Protection against Bovine Respiratory Syncytial Virus Afforded by Maternal Antibodies from Cows Immunized with an Inactivated Vaccine
Gilles Meyer,
Charlotte Foret-Lucas,
Maxence Delverdier,
Antoine Cuquemelle,
Aurélie Secula,
Hervé Cassard
Affiliations
Gilles Meyer
Interactions Hôtes-Agents Pathogènes (IHAP), Université de Toulouse, INRAE (Institut National de Recherche pour L’agriculture, L’alimentation et L’environnement), ENVT (Ecole Nationale Vétérinaire de Toulouse), 31100 Toulouse, France
Charlotte Foret-Lucas
Interactions Hôtes-Agents Pathogènes (IHAP), Université de Toulouse, INRAE (Institut National de Recherche pour L’agriculture, L’alimentation et L’environnement), ENVT (Ecole Nationale Vétérinaire de Toulouse), 31100 Toulouse, France
Maxence Delverdier
Interactions Hôtes-Agents Pathogènes (IHAP), Université de Toulouse, INRAE (Institut National de Recherche pour L’agriculture, L’alimentation et L’environnement), ENVT (Ecole Nationale Vétérinaire de Toulouse), 31100 Toulouse, France
Antoine Cuquemelle
Interactions Hôtes-Agents Pathogènes (IHAP), Université de Toulouse, INRAE (Institut National de Recherche pour L’agriculture, L’alimentation et L’environnement), ENVT (Ecole Nationale Vétérinaire de Toulouse), 31100 Toulouse, France
Aurélie Secula
Interactions Hôtes-Agents Pathogènes (IHAP), Université de Toulouse, INRAE (Institut National de Recherche pour L’agriculture, L’alimentation et L’environnement), ENVT (Ecole Nationale Vétérinaire de Toulouse), 31100 Toulouse, France
Hervé Cassard
Interactions Hôtes-Agents Pathogènes (IHAP), Université de Toulouse, INRAE (Institut National de Recherche pour L’agriculture, L’alimentation et L’environnement), ENVT (Ecole Nationale Vétérinaire de Toulouse), 31100 Toulouse, France
The passive protection afforded by the colostrum from cattle that were vaccinated prepartum with an inactivated combination vaccine against the bovine respiratory syncytial virus (BRSV) was evaluated after an experimental challenge of calves. Pregnant cows without or with a low ELISA and neutralizing BRSV antibody titers were twice vaccinated or not vaccinated, the last immunization being at one month prior to calving. Vaccination was followed by a rapid increase in BRSV antibody titers after the second immunization. Twenty-eightnewborn calves were fed during the 6 h following birth, with 4 L of colostrum sourced from vaccinated cows (14 vaccine calves) or non-vaccinated cows (14 control calves) and were challenged with BRSV at 21 days of age. We showed that maternal immunity to BRSV provides a significant reduction in the clinical signs of BRSV in calves, especially for severe clinical forms. This protection was correlated with reduced BRSV detection in the lower respiratory tract but not in nasal swabs, indicating an absence of protection against BRSV nasal excretion. Finally, transcriptomic assays in bronchoalveolar lavages showed no statistical differences between groups for chemokine and cytokine mRNA transcriptions, with the exception of the overexpression of IL-9 at days 6 and 10 post-challenge, and a severe downregulation of CXCL-1 at day 3 post-challenge, in the vaccine group.