A major cell wall lipopeptide of Mycobacterium avium subspecies paratuberculosis

被引:24
作者
Eckstein, TM
Chandrasekaran, S
Mahapatra, S
McNeil, MR
Chatterjee, D
Rithner, CD
Ryan, PW
Belisle, JT
Inamine, JM
机构
[1] Colorado State Univ, Dept Microbiol Immunol & Pathol, Ft Collins, CO 80523 USA
[2] Colorado State Univ, Macromol Res Facil, Ft Collins, CO 80523 USA
[3] Colorado State Univ, Dept Chem, Ft Collins, CO 80523 USA
关键词
D O I
10.1074/jbc.M512465200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mycobacterium avium subspecies paratuberculosis (MAP), the causative agent of Johne disease in cattle and other ruminants, is proposed to be at least one of the causes of Crohn disease in humans. MAP and Mycobacterium avium subspecies avium, a closely related opportunistic environmental bacterium, share 95% of their genes and exhibit homologies of more than 99% between these genes. The identification of molecules specific for MAP is essential for understanding its pathogenicity and for development of useful diagnostic tools. The application of gas chromatography, mass spectrometry, and nuclear magnetic resonance led to the structural identification of a major cell wall lipopeptide of MAP, termed Para-LP-01, defined as C20 fatty acyl-D-Phe-N-Me-L-Val-L-Ile-L-Phe-L-Ala methyl ester. Variations of this lipopeptide with different fatty acyl moieties (C16 fatty acyl through C17, C18, C19, C21 to C22) were also identified. Besides the specificity of this lipopeptide for MAP, the presence of an N-Me-L-valine represents the first reported N-methylated amino acid within an immunogenic lipopeptide of mycobacteria. Sera from animals with Johne disease, but not sera from uninfected cattle, reacted with this lipopeptide, indicating potential biological importance.
引用
收藏
页码:5209 / 5215
页数:7
相关论文
共 31 条
[1]   DETERMINATION OF AMINO ACID SEQUENCES IN OLIGOPEPTIDES BY MASS SPECTROMETRY .I. STRUCTURE OF FORTUITINE AN ACYLNONAPEPTIDE METHYL ESTER [J].
BARBER, M ;
JOLLES, P ;
VILKAS, E ;
LEDERER, E .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1965, 18 (04) :469-&
[2]   IMMUNOGENICITY OF TYPE-SPECIFIC C-MYCOSIDE GLYCOPEPTIDOLIPIDS OF MYCOBACTERIA [J].
BARROW, WW ;
BRENNAN, PJ .
INFECTION AND IMMUNITY, 1982, 36 (02) :678-684
[3]  
BARTOS M, 2005, J MICROBIOL METHODS
[4]  
BELISLE JT, 1993, J BIOL CHEM, V268, P10510
[5]   MONOCLONAL-ANTIBODIES TO THE MULTIENZYME ENNIATIN SYNTHETASE - PRODUCTION AND USE IN STRUCTURAL STUDIES [J].
BILLICH, A ;
ZOCHER, R ;
KLEINKAUF, H ;
BRAUN, DG ;
LAVANCHY, D ;
HOCHKEPPEL, HK .
BIOLOGICAL CHEMISTRY HOPPE-SEYLER, 1987, 368 (05) :521-529
[6]  
CANGELOSI GA, 2004, PATHOGENIC MYCOBACTE, P39
[7]   Johne's disease, inflammatory bowel disease, and Mycobacterium paratuberculosis [J].
Chacon, O ;
Bermudez, LE ;
Barletta, RG .
ANNUAL REVIEW OF MICROBIOLOGY, 2004, 58 :329-363
[8]   The surface glycopeptidolipids of mycobacteria: structures and biological of properties [J].
Chatterjee, D ;
Khoo, KH .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2001, 58 (14) :2018-2042
[9]   A SIMPLE AND RAPID METHOD FOR THE PERMETHYLATION OF CARBOHYDRATES [J].
CIUCANU, I ;
KEREK, F .
CARBOHYDRATE RESEARCH, 1984, 131 (02) :209-217
[10]   PRELIMINARY EVALUATION OF A MYCOBACTERIUM-TUBERCULOSIS LIPOOLIGOSACCHARIDE (LOS) ANTIGEN IN THE SEROLOGICAL DIAGNOSIS OF TUBERCULOSIS IN HIV-SEROPOSITIVE AND SERONEGATIVE PATIENTS [J].
DALEINE, G ;
LAGRANGE, PH .
TUBERCLE AND LUNG DISEASE, 1995, 76 (03) :234-239