A conventional polymerase chain reaction-based method for the diagnosis of human schistosomiasis in stool samples from individuals in a low-endemicity area
The aim of this study was to evaluate the efficacy of a polymerase chain reaction (PCR)-based method to detect Schistosoma mansoni DNA in stool samples from individuals living in a low-endemicity area in Brazil. Of the 125 initial stool samples, 80 were ELISA reactive and eggs were identified in 19...
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Published in | Memórias do Instituto Oswaldo Cruz Vol. 108; no. 8 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Fundação Oswaldo Cruz, Fiocruz
17.02.2015
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Subjects | |
Online Access | Get full text |
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Summary: | The aim of this study was to evaluate the efficacy of a polymerase
chain reaction (PCR)-based method to detect Schistosoma mansoni DNA
in stool samples from individuals living in a low-endemicity area in
Brazil. Of the 125 initial stool samples, 80 were ELISA reactive and
eggs were identified in 19 of the samples by parasitological
examination. For the PCR evaluations, 56 stool samples were selected
and divided into five groups. Groups I-IV were scored negative for S.
mansoni eggs by parasitological examination. Groups I and II were ELISA
reactive, whereas Groups III and IV were ELISA nonreactive. Groups II
and III were positive for other intestinal parasites. PCR testing
scored eight samples as positive from these four groups. Group V
represented the S. mansoni-positive group and it included
ELISA-reactive samples that were scored positive for S. mansoni by one
or more parasitological examinations (6/19 were positive by Kato-Katz
method, 9/17 by saline gradient and 10/13 by Helmintex®). PCR
scored 13 of these 19 samples as positive for S. mansoni. We conclude
that while none of these methods yielded 100% sensitivity, a
combination of techniques should be effective for improving the
detection of S. mansoni infection in low-endemicity areas. |
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ISSN: | 1678-8060 |