Abstract
Outbreaks of bovine pleuropneumonia caused by small-colony strains of Mycoplasma mycoides subsp. mycoides occur in Africa, and vaccination is used for control. Since protein subunits are needed to improve multivalent vaccines, monoclonal antibodies (MAbs) were made to facilitate protein identification and isolation. Eleven immunoglobulin M MAbs derived from mouse spleen donors immunized with disrupted whole organisms bound periodate-sensitive epitopes on externally exposed polysaccharide. Seven of these MAbs caused in vitro growth inhibition of M. mycoides subsp. mycoides; however, reaction with carbohydrate epitopes prevented their use in identifying proteins. Ten additional MAbs from mouse spleen donors immunized with Triton X-114-phase integral membrane proteins reacted with periodate-insensitive, proteinase K-sensitive epitopes. These MAbs were classified into three groups based on immunoblots of Triton X-114-phase proteins. One group reacted with 96-, 16-, and 15-kDa proteins. Another group reacted with 26-, 21-, and 16-kDa proteins, while a third group reacted only with 26- and 21-kDa proteins. One MAb from each group reacted with trypsinsensitive epitopes on live organisms, yet none caused in vitro growth inhibition. Representative MAbs reacted with all small-colony strains in immunoblots and did not react with large colony strains. However, these MAbs were not specific for small-colony strains, as proteins from two other M. mycoides cluster organisms were identified. Nevertheless, MAbs to surface-exposed epitopes on integral membrane proteins will be useful for isolation of these proteins for immunization, since one or more might induce growth-inhibiting antibodies or other protective responses.
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- Avakian A. P., Kleven S. H., Ley D. H. Comparison of Mycoplasma gallisepticum strains and identification of immunogenic integral membrane proteins with Triton X-114 by immunoblotting. Vet Microbiol. 1991 Nov;29(3-4):319–328. doi: 10.1016/0378-1135(91)90139-7. [DOI] [PubMed] [Google Scholar]
- BROWN R. D., GOURLAY R. N., MACLEOD A. K. THE PRODUCTION OF T1 BROTH CULTURE CONTAGIOUS BOVINE PLEUROPNEUMONIA VACCINE. Bull Epizoot Dis Afr. 1965 Jun;13:149–155. [PubMed] [Google Scholar]
- Bashiruddin J. B., Nicholas R. A., Santini F. G., Ready R. A., Woodward M. J., Taylor T. K. Use of the polymerase chain reaction to detect mycoplasma DNA in cattle with contagious bovine pleuropneumonia. Vet Rec. 1994 Mar 5;134(10):240–241. doi: 10.1136/vr.134.10.240. [DOI] [PubMed] [Google Scholar]
- Bordier C. Phase separation of integral membrane proteins in Triton X-114 solution. J Biol Chem. 1981 Feb 25;256(4):1604–1607. [PubMed] [Google Scholar]
- Brocchi E., Gamba D., Poumarat F., Martel J. L., De Simone F. Improvements in the diagnosis of contagious bovine pleuropneumonia through the use of monoclonal antibodies. Rev Sci Tech. 1993 Jun;12(2):559–570. doi: 10.20506/rst.12.2.702. [DOI] [PubMed] [Google Scholar]
- Buttery S. H., Lloyd L. C., Titchen D. A. Acute respiratory, circulatory and pathological changes in the calf after intravenous injections of the galactan from Mycoplasma mycoides subsp. mycoides. J Med Microbiol. 1976 Nov;9(4):379–391. doi: 10.1099/00222615-9-4-379. [DOI] [PubMed] [Google Scholar]
- CLYDE W. A., Jr MYCOPLASMA SPECIES IDENTIFICATION BASED UPON GROWTH INHIBITION BY SPECIFIC ANTISERA. J Immunol. 1964 Jun;92:958–965. [PubMed] [Google Scholar]
- Davies G., Gilbert F. R. Contagious bovine pleuropneumonia vaccination in East Africa. Bull Epizoot Dis Afr. 1969 Mar;17(1):21–26. [PubMed] [Google Scholar]
- EDWARD D. G., FREUNDT E. A. The classification and nomenclature of organisms of the pleuropneumonia group. J Gen Microbiol. 1956 Feb;14(1):197–207. doi: 10.1099/00221287-14-1-197. [DOI] [PubMed] [Google Scholar]
- Garba S. A., Terry R. J. Immunogenicity of oil-based contagious bovine pleuropneumonia vaccine in cattle. Vaccine. 1986 Dec;4(4):266–270. doi: 10.1016/0264-410x(86)90142-8. [DOI] [PubMed] [Google Scholar]
- Garba S. A., Terry R. J., Lamorde A. G. Effect of booster dose on the immunity of cattle to mycoplasma vaccines. Vet Rec. 1991 Feb 16;128(7):155–156. doi: 10.1136/vr.128.7.155. [DOI] [PubMed] [Google Scholar]
- Gourlay R. N. Contagious bovine pleuropneumonia-protection following natural infection and vaccination. Dev Biol Stand. 1975;28:586–589. [PubMed] [Google Scholar]
- Gourlay R. N., Thrower K. J. Morphology of Mycoplasma mycoides thread-phase growth. J Gen Microbiol. 1968 Nov;54(1):155–159. doi: 10.1099/00221287-54-1-155. [DOI] [PubMed] [Google Scholar]
- Gray M. A., Simam P., Smith G. R. Observations on experimental inactivated vaccines for contagious bovine pleuropneumonia. J Hyg (Lond) 1986 Oct;97(2):305–315. doi: 10.1017/s0022172400065402. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Helenius A., Simons K. Solubilization of membranes by detergents. Biochim Biophys Acta. 1975 Mar 25;415(1):29–79. doi: 10.1016/0304-4157(75)90016-7. [DOI] [PubMed] [Google Scholar]
- Hwang Y. S., Panangala V. S., Rossi C. R., Giambrone J. J., Lauerman L. H. Monoclonal antibodies that recognize specific antigens of Mycoplasma gallisepticum and M. synoviae. Avian Dis. 1989 Jan-Mar;33(1):42–52. [PubMed] [Google Scholar]
- Levisohn S., Davidson I., Caro Vergara M. R., Rapoport E. Use of an ELISA for differential diagnosis of Mycoplasma agalactiae and M mycoides subspecies mycoides (LC) in naturally infected goat herds. Res Vet Sci. 1991 Jul;51(1):66–71. doi: 10.1016/0034-5288(91)90033-k. [DOI] [PubMed] [Google Scholar]
- Levisohn S., Razin S. Isolation, ultrastructure and antigenicity of Mycoplasma gallisepticum membranes. J Hyg (Lond) 1973 Dec;71(4):725–737. doi: 10.1017/s0022172400022981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Masiga W. N., Roberts D. H., Kakoma I., Rurangirwa F. R. Passive immunity to contagious bovine pleuropneumonia. Res Vet Sci. 1975 Nov;19(3):330–332. [PubMed] [Google Scholar]
- Masiga W. N., Windsor R. S. Immunity to contagious bovine pleuropneumonia. Vet Rec. 1975 Nov 1;97(18):350–351. doi: 10.1136/vr.97.18.350. [DOI] [PubMed] [Google Scholar]
- Masiga W. N., Windsor R. S. The efficacy of T1 strain broth culture vaccine against contagious bovine pleuropneumonia: the effect of revaccination of cattle 6 months and 1 year after primary vaccination and prolonged exposure. Bull Epizoot Dis Afr. 1974 Mar;22(1):27–31. [PubMed] [Google Scholar]
- Nicholas R. A., Bashiruddin J. B. Mycoplasma mycoides subspecies mycoides (small colony variant): the agent of contagious bovine pleuropneumonia and member of the "Mycoplasma mycoides cluster". J Comp Pathol. 1995 Jul;113(1):1–27. doi: 10.1016/s0021-9975(05)80065-9. [DOI] [PubMed] [Google Scholar]
- Olson L. D., Shane S. W., Karpas A. A., Cunningham T. M., Probst P. S., Barile M. F. Monoclonal antibodies to surface antigens of a pathogenic Mycoplasma hominis strain. Infect Immun. 1991 May;59(5):1683–1689. doi: 10.1128/iai.59.5.1683-1689.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Plackett P., Buttery S. H. A galactofuranose disaccharide from the galactan of Mycoplasma mycoides. Biochem J. 1964 Jan;90(1):201–205. doi: 10.1042/bj0900201. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Poumarat F., Longchambon D., Martel J. L. Application of dot immunobinding on membrane filtration (MF dot) to the study of relationships within "M. mycoides cluster" and within "glucose and arginine-negative cluster" of ruminant mycoplasmas. Vet Microbiol. 1992 Oct;32(3-4):375–390. doi: 10.1016/0378-1135(92)90159-q. [DOI] [PubMed] [Google Scholar]
- Provost A., Borredon C., Queval R. Recherches immunologiques sur la péripneumonie. XI. Un vaccin vivant mixte antibovipestique-antiperipneumonique inocule en un seul temps. Conception, production, controles. Rev Elev Med Vet Pays Trop. 1970;23(2):143–162. [PubMed] [Google Scholar]
- Riethman H. C., Boyer M. J., Wise K. S. Triton X-114 phase fractionation of an integral membrane surface protein mediating monoclonal antibody killing of Mycoplasma hyorhinis. Infect Immun. 1987 May;55(5):1094–1100. doi: 10.1128/iai.55.5.1094-1100.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rurangirwa F. R., Wambugu A., Kihara S. M., McGuire T. C. A Mycoplasma strain F38 growth-inhibiting monoclonal antibody (WM-25) identifies an epitope on a surface-exposed polysaccharide antigen. Infect Immun. 1995 Apr;63(4):1415–1420. doi: 10.1128/iai.63.4.1415-1420.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Smith P. K., Krohn R. I., Hermanson G. T., Mallia A. K., Gartner F. H., Provenzano M. D., Fujimoto E. K., Goeke N. M., Olson B. J., Klenk D. C. Measurement of protein using bicinchoninic acid. Anal Biochem. 1985 Oct;150(1):76–85. doi: 10.1016/0003-2697(85)90442-7. [DOI] [PubMed] [Google Scholar]
- Tanford C., Reynolds J. A. Characterization of membrane proteins in detergent solutions. Biochim Biophys Acta. 1976 Oct 26;457(2):133–170. doi: 10.1016/0304-4157(76)90009-5. [DOI] [PubMed] [Google Scholar]
- Taylor T. K., Bashiruddin J. B., Gould A. R. Application of a diagnostic DNA probe for the differentiation of the two types of Mycoplasma mycoides subspecies mycoides. Res Vet Sci. 1992 Sep;53(2):154–159. doi: 10.1016/0034-5288(92)90103-9. [DOI] [PubMed] [Google Scholar]
- Taylor T. K., Bashiruddin J. B., Gould A. R. Relationships between members of the Mycoplasma mycoides cluster as shown by DNA probes and sequence analysis. Int J Syst Bacteriol. 1992 Oct;42(4):593–601. doi: 10.1099/00207713-42-4-593. [DOI] [PubMed] [Google Scholar]
- 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):4350–4354. doi: 10.1073/pnas.76.9.4350. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Whittlestone P. Immunity to mycoplasmas causing respiratory diseases in man and animals. Adv Vet Sci Comp Med. 1976;20:277–307. [PubMed] [Google Scholar]
- Woodward M. P., Young W. W., Jr, Bloodgood R. A. Detection of monoclonal antibodies specific for carbohydrate epitopes using periodate oxidation. J Immunol Methods. 1985 Apr 8;78(1):143–153. doi: 10.1016/0022-1759(85)90337-0. [DOI] [PubMed] [Google Scholar]