Characterization of a Sarcocystis neurona isolate (SN6) from a naturally infected horse from Oregon.
Abstract: An isolate of Sarcocystis neurona (SN6) was obtained from the spinal cord of a horse from Oregon with neurologic signs. The parasite was isolated in cultures of bovine monocytes and equine spleen cells. The parasite divided by endopolygeny and completed at least one asexual cycle in cell cultures in three days. Two gamma interferon knockout mice inoculated with cell culture-derived merozoites became ill 35 d later and S. neurona schizonts and merozoites were found in encephalitic lesions. The parasite in tissue sections of mice reacted with S. neurona-specific antibodies and S. neurona was reisolated from the brain of knockout mice.
Publication Date: 1999-10-16 PubMed ID: 10519218DOI: 10.1111/j.1550-7408.1999.tb06067.xGoogle Scholar: Lookup
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- Case Reports
- Journal Article
- Animal Health
- Cell Culture
- Clinical Pathology
- Diagnosis
- Disease
- Disease Diagnosis
- Equine Diseases
- Equine Health
- Equine Protozoal Myeloencephalitis
- Experimental Methods
- Genetics
- Horses
- Immunology
- Infection
- Infectious Disease
- Neurological Diseases
- Parasites
- Sarcocystis
- Veterinary Care
- Veterinary Medicine
- Veterinary Research
Summary
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The research article covers the study of the isolation of a Sarcocystis neurona (SN6) parasite from the spinal cord of a neurologically impaired horse from Oregon. The parasite was cultured in bovine monocytes and equine spleen cells, and was later found in the lesions of gamma interferon knockout mice.
Introduction
Sarcocystis neurona is a parasite often linked to severe neurological diseases in horses. The study primarily focuses on the identification and isolation of a particular isolate of this parasite, SN6, from a horse displaying neurological signs.
Isolation and Culture of The Parasite
- The SN6 isolate was extracted from the spinal cord of the affected horse from Oregon.
- It was then placed in cultures of bovine monocytes (a type of white blood cell) and equine spleen cells for growth and multiplication.
Parasite Reproduction Study
- The parasite’s reproduction process was then observed, through a process known as endopolygeny, where one parent cell multiplies into many.
- This process was found to complete at least one asexual cycle in cell cultures in three days, providing an insight into the replication dynamics of the parasite.
Transmission to Mice
- Post the observation in cell culture, the parasite was then introduced to gamma interferon knockout mice, to investigate the transmission process.
- The mice, inoculated with merozoites (a form of the parasite) derived from the cell culture, showed signs of illness 35 days post the introduction.
- Post-mortem examination of the affected mice revealed the presence of S. neurona schizonts and merozoites within lesions in the brain, confirming the transmissibility of the parasites.
Confirmation of The Parasite
- The infiltrated tissue sections of the mice brains reacted with S. neurona-specific antibodies, confirming the identity of the parasite.
- Further, S. neurona was also reisolated from the brain of the affected mice, providing an additional confirmation of the parasite’s presence and its replicative continuity within a host.
Cite This Article
APA
Dubey JP, Mattson DE, Speer CA, Baker RJ, Mulrooney DM, Tornquist SJ, Hamir AN, Gerros TC.
(1999).
Characterization of a Sarcocystis neurona isolate (SN6) from a naturally infected horse from Oregon.
J Eukaryot Microbiol, 46(5), 500-506.
https://doi.org/10.1111/j.1550-7408.1999.tb06067.x Publication
Researcher Affiliations
- United States Department of Agriculture, Agricultural Research Service, Beltsville Agricultural Research Center, Maryland 20705-2350, USA. Jdubey@lpsi.barc.usda.gov
MeSH Terms
- Animals
- Cattle
- Cells, Cultured
- Encephalomyelitis / parasitology
- Encephalomyelitis / veterinary
- Horse Diseases / parasitology
- Horses / parasitology
- Immunoblotting
- Immunocompromised Host
- Male
- Mice
- Oregon
- Rabbits
- Sarcocystis / growth & development
- Sarcocystis / isolation & purification
- Sarcocystis / pathogenicity
- Sarcocystosis / parasitology
- Sarcocystosis / veterinary
- Spinal Cord / parasitology
Citations
This article has been cited 4 times.- Ojo KK, Dangoudoubiyam S, Verma SK, Scheele S, DeRocher AE, Yeargan M, Choi R, Smith TR, Rivas KL, Hulverson MA, Barrett LK, Fan E, Maly DJ, Parsons M, Dubey JP, Howe DK, Van Voorhis WC. Selective inhibition of Sarcocystis neurona calcium-dependent protein kinase 1 for equine protozoal myeloencephalitis therapy. Int J Parasitol 2016 Dec;46(13-14):871-880.
- Verma SK, Lindsay DS, Rosenthal BM, Dubey JP. Ancient, globally distributed lineage of Sarcocystis from sporocysts of the Eastern rat snake (Pantherophis alleghaniensis) and its relation to neurological sequalae in intermediate hosts. Parasitol Res 2016 Jul;115(7):2697-704.
- Dubey JP, Howe DK, Furr M, Saville WJ, Marsh AE, Reed SM, Grigg ME. An update on Sarcocystis neurona infections in animals and equine protozoal myeloencephalitis (EPM). Vet Parasitol 2015 Apr 15;209(1-2):1-42.
- Ellison S, Witonsky S. Evidence that antibodies against recombinant SnSAG1 of Sarcocystis neurona merozoites are involved in infection and immunity in equine protozoal myeloencephalitis. Can J Vet Res 2009 Jul;73(3):176-83.
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