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Subfamily I Treponema pallidum repeat protein family: sequence variation and immunity.

TitleSubfamily I Treponema pallidum repeat protein family: sequence variation and immunity.
Publication TypeJournal Article
Year of Publication2004
AuthorsSun, ES, Molini, BJ, Barrett, LK, Centurion-Lara, A, Lukehart, SA, Van Voorhis, WC
JournalMicrobes Infect
Volume6
Issue8
Pagination725-37
Date Published2004 Jul
ISSN1286-4579
KeywordsAmino Acid Sequence, Animals, Antibodies, Bacterial, Antigenic Variation, Bacterial Outer Membrane Proteins, Colony Count, Microbial, Conserved Sequence, Disease Models, Animal, DNA, Bacterial, Genes, Bacterial, Immunization, Lymphocyte Activation, Molecular Sequence Data, Polymorphism, Genetic, Rabbits, Sequence Alignment, Sequence Analysis, DNA, Syphilis, Cutaneous, Treponema pallidum
Abstract

A 12-membered Treponema pallidum repeat (Tpr) protein family has been identified in T. pallidum subsp. pallidum, the causative agent of syphilis. The subfamily I Tpr proteins (C, D, F, and I) possess conserved sequence at the N- and C-termini and central regions that differentiate the members. These proteins may be important in the immune response during syphilis infection and in protective immunity. Strong antibody responses have been observed toward some of the subfamily I Tpr proteins during infection with different syphilis isolates. Some sequence variation has also been identified in one subfamily I Tpr member, TprD, among T. pallidum subsp. pallidum isolates. In this study, we examined sequences in the remaining subfamily I Tpr proteins among strains. Both TprF and TprI were conserved among T. pallidum subsp. pallidum isolates. While some heterogeneity was identified in TprC. We further examined the immune response and protective capacity of TprF protein in this paper. We demonstrate that the N-terminal conserved region of the subfamily I Tpr proteins elicits strong antibody and T-cell responses during infection, and immunization with this region attenuates syphilitic lesion development upon infectious challenge.

DOI10.1016/j.micinf.2004.04.001
Alternate JournalMicrobes Infect.
PubMed ID15207819