The hypothetical protein CT813 is localized in the Chlamydia trachomatis inclusion membrane and is immunogenic in women urogenitally infected with C-trachomatis

被引:57
作者
Chen, Chaoqun
Chen, Ding
Sharma, Jyotika
Cheng, Wen
Zhong, Youmin
Liu, Kaiyang
Jensen, Jani
Shain, Rochelle
Arulanandam, Bernard
Zhong, Guangming
机构
[1] Univ Texas, Hlth Sci Ctr, Dept Microbiol & Immunol, San Antonio, TX 78229 USA
[2] Univ Texas, Hlth Sci Ctr, Dept Obstet & Genecol, San Antonio, TX 78229 USA
[3] Univ Texas, Dept Biol, San Antonio, TX 78249 USA
关键词
D O I
10.1128/IAI.00081-06
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Using antibodies raised with chlamydial fusion proteins, we have localized a protein encoded by hypothetical open reading frame CT813 in the inclusion membrane of Chlamydia trachomatis. The detection of the C. trachomatis inclusion membrane by an anti-CT813 antibody was blocked by the CT813 protein but not unrelated fusion proteins. The CT813 protein was detected as early as 12 h after chlamydial infection and was present in the inclusion membrane during the entire growth cycle. All tested serovars from C. trachomatis but not other chlamydial species expressed the CT813 protein. Exogenously expressed CT813 protein in HeLa cells displayed a cytoskeleton-like structure similar to but not overlapping with host cell intermediate filaments, suggesting that the CT813 protein is able to either polymerize or associate with host cell cytoskeletal structures. Finally, women with C. trachomatis urogenital infection developed high titers of antibodies to the CT813 protein, demonstrating that the CT813 protein is not only expressed but also immunogenic during chlamydial infection in humans. In all, the CT813 protein is an inclusion membrane protein unique to C. trachomatis species and has the potential to interact with host cells and induce host immune responses during natural infection. Thus, the CT813 protein may represent an important candidate for understanding C. trachomatis pathogenesis and developing intervention and prevention strategies for controlling C. trachomatis infection.
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页码:4826 / 4840
页数:15
相关论文
共 74 条
[1]   Chlamydial development is blocked in host cells transfected with Chlamydophila caviae incA -: art. no. 24 [J].
Alzhanov, D ;
Barnes, J ;
Hruby, DE ;
Rockey, DD .
BMC MICROBIOLOGY, 2004, 4 (1)
[2]   MAPPING ANTIGENIC DOMAINS EXPRESSED BY CHLAMYDIA-TRACHOMATIS MAJOR OUTER-MEMBRANE PROTEIN GENES [J].
BAEHR, W ;
ZHANG, YX ;
JOSEPH, T ;
SU, H ;
NANO, FE ;
EVERETT, KDE ;
CALDWELL, HD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (11) :4000-4004
[3]  
Bannantine JP, 2000, CELL MICROBIOL, V2, P35
[4]   Tandem genes of Chlamydia psittaci that encode proteins localized to the inclusion membrane [J].
Bannantine, JP ;
Rockey, DD ;
Hackstadt, T .
MOLECULAR MICROBIOLOGY, 1998, 28 (05) :1017-1026
[5]   Chlamydia trachomatis IncA is localized to the inclusion membrane and is recognized by antisera from infected humans and primates [J].
Bannantine, JP ;
Stamm, WE ;
Suchland, RJ ;
Rockey, DD .
INFECTION AND IMMUNITY, 1998, 66 (12) :6017-6021
[6]   Role of neutrophils in controlling early stages of a Chlamydia trachomatis infection [J].
Barteneva, N ;
Theodor, I ;
Peterson, EM ;
delaMaza, LM .
INFECTION AND IMMUNITY, 1996, 64 (11) :4830-4833
[7]   Epidemic lymphogranuloma venereum during epidemics of crack cocaine use and HIV infection in the Bahamas [J].
Bauwens, JE ;
Orlander, H ;
Gomez, MP ;
Lampe, M ;
Morse, S ;
Stamm, WE ;
Cone, R ;
Ashley, R ;
Swenson, P ;
Holmes, KK .
SEXUALLY TRANSMITTED DISEASES, 2002, 29 (05) :253-258
[8]   Genomic transcriptional profiling of the developmental cycle of Chlamydia trachomatis [J].
Belland, RJ ;
Zhong, GM ;
Crane, DD ;
Hogan, D ;
Sturdevant, D ;
Sharma, J ;
Beatty, WL ;
Caldwell, HD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (14) :8478-8483
[9]   Golgi-dependent transport of cholesterol to the Chlamydia trachomatis inclusion [J].
Carabeo, RA ;
Mead, DJ ;
Hackstadt, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (11) :6771-6776
[10]   PROTECTIVE EFFICACY OF MAJOR OUTER-MEMBRANE PROTEIN-SPECIFIC IMMUNOGLOBULIN-A (IGA) AND IGG MONOCLONAL-ANTIBODIES IN A MURINE MODEL OF CHLAMYDIA-TRACHOMATIS GENITAL-TRACT INFECTION [J].
COTTER, TW ;
MENG, Q ;
SHEN, ZL ;
ZHANG, YX ;
SU, H ;
CALDWELL, HD .
INFECTION AND IMMUNITY, 1995, 63 (12) :4704-4714