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Amino Acid Polymorphisms Within the Entire HCV NS5A Region in Estonian Chronic HCV 1b Patients With Different Treatment Response
A substantial proportion of hepatitis C virus (HCV)-1b infected patients do not response to pegylated interferon-α plus ribavirin (PegIFNα/RBV) combination therapy that was partially associated with mutations in the non-structural 5A (NS5A) protein. Analysis of NS5A polymorphisms in HCV genotype 1b...
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Published in: | Hepatitis monthly 2013-12, Vol.13 (12), p.e14481-e14481 |
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creator | Kuznetsova, Tatiana Tallo, Tatjana Brjalin, Vadim Reshetnjak, Irina Salupere, Riina Priimagi, Ljudmilla Katargina, Olga Smirnova, Maria Jansons, Juris Tefanova, Valentina |
description | A substantial proportion of hepatitis C virus (HCV)-1b infected patients do not response to pegylated interferon-α plus ribavirin (PegIFNα/RBV) combination therapy that was partially associated with mutations in the non-structural 5A (NS5A) protein.
Analysis of NS5A polymorphisms in HCV genotype 1b pre-treatment serum samples from Estonian patients and their effect on the treatment response.
Twenty-nine complete NS5A sequences obtained from patients with chronic HCV-1b infection who had received combined therapy with PegIFNα-2a/RBV were analyzed and compared with the prototype strain HCV-J. Twelve patients achieved a sustained virological response (SVR), 15 were non-SVR and 2 patients stopped treatment because of side effects.
No significant difference in total number of amino acid mutations was observed between isolates from SVR and non-SVR patients in any known regions of the NS5A protein. However, specific amino acid substitutions at positions 1989 and 2283 correlated significantly with SVR, mutations at positions 1979, 2107, 2171 and 2382 were associated with non-response to treatment and amino acid substitution at position 2319 was observed in relapsers. At phylogenetic analysis, NS5A nucleotide sequences have been subdivided into four groups characterized by the different treatment response. Twenty-four novel nucleotide polymorphisms and 11 novel amino acid polymorphisms were identified based on the phylogenetic tree topology.
Specific amino acid substitutions correlating with the treatment response were found. Polymorphisms revealed by phylogenetic analysis may define the signature patterns for treatment susceptible and treatment resistant strains prevalent in Estonia. |
doi_str_mv | 10.5812/hepatmon.14481 |
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Analysis of NS5A polymorphisms in HCV genotype 1b pre-treatment serum samples from Estonian patients and their effect on the treatment response.
Twenty-nine complete NS5A sequences obtained from patients with chronic HCV-1b infection who had received combined therapy with PegIFNα-2a/RBV were analyzed and compared with the prototype strain HCV-J. Twelve patients achieved a sustained virological response (SVR), 15 were non-SVR and 2 patients stopped treatment because of side effects.
No significant difference in total number of amino acid mutations was observed between isolates from SVR and non-SVR patients in any known regions of the NS5A protein. However, specific amino acid substitutions at positions 1989 and 2283 correlated significantly with SVR, mutations at positions 1979, 2107, 2171 and 2382 were associated with non-response to treatment and amino acid substitution at position 2319 was observed in relapsers. At phylogenetic analysis, NS5A nucleotide sequences have been subdivided into four groups characterized by the different treatment response. Twenty-four novel nucleotide polymorphisms and 11 novel amino acid polymorphisms were identified based on the phylogenetic tree topology.
Specific amino acid substitutions correlating with the treatment response were found. Polymorphisms revealed by phylogenetic analysis may define the signature patterns for treatment susceptible and treatment resistant strains prevalent in Estonia.</description><identifier>ISSN: 1735-143X</identifier><identifier>EISSN: 1735-3408</identifier><identifier>DOI: 10.5812/hepatmon.14481</identifier><identifier>PMID: 24358043</identifier><language>eng</language><publisher>Iran: Tehran Hepatitis Center</publisher><ispartof>Hepatitis monthly, 2013-12, Vol.13 (12), p.e14481-e14481</ispartof><rights>Copyright Tehran Hepatitis Center Dec 2013</rights><rights>Copyright © 2013, Kowsar Corp. 2013</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c418t-fb783c08fd3eaf0fc9b9e3690d117ca72aee5930c6ef65f4dfcd9f94b9002d6a3</citedby><cites>FETCH-LOGICAL-c418t-fb783c08fd3eaf0fc9b9e3690d117ca72aee5930c6ef65f4dfcd9f94b9002d6a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3867023/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3867023/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,725,778,782,883,27907,27908,53774,53776</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24358043$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kuznetsova, Tatiana</creatorcontrib><creatorcontrib>Tallo, Tatjana</creatorcontrib><creatorcontrib>Brjalin, Vadim</creatorcontrib><creatorcontrib>Reshetnjak, Irina</creatorcontrib><creatorcontrib>Salupere, Riina</creatorcontrib><creatorcontrib>Priimagi, Ljudmilla</creatorcontrib><creatorcontrib>Katargina, Olga</creatorcontrib><creatorcontrib>Smirnova, Maria</creatorcontrib><creatorcontrib>Jansons, Juris</creatorcontrib><creatorcontrib>Tefanova, Valentina</creatorcontrib><title>Amino Acid Polymorphisms Within the Entire HCV NS5A Region in Estonian Chronic HCV 1b Patients With Different Treatment Response</title><title>Hepatitis monthly</title><addtitle>Hepat Mon</addtitle><description>A substantial proportion of hepatitis C virus (HCV)-1b infected patients do not response to pegylated interferon-α plus ribavirin (PegIFNα/RBV) combination therapy that was partially associated with mutations in the non-structural 5A (NS5A) protein.
Analysis of NS5A polymorphisms in HCV genotype 1b pre-treatment serum samples from Estonian patients and their effect on the treatment response.
Twenty-nine complete NS5A sequences obtained from patients with chronic HCV-1b infection who had received combined therapy with PegIFNα-2a/RBV were analyzed and compared with the prototype strain HCV-J. Twelve patients achieved a sustained virological response (SVR), 15 were non-SVR and 2 patients stopped treatment because of side effects.
No significant difference in total number of amino acid mutations was observed between isolates from SVR and non-SVR patients in any known regions of the NS5A protein. However, specific amino acid substitutions at positions 1989 and 2283 correlated significantly with SVR, mutations at positions 1979, 2107, 2171 and 2382 were associated with non-response to treatment and amino acid substitution at position 2319 was observed in relapsers. At phylogenetic analysis, NS5A nucleotide sequences have been subdivided into four groups characterized by the different treatment response. Twenty-four novel nucleotide polymorphisms and 11 novel amino acid polymorphisms were identified based on the phylogenetic tree topology.
Specific amino acid substitutions correlating with the treatment response were found. Polymorphisms revealed by phylogenetic analysis may define the signature patterns for treatment susceptible and treatment resistant strains prevalent in Estonia.</description><issn>1735-143X</issn><issn>1735-3408</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNpdkc1v1DAQxS1ERUvhyhFZ4sJlFzt24viCtFoWilSVqpSPm-U448ZVYqe2F6k3_nTc7rYCTn7W_ObpjR5CryhZ1i2t3g0w6zwFv6Sct_QJOqKC1QvGSft0rylnPw_R85SuCalbIqpn6LDirEjOjtDv1eR8wCvjenwextspxHlwaUr4h8uD8zgPgDc-uwj4ZP0dn32tV_gCrlzwuEw3KQfvtMfrIRZh7hna4XOdHfi8c8EfnLUQyx9fRihx79QFpDn4BC_QgdVjgpf79xh9-7i5XJ8sTr98-rxenS4Mp21e2E60zJDW9gy0JdbITgJrJOkpFUaLSgPUkhHTgG1qy3tremkl7yQhVd9odoze73znbTdBb0qGqEc1RzfpeKuCdurfiXeDugq_FGsbQSpWDN7uDWK42ULKanLJwDhqD2GbFOWSCEZl0xT0zX_oddhGX84rlKhZxbiQhVruKBNDShHsYxhK1F256qFcdV9uWXj99wmP-EOb7A9rFaO8</recordid><startdate>20131214</startdate><enddate>20131214</enddate><creator>Kuznetsova, Tatiana</creator><creator>Tallo, Tatjana</creator><creator>Brjalin, Vadim</creator><creator>Reshetnjak, Irina</creator><creator>Salupere, Riina</creator><creator>Priimagi, Ljudmilla</creator><creator>Katargina, Olga</creator><creator>Smirnova, Maria</creator><creator>Jansons, Juris</creator><creator>Tefanova, Valentina</creator><general>Tehran Hepatitis Center</general><general>Kowsar</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>CWDGH</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20131214</creationdate><title>Amino Acid Polymorphisms Within the Entire HCV NS5A Region in Estonian Chronic HCV 1b Patients With Different Treatment Response</title><author>Kuznetsova, Tatiana ; Tallo, Tatjana ; Brjalin, Vadim ; Reshetnjak, Irina ; Salupere, Riina ; Priimagi, Ljudmilla ; Katargina, Olga ; Smirnova, Maria ; Jansons, Juris ; Tefanova, Valentina</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c418t-fb783c08fd3eaf0fc9b9e3690d117ca72aee5930c6ef65f4dfcd9f94b9002d6a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Kuznetsova, Tatiana</creatorcontrib><creatorcontrib>Tallo, Tatjana</creatorcontrib><creatorcontrib>Brjalin, Vadim</creatorcontrib><creatorcontrib>Reshetnjak, Irina</creatorcontrib><creatorcontrib>Salupere, Riina</creatorcontrib><creatorcontrib>Priimagi, Ljudmilla</creatorcontrib><creatorcontrib>Katargina, Olga</creatorcontrib><creatorcontrib>Smirnova, Maria</creatorcontrib><creatorcontrib>Jansons, Juris</creatorcontrib><creatorcontrib>Tefanova, Valentina</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Middle East & Africa Database</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Hepatitis monthly</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kuznetsova, Tatiana</au><au>Tallo, Tatjana</au><au>Brjalin, Vadim</au><au>Reshetnjak, Irina</au><au>Salupere, Riina</au><au>Priimagi, Ljudmilla</au><au>Katargina, Olga</au><au>Smirnova, Maria</au><au>Jansons, Juris</au><au>Tefanova, Valentina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Amino Acid Polymorphisms Within the Entire HCV NS5A Region in Estonian Chronic HCV 1b Patients With Different Treatment Response</atitle><jtitle>Hepatitis monthly</jtitle><addtitle>Hepat Mon</addtitle><date>2013-12-14</date><risdate>2013</risdate><volume>13</volume><issue>12</issue><spage>e14481</spage><epage>e14481</epage><pages>e14481-e14481</pages><issn>1735-143X</issn><eissn>1735-3408</eissn><abstract>A substantial proportion of hepatitis C virus (HCV)-1b infected patients do not response to pegylated interferon-α plus ribavirin (PegIFNα/RBV) combination therapy that was partially associated with mutations in the non-structural 5A (NS5A) protein.
Analysis of NS5A polymorphisms in HCV genotype 1b pre-treatment serum samples from Estonian patients and their effect on the treatment response.
Twenty-nine complete NS5A sequences obtained from patients with chronic HCV-1b infection who had received combined therapy with PegIFNα-2a/RBV were analyzed and compared with the prototype strain HCV-J. Twelve patients achieved a sustained virological response (SVR), 15 were non-SVR and 2 patients stopped treatment because of side effects.
No significant difference in total number of amino acid mutations was observed between isolates from SVR and non-SVR patients in any known regions of the NS5A protein. However, specific amino acid substitutions at positions 1989 and 2283 correlated significantly with SVR, mutations at positions 1979, 2107, 2171 and 2382 were associated with non-response to treatment and amino acid substitution at position 2319 was observed in relapsers. At phylogenetic analysis, NS5A nucleotide sequences have been subdivided into four groups characterized by the different treatment response. Twenty-four novel nucleotide polymorphisms and 11 novel amino acid polymorphisms were identified based on the phylogenetic tree topology.
Specific amino acid substitutions correlating with the treatment response were found. Polymorphisms revealed by phylogenetic analysis may define the signature patterns for treatment susceptible and treatment resistant strains prevalent in Estonia.</abstract><cop>Iran</cop><pub>Tehran Hepatitis Center</pub><pmid>24358043</pmid><doi>10.5812/hepatmon.14481</doi><oa>free_for_read</oa></addata></record> |
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title | Amino Acid Polymorphisms Within the Entire HCV NS5A Region in Estonian Chronic HCV 1b Patients With Different Treatment Response |
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