Visible and rapid detection of feline chaphamaparvovirus using multienzyme isothermal rapid amplification and lateral flow dipstick assay

被引:0
|
作者
Ji, Jun [1 ]
Mu, Xinhao [1 ]
Pan, Shunshun [1 ]
Xu, Xin [1 ]
Zhang, Shiyuan [1 ]
Huang, Honghui [1 ]
Li, Ying [1 ]
Bi, Yingzuo [2 ]
Yao, Lunguang [1 ]
机构
[1] Nanyang Normal Univ, Henan Prov Engn & Technol Ctr Anim Dis Diag & Inte, Henan Key Lab Insect Biol Funiu Mt, Nanyang, Peoples R China
[2] South China Agr Univ, Coll Anim Sci & Vet Med, Guangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
FeChPV; MIRA-LFD; detection; sensitivity; simplicity; PCR;
D O I
10.3389/fcimb.2025.1490948
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Feline chaphamaparvovirus (FeChPV) is a novel parvovirus previously reported in Canadian cats and Chinese dogs with diarrhea in 2019 and 2020, respectively. Herein, we aimed to establish a simple detection method for FeChPV in field clinics. The primers and probes for the multienzyme isothermal rapid amplification and lateral flow dipstick (MIRA-LFD) assay were designed to target the conserved regions of the FeChPV genome and determine the optimal reaction temperature and time. Without relying on precision instruments, FeChPV detection using the MIRA-LFD assay was completed within 20 min at 37 degrees C, without any cross-reaction with other reference viruses. The newly established MIRA-LFD assay had a detection limit of 32.3 copies/mu L, which was 10-fold lower than that of the nested polymerase chain reaction (PCR) assay. Furthermore, the MIRA-LFD assay detected 29 FeChPV-positive samples among 417 cats with diarrhea, providing a slightly higher positivity rate than the nested PCR assay. These results indicate that the newly developed MIRA-LFD assay for FeChPV detection is an efficient, economical, reliable, and simple method that can help in the early prevention and control of FeChPV infection.
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页数:7
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