GLYCOPEPTIDE SUSCEPTIBILITY AMONG STAPHYLOCOCCI AND ENTEROCOCCI ISOLATES FROM SULAIMANI HEALTH LABORATORIES

Authors

  • Razaw Mofaq Rashid Kurdistan Board Medical Studies Candidate, Public Health Laboratory, Sulaimani Directorate of Health, Kurdistan Region, Iraq.
  • Sherko A. Omer Department of Microbiology, College of Medicine, University of Sulaimani, Kurdistan Region, Iraq.

DOI:

https://doi.org/10.17656/jsmc.10176

Keywords:

Glycopeptide susceptibility, S. aureus, CoNS, enterococci, Sulaimani

Abstract

Background

Glycopeptide antibiotics are bactericidal agents that inhibit late stage bacterial cell wall peptidoglycan synthesis in Gram-positive bacteria. They are used for multiresistant Gram-positive cocci infection such as staphylococci and enterococci.

Objectives 

To determine glycopeptide susceptibility among staphylococci and enterococci isolates from Sulaimani city health laboratories and find combined methicillin and vancomycin resistance among S. aureus isolates.

Materials and Methods

Isolates of staphylococci and enterococci were collected from different hospital laboratories and community health laboratories in Sulaimani city. Staphylococci were differentiated based on coagulase test while enterococci species were determined using Vitek 2 ®automated system. Antimicrobial susceptibility test was preformed according to the Bauer-Kirby disk diffusion method using vancomycin, teicoplanin, amoxicillin-clavulanate, cefoxitin, methicillin, erythromycin, amikacin, gentamicin and netilmicin disks. The susceptibility was determined according to the Performance Standards for Antimicrobial Disk Susceptibility Tests.

Results

A total of 207 isolates of staphylococci and enterococci were collected from six hospital laboratories and two community health laboratories in Sulaimani city. The isolates were 146 Staphylococcus aureus, 36 coagulase-negative staphylococci (CoNS) and 25 enterococci isolates. The isolates were from inpatients 182 (87.9%), the other 25 (12.1%) were from outpatients submitting their specimens to community health laboratories. Resistance to vancomycin was detected in one isolate of each S. aureus (0.7%), CoNS (2.8%) andenterococci species (4%). For teicoplanin, one S. aureus isolate showed intermediate response (0.7) and two isolates (1.4%) were resistant. One isolate of each CoNS (2.8%) and enterococci spp. (4%) was resistant to teicoplanin. One MRSA isolate (1.25%) was resistant to vancomycin and combined resistance to both vancomycin and teicoplanin was detected in three isolates. 

Conclusion

Glycopeptide resistance was reported in staphylococci and enterococci but was uncommon. The reported resistance advises regular observation and monitoring the antibiotic susceptibility and strict antibiotic policy. Glycopeptide alternative still can be used in treatment of some Gram-positive infections, this may delay the emergence and spread of glycopeptide resistance.

References

Reynolds PE. Structure, biochemistry and mechanism of action of glycopeptide antibiotics. European Journal of Clinical Microbiology & Infectious Diseases. 1989;8(11):943-50. DOI: https://doi.org/10.1007/BF01967563

Dancer SJ. Glycopeptide resistance in Staphylococcus aureus. Journal of Antimicrobial Chemotherapy. 2003;51(5):1309-11. DOI: https://doi.org/10.1093/jac/dkg196

Pottinger P, Reller LB, Ryan KJ. Antibacterial Agents and Resistance. In: Ryan KJ, Ray CG, editors. Sherris Medical Microbiology. Sixth ed. New York: Mcgraw-hill; 2014.

Murray BE, Arias CA, C. NE. Glycopeptides (Vancomycin and Teicoplanin), Streptogramins (Quinupristin-Dalfopristin), Lipopeptides (Daptomycin), and Lipoglycopeptides (Telavancin). In: Bennett JE, Dolin R, Blaster MJ, editors. Mandell, Douglas, and Bennett’s Principles and Practice of INFECTIOUS DISEASES. 1. Eighth Edition ed. Philadelphia, PA: Saunders, Elsevier; 2015. p. 437-00. DOI: https://doi.org/10.1016/B978-1-4557-4801-3.00030-8

Ahlstrand E, Svensson K, Persson L, Tidefelt U, Söderquist B. Glycopeptide resistance in coagulase-negative staphylococci isolated in blood cultures from patients with hematological malignancies during three decades. European journal of clinical microbiology & infectious diseases. 2011;30(11):1349-54. DOI: https://doi.org/10.1007/s10096-011-1228-8

Schwalbe RS, Stapleton JT, Gilligan PH. Emergence of vancomycin resistance in coagulase-negative staphylococci. New England Journal of Medicine. 1987;316(15):927-31. DOI: https://doi.org/10.1056/NEJM198704093161507

Ploy MC, Grelaud C, Martin C, de Lumley L, Denis F. First clinical isolate of vancomycin-intermediate Staphylococcus aureus in a French hospital. Lancet (London, England). 1998;351(9110):1212. DOI: https://doi.org/10.1016/S0140-6736(05)79166-2

Hiramatsu K, Hanaki H, Ino T, Yabuta K, Oguri T, Tenover FC. Methicillin-resistant Staphylococcus aureus clinical strain with reduced vancomycin susceptibility. The Journal of antimicrobial chemotherapy. 1997;40(1):135-6. DOI: https://doi.org/10.1093/jac/40.1.135

Report MaMW. Staphylococcus aureus with reduced susceptibility to vancomycin--United States, 1997. MMWR Morb Mortal Wkly Rep. 1997;46(33):765-6.

Cetinkaya Y, Falk P, Mayhall CG. Vancomycin-resistant enterococci. Clinical microbiology reviews. 2000;13(4):686-707. DOI: https://doi.org/10.1128/CMR.13.4.686

Sujatha S, Praharaj I. Glycopeptide Resistance in Gram-Positive Cocci: A Review. Interdisciplinary Perspectives on Infectious Diseases. 2012;2012:10. DOI: https://doi.org/10.1155/2012/781679

Cosgrove S, Carroll K, Perl T. Staphylococcus aureus with reduced susceptibility to vancomycin. Clinical infectious diseases. 2004;39(4):539-45. DOI: https://doi.org/10.1086/422458

Walsh TR, Howe RA. The prevalence and mechanisms of vancomycin resistance in Staphylococcus aureus. Annual Reviews in Microbiology. 2002;56(1):657-75. DOI: https://doi.org/10.1146/annurev.micro.56.012302.160806

Srinivasan A, Dick JD, Perl TM. Vancomycin resistance in staphylococci. Clinical microbiology reviews. 2002;15(3):430-8. DOI: https://doi.org/10.1128/CMR.15.3.430-438.2002

Rogers KL, Fey PD, Rupp ME. Coagulase-negative staphylococcal infections. Infectious disease clinics of North America. 2009;23(1):73-98. DOI: https://doi.org/10.1016/j.idc.2008.10.001

Fainstein V, LeBlanc B, Bodey GP. Comparative in vitro study of teichomycin A2. Antimicrobial agents and chemotherapy. 1983;23(3):497-9. DOI: https://doi.org/10.1128/AAC.23.3.497

Wilson A, O'hare M, Felmingham D, Grüneberg R. Teicoplanin-resistant coagulase-negative staphylococcus. The Lancet. 1986;328(8513):973. DOI: https://doi.org/10.1016/S0140-6736(86)90622-7

Bene VED, John JF, Twitty JA, Lewis JW. Anti-staphylococcal activity of teicoplanin, vancomycin, and other antimicrobial agents: the significance of methicillin resistance. The Journal of infectious diseases. 1986;154(2):349-52. DOI: https://doi.org/10.1093/infdis/154.2.349

Veach L, Pfaller M, Barrett M, Koontz F, Wenzel R. Vancomycin resistance in Staphylococcus haemolyticus causing colonization and bloodstream infection. Journal of clinical microbiology. 1990;28(9):2064-8. DOI: https://doi.org/10.1128/jcm.28.9.2064-2068.1990

Sanyal D, Johnson A, George R, Cookson B, Williams A. Peritonitis due to vancomycin-resistant Staphylococcus epidermidis. The Lancet. 1991;337(8732):54. DOI: https://doi.org/10.1016/0140-6736(91)93375-J

Appelbaum PC. The emergence of vancomycin-intermediate and vancomycin-resistant Staphylococcus aureus. Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases. 2006;12 Suppl 1:16-23. DOI: https://doi.org/10.1111/j.1469-0691.2006.01344.x

Tiwari HK, Sen MR. Emergence of vancomycin resistant Staphylococcus aureus (VRSA) from a tertiary care hospital from northern part of India. BMC Infectious diseases. 2006;6(1):156. DOI: https://doi.org/10.1186/1471-2334-6-156

Showsh SA, De Boever EH, Clewell DB. Vancomycin resistance plasmid in Enterococcus faecalis that encodes sensitivity to a sex pheromone also produced by Staphylococcus aureus. Antimicrobial agents and chemotherapy. 2001;45(7):2177-8. DOI: https://doi.org/10.1128/AAC.45.7.2177-2178.2001

Billot-Klein D, Gutmann L, Bryant D, Bell D, Van Heijenoort J, Grewal J, et al. Peptidoglycan synthesis and structure in Staphylococcus haemolyticus expressing increasing levels of resistance to glycopeptide antibiotics. Journal of bacteriology. 1996;178(15):4696-703. DOI: https://doi.org/10.1128/jb.178.15.4696-4703.1996

Leclercq R, Derlot E, Duval J, Courvalin P. Plasmid-mediated resistance to vancomycin and teicoplanin in Enterococcus faecium. New England Journal of Medicine. 1988;319(3):157-61. DOI: https://doi.org/10.1056/NEJM198807213190307

Méndez-Álvarez S, Pérez-Hernández X, Claverie-Martín F. Glycopeptide resistance in enterococci. International Microbiology. 2000;3(2):71-80.

Foster T. Staphylococcus. In: Baron S, editor. Medical Microbiology Fourth ed. Texas: University of Texas Medical Branch at Galveston, Galveston, Texas; 1996.

Bauer A, Kirby W, Sherris JC, Turck M. Antibiotic susceptibility testing by a standardized single disk method. American journal of clinical pathology. 1966;45(4):493. DOI: https://doi.org/10.1093/ajcp/45.4_ts.493

Performance Standards for Antimicrobial Susceptibility Testing M100; Twenty-Fifth Informational Supplement. Wayne, PA: CLSI; 2015

Performance Standards for Antimicrobial Susceptibility Testing M100; Seventeenth Informational Supplement. Wayne, PA: CLSI;2007.

Sievert DM, Ricks P, Edwards JR, Schneider A, Patel J, Srinivasan A, et al. Antimicrobial-resistant pathogens associated with healthcare-associated infections summary of data reported to the National Healthcare Safety Network at the Centers for Disease Control and Prevention, 2009–2010. Infection Control & Hospital Epidemiology. 2013;34(1):1-14. DOI: https://doi.org/10.1086/668770

Zhanel GG, Adam HJ, Baxter MR, Fuller J, Nichol KA, Denisuik AJ, et al. Antimicrobial susceptibility of 22746 pathogens from Canadian hospitals: results of the CANWARD 2007–11 study. Journal of Antimicrobial Chemotherapy. 2013;68(suppl_1):i7-i22. DOI: https://doi.org/10.1093/jac/dkt022

O’Driscoll T, Crank CW. Vancomycin-resistant enterococcal infections: epidemiology, clinical manifestations, and optimal management. Infection and drug resistance. 2015;8:217. DOI: https://doi.org/10.2147/IDR.S54125

Bhamare B, Karmarkar A, Iyer V, Bhardwaj R, Deshpande S, Kagal A. Study of prevalence of methicillin and vancomycin resistance in multidrug resistant coagulase negative staphylococci. International J of Healthcare and Biomedical Research. 2014;2(3):67-72.

Aligholi M, Emaneini M, Jabalameli F, Shahsavan S, Dabiri H, Sedaght H. Emergence of high-level vancomycin-resistant Staphylococcus aureus in the Imam Khomeini Hospital in Tehran. Medical Principles and Practice. 2008;17(5):432-4. DOI: https://doi.org/10.1159/000141513

Al-Dahbi AM, Al-Mathkhury HJ. Distribution of Methicillin Resistant Staphylococcus aureus in Iraqi patients and Healthcare Workers. Iraqi J Sci. 2013;54(2):293-300.

Walters MS, Eggers P, Albrecht V, Travis T, Lonsway D, Hovan G, et al. Vancomycin-Resistant Staphylococcus aureus - Delaware, 2015. MMWR Morb Mortal Wkly Rep. 2015;64(37):1056. DOI: https://doi.org/10.15585/mmwr.mm6437a6

Jalal SM, Omer SA, Anwer KA. Bacteriological and PCR Detection of pvl, msrA and mecA Genes among Staphylococcus aureus isolated from Burn Wounds. Sulaimani, Iraq: University of Sulaimani, College of Medicine; 2017.

Davoudi A, Najafi N, Alian S, Tayebi A, Ahangarkani F, Rouhi S, et al. Resistance pattern of antibiotics in patient underwent open heart surgery with nosocomial infection in North of Iran. Global journal of health science. 2016;8(2):288. DOI: https://doi.org/10.5539/gjhs.v8n2p288

Tiemersma EW, Bronzwaer SL, Lyytikäinen O, Degener JE, Schrijnemakers P, Bruinsma N, et al. Methicillin-resistant Staphylococcus aureus in Europe, 1999–2002. Emerging infectious diseases. 2004;10(9):1627. DOI: https://doi.org/10.3201/eid1009.040069

Pichler G, Pux C, Babeluk R, Hermann B, Stoiser E, De Campo A, et al. MRSA prevalence rates detected in a tertiary care hospital in Austria and successful treatment of MRSA positive patients applying a decontamination regime with octenidine. European Journal of Clinical Microbiology & Infectious Diseases. 2018;37(1):21-7. DOI: https://doi.org/10.1007/s10096-017-3095-4

Flournoy D, Robinson M. In vitro antimicrobial susceptibilities of 349 methicillin-resistant Staphylococcus aureus isolates from veterans. Methods and findings in experimental and clinical pharmacology. 1990;12(8):541-4.

Published

2018-12-21

How to Cite

1.
Rashid R, Omer S. GLYCOPEPTIDE SUSCEPTIBILITY AMONG STAPHYLOCOCCI AND ENTEROCOCCI ISOLATES FROM SULAIMANI HEALTH LABORATORIES. JSMC [Internet]. 2018 Dec. 21 [cited 2024 Jul. 3];8(4):251-9. Available from: https://jsmc.univsul.edu.iq/index.php/jsmc/article/view/jsmc-10176

Similar Articles

1-10 of 402

You may also start an advanced similarity search for this article.

Most read articles by the same author(s)

1 2 > >>