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Protective efficacy of recombinant bacterin vaccine against botulism in cattle

Authors :
Paula Fonseca Finger
Cleideanny C. Galvão
Ângela Nunes Moreira
Fabricio Rochedo Conceição
Carlos Eduardo Pouey da Cunha
Denis Y. Otaka
Marcos Roberto Alves Ferreira
Rafael Rodrigues Rodrigues
Carolina Georg Magalhães
Clóvis Moreira
Felipe Masiero Salvarani
Source :
Vaccine. 38(11)
Publication Year :
2019

Abstract

Botulism is a paralytic disease caused by the intoxication of neurotoxins produced by Clostridium botulinum. Among the seven immunologically distinct serotypes of neurotoxins (BoNTs A − G), serotypes C and D, or a chimeric fusion termed C/D or D/C, are responsible for animal botulism. The most effective way to prevent botulism in cattle is through vaccination; however, the commercially available vaccines produced by detoxification of native neurotoxins are time-consuming and hazardous. To overcome these drawbacks, a non-toxic recombinant vaccine was developed as an alternative. In this study, the recombinant protein vaccine was produced using an Escherichia coli cell-based system. The formaldehyde-inactivated E. coli is able to induce 7.45 ± 1.77 and 6.6 ± 1.28 IU/mL neutralizing mean titers against BoNTs C and D in cattle, respectively, determined by mouse neutralization bioassay, and was deemed protective by the Brazilian legislation. Moreover, when the levels of anti-BoNT/C and D were compared with those achieved by the recombinant purified vaccines, no significant statistical difference was observed. Cattle vaccinated with the commercial vaccine developed 1.33 and 3.33 IU/mL neutralizing mean titers against BoNT serotypes C and D, respectively. To the best of our knowledge, this study is the first report on recombinant E. coli bacterin vaccine against botulism. The vaccine was safe and effective in generating protective antibodies and, thus, represents an industry-friendly alternative for the prevention of cattle botulism.

Details

ISSN :
18732518
Volume :
38
Issue :
11
Database :
OpenAIRE
Journal :
Vaccine
Accession number :
edsair.doi.dedup.....97d86be35a5eb26d73ae67aa50e45f91