Sec. Leary et al., ACTIVE IMMUNIZATION WITH RECOMBINANT V-ANTIGEN FROM YERSINIA-PESTIS PROTECTS MICE AGAINST PLAGUE, Infection and immunity, 63(8), 1995, pp. 2854-2858
The gene encoding V antigen from Yersinia pestis was cloned into the p
lasmid expression vector pGEX-5X-2. When electroporated into Escherich
ia coli JM109, the recombinant expressed V antigen as a stable fusion
protein with glutathione S-transferase. The glutathione S-transferase-
V fusion protein was isolated from recombinant E. coli and cleaved wit
h factor Xa to yield purified V antigen as a stable product Recombinan
t V antigen was inoculated intraperitoneally into mice and shown to in
duce a protective immune response against a subcutaneous challenge wit
h 3.74 x 10(6) CFU of virulent Y. pestis. Protection correlated with t
he induction of a high titer of serum antibodies and a T-cell response
specific for recombinant V antigen. These results indicate that V ant
igen should be a major component of an improved vaccine for plague.