Detection and genotyping of TT virus in healthy and subjects with HBV or HCV in different populations in the United Arab Emirates
TT virus (TTV) and TTV‐like viruses (TTVLs) have been reported to be associated with non‐A–E hepatitis. To determine the rate of infection and genotypic characteristics of TTV in the United Arab Emirates (UAE), a total of 449 serum samples representing different populations in the UAE and comprising...
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Veröffentlicht in: | Journal of medical virology 2004-03, Vol.72 (3), p.502-508 |
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Zusammenfassung: | TT virus (TTV) and TTV‐like viruses (TTVLs) have been reported to be associated with non‐A–E hepatitis. To determine the rate of infection and genotypic characteristics of TTV in the United Arab Emirates (UAE), a total of 449 serum samples representing different populations in the UAE and comprising healthy as well as patients positive for HBsAg and HCV were screened. National subjects (n = 200) and non‐nationals residing in the UAE (n = 249) were tested by PCR. The results obtained showed that the rate of TTV infection in healthy nationals, and those with HBsAg or antibody to HCV were 34.9, 97.9, and 95.7, respectively, compared to 89.1% (115/129), 89.2% (66/74), and 84.8% (39/46), respectively, in non‐nationals. Sequence analysis of the untranslated region (UTR) using 71 clones generated from the PCR products of eight serum samples from healthy individuals (four nationals and four non‐nationals) showed that 83.1% of the TTV clones were classified into groups 1–4, whereas 16.9% into possibly new genotype(s). The analysis also revealed that healthy national subjects carried multiple viruses. Phylogenetic analysis of representative sequences revealed clustering of clones into at least five major groups. Also, when compared to reference genotypes (from GenBank), two of our clones belonged to two previously identified genotypes. Non‐significant gender differences were seen in all ethnic groups studied (P > 0.05). In conclusion, the rate of TTV infection in the UAE nationals is significantly lower (P |
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ISSN: | 0146-6615 1096-9071 |
DOI: | 10.1002/jmv.20017 |