| Literature DB >> 34662861 |
Kantapong Iamrod1, Apisit Chaidee1,2, Rucksak Rucksaken3, Kulthida Y Kopolrat1,2, Chanika Worasith1,2, Phattharaphon Wongphutorn2,4, Kitti Intuyod2,5, Somchai Pinlaor1,2, Jiraporn Sithithaworn6, Paiboon Sithithaworn1,2, Nuttanan Hongsrichan1,2.
Abstract
Human strongyloidiasis is one of the neglected tropical diseases caused by infection with soil-transmitted helminth Strongyloides stercoralis. Conventional stool examination, a method commonly used for diagnosis of S. stercoralis, has low sensitivity, especially in the case of light infections. Herein, we developed the droplet digital polymerase chain reaction (ddPCR) assay to detect S. stercoralis larvae in stool and compared its performance with real-time PCR and stool examination techniques (formalin ethyl-acetate concentration technique [FECT] and agar plate culture [APC]). The ddPCR results showed 98% sensitivity and 90% specificity, and real-time PCR showed 82% sensitivity and 76.7% specificity when compared with the microscopic methods. Moreover, ddPCR could detect a single S. stercoralis larva in feces, and cross-reactions with other parasites were not observed. In conclusion, a novel ddPCR method exhibited high sensitivity and specificity for detection of S. stercoralis in stool samples. This technique may help to improve diagnosis, particularly in cases with light infection. In addition, ddPCR technique might be useful for screening patients before starting immunosuppressive drug therapy, and follow-up after treatment of strongyloidiasis.Entities:
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Year: 2021 PMID: 34662861 PMCID: PMC8733496 DOI: 10.4269/ajtmh.21-0729
Source DB: PubMed Journal: Am J Trop Med Hyg ISSN: 0002-9637 Impact factor: 3.707