Journals / Turkish Journal of Medical Sciences / 2009 / Cilt: 39 - Sayı: 6

Molecular typing of methicillin-resistant Staphylococcus aureus isolated from bloodstream infections in a university hospital

Pages
959–968
Publication Date
2009-06-01
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Conclusion: Our findings indicated that MRSA bloodstream infections in our hospital were not originated from any predominant clone and AP-PCR typing can be used to screen clonal relatedness of these strains.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Aim: Bloodstream infections due to methicillin-resistant Staphyococcus aureus (MRSA) strains are one of the major problems in many hospitals.
📊
Key Findings & Data:Materials and methods: A total of 37 consecutive MRSA strains were identified from the blood cultures from January to December 2003.
💡
Conclusion & Impact:Conclusion: Our findings indicated that MRSA bloodstream infections in our hospital were not originated from any predominant clone and AP-PCR typing can be used to screen clonal relatedness of these strains.
🔬Design:Research Article
📍Scope:2003 Verileri
⚙️Variables:Key words: Methicillin-resistant Staphyococcus aureus · bloodstream infections · AP-PCR

Abstract

Aim: Bloodstream infections due to methicillin-resistant Staphyococcus aureus (MRSA) strains are one of the major problems in many hospitals. Molecular typing provides very useful information about the origin and the spreading ways of strains. The aim of the present study is to assess the clonal relationship amongst MRSA strains isolated from bloodstream infections of patients in Turgut Özal Medical Center, İnönü University in Turkey. Materials and methods: A total of 37 consecutive MRSA strains were identified from the blood cultures from January to December 2003. Methicillin resistance was confirmed with amplification of the mecA gene by polymerase chain reaction (PCR). Clonal relatedness of the strains was investigated by arbitrarily primed polymerase chain reaction (AP-PCR) and pulsed-field gel electrophoresis (PFGE). Results: Of the 37 mecA positive S. aureus strains identified in a 1-year period, 29 (78.3%) were from intensive care units (ICUs) and the remaining 6 from other wards. The MRSA strains were resistant to most clinically useful anti-staphylococcal agents. AP-PCR and PFGE typing methods indicated that 67.6% and 60.7% of the typed strains were clonally related, respectively. Clonally related strains were not restricted in a specific clinic and period. Conclusion: Our findings indicated that MRSA bloodstream infections in our hospital were not originated from any predominant clone and AP-PCR typing can be used to screen clonal relatedness of these strains. The present data showed that there was no predominant MRSA clone in our hospital. However, because of the high rates of MRSA and clonally related strains, the infection control practices were reconsidered and more strict rules were proposed to the infection control committee to eliminate the spread of these strains between wards in our hospital.

Özet

Aim: Bloodstream infections due to methicillin-resistant Staphyococcus aureus (MRSA) strains are one of the major problems in many hospitals. Molecular typing provides very useful information about the origin and the spreading ways of strains. The aim of the present study is to assess the clonal relationship amongst MRSA strains isolated from bloodstream infections of patients in Turgut Özal Medical Center, İnönü University in Turkey. Materials and methods: A total of 37 consecutive MRSA strains were identified from the blood cultures from January to December 2003. Methicillin resistance was confirmed with amplification of the mecA gene by polymerase chain reaction (PCR). Clonal relatedness of the strains was investigated by arbitrarily primed polymerase chain reaction (AP-PCR) and pulsed-field gel electrophoresis (PFGE). Results: Of the 37 mecA positive S. aureus strains identified in a 1-year period, 29 (78.3%) were from intensive care units (ICUs) and the remaining 6 from other wards. The MRSA strains were resistant to most clinically useful anti-staphylococcal agents. AP-PCR and PFGE typing methods indicated that 67.6% and 60.7% of the typed strains were clonally related, respectively. Clonally related strains were not restricted in a specific clinic and period. Conclusion: Our findings indicated that MRSA bloodstream infections in our hospital were not originated from any predominant clone and AP-PCR typing can be used to screen clonal relatedness of these strains. The present data showed that there was no predominant MRSA clone in our hospital. However, because of the high rates of MRSA and clonally related strains, the infection control practices were reconsidered and more strict rules were proposed to the infection control committee to eliminate the spread of these strains between wards in our hospital.

🔖

Cite This Article

YETKİN, G. (2009). Molecular typing of methicillin-resistant Staphylococcus aureus isolated from bloodstream infections in a university hospital. Turkish Journal of Medical Sciences, Cilt: 39 - Sayı: 6, 959–968. https://ajindex.com/articles/114044

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (8)

  1. De Lencastre H, Tomasz A. Reassessment of the number of auxiliary genes essential for high-level methicillin resistance in S. aureus. Antimicrob. Agents Chemother 1994; 38: 2590–8. Chambers HF. Methicillin resistance in staphylococci: molecular and biochemical basis and clinical implications. Clin Microbiol Rev 1997; 10: 781–91.
  2. Brumfitt W, Hamilton-Miller T. Methicillin-resistant Staphylococcus aureus. New Engl J Med 1990; 320: 1188–96.
  3. Diederen BMW, Kluytmans JAJW. The emergence of infections with community-associated methicillin resistant Staphylococcus aureus. J Infection 2006; 52:157-68. Appelbaum P.C. MRSA- the tip of the iceberg. Clin Microbiol Infect 2006;12(Suppl.2):3-10.
  4. Belkum A, Kluytmans J, Leeuwen W, Bax R, Quint W, Peters E et al. Multicenter evaluation of arbitrarily primed PCR for typing of Staphylococcus aureus strain. J Clin Microbiol 1995; 33: 1537-47.
  5. Guducuoglu H, Ayan M, Durmaz R, Berktas M, Bozkurt H, Bayraktar Y. Epidemiological analysis of Staphylococcus aureus strains from nasal carriers in a teaching hospital. New Microbiol 2002; 25: 421-6.
  6. Tekerekoglu MS, Ay S, Otlu B, Ciçek A, Kayabaş U, Durmaz R.Molecular epidemiology of methicillin-resistant Staphylococcus aureus isolates from clinical specimens of patients with nosocomial infection: are there unnoticed silent outbreaks? New Microbiol. 2007; 30(2):131-7.
  7. Zee A, Verbakel H, Zon JC, Frenay I, van Belkum A, Peeters M et al. Moleculer genotyping of Staphylococcus aureus strains: Comparison of repetitive element sequence based PCR with various typing methods and isolation of a novel epidemicity marker. J Clin Microbiol 1999; 37:342-9.
  8. Cetinkaya Y, Kocagoz S, Hayran M, Uzun O, Akova M, Gursu G et al. Analysis of a mini outbreak of methicillin resistant Staphylococcus aureus in a surgical ward by using arbitrarily primed polymerase chain reaction. J Chemother 2000; 12: 13844. Goering RV. Persing, DH Tenover, FC Versalovic, J Tang, YW Unger, ER Relman, DA White. Pulsed-field gel electrophoresis. Eds. Molecular Microbiology:Diagnostic Principles and Practice. American Society for Microbiology Washington DC: 2004.p.185-69. Clinical and Laboratory Standards Institute. Performance Standards for Antimicrobial Susceptibility Testing. 2005 Document M100-S15. 5th Informational Supplement. Wayne, PA: CLSI. National Committee for Clinical Laboratory Standards. Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically. Approved standard M100– S13(M7). National