Literature DB >> 3520447

Analysis of antigen switching rates in Trypanosoma brucei.

G S Lamont, R S Tucker, G A Cross.   

Abstract

Previously quoted figures for the frequency of antigen switching in Trypanosoma brucei are based on incorrect assumptions. In order to determine the correct switching frequency, an equation was derived that takes the growth rates of the newly expressed antigen types into consideration as well as the proportion of switched trypanosomes and the number of generations since the population was antigenically homogeneous. When this equation was applied to published in vitro data, variable values were obtained for the switching frequency in clonal populations originally expressing one antigen type. The calculated most likely switching frequencies ranged from 1.4 X 10(-7) to 3.5 X 10(-6). This variation was probably caused by differences in the growth rates of the new antigen types in the population and failure to detect slow growing variants. To overcome these problems, an experimental procedure was developed to analyse the switching frequency in vitro. Trypanosomes were cloned and grown in parallel cultures. After an appropriate number of generations, cells expressing the original antigen type were destroyed and, from the proportion of cultures that contained new antigen types, the switching frequency was calculated. The technique minimized subculturing or other procedures that could distort the results. Although the method was optimized for analysing switching frequency, the values differed between experiments, ranging from 2.2 X 10(-7) to 2.6 X 10(-6) for one variant. Possible causes for the variations in switching frequency are discussed.

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Year:  1986        PMID: 3520447     DOI: 10.1017/s003118200006412x

Source DB:  PubMed          Journal:  Parasitology        ISSN: 0031-1820            Impact factor:   3.234


  25 in total

1.  Targeting the variable surface of African trypanosomes with variant surface glycoprotein-specific, serum-stable RNA aptamers.

Authors:  Mihaela Lorger; Markus Engstler; Matthias Homann; H Ulrich Göringer
Journal:  Eukaryot Cell       Date:  2003-02

2.  High-efficiency clonal growth of bloodstream- and insect-form Trypanosoma brucei on agarose plates.

Authors:  V B Carruthers; G A Cross
Journal:  Proc Natl Acad Sci U S A       Date:  1992-09-15       Impact factor: 11.205

3.  Consequences of telomere shortening at an active VSG expression site in telomerase-deficient Trypanosoma brucei.

Authors:  Oliver Dreesen; George A M Cross
Journal:  Eukaryot Cell       Date:  2006-10-27

4.  Trypanosome variant surface glycoprotein transfer to target membranes: a model for the pathogenesis of trypanosomiasis.

Authors:  M R Rifkin; F R Landsberger
Journal:  Proc Natl Acad Sci U S A       Date:  1990-01       Impact factor: 11.205

5.  Predominance of duplicative VSG gene conversion in antigenic variation in African trypanosomes.

Authors:  N P Robinson; N Burman; S E Melville; J D Barry
Journal:  Mol Cell Biol       Date:  1999-09       Impact factor: 4.272

6.  Sequence divergence in a family of variant surface glycoprotein genes from trypanosomes: coding region hypervariability and downstream recombinogenic repeats.

Authors:  M C Field; J C Boothroyd
Journal:  J Mol Evol       Date:  1996-05       Impact factor: 2.395

7.  DNA rearrangements associated with multiple consecutive directed antigenic switches in Trypanosoma brucei.

Authors:  M Navarro; G A Cross
Journal:  Mol Cell Biol       Date:  1996-07       Impact factor: 4.272

8.  Gene conversions mediating antigenic variation in Trypanosoma brucei can occur in variant surface glycoprotein expression sites lacking 70-base-pair repeat sequences.

Authors:  R McCulloch; G Rudenko; P Borst
Journal:  Mol Cell Biol       Date:  1997-02       Impact factor: 4.272

9.  Developmental regulation of a novel repetitive protein of Trypanosoma brucei.

Authors:  M R Mowatt; C E Clayton
Journal:  Mol Cell Biol       Date:  1987-08       Impact factor: 4.272

10.  Improved separation of chromosome-sized DNA from Trypanosoma brucei, stock 427-60.

Authors:  L H Van der Ploeg; C L Smith; R I Polvere; K M Gottesdiener
Journal:  Nucleic Acids Res       Date:  1989-04-25       Impact factor: 16.971

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