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开发一种用于鸡传染性法氏囊病抗体血清学检测的内部间接酶联免疫吸附测定试剂盒。

Development of an in-house indirect ELISA kit for the serological detection of antibodies against infectious bursal disease in chickens.

作者信息

Hurisa Takele Tesgera, Abayneh Takele, Sori Teshale, Chengh Guohua, Fang Yongxiang, Bayisa Berecha, Akalu Mirtneh, Sherefa Kedir, Ayele Getu, Geresu Adugna, Dinka Hunduma, Mokonnin Mulatu, Bulto Warkisa Chala, Negi Teferi Degefa, Demeke Berhan, Yami Megersa Mindaye, Jemal Mohammed, Legesse Abinet, Tesfaye Yeneneh, Zeleke Amde

机构信息

National Veterinary Institute, Bishoftu, Ethiopia.

出版信息

BMC Vet Res. 2025 Apr 27;21(1):293. doi: 10.1186/s12917-025-04756-2.

Abstract

Infectious bursal disease is a highly contagious disease of young chickens caused by the infectious bursal disease virus. This disease poses an important threat to the commercial poultry industry globally. This study was designed to develop an In-House Indirect Enzyme-Linked Immune Sorbent Assay Kit for the serological detection of antibodies against infectious bursal disease viruses. An infectious bursal disease virus antigen dilution (1:2), sample serum (1:500), and mouse anti-chicken immunoglobulin G (IgG) labeled with horseradish peroxidase (HRP) (1:2,000) were used in this assay. The calculated cutoff value was 0.24. This in-house indirect ELISA method was compared with a commercial ELISA kit for the detection of antibodies against infectious bursal disease virus in chickens. The performance of the newly developed and commercial ELISA kit was evaluated as described by Samad et al. (1994). The sensitivity and specificity of the current ELISA method were 98% (95% CI: 92.96-99.76) and 97% (95% CI: 91.48-99.38), respectively. The average intra-assay % CV of the triplet of 2 samples was 7.6, and interassay comparisons indicated a CV of 5.45%. As indicated by the results, we described a valuable and cost-effective, sensitive and specific in-house indirect ELISA kit for the serological diagnosis of infectious bursal disease in Ethiopia.

摘要

传染性法氏囊病是由传染性法氏囊病病毒引起的幼鸡高度传染性疾病。这种疾病对全球商业家禽业构成重大威胁。本研究旨在开发一种用于血清学检测传染性法氏囊病病毒抗体的内部间接酶联免疫吸附测定试剂盒。该测定中使用了传染性法氏囊病病毒抗原稀释液(1:2)、样品血清(1:500)和用辣根过氧化物酶(HRP)标记的小鼠抗鸡免疫球蛋白G(IgG)(1:2000)。计算得出的临界值为0.24。将这种内部间接ELISA方法与一种用于检测鸡传染性法氏囊病病毒抗体的商业ELISA试剂盒进行比较。按照Samad等人(1994年)所述方法评估新开发的ELISA试剂盒和商业ELISA试剂盒的性能。当前ELISA方法的敏感性和特异性分别为98%(95%置信区间:92.96 - 99.76)和97%(95%置信区间:91.48 - 99.38)。2个样品的三重检测中,平均批内变异系数(%CV)为7.6,批间比较显示变异系数为5.45%。结果表明,我们描述了一种用于埃塞俄比亚传染性法氏囊病血清学诊断的有价值、经济高效、灵敏且特异的内部间接ELISA试剂盒。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e12a/12034110/92eedcd31d01/12917_2025_4756_Fig1_HTML.jpg

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