Protection against Bovine Respiratory Syncytial Virus Afforded by Maternal Antibodies from Cows Immunized with an Inactivated Vaccine

被引:3
作者
Meyer, Gilles [1 ]
Foret-Lucas, Charlotte [1 ]
Delverdier, Maxence [1 ]
Cuquemelle, Antoine [1 ]
Secula, Aurelie [1 ]
Cassard, Herve [1 ]
机构
[1] Univ Toulouse, ENVT Ecole Natl Vet Toulouse, INRAE Inst Natl Rech Agr Alimentat & Environm, Interact Hotes Agents Pathogenes IHAP, F-31100 Toulouse, France
关键词
BRSV; vaccination; cattle; colostrum; maternal immunity; BRD; NEUTRALIZING ANTIBODIES; MANNHEIMIA-HAEMOLYTICA; MEMORY RESPONSES; DAIRY-HERD; CALVES; INFECTION; COLOSTRUM; EFFICACY; HERPESVIRUS-1; INTERLEUKIN-9;
D O I
10.3390/vaccines11010141
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
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