Differential diagnosis of the infection caused by wild-type or CD2v-deleted ASFV strains by quantum dots-based immunochromatographic assay

被引:11
作者
Niu, Yan [1 ]
Zhang, Gaiping [1 ,2 ]
Zhou, Jingming [1 ,3 ]
Liu, Hongliang [1 ,3 ]
Chen, Yumei [1 ,3 ]
Ding, Peiyang [1 ]
Qi, Yanhua [1 ]
Liang, Chao [1 ]
Zhu, Xifang [1 ]
Wang, Aiping [1 ,3 ]
机构
[1] Zhengzhou Univ, Sch Life Sci, Zhengzhou 450001, Henan, Peoples R China
[2] Henan Agr Univ, Zhengzhou, Henan, Peoples R China
[3] Henan Zhongze Biol Engn Co LTD, Zhengzhou, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
ASFV; fluorescent immunochromatographic assay; CD2v protein; antibody detection; differential diagnosis;
D O I
10.1111/lam.13691
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
African swine fever (ASF), a highly contagious and lethal disease, poses a tremendous threat and burden to the swine industry worldwide. Lack of available vaccines or treatments leaves rapid diagnosis as the key tool to control the disease. Quantum dots (QDs) are unique fluorescent semiconductor nanoparticles, highly versatile for biological applications. In this study, we developed a quantum dots-based fluorescent immunochromatographic assay (QDs-FICA) using CD2v as the diagnosis antigen to detect ASFV antibodies. The titre of the test strip was 1 : 5 center dot 12 x 10(5). In addition, the strip was highly specific to anti-ASFV serum and had no cross-reaction with CSFV, PPV, PRRSV, PCV-2, PRV and FMDV. Moreover, a comparative test of 71 clinical samples showed that the coincidence rate was 85 center dot 92% between the test strip and the commercial ELISA kit (coated with p30, p62 and p72). The QDs-FICA can be used to detect ASFV antibodies, which is meaningful for the surveillance, control and purification of ASF.
引用
收藏
页码:1001 / 1007
页数:7
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