Analyze Diet
Infection and immunity1998; 66(5); 1834-1838; doi: 10.1128/IAI.66.5.1834-1838.1998

Evidence that surface proteins Sn14 and Sn16 of Sarcocystis neurona merozoites are involved in infection and immunity.

Abstract: Sarcocystis neurona is the etiologic agent of equine protozoal myeloencephalitis (EPM). Based on an analysis of 25,000 equine serum and cerebrospinal fluid (CSF) samples, including samples from horses with neurologic signs typical of EPM or with histologically or parasitologically confirmed EPM, four major immunoblot band patterns have been identified. Twenty-three serum and CSF samples representing each of the four immunoblot patterns were selected from 220 samples from horses with neurologic signs resembling EPM and examined for inhibitory effects on the infectivity of S. neurona by an in vitro neutralization assay. A high correlation between immunoblot band pattern and neutralizing activity was detected. Two proteins, Sn14 and Sn16 (14 and 16 kDa, respectively), appeared to be important for in vitro infection. A combination of the results of surface protein labeling, immunoprecipitation, Western blotting, and trypsin digestion suggests that these molecules are surface proteins and may be useful components of a vaccine against S. neurona infection. Although S. neurona is an obligate intracellular parasite, it is potentially a target for specific antibodies which may lyse merozoites via complement or inhibit their attachment and penetration to host cells.
Publication Date: 1998-05-09 PubMed ID: 9573058PubMed Central: PMC108132DOI: 10.1128/IAI.66.5.1834-1838.1998Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This research article explores the role of surface proteins Sn14 and Sn16 in the infection and immune response related to Sarcocystis neurona, the causative agent of equine protozoal myeloencephalitis.

Understanding the Research Objectives

  • The study attempts to understand the role of surface proteins in the life cycle of Sarcocystis neurona, a parasite that causes equine protozoal myeloencephalitis.
  • By analyzing equine serum and cerebrospinal fluid (CSF) samples, four major immunoblot band patterns were identified indicating potential variations in immune response.
  • The researchers were interested in the neutralizing activity of these samples, hinting at how the immune system of horses could potentially hinder the infectivity of S. neurona.

Methods and Analysis

  • Samples were checked for their effect on S. neurona’s infectivity through an in vitro neutralization assay.
  • Proteins Sn14 and Sn16 were singled out as having a high correlation with neutralizing activity, suggesting their critical role in the infection process.
  • A combination of several lab techniques like surface protein labeling, immunoprecipitation, Western blotting, and trypsin digestion were used to understand the role of these proteins better.

Key Findings

  • The study found that proteins Sn14 and Sn16 appear to be important for in vitro infection, possibly serving as the main agents for the parasite to invade host cells.
  • The research also suggests that these proteins are likely located on the parasite’s surface which makes them accessible targets for antibodies that could neutralize the pathogen.

Implications of the Study

  • This research provides new insights into how S. neurona can infect its host, offering potential new approaches for controlling or preventing the disease.
  • Understanding the role of surface proteins could help scientists develop a vaccine against S. neurona infection, potentially reducing its widespread impact on horse populations.

Cite This Article

APA
Liang FT, Granstrom DE, Zhao XM, Timoney JF. (1998). Evidence that surface proteins Sn14 and Sn16 of Sarcocystis neurona merozoites are involved in infection and immunity. Infect Immun, 66(5), 1834-1838. https://doi.org/10.1128/IAI.66.5.1834-1838.1998

Publication

ISSN: 0019-9567
NlmUniqueID: 0246127
Country: United States
Language: English
Volume: 66
Issue: 5
Pages: 1834-1838

Researcher Affiliations

Liang, F T
  • Gluck Equine Research Center, Department of Veterinary Science, University of Kentucky, Lexington 40546-0099, USA.
Granstrom, D E
    Zhao, X M
      Timoney, J F

        MeSH Terms

        • Animals
        • Antibodies, Protozoan / immunology
        • Encephalitis / immunology
        • Encephalitis / veterinary
        • Horse Diseases / immunology
        • Horses
        • Immunoblotting
        • Membrane Proteins / immunology
        • Neutralization Tests
        • Precipitin Tests
        • Protozoan Proteins / analysis
        • Protozoan Proteins / immunology
        • Sarcocystis / immunology
        • Sarcocystosis / immunology
        • Sarcocystosis / veterinary
        • Trypsin / pharmacology

        References

        This article includes 39 references
        1. Alves MJ, Abuin G, Kuwajima VY, Colli W. Partial inhibition of trypomastigote entry into cultured mammalian cells by monoclonal antibodies against a surface glycoprotein of Trypanosoma cruzi.. Mol Biochem Parasitol 1986 Oct;21(1):75-82.
          pubmed: 3534565doi: 10.1016/0166-6851(86)90081-2google scholar: lookup
        2. Bannister LH, Mitchell GH, Butcher GA, Dennis ED. Lamellar membranes associated with rhoptries in erythrocytic merozoites of Plasmodium knowlesi: a clue to the mechanism of invasion.. Parasitology 1986 Apr;92 ( Pt 2):291-303.
          pubmed: 2423944doi: 10.1017/s0031182000064064google scholar: lookup
        3. Lombardo de Barros CS, de Barros SS, dos Santos MN. Equine protozoal myeloencephalitis in southern Brazil.. Vet Rec 1986 Sep 13;119(11):283-4.
          pubmed: 3776029doi: 10.1136/vr.119.11.283google scholar: lookup
        4. Beech J, Dodd DC. Toxoplasma-like encephalomyelitis in the horse.. Vet Pathol 1974;11(1):87-96.
          pubmed: 4215208doi: 10.1177/030098587401100110google scholar: lookup
        5. Bentz BG, Granstrom DE, Stamper S. Seroprevalence of antibodies to Sarcocystis neurona in horses residing in a county of southeastern Pennsylvania.. J Am Vet Med Assoc 1997 Feb 15;210(4):517-8.
          pubmed: 9040838
        6. Blythe LL, Granstrom DE, Hansen DE, Walker LL, Bartlett J, Stamper S. Seroprevalence of antibodies to Sarcocystis neurona in horses residing in Oregon.. J Am Vet Med Assoc 1997 Feb 15;210(4):525-7.
          pubmed: 9040840
        7. Boy MG, Galligan DT, Divers TJ. Protozoal encephalomyelitis in horses: 82 cases (1972-1986).. J Am Vet Med Assoc 1990 Feb 15;196(4):632-4.
          pubmed: 2303389
        8. Cole SR, Ashman LK, Ey PL. Biotinylation: an alternative to radioiodination for the identification of cell surface antigens in immunoprecipitates.. Mol Immunol 1987 Jul;24(7):699-705.
          pubmed: 3309626doi: 10.1016/0161-5890(87)90051-4google scholar: lookup
        9. Coppel RL. Repeat structures in a Plasmodium falciparum protein (MESA) that binds human erythrocyte protein 4.1.. Mol Biochem Parasitol 1992 Feb;50(2):335-47.
          pubmed: 1741020doi: 10.1016/0166-6851(92)90231-8google scholar: lookup
        10. Davis SW, Daft BN, Dubey JP. Sarcocystis neurona cultured in vitro from a horse with equine protozoal myelitis.. Equine Vet J 1991 Jul;23(4):315-7.
        11. Davis SW, Speer CA, Dubey JP. In vitro cultivation of Sarcocystis neurona from the spinal cord of a horse with equine protozoal myelitis.. J Parasitol 1991 Oct;77(5):789-92.
          pubmed: 1919932
        12. Doyle PS, Crabb J, Petersen C. Anti-Cryptosporidium parvum antibodies inhibit infectivity in vitro and in vivo.. Infect Immun 1993 Oct;61(10):4079-84.
        13. Dubey JP, Davis GW, Koestner A, Kiryu K. Equine encephalomyelitis due to a protozoan parasite resembling Toxoplasma gondii.. J Am Vet Med Assoc 1974 Aug 1;165(3):249-55.
          pubmed: 4845678
        14. Dubey JP, Davis SW, Speer CA, Bowman DD, de Lahunta A, Granstrom DE, Topper MJ, Hamir AN, Cummings JF, Suter MM. Sarcocystis neurona n. sp. (Protozoa: Apicomplexa), the etiologic agent of equine protozoal myeloencephalitis.. J Parasitol 1991 Apr;77(2):212-8.
          pubmed: 1901359
        15. Fayer R, Mayhew IG, Baird JD, Dill SG, Foreman JH, Fox JC, Higgins RJ, Reed SM, Ruoff WW, Sweeney RW. Epidemiology of equine protozoal myeloencephalitis in North America based on histologically confirmed cases. A report.. J Vet Intern Med 1990 Mar-Apr;4(2):54-7.
        16. Granstrom DE, Alvarez O Jr, Dubey JP, Comer PF, Williams NM. Equine protozoal myelitis in Panamanian horses and isolation of Sarcocystis neurona.. J Parasitol 1992 Oct;78(5):909-12.
          pubmed: 1403437
        17. Granstrom DE, Dubey JP, Davis SW, Fayer R, Fox JC, Poonacha KB, Giles RC, Comer PF. Equine protozoal myeloencephalitis: antigen analysis of cultured Sarcocystis neurona merozoites.. J Vet Diagn Invest 1993 Jan;5(1):88-90.
          pubmed: 8466988doi: 10.1177/104063879300500118google scholar: lookup
        18. Granstrom D E, Reed S M. Equine protozoal myeloencephalitis. Equine Pract 1994;16:23–26.
        19. Granstrom D E, Dubey J P, Giles R C, Gajadhar A A, Fenger C K. Equine protozoal myeloencephalitis: biology and epidemiology. In: Nakajima H, Plowright W, editors. Proceeding, 7th International Conference on Equine Infectious Diseases 1994, Tokyo, Japan. Newmarket, England: R&W Publications Ltd.; 1994. pp. 109–111.
        20. Granstrom D E. Equine protozoal myeloencephalitis testing: review of 1993 and 1994. Proc Am Assoc Equine Pract 1995;41:218–219.
        21. Granstrom DE. Recent advances in the laboratory diagnosis of equine parasitic diseases.. Vet Clin North Am Equine Pract 1995 Dec;11(3):437-42.
        22. Hamir AN, Moser G, Galligan DT, Davis SW, Granstrom DE, Dubey JP. Immunohistochemical study to demonstrate Sarcocystis neurona in equine protozoal myeloencephalitis.. J Vet Diagn Invest 1993 Jul;5(3):418-22.
          pubmed: 8373858doi: 10.1177/104063879300500320google scholar: lookup
        23. Hines SA, Palmer GH, Jasmer DP, Goff WL, McElwain TF. Immunization of cattle with recombinant Babesia bovis merozoite surface antigen-1.. Infect Immun 1995 Jan;63(1):349-52.
          pmc: PMC172999pubmed: 7806376doi: 10.1128/iai.63.1.349-352.1995google scholar: lookup
        24. Hollingdale MR, Nardin EH, Tharavanij S, Schwartz AL, Nussenzweig RS. Inhibition of entry of Plasmodium falciparum and P. vivax sporozoites into cultured cells; an in vitro assay of protective antibodies.. J Immunol 1984 Feb;132(2):909-13.
          pubmed: 6317752
        25. Laemmli UK. Cleavage of structural proteins during the assembly of the head of bacteriophage T4.. Nature 1970 Aug 15;227(5259):680-5.
          pubmed: 5432063doi: 10.1038/227680a0google scholar: lookup
        26. Masri MD, Alda JL, Dubey JP. Sarcocystis neurona-associated ataxia in horses in Brazil.. Vet Parasitol 1992 Oct;44(3-4):311-4.
          pubmed: 1466140doi: 10.1016/0304-4017(92)90128-vgoogle scholar: lookup
        27. Mineo JR, McLeod R, Mack D, Smith J, Khan IA, Ely KH, Kasper LH. Antibodies to Toxoplasma gondii major surface protein (SAG-1, P30) inhibit infection of host cells and are produced in murine intestine after peroral infection.. J Immunol 1993 May 1;150(9):3951-64.
          pubmed: 7682587
        28. Perkins ME. Rhoptry organelles of apicomplexan parasites.. Parasitol Today 1992 Jan;8(1):28-32.
          pubmed: 15463523doi: 10.1016/0169-4758(92)90308-ogoogle scholar: lookup
        29. Petersen C, Gut J, Doyle PS, Crabb JH, Nelson RG, Leech JH. Characterization of a > 900,000-M(r) Cryptosporidium parvum sporozoite glycoprotein recognized by protective hyperimmune bovine colostral immunoglobulin.. Infect Immun 1992 Dec;60(12):5132-8.
        30. Sam-Yellowe TY, Shio H, Perkins ME. Secretion of Plasmodium falciparum rhoptry protein into the plasma membrane of host erythrocytes.. J Cell Biol 1988 May;106(5):1507-13.
          pmc: PMC2115054pubmed: 2453514doi: 10.1083/jcb.106.5.1507google scholar: lookup
        31. Saul A. Kinetic constraints on the development of a malaria vaccine.. Parasite Immunol 1987 Jan;9(1):1-9.
        32. Saville WJ, Reed SM, Granstrom DE, Hinchcliff KW, Kohn CW, Wittum TE, Stamper S. Seroprevalence of antibodies to Sarcocystis neurona in horses residing in Ohio.. J Am Vet Med Assoc 1997 Feb 15;210(4):519-24.
          pubmed: 9040839
        33. Schofield L, Bushell GR, Cooper JA, Saul AJ, Upcroft JA, Kidson C. A rhoptry antigen of Plasmodium falciparum contains conserved and variable epitopes recognized by inhibitory monoclonal antibodies.. Mol Biochem Parasitol 1986 Feb;18(2):183-95.
          pubmed: 2421161doi: 10.1016/0166-6851(86)90037-xgoogle scholar: lookup
        34. Schwartzman JD. Inhibition of a penetration-enhancing factor of Toxoplasma gondii by monoclonal antibodies specific for rhoptries.. Infect Immun 1986 Mar;51(3):760-4.
          pmc: PMC260962pubmed: 3512433doi: 10.1128/iai.51.3.760-764.1986google scholar: lookup
        35. Stewart MJ, Schulman S, Vanderberg JP. Rhoptry secretion of membranous whorls by Plasmodium falciparum merozoites.. Am J Trop Med Hyg 1986 Jan;35(1):37-44.
          pubmed: 3511750doi: 10.4269/ajtmh.1986.35.37google scholar: lookup
        36. Tilley M, Fayer R, Guidry A, Upton SJ, Blagburn BL. Cryptosporidium parvum (Apicomplexa: Cryptosporidiidae) oocyst and sporozoite antigens recognized by bovine colostral antibodies.. Infect Immun 1990 Sep;58(9):2966-71.
        37. Towbin H, Staehelin T, Gordon J. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.. Proc Natl Acad Sci U S A 1979 Sep;76(9):4350-4.
          pmc: PMC411572pubmed: 388439doi: 10.1073/pnas.76.9.4350google scholar: lookup
        38. Tzipori S, Roberton D, Cooper DA, White L. Chronic cryptosporidial diarrhoea and hyperimmune cow colostrum.. Lancet 1987 Aug 8;2(8554):344-5.
          pubmed: 2886815doi: 10.1016/s0140-6736(87)90944-5google scholar: lookup
        39. Yoshida N, Mortara RA, Araguth MF, Gonzalez JC, Russo M. Metacyclic neutralizing effect of monoclonal antibody 10D8 directed to the 35- and 50-kilodalton surface glycoconjugates of Trypanosoma cruzi.. Infect Immun 1989 Jun;57(6):1663-7.

        Citations

        This article has been cited 5 times.
        1. Nadzirah TTI, Yik FM, Ling LY. Seroprevalence of Sarcocystis falcatula in Two Islands of Malaysia using Recombinant Surface Antigen 4.. Korean J Parasitol 2020 Feb;58(1):1-5.
          doi: 10.3347/kjp.2020.58.1.1pubmed: 32145721google scholar: lookup
        2. Lesniak I, Heckmann I, Franz M, Greenwood AD, Heitlinger E, Hofer H, Krone O. Recolonizing gray wolves increase parasite infection risk in their prey.. Ecol Evol 2018 Feb;8(4):2160-2170.
          doi: 10.1002/ece3.3839pubmed: 29468033google scholar: lookup
        3. 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.
          doi: 10.1016/j.vetpar.2015.01.026pubmed: 25737052google scholar: lookup
        4. 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.
          pubmed: 19794889
        5. Howe DK, Gaji RY, Mroz-Barrett M, Gubbels MJ, Striepen B, Stamper S. Sarcocystis neurona merozoites express a family of immunogenic surface antigens that are orthologues of the Toxoplasma gondii surface antigens (SAGs) and SAG-related sequences.. Infect Immun 2005 Feb;73(2):1023-33.