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Nested-PCR assay for detection of Schistosoma japonicum infection in domestic animals

机译:巢式PCR检测家禽日本血吸虫感染

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BackgroundSchistosomiasis japonica is a common zoonosis. Domestic animals are the primary source of infection and play an important role in disease transmission. The prevalence and infectivity of this disease in domestic animals in China have significantly decreased and, for this reason, diagnostics with a higher sensitivity have become increasingly necessary. It was reported that polymerase chain reaction (PCR)-based methods could be used to detect schistosome infection in humans and animals and presented a high sensitivity and specificity. The present study aimed to develop a PCR-based method for detection of Schistosoma japonicum infection in domestic animals. MethodsA specific nested-PCR assay was developed to detect S. japonicum infection in domestic animals via amplification of a 231-bp DNA fragment of retrotransposon SjR2. The developed assay was first used in sera and dry blood filter paper (DBFP) from goats and buffaloes at different time points of infection. Then, 78 DBFPs from 39 artificially-infected bovines at 14 and 28?days post-infection and 42 DBFPs from schistosome-negative bovines from the city of Huangshan in the Anhui province were used to evaluate the diagnostic validity. Furthermore, this assay was used to detect S. japonicum infection in domestic animals in Dongzhi and Wangjiang counties. ResultsThe expected PCR product was detected in eggs and adult worms of S. japonicum and blood samples from S. japonicum -infected goats and water buffaloes, but not from Fasciola and Haemonchus contortus worms. The nested-PCR assay could detect the target S. japonicum DNA in DBFPs from goats and buffaloes after day 3 post-infection. The sensitivity in buffaloes at 14 and 28?days post-infection was 92.30% (36/39) and 100% (39/39), respectively. The specificity was 97.60% (41/42). The positivity rates in Dongzhi and Wangjiang counties were 6.00% and 8.00% in bovines and 22.00% and 16.67% in goats, respectively. The positivity rates in goats in both counties were higher than those in bovines with a significant difference in Dongzhi County but not in Wangjiang County ( P P =?0.23, respectively). ConclusionsOur results suggest that the developed nested-PCR assay may be used for the diagnosis of S. japonicum infection in domestic animals, and the control of S. japonicum infection in goats should be paid more attention.
机译:背景日本血吸虫病是一种常见的人畜共患病。家畜是主要的感染源,在疾病传播中起重要作用。在中国,这种疾病在家畜中的流行和传染性已大大降低,因此,越来越需要具有更高敏感性的诊断方法。据报道,基于聚合酶链反应(PCR)的方法可用于检测人和动物中的血吸虫感染,并具有很高的灵敏度和特异性。本研究旨在开发一种基于PCR的方法来检测日本血吸虫在家畜中的感染。方法建立了特异性的巢式PCR检测法,通过扩增反转录转座子SjR2的231bp DNA片段来检测家畜中的日本血吸虫感染。所开发的测定法首先在感染的不同时间点用于山羊和水牛的血清和干血滤纸(DBFP)中。然后,使用39只人工感染的牛在感染后14天和28天的78个DBFP和来自黄山市血吸虫病阴性的牛的42个DBFP来评估诊断的有效性。此外,该测定法还用于检测东直县和望江县家畜中的日本血吸虫感染。结果在日本血吸虫的卵和成虫中以及感染日本血吸虫的山羊和水牛的血样中检出了预期的PCR产物,但在Fasciola和Haemonchus contortus蠕虫中未检出。感染后第3天,巢式PCR检测可以检测山羊和水牛的DBFP中的日本血吸虫DNA。感染后14天和28天,水牛的敏感性分别为92.30%(36/39)和100%(39/39)。特异性为97.60%(41/42)。东直县和望江县的阳性率在牛中分别为6.00%和8.00%,在山羊中分别为22.00%和16.67%。两个县的山羊的阳性率均高于牛,东直县的差异较大,望江县的差异无统计学意义(分别为P = 0.23)。结论我们的结果表明,开发的巢式PCR检测方法可用于诊断家畜中的日本血吸虫感染,并应更加注意控制山羊的日本血吸虫感染。

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