Prevalence of Staphylococcal bloodstream infections and its antibiogram from a tertiary-care hospital in India: A cross-sectional study

  • Moumita Sardar Department of Microbiology, Faculty of Medicine and Health Sciences, SGT University, Haryana, India
  • Mukesh Sharma Department of Microbiology, Faculty of Medicine and Health Sciences, SGT University, Haryana, India
  • Manisha Khandait Department of Microbiology, Faculty of Medicine and Health Sciences, SGT University, Haryana, India
  • Pinky Bhardwaj Department of Microbiology, Faculty of Medicine and Health Sciences, SGT University, Haryana, India
  • Ronika Kurichh Faculty of Medicine and Health Sciences, SGT University, Haryana, India
  • Leimapokpam Sumitra Devi Department of Microbiology, Faculty of Medicine and Health Sciences, SGT University, Haryana, India
Keywords: Bloodstream infections, Staphylococcus aureus, CoNS, MRSA, antibiogram

Abstract

Background: Bloodstream infections (BSIs) can cause self-limiting infections that recover within one to two days in healthy individuals to life-threatening sepsis in those with predisposing conditions.

Aim: The present study aimed to assess the frequency and antibiogram of Staphylococcus spp. isolated from blood culture and further detect methicillin resistance and vancomycin resistance among the isolates.

Methods: A total of 120 Staphylococcus species isolated over a period of six months from patients with BSIs were included in the study. In addition to antibiogram, vancomycin resistance was also determined using vancomycin screen agar test and E-test for determination of minimum inhibitory concentration (MIC).

Results: Among the Staphylococcal isolates (n= 120), comprising of S. aureus (66.7%, n= 80) and coagulase negative Staphylococci (CoNS) (33.3%, n= 40), a total of 56 (70%) S. aureus and 24 (60%) CoNS isolates were detected as methicillin-resistant. Of the methicillin resistant CoNS, 33.3% (n=6), 50% (n=6) and 40% (n= 4) were methicillin resistant S. epidermidis, S. haemolyticus and S. hominis, respectively.  All the Staphylococcal isolates were susceptible to linezolid and minocycline. Of the MRSA isolates, two strains were found to be resistant to vancomycin by Kirby Bauer’s disc diffusion method. Additionally, D-test was done for the MRSA strains (n= 56), of which 20 (35.7%) exhibited inducible clindamycin resistance.

Conclusion: This study highlights the increasing methicillin resistance in staphylococcal blood isolates. Resistance to majority of the antibiotics including vancomycin, the drug of choice for treatment of infections caused by MRSA strains, has reached alarming levels and continues to increase.

References

Khurana S, Bhardwaj N, Kumari M, Malhotra R, Mathur P. Prevalence, etiology and antibiotic resistance profiles of bacterial bloodstream infections in a tertiary care hospital in Northern India: a 4-year study. J Lab Physicians. 2018; 10: 426-31.

Kwiecinski JM, Horswill AR. Staphylococcus aureus bloodstream infections: pathogenesis and regulatory mechanisms. Curr Opin Microbiol. 2020; 53: 51-60.

Lamy B, Dargere S, Arendrup MC, Parienti JJ, Tattevin P. How to optimize the use of blood cultures for the diagnosis of bloodstream infections? A state-of-the art. Front Microbiol. 2016; 7: 697.

Hoenigl M, Wagner J, Raggam RB, Prueller F, Prattes J, Eigl S, et al. Characteristics of hospital acquired and community- onset blood stream infections, South East Austria. Plos One. 2014; 9: e104702.

Johnson J, Robinson ML, Rajput UC, Valvi C, Kinikar A, Parikh TB, et al. High burden of bloodstream infections associated with antimicrobial resistance and mortality in the neonatal intensive care unit in Pune, India. Clin Infect Dis. 2021; 73: 271-80.

Wu SW, De Lencastre H, Tomasz A. Recruitment of the mecA gene homologue of Staphylococcus sciuri into a resistance determinant and expression of the resistant phenotype in Staphylococcus aureus. J Bacteriol Res. 2001; 183: 2417-24.

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.

Rubinstein E, Keynan Y. Vancomycin revisited - 60 years later. Front Public Health. 2014; 2: 217.

Hiramatsu K, Hanaki H, Ino T, Yabuta K, Oguri T, Tenover FC. Methicillin resistant Staphylococcus aureus clinical strain with reduced vancomycin susceptibility. J Antimicrob Chemother. 1997; 40: 135-6.

Centers for Disease Control and Prevention (CDC). Staphylococcus aureus resistant to vancomycin-United States, 2002. MMWR Morb Mortal Wkly Rep. 2002; 51: 565-7.

Tiwari HK, Sen MR. Emergence of vancomycin resistant Staphylococcus aureus (VRSA) from a tertiary care hospital from northern part of India. BMC Infect Dis. 2006; 6: 1-6.

Palazzo ICV, Araujo MLC, Darini ALC. First Report of vancomycin-resistant Staphylococci isolated from healthy carriers in Brazil. J Clin Microbiol. 2005; 43: 179-185.

Collee JG, Miles RS, Watt B. Tests for the identification of bacteria. Mackie TJ, McCartney JE. Mackie & McCartney practical medical microbiology. 14th ed. New York: Churchill Livingstone, 1996. Pp 131-50.

Clinical and Laboratory Standards Institute (CLSI). Performance Standards for Antimicrobial Susceptibility Testing: 30th Informational supplement M100-S30. Wayne PA: Clinical and Laboratory Standard Institute; 2020.

Clinical and Laboratory Standards Institute (CLSI). Performance Standards for Antimicrobial Susceptibility Testing. 22nd Informational Supplement. M100-S22. 2014; 32(1).

Mathur P, Varghese P, Tak V, Gunjiyal J, Lalwani S, Kumar S, et al. Epidemiology of blood stream infections at a level-1 trauma care center of India. J Lab Physicians. 2014; 6: 22-7.

Tak V, Mathur P, Lalwani S, Misra MC. Staphylococcal blood stream infections: epidemiology, resistance pattern and outcome at a level 1 Indian trauma care center. J Lab Physicians. 2013; 5: 46-50.

Saeed A, Ahsan F, Nawaz M, Iqbal K, Rehman KU, Ijaz T. Incidence of vancomycin resistant phenotype of the methicillin resistant Staphylococcus aureus isolated from a tertiary care hospital in Lahore. Antibiotics. 2019; 9: 3.

Kulshrestha A, Anamika V, Mrithunjay K, Dalal A, Manish K. A study on the prevalence of vancomycin resistant and intermediate Staphylococcus aureus isolated from various clinical specimen in a tertiary care hospital and detection of their MIC values by E-test. Int J Med Microbiol Trop Dis. 2017; 3: 119-25.

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

Vasudeva N, Nirwan PS, Shrivastava P. Bloodstream infections and antimicrobial sensitivity patterns in a tertiary care hospital of India. Ther Adv Infect Dis. 2016; 3: 119-27.

Gohel K, Jojera A, Soni S, Gang S, Sabnis R, Desai M. Bacteriological profile and drug resistance patterns of blood culture isolates in a tertiary care nephrourology teaching institute. BioMed Res Int. 2014; 7; 2014.

Mamtora D, Saseedharan S, Bhalekar P, Katakdhond S. Microbiological profile and antibiotic susceptibility pattern of Gram-positive isolates at a tertiary care hospital. J Lab Physicians. 2019; 11: 144-8.

Singh S, Dhawan B, Kapil A, Kabra SK, Suri A, Sreenivas V, et al. Coagulase- negative staphylococci causing blood stream infection at an Indian tertiary care hospital: prevalence, antimicrobial resistance and molecular characterization. Indian J Med Microbiol 2016; 34: 500-5.

Kim CJ, Kim HB, Oh Md., Kim Y, Kim A, Oh SH, et al. The burden of nosocomial staphylococcus aureus bloodstream infection in South Korea: a prospective hospital-based nationwide study. BMC Infect Dis. 2014; 14: 590.

Solanki R, Javadekar TB. Incidence of vancomycin resistant staphylococci from various clinical isolates in a tertiary care hospital. Natl Lab Med. 2012; 1: 23-5.

Khadri H, Alzohairy M. Prevalence and antibiotic susceptibility pattern of methicillin- resistant and coagulase-negative staphylococci in a tertiary care hospital in India. Int J Med Sci. 2010; 2: 116-20.

Mir AB. Prevalence and antimicrobial susceptibility of methicillin resistant Staphylococcus aureus and coagulase-negative staphylococci in a tertiary care hospital. Asian J Pharm Clin Res. 2013; 6: 231-4.

Maharath A, Ahmed MS. Bacterial etiology of bloodstream infections and antimicrobial resistance patterns from a tertiary care hospital in Male, Maldives. Int J Microbiol. 2021; 2021: Article ID 3088202.

Singh L, Cariappa MP, Das NK. Drug sensitivity pattern of various Staphylococcus species isolated at a tertiary care hospital. Med J Armed Forces India. 2016; 72: 62-6.

Birru M, Woldemariam M, Manilal A, Aklilu A, Tsalla T, Mitiku A, et al. Bacterial profile, antimicrobial susceptibility patterns, and associated factors among bloodstream infection suspected patients attending Arba Minch General Hospital, Ethiopia. Sci Rep. 2021; 11: 15882.

Wasihun AG, Wlekidan LN, Gebremariam SA, Dejene TA, Welderufael Al, Haile TD, et al. Bacteriological profile and antimicrobial susceptibility patterns of blood culture isolates among febrile patients in Mekelle Hospital, Northern Ethiopia. SpringerPlus. 2015; 4: 1-7.

Zhang Z, Sun Z, Tian L. Antimicrobial resistance among pathogens causing bloodstream infections: A multicenter surveillance report over 20 years (1998– 2017). Infect Drug Resist. 2022; 15: 249-60.

Yadav A, Sharma A, Deep A. Vancomycin resistance in clinical isolates of methicillin resistance Staphylococcus aureus from a tertiary care hospital. Saudi J Pathol Microbiol. 2018; 3: 398-401.

Maheshwari M, Malhotra VL, Devi LS, Broor S. Prevalence of inducible clindamycin resistance in Staphylococcus aureus isolates in a peri-urban hospital in Haryana. Indian J Health Sci Care. 2017; 4: 57-61.

Mehta M, Dutta P, Gupta V. Antimicrobial susceptibility pattern of blood isolates from a teaching hospital in North India. Jpn J Infect Dis. 2005; 58: 174.

Rybak MJ, Vidaillac C, Sader HS, Rhomberg PR, Salimnia H, Briski LE, et al. Evaluation of vancomycin susceptibility testing for methicillin-resistant Staphylococcus aureus: comparison of E-test and three automated testing methods. J Clin Microbiol. 2013; 51: 2077-81.

Published
2025-12-31