Department of Veterinary Science, National Institute of Infectious Diseases, 1-23-1 Toyama, Shinjuku, Tokyo, 162-8640, Japan.
Department of Veterinary Science, National Institute of Infectious Diseases, 1-23-1 Toyama, Shinjuku, Tokyo, 162-8640, Japan.
J Virol Methods. 2019 Jul;269:83-87. doi: 10.1016/j.jviromet.2019.03.009. Epub 2019 Apr 5.
A novel indirect fluorescent antibody test (IFAT) for detection of IgM against Nipah virus (NiV) was developed using HeLa 229 cells expressing recombinant NiV nucleocapsid protein (NiV-N). The NiV IFAT was evaluated using three panels of sera: a) experimentally produced sera from NiV-N-immunized/pre-immunized macaques, b) post-infection human sera associated with a Nipah disease outbreak in the Philippines in 2014, and c) human sera from a non-exposed Malaysian population. Immunized macaque sera showed a characteristic granular staining pattern of the NiV-N expressed antigen in HeLa 229 cells, which was readily distinguished from negative-binding results of the pre-immunized macaque sera. The IgM antibody titers in sequential serum samples (n = 7) obtained from three Nipah patients correlated well with previously published results using conventional IgM capture ELISA and SNT serology. The 90 human serum samples from unexposed persons were unreactive by IFAT. The IFAT utilizing NiV-N-expressing HeLa 229 cells to detect IgM antibody in an early stage of NiV infection is an effective approach, which could be utilized readily in local laboratories to complement other capabilities in NiV-affected countries.
一种用于检测尼帕病毒(NiV)IgM 的新型间接荧光抗体试验(IFAT)已被开发出来,该试验使用表达重组 NiV 核衣壳蛋白(NiV-N)的 HeLa 229 细胞。使用三个血清面板评估了 NiV IFAT:a)来自 NiV-N 免疫/预免疫猕猴的实验产生的血清,b)与 2014 年菲律宾尼帕病爆发相关的感染后人类血清,c)来自未暴露的马来西亚人群的人类血清。免疫猕猴血清在 HeLa 229 细胞中显示出 NiV-N 表达抗原的特征性颗粒状染色模式,这与预免疫猕猴血清的阴性结合结果明显区分开来。从三名尼帕病患者获得的连续血清样本(n=7)中的 IgM 抗体滴度与使用传统 IgM 捕获 ELISA 和 SNT 血清学获得的先前发表的结果很好地相关。90 份来自未暴露人群的人血清样本在 IFAT 中无反应。使用表达 NiV-N 的 HeLa 229 细胞检测 NiV 感染早期 IgM 抗体的 IFAT 是一种有效的方法,可在当地实验室中广泛使用,以补充受 NiV 影响国家的其他能力。