Yoshimatsu K, Arikawa J, Kariwa H
Institute of Immunological Science, Faculty of Veterinary Medicine, Hokkaido University, Sapporo, Japan.
J Vet Med Sci. 1993 Dec;55(6):1047-50. doi: 10.1292/jvms.55.1047.
Recombinant baculovirus-infected insect cells which expressed recombinant protein, analogous to the nucleocapsid protein (NP) of Seoul type hantavirus, strain SR-11 (rNP-SR-Sf9) were applied to the indirect immunofluorescent antibody (IFA) test. The rNP-SR-Sf9 reacted with anti NP MAb clones which recognized strain specific or hantavirus common epitopes in the IFA test. The recombinant antigen was detected by antibodies to 3 serotypes of hantaviruses (Hantaan 76-118, SR-11, Puumala). Antibody titers of a group of experimentally infected mouse and urban rat sera using rNP-SR-Sf9 and strain SR-11-infected Vero cell antigens were mutual correlative. These results indicated that the rNP-SR-Sf9 were an effective and safety substitute for Vero E6 cells in the IFA test for serosurveys of hantavirus infection.
表达重组蛋白的重组杆状病毒感染昆虫细胞,该重组蛋白类似于汉城型汉坦病毒SR - 11株的核衣壳蛋白(NP)(rNP - SR - Sf9),被应用于间接免疫荧光抗体(IFA)检测。在IFA检测中,rNP - SR - Sf9与识别毒株特异性或汉坦病毒共同表位的抗NP单克隆抗体克隆发生反应。该重组抗原可被3种汉坦病毒血清型(汉滩病毒76 - 118、SR - 11、普马拉病毒)的抗体检测到。使用rNP - SR - Sf9和SR - 11毒株感染的Vero细胞抗原,一组经实验感染的小鼠和城市大鼠血清的抗体滴度呈相互关联。这些结果表明,在汉坦病毒感染血清学调查的IFA检测中,rNP - SR - Sf9是Vero E6细胞的有效且安全的替代物。