2004
DOI: 10.1016/j.meegid.2003.12.003
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Genetic variability between Trichomonas vaginalis isolates and correlation with clinical presentation

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Cited by 30 publications
(16 citation statements)
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“…Currently, there is no "gold standard" method for genotyping isolates of T. vaginalis. A number of methods have been used in previous attempts to characterize the genetic diversity and population structure of T. vaginalis including isoenzyme analysis, repetitive sequence hybridization, random amplified polymorphic DNA, restriction fragment length polymorphism (RFLP), sequence polymorphisms in rRNA genes and intergenic regions, pulsed-field gel electrophoresis, and antigenic characterization (3,17,26,43,49,50,58,60,64,65). These methods have variable levels of reproducibility and precision in determining the genetic relatedness of isolates.…”
mentioning
confidence: 99%
“…Currently, there is no "gold standard" method for genotyping isolates of T. vaginalis. A number of methods have been used in previous attempts to characterize the genetic diversity and population structure of T. vaginalis including isoenzyme analysis, repetitive sequence hybridization, random amplified polymorphic DNA, restriction fragment length polymorphism (RFLP), sequence polymorphisms in rRNA genes and intergenic regions, pulsed-field gel electrophoresis, and antigenic characterization (3,17,26,43,49,50,58,60,64,65). These methods have variable levels of reproducibility and precision in determining the genetic relatedness of isolates.…”
mentioning
confidence: 99%
“…The isolate T-H7 of T. vaginalis was axenized from a symptomatic woman following the methodology described by Rojas et al (2004). Parasites were cultured in TYI (Diamond et al 1978) supplemented with heat-inactivated bovine serum at a final concentration of 10%, under anaerobic conditions, at 37 C. Cultures at exponential phase were used for the experiments.…”
Section: Parasites Culturesmentioning
confidence: 99%
“…Initial investigations into T. vaginalis genetic diversity used RAPD analysis (Rapid Amplification of Polymorphic DNA) 7 . Drawbacks of this method are a lack of reproducibility between laboratories and a requirement for DNA from axenic organisms, since DNA from any source can act as a template for amplification when using random primer annealing.…”
Section: Introductionmentioning
confidence: 99%