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检测野生啮齿动物中的拉沙病毒反应性 IgG 抗体:捕获酶联免疫测定法的验证。

Detection of Lassa Virus-Reactive IgG Antibodies in Wild Rodents: Validation of a Capture Enzyme-Linked Immunological Assay.

机构信息

Bernhard Nocht Institute for Tropical Medicine, 20359 Hamburg, Germany.

Natural History Museum, Obafemi Awolowo University, Ile Ife HO220005, Nigeria.

出版信息

Viruses. 2022 May 7;14(5):993. doi: 10.3390/v14050993.

Abstract

The aim of this study was to evaluate the use of a capture enzyme-linked immunosorbent assay (ELISA) for the detection of LASV-reactive IgG antibodies in rodents. The assay was used for laboratory-bred rodents, as well as for animals caught in the wild in various regions of West Africa. The ELISA reached an accuracy of 97.1% in samples of known exposure, and a comparison to an immunofluorescence assay (IFA) revealed a very strong agreement between the ELISA and IFA results (Cohen's kappa of 0.81). The agreement is valid in Nigeria, and in Guinea and Sierra Leone where the lineages II and IV are circulating, respectively. Altogether, these results indicate that this capture ELISA is suitable for LASV IgG serostatus determination in rodents as an alternative to IFA. This assay will be a strong, accurate, and semi-quantitative alternative for rodent seroprevalence studies that does not depend on biosafety level 4 infrastructures, providing great benefits for ecology and epidemiology studies of Lassa fever, a disease listed on the Research and Development Blueprint of the WHO.

摘要

本研究旨在评估捕获酶联免疫吸附测定(ELISA)在检测啮齿动物中 LASV 反应性 IgG 抗体中的应用。该检测方法用于实验室饲养的啮齿动物,以及在西非不同地区野外捕获的动物。在已知暴露的样本中,ELISA 的准确性达到 97.1%,与免疫荧光测定(IFA)的比较显示 ELISA 和 IFA 结果之间具有很强的一致性(Cohen 的 kappa 值为 0.81)。该一致性在尼日利亚以及分别流行谱系 II 和 IV 的几内亚和塞拉利昂有效。总的来说,这些结果表明,这种捕获 ELISA 适合作为 IFA 的替代方法,用于确定啮齿动物中的 LASV IgG 血清状态。该检测方法将成为一种强大、准确和半定量的替代方法,用于啮齿动物血清流行率研究,而不需要依赖生物安全 4 级基础设施,为生态和流行病学研究拉沙热(一种被世界卫生组织研发蓝图列为疾病)带来了巨大的好处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f7c/9147821/f146e2ff5cad/viruses-14-00993-g001.jpg

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