1887

Abstract

Cord factor (trehalose 6,6′-dimycolate, TDM) is an unique glycolipid with a trehalose and two molecules of mycolic acids in the mycobacterial cell envelope. Since TDM consists of two molecules of very long branched-chain 3-hydroxy fatty acids, the molecular mass ranges widely and in a complex manner. To characterize the molecular structure of TDM precisely and simply, an attempt was made to determine the mycolic acid subclasses of TDM and the molecular species composition of intact TDM by matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry for the first time. The results showed that less than 1 μg mycolic acid methyl ester of TDM from nine representative species of mycobacteria and TDM from the same species was sufficient to obtain well-resolved mass spectra composed of pseudomolecular ions [+Na]. Although the mass ion distribution was extremely diverse, the molecular species of each TDM was identified clearly by constructing a molecular ion matrix consisting of the combination of two molecules of mycolic acids. The results showed a marked difference in the molecular structure of TDM among mycobacterial species and subspecies. TDM from (HRv and Aoyama B) showed a distinctive mass pattern and consisted of over 60 molecular ions with -, methoxy- and ketomycolate. TDM from BCG Tokyo 172 similarly showed over 35 molecular ions, but that from BCG Connaught showed simpler molecular ion clusters consisting of less than 35 molecular species due to a complete lack of methoxymycolate. Mass ions due to TDM from BCG Connaught and showed a biphasic distribution, but the two major peaks of TDM from were shifted up two or three carbon units higher compared with BCG Connaught. Within the rapid grower group, in TDM consisting of -, keto- and wax ester mycolate from and , the mass ion distribution due to polar mycolates was shifted lower than that from the group. Since the physico-chemical properties and antigenic structure of mycolic acid of TDM affect the host immune responses profoundly, the molecular characterization of TDM by MALDI-TOF mass analysis may give very useful information on the relationship of glycolipid structure to its biological activity.

Loading

Article metrics loading...

/content/journal/micro/10.1099/mic.0.28158-0
2005-10-01
2024-04-24
Loading full text...

Full text loading...

/deliver/fulltext/micro/151/10/3403.html?itemId=/content/journal/micro/10.1099/mic.0.28158-0&mimeType=html&fmt=ahah

References

  1. Barry C. E. 3rd, Lee R. E., Mdluli K., Sampson A. E., Schroeder B. G., Slayden R. A, Yuan Y. 1998; Mycolic acids: structure, biosynthesis and physiological functions. Prog Lipid Res 37:143–179 [CrossRef]
    [Google Scholar]
  2. Beckman E. M., Porcelli S. A., Morita C. T., Behar S. M., Furlong S. T., Brenner M. B. 1994; Recognition of a lipid antigen by CD1-restricted αβ + T cells. Nature 372:691–694 [CrossRef]
    [Google Scholar]
  3. Bloch H. 1950; Studies on the virulence of tubercle bacilli; the relationship of the physiological state of the organisms to their pathogenicity. J Exp Med 92:507–526 [CrossRef]
    [Google Scholar]
  4. Crowe L. M., Spargo B. J., Ioneda T., Beaman B. L., Crowe J. H. 1994; Interaction of cord factor ( α , α ′-trehalose-6,6′-dimycolate) with phospholipids. Biochim Biophys Acta 119453–60 [CrossRef]
    [Google Scholar]
  5. Dubnau E., Chan J., Raynaud C., Mohan V. P., Quemard A., Smith I, Daffé M., Lanéelle M. A., Yu K. 2000; Oxygenated mycolic acids are necessary for virulence of Mycobacterium tuberculosis in mice. Mol Microbiol 36:630–637
    [Google Scholar]
  6. Enomoto K., Oka S., Fujiwara N., Okamoto T., Okuda Y., Maekura R., Kuroki T., Yano I. 1998; Rapid serodiagnosis of Mycobacterium avium-intracellulare complex infection by ELISA with cord factor (trehalose 6,6′-dimycolate), and serotyping using the glycopeptidolipid antigen. Microbiol Immunol 42:689–696 [CrossRef]
    [Google Scholar]
  7. Fujita Y., Naka T., Doi T., Yano I. 2005; Direct molecular mass determination of trehalose monomycolate from 11 species of mycobacteria by MALDI-TOF mass spectrometry. Microbiology 151:1443–1452 [CrossRef]
    [Google Scholar]
  8. Gotoh K., Mitsuyama M., Imaizumi S., Kawamura I., Yano I. 1991; Mycolic acid-containing glycolipid as a possible virulence factor of Rhodococcus equi for mice. Microbiol Immunol 35:175–185 [CrossRef]
    [Google Scholar]
  9. Liu J., Barry C. E. 3rd, Besra G. S., Nikaido H. 1996; Mycolic acid structure determines the fluidity of the mycobacterial cell wall. J Biol Chem 271:29545–29551 [CrossRef]
    [Google Scholar]
  10. Minnikin D. E. 1982; Lipids: complex lipids, their chemistry, biosynthesis and roles. Part I: physiology of the mycobacteria. In The Biology of the Mycobacteria pp. 95–184 Edited by Ratledge C., Stanford J. London: Academic Press;
    [Google Scholar]
  11. Minnikin D. E. 1988; Isolation and purification of mycobacterial wall lipids. In Bacterial Cell Surface Techniques pp. 125–135 Edited by Hancock I. C., Poxton I. R. Chichester: Wiley;
    [Google Scholar]
  12. Minnikin D. E., Parlett J. H., Magnusson M., Ridell M., Lind A. 1984; Mycolic acid patterns of representatives of Mycobacterium bovis BCG. J Gen Microbiol 130:2733–2736
    [Google Scholar]
  13. Moody D. B., Reinhold B. B., Guy M. R. 9 other authors 1997; Structural requirements for glycolipid antigen recognition by CD1b-restricted T cells. Science 278:283–286 [CrossRef]
    [Google Scholar]
  14. Moody D. B., Reinhold B. B., Reinhold V. N., Besra G. S., Porcelli S. A. 1999; Uptake and processing of glycosylated mycolates for presentation to CD1b-restricted T cells. Immunol Lett 65:85–91 [CrossRef]
    [Google Scholar]
  15. Niazi K., Chiu M., Mendoza R. 8 other authors 2001; The A′ and F′ pockets of human CD1b are both required for optimal presentation of lipid antigens to T cells. J Immunol 166:2562–2570 [CrossRef]
    [Google Scholar]
  16. Noll H., Bloch H., Asselineau J., Lederer E. 1956; The chemical structure of the cord factor of Mycobacterium tuberculosis . Biochim Biophys Acta 20:299–309 [CrossRef]
    [Google Scholar]
  17. Oswald I. P., Dozois C. M., Petit J. F., Lemaire G. 1997; Interleukin-12 synthesis is a required step in trehalose dimycolate-induced activation of mouse peritoneal macrophages. Infect Immun 65:1364–1369
    [Google Scholar]
  18. Pan J., Fujiwara N., Oka S., Maekura R., Ogura T., Yano I. 1999; Anti-cord factor (trehalose 6,6′-dimycolate) IgG antibody in tuberculosis patients recognizes mycolic acid subclasses. Microbiol Immunol 43:863–869 [CrossRef]
    [Google Scholar]
  19. Rastogi N., Legrand E., Sola C. 2001; The mycobacteria: an introduction to nomenclature and pathogenesis. Rev Sci Tech 20:21–54
    [Google Scholar]
  20. Ryll R., Kumazawa Y., Yano I. 2001a; Immunological properties of trehalose dimycolate (cord factor) and other mycolic acid-containing glycolipids – a review. Microbiol Immunol 45:801–811 [CrossRef]
    [Google Scholar]
  21. Ryll R., Watanabe K., Fujiwara N., Takimoto H., Hasunuma R., Kumazawa Y., Okada M., Yano I. 2001b; Mycobacterial cord factor, but not sulfolipid, causes depletion of NKT cells and upregulation of CD1d1 on murine macrophages. Microbes Infect 3:611–619 [CrossRef]
    [Google Scholar]
  22. Spargo B. J., Crowe L. M., Ioneda T., Beaman B. L., Crowe J. H. 1991; Cord factor ( α , α -trehalose 6,6′-dimycolate) inhibits fusion between phospholipid vesicles. Proc Natl Acad Sci U S A 88:737–740 [CrossRef]
    [Google Scholar]
  23. Toriyama S., Imaizumi S., Tomiyasu I., Masui M., Yano I. 1982; Incorporation of 18O into long-chain, secondary alcohols derived from ester mycolic acids in Mycobacterium phlei . Biochim Biophys Acta 712:427–429 [CrossRef]
    [Google Scholar]
  24. Ueda S., Fujiwara N., Naka T., Sakaguchi I., Ozeki Y., Yano I., Kasama T., Kobayashi K. 2001; Structure-activity relationship of mycoloyl glycolipids derived from Rhodococcus . sp– 4306 Microb Pathog 30:91–99 [CrossRef]
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/micro/10.1099/mic.0.28158-0
Loading
/content/journal/micro/10.1099/mic.0.28158-0
Loading

Data & Media loading...

This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error