Autor: |
Godoy, Naiane Lima, de Moraes, Jonathan Ballico, de Castro, Cynthia Aparecida, Santana, Jhonne Pedro Pedott, Zangirolami, Teresa Cristina, Silva, Adilson José da, Novo-Mansur, Maria Teresa Marques, de Freitas Anibal, Fernanda |
Předmět: |
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Zdroj: |
Cellular Physiology & Biochemistry (Cell Physiol Biochem Press GmbH & Co. KG); 2023, Vol. 57 Issue 5, p379-394, 16p |
Abstrakt: |
Background/Aims: Swine erysipelas is a disease caused by Erysipelothrix rhusiopathiae, a Gram-positive bacillus, which has great economic importance because it leads to the loss of the swine herd. To control this disease, animals are immunized with a cellular vaccine of killed or attenuated E. rhusiopathiae, but even with herd vaccination, cases of swine erysipelas outbreaks have been reported in the United States, China and Japan, leading to the search for other antigenic components of the bacteria that may promote greater protection against E. rhusiopathiae. The surface protein SpaA from E. rhusiopathiae has been shown to be a candidate to constitute a subunit vaccine, since it has already been reported to induce a host immune response against the bacterium. DnaK, a hsp70 molecular chaperone, also seems to be a good candidate in the composition of a vaccine, as it has been demonstrated to be an antigenic protein of the bacteria. Methods: This work evaluated the immunogenicity and protection induced by the E. rhusiopathiae SpaA and DnaK recombinant proteins in a murine model, by intramuscular administration to mice with two doses of 100 µg at 21-day interval between them. The candidate proteins were tested either separately and together, compared with the commercial vaccine and the non-vaccination condition, and mice were challenged with a virulent strain of E. rhusiopathiae. Serum was collected to assess the produced antibodies and peripheral blood cells, whereas spleen and kidney tissues were assayed for E. rhusiopathiae [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
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