| Literature DB >> 23688803 |
Ning Wang1, De-Sheng Li, Xuan Zhou, Yue Xie, Yi-Nan Liang, Cheng-Dong Wang, Hua Yu, Shi-Jie Chen, Yu-Bo Yan, Xiao-Bin Gu, Shu-Xian Wang, Xue-Rong Peng, Guang-You Yang.
Abstract
Baylisascaris schroederi is one of the most common intestinal nematodes in giant pandas. It can cause severe baylisascariasis which is highly infectious in its natural hosts. A rapid and reliable diagnosis of parasite infections is crucial to protect giant pandas, as well as for environmental monitoring and disease surveillance. Here, we established a specific PCR assay for B. schroederi detection which was targeting a 331-bp long fragment of the mitochondrial cytochrome c oxidase subunit II (COII) gene. Fifty fresh fecal samples collected from captive giant pandas were tested by the established PCR assay and the traditional flotation technique. DNA extracted from a single B. schroederi egg could be successfully amplified, while no cross-reactivity was found with DNA from Ancylostoma caninum eggs. The detection rate of the PCR assay was 68%, which was higher than that of the traditional egg flotation (46%). Our findings demonstrated that the PCR assay is sensitive and specific for the detection and identification of B. schroederi eggs. Therefore, it could become a useful tool for the investigation of B. schroederi infections in giant pandas.Entities:
Keywords: Baylisascaris schroederi; Cytochrome c oxidase subunit II gene; Eggs; Giant panda; PCR
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Year: 2013 PMID: 23688803 DOI: 10.1016/j.parint.2013.05.004
Source DB: PubMed Journal: Parasitol Int ISSN: 1383-5769 Impact factor: 2.230