Abstract

BackgroundBovine babesiosis is caused by apicomplexan pathogens of the genus Babesia such as B. bigemina and B. bovis. These tick-borne pathogens have a complex life-cycle involving asexual multiplication in vertebrate hosts and sexual reproduction in invertebrate vectors. In the tick midgut, extracellular Babesia parasites transform into gametes that fuse to form zygotes. Understanding the mechanisms that underlie formation of extracellular Babesia tick stages is an important step towards developing control strategies for preventing tick infection and subsequent parasite transmission.ResultsWe induced B. bigemina sexual stages in vitro by exposing parasites to Tris 2-carboxyethyl phosphine (TCEP). Subsequently, we identified a novel putative methyltransferase gene (BBBOND_0204030) that is expressed uniquely in all B. bigemina tick stages but not in blood stages. In vitro TCEP-exposed B. bigemina presented diverse morphology including parasites with long projections, round forms and clusters of round forms indicative of sexual stage induction. We confirmed the development of sexual stages by detecting upregulation of previously defined B. bigemina sexual stage marker genes, ccp2 and 3, and their respective protein expression in TCEP-induced B. bigemina cultures. Next, transcription analysis of in vitro TCEP-induced B. bigemina culture based on an in silico derived list of homologs of Plasmodium falciparum gamete-specific genes demonstrated differential expression of the gene BBBOND_0204030 in induced cells. Further examination of ex vivo infected ticks demonstrated that BBBOND_0204030 is transcribed by multiple stages of B. bigemina during parasite development in tick midgut, ovary and hemolymph. Interestingly, ex vivo results confirmed our in vitro observation that blood stages of B. bigemina do not express BBBOND_0204030 and validated the in vitro system of inducing sexual stages.ConclusionsHerein we describe the identification of a B. bigemina gene transcribed exclusively by parasites infecting ticks using a novel method of inducing B. bigemina sexual stages in vitro. We propose that this gene can be used as a marker for parasite development within the tick vector. Together, these tools will facilitate our understanding of parasite-tick interactions, the identification of novel vaccine targets and, consequently, the development of additional strategies to control bovine babesiosis.

Highlights

  • Bovine babesiosis is caused by apicomplexan pathogens of the genus Babesia such as B. bigemina and B. bovis

  • Babesia bigemina is more prevalent than other Babesia parasites because it is transmitted by several tick species including Rhipicephalus microplus, R. annulatus, R. appendiculatus, R. evertsi, Boophilus decoloratus and B. geigyi, as well as multiple stages of these ticks, including nymph and adult stages [1,2,3,4,5]

  • We describe the use of Tris 2-carboxyethyl phosphine (TCEP) to consistently induce B. bigemina sexual stages in vitro

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Summary

Introduction

Bovine babesiosis is caused by apicomplexan pathogens of the genus Babesia such as B. bigemina and B. bovis These tick-borne pathogens have a complex life-cycle involving asexual multiplication in vertebrate hosts and sexual reproduction in invertebrate vectors. Babesia bigemina and B. bovis are the main causative agents of cattle tick fever in tropical and subtropical regions. This disease has a negative economic impact on the cattle industry due to the cost of treatment, morbidity and mortality. Similar to Plasmodium spp., the causative agent of malaria, B. bigemina has a complex life-cycle, including asexual reproduction in the mammalian host and sexual reproduction in the tick host. The B. bigemina life-cycle in the mammalian host begins when infected nymphs or adults of the tick vector feed on a bovine. There remain fundamental knowledge gaps regarding the role of B. bigemina tick stage genes involved in parasite development within the arthropod vector

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