Abstract

Simple SummaryWe review the efforts to develop a vaccine against neosporosis, caused by the apicomplexan parasite Neospora caninum. Vertical transmission is the main mode of infection, and can lead to stillbirth, abortion, or birth of weak calves. We provide information on the biology of Neospora caninum and on the disease caused by this parasite, and summarize the current understanding on how the host deals with infection. We review studies on live- and subunit-vaccines, and demonstrate advantages and setbacks in the use of small laboratory animal models in investigations on a disease with high relevance in cattle.Neosporosis, caused by the apicomplexan parasite Neospora caninum, represents one of the economically most important causes of abortion in cattle. During pregnancy, the parasite infects the placental tissue and the fetus, which can lead to stillbirth, abortion, or birth of weak calves. Alternatively, calves are born without clinical symptoms, but they can carry over the parasite to the next generation. In addition, N. caninum causes neuromuscular disease in dogs. The economic importance of neosporosis has prompted researchers to invest in the development of measures to prevent infection of cattle by vaccination. A good vaccine must stimulate protective cellular immune responses as well as antibody responses at mucosal sites and, systemically, must activate T-helper cells to produce relevant cytokines, and must elicit specific antibodies that aid in limiting parasite proliferation, e.g., by interference with host cell invasion, activation of complement, and/or opsonization of parasites to have them killed by macrophages. Different types of vaccines have been investigated, either in bovines or in the mouse model. These include live vaccines such as naturally less virulent isolates of N. caninum, attenuated strains generated by irradiation or chemical means, or genetically modified transgenic strains. Live vaccines were shown to be very effective; however, there are serious disadvantages in terms of safety, costs of production, and stability of the final product. Subunit vaccines have been intensively studied, as they would have clear advantages such as reduced costs in production, processing and storage, increased stability and shelf life. The parasite antigens involved in adhesion and invasion of host cells, such as surface constituents, microneme-, rhoptry- and dense granule-components represent interesting targets. Subunit vaccines have been applied as bacterially expressed recombinant antigens or as DNA vaccines. Besides monovalent vaccines also polyvalent combinations of different antigens have been used, providing increased protection. Vaccines have been combined with immunostimulating carriers and, more recently, chimeric vaccines, incorporating immuno-relevant domains of several antigens into a single protein, have been developed.

Highlights

  • Neospora caninum is an apicomplexan, which belongs to the family of Sarcocystidae

  • Neospora caninum is the causative agent of neosporosis, a serious illness associated with abortion, stillbirth and maternal infertility in cattle and neurological disease in dogs

  • The first hint that an approach employing a complex mixture of antigens could confer protection against neosporosis was provided by Liddell et al [45], which showed that immunization with a killed tachyzoite lysate prevented fetal infection in Balb/c mice

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Summary

Introduction

Neospora caninum is an apicomplexan, which belongs to the family of Sarcocystidae. The parasite is distributed worldwide and infects a broad range of animals including cattle, sheep, goats, deer, horses and dogs. In an immune-competent host, tachyzoites are attacked and largely eliminated by the host immune response, and this could be one of the factors which trigger stage conversion to the bradyzoite stage [16] In special situations, such as pregnancy, recrudescence can occur, bradyzoites get reactivated, and the loss of an efficient Th-1 response of a pregnant dam can lead to limited suppression of the cell mediated immunity which normally keeps tachyzoite proliferation in check [16]. This temporary break in host immunity, which normally does not cause clinical disease in the dam, can lead to transplacental infection of the fetus and abortion

Neosporosis
Vaccines Against Neosporosis
Parasite Antigens Involved in Host Cell Invasion as Potential Vaccine Targets
Killed Tachyzoite Lysates
Live-Attenuated Vaccines
Subunit Vaccines
Chimeric Vaccines
Findings
Conclusions

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