Cloning and comparison of fliC genes and identification of glycosylation in the flagellin of Pseudomonas aeruginosa a-type strains

被引:97
作者
Brimer, CD [1 ]
Montie, TC [1 ]
机构
[1] Univ Tennessee, Dept Microbiol, Knoxville, TN 37996 USA
关键词
D O I
10.1128/JB.180.12.3209-3217.1998
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Pseudomonas aeruginosa a-type strains produce flagellin proteins which vary in molecular weight between strains. To compare the properties of a-type flagellins, the flagellin genes of several Pseudomonas aeruginosa a-type strains, as determined by interaction with specific anti-a monoclonal antibody, were cloned and sequenced, PCR amplification of the a-type flagellin gene fragments from five strains each yielded a 1.02-kb product, indicating that the gene size is not likely to be responsible for the observed molecular weight differences among the a-type strains, The flagellin amino acid sequences of several a-type strains (170018, 5933, 5939, and PAK) were compared, and that of 170018 was compared with that of PAO1, a b-type strain, The former comparisons revealed that a-type strains are similar in amino acid sequence, while the latter comparison revealed differences between 170018 and PAO1. Posttranslational modification was explored for its contribution to the observed differences in molecular weight among the a-type strains, A biotin-hydrazide glycosylation assay was performed on the flagellins of three a-type strains (170018, 5933, and 5939) and one b-type strain (M2), revealing a positive glycosylation reaction for strains 5933 and 5939 and a negative reaction for 170018 and M2, Deglycosylation of the flagellin proteins with trifluoromethanesulfonic acid (TFMS) confirmed the glycosylation results, A molecular weight shift was observed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis for the TFMS-treated flagellins of 5933 and 5939, These results indicate that the molecular weight discrepancies observed for the a-type flagellins can be attributed, at least in part, to glycosylation of the protein, Anti-a flagellin monoclonal antibody reacted with the TFMS-treated flagellins, suggesting that the glycosyl groups are not a necessary component of the epitope for the human anti-a monoclonal antibody, Comparisons between a-type sequences and a b-type sequence (PAO1) will aid in delineation of the epitope for this monoclonal antibody.
引用
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页码:3209 / 3217
页数:9
相关论文
共 47 条
  • [1] ELECTROPHORETIC SEPARATION AND MOLECULAR-WEIGHT CHARACTERIZATION OF PSEUDOMONAS-AERUGINOSA H-ANTIGEN FLAGELLINS
    ALLISON, JS
    DAWSON, M
    DRAKE, D
    MONTIE, TC
    [J]. INFECTION AND IMMUNITY, 1985, 49 (03) : 770 - 774
  • [2] VARIATION IN ANTIGENICITY AND MOLECULAR-WEIGHT OF CAMPYLOBACTER-COLI VC167 FLAGELLIN IN DIFFERENT GENETIC BACKGROUNDS
    ALM, RA
    GUERRY, P
    POWER, ME
    TRUST, TJ
    [J]. JOURNAL OF BACTERIOLOGY, 1992, 174 (13) : 4230 - 4238
  • [3] EPSILON-N-METHYL-LYSINE IN BACTERIAL FLAGELLAR PROTEIN
    AMBLER, RP
    REES, MW
    [J]. NATURE, 1959, 184 (4679) : 56 - 57
  • [4] ANSORG R, 1978, ZENTBL BAKTERIOL P 1, V224, P228
  • [5] *APPL BIOS INC, 1995, ABI PRISM DYE TERMIN
  • [6] *APPL BIOS INC, 1991, US B APPL BIOS INC, V18
  • [7] BEHAVIORAL-RESPONSES IN BACTERIA
    ARMITAGE, JP
    [J]. ANNUAL REVIEW OF PHYSIOLOGY, 1992, 54 : 683 - 714
  • [8] BAKER B S, 1983, Microbios Letters, V23, P7
  • [9] FLAGELLAR STRUCTURE AND HYPERTHERMOPHILY - ANALYSIS OF A SINGLE FLAGELLIN GENE AND ITS PRODUCT IN AQUIFEX PYROPHILUS
    BEHAMMER, W
    SHAO, ZX
    MAGES, W
    RACHEL, R
    STETTER, KO
    SCHMITT, R
    [J]. JOURNAL OF BACTERIOLOGY, 1995, 177 (22) : 6630 - 6637
  • [10] ISOLATION AND CHARACTERIZATION OF PSEUDOMONAS-PSEUDOMALLEI FLAGELLIN PROTEINS
    BRETT, PJ
    MAH, DCW
    WOODS, DE
    [J]. INFECTION AND IMMUNITY, 1994, 62 (05) : 1914 - 1919