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Genome Analysis of Treponema Pallidum Subsp. Pallidum and Subsp. Pertenue Strains: Most of the Genetic Differences Are Localized in Six Regions

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Journal PLoS One
Date 2011 Jan 7
PMID 21209953
Citations 37
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Abstract

The genomes of eight treponemes including T. p. pallidum strains (Nichols, SS14, DAL-1 and Mexico A), T. p. pertenue strains (Samoa D, CDC-2 and Gauthier), and the Fribourg-Blanc isolate, were amplified in 133 overlapping amplicons, and the restriction patterns of these fragments were compared. The approximate sizes of the genomes investigated based on this whole genome fingerprinting (WGF) analysis ranged from 1139.3-1140.4 kb, with the estimated genome sequence identity of 99.57-99.98% in the homologous genome regions. Restriction target site analysis, detecting the presence of 1773 individual restriction sites found in the reference Nichols genome, revealed a high genome structure similarity of all strains. The unclassified simian Fribourg-Blanc isolate was more closely related to T. p. pertenue than to T. p. pallidum strains. Most of the genetic differences between T. p. pallidum and T. p. pertenue strains were accumulated in six genomic regions. These genome differences likely contribute to the observed differences in pathogenicity between T. p. pallidum and T. p. pertenue strains. These regions of sequence divergence could be used for the molecular detection and discrimination of syphilis and yaws strains.

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References
1.
Wendel Jr G, Sanchez P, Peters M, Harstad T, Potter L, Norgard M . Identification of Treponema pallidum in amniotic fluid and fetal blood from pregnancies complicated by congenital syphilis. Obstet Gynecol. 1991; 78(5 Pt 2):890-5. View

2.
Hackett C . ON THE ORIGIN OF THE HUMAN TREPONEMATOSES (PINTA, YAWS, ENDEMIC SYPHILIS AND VENEREAL SYPHILIS). Bull World Health Organ. 1963; 29:7-41. PMC: 2554777. View

3.
GASTINEL P, Vaisman A, Hamelin A, DUNOYER F . [Study of a recently isolated strain of Treponema pertenue]. Ann Dermatol Syphiligr (Paris). 1963; 90:155-61. View

4.
Harper K, Ocampo P, Steiner B, George R, Silverman M, Bolotin S . On the origin of the treponematoses: a phylogenetic approach. PLoS Negl Trop Dis. 2008; 2(1):e148. PMC: 2217670. DOI: 10.1371/journal.pntd.0000148. View

5.
Stamm L, Kerner Jr T, Bankaitis V, Bassford Jr P . Identification and preliminary characterization of Treponema pallidum protein antigens expressed in Escherichia coli. Infect Immun. 1983; 41(2):709-21. PMC: 264700. DOI: 10.1128/iai.41.2.709-721.1983. View