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Theileria taurotragi infection

Theileria taurotragi infection

Previous Authors: J A LAWRENCE AND S M WILLIAMSON

Current Authors:
J A LAWRENCE - Extraordinary Professor, DPhil, BSc, MRCVS (ret.), DTVM, Department of Paraclinical Veterinary Science, University of Zimbabwe, Harare, Zimbabwe 
B J MANS - Principal Researcher, BSc, BSc (Hons) Biochemistry, MSc (Biochemistry), PhD (Biochemistry), Agricultural Research Council, Onderstepoort Veterinary Research, 100 Old Soutpan Road, Pretoria, Gauteng, 0110, South Africa

Introduction

Theileria taurotragi was first described by Martin and Brocklesby19 in 1960, under the name Cytauxzoon taurotragi, as a benign parasite of the eland (Taurotragus oryx). It was subsequently demonstrated that the parasite was readily transmissible to the ox, in which it caused a transient febrile reaction,35 and it became clear that T. taurotragi was one of the benign theilerial parasites of cattle which had been known collectively as Theileria mutans since the beginning of the twentieth century.31 The disease it causes was first described by Neitz22 in 1957, when it was mistaken for a mild form of T. mutans infection transmitted by Rhipicephalus appendiculatus. The parasite is widely distributed through eastern and southern Africa, and in addition to the ox and the eland it will infect sheep and goats under experimental conditions but does not produce piroplasms.22, 33 It  also infects cell lines from a number of other species of Bovidae in vitro.30 The main significance of Theileria taurotragi is the confusion that it causes in the differential diagnosis of mild reactions to Theileria parva, although it can occasionally be responsible for cases of cerebral theileriosis (Turning sickness). Theileria parva and T. taurotragi both utilise the same tick vector, Rhipicephalus appendiculatus, and antibodies to T. taurotragi cross-react in the T. parva immunofluorescent antibody test (IFAT) 17, which has complicated epidemiological studies on T. parva.

Aetiology and life cycle

The morphological and biological characteristics of T. taurotragi are generally similar to those of T. parva, but the ultrastruture of the merozoites in bovine brain is different 6. In the eland, bars and veils found in the erythrocytes are associated with the piroplasms, 36 but these structures are not present in the ox. The parasite is transmitted by R. appendiculatus and Rhipicephalus evertsi evertsi, 32 Rhipicephalus pulchellus4 and Rhipicephalus zambeziensis.14 Recovered cattle remain carriers for at least 11 months.13 The schizonts stimulate transformation of host cells to a limited extent, but the target cells have not been identified. The schizonts can be cultured in vitro in lymphoblasts, as with T. parva.29 Infection can be transmitted readily between cattle by intravenous inoculation of 100 ml of blood, which suggests that intra-erythrocytic division and invasion of new erythrocytes occurs.9

Epidemiology

Theileria taurotragi has been recorded from eastern, central and southern Africa and has been confirmed with molecular methods in Botswana 2, 21, 23, Kenya, Mozambique 20, Nigeria 16, Rwanda 1, South Africa 37, Sudan 28, Tanzania 6, Uganda 24, 25, Zambia 12 and Zimbabwe 1. This corresponds with the range of R. appendiculatus, but its other vector ticks are also found throughout this region 34. Theileria parva also occurs in most of these areas, indicating an overlap in geographic distribution.  Reverse line blot analysis has allowed estimations of prevalence for T. taurotragi, which may be as high as 76% 24. Older cattle generally have a higher prevalence, reflecting infection over time; indigenous cattle breeds seem to be more resistant to infection than exotic or cross-breeds; and cattle grazing inside wildlife reserves have a higher prevalence compared to cattle grazing outside, as a result of contact with eland, which show higher levels of infection than cattle 24. Theileria taurotragi seems to be cattle and eland specific, although it has also been detected in bushbuck (Tragelaphus sylvaticus) in Uganda 24. Extensive screening of African buffalo (Syncerus caffer) has not detected T. taurotragi to date 18, 24, 26.  A single report of the detection of T. taurotragi in four African buffalo, used a multiplex real-time PCR, could not be confirmed with sequencing 7.  While mixed infections of T. parva and T. taurotragi in cattle are common where parasites are sympatric, this is probably due to maintenance of both parasites in cattle or the overlap in geographic distribution of African buffalo and eland 15.

Clinical signs

Infection of cattle with T. taurotragi results in a mild febrile reaction of 1 to 14 days’ duration commencing after an incubation period of 10 to 21 days.5, 13 Slight enlargement of superficial lymph nodes, especially the parotid lymph nodes draining the ears on which infected ticks have fed, is present, but there is no evidence of anorexia or other clinical signs. Toxicosis, resulting from heavy infestation with R. appendiculatus, exhibits similar signs and may occur with and overshadow the reaction to the Theileria. The parasite may occasionally cause nervous signs associated with cerebral infarction (Turning sickness).

Infection in sheep is benign. In eland the parasite sometimes causes severe or fatal disease.10

Pathogenesis and pathology

Theileria taurotragi stimulates lymphoid proliferation in the same way as T. parva, but to a very limited extent. Enlargement of lymph nodes is the only lesion to be expected, except in the case of cerebral infarction.

Diagnosis and differential diagnosis

Theileria taurotragi infection may be suspected when a mild febrile reaction, with enlargement of superficial lymph nodes, occurs in cattle exposed to Rhipicephalus infestation, and schizonts are demonstrated in lymph node smears.

Differentiation of infection with T. taurotragi from infection with T. parva has been discussed previously in relation to East Coast fever (East Coast fever) and turning sickness (Turning sickness). The T. parva-specific enzyme-linked immunosorbent assay (ELISA), unlike the IFAT, does not suffer from cross-reactions with antibodies to T. taurotragi, and several immunological and molecular tools exist which can distinguish the two parasites. For example, one of the anti-schizont monoclonal antibodies in the monoclonal antibody panel used to characterize cell cultures of isolates of Theileria reacts exclusively with T. taurotragi.3 Reverse line blot analysis can distinguish between T. parva and T. taurotragi and detect co-infections 11.  When T. parva infection needs to be differentiated, a variety of specific conventional or real-time PCR assays can be used to exclude its presence 17.

Control

As T. taurotragi is usually a benign parasite, there are no indications for its treatment or control.

References

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