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Genetic characterization of hepatitis C virus strains in Estonia: Fluctuations in the predominating subtype with time

Tatjana TalloDepartment of Virology, National Institute for Health Development, Hiiu 42, 11619 Tallinn, EstoniaHeléne NorderDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institute, Stockholm, SwedenValentina TefanovaDepartment of Virology, National Institute for Health Development, Hiiu 42, 11619 Tallinn, EstoniaTõnu KrispinDepartment of Microbiology, University of Tartu, Tartu, EstoniaJelena SchmidtDepartment for Infectious Disease, Ida-Viru Central Hospital, Kohtla-Järve, EstoniaMadis IlmojaNephrology Department and Haemodialysis Unit, Tallinn-West Central Hospital, Tallinn, EstoniaKaren OrgulasDepartment of Oncohaematology, Tallinn Children's Hospital, EstoniaKaije PruunsildDepartment of Oncohaematology, Tallinn Children's Hospital, EstoniaLudmilla PriimägiDepartment of Virology, National Institute for Health Development, Hiiu 42, 11619 Tallinn, EstoniaLars O. MagniusDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institute, Stockholm, Sweden
2007en
ABI

Аннотация

During the last decade, there has been a dramatic increase in intravenous drug use in young adults in Estonia with an increased incidence of both hepatitis B and C as a consequence. Since genetic data are limited regarding hepatitis C virus (HCV) strains in Estonia, the aim of the study was to characterize HCV strains in different risk groups to determine their relatedness to strains from other geographical regions. Three hundred fifty-three anti-HCV positive sera collected during 1994-2004 from hospitalized patients, blood donors and health care workers were used as source of HCV RNA. Two hundred nine (59%) of the sera were positive for HCV RNA by PCR directed to the 5'-UTR region. For 174 strains the HCV subtype was determined by analyses of the NS5B and/or the 5'UTR-core regions. 1b (71%) was the most common subtype followed by 3a (24%), 2c (2%), 1a (1%), and 2a (1%). The 1b and 3a strains were similar to strains from other regions of the former USSR. Within genotype 1b there were several HCV lineages. However, for 3a there seemed to be two separate introductions into Estonia. There was a relative shift from subtype 1b to 3a in 1999-2000 with a further replacement of 3a with 1b in intravenous drug users in 2001 and onwards (P < 0.05). However, both subtypes were found to co-circulate in the community independent of risk factors. One patient was infected with the 2k/1b recombinant presumed to originate from St. Petersburg being the first isolate of this recombinant recovered outside Russia.

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