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. 1987 Mar;55(3):711–715. doi: 10.1128/iai.55.3.711-715.1987

Production and characterization of serovar-specific monoclonal antibodies to serovars 4, 8, and 9 of Mycobacterium intracellulare.

K Nishimori, H Yugi, M Naiki, T Sugimura, Y Tanaka, I Nonomura, Y Yokomizo, S Kubo
PMCID: PMC260398  PMID: 3818094

Abstract

Serovar-specific monoclonal antibodies against Mycobacterium avium-Mycobacterium intracellulare-Mycobacterium scrofulaceum complex serovars 4, 8, and 9 were prepared. Nine, four, and one monoclonal antibodies, respectively, to the serovars were prepared by the usual cell fusion technique. All nine monoclonal antibodies to serovar 4 were monospecific for their homologous serovar and reacted with several native glycopeptidolipids (GPLs) and one major deacylated GPL from the homologous serovar. One of the four monoclonal antibodies to serovar 8 seemed to be monospecific for its homologous serovar, but the other cross-reacted with serovar 6 because serovar 6 organisms contain the same components as does the major deacylated GPL from serovar 8. One monoclonal antibody to serovar 9 was monospecific for its homologous serovar and reacted with one of the two major deacylated GPLs from this serovar. These antibody preparations proved useful for serovar identification.

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Selected References

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  1. Barrow W. W., Brennan P. J. Immunogenicity of type-specific C-mycoside glycopeptidolipids of mycobacteria. Infect Immun. 1982 May;36(2):678–684. doi: 10.1128/iai.36.2.678-684.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Brennan P. J., Goren M. B. Structural studies on the type-specific antigens and lipids of the mycobacterium avium. Mycobacterium intracellulare. Mycobacterium scrofulaceum serocomplex. Mycobacterium intracellulare serotype 9. J Biol Chem. 1979 May 25;254(10):4205–4211. [PubMed] [Google Scholar]
  3. Brennan P. J., Heifets M., Ullom B. P. Thin-layer chromatography of lipid antigens as a means of identifying nontuberculous mycobacteria. J Clin Microbiol. 1982 Mar;15(3):447–455. doi: 10.1128/jcm.15.3.447-455.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Brennan P. J., Mayer H., Aspinall G. O., Nam Shin J. E. Structures of the glycopeptidolipid antigens from serovars in the Mycobacterium avium/Mycobacterium intracellulare/Mycobacterium scrofulaceum serocomplex. Eur J Biochem. 1981 Mar 16;115(1):7–15. doi: 10.1111/j.1432-1033.1981.tb06190.x. [DOI] [PubMed] [Google Scholar]
  5. Brennan P. J., Souhrada M., Ullom B., McClatchy J. K., Goren M. B. Identification of atypical mycobacteria by thin-layer chromatography of their surface antigens. J Clin Microbiol. 1978 Oct;8(4):374–379. doi: 10.1128/jcm.8.4.374-379.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Cheresh D. A., Varki A. P., Varki N. M., Stallcup W. B., Levine J., Reisfeld R. A. A monoclonal antibody recognizes an O-acylated sialic acid in a human melanoma-associated ganglioside. J Biol Chem. 1984 Jun 25;259(12):7453–7459. [PubMed] [Google Scholar]
  7. Fredman P., Jeansson S., Lycke E., Svennerholm L. A monoclonal antibody reacting specifically with ganglioside GD1b in human brain. FEBS Lett. 1985 Sep 9;189(1):23–26. doi: 10.1016/0014-5793(85)80834-6. [DOI] [PubMed] [Google Scholar]
  8. Hakomori S., Nudelman E., Levery S. B., Patterson C. M. Human cancer-associated gangliosides defined by a monoclonal antibody (IB9) directed to sialosyl alpha 2 leads to 6 galactosyl residue: a preliminary note. Biochem Biophys Res Commun. 1983 Jun 29;113(3):791–798. doi: 10.1016/0006-291x(83)91069-0. [DOI] [PubMed] [Google Scholar]
  9. Higashi H., Fukui Y., Ueda S., Kato S., Hirabayashi Y., Matsumoto M., Naiki M. Sensitive enzyme-immunostaining and densitometric determination on thin-layer chromatography of N-glycolylneuraminic acid-containing glycosphingolipids, Hanganutziu-Deicher antigens. J Biochem. 1984 May;95(5):1517–1520. doi: 10.1093/oxfordjournals.jbchem.a134760. [DOI] [PubMed] [Google Scholar]
  10. Kannagi R., Cochran N. A., Ishigami F., Hakomori S., Andrews P. W., Knowles B. B., Solter D. Stage-specific embryonic antigens (SSEA-3 and -4) are epitopes of a unique globo-series ganglioside isolated from human teratocarcinoma cells. EMBO J. 1983;2(12):2355–2361. doi: 10.1002/j.1460-2075.1983.tb01746.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Marks J., Jenkins P. A., Schaefer W. B. Thin-layer chromatography of mycobacterial lipids as an aid to classification: technical improvements: mycobacterium avium, M. intracellulare (Battey bacilli). Tubercle. 1971 Sep;52(3):219–225. doi: 10.1016/0041-3879(71)90044-4. [DOI] [PubMed] [Google Scholar]
  12. Masaki S., Shimizu K., Cho N., Hirose T. Isolation of mycobacteria from lymph nodes of pigs and their environment. Nihon Juigaku Zasshi. 1982 Apr;44(2):213–221. doi: 10.1292/jvms1939.44.213. [DOI] [PubMed] [Google Scholar]
  13. Miyoshi I., Higashi H., Hirabayashi Y., Kato S., Naiki M. Detection of 4-O-acetyl-N-glycolylneuraminyl lactosylceramide as one of tumor-associated antigens in human colon cancer tissues by specific antibody. Mol Immunol. 1986 Jun;23(6):631–638. doi: 10.1016/0161-5890(86)90100-8. [DOI] [PubMed] [Google Scholar]
  14. Naiki M., Kato M. Immunological identification of blood group Pk antigen on normal human erythrocytes and isolation of anti-Pk with different affinity. Vox Sang. 1979;37(1):30–38. doi: 10.1111/j.1423-0410.1979.tb02265.x. [DOI] [PubMed] [Google Scholar]
  15. Orskov F., Orskov I., Sutton A., Schneerson R., Lin W., Egan W., Hoff G. E., Robbins J. B. Form variation in Escherichia coli K1: determined by O-acetylation of the capsular polysaccharide. J Exp Med. 1979 Mar 1;149(3):669–685. doi: 10.1084/jem.149.3.669. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Schaefer W. B. Serologic identification and classification of the atypical mycobacteria by their agglutination. Am Rev Respir Dis. 1965 Dec;92(6):85–93. doi: 10.1164/arrd.1965.92.6P2.85. [DOI] [PubMed] [Google Scholar]
  17. TSUKAMURA M. Differentiationof mycobacterium tuberculosis from other mycobacteria by sodium salicylate susceptiblity. Am Rev Respir Dis. 1962 Jul;86:81–83. doi: 10.1164/arrd.1962.86.1.81. [DOI] [PubMed] [Google Scholar]
  18. Voller A., Bidwell D. E., Bartlett A. Enzyme immunoassays in diagnostic medicine. Theory and practice. Bull World Health Organ. 1976;53(1):55–65. [PMC free article] [PubMed] [Google Scholar]
  19. Yanagihara D. L., Barr V. L., Knisley C. V., Tsang A. Y., McClatchy J. K., Brennan P. J. Enzyme-linked immunosorbent assay of glycolipid antigens for identification of mycobacteria. J Clin Microbiol. 1985 Apr;21(4):569–574. doi: 10.1128/jcm.21.4.569-574.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Young W. W., Jr, MacDonald E. M., Nowinski R. C., Hakomori S. I. Production of monoclonal antibodies specific for two distinct steric portions of the glycolipid ganglio-N-triosylceramide (asialo GM2). J Exp Med. 1979 Oct 1;150(4):1008–1019. doi: 10.1084/jem.150.4.1008. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Young W. W., Jr, Portoukalian J., Hakomori S. Two monoclonal anticarbohydrate antibodies directed to glycosphingolipids with a lacto-N-glycosyl type II chain. J Biol Chem. 1981 Nov 10;256(21):10967–10972. [PubMed] [Google Scholar]
  22. Yugi H., Nemoto H., Watanabe K. Senotypes of Mycobacterium intracellulare of porcine origin. Natl Inst Anim Health Q (Tokyo) 1972 Fall;12(3):168–169. [PubMed] [Google Scholar]

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