Rapid detection of Opisthorchis viverrini and Strongyloides stercoralis in human fecal samples using a duplex real-time PCR and melting curve analysis

被引:38
作者
Janwan, Penchom [1 ,2 ]
Intapan, Pewpan M. [1 ,2 ]
Thanchomnang, Tongjit [2 ,5 ]
Lulitanond, Viraphong [2 ,3 ]
Anamnart, Witthaya [4 ]
Maleewong, Wanchai [1 ,2 ]
机构
[1] Khon Kaen Univ, Dept Parasitol, Fac Med, Khon Kaen 40002, Thailand
[2] Khon Kaen Univ, Res & Diagnost Ctr Emerging Infect Dis, Khon Kaen 40002, Thailand
[3] Khon Kaen Univ, Dept Microbiol, Fac Med, Khon Kaen 40002, Thailand
[4] Walailak Univ, Sch Allied Hlth Sci & Publ Hlth, Dept Med Technol, Thasala 80160, Nakhon Si Thamm, Thailand
[5] Mahasarakham Univ, Fac Med, Maha Sarakham 44000, Thailand
关键词
CLONORCHIS-SINENSIS; STOOL SPECIMENS; DIAGNOSIS; EPIDEMIOLOGY; INFECTIONS; EXCRETION; LARVAE; SNAILS; ASIA;
D O I
10.1007/s00436-011-2419-z
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Human opisthorchiasis caused by the liver fluke Opisthorchis viverrini is an endemic disease in Southeast Asian countries including the Lao People's Democratic Republic, Cambodia, Vietnam, and Thailand. Infection with the soil-transmitted roundworm Strongyloides stercoralis is an important problem worldwide. In some areas, both parasitic infections are reported as co-infections. A duplex real-time fluorescence resonance energy transfer (FRET) PCR merged with melting curve analysis was developed for the rapid detection of O. viverrini and S. stercoralis in human fecal samples. Duplex real-time FRET PCR is based on fluorescence melting curve analysis of a hybrid of amplicons generated from two genera of DNA elements: the 162 bp pOV-A6 DNA sequence specific to O. viverrini and the 244 bp 18S rRNA sequence specific to S. stercoralis, and two pairs of specific fluorophore-labeled probes. Both O. viverrini and S. stercoralis can be differentially detected in infected human fecal samples by this process through their different fluorescence channels and melting temperatures. Detection limit of the method was as little as two O. viverrini eggs and four S. stercoralis larvae in 100 mg of fecal sample. The assay could distinguish the DNA of both parasites from the DNA of negative fecal samples and fecal samples with other parasite materials, as well as from the DNA of human leukocytes and other control parasites. The technique showed 100% sensitivity and specificity. The introduced duplex real-time FRET PCR can reduce labor time and reagent costs and is not prone to carry over contamination. The method is important for simultaneous detection especially in areas where both parasites overlap incidence and is useful as the screening tool in the returning travelers and immigrants to industrialized countries where number of samples in the diagnostic units will become increasing.
引用
收藏
页码:1593 / 1601
页数:9
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