## Abstract Hepatitis C virus (HCV) subtypes were determined in 125 Iranian patients by phylogenetic analysis within the NS5B or 5′‐UTR/core regions. Subtypes 1a and 3a were predominant accounting for 47 and 36%, whereas 1b and 4 accounted for 8 and 7%. This subtype distribution differs from that o
Molecular and phylogenetic analysis of human influenza virus among Iranian patients in Shiraz, Iran
✍ Scribed by Mahsa Shahidi; Masoumeh Tavassoti Kheiri; Samad Amini-Bavil-Olyaee; Masoud Hosseini; Afagh Moattari; Mansoureh Tabatabaeian; Rouzbeh Bashar; Ramin Sarrami-Forooshani; Fereidoun Mahboudi
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 217 KB
- Volume
- 79
- Category
- Article
- ISSN
- 0146-6615
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✦ Synopsis
Abstract
Influenza is a viral respiratory pathogen responsible for frequent seasonal epidemics. There are currently three major human influenza viruses in global circulation namely A/H1N1, A/H3N2, and B. The objective of this study was to determine the human influenza virus genotypes in Shiraz, the capital of the Fars province of Iran. Three hundred patients suspected with human influenza virus infection were enrolled in this survey (2004–2005). The throat samples were cultured and titrated by hemagglutination (HA) assay. Typing and subtyping were performed by an in‐house developed multiplex RT–PCR. Moreover, the phylogenetic analysis was carried out for HA gene. A total of 24 samples were found to be positive for human influenza virus infection, 17 H1N1 and 7 H3N2. These results were in agreement with the HI assay. The phylogenetic analysis results revealed that the Iranian H1N1 isolated were close to the A/New Caledonia/20/99 vaccine strain genetically and the Iranian H3N2 isolates were also related closely to the Fujian/411/021 and California/7/2004 vaccine strains. However, a slight genetic drift was found in these isolates. In conclusion, it was demonstrated that both influenza A subtypes A/H1N1 and A/H3N2 were dominant among Iranian patients in Shiraz during the 2004/5 winter season. J. Med. Virol. 79: 803–810, 2007. © 2007 Wiley‐Liss, Inc.
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