Abstract

BackgroundEast Coast fever (ECF) is a devastating disease of cattle and a significant constraint to improvement of livestock production in sub-Saharan Africa. The protozoan parasite causing ECF, Theileria parva, undergoes obligate sexual stage development in its tick vector Rhipicephalus appendiculatus. Tick-borne acquisition and transmission occurs transstadially; larval and nymphal ticks acquire infection while feeding and transmit to cattle when they feed after molting to the next stage. Much of the current knowledge relating to tick-borne acquisition and transmission of T. parva has been derived from studies performed during acute infections where parasitemia is high. In contrast, tick-borne transmission during the low-level persistent infections characteristic of endemic transmission cycles is rarely studied.MethodsCattle were infected with one of two stocks of T. parva (Muguga or Marikebuni). Four months post-infection when parasites were no longer detectable in peripheral blood by PCR, 500 R. appendiculatus nymphs were fed to repletion on each of the cattle. After they molted to the adult stage, 20 or 200 ticks, respectively, were fed on two naïve cattle for each of the parasite stocks. After adult ticks fed to repletion, cattle were tested for T. parva infection by nested PCR and dot blot hybridization.ResultsOnce they had molted to adults the ticks that had fed as nymphs on Muguga and Marikebuni infected cattle successfully transmitted Theileria parva to all naïve cattle, even though T. parva infection was not detectable by nested PCR on salivary gland genomic DNA of a sample of individual ticks. However, a salivary gland homogenate from a single Marikebuni infected tick was able to infect primary bovine lymphocytes. Infection was detected by nested p104 PCR in 3 of 4 calves and detected in all 4 calves by T. parva 18S nested PCR/dot blot hybridization.ConclusionWe show that R. appendiculatus ticks are able to acquire T. parva parasites from infected cattle even in the absence of detectable parasitemia. Although infection was undetectable in a sample of individual ticks, cumulatively as few as 20 ticks were able to transmit T. parva to naïve cattle. These results have important implications for our understanding of T. parva transmission by R. appendiculatus in ECF endemic regions.

Highlights

  • East Coast fever (ECF) is a devastating disease of cattle and a significant constraint to improvement of livestock production in sub-Saharan Africa

  • Acute infection of cattle with Theileria parva causes a severe lympho-proliferative disease known as East Coast fever (ECF), one of the most significant tick-borne diseases of cattle in Africa [1,2,3]

  • In order to better understand the natural transmission dynamics that cattle might experience in the field we investigated the ability of R. appendiculatus ticks to transmit either the Muguga or the Marikebuni stock parasites to naïve cattle after feeding on persistently infected animals with no detectable parasitemia

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Summary

Introduction

East Coast fever (ECF) is a devastating disease of cattle and a significant constraint to improvement of livestock production in sub-Saharan Africa. The protozoan parasite causing ECF, Theileria parva, undergoes obligate sexual stage development in its tick vector Rhipicephalus appendiculatus. Much of the current knowledge relating to tick-borne acquisition and transmission of T. parva has been derived from studies performed during acute infections where parasitemia is high. Acute infection of cattle with Theileria parva causes a severe lympho-proliferative disease known as East Coast fever (ECF), one of the most significant tick-borne diseases of cattle in Africa [1,2,3]. Transmission of T. parva to domestic cattle occurs during the feeding of the infected tick vector, Rhipicephalus appendiculatus. Theileria parva sporozoites are released, together with saliva, from tick salivary glands into the feeding site where they infect bovine lymphocytes and develop into the schizont stage, transforming the cells leading to a clonal expansion of schizont-infected lymphocytes. The persistent infectious state is thought to be maintained through the slow continuous proliferation of schizont-infected cells, events governing this process, or where the schizont infected cells reside are poorly understood [1]

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