Ultra-rapid and sensitive detection of African swine fever virus using multiple cross displacement amplification combined with nanoparticle-based lateral flow biosensor

被引:0
|
作者
Mao, Sha [1 ,2 ,3 ,4 ]
Zhang, Renjun [5 ]
Yang, Xinggui [1 ]
Huang, Junfei [1 ]
Kang, Yingqian [2 ,3 ,4 ]
Wang, Yi [6 ]
Chen, Hong [7 ]
Li, Shijun [1 ,2 ,3 ,4 ]
机构
[1] Guizhou Prov Ctr Dis Control & Prevent, Guiyang, Guizhou, Peoples R China
[2] Guizhou Med Univ, Key Lab Environm Pollut Monitoring & Dis Control, Minist Educ Guizhou, Guiyang, Guizhou, Peoples R China
[3] Guizhou Med Univ, Sch Basic Med Sci, Guiyang, Guizhou, Peoples R China
[4] Guizhou Med Univ, Inst One Hlth Res, Guiyang, Guizhou, Peoples R China
[5] Guizhou Prov Ctr Anim Dis Control & Prevent, Guiyang, Guizhou, Peoples R China
[6] Capital Inst Pediat, Expt Res Ctr, Beijing, Peoples R China
[7] EPINTEK Guiyang Ltd, Guiyang, Guizhou, Peoples R China
关键词
African swine fever virus; multiple cross displacement amplification; nanoparticle-based lateral flow biosensor; ASFV-MCDA-LFB; point-of-care testing; VISUAL DETECTION; ASSAY;
D O I
10.3389/fmicb.2024.1403577
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
African swine fever (ASF) is a devastating disease that can kill almost all infected pigs, causing great damage to the pig industry and destabilizing the global economy. Here, we developed a specific assay that combined multiple cross-displacement amplification (MCDA) with a nanoparticle-based lateral flow biosensor (LFB) for early and rapid identification of the African swine fever virus (ASFV-MCDA-LFB). We first designed a set of MCDA primers to recognize 10 different regions of the target ASFV B646L gene. Subsequently, the MCDA reaction was monitored with various methods: MG chromogenic reagents, agarose gel electrophoresis, real-time turbidity, and LFB. The ASFV-MCDA-LFB assay was optimized and evaluated with target nucleic acid templates extracted from various pathogens and simulated whole blood samples. As a result, the detection of limit (LOD) of the ASFV assay was 200 copies/reaction within 30 min, and no cross-reaction were observed with other non-ASFV viruses and common pathogens in this study. The evaluation assays demonstrated that the ASFV-MCDA-LFB method here is rapid, objective, easy-to-use, and low-cost detection method which can be used as a diagnostic or screening tool with competitive potential for point-of-care testing (POCT) of ASFV.
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页数:12
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