The use of RT-PCR for determination of separate end-points for the strains IB H120 and IB D274 in titration of the combination vaccine Poulvac IB® primer

• Published in: Journal of virological methods 2013-11, Vol.193 (2), p.508-511
• Main Authors: Geerligs, H.J., Meinders, C.A.M., Snel, J., Duyves, W.
• Format: Article
• Language: English
• Subjects: Animals; chicken eggs; Chickens; Coronavirus Infections - prevention & control; Coronavirus Infections - veterinary; Eggs; End-point; freeze drying; infectious bronchitis; Infectious bronchitis virus - genetics; Infectious bronchitis virus - isolation & purification; Live combination vaccine; PCR; Poultry; Poultry Diseases - prevention & control; reverse transcriptase polymerase chain reaction; Reverse Transcriptase Polymerase Chain Reaction - methods; Titration; Vaccine Potency; vaccines; Vaccines, Attenuated - immunology; Vaccines, Combined - immunology; Viral Load; Viral Vaccines - immunology; viruses
• ISSN: 0166-0934; 1879-0984
• DOI: 10.1016/j.jviromet.2013.06.029

•Reading of live virus titrations by PCR.•Determination of endpoints for different viruses in one titration by PCR.•Similarity of titration results of reading by visual examination and reading by PCR. Poulvac IB® Primer is a lyophilized vaccine containing two attenuated infectious bronchitis strains in one vial, IB H120 and IB D274. For quantification of the viral content of the vaccine, dilution series of the final product are inoculated in embryonated chicken eggs. After the incubation period of seven days standard practice is for the embryos to be taken from each egg and examined visually for IB specific lesions; these readings are used to determine an end-point in viral titrations. The result is a titre value to which both strains contribute. However, it is not clear what the live virus titre is for strain IB H120 and for strain IB D274. In order to determine end-points in the titration for each of the two strains, we collected the allantoic fluids from each egg after the incubation period and tested these for the presence of IB H120 and IB D274 by a strain specific reverse phase PCR. Based on the data obtained by PCR we were able to determine an end-point for each of the two strains. For a given commercial batch of Poulvac IB primer we determined titres of 106.31 EID50 per vial for IB H120 and 106.59 EID50 for IB D274 using PCR for end-point determination. These end-points matched well with the end-point determined for both strains cumulatively after visual examination, i.e. 106.67 EID50 per vial. It is concluded that PCR is a suitable means to determine end-points in titrations of live viruses.