2001
DOI: 10.1002/1096-9071(20000201)63:2<189::aid-jmv1014>3.0.co;2-h
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TT virus levels in the plasma of infected individuals with different hepatic and extrahepatic pathology

Abstract: TT virus (TTV) infection is extremely widespread in the general population. A sensitive real-time PCR assay was developed that quantitated accurately the most prevalent TTV genotypes in Italy. When used to test 217 individuals for TTV viraemia, the overall prevalence was 94%. Viraemia levels varied widely amongst individual subjects, with no major differences related to gender or age. The highest TTV titres were in haemophiliacs and in patients with non-A-E hepatitis, but they did not differ from the group wit… Show more

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Cited by 53 publications
(23 citation statements)
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“…Genomic DNA was extracted from buffy coat cells by using the QIAamp DNA Blood Mini kit (Qiagen, Milan, Italy). Provirus DNA was quantitated by amplifying 0.3 to 0.6 g of extracted DNA by TM-PCR on the ABI Prism 7700 Sequence Detection System (Applied Biosystems, Monza, Italy), with 900 nM M2-S sense primer (AGACC GCTGCCCTATTTCACT; nucleotide positions 1296 to 1316 and referred to as FIV-Petaluma [59]), 300 nM M2-AS antisense primer (TTCTGGCTGGTGCA AATCTG; nucleotides 1367 to 1386), and 100 nM M2-P probe (TGCCTGTTG TTCTTGAGTTAATCCTATTCCCA; nucleotides 1330 to 1359) and under conditions described elsewhere (52). The standard curve was generated by coamplifying serial 10-fold dilutions (10 2 to 10 7 ) of pGEM-M2 plasmid containing the whole p25 region of FIV-M2.…”
Section: Methodsmentioning
confidence: 99%
“…Genomic DNA was extracted from buffy coat cells by using the QIAamp DNA Blood Mini kit (Qiagen, Milan, Italy). Provirus DNA was quantitated by amplifying 0.3 to 0.6 g of extracted DNA by TM-PCR on the ABI Prism 7700 Sequence Detection System (Applied Biosystems, Monza, Italy), with 900 nM M2-S sense primer (AGACC GCTGCCCTATTTCACT; nucleotide positions 1296 to 1316 and referred to as FIV-Petaluma [59]), 300 nM M2-AS antisense primer (TTCTGGCTGGTGCA AATCTG; nucleotides 1367 to 1386), and 100 nM M2-P probe (TGCCTGTTG TTCTTGAGTTAATCCTATTCCCA; nucleotides 1330 to 1359) and under conditions described elsewhere (52). The standard curve was generated by coamplifying serial 10-fold dilutions (10 2 to 10 7 ) of pGEM-M2 plasmid containing the whole p25 region of FIV-M2.…”
Section: Methodsmentioning
confidence: 99%
“…In people who have received multiple blood transfusions the virus is almost universally present with more than one subtype in each individual. Table 1 demonstrates the countrywide prevalence of TTV infection in different categories of populations including both healthy persons and patients with various types of diseases [62][63][64][65][66][67][68][69][70][71][72][73][74][75] .…”
Section: Epidemiologymentioning
confidence: 99%
“…The epidemiology and pathogenic potential of TTV is poorly understood. In several studies, however, the viral genome has been detected at comparable prevalence rates in the blood of healthy persons and patients and this led to the hypothesis that TTV might be essentially non-pathogenic in nature [18] . TTV can be transmitted by parenteral route, although its role in causing post-transfusion hepatitis has not been established.…”
Section: Introductionmentioning
confidence: 99%