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Infection and Immunity, November 2000, p. 6482-6486, Vol. 68, No. 11
Program in Infectious Diseases, Department of
Epidemiology, School of Public Health, University of North Carolina,
Chapel Hill, North Carolina 27599-7400
Received 17 May 2000/Returned for modification 24 July
2000/Accepted 18 August 2000
Syphilis is a chronic infection with early relapses that are
hypothesized to result from the emergence of phenotypic variants of
Treponema pallidum. Recent studies demonstrated that TprK, a target of protective immunity, is heterogeneous in several T. pallidum strains, but not in Nichols strain Seattle (A. Centurion-Lara, C. Godornes, C. Castro, W. C. Van Voorhis, and
S. A. Lukehart, Infect. Immun. 68:824-831, 2000). Analysis of
PCR-amplified tprK from Nichols strain UNC and Street
strain 14 treponemes showed that TprK has seven regions of intrastrain
heterogeneity resulting from amino acid substitutions, insertions, and
deletions. In contrast, analysis of PCR-amplified tprJ
showed little intrastrain or interstrain heterogeneity. Reverse
transcriptase PCR analysis demonstrated that mRNA transcripts
representing unique polymorphic TprK proteins are present during
syphilitic infection. Southern hybridization confirmed that Nichols
strain UNC and Street strain 14 each contain a single copy of
tprK, indicating that intrastrain heterogeneity is due to
the presence of multiple treponemal subpopulations which contain a
variant form of tprK.
0019-9567/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
The Sequence-Variable, Single-Copy tprK
Gene of Treponema pallidum Nichols Strain UNC and Street
Strain 14 Encodes Heterogeneous TprK Proteins
*
Corresponding author. Mailing address: Program in
Infectious Diseases, Department of Epidemiology, School of Public
Health, University of North Carolina, Chapel Hill, NC 27599-7400. Phone: (919) 966-3882. Fax: (919) 966-2089. E-mail:
lstamm{at}emailunc.edu.
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