Stulberg Alyssa, Barry Christina, Robinson Alyssia, Mueller Nicole, Bello Alexander, Wood Heidi
Public Health Agency of Canada (PHAC), Winnipeg, MB, Canada.
Methods Mol Biol. 2025;2893:25-35. doi: 10.1007/978-1-0716-4338-9_3.
The California serogroup (CSG) viruses are orthobunyaviruses endemic in North America and responsible for the second most common cause of mosquito-borne viral encephalitis in the United States. As the CSG viruses have been neglected and are poorly studied, there are no commercial diagnostic serological assays or reagents available for detection. Therefore, diagnostic laboratories have had to rely on the development of their own in-house serological assays. To develop serological assays, antigenic materials such as recombinant protein, virus-like particles (VLP), or inactivated virus can be used in the IgM antibody capture enzyme-linked immunosorbent assay (MAC-ELISA) to detect CSG virus-specific IgM antibodies. All positive MAC-ELISA results should be confirmed by a well-defined gold standard test method such as the plaque-reduction neutralization test (PRNT).
加利福尼亚血清群(CSG)病毒是北美洲特有的正布尼亚病毒,是美国蚊媒病毒性脑炎的第二大常见病因。由于CSG病毒一直被忽视且研究较少,目前尚无用于检测的商业诊断血清学检测方法或试剂。因此,诊断实验室不得不依靠自行开发内部血清学检测方法。为了开发血清学检测方法,可以在IgM抗体捕获酶联免疫吸附测定(MAC-ELISA)中使用重组蛋白、病毒样颗粒(VLP)或灭活病毒等抗原材料来检测CSG病毒特异性IgM抗体。所有MAC-ELISA阳性结果都应通过明确的金标准检测方法进行确认,如蚀斑减少中和试验(PRNT)。