Volume 67, Issue 3 , Pages 239-245, July 2010
Evaluation of a real-time polymerase chain reaction assay for the detection of Dientamoeba fragilis☆
Abstract
The diagnostic value of a real-time polymerase chain reaction (PCR) assay targeting the 5.8S rDNA of Dientamoeba fragilis was investigated as compared with conventional parasitologic methods including cultivation testing 959 fecal samples from 491 patients attending a tertiary-care hospital and suspected of having an intestinal parasitosis. The real-time PCR assay revealed 117 additional D. fragilis-positive samples as compared with conventional methods, showing 100% sensitivity and specificity in our experience. On the whole, D. fragilis infection was detected in 186 samples from 105 patients (21.4%, third in frequency among the diagnosed intestinal parasitoses). The evaluated real-time PCR assay represents an effective tool to obtain both an accurate diagnosis and a reliable epidemiologic picture of dientamoebiasis.
Keywords: Real-time PCR, Diagnosis, Dientamoeba fragilis, Parasitosis
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☆ A.C. and C.G. conceived and designed the experiments. A.C., C.G., S.M., S.P., and G.P. performed the experiments. A.C. and S.R. performed conventional parasitological diagnostic methods. S.M., F.G., and N.M. performed sequencing. C.G. and S.M. did the sequence analysis. A.C., C.G., and S.M. wrote the paper. G.D. and C.C. conducted scientific supervision of the manuscript.
PII: S0732-8893(10)00052-0
doi:10.1016/j.diagmicrobio.2010.02.016
© 2010 Elsevier Inc. All rights reserved.
Volume 67, Issue 3 , Pages 239-245, July 2010
