Immunization with recombinant beta-tubulin from Trypanosoma evansi induced protection against T-evansi, T-equiperdum and T-b. brucei infection in mice
Immunization with recombinant beta-tubulin from Trypanosoma evansi induced protection against T-evansi, T-equiperdum and T-b. brucei infection in mice
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DOI:
10.1111/j.1365-3024.2006.00933.x
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发表时间:
2007-04-01
影响因子:
2.2
通讯作者:
Lun, Z. -R.
中科院分区:
文献类型:
--
作者:
Li, S. -Q.;Fung, M. -C.;Lun, Z. -R.
The beta-tubulin gene of Trypanosoma evansi (STIB 806) was cloned and expressed in Escherichia coli. The predicted amino acid sequence of T. evansi beta-tubulin shows 100%, 99.8%, 99.1%, and 98.6% homology with T. equiperdum, T. b. brucei, T. cruzi and T. danilewskyi, respectively, but is diverse from that of T. cyclops, showing only 51.6% of homology. Recombinant beta-tubulin was expressed as inclusion bodies in E. coli. It was purified and renatured for immunological studies. Mice immunized with the renatured recombinant beta-tubulin were protected from lethal challenge with T. evansi STIB 806, T. equiperdum STIB 818 and T. b. brucei STIB 940, showing 83.3%, 70% and 76.7% protection, respectively. Serum collected from the rabbit immunized with recombinant beta-tubulin inhibited the growth of T. evansi, T. equiperdum and T. b. brucei in vitro. Serum from mice and rabbits immunized with recombinant beta-tubulin recognized only T. evansi beta-tubulin and not mouse beta-tubulin. The results of this study demonstrated that the recombinant T. evansi beta-tubulin is a potential candidate for the development of a vaccine to prevent animal trypanosomiasis caused by these three trypanosome species.