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Infection and Immunity, November 2006, p. 6244-6251, Vol. 74, No. 11
0019-9567/06/$08.00+0 doi:10.1128/IAI.00827-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
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Departments of Pathobiology,1 Medicine, University of Washington, Seattle, Washington2
Received 22 May 2006/ Returned for modification 25 June 2006/ Accepted 11 August 2006
The tprK gene in the syphilis spirochete, Treponema pallidum subsp. pallidum, undergoes antigenic variation in seven variable (V) regions. tprK is highly variable within T. pallidum strains, and a method has been developed to derive clones of T. pallidum that express a single, unique tprK sequence. Rabbits were infected with three different T. pallidum clones or the parent strain from which the clones were derived, and their sera were examined by immunoassay for antibody reactivity against synthetic peptides representing the TprK V regions from each clone. The parent strain expresses many different V region sequences, and infection with this strain induced antibody responses against a wide variety of V regions. In rabbits infected with the Chicago C clone, antibodies developed against all of the V regions except V1, while antibodies developed against only V5, V6, and V7 in Chicago A-infected rabbits. During Chicago B infection, antibodies developed against all of the V regions except V1 and V3. Antibodies were highly specific for the V regions of the infecting clone, and cross-reactivity was rare. The demonstration that the V regions elicit a variant-specific antibody response supports the hypothesis that TprK variants may help organisms to avoid the developing immune response in infected individuals, contributing to the ability of T. pallidum to establish chronic infection.
Published ahead of print on 21 August 2006.
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