Literature DB >> 6098033

Purification of Treponema pallidum, Nichols strain, by Percoll density gradient centrifugation.

P A Hanff, S J Norris, M A Lovett, J N Miller.   

Abstract

The purification of motile and virulent Treponema pallidum, Nichols strain, from rabbit testicular tissue is reported. Suspensions of T. pallidum were overlayed onto 20-ml cushions of 43% Percoll and in-situ density gradients were formed by centrifugation at 34,800 g for 30 min. Gradient fractionation indicated that T. pallidum banded at a density of 1.051 g/cc3 and that soluble proteineous testicular components remained in the upper portion of the gradient. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) confirmed the removal of host testicular and serum components. Purified suspensions of T. pallidum were greater than 95% actively motile and fully virulent, and greater than 50% motility could be maintained in vitro for up to five days. As determined by electron microscopy, Percoll-purified T. pallidum was structurally unaltered and contained much less tissue debris than did crude extracts or T. pallidum prepared by differential centrifugation. The Percoll purification method has been applied successfully to physiology, recombinant DNA, and antigenic structure studies, and to the preparation of antigen for the fluorescent treponemal antibody-absorbed (FTA-Abs) test for syphilis.

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Year:  1984        PMID: 6098033     DOI: 10.1097/00007435-198410000-00003

Source DB:  PubMed          Journal:  Sex Transm Dis        ISSN: 0148-5717            Impact factor:   2.830


  61 in total

1.  BAC library of T. pallidum DNA in E. coli.

Authors:  David Smajs; Matthew McKevitt; Ling Wang; Jerrilyn K Howell; Steven J Norris; Timothy Palzkill; George M Weinstock
Journal:  Genome Res       Date:  2002-03       Impact factor: 9.043

2.  Membrane topology and cellular location of the Treponema pallidum glycerophosphodiester phosphodiesterase (GlpQ) ortholog.

Authors:  D V Shevchenko; T J Sellati; D L Cox; O V Shevchenko; E J Robinson; J D Radolf
Journal:  Infect Immun       Date:  1999-05       Impact factor: 3.441

3.  Characterization of the cytoplasmic filament protein gene (cfpA) of Treponema pallidum subsp. pallidum.

Authors:  Y You; S Elmore; L L Colton; C Mackenzie; J K Stoops; G M Weinstock; S J Norris
Journal:  J Bacteriol       Date:  1996-06       Impact factor: 3.490

4.  Identification of homologs for thioredoxin, peptidyl prolyl cis-trans isomerase, and glycerophosphodiester phosphodiesterase in outer membrane fractions from Treponema pallidum, the syphilis spirochete.

Authors:  D V Shevchenko; D R Akins; E J Robinson; M Li; O V Shevchenko; J D Radolf
Journal:  Infect Immun       Date:  1997-10       Impact factor: 3.441

5.  Humoral response of the mouse to Treponema pallidum.

Authors:  J M Saunders; J D Folds
Journal:  Genitourin Med       Date:  1985-08

6.  Characterization of outer membranes isolated from Treponema pallidum, the syphilis spirochete.

Authors:  J D Radolf; E J Robinson; K W Bourell; D R Akins; S F Porcella; L M Weigel; J D Jones; M V Norgard
Journal:  Infect Immun       Date:  1995-11       Impact factor: 3.441

7.  Flagellins, but not endoflagellar sheath proteins, of Treponema pallidum and of pathogen-related oral spirochetes are glycosylated.

Authors:  C Wyss
Journal:  Infect Immun       Date:  1998-12       Impact factor: 3.441

8.  The outer membrane, not a coat of host proteins, limits antigenicity of virulent Treponema pallidum.

Authors:  D L Cox; P Chang; A W McDowall; J D Radolf
Journal:  Infect Immun       Date:  1992-03       Impact factor: 3.441

9.  Treponemal infection specifically enhances node T-cell regulation of macrophage activity.

Authors:  D R Tabor; O Bagasra; R F Jacobs
Journal:  Infect Immun       Date:  1986-10       Impact factor: 3.441

10.  Antibody-independent interactions of fibronectin, C1q, and human neutrophils with Treponema pallidum.

Authors:  R E Baughn
Journal:  Infect Immun       Date:  1986-11       Impact factor: 3.441

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