Differential Opa specificities for CD66 receptors influence tissue interactions and cellular response to Neisseria gonorrhoeae

被引:125
作者
Gray-Owen, SD
Lorenzen, DR
Haude, A
Meyer, TF
Dehio, C
机构
[1] Max Planck Inst Biol, Infekt Biol Abt, D-72076 Tubingen, Germany
[2] Max Planck Inst Infekt Biol, Mol Biol Abt, D-10117 Berlin, Germany
关键词
D O I
10.1046/j.1365-2958.1997.6342006.x
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
The ability of all 11 variable opacity (Opa) proteins encoded by Neisseria gonorrhoeae MS11 to interact directly with the five CD66 antigens was determined. Transfected HeLa cell lines expressing individual CD66 antigens were infected with recombinant N. gonorrhoeae and Escherichia coli strains expressing defined Opas. Based upon the ability of these bacteria to bind and invade and to isolate specifically CD66 antigens from detergent-soluble extracts of the corresponding cell lines, distinct specificity groups of Opa interaction with CD66 were seen. Defining these specificity groups allowed us to assign a specific function for CD66a in the Opa-mediated interaction of gonococci with two different target cell types, which are both known to co-express multiple CD66 antigens. The competence of individual Opas to interact with CD66a was strictly correlated with their ability to induce an oxidative response by polymorphonuclear neutrophils. The same Opa specificity was observed for the level of gonococcal binding to primary endothelial cells after stimulation with TNF alpha, which was shown to increase the expression of CD66a rather than CD66e. As CD66e alone is expressed on other target tissues of gonococcal pathogenicity, Opa variation probably contributes to the cell tropism displayed by gonococci.
引用
收藏
页码:971 / 980
页数:10
相关论文
共 52 条
[1]   PURIFICATION AND CHARACTERIZATION OF 8 CLASS-5 OUTER-MEMBRANE PROTEIN VARIANTS FROM A CLONE OF NEISSERIA-MENINGITIDIS SEROGROUP-A [J].
ACHTMAN, M ;
NEIBERT, M ;
CROWE, BA ;
STRITTMATTER, W ;
KUSECEK, B ;
WEYSE, E ;
WALSH, MJ ;
SLAWIG, B ;
MORELLI, G ;
MOLL, A ;
BLAKE, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 168 (02) :507-525
[2]   Association of biliary glycoprotein with protein tyrosine phosphatase SHP-1 in malignant colon epithelial cells [J].
Beauchemin, N ;
Kunath, T ;
Robitaille, J ;
Chow, B ;
Turbide, C ;
Daniels, E ;
Veillette, A .
ONCOGENE, 1997, 14 (07) :783-790
[3]   HUMAN NEUTROPHIL RESPONSE TO RECOMBINANT NEISSERIAL OPA PROTEINS [J].
BELLAND, RJ ;
CHEN, T ;
SWANSON, J ;
FISCHER, SH .
MOLECULAR MICROBIOLOGY, 1992, 6 (13) :1729-1737
[4]  
BERLING B, 1990, CANCER RES, V50, P6534
[5]   THE OPACITY PROTEINS OF NEISSERIA-GONORRHOEAE STRAIN MS11 ARE ENCODED BY A FAMILY OF 11 COMPLETE GENES [J].
BHAT, KS ;
GIBBS, CP ;
BARRERA, O ;
MORRISON, SG ;
JAHNIG, F ;
STERN, A ;
KUPSCH, EM ;
MEYER, TF ;
SWANSON, J .
MOLECULAR MICROBIOLOGY, 1991, 5 (08) :1889-1901
[6]   Differential recognition of members of the carcinoembryonic antigen family by Opa variants of Neisseria gonorrhoeae [J].
Bos, MP ;
Grunert, F ;
Belland, RJ .
INFECTION AND IMMUNITY, 1997, 65 (06) :2353-2361
[7]   NEUTROPHILS CAN GENERATE THEIR ACTIVATOR NEUTROPHIL-ACTIVATING PEPTIDE-2 BY PROTEOLYTIC CLEAVAGE OF PLATELET-DERIVED CONNECTIVE TISSUE-ACTIVATING PEPTIDE-III [J].
BRANDT, E ;
VANDAMME, J ;
FLAD, HD .
CYTOKINE, 1991, 3 (04) :311-321
[8]   ADHERENCE OF PILUS(-) OPA(+) GONOCOCCI TO EPITHELIAL-CELLS IN-VITRO INVOLVES HEPARAN-SULFATE [J].
CHEN, T ;
BELLAND, RJ ;
WILSON, J ;
SWANSON, J .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (02) :511-517
[9]   Several carcinoembryonic antigens (CD66) serve as receptors for gonococcal opacity proteins [J].
Chen, T ;
Grunert, F ;
MedinaMarino, A ;
Gotschlich, EC .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (09) :1557-1564
[10]   CGM1a antigen of neutrophils, a receptor of gonococcal opacity proteins [J].
Chen, T ;
Gotschlich, EC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (25) :14851-14856