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. 1995 Mar;33(3):675–679. doi: 10.1128/jcm.33.3.675-679.1995

Detection of Anaplasma ovis infection in goats by major surface protein 5 competitive inhibition enzyme-linked immunosorbent assay.

L W Ndung'u 1, C Aguirre 1, F R Rurangirwa 1, T F McElwain 1, T C McGuire 1, D P Knowles 1, G H Palmer 1
PMCID: PMC228012  PMID: 7538510

Abstract

A competitive inhibition enzyme-linked immunosorbent assay (ELISA) based on a major surface protein 5 (MSP5) B-cell epitope conserved among Anaplasma species was used to detect goats infected with Anaplasma ovis. We examined strains of A. ovis isolated from goats in Kenya and demonstrated that MSP5 and the target B-cell epitope, bound by monoclonal antibody ANAF16C1, were conserved. Sera from 149 goats in four regions of Kenya and from 302 goats in six U.S. states were tested for the presence of epitope-specific antibodies with the MSP5 competitive inhibition ELISA. Evidence that the assay can be used to detect A. ovis-infected goats includes the following: (i) 53 goats raised in confinement with arthropod control were all seronegative; (ii) six goats experimentally infected with A. ovis seroconverted at the same time that they developed detectable rickettsemia; (iii) seroconverted goats remained seropositive, consistent with the persistence of A. ovis in goats and the presence of anti-MSP5 antibody in cattle persistently infected with Anaplasma marginale; and (iv) 119 of 127 known A. ovis-infected goats in Kenya were seropositive. A. ovis infection, as determined serologically and by demonstration of infected erythrocytes, in goats from the four regions in Kenya was highly prevalent. In contrast, despite the presence of A. ovis and competent arthropod vectors in the United States, the prevalence of infection appeared to be very low. The high prevalence in Kenya and the occurrence of anemia in persistently infected goats may be impediments to current efforts to increase milk yields on small farms.

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Selected References

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  1. Allred D. R., McGuire T. C., Palmer G. H., Leib S. R., Harkins T. M., McElwain T. F., Barbet A. F. Molecular basis for surface antigen size polymorphisms and conservation of a neutralization-sensitive epitope in Anaplasma marginale. Proc Natl Acad Sci U S A. 1990 Apr;87(8):3220–3224. doi: 10.1073/pnas.87.8.3220. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Eriks I. S., Palmer G. H., McGuire T. C., Allred D. R., Barbet A. F. Detection and quantitation of Anaplasma marginale in carrier cattle by using a nucleic acid probe. J Clin Microbiol. 1989 Feb;27(2):279–284. doi: 10.1128/jcm.27.2.279-284.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Eriks I. S., Stiller D., Goff W. L., Panton M., Parish S. M., McElwain T. F., Palmer G. H. Molecular and biological characterization of a newly isolated Anaplasma marginale strain. J Vet Diagn Invest. 1994 Oct;6(4):435–441. doi: 10.1177/104063879400600406. [DOI] [PubMed] [Google Scholar]
  4. Eriks I. S., Stiller D., Palmer G. H. Impact of persistent Anaplasma marginale rickettsemia on tick infection and transmission. J Clin Microbiol. 1993 Aug;31(8):2091–2096. doi: 10.1128/jcm.31.8.2091-2096.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Kocan K. M., Stiller D. Development of Anaplasma ovis (Rickettsiales: Anaplasmataceae) in male Dermacentor andersoni (Acari: Ixodidae) transferred from infected to susceptible sheep. J Med Entomol. 1992 Jan;29(1):98–107. doi: 10.1093/jmedent/29.1.98. [DOI] [PubMed] [Google Scholar]
  6. Love J. N. Cryogenic preservation of Anaplasma marginale with Dimethyl sulfoxide. Am J Vet Res. 1972 Dec;33(12):2557–2560. [PubMed] [Google Scholar]
  7. Magonigle R. A., Eckblad W. P., Lincoln S. D., Frank F. W. Anaplasma ovis in Idaho sheep. Am J Vet Res. 1981 Feb;42(2):199–201. [PubMed] [Google Scholar]
  8. McGuire T. C., Davis W. C., Brassfield A. L., McElwain T. F., Palmer G. H. Identification of Anaplasma marginale long-term carrier cattle by detection of serum antibody to isolated MSP-3. J Clin Microbiol. 1991 Apr;29(4):788–793. doi: 10.1128/jcm.29.4.788-793.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. McGuire T. C., Palmer G. H., Goff W. L., Johnson M. I., Davis W. C. Common and isolate-restricted antigens of Anaplasma marginale detected with monoclonal antibodies. Infect Immun. 1984 Sep;45(3):697–700. doi: 10.1128/iai.45.3.697-700.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Mohan R. N., Pathak R. C. Prevalence of anaplasmosis in ruminants in Northern India. Indian Vet J. 1966 Aug;43(8):685–689. [PubMed] [Google Scholar]
  11. Neitz W. O. Anaplasma ovis infection. Bull Off Int Epizoot. 1968 May;70(1):359–365. [PubMed] [Google Scholar]
  12. Palmer G. H., Barbet A. F., Musoke A. J., Katende J. M., Rurangirwa F., Shkap V., Pipano E., Davis W. C., McGuire T. C. Recognition of conserved surface protein epitopes on Anaplasma centrale and Anaplasma marginale isolates from Israel, Kenya and the United States. Int J Parasitol. 1988 Feb;18(1):33–38. doi: 10.1016/0020-7519(88)90033-1. [DOI] [PubMed] [Google Scholar]
  13. Palmer G. H., McGuire T. C. Immune serum against Anaplasma marginale initial bodies neutralizes infectivity for cattle. J Immunol. 1984 Aug;133(2):1010–1015. [PubMed] [Google Scholar]
  14. RYFF J. F., WEIBEL J. L., THOMAS G. M. RELATIONSHIP OF OVINE TO BOVINE ANAPLASMOSIS. Cornell Vet. 1964 Jul;54:407–414. [PubMed] [Google Scholar]
  15. SPLITTER E. J., ANTHONY H. D., TWIEHAUS M. J. Anaplasma ovis in the United States; experimental studies with sheep and goats. Am J Vet Res. 1956 Jul;17(64):487–491. [PubMed] [Google Scholar]
  16. SPLITTER E. J., TWIEHAUS M. J., CASTRO E. R. Anaplasmosis in sheep in the United States. J Am Vet Med Assoc. 1955 Sep;127(942):244–245. [PubMed] [Google Scholar]
  17. Shompole S., Waghela S. D., Rurangirwa F. R., McGuire T. C. Cloned DNA probes identify Anaplasma ovis in goats and reveal a high prevalence of infection. J Clin Microbiol. 1989 Dec;27(12):2730–2735. doi: 10.1128/jcm.27.12.2730-2735.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Sinha G. K., Pathak R. C. Anaplasmosis in goat and sheep. Indian Vet J. 1966 Jun;43(6):490–493. [PubMed] [Google Scholar]
  19. Tebele N., McGuire T. C., Palmer G. H. Induction of protective immunity by using Anaplasma marginale initial body membranes. Infect Immun. 1991 Sep;59(9):3199–3204. doi: 10.1128/iai.59.9.3199-3204.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Visser E. S., McGuire T. C., Palmer G. H., Davis W. C., Shkap V., Pipano E., Knowles D. P., Jr The Anaplasma marginale msp5 gene encodes a 19-kilodalton protein conserved in all recognized Anaplasma species. Infect Immun. 1992 Dec;60(12):5139–5144. doi: 10.1128/iai.60.12.5139-5144.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Zwart D., Buys J. Studies on Anaplasma ovis infection. II. Pathogenicity of a Nigerian goat strain for Dutch sheep and goats. Bull Epizoot Dis Afr. 1968 Mar;16(1):73–80. [PubMed] [Google Scholar]

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