1997
DOI: 10.1590/s0100-879x1997000300006
|View full text |Cite
|
Sign up to set email alerts
|

Genomic characterization of Brazilian hepatitis C virus genotypes 1a and 1b

Abstract: Parts of 5' non-coding (5' NC) and of E1 envelope regions of the hepatitis C virus (HCV) genome were amplified from sera of 26 Brazilian anti-HCV antibody-positive patients using the reverse transcription-polymerase chain reaction (RT-PCR). Fourteen samples were PCR positive with primers from the 5' NC region and 8 of them were also positive with primers from the E1 region. A genomic segment of 176 bp from the E1 region of 7 isolates was directly sequenced from PCR products. The sequences were compared with th… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
28
0
2

Year Published

2002
2002
2019
2019

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 35 publications
(30 citation statements)
references
References 33 publications
(28 reference statements)
0
28
0
2
Order By: Relevance
“…Detection and genotyping of HCV RNA -All samples were submitted to RNA extraction, reverse transcription, and a nested PCR with primers complementary to the conserved area of the 5' non-coding region of HCV, essentially as described by Ginabreda et al (1997). Positive samples were genotyped by line probe assay (INNO-LiPA HCV, Innogenetics NV, Ghent, Belgium).…”
Section: Methodsmentioning
confidence: 99%
“…Detection and genotyping of HCV RNA -All samples were submitted to RNA extraction, reverse transcription, and a nested PCR with primers complementary to the conserved area of the 5' non-coding region of HCV, essentially as described by Ginabreda et al (1997). Positive samples were genotyped by line probe assay (INNO-LiPA HCV, Innogenetics NV, Ghent, Belgium).…”
Section: Methodsmentioning
confidence: 99%
“…Sixty-six anti-HCV positive samples were subjected to RNA extraction by the commercially standardized reagents (QIAamp Viral RNA Mini Kit, Qiagen, Hilden, Germany) according to the manufacturer's instructions, followed by reverse transcription, as described by GINABREDA et al 11 . cDNA was amplified using the primers complementary to the conserved area of the 5' NC and NS5B regions and PCR conditions described by GINABREDA et al 11 and SANDRES-SAUNÉ et al 21 , respectively.…”
mentioning
confidence: 99%
“…cDNA was amplified using the primers complementary to the conserved area of the 5' NC and NS5B regions and PCR conditions described by GINABREDA et al 11 and SANDRES-SAUNÉ et al 21 , respectively.…”
mentioning
confidence: 99%
“…Positive samples were retested for confirmation using a line immunoassay (INNO-LIA HCV Ab III, Innogenetics). All samples were submitted to RNA extraction, reverse transcription, and a nested PCR with primers complementary to the conserved area of the 5' non-coding region of HCV, essentially as describe by Ginabreda et al (1997). Prevalence and 95% confidence intervals (95% CI) were calculated.…”
mentioning
confidence: 99%