Polymorphism of the TT virus and its frequency in Polish blood donors

Objective To determine, in Polish blood donors, the frequency of TT virus (TTV) using different primers and the sequence diversity of TTV genotypes. Materials and Methods Two‐hundred blood donors were studied. TTV DNA was detected by the polymerase chain reaction (PCR) using primers for the coding (...

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Bibliographic Details
Published inVox sanguinis Vol. 82; no. 4; pp. 177 - 181
Main Authors Grabarczyk, P., Brojer, E.
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Science Ltd 01.05.2002
Blackwell
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Summary:Objective To determine, in Polish blood donors, the frequency of TT virus (TTV) using different primers and the sequence diversity of TTV genotypes. Materials and Methods Two‐hundred blood donors were studied. TTV DNA was detected by the polymerase chain reaction (PCR) using primers for the coding (ORF1) and non‐coding (NC) regions. Twenty isolates were genotyped by sequencing the ORF1 fragment. Results TTV DNA was detected in 78% of donors using NC primers and in 10% using ORF1 primers. The frequency of TTV DNA detection by NC primers was observed to increase with donor age, whereas the frequency of detection by ORF primers did not differ between various age‐groups. The nucleotide sequence homology of Polish TTV isolates ranged from 59 to 99%. Three genotypes (1b, 2b and 2c) were identified. Conclusions The frequency of TTV detection depends on the primers used for the PCR. Using the NC primers the virus is detected in the majority of donors, whereas the ORF1 primers strongly underestimate the prevalence of TTV. The frequency of TTV DNA increases with age. Polish TTV isolates are highly polymorphic and are classified as 1b, 2b and 2c.
Bibliography:ark:/67375/WNG-HZD31B7N-K
istex:6E5B21612A5A7F00608E43B5FFD11CF00586D308
ArticleID:VOX178
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0042-9007
1423-0410
DOI:10.1046/j.1423-0410.2002.00178.x