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Evaluation of the protective effect of a prime-boost strategy with plasmid DNA followed by recombinant adenovirus expressing BmAMA1 as vaccines against Babesia microti infection in hamster

  • Guanbo Wang , Longzheng Yu , Artemis Efstratiou , Paul Franck Adjou Moumouni , Mingming Liu , Huanping Guo , Yang Gao , Shinuo Cao , Mo Zhou , Jixu Li , Aaron Edmond Ringo and Xuenan Xuan EMAIL logo
Published/Copyright: April 13, 2018
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Abstract

In the present study, we have investigated the protective effect of a heterologous prime-boost strategy with priming plasmid DNA followed by recombinant adenovirus, both expressing BmAMA1, against Babesia microti infection. Four groups consisting of 3 hamsters per group were immunized with pBmAMA1/Ad5BmAMA1, pNull/Ad5BmAMA1, pBmAMA1/Ad5Null and pNull/Ad5Null, followed by challenge infection with B. microti. Our results showed that hamsters immunized with plasmid and adenovirus expressing BmAMA1 developed a robust IgG and IgG2a antibody response against BmAMA1, suggesting the DNA vaccine or viral vector vaccine tend to induce a Th1-biased response. Compared to the control hamsters, the hamsters vaccinated either with the prime-boost strategy or one of the two “vaccines” exhibited no significant protection against B. microti challenge. Although a slight difference in terms of parasitemia and hematocrit values at days 14–16 post challenge infection was observed, no other statistical difference was detected. Our results indicate that the prime-boost vaccination strategy of injection of plasmid and adenovirus expressing BmAMA1 is not efficient in protecting against B. microti infection.

Acknowledgements

This study was supported by a Grant-in-Aid for Scientific Research, from the Ministry of Education, Culture, Sports, Science of Technology of Japan.

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Received: 2017-6-30
Revised: 2018-2-10
Accepted: 2018-3-5
Published Online: 2018-4-13
Published in Print: 2018-6-26

© 2018 W. Stefański Institute of Parasitology, PAS

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