Development of an antigen-ELISA and a colloidal gold-based immunochromatographic strip based on monoclonal antibodies for detection of avian influenza A(H5) viruses

被引:1
|
作者
Xiao, Yixin
Yang, Fan
Liu, Fumin
Cheng, Linfang
Yao, Hangping
Wu, Nanping
Wu, Haibo [1 ,2 ]
机构
[1] Zhejiang Univ, Sch Med, Affiliated Hosp 1, State Key Lab Diag & Treatment Infect Dis, 79 Qingchun Rd, Hangzhou 310003, Zhejiang, Peoples R China
[2] Zhejiang Univ, Sch Med, Affiliated Hosp 1, Natl Clin Res Ctr Infect Dis, 79 Qingchun Rd, Hangzhou 310003, Zhejiang, Peoples R China
关键词
avian influenza A(H5) virus; ELISA; immunochromatographic strip; sensitivity; specificity; LINKED-IMMUNOSORBENT-ASSAY; PATHOGENICITY; EVOLUTION; H5N1;
D O I
10.1177/10406387211027538
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Avian influenza A(H5) viruses (avian IAVs) pose a major threat to the economy and public health. We developed an antigen-ELISA (ag-ELISA) and a colloidal gold-based immunochromatographic strip for the rapid detection of avian A(H5) viruses. Both detection methods displayed no cross-reactivity with other viruses (e.g., other avian IAVs, infectious bursal disease virus, Newcastle disease virus, infectious bronchitis virus, avian paramyxovirus). The ag-ELISA was sensitive down to 0.5 hemagglutinin (HA) units/100 mu L of avian A(H5) viruses and 7.5 ng/mL of purified H5 HA proteins. The immunochromatographic strip was sensitive down to 1 HA unit/100 mu L of avian A(H5) viruses. Both detection methods exhibited good reproducibility with CVs < 10%. For 200 random poultry samples, the sensitivity and specificity of the ag-ELISA were 92.6% and 98.8%, respectively, and for test strips were 88.9% and 98.3%, respectively. Both detection methods displayed high specificity, sensitivity, and stability, making them suitable for rapid detection and field investigation of avian A(H5) viruses.
引用
收藏
页码:969 / 974
页数:6
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