Literature DB >> 3544252

Serum requirement for the multiplication of Treponema pallidum in a tissue-culture system: association of growth-promoting activity with the protein fraction.

S J Norris, D G Edmondson.   

Abstract

The nature of the serum requirement of Treponema pallidum subspecies pallidum (Nichols strain) was examined in a culture system utilizing Sf1Ep cottontail rabbit cells. In this system, significant multiplication of treponemes occurs in the presence of select lots of fetal bovine serum (FBS) or calf serum (CS) at concentrations of greater than or equal to 5% (vol/vol). Heat-inactivation of the serum greatly enhances treponemal multiplication, and normal human serum was found to be as effective as FBS in supporting the growth of T. pallidum. The protein fraction of FBS obtained by membrane ultrafiltration was capable of supporting the multiplication of T. pallidum when added to the basal tissue culture medium; an average increase of 23-fold was observed in these cultures, as compared with a mean increase of 25-fold in the 20% FBS controls. In contrast, the ultrafiltrate fraction of FBS (consisting of compounds with molecular weights of less than 10,000 daltons) did not support either growth or the retention of motility. Proteins precipitable with 25% (wt/vol) polyethylene glycol (i.e., albumin, transferrin, ceruloplasmin, and other proteins) also promoted the growth of T. pallidum. This observation provides further evidence that the required serum components are associated with the protein fraction.

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Year:  1986        PMID: 3544252     DOI: 10.1097/00007435-198610000-00001

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


  8 in total

1.  In vitro culture system to determine MICs and MBCs of antimicrobial agents against Treponema pallidum subsp. pallidum (Nichols strain).

Authors:  S J Norris; D G Edmondson
Journal:  Antimicrob Agents Chemother       Date:  1988-01       Impact factor: 5.191

2.  Complementation of an Escherichia coli proC mutation by a gene cloned from Treponema pallidum.

Authors:  F C Gherardini; M M Hobbs; L V Stamm; P J Bassford
Journal:  J Bacteriol       Date:  1990-06       Impact factor: 3.490

3.  High- and low-infectivity phenotypes of clonal populations of in vitro-cultured Borrelia burgdorferi.

Authors:  S J Norris; J K Howell; S A Garza; M S Ferdows; A G Barbour
Journal:  Infect Immun       Date:  1995-06       Impact factor: 3.441

4.  Characterization of the low-molecular-mass proteins of virulent Treponema pallidum.

Authors:  L V Stamm; E A Parrish
Journal:  Infect Immun       Date:  1994-01       Impact factor: 3.441

Review 5.  Polypeptides of Treponema pallidum: progress toward understanding their structural, functional, and immunologic roles. Treponema Pallidum Polypeptide Research Group.

Authors:  S J Norris
Journal:  Microbiol Rev       Date:  1993-09

6.  Heterologous expression of the Treponema pallidum laminin-binding adhesin Tp0751 in the culturable spirochete Treponema phagedenis.

Authors:  Caroline E Cameron; Janelle M Y Kuroiwa; Mitsunori Yamada; Teresa Francescutti; Bo Chi; Howard K Kuramitsu
Journal:  J Bacteriol       Date:  2008-02-08       Impact factor: 3.490

7.  Long-Term In Vitro Culture of the Syphilis Spirochete Treponema pallidum subsp. pallidum.

Authors:  Diane G Edmondson; Bo Hu; Steven J Norris
Journal:  mBio       Date:  2018-06-26       Impact factor: 7.867

8.  In Vitro Cultivation of the Syphilis Spirochete Treponema pallidum.

Authors:  Diane G Edmondson; Steven J Norris
Journal:  Curr Protoc       Date:  2021-02
  8 in total

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