khartoum State, Sudan. American Journal of Microbiological Research, 2016; 4(2):56-60.
47. Dhanalakshmi TA, Umapathy BL and Mohan DR. Prevalence of Methicillin, Vancomycin and Multidrug Resistance among Staphylococcus aureus. Journal of Clinical and Diagnostic Research. 2012 August, Vol-6(6): 974-977
48. Shittu AO, Oken K, Adesida S, Oyedara O, Witte W, Strommenger B et al. Antibiotic resistance and molecular epidemiology of Staphylococcus aureus in Nigeria. BMCMicrobiol, 2011; 11: 8.
49. Arora S, Devi P, Arora U, Devi B. Prevalence of methicillin resistance Staphylococcus Aureus (MRSA) in a tertiary care hospital in Northern India. India J Lab Physician, 2010; 2(2):78-81.
50. Taj Y, Abdullah FE, Kazmi SU. Current pattern of antibiotic resistance in Staphylococcus aureus clinical isolates and the emergence of vancomycin resistance. Journal of the College of Physicians and Surgeons-Pakistan: JCPSP, 2010; 20:728-32
51. Pathak A, Marothi Y, Iyer RV, Singh B, Sharma M, Eriksson B, Macaden R et al. Nasal carriage and antimicrobial susceptibility of Staphylococcus aureus in healthy preschool children in Ujjain, India. BMC Pediatrics, 2010; 10:100.
52. Tefera S, Awoke T, Mekonnen D. Methicillin and vancomycin resistant Staphylococcus aureus and associated factors from surgical ward inpatients at Debre Markos Referral Hospital, Northwest Ethiopia. Infect Drug Resist. 2021;14:3053–3062.
53. Aouati H, Hadjadj L, Aouati F, et al. Emergence of methicillin-resistant Staphylococcus aureus ST239/241 SCCmec-III Mercury in Eastern Algeria. Pathogens. 2021;10:1503.
54. Abd El-Hamid MI, Sewid AH, Samir M, et al. Clonal Diversity and Epidemiological Characteristics of ST239-MRSA Strains. Front Cell Infect Microbiol. 2022;12:782045.

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