Shiga toxoid chimeric proteins
A chimeric Shiga toxoid according to the invention contains an enzymatically-inactivated StxA subunit and a native StxB subunit. This hybrid Shiga toxoid induces the production of broadly cross-reactive species of antibodies against Shiga toxin following immunization. The StxA subunit is modified so that it is enzymatically inactive. The invention thus encompasses the Shiga toxoid or fragments thereof and the nucleic acid sequence of the Shiga toxoid or fragments thereof. The invention further encompasses the production of a Shiga toxoid, the production of antibodies using the Shiga toxoid and methods of productions, and an immunogenic composition containing the Shiga toxoid.
1. A chimeric protein selected from the group consisting of:
(i) a chimeric protein comprising SEQ ID NO: 2,
(ii) a chimeric protein encoded by the nucleic acid sequence of SEQ ID NO: 1, and
(iii) a chimeric protein comprising SEQ ID NO: 2 and SEQ ID NO: 3.
2. A method of generating antibodies capable of binding to Stx comprising administering a chimeric protein of claim 1 to a mammal.
3. The method of claim 2 , wherein the mammal is a human.
4. The method of claim 3 , wherein the human is suffering from diarrhea.
5. The method of claim 3 , wherein the human is suffering from hemolytic uremic syndrome.
6. A method of preventing hemolytic uremic syndrome in a mammal comprising administering a composition comprising the chimeric protein of claim 1 .
7. A method of preventing diarrhea associated with Shiga toxin-producing Escherichia coli infection in a mammal comprising administering a composition comprising the chimeric protein of claim 1 .
8. The chimeric protein of claim 1 , wherein the chimeric protein is capable of inducing the production of broadly cross-reactive species of antibodies against shiga-like toxin 1 (Stx1) and shiga-like toxin 2 (Stx2) following immunization.
9. A composition comprising the chimeric protein of claim 1 .
10. The composition of claim 9 , further comprising a pharmaceutically acceptable carrier.
11. The composition of claim 9 , further comprising an adjuvant.
12. The composition of claim 9 , wherein said composition is suitable for administration to a human.