Experimental Infection of Calves with Transfected Attenuated Babesia bovis Expressing the Rhipicephalus microplus Bm86 Antigen and eGFP Marker: Preliminary Studies towards a Dual Anti-Tick/Babesia Vaccine
Bovine babesiosis, caused by and , is a major tick-borne disease of cattle with global economic impact. The disease can be prevented using integrated control measures including attenuated vaccines, babesicidal drugs, and tick control approaches. Vaccination of cattle with the Bm86-based recombinant...
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Published in: | Pathogens (Basel) Vol. 10; no. 2; p. 135 |
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Main Authors: | , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Switzerland
MDPI AG
29-01-2021
MDPI |
Subjects: | |
Online Access: | Get full text |
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Summary: | Bovine babesiosis, caused by
and
, is a major tick-borne disease of cattle with global economic impact. The disease can be prevented using integrated control measures including attenuated
vaccines, babesicidal drugs, and tick control approaches. Vaccination of cattle with the
Bm86-based recombinant vaccine reduces the fitness of
and
, but several booster inoculations are required to maintain protection. Herein, we generated a stable transfected strain of
expressing an enhanced GFP (eGFP) and a chimeric version of Bm86 (
/Bm86/eGFP). The eGFP was expressed in the parasite cytoplasm, whereas Bm86 was displayed on the surface of merozoites. Three splenectomized calves experimentally infected with
/Bm86/eGFP showed mild signs of acute disease and developed long-lasting antibody responses to
and native Bm86. No evidence of sequestration of parasites in the cerebral capillaries was found upon postmortem analysis, confirming attenuation of the strain. This is the first report of transfected
expressing the tick antigen Bm86 on the merozoite surface that elicits an antibody response to native Bm86. These results represent a proof of concept for a novel live, attenuated, tagged dual-vaccine approach to attempt simultaneous control of babesiosis and tick infestation. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 These authors contribute equally to this work. |
ISSN: | 2076-0817 2076-0817 |
DOI: | 10.3390/pathogens10020135 |