DETECTION OF HELICOBACTER-PYLORI IN STOOL SPECIMENS BY PCR AND ANTIGEN ENZYME-IMMUNOASSAY

Citation
A. Makristathis et al., DETECTION OF HELICOBACTER-PYLORI IN STOOL SPECIMENS BY PCR AND ANTIGEN ENZYME-IMMUNOASSAY, Journal of clinical microbiology, 36(9), 1998, pp. 2772-2774
Citations number
12
Categorie Soggetti
Microbiology
ISSN journal
00951137
Volume
36
Issue
9
Year of publication
1998
Pages
2772 - 2774
Database
ISI
SICI code
0095-1137(1998)36:9<2772:DOHISS>2.0.ZU;2-B
Abstract
A highly sensitive seminested PCR assay to detect Helicobacter pylori DNA in feces was developed. PCR with stool specimens and a novel antig en enzyme immunoassay (EIA) for H. pylori detection in feces were eval uated as diagnostic tools and in follow-up with samples from 63 infect ed and 37 noninfected persons. Infected individuals received eradicati on therapy followed by endoscopic follow-up 35 days after the start of treatment. At that time, a second stool specimen was obtained from 55 of these patients. Before eradication, the sensitivity of BCR was 93. 7% and that of EIA 88.9%. Specificities were 100 and 94.6%, respective ly. Of the 55 follow-up specimens, 41 originated from patients from wh om H. pylori had been eradicated. Of these, 21 were still positive by PCR and 13 were positive by EPA, indicating that 1 month may be too sh ort a period for follow-up evaluation of stool specimens by these test s.