| Literature DB >> 28268185 |
Jing Xu1, Zhong Liang Duan2, Zhi Xun Guan3, Yan Yan Wang4, Cai Lin5, Ting Ting Zhang6, Hui Qin Zhang7, Ximei Qian8, Chao Ming Xia9.
Abstract
Currently in China, the schistosomiasis control program has shifted its focus from transmission control to the elimination of the disease. Effective forecast and surveillance systems of schistiosomiasis are of great importance for issuing timely and early warnings on risk of infection, and therefore implementing preventive measures to avoid infection. There is great demand in more sensitive and specific methods to improve the surveillance system for early detection of S. japonicum infection in sentinel mice. In this study, we reported a sensitive nested-PCR assay targeting a 303-bp fragment from highly repetitive retrotransposon SjCHGCS19 to detect the S. japonicum DNA in sera of experimental mice. Meanwhile, detection efficacy of the nested-PCR was compared with two conventional methods for field monitoring schistosomiasis such as ELISA and IHA. The nested-PCR assay could detect the specific DNA at 3-day post-infection in sera of mice with 5 cercariae infection, while for ELISA and IHA, both show negative results even after 2 weeks post-infection in mice with 20 cercariae infection. Our results demonstrated the DNA-based assay was more sensitive to make early diagnosis of S. japonicum infection in sentinel mice models, which will improve the early-warning ability of schistosomiasis surveillance system.Entities:
Keywords: Diagnosis; Schistosomiasis; SjCHGCS19; Surveillance
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Year: 2017 PMID: 28268185 DOI: 10.1016/j.exppara.2016.12.010
Source DB: PubMed Journal: Exp Parasitol ISSN: 0014-4894 Impact factor: 2.011