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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Two sequential PCR amplifications for detection of Schistosoma mansoni in stool samples with low parasite load

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Author(s):
Carvalho do Espirito-Santo, Maria Cristina [1] ; Alvarado-Mora, Monica Viviana [2] ; Silva Pinto, Pedro Luiz [3] ; Carrilho, Flair Jose ; Rebello Pinho, Joao Renato [2] ; Borges Gryschek, Ronaldo Cesar [1]
Total Authors: 6
Affiliation:
[1] Univ Sao Paulo, Sch Med, Dept Infect & Parasit Dis, Sao Paulo - Brazil
[2] Univ Sao Paulo, Sch Med, Lab Gastroenterol & Hepatol, Inst Trop Med, Dept Gastroenterol, Sao Paulo - Brazil
[3] Adolfo Lutz Inst, Enteroparasitosis Sect, Parasitol & Mycol Div, Sao Paulo - Brazil
Total Affiliations: 3
Document type: Journal article
Source: Revista do Instituto de Medicina Tropical de São Paulo; v. 54, n. 5, p. 245-248, SEP-OCT 2012.
Web of Science Citations: 6
Abstract

Schistosomiasis constitutes a major public health problem, with an estimated 200 million individuals infected worldwide and 700 million people living in risk areas. In Brazil there are areas of high, medium and low endemicity. Studies have shown that in endemic areas with a low prevalence of Schistosoma infection the sensitivity of parasitological methods is clearly reduced. Consequently diagnosis is often impeded due to the presence of false-negative results. The aim of this study is to present the PCR reamplification (Re-PCR) protocol for the detection of Schistosoma mansoni in samples with low parasite load (with less than 100 eggs per gram (epg) of feces). Three methods were used for the lysis of the envelopes of the S. mansoni eggs and two techniques of DNA extraction were carried out. Extracted DNA was quantified, and the results suggested that the extraction technique, which mixed glass beads with a guanidine isothiocyanate/phenol/chloroform (GT) solution, produced good results. PCR reamplification was conducted and detection sensitivity was found to be five eggs per 500 mg of artificially marked feces. The results achieved using these methods suggest that they are potentially viable for the detection of Schistosoma infection with low parasite load. (AU)