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本文引用的文献

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Development of an antigen-capture enzyme-linked immunosorbent assay and immunochromatographic strip based on monoclonal antibodies for detection of H6 avian influenza viruses.基于单克隆抗体的 H6 禽流感病毒抗原捕获酶联免疫吸附试验和免疫层析条的研制。
Arch Virol. 2020 May;165(5):1129-1139. doi: 10.1007/s00705-020-04602-w. Epub 2020 Mar 27.
2
The Pattern of Highly Pathogenic Avian Influenza H5N1 Outbreaks in South Asia.南亚高致病性禽流感H5N1疫情模式
Trop Med Infect Dis. 2019 Nov 27;4(4):138. doi: 10.3390/tropicalmed4040138.
3
Development of a HA1-specific enzyme-linked immunosorbent assay against pandemic influenza virus A H1N1.针对甲型H1N1大流行性流感病毒的HA1特异性酶联免疫吸附测定法的开发。
Clin Exp Vaccine Res. 2019 Jan;8(1):70-76. doi: 10.7774/cevr.2019.8.1.70. Epub 2019 Jan 31.
4
A sandwich ELISA for detecting the hemagglutinin of avian influenza A (H10N8) virus.用于检测甲型流感病毒(H10N8)血凝素的夹心 ELISA 方法。
J Med Virol. 2019 May;91(5):877-880. doi: 10.1002/jmv.25387. Epub 2019 Jan 10.
5
Development of a Colloidal Gold-Based Immunochromatographic Strip for Rapid Detection of H7N9 Influenza Viruses.用于快速检测H7N9流感病毒的胶体金免疫层析试纸条的研制
Front Microbiol. 2018 Aug 31;9:2069. doi: 10.3389/fmicb.2018.02069. eCollection 2018.
6
Clinical and Immunological Characteristics of Human Infections With H5N6 Avian Influenza Virus.人感染 H5N6 禽流感病毒的临床和免疫学特征。
Clin Infect Dis. 2019 Mar 19;68(7):1100-1109. doi: 10.1093/cid/ciy681.
7
Monoclonal antibody-based colloid gold immunochromatographic strip for the rapid detection of Tomato zonate spot tospovirus.基于单克隆抗体的胶体金免疫层析条用于快速检测番茄环斑病毒。
Virol J. 2018 Jan 18;15(1):15. doi: 10.1186/s12985-018-0919-5.
8
Multiplex Reverse Transcription-PCR for Simultaneous Surveillance of Influenza A and B Viruses.多重逆转录聚合酶链反应同时监测甲型和乙型流感病毒。
J Clin Microbiol. 2017 Dec;55(12):3492-3501. doi: 10.1128/JCM.00957-17. Epub 2017 Oct 4.
9
Evolution, global spread, and pathogenicity of highly pathogenic avian influenza H5Nx clade 2.3.4.4.高致病性禽流感H5Nx进化分支2.3.4.4的进化、全球传播及致病性
J Vet Sci. 2017 Aug 31;18(S1):269-280. doi: 10.4142/jvs.2017.18.S1.269.
10
Rapid and broad detection of H5 hemagglutinin by an immunochromatographic kit using novel monoclonal antibody against highly pathogenic avian influenza virus belonging to the genetic clade 2.3.4.4.使用针对遗传分支2.3.4.4的高致病性禽流感病毒的新型单克隆抗体的免疫层析试剂盒对H5血凝素进行快速广泛检测。
PLoS One. 2017 Aug 7;12(8):e0182228. doi: 10.1371/journal.pone.0182228. eCollection 2017.

基于单克隆抗体的禽流感 A(H5)病毒抗原 ELISA 检测方法和胶体金免疫层析试纸条的研制。

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

机构信息

State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, and National Clinical Research Center for Infectious Diseases, the First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.

出版信息

J Vet Diagn Invest. 2021 Sep;33(5):969-974. doi: 10.1177/10406387211027538. Epub 2021 Jun 24.

DOI:10.1177/10406387211027538
PMID:34166136
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8366253/
Abstract

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 µL 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 µL 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.

摘要

甲型流感病毒(avian IAVs)对经济和公共卫生构成重大威胁。我们开发了一种抗原酶联免疫吸附试验(ag-ELISA)和胶体金免疫层析条,用于快速检测禽甲型 H5 病毒。这两种检测方法均与其他病毒(如其他禽 IAV、传染性法氏囊病病毒、新城疫病毒、传染性支气管炎病毒、禽副黏病毒)无交叉反应。ag-ELISA 的检测下限低至 0.5 血凝素(HA)单位/100µL 的禽甲型 H5 病毒和 7.5ng/mL 的纯化 H5 HA 蛋白。免疫层析条的检测下限低至 1HA 单位/100µL 的禽甲型 H5 病毒。这两种检测方法的重现性均良好,变异系数(CV)<10%。对于 200 份随机禽样,ag-ELISA 的敏感性和特异性分别为 92.6%和 98.8%,而测试条的敏感性和特异性分别为 88.9%和 98.3%。这两种检测方法均具有高度的特异性、敏感性和稳定性,适用于禽甲型 H5 病毒的快速检测和现场调查。