Effect of intermittent oral administration of ponazuril on experimental Sarcocystis neurona infection of horses

Robert J. MacKay Department of Large Animal Clinical Sciences, University of Florida, Gainesville, FL 32610.

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Susan T. Tanhauser Department of Large Animal Clinical Sciences, University of Florida, Gainesville, FL 32610.

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Karen D. Gillis Department of Large Animal Clinical Sciences, University of Florida, Gainesville, FL 32610.

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Ian G. Mayhew Department of Veterinary Clinical Studies, Easter Bush Veterinary Centre, University of Edinburgh, Roslin, Midlothian EH25 9RG, Scotland.

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Tom J. Kennedy Bayer Animal Health, Merriam, KS 66202.

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 PhD

Abstract

Objective—To evaluate the effect of intermittent oral administration of ponazuril on immunoconversion against Sarcocystis neurona in horses inoculated intragastrically with S neurona sporocysts.

Animals—20 healthy horses that were seronegative for S neurona–specific IgG.

Procedures—5 control horses were neither inoculated with sporocysts nor treated. Other horses (5 horses/group) each received 612,500 S neurona sporocysts via nasogastric tube (day 0) and were not treated or were administered ponazuril (20 mg/kg, PO) every 7 days (beginning on day 5) or every 14 days (beginning on day 12) for 12 weeks. Blood and CSF samples were collected on day – 1 and then every 14 days after challenge for western blot assessment of immunoconversion. Clinical signs of equine protozoal myeloencephalitis (EPM) were monitored, and tissues were examined histologically after euthanasia.

Results—Sera from all challenged horses yielded positive western blot results within 56 days. Immunoconversion in CSF was detected in only 2 of 5 horses that were treated weekly; all other challenged horses immunoconverted within 84 days. Weekly administration of ponazuril significantly reduced the antibody response against the S neurona 17-kd antigen in CSF. Neurologic signs consistent with EPM did not develop in any group; likewise, histologic examination of CNS tissue did not reveal protozoa or consistent degenerative or inflammatory changes.

Conclusions and Clinical Relevance—Administration of ponazuril every 7 days, but not every 14 days, significantly decreased intrathecal anti–S neurona antibody responses in horses inoculated with S neurona sporocysts. Protocols involving intermittent administration of ponazuril may have application in prevention of EPM.

Abstract

Objective—To evaluate the effect of intermittent oral administration of ponazuril on immunoconversion against Sarcocystis neurona in horses inoculated intragastrically with S neurona sporocysts.

Animals—20 healthy horses that were seronegative for S neurona–specific IgG.

Procedures—5 control horses were neither inoculated with sporocysts nor treated. Other horses (5 horses/group) each received 612,500 S neurona sporocysts via nasogastric tube (day 0) and were not treated or were administered ponazuril (20 mg/kg, PO) every 7 days (beginning on day 5) or every 14 days (beginning on day 12) for 12 weeks. Blood and CSF samples were collected on day – 1 and then every 14 days after challenge for western blot assessment of immunoconversion. Clinical signs of equine protozoal myeloencephalitis (EPM) were monitored, and tissues were examined histologically after euthanasia.

Results—Sera from all challenged horses yielded positive western blot results within 56 days. Immunoconversion in CSF was detected in only 2 of 5 horses that were treated weekly; all other challenged horses immunoconverted within 84 days. Weekly administration of ponazuril significantly reduced the antibody response against the S neurona 17-kd antigen in CSF. Neurologic signs consistent with EPM did not develop in any group; likewise, histologic examination of CNS tissue did not reveal protozoa or consistent degenerative or inflammatory changes.

Conclusions and Clinical Relevance—Administration of ponazuril every 7 days, but not every 14 days, significantly decreased intrathecal anti–S neurona antibody responses in horses inoculated with S neurona sporocysts. Protocols involving intermittent administration of ponazuril may have application in prevention of EPM.

Contributor Notes

Dr. Tanhauser's present address is Newberry Equine Veterinary Service, 1210 SW 218th St, Newberry, FL 32669.

Dr. Gillis' present address is Environmental Health and Safety, University of Florida, Gainesville, FL 32611.

Dr. Mayhew's present address is Institute of Veterinary, Animal and Biomedical Sciences, Massey University, Palmerston North, New Zealand.

Dr. Kennedy's present address is Farnam Companies, 3851 N 28th St, Phoenix, AZ 85013.

Supported by Bayer Animal Health.

Address correspondence to Dr. MacKay.
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