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Research Article | Volume 3 Issue 1 (Jan-June, 2024) | Pages 1 - 6
Methicillin and Inducible Clindamycin resistance among Staphylococcus species isolated from Surgical site infections
 ,
 ,
Under a Creative Commons license
Open Access
Received
Feb. 14, 2024
Revised
March 7, 2024
Accepted
June 4, 2024
Published
June 30, 2024
Abstract
Surgical site infections, Staphylococcus aureus, Coagulase Negative Staphylococci, antibiotic resistance, infection control
Keywords
INTRODUCTION

Surgical site infection(SSI) is major problem in in clinical aspects instead of technical advances in infection control and surgical practices[1]. SSI as infection occurring within 30 days or in some specific surgeries 90 days after a surgical operation[2].  SSI causes increase in the treatment cost, length of hospital stay and significant morbidity and mortality[3]. SSI can be caused by increasing prevalence of some multi drug resistant gram positive organisms like Methicillin resistant Staphylococcus aureus (MRSA), Coagulase Negative Staphylococci, Vancomycin Resistant Enterococci (VRE). The aim of the study is to evaluate the occurrence of SSI, associated with gram positive microorganisms and their drug sensitivity pattern at our tertiary care centre.

MATERIAL AND METHODS:

This was a descriptive (Cross-sectional) study conducted in the Department of Microbiology at a tertiary care centre in Central India  from November 2020 to December 2022 with approval from institute ethical committee and informed consent was obtained from the subjects.

A total of 241 samples were collected from SSI cases with complaint of pain, swelling, redness, discharge, delayed or non-healing wound and processed as per standard microbiological techniques[4]. Antimicrobial susceptibility testing was performed as per CLSI 2020[5].

Results:

Out of 220 culture positive samples; 175 showed monomicrobial growth and 45 showed polymicrobial growth. Among SSI cases with each polymicrobial growth, two isolates were grown in culture positive samples.

Out of 265 isolates most common isolated gram positive  organism was Staphylococcus aureus 36(13.59%) followed by CoNS 12(4.53%) and Enterococcus faecalis 5(1.89%) and others were gram negative organisms.

All the 36 Staphylococcus aureus isolates were sensitive to Vancomycin and Linezolid. Maximum resistance was shown towards Penicillin i.e. 31(86.11%) (Table1).

Among 12 isolates of CoNS, all the isolates were found to be sensitive to Vancomycin and Linezolid. 10(83.33%) isolates were resistant to Penicillin and 2(16.67%) isolates were found to be resistant to Clindamycin.(Table 1)

12 (33.33%) S. aureus isolates were found to be resistant to Methicillin while among 12 CoNS isolates, 2(16.67%) were Methicillin resistant. Among 18 S. aureus isolates;9(25%) isolates had shown Inducible Clindamycin resistance. (Table 2)

 

Table 1: Antimicrobial resistance in Staphylococcus species

Groups

Antibiotics

Staphylococcus aureus

n=36(%)

CoNS

n=12(%)

Gro up A

Erythromycin

21(58.33)

3(25)

Clindamycin

20(55.56)

2(16.67)

Cefoxitin

12(33.33)

2(16.67)

Penicillin G

31(86.11)

10(83.33)

Group B

Linezolid

0

0

Tetracycline

22(61.11)

4(33.33)

Vancomycin*

0

0

Group C

Chloramphenicol

13(36.11)

3(25)

Ciprofloxacin

15(41.67)

5(41.67)

Gentamicin

17(47.22)

4(33.33)

*Sensitivity by MIC(E-test) method

Table 2: Methicillin resistant and Inducible Clindamycin resistant in Staphylococcal species:

Staphylococcal species

MRSA

ICR

S. aureus(n=36)

12 (33.33)

9(25)

CoNS (n=12)

2 (16.67)

0

 

 

Discussion:

Out of 220 culture positive samples, 175 showed monomicrobial growth and 45 showed polymicrobial growth. Among SSI cases with each polymicrobial growth, two isolates were grown in culture positive samples.

Out of total 265 isolated organisms from culture positive SSI cases, most common gram positive organism isolated was S. aureus (13.59%). Similar finding were reported by Dessie et al[6]  22.4% and Mehta et al [7]  27.84% in their studies.

Coagulase negative staphylococci was isolated in 4.53% culture positive SSIs cases. This is comparable to the study by Dessie et al2[6] who reported 8.2% and Verma et al[8] reported 3.48%.

Among 36 isolates of S.aureus, all the isolates were found to be sensitive to Vancomycin and Linezolid, while 86.11% of Staphylococcal isolates were resistant to Penicillin. Similar results for 100% sensitivity to Vancomycin and Linezolid have been published by multiple studies like Siddiqui et al, [11] and Narula et al[12].

In present study, all the 12 isolates of Coagulase negative staphylococci (CoNS) were found sensitive to Vancomycin and Linezolid while 16.67% isolates were resistant to Clindamycin and Cefoxitin both respectively. It is comparable to Budhani et al[13] that shows 97.8% CoNS were sensitive to Linezolid followed by Vancomycin (96.8%), and Gentamicin (85.6%) while 40.5% isolates were resistant to Cefoxitin.

Percentage of MRSA in  present study is 12 (33.33%). Among CoNS, two(16.67%) were detected as MRCoNS. It was found that all the methicillin resistant strains (100%) were sensitive to Vancomycin and Linezolid comparable with studies by Jain et al [14] who reported 48.78% and Negi et al[1]  reported 15.7% of MRSA in their study.

In present study, 9(25%) isolates of S. aureus isolates were detected as ICR  while a study by Eksi et al[15] detected in 6.9%  MRSA strains and Mokta et al[16] reported ICR 28.39%,

Conclusions:

Most of the pathogens associated with the SSIs among gram positive organisms in the study is S. aureus. Among these, 33.33% are MRSA which showed multidrug resistance pattern and 25% were inducible Clindamycin resistant. These isolates were showing least resistance pattern toward Vancomycin and linezolid while Maximum resistance was shown towards Penicillin i.e. 31(86.11%) while 12 (33.33%) isolates were found to be resistant to Cefoxitin. Reduction in  SSI  infection rate reduces  the wastage of healthcare resources, patient morbidity and mortality. This would be supported with proper infection control measures and  antibiotic policy. Infection by Multidrug-resistant bacteria enhances the need for antibiotic stewardship policy in hospitals.

References
  1. Negi V, Pal S, Juyal D, Sharma MK, Sharma N. Bacteriological profile of surgical site infections and their antibiogram: A study from resource constrained rural setting of Uttarakhand state, India. Journal of clinical and diagnostic research: JCDR. 2015;9(10):17.https://doi.org/ 10.7860/JCDR/2015/15342.6698

  2. Centre for Disease Control. National nosocomial infections study quarterly report, first and second quarters 1973. Atlanta, CDC 1974.

  3. Suchitra JB, Lakshmidevi N. Surgical site infections: Assessing risk factors, outcomes and antimicrobial sensitivity patterns. Afr. J. Microbiol. Res., 2009: 3(4): 175-79. 

  4. Collee J, Duguid J, Fraser A, Marmion B, Simmons A. Specimen Collection and Transport Mackie and Mc Cartney Practical Medical Microbiology. 2006:95-111.
  5. CLSI. Clinical and Laboratory Standards Institute, M100 Performance Standards for Antimicrobial Susceptibility Testing. 30th ed. USA: CLSI Wayne, PA; 2020.
  6. Dessie W, Mulugeta G, Fentaw S, Mihret A, Hassen M, Abebe E. Pattern of bacterial pathogens and their susceptibility isolated from surgical site infections at selected referral hospitals, Addis Ababa, Ethiopia. International journal of microbiology. 2016.
  7. Mehta S, Sahni N, Singh V, Bunger R, Garg T, Shinu P. Nosocomial Wound Infection amongst Post Operative Patients and their Antibiograms at Tertiary Care Hospital in India. African Journal of Clinical and Experimental Microbiology. 2014;15(2):60-8.
  8. Verma AK, Kapoor A, Bhargava A. Antimicrobial susceptibility pattern of bacterial isolates from surgical wound infections in tertiary care hospital in Allahabad, India. Internet Journal of Medical Update-EJOURNAL. 2012;7(1).
  9. Siddiqui N, Nandkar S, Khaparkuntikar M, Gaikwad A. Surveillance of post-operative wound infections along with their bacteriological profile and antibiotic sensitivity pattern at government cancer hospital, Aurangabad, India. Int J Curr Microbiol Appl Sci. 2017;6:595-600.
  10. Narula H, Chikara G, Gupta P. A prospective study on bacteriological profile and antibiogram of postoperative wound infections in a tertiary care hospital in Western Rajasthan. Journal of Family Medicine and Primary Care. 2020;9(4):1927.
  11. Budhani D, Kumar S, Sayal P, Singh S. Bacteriological profile and antibiogram of surgical site infection/postoperative wound infection. IJMRR. 2016;4(11):1994-9.
  12. Jain K, Chavan NS, Jain S. Bacteriological profile of post-surgical wound infection along with special reference to MRSA in central India, Indore. Int J Intg Med Sci. 2014;1(1):9-13.
  13. Eksi F, Gayyurhan ED, Bayram A, Karsligil T. Determination of antimicrobial susceptibility patterns and inducible clindamycin resistance in Staphylococcus aureus strains recovered from southeastern Turkey. Journal of Microbiology, Immunology and Infection. 2011;44(1):57-62.
  14. Mokta KK, Verma S, Chauhan D, Ganju SA, Singh D, Kanga A, et al. Inducible clindamycin resistance among clinical isolates of Staphylococcus aureus from Sub Himalayan Region of India. Journal of Clinical and Diagnostic Research: JCDR. 2015;9(8):DC20.
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