| Literature DB >> 31765721 |
Tom Willems1, Annebel De Vleeschauwer1, Mariano Perez-Filgueira2, Yanmin Li3, Anna Ludi4, David Lefebvre1, Ginette Wilsden4, Bob Statham4, Bernd Haas5, Nora Mattion6, Blanca Robiolo6, Claudia Beascoechea Perez7, Eduardo Maradei7, Eliana Smitsaart8, José La Torre6, Kris De Clercq9.
Abstract
Foot-and-mouth disease virus (FMDV) is a highly variable RNA virus existing as seven different serotypes. The antigenic variability between and within serotypes can limit the cross-reactivity and therefore the in vivo cross-protection of vaccines. Selection of appropriate vaccine strains is crucial in the control of FMD. Determination of indirect relationships (r1-value) between potential vaccine strains and field strains based on antibody responses against both are routinely used for vaccine matching purposes. Aiming at the investigation of the repeatability, reproducibility and comparability of r1-value determination within and between laboratories and serological tests, a small scale vaccine matching ring test for FMDV serotype A was organized. Well-characterized serum pools from cattle vaccinated with a monovalent A24/Cruzeiro/Brazil/55 (A24) FMD vaccine with known in vivo protection status (homologous and heterologous) were distributed to four laboratories to determine r1-values for the heterologous FMD strains A81/Argentina/87, A/Argentina/2000 and A/Argentina/2001 using the virus neutralization tests (VNT) and liquid phase blocking ELISA (LPBE). Within laboratories, the repeatability of r1-value determination was high for both antibody assays. VNT resulted in reproducible and comparable r1-values between laboratories, indicative of a lack of antigenic relatedness between the A24 strain and the heterologous strains tested in this work, thus corresponding to some of the in vivo findings with these strains. Using LPBE, similar trends in r1-values were observed in all laboratories, but the overall reproducibility was lower than with VNT. Inconsistencies between laboratories may at least in part be attributed to differences in LPBE protocols as well as the in preexisting information generated in each laboratory (such as antibody titer-protection correlation curves). To gain more insight in the LPBE-derived r1-values standard bovine control sera were included in the antibody assays performed in each laboratory and a standardization exercise was performed.Entities:
Keywords: (r1)-value; Foot-and-mouth disease virus; Liquid phase blocking ELISA (LPBE); Vaccine matching; Virus neutralization test (VNT)
Year: 2019 PMID: 31765721 DOI: 10.1016/j.jviromet.2019.113786
Source DB: PubMed Journal: J Virol Methods ISSN: 0166-0934 Impact factor: 2.014