Antigenic Diversity in Theileria parva Populations From Sympatric Cattle and African Buffalo Analyzed Using Long Read Sequencing

East Coast fever (ECF) in cattle is caused by the Apicomplexan protozoan parasite Theileria parva, transmitted by the three-host tick Rhipicephalus appendiculatus. The African buffalo (Syncerus caffer) is the natural host for T. parva but does not suffer disease, whereas ECF is often fatal in cattle. The genetic relationship between T. parva populations circulating in cattle and buffalo is poorly understood, and has not been studied in sympatric buffalo and cattle. This study aimed to determine the genetic diversity of T. parva populations in cattle and buffalo, in an area where livestock co-exist with buffalo adjacent to the Serengeti National Park, Tanzania. Three T. parva antigens (Tp1, Tp4, and Tp16), known to be recognized by CD8+ and CD4+ T cells in immunized cattle, were used to characterize genetic diversity of T. parva in cattle (n = 126) and buffalo samples (n = 22). Long read (PacBio) sequencing was used to generate full or near-full length allelic sequences. Patterns of diversity were similar across all three antigens, with allelic diversity being significantly greater in buffalo-derived parasites compared to cattle-derived (e.g., for Tp1 median cattle allele count was 9, and 81.5 for buffalo), with very few alleles shared between species (8 of 651 alleles were shared for Tp1). Most alleles were unique to buffalo with a smaller proportion unique to cattle (412 buffalo unique vs. 231 cattle-unique for Tp1). There were indications of population substructuring, with one allelic cluster of Tp1 representing alleles found in both cattle and buffalo (including the TpM reference genome allele), and another containing predominantly only alleles deriving from buffalo. These data illustrate the complex interplay between T. parva populations in buffalo and cattle, revealing the significant genetic diversity in the buffalo T. parva population, the limited sharing of parasite genotypes between the host species, and highlight that a subpopulation of T. parva is maintained by transmission within cattle. The data indicate that fuller understanding of buffalo T. parva population dynamics is needed, as only a comprehensive appreciation of the population genetics of T. parva populations will enable assessment of buffalo-derived infection risk in cattle, and how this may impact upon control measures such as vaccination.

[1]  A. Musoke,et al.  Sequence diversity of cytotoxic T cell antigens and satellite marker analysis of Theileria parva informs the immunization against East Coast fever in Rwanda , 2020, Parasites & Vectors.

[2]  C. Sugimoto,et al.  Genetic Diversity and Sequence Polymorphism of Two Genes Encoding Theileria parva Antigens Recognized by CD8+ T Cells among Vaccinated and Unvaccinated Cattle in Malawi , 2020, Pathogens.

[3]  Olukemi O. Ifeonu,et al.  Capture-based enrichment of Theileria parva DNA enables full genome assembly of first buffalo-derived strain and reveals exceptional intra-specific genetic diversity , 2020, bioRxiv.

[4]  A. Nanteza,et al.  Antigen gene and variable number tandem repeat (VNTR) diversity in Theileria parva parasites from Ankole cattle in south-western Uganda: Evidence for conservation in antigen gene sequences combined with extensive polymorphism at VNTR loci. , 2020, Transboundary and emerging diseases.

[5]  W. Morrison,et al.  Theileria parva: a parasite of African buffalo, which has adapted to infect and undergo transmission in cattle , 2020, International journal for parasitology.

[6]  A. Djikeng,et al.  Genetic and antigenic variation of the bovine tick-borne pathogen Theileria parva in the Great Lakes region of Central Africa , 2019, Parasites & Vectors.

[7]  Olukemi O. Ifeonu,et al.  Re-annotation of the Theileria parva genome refines 53% of the proteome and uncovers essential components of N-glycosylation, a conserved pathway in many organisms , 2019, BMC Genomics.

[8]  M. Simuunza,et al.  Diversity of two Theileria parva CD8+ antigens in cattle and buffalo-derived parasites in Tanzania. , 2019, Ticks and tick-borne diseases.

[9]  S. Cleaveland,et al.  Waves of endemic foot-and-mouth disease in eastern Africa suggest feasibility of proactive vaccination approaches , 2018, Nature Ecology & Evolution.

[10]  W. Weir,et al.  Ancient diversity and geographical sub-structuring in African buffalo Theileria parva populations revealed through metagenetic analysis of antigen-encoding loci☆ , 2018, International journal for parasitology.

[11]  O. Hanotte,et al.  The genome landscape of indigenous African cattle , 2017, Genome Biology.

[12]  Paolo Piazza,et al.  Comprehensive comparison of Pacific Biosciences and Oxford Nanopore Technologies and their applications to transcriptome analysis , 2017, F1000Research.

[13]  W. Weir,et al.  The African buffalo parasite Theileria. sp. (buffalo) can infect and immortalize cattle leukocytes and encodes divergent orthologues of Theileria parva antigen genes , 2015, International journal for parasitology. Parasites and wildlife.

[14]  George P. Omondi,et al.  Exposure of vaccinated and naive cattle to natural challenge from buffalo-derived Theileria parva , 2015, International journal for parasitology. Parasites and wildlife.

[15]  R. Skilton,et al.  Genetic and antigenic diversity of Theileria parva in cattle in Eastern and Southern zones of Tanzania. A study to support control of East Coast fever , 2014, Parasitology.

[16]  T. Abe,et al.  Whole-Genome Sequencing of Theileria parva Strains Provides Insight into Parasite Migration and Diversification in the African Continent , 2013, DNA research : an international journal for rapid publication of reports on genes and genomes.

[17]  U. Certa,et al.  High-resolution genotyping and mapping of recombination and gene conversion in the protozoan Theileria parva using whole genome sequencing , 2012, BMC Genomics.

[18]  V. Radeloff,et al.  Land-cover change and human population trends in the greater Serengeti ecosystem from 1984–2003 , 2012 .

[19]  W. Weir,et al.  Escape from CD8+ T Cell Response by Natural Variants of an Immunodominant Epitope from Theileria parva Is Predominantly Due to Loss of TCR Recognition , 2011, The Journal of Immunology.

[20]  A. Tait,et al.  Theileria parva genetic diversity and haemoparasite prevalence in cattle and wildlife in and around Lake Mburo National Park in Uganda , 2011, Parasitology Research.

[21]  D. McKeever,et al.  Construction of a genetic map for Theileria parva: Identification of hotspots of recombination , 2011, International journal for parasitology.

[22]  Joana C. Silva,et al.  Two Theileria parva CD8 T Cell Antigen Genes Are More Variable in Buffalo than Cattle Parasites, but Differ in Pattern of Sequence Diversity , 2011, PloS one.

[23]  W. Weir,et al.  Haemoparasite prevalence and Theileria parva strain diversity in Cape buffalo (Syncerus caffer) in Uganda. , 2011, Veterinary parasitology.

[24]  J. Rushton,et al.  Assessing the impact of East Coast Fever immunisation by the infection and treatment method in Tanzanian pastoralist systems. , 2010, Preventive veterinary medicine.

[25]  J. Sunter,et al.  A nested PCR assay exhibits enhanced sensitivity for detection of Theileria parva infections in bovine blood samples from carrier animals , 2010, Parasitology Research.

[26]  D. McKeever,et al.  CD8+ T-cell responses to Theileria parva are preferentially directed to a single dominant antigen: Implications for parasite strain-specific immunity , 2009, European Journal of Immunology.

[27]  D. Knowles,et al.  Quantification of Theileria parva in Rhipicephalus appendiculatus (Acari: Ixodidae) Confirms Differences in Infection Between Selected Tick Strains , 2009, Journal of medical entomology.

[28]  G. Di Giulio,et al.  Live immunization against East Coast fever--current status. , 2009, Trends in parasitology.

[29]  D. McKeever,et al.  Characterization of the Fine Specificity of Bovine CD8 T-Cell Responses to Defined Antigens from the Protozoan Parasite Theileria parva , 2007, Infection and Immunity.

[30]  D. McKeever,et al.  Current status of vaccine development against Theileria parasites , 2006, Parasitology.

[31]  N. J. Tonukari,et al.  Theileria parva candidate vaccine antigens recognized by immune bovine cytotoxic T lymphocytes. , 2006, Proceedings of the National Academy of Sciences of the United States of America.

[32]  A. Tait,et al.  Population genetic analysis and sub-structuring of Theileria parva in Uganda. , 2005, Molecular and biochemical parasitology.

[33]  Daniel G. Bradley,et al.  African Pastoralism: Genetic Imprints of Origins and Migrations , 2002, Science.

[34]  R. Bishop,et al.  The persistence of Theileria parva infection in cattle immunized using two stocks which differ in their ability to induce a carrier state: analysis using a novel blood spot PCR assay , 2002, Parasitology.

[35]  J. McDermott,et al.  Differences in the epidemiology of theileriosis on smallholder dairy farms in contrasting agro-ecological and grazing strata of highland Kenya , 2000, Epidemiology and Infection.

[36]  S. Kemp,et al.  Parasite strain specificity of bovine cytotoxic T cell responses to Theileria parva is determined primarily by immunodominance. , 1995, Journal of immunology.

[37]  W. Morrison,et al.  Parasite strain specificity of precursor cytotoxic T cells in individual animals correlates with cross-protection in cattle challenged with Theileria parva , 1995, Infection and immunity.

[38]  R. Bishop,et al.  Molecular characterization of Theileria parasites: application to the epidemiology of theileriosis in Zimbabwe , 1994, Parasitology.

[39]  D. Stagg,et al.  Transformation of Theileria parva derived from African buffalo (Syncerus caffer) by tick passage in cattle and its use in infection and treatment immunization. , 1992, Veterinary parasitology.

[40]  C. Mpangala,et al.  Exposure of Ankole and crossbred cattle to theileriosis in Rwanda , 1991, Tropical Animal Health and Production.

[41]  D. McKeever,et al.  Theileria parva: the nature of the immune response and its significance for immunoprophylaxis. , 1990, Revue scientifique et technique.

[42]  C. O'Callaghan,et al.  Characterization of buffalo-derived theilerial parasites with monoclonal antibodies and DNA probes , 1989, Parasitology.

[43]  J. Grootenhuis,et al.  Evaluation of cytotoxic lymphocytes and their parasite strain specificity from African buffalo infected with Theileria parva , 1988, Parasite immunology.

[44]  E. Taracha,et al.  Effect of timing and intensity of challenge following immunization against East Coast fever. , 1987, Veterinary parasitology.

[45]  M. P. Cunningham,et al.  Maintenance of Theileria parva parva infection in an endemic area of Kenya , 1986, Parasitology.

[46]  J. Grootenhuis,et al.  Further studies on the immunization of cattle against Theileria lawrencei by infection and chemoprophylaxis , 1979 .

[47]  J. Bier [Immunology of infections]. , 1978, Deutsche zahnarztliche Zeitschrift.

[48]  M. P. Cunningham,et al.  Exposure of immunized cattle to prolonged natural challenge of Theileria lawrencei derived from African buffalo (Syncerus caffer) , 1977 .

[49]  G. Uilenberg,et al.  Studies on Theileriidae (Sporozoa) in Tanzania. VIII. Experiments with African buffalo (Syncerus caffer). , 1977, Tropenmedizin und Parasitologie.

[50]  G. Uilenberg,et al.  Studies on Theileriidae (Sporozoa) in Tanzania. I. Tick transmission of Haematoxenus veliferus. , 1976, Tropenmedizin und Parasitologie.

[51]  M. P. Cunningham,et al.  East coast fever: 3. Chemoprophylactic immunization of cattle using oxytetracycline and a combination of theilerial strains , 1975 .

[52]  M. J. Burridge,et al.  East coast fever: 1. Chemoprophylactic immunization of cattle against Theileria parva (Muguga) and five theilerial strains , 1975 .

[53]  M. J. Burridge,et al.  East coast fever: 2. Cross-immunity trials with a Kenya strain of Theileria lawrencei , 1975 .

[54]  A. Young,et al.  Transmission ofTheileria lawrencei (Serengeti) by the ixodid tick,Rhipicephalus appendiculatus , 1973, Tropical Animal Health and Production.

[55]  S. Morzaria,et al.  Duration of immunity to East Coast fever (Theileria parva infection of cattle) , 1972, Parasitology.

[56]  D. W. Brocklesby,et al.  The Passage of “ Theileria Lawrencei (Kenya)” Through Cattle 1 1This paper is based on part of a thesis submitted by D. W. B. to the University of Zurich for the degree of Dr. Vet. Med. , 1966 .

[57]  G. Scott,et al.  Morbidity and Mortality Rates in East Coast Fever (Theileria Parva Infection) and their Application to Drug Screening Procedures , 1961 .

[58]  K. Au,et al.  Comprehensive comparison of Pacific Biosciences and Oxford Nanopore Technologies and their applications to transcriptome analysis. , 2017, F1000Research.

[59]  S. Cleaveland,et al.  Patterns of Foot-and-Mouth Disease Virus Distribution in Africa: The Role of Livestock and Wildlife in Virus Emergence , 2014 .

[60]  D. McKeever,et al.  Immunology of infections with Theileria parva in cattle. , 1998, Chemical immunology.

[61]  W. Brown,et al.  Theileria parva in cattle , 1989 .

[62]  D. Radley Infection and Treatment Method of Immunization Against Theileriosis , 1981 .

[63]  J. Wilde East Coast fever. , 1967, Advances in veterinary science.