Development and validation of an in vitro titrimetric method for determination of classical swine fever viruses in PK-15 cells

• Published in: Journal of immunological methods Vol. 508; p. 113321
• Main Authors: Dhar, Pronab, Das, Subash Chandra, Manu, M., Mahapatra, Chayna Singha, Latheef, Shyma K.
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 01-09-2022
• Subjects: Classical swine fever virus; Fluorescent antibody test; Immunofluorescence; PK-15 cells; Virus titration; Virus titration; PK-15 cells; Classical swine fever virus; Immunofluorescence; Fluorescent antibody test
• ISSN: 0022-1759; 1872-7905
• DOI: 10.1016/j.jim.2022.113321

Classical swine fever (CSF) is a highly contagious notifiable disease of pigs caused by CSF virus of Flaviviridae family. Previously, lapinized vaccines were used for the disease control, which has now been replaced with cell culture vaccines. Determination of virus titre is the key factor for development and quality control testing of classical swine fever (CSF) cell culture vaccines. Since CSFV is a non- cytopathic virus, an accurate method for the titration of this virus in cell culture has not yet been reported. Here we present a full proof method of titration of CSF cell culture viruses employing Fluorescent Antibody Technique (FAT) in 24 well plate cover slip culture of PK-15 cells. CSFV monoclonal antibodies (Mab) used in the test bind to the CSF virus particles in the cell cytoplasm of the infected cells and the immune-fluorescence signal is produced by subsequent binding of FITC conjugate with Mab. In this newly developed method, apple green fluorescence is observed in the cytoplasm of the infected cells as the virus multiplies only in the cytoplasm. The nucleus as well as the uninfected cells cytoplasm is stained red without any traces of green fluorescence. Thus, the test clearly differentiates a CSFV infected cell from the uninfected cells in the vicinity, if any, and also from the uninfected controls. The test can also quantify the accurate titres of CSF live viruses in the cell culture vaccines and hence it has wide application in routine virus titration applied for manufacturing of CSF cell culture vaccines, determination of accurate multiplicity of infection (m.o.i.) during infection and quality control of vaccines by the testing laboratories.
Schematic representation of the steps followed for virus titration in cover-slip cultures in 24 well plate and performing FAT staining of the infected cells. [Display omitted]