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Research Project: Control Strategies for Bovine Babesiosis

Location: Animal Disease Research

Title: Vaccination of cattle with the Babesia bovis sexual-stage protein HAP2 abrogates parasite transmission by Rhipicephalus microplus ticks

Author
item SILVA, MARTA - Washington State University
item BASTOS, REGINALDO - Washington State University
item LAUGHERY, JACOB - Washington State University
item ALZAN, HEBA - Washington State University
item RATHINASAMY, VIGNESH - James Cook University
item COOKE, BRIAN - James Cook University
item Suarez, Carlos

Submitted to: NPJ Vaccines
Publication Type: Peer Reviewed Journal
Publication Acceptance Date: 9/15/2023
Publication Date: 9/27/2023
Citation: Silva, M.G., Bastos, R.G., Laughery, J.M., Alzan, H.F., Rathinasamy, V.A., Cooke, B.M., Suarez, C.E. 2023. Vaccination of cattle with the Babesia bovis sexual-stage protein HAP2 abrogates parasite transmission by Rhipicephalus microplus ticks. NPJ Vaccines. Vaccines 8, 140. https://doi.org/10.1038/s41541-023-00741-8.
DOI: https://doi.org/10.1038/s41541-023-00741-8

Interpretive Summary: New methods for the control of bovine babesiosis, a poorly-controlled tick-borne disease of global impact caused by Babesia bovis, are urgently needed. Babesia parasites have a sexual cycle of reproduction that occurs in the midgut of the tick vector after a blood meal on a Babesia-infected animal. One possible strategy for intervention is the creation of vaccines that are able to block the transmission of the parasite by ther tick vectors (known as transmission blocking vaccines, or TBV). Hereby we took advantage of the expression of a widely conserved gametocyte protein termed HAP2, which is is uniquely expressed on the surface of B. bovis sexual stage parasites, and is a candidate for transmission-blocking vaccines (TBV). In this study, we tested whether vaccination of calves with recombinant HAP2 (rHAP2) interferes with transmission of B. bovis by competent ticks in a cattle vaccination trial that included tick aquisition and tick transmission stages. Calves vaccinated with rHAP2 (n=3), but not control animals (n=3) developed antibodies specific to the vaccine antigen. Overall, the results of the vaccination trial demosntrated that parasite tick-transmission was blocked in thse animals vaccinated with the rHAP2 antigen, which confirmed HAP2 as a prime TBV candidate against infection of cattle by B. bovis.

Technical Abstract: The apicomplexan parasite Babesia bovis is responsible for bovine babesiosis, a poorly controlled tick-borne disease of global impact. The widely conserved gametocyte protein HAPLESS2/GCS1 (HAP2) is uniquely expressed on the surface of B. bovis sexual stage parasites and is a candidate for transmission-blocking vaccines (TBV). Here, we tested whether vaccination of calves with recombinant HAP2 (rHAP2) interferes with the transmission of B. bovis by competent ticks. Calves vaccinated with rHAP2 (n'='3), but not control animals (n'='3) developed antibodies specific to the vaccine antigen. Vaccinated and control animals were infested with Rhipicephalus microplus larvae and subsequently infected with virulent blood stage B. bovis parasites by needle inoculation, with all animals developing clinical signs of acute babesiosis. Engorged female ticks fed on the infected calves were collected for oviposition, hatching, and obtention of larvae. Transmission feeding was then conducted using pools of larvae derived from ticks fed on rHAP2-vaccinated or control calves. Recipient calves (n'='3) exposed to larvae derived from control animals, but none of the recipient calves (n'='3) challenged with larvae from ticks fed on rHAP2-vaccinated animals, developed signs of acute babesiosis within 11 days after tick infestation. Antibodies against B. bovis antigens and parasite DNA were found in all control recipient animals, but not in any of the calves exposed to larvae derived from HAP2-vaccinated animals, consistent with the absence of B. bovis infection via tick transmission. Overall, our results are consistent with the abrogation of parasite tick transmission in rHAP2-vaccinated calves, confirming this antigen as a prime TBV candidate against B. bovis.