TY - JOUR
T1 - Characterization of the immune response and evaluation of the protective capacity of rSsnA against Streptococcus suis infection in pigs
AU - Gómez-Gascón, Lidia
AU - Cardoso-Toset, Fernando
AU - Tarradas, Carmen
AU - Gómez-Laguna, Jaime
AU - Maldonado, Alfonso
AU - Nielsen, Jens
AU - Olaya-Abril, Alfonso
AU - Rodríguez-Ortega, Manuel J
AU - Luque, Inmaculada
PY - 2016
Y1 - 2016
N2 - The efforts made to develop vaccines against Streptococcus suis have failed because of lack of common antigens cross-reactive against different serotypes of this species. The cell wall-anchored proteins can be good vaccine candidates due to their high expression and accessibility to antibodies, among these, a cell-wall protein, DNA-nuclease (SsnA), present in most of the S. suis serotypes and clinical isolates collected from infected pigs, was selected. An experimental challenge against S. suis serotype 2 in a pig model was used to validate the efficacy of recombinant SsnA combined with aluminium hydroxide plus Quil A as adjuvants, previously tested in mice by our research group with good results. In our study, clinical characteristics, bacterial load and spread, haematological and immunological parameters and the antibody response, including the opsonophagocytosis analysis of the sera were evaluated. Moreover the composition of peripheral blood leukocyte populations was studied in infected animals. The results show that the immunization of piglets with rSsnA elicits a significant humoral antibody response. However, the antibody response is not reflected in protection of pigs that are challenged with a virulent strain in our conventional vaccination model. Further studies are necessary to evaluate the use of rSsnA as a vaccine candidate for swine.
AB - The efforts made to develop vaccines against Streptococcus suis have failed because of lack of common antigens cross-reactive against different serotypes of this species. The cell wall-anchored proteins can be good vaccine candidates due to their high expression and accessibility to antibodies, among these, a cell-wall protein, DNA-nuclease (SsnA), present in most of the S. suis serotypes and clinical isolates collected from infected pigs, was selected. An experimental challenge against S. suis serotype 2 in a pig model was used to validate the efficacy of recombinant SsnA combined with aluminium hydroxide plus Quil A as adjuvants, previously tested in mice by our research group with good results. In our study, clinical characteristics, bacterial load and spread, haematological and immunological parameters and the antibody response, including the opsonophagocytosis analysis of the sera were evaluated. Moreover the composition of peripheral blood leukocyte populations was studied in infected animals. The results show that the immunization of piglets with rSsnA elicits a significant humoral antibody response. However, the antibody response is not reflected in protection of pigs that are challenged with a virulent strain in our conventional vaccination model. Further studies are necessary to evaluate the use of rSsnA as a vaccine candidate for swine.
KW - Adjuvants
KW - Pig model
KW - S. suis
KW - rSsnA
U2 - 10.1016/j.cimid.2016.06.001
DO - 10.1016/j.cimid.2016.06.001
M3 - Journal article
C2 - 27477507
SN - 0147-9571
VL - 47
SP - 52
EP - 59
JO - Comparative Immunology, Microbiology & Infectious Diseases
JF - Comparative Immunology, Microbiology & Infectious Diseases
ER -