Use of primate model system to identify Chlamydia trachomatis protein antigens recognized uniquely in the context of infection.

TitleUse of primate model system to identify Chlamydia trachomatis protein antigens recognized uniquely in the context of infection.
Publication TypeJournal Article
Year of Publication1999
AuthorsBannantine JP, Rockey DD
JournalMicrobiology (Reading, England)
Volume145 ( Pt 8)
Pagination2077-85
Date Published1999 Aug
ISSN1350-0872
KeywordsAnimals, Antibodies, Bacterial, Antigens, Bacterial, ATP-Binding Cassette Transporters, Bacterial Proteins, Chlamydia Infections, Chlamydia trachomatis, Disease Models, Animal, Genital Diseases, Male, Guinea Pigs, Humans, Immunoblotting, Macaca fascicularis, Male, Microscopy, Fluorescence, Molecular Sequence Data, Periplasmic Binding Proteins, Recombinant Fusion Proteins
Abstract

A primate model system was used to identify Chlamydia trachomatis antigens uniquely recognized in the context of infection. Serum antibody titres were measured in cynomolgus monkeys challenged urethrally with C. trachomatis serovar L2 elementary bodies (EBs). High-titre sera from these primates were used, in parallel with antisera against killed C. trachomatis EBs, to differentially screen an expression library of C. trachomatis serovar L2 DNA. Four clones were recognized only by antisera from infected monkeys. Sequence analysis revealed that three of these immunoreactive clones overlap a common ORF, designated ORF D242 (encoding p242), in the C. trachomatis genome database. The fourth clone contains two complete ORFs, each encoding 32 kDa proteins that share identity with Treponema pallidum TroA and TroB (ORFs D067 and D068 in the C. trachomatis database, respectively). Immunoblot analysis of Escherichia coli lysates expressing C. trachomatis TroA, TroB and p242 fusion proteins showed that p242 and TroA, but not TroB, were detected by the sera collected from infected primates. Antibodies directed at TroA and p242 were also detected in sera from several C. trachomatis-infected patients, demonstrating that these proteins are also recognized by humans following infection. Immunoblot analysis with antibody against TroA and p242 also demonstrated that both antigens are present in higher abundance in infected ChoK1 cells relative to purified C. trachomatis EBs. Immunofluorescence microscopy shows that TroA and p242 are both localized to intracellular developmental forms at the margins of growing inclusions. Collectively, these studies identify two C. trachomatis proteins that are under-represented in EBs and are recognized uniquely in the context of infection.

Alternate JournalMicrobiology (Reading, Engl.)