Dergiler / Turkish Journal of Medical Sciences / 2011 / Cilt: 41 - Sayı: 2

Investigation of toxin genes in Staphylococcus aureus strains isolated in Mustafa Kemal University Hospital

Sayfa
343–352
Yayın Tarihi
2022-11-05
DOI
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Conclusion: Our results have revealed that toxin genes were very prevalent among S. aureus isolates, and the toxigenic isolates were independent of the genotypes obtained by PCR-RFLP of the coa gene (P > 0.05).

📌 3 Maddede Bu Makale

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Amaç & Hipotez:The aim of this study was to investigate the presence of genes encoding staphylococcal enterotoxins (SEs), exfoliative toxins (ETAs, ETBs), and toxic shock syndrome toxin-1 (TSST-1) by polymerase chain reaction (PCR) in Staphylococcus aureus strains isolated from various clinical samples from the Mustafa Kemal University Hospital.
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Temel Bulgular & Veri:Materials and methods: A total of 120 S. aureus strains isolated from various clinical samples (blood, wounds, urine, conjuctival swabs, and tracheal aspirate) over a 1 year period, 2007-2008, were used in this study.
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Sonuç & Katkı:Conclusion: Our results have revealed that toxin genes were very prevalent among S. aureus isolates, and the toxigenic isolates were independent of the genotypes obtained by PCR-RFLP of the coa gene (P > 0.05).
🔬Tür:Araştırma Makalesi
📍Kapsam:2007-2008 Verileri
⚙️Değişkenler:Key words: Staphylococcus aureus · toxin genes · PCR-RFLP

Özet

The aim of this study was to investigate the presence of genes encoding staphylococcal enterotoxins (SEs), exfoliative toxins (ETAs, ETBs), and toxic shock syndrome toxin-1 (TSST-1) by polymerase chain reaction (PCR) in Staphylococcus aureus strains isolated from various clinical samples from the Mustafa Kemal University Hospital. In addition, PCR-based restriction fragment length polymorphism (RFLP) analysis of the coa gene was employed to genotype the isolates. Materials and methods: A total of 120 S. aureus strains isolated from various clinical samples (blood, wounds, urine, conjuctival swabs, and tracheal aspirate) over a 1 year period, 2007-2008, were used in this study. Results: Almost 65.8% of the isolates possessed at least one toxin gene. The genes most frequently found were seg-sei (40.8%), followed by sea (30%) and eta (19.2%). Overall, 35 toxin genotypes were observed, among which the genotypes seg-sei, sea-seg-sei, and sea-see predominated at the rate of 8.3%, 5.8%, and 5%, respectively. Four coagulase genotype patterns were observed, with molecular sizes ranging from 570 to 970 bp. Coa-based RFLP analysis revealed 7 different patterns using AluI. Conclusion: Our results have revealed that toxin genes were very prevalent among S. aureus isolates, and the toxigenic isolates were independent of the genotypes obtained by PCR-RFLP of the coa gene (P > 0.05).

Abstract

The aim of this study was to investigate the presence of genes encoding staphylococcal enterotoxins (SEs), exfoliative toxins (ETAs, ETBs), and toxic shock syndrome toxin-1 (TSST-1) by polymerase chain reaction (PCR) in Staphylococcus aureus strains isolated from various clinical samples from the Mustafa Kemal University Hospital. In addition, PCR-based restriction fragment length polymorphism (RFLP) analysis of the coa gene was employed to genotype the isolates. Materials and methods: A total of 120 S. aureus strains isolated from various clinical samples (blood, wounds, urine, conjuctival swabs, and tracheal aspirate) over a 1 year period, 2007-2008, were used in this study. Results: Almost 65.8% of the isolates possessed at least one toxin gene. The genes most frequently found were seg-sei (40.8%), followed by sea (30%) and eta (19.2%). Overall, 35 toxin genotypes were observed, among which the genotypes seg-sei, sea-seg-sei, and sea-see predominated at the rate of 8.3%, 5.8%, and 5%, respectively. Four coagulase genotype patterns were observed, with molecular sizes ranging from 570 to 970 bp. Coa-based RFLP analysis revealed 7 different patterns using AluI. Conclusion: Our results have revealed that toxin genes were very prevalent among S. aureus isolates, and the toxigenic isolates were independent of the genotypes obtained by PCR-RFLP of the coa gene (P > 0.05).

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Bu Makaleye Atıf Yap

DEMİR, C., DURAN, N., ÖZER, B., ASLANTAŞ, Ö., OCAK, S. (2022). Investigation of toxin genes in Staphylococcus aureus strains isolated in Mustafa Kemal University Hospital. Turkish Journal of Medical Sciences, Cilt: 41 - Sayı: 2, 343–352. https://ajindex.com/articles/611368

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Kaynakça (10)

  1. Balaban N, Rasooly A. Staphylococcal enterotoxins. Int J Food Microbiol 2000; 61: 1-10. Kotb M. Bacterial pyrogenic exotoxins as superantigens. Clin Microbiol 1995; 8: 411-426.
  2. Lina G, Bohach GA, Nair SP, Hiramatsu K, Jouvin-Marche E, Mariuzza R. Standard nomenclature for the superantigens expressed by Staphylococcus. J Infect Dis 2004; 189: 2334- 2336. Omoe K, Imanishi K, Hu DL, Kato H, Fugane Y, Abe Y et al. Characterization of novel staphylococcal enterotoxin-like toxin type P. Infect Immun 2005; 73: 5540–5546.
  3. Omoe K, Hu DL, Takahashi-Omoe H, Nakane A, Shinagawa K. Identifi cation and characterization of a new staphylococcal enterotoxin-related putative toxin encoded by two kinds of plasmids. Infect Immun 2003; 71: 6088- 6094. Leterte C, Perelle S, Dilaser F, Fach P. Identifi cation of a new putative enterotoxin SEU encoded by the egc cluster of Staphylococcus aureus. J Appl Microbiol 2003; 95: 38-43.
  4. Orwin PM, Fitzgerald JR, Leung DY, Gutierrez JA. Bohach GA, Schlievert PM. Characterization of Staphylococcus aureus enterotoxin L. J Clin Microbiol 2003; 71: 2916-2919.
  5. Omoe K, Ishikawa M, Shimoda Y, Hu DL, Ueda S, Shinagawa K. Detection of seg, seh, and sei genes in Staphylococcus aureus isolates and determination of the enterotoxin productivities of S. aureus isolates harboring seg, seh, or sei genes. J Clin Microbiol 2002; 40: 857-862.
  6. Yarwood JM, McCormick JK, Paustian ML, Orwin PM, Kapur V, Schlievert PM. Characterization and expression analysis of Staphylococcus aureus pathogenicity island 3: implications for the evolution of staphylococcal pathogenicity island. J Biol Chem 2000; 277: 13138-13147.
  7. Orwin PM, Leung DY, Donahue HL, Novick RP, Schlievert PM. Biochemical and biological properties of staphylococcal enterotoxin K. Infect Immun 2001; 69: 360- 366. Jarraud S, Peyrat MA, Lim A, Tristan A, Bes M, Mougel C et al. egc, a highly prevalent operon of enterotoxin gene, forms a putative nursery of superantigens in Staphylococcus aureus. J Immunol 2001; 166: 669-677.
  8. Su YC, Wong AC. Identifi cation and purifi cation of a new staphylococcal enterotoxin, H. Appl Environ Microbiol 1995; 61: 1438-1443.
  9. Tenover FC, Arbeit R, Archer G. Biddle J, Byrne S, Goering R et al. Comparison of traditional and molecular methods of typing isolates of Staphylococcus aureus. J Clin Microbiol 1994; 32: 407-415.
  10. Goh SH, Bryne SK, Zhang JL, Chow AW. Molecular typing of Staphylococcus aureus on the basis of coagulase gene polymorphisms. J Clin Microbiol 1992; 30: 1642-1645