The major goals of veterinary vaccines are to improve the health and welfare of companion animals, increase production of livestock in a cost-effective manner, and prevent animal-to-human transmission from both domestic animals and wildlife. These diverse aims have led to different approaches to the development of veterinary vaccines from crude but effective whole-pathogen preparations to molecularly defined subunit vaccines, genetically engineered organisms or chimeras, vectored antigen formulations, and naked DNA injections. The final successful outcome of vaccine research and development is the generation of a product that will be available in the marketplace or that will be used in the field to achieve desired outcomes. As detailed in this review, successful veterinary vaccines have been produced against viral, bacterial, protozoal, and multicellular pathogens, which in many ways have led the field in the application and adaptation of novel technologies. These veterinary vaccines have had, and continue to have, a major impact not only on animal health and production but also on human health through increasing safe food supplies and preventing animal-to-human transmission of infectious diseases. The continued interaction between animals and human researchers and health professionals will be of major importance for adapting new technologies, providing animal models of disease, and confronting new and emerging infectious diseases.

Current Status of Veterinary Vaccines

Babesia bovis is an apicomplexan tick-transmitted pathogen of cattle imposing a global risk and severe constraints to livestock health and economic development. The complete genome sequence was undertaken to facilitate vaccine antigen discovery, and to allow for comparative analysis with the related apicomplexan hemoprotozoa Theileria parva and Plasmodium falciparum. At 8.2 Mbp, the B. bovis genome is similar in size to that of Theileria spp. Structural features of the B. bovis and T. parva genomes are remarkably similar, and extensive synteny is present despite several chromosomal rearrangements. In contrast, B. bovis and P. falciparum, which have similar clinical and pathological features, have major differences in genome size, chromosome number, and gene complement. Chromosomal synteny with P. falciparum is limited to microregions. The B. bovis genome sequence has allowed wide scale analyses of the polymorphic variant erythrocyte surface antigen protein (ves1 gene) family that, similar to the P. falciparum var genes, is postulated to play a role in cytoadhesion, sequestration, and immune evasion. The ∼150 ves1 genes are found in clusters that are distributed throughout each chromosome, with an increased concentration adjacent to a physical gap on chromosome 1 that contains multiple ves1-like sequences. ves1 clusters are frequently linked to a novel family of variant genes termed smorfs that may themselves contribute to immune evasion, may play a role in variant erythrocyte surface antigen protein biology, or both. Initial expression analysis of ves1 and smorf genes indicates coincident transcription of multiple variants. B. bovis displays a limited metabolic potential, with numerous missing pathways, including two pathways previously described for the P. falciparum apicoplast. This reduced metabolic potential is reflected in the B. bovis apicoplast, which appears to have fewer nuclear genes targeted to it than other apicoplast containing organisms. Finally, comparative analyses have identified several novel vaccine candidates including a positional homolog of p67 and SPAG-1, Theileria sporozoite antigens targeted for vaccine development. The genome sequence provides a greater understanding of B. bovis metabolism and potential avenues for drug therapies and vaccine development.

/pdf/genome-sequence-of-babesia-bovis-and-comparative-analysis-of-3cqfocverm.pdf

Genome sequence of Babesia bovis and comparative analysis of apicomplexan hemoprotozoa.

/pdf/evolution-and-genetic-diversity-of-theileria-3qwo7vmygl.pdf

Evolution and genetic diversity of Theileria.

A review of reverse vaccinology approaches for the development of vaccines against ticks and tick borne diseases.

The evolution of Antarctic climate from a Cretaceous greenhouse into the Neogene icehouse is captured within a rich record of fossil leaves, wood, pollen, and flowers from the Antarctic Peninsula and the Transantarctic Mountains. About 85 million years ago, during the mid-Late Cretaceous, flowering plants thrived in subtropical climates in Antarctica. Analysis of their leaves and flowers, many of which were ancestors of plants that live in the tropics today, indicates that summer temperatures averaged 20°C during this global thermal maximum. After the Paleocene (~60 Ma) warmth-loving plants gradually lost their place in the vegetation and were replaced by floras dominated by araucarian conifers (monkey puzzles) and the southern beech Nothofagus, which tolerated freezing winters. Plants hung on tenaciously in high latitudes, even after ice sheets covered the land, and during periods of interglacial warmth in the Neogene small dwarf plants survived in tundra-like conditions within 500 km of the South Pole.

/pdf/100-million-years-of-antarctic-climate-evolution-evidence-aa8ec1qkqa.pdf

100 Million Years of Antarctic Climate Evolution: Evidence from Fossil Plants

East Coast fever, caused by the tick-borne intracellular apicomplexan parasite Theileria parva, is a highly fatal lymphoproliferative disease of cattle. The pathogenic schizont-induced lymphocyte transformation is a unique cancer-like condition that is reversible with parasite removal. Schizont-infected cell-directed CD8(+) cytotoxic T lymphocytes (CTL) constitute the dominant protective bovine immune response after a single exposure to infection. However, the schizont antigens targeted by T. parva-specific CTL are undefined. Here we show the identification of five candidate vaccine antigens that are the targets of MHC class I-restricted CD8(+) CTL from immune cattle. CD8(+) T cell responses to these antigens were boosted in T. parva-immune cattle resolving a challenge infection and, when used to immunize naive cattle, induced CTL responses that significantly correlated with survival from a lethal parasite challenge. These data provide a basis for developing a CTL-targeted anti-East Coast fever subunit vaccine. In addition, orthologs of these antigens may be vaccine targets for other apicomplexan parasites.

https://www.pnas.org/content/pnas/103/9/3286.full.pdf

Theileria parva candidate vaccine antigens recognized by immune bovine cytotoxic T lymphocytes

Exploiting host immunity and parasite genomics to develop a robust sub-unit vaccine against East Coast fever in cattle - where are we?

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Theileria parva candidate vaccine antigens recognized by immune bovine cytotoxic T lymphocytes

Exploiting host immunity and parasite genomics to develop a robust sub-unit vaccine against East Coast fever in cattle - where are we?