Detection of enterotoxin DNA in Staphylococcus aureus strains obtained from the middle meatus in controls and nasal polyp patients

被引:33
作者
Van Zele, Thibaut [1 ]
Vaneechoutte, Mario [2 ]
Holtappels, Gabriele [1 ]
Gevaert, Philippe [1 ]
van Cauwenberge, P. [1 ]
Bachert, Claus [1 ]
机构
[1] Ghent Univ Hosp, Dept Ear Nose & Throat, Upper Airways Res Lab, B-9000 Ghent, Belgium
[2] Ghent Univ Hosp, Dept Clin Chem Microbiol & Immunol, B-9000 Ghent, Belgium
来源
AMERICAN JOURNAL OF RHINOLOGY | 2008年 / 22卷 / 03期
关键词
chronic rhinosinusitis; enterotoxin; nasal polyposis; PCR; Staphylococcus aureus; superantigen;
D O I
10.2500/ajr.2008.22.3161
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Background: Recent findings indicate that Staphylococcus aureus and its products may be involved in the modification of nasal polyposis. The purpose of this study was to investigate the presence of S. aureus enterotoxin genes and the agr subtype in bacterial DNA of S. aureus strains isolated from the middle meatus of nasal polyp and control patients. Methods: S. aureus strains were isolated from nasal polyp patients and controls. The strains were screened using PCR for their agr subtype, classic superantigens (SEA, SEB, SEC, SED or TSST-1), the egc cluster (SEG, SEI, SEM, SEN, and SEO and other enterotoxins (SEE, SEH, SEJ, SEK, and SEL) distinct from the egc locus. Results: Seventy-five percent of S. aureus strains had at least one enterotoxin in their DNA. The egc gene cluster was identified in 27 (67.5%) strains. At least one classic enterotoxin gene was present in 42.5% of the strains. Interestingly, there were no differences in enterotoxin genes between S. aureus strains isolated from controls compared with nasal polyposis patients. In controls, an equal distribution among the four agr groups was found, while 73% of the NPs strains belonged to agr groups I and II. Conclusion: In this study we found no significant difference between strains from nasal polyp patients and controls in the presence of enterotoxin genes. However, in NPs, a higher number of strains belonged to agr I or II, which are associated with strains causing enterotoxin-mediated disease.
引用
收藏
页码:223 / 227
页数:5
相关论文
共 28 条
[21]   High prevalence of superantigens associated with the egc locus in Staphylococcus aureus isolates from patients with atopic eczema [J].
Mempel, M ;
Lina, G ;
Hojka, M ;
Schnopp, C ;
Seidl, HP ;
Schäfer, T ;
Ring, J ;
Vandenesch, F ;
Abeck, D .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2003, 22 (05) :306-309
[22]   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].
Omoe, K ;
Ishikawa, M ;
Shimoda, Y ;
Hu, DL ;
Ueda, S ;
Shinagawa, K .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (03) :857-862
[23]   EVALUATION OF A COMMERCIAL ENZYME-IMMUNOASSAY KIT (RIDASCREEN) FOR DETECTION OF STAPHYLOCOCCAL ENTEROTOXINS A, B, C, D, AND E IN FOODS [J].
PARK, CE ;
AKHTAR, M ;
RAYMAN, MK .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1994, 60 (02) :677-681
[24]  
SAMBROOK J, 1989, MOL CLONING LABORATO, pCH6
[25]   ENVIRONMENTAL-FACTORS AFFECTING TOXIC SHOCK SYNDROME TOXIN-1 (TSST-1) SYNTHESIS [J].
SARAFIAN, SK ;
MORSE, SA .
JOURNAL OF MEDICAL MICROBIOLOGY, 1987, 24 (01) :75-81
[26]   Specific immunoglobulin E for staphylococcal enterotoxins in nasal polyps from patients with aspirin-intolerant asthma [J].
Suh, YJ ;
Yoon, SH ;
Sampson, AP ;
Kim, HJ ;
Kim, SH ;
Nahm, DH ;
Suh, CH ;
Park, HS .
CLINICAL AND EXPERIMENTAL ALLERGY, 2004, 34 (08) :1270-1275
[27]   Differentiation of chronic sinus diseases by measurement of inflammatory mediators [J].
Van Zele, T. ;
Claeys, S. ;
Gevaert, P. ;
Van Maele, G. ;
Holtappels, G. ;
Van Cauwenberge, P. ;
Bachert, C. .
ALLERGY, 2006, 61 (11) :1280-1289
[28]   Staphylococcus aureus colonization and IgE antibody formation to enterotoxins is increased in nasal polyposis [J].
Van Zele, T ;
Gevaert, P ;
Watelet, JB ;
Claeys, C ;
van Cauwenberge, P ;
Bachert, C .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2004, 114 (04) :981-983