Replication-independent reduction in the number and diversity of recombinant progeny viruses in chickens vaccinated with an attenuated infectious laryngotracheitis vaccine

Loncoman, Carlos A.; Hartley, Carol A.; Coppo, Mauricio J. C.; Browning, Glenn F.; Quinteros, Jose A.; Diaz-Mendez, Andres; Thilakarathne, Dulari; Fakhri, Omid; Vaz, Paola K.; Devlin, Joanne M.

Abstract

Recombination is closely linked with virus replication and is an important mechanism that contributes to genome diversification and evolution in alphaherpesviruses. Infectious laryngotracheitis (ILTV; Gallid alphaherpesvirus 1) is an alphaherpesvirus that causes respiratory disease in poultry. In the past, natural (field) recombination events between different strains of ILTV generated virulent recombinant viruses that have caused severe disease and economic loss in poultry industries. In this study, chickens were vaccinated with attenuated ILTV vaccines to examine the effect of vaccination on viral recombination and diversity following subsequent co-inoculation with two field strains of ILTV. Two of the vaccines (SA2 and A20) prevented ILTV replication in the trachea after challenge, but the level of viral replication after co-infection in birds that received the Serva ILTV vaccine strain did not differ from that of the mock-vaccinated (control) birds. Even though the levels of viral replication were similar in the two groups, the number of recombinant progeny viruses and the level of viral diversity were significantly lower in the Serva-vaccinated birds than in mock-vaccinated birds. In both the mock-vaccinated and Serva-vaccinated groups, a high proportion of recombinant viruses were detected in naive in-contact chickens that were housed with the co-inoculated birds. Our results indicate that vaccination can limit the number and diversity of recombinant progeny viruses in a manner that is independent of the level of virus replication. It is possible that immune responses induced by vaccination can select for virus genotypes that replicate well under the pressure of the host immune response. (C) 2018 Elsevier Ltd. All rights reserved.

Más información

Título según WOS: ID WOS:000445984000006 Not found in local WOS DB
Título de la Revista: VACCINE
Volumen: 36
Número: 38
Editorial: ELSEVIER SCI LTD
Fecha de publicación: 2018
Página de inicio: 5709
Página final: 5716
DOI:

10.1016/j.vaccine.2018.08.012

Notas: ISI