Prevalence of Tropheryma whipplei DNA in patients with various gastrointestinal diseases and in healthy controls

被引:42
作者
Amsler, L
Bauerfeind, P
Nigg, C
Maibach, RC
Steffen, R
Altwegg, M
机构
[1] Univ Zurich, Dept Med Microbiol, CH-8028 Zurich, Switzerland
[2] Swiss Fed Off Publ Hlth, CH-3003 Bern, Switzerland
[3] Univ Zurich, Inst Social & Prevent Med, CH-8028 Zurich, Switzerland
[4] Univ Zurich Hosp, Med Policlin, CH-8091 Zurich, Switzerland
[5] Univ Zurich Hosp, Div Gastroenterol, CH-8091 Zurich, Switzerland
关键词
D O I
10.1007/s15010-002-3083-0
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Little is known about the epidemiology of Tropheryma whipplei and its prevalence in people without clinical signs of Whipple's disease. Patients and Methods: We screened 239 patients with various gastrointestinal diseases for T. whipplei DNA and compared them with 215 healthy controls in order to check whether T. whipplei might be a risk factor for common gastrointestinal problems or diseases. We detected the 16S rDNA of T. whipplei in salivary and stool samples using a specific seminested PCR. Results: The prevalence of T. whipplei DNA in patients and in controls was 4.2% (95% CI 2.0-7.6%) and 7.0% (95% CI 4.0-11.3%), respectively. None of the different gastrointestinal diseases was associated with a higher rate of PCR-positive tests, except for the group of patients with reflux syndrome. Five out of 43 patients with reflux were found to be positive, with all five being positive in the salivary sample. This is in contrast to our findings in carriers without reflux with mainly positive stool samples (p < 0.01). Conclusion: We conclude that the asymptomatic carder state of T. whipplei indeed exists and that it is much more frequent than the rare Whipple's disease. The higher prevalence of T whipplei DNA in the saliva of patients with reflux syndrome suggests that the stomach might be the habitat of the organism.
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页码:81 / 85
页数:5
相关论文
共 27 条
[1]  
Brändle M, 1999, CLIN ENDOCRINOL, V50, P399
[2]  
DOBBINS WO, 1985, Q J MED, V56, P523
[3]   Whipple's disease and "Tropheryma whippelii" [J].
Dutly, F ;
Altwegg, M .
CLINICAL MICROBIOLOGY REVIEWS, 2001, 14 (03) :561-+
[4]   Tropheryma whippelii DNA in saliva of patients without Whipple's disease [J].
Dutly, F ;
Hinrikson, HP ;
Seidel, T ;
Morgenegg, S ;
Altwegg, M ;
Bauerfeind, P .
INFECTION, 2000, 28 (04) :219-222
[5]   PCR-positive tests for Tropheryma whippelii in patients without Whipple's disease [J].
Ehrbar, HU ;
Bauerfeind, P ;
Dutly, F ;
Koelz, HR ;
Altwegg, M .
LANCET, 1999, 353 (9171) :2214-2214
[6]   Quantitative detection of Tropheryma whipplei DNA by real-time PCR [J].
Fenollar, F ;
Fournier, PE ;
Raoult, D ;
Gérolami, R ;
Lepidi, H ;
Poyart, C .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (03) :1119-1120
[7]   A case of aortic valve disease associated with Tropheryma whippelii infection in the absence of other signs of Whipple's disease [J].
Geissdörfer, W ;
Wittmann, I ;
Seitz, G ;
Cesnjevar, R ;
Röllinghoff, M ;
Schoerner, C ;
Bogdan, C .
INFECTION, 2001, 29 (01) :44-47
[8]   Whipple endocarditis without overt gastrointestinal disease:: Report of four cases [J].
Gubler, JGH ;
Kuster, M ;
Dutly, F ;
Bannwart, F ;
Krause, M ;
Vögelin, HP ;
Garzoli, G ;
Altwegg, M .
ANNALS OF INTERNAL MEDICINE, 1999, 131 (02) :112-116
[9]   Detection of three different types of 'Tropheryma whippelii' directly from clinical specimens by sequencing, single-strand conformation polymorphism (SSCP) analysis and type-specific PCR of their 16S-23S ribosomal intergenic spacer region [J].
Hinrikson, HP ;
Dutly, F ;
Nair, S ;
Altwegg, M .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1999, 49 :1701-1706
[10]   Evaluation of a specific nested PCR targeting domain III of the 23S rRNA gene of "Tropheryma whippelii" and proposal of a classification system for its molecular variants [J].
Hinrikson, HP ;
Dutly, F ;
Altwegg, M .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (02) :595-599