A recombinant nucleocapsid protein of Hantaan virus (HTN) 76-118 strain expressed in E. coli was applied as a serodiagnostic antigen in an enzyme-linked immunosorbent assay (rHTN-ELISA) for detection of hantavirus antibody in rat sera. The sensitivity and specificity of the rHTN-ELISA were compared with those of the indirect immunofluoresent assay (IFA) using virus-infected cells. The sensitivity of rHTN-ELISA was similar to that of the IFA both in experimentally SR- 11 infected rat and naturally infected rat sera. Sera showing a low antibody titer in IFA and suspected to be negative by other methods were also found to be negative in rHTN-ELISA. These results indicate that rHTN-ELISA is effective as a screening method for serodiagnosis of hantaviruses, because of its high sensitivity, specificity, safety and suitability for processing large number of samples. Copyright © 2003 Japanese Association for Laboratory Animal Science.
CITATION STYLE
Takakura, A., Goto, K., Itoh, T., Yoshimatsu, K., Takashima, I., & Arikawa, J. (2003). Establishment of an enzyme-linked immunosorbent assay for detection of Hantavirus antibody of rats using a recombinant of nucleocapsid protein expressed in Escherichia coli. Experimental Animals, 52(1), 25–30. https://doi.org/10.1538/expanim.52.25
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