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实时荧光共振能量转移聚合酶链反应法结合探针杂交检测老挝人民民主共和国感染华支睾吸虫的双脐螺中华支睾吸虫的分子证据。

Molecular evidence of Opisthorchis viverrini in infected bithyniid snails in the Lao People's Democratic Republic by specific hybridization probe-based real-time fluorescence resonance energy transfer PCR method.

机构信息

Applied Malacology Center, Department of Social and Environmental Medicine, Faculty of Tropical Medicine, Mahidol University, Bangkok, 10400, Thailand.

出版信息

Parasitol Res. 2011 Apr;108(4):973-8. doi: 10.1007/s00436-010-2140-3. Epub 2010 Nov 11.

Abstract

Naturally occurring bithyniid snails, Bithynia siamensis goniomphalos (Prosobranchia: Bithyniidae), and their intermediate hosts were sampled from Khammouane Province, the Lao People's Democratic Republic, and the prevalence of the carcinogenic human liver fluke, Opisthorchis viverrini, was examined. The presence of O. viverrini cercariae in snails was examined by cercarial shedding test and then confirmed by specific hybridization probe-based real-time fluorescence resonance energy transfer (FRET) PCR method. The real-time FRET PCR method is based on a fluorescence melting curve analysis of a hybrid between an amplicon produced from the pOV-A6 specific sequence (Genbank accession no. S80278), a 162-bp repeated sequence specific to O. viverrini, and specific fluorophore-labeled probes. Mean melting temperature of O. viverrini DNA from the cercariae and each of two positive snails by shedding test was 66.3 ± 0.1. The O. viverrini infection rate in snails was 2.47% (2/81) by cercarial shedding test but was 8.52% (4/47) by real-time FRET PCR method. The real-time FRET PCR method is rapid and effective in examining a large number of snail samples simultaneously. Validation using molecular evidence from this procedure provides another tool for surveying the prevalence of O. viverrini-infected snails in Southeast Asian countries.

摘要

从老挝人民民主共和国的甘蒙省采集了天然双壳贝类蜗牛、暹罗双壳贝(腹足纲:双壳贝科)及其中间宿主,并检查了致癌性肝吸虫、麝猫后睾吸虫的流行情况。通过排放试验检查蜗牛中麝猫后睾吸虫尾蚴的存在,然后通过基于特异性杂交探针的实时荧光共振能量转移(FRET)PCR 方法进行确认。实时 FRET PCR 方法基于扩增子与特异性荧光标记探针之间杂交的荧光熔解曲线分析,该扩增子来自 pOV-A6 特异性序列(Genbank 登录号 S80278),是麝猫后睾吸虫特有的 162 个重复序列。从尾蚴和通过排放试验的两个阳性蜗牛中获得的麝猫后睾吸虫 DNA 的平均熔解温度分别为 66.3 ± 0.1°C。通过排放试验检测到蜗牛的麝猫后睾吸虫感染率为 2.47%(2/81),而通过实时 FRET PCR 方法为 8.52%(4/47)。实时 FRET PCR 方法可快速有效地同时检查大量蜗牛样本。使用该程序的分子证据进行验证为调查东南亚国家麝猫后睾吸虫感染蜗牛的流行情况提供了另一种工具。

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