TY - JOUR
T1 - Immune responses to Streptococcus sobrinus surface protein antigen A expressed by recombinant Salmonella typhimurium
AU - Doggett, T. A.
AU - Jagusztyn-Krynicka, E. K.
AU - Curtiss, R.
PY - 1993
Y1 - 1993
N2 - In this study, we used a vaccine strain of Salmonella typhimurium to express antigenic determinants of the SpaA antigen of Streptococcus sobrinus, which is involved in the caries-forming process. We cloned either a single repeat (pYA2901) or three tandem repeats (pYA2905) of the 0.48-kb fragment of the spaA gene, which codes for an important component of the SpaA protein, plus a 1.2-kb minor antigenic determinant and measured the resulting immune responses to SpaA in orally immunized BALB/c mice. The single or triple repeat of the spaA gene fragment was inserted into the Asd+ vector pYA292 and was transformed into the S. typhimurium Δcya Δcrp vaccine strain χ4072 containing Δasd in the chromosome. Female BALB/c mice were then orally immunized with two doses of the S. typhimurium containing either of the two SpaA constructs, and the immune responses to the expressed SpaA protein were assessed. Significant serum immunoglobulin G (IgG) anti-SpaA titers were detected in mice immunized with χ4072(pYA2905) but not χ4072(pYA2901). Salivary anti-SpaA IgA titers were minimal and were only detected in mice immunized with S. typhimurium expressing the SpaA encoded by pYA2905. Intestinal anti-SpaA IgA titers, however, were detected in both groups of mice, particularly in mice immunized with χ4072(pYA2905). An oral booster 26 weeks after the initial series of immunizations resulted in increased serum IgG titers in both χ4072(pYA2901)- and χ4072(pYA2905)-immunized animals, particularly in the χ4072(pYA2905)-immunized animals. No anamnestic IgA response was detected in the saliva following the booster immunization.
AB - In this study, we used a vaccine strain of Salmonella typhimurium to express antigenic determinants of the SpaA antigen of Streptococcus sobrinus, which is involved in the caries-forming process. We cloned either a single repeat (pYA2901) or three tandem repeats (pYA2905) of the 0.48-kb fragment of the spaA gene, which codes for an important component of the SpaA protein, plus a 1.2-kb minor antigenic determinant and measured the resulting immune responses to SpaA in orally immunized BALB/c mice. The single or triple repeat of the spaA gene fragment was inserted into the Asd+ vector pYA292 and was transformed into the S. typhimurium Δcya Δcrp vaccine strain χ4072 containing Δasd in the chromosome. Female BALB/c mice were then orally immunized with two doses of the S. typhimurium containing either of the two SpaA constructs, and the immune responses to the expressed SpaA protein were assessed. Significant serum immunoglobulin G (IgG) anti-SpaA titers were detected in mice immunized with χ4072(pYA2905) but not χ4072(pYA2901). Salivary anti-SpaA IgA titers were minimal and were only detected in mice immunized with S. typhimurium expressing the SpaA encoded by pYA2905. Intestinal anti-SpaA IgA titers, however, were detected in both groups of mice, particularly in mice immunized with χ4072(pYA2905). An oral booster 26 weeks after the initial series of immunizations resulted in increased serum IgG titers in both χ4072(pYA2901)- and χ4072(pYA2905)-immunized animals, particularly in the χ4072(pYA2905)-immunized animals. No anamnestic IgA response was detected in the saliva following the booster immunization.
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M3 - Article
C2 - 8478075
AN - SCOPUS:0027173915
VL - 61
SP - 1859
EP - 1866
JO - Infection and Immunity
JF - Infection and Immunity
SN - 0019-9567
IS - 5
ER -