Analysis of influenza A/H3N2 neuraminidase genes obtained from influenza patients in the 2011/12 and 2012/13 seasons in Japan
Influenza virus has neuraminidase (NA), a surface protein with enzymatic activity that is essential for virus replication. Mutation may affect the effectiveness of NA inhibitors that are used for the treatment of influenza patients. In this study, we determined the NA gene sequences from the clinica...
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Veröffentlicht in: | Fukuoka igaku zasshi = Hukuoka acta medica 2015-01, Vol.106 (1), p.16-22 |
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creator | Ikematsu, Hideyuki Chong, Yong Shirane, Kenjiro Toh, Hidehiro Sasaki, Hiroyuki Koga, Yui Urata, Michiyo Hotta, Taeko Uchiumi, Takeshi Kang, Donchon |
description | Influenza virus has neuraminidase (NA), a surface protein with enzymatic activity that is essential for virus replication. Mutation may affect the effectiveness of NA inhibitors that are used for the treatment of influenza patients. In this study, we determined the NA gene sequences from the clinical isolates of influenza patients to examine the chronological genetic changes and the relation to drug susceptibility.
For 96 A/H3N2 virus isolates the 50% inhibitory concentration (IC50) (48 each from the 2011-12 and 12-13 influenza seasons) was measured. RT-PCR was done with extracted viral RNA, followed by nucleotide sequencing.
One putative amino acid mutation, D151N, was found in an NA activity-related cite in five of ninety-six tested isolate. The mutation did not affect the IC50 value. The mutations identified at amino acid positions 387 and 400 were statistically correlated with an increased IC50 value, although the change was less than ten times, suggesting no significant difference in the clinical effectiveness. A small number .of isolates showed mutation in the T and/or B cell epitope region of NA.
No mutation that affected the IC50 value or effectiveness of NAIs was detected. Antigenic mutations of NA, which influence the selection of epidemic strains, were not determined. Continuous observation will be necessary to further clarify the genetic features of NA. |
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For 96 A/H3N2 virus isolates the 50% inhibitory concentration (IC50) (48 each from the 2011-12 and 12-13 influenza seasons) was measured. RT-PCR was done with extracted viral RNA, followed by nucleotide sequencing.
One putative amino acid mutation, D151N, was found in an NA activity-related cite in five of ninety-six tested isolate. The mutation did not affect the IC50 value. The mutations identified at amino acid positions 387 and 400 were statistically correlated with an increased IC50 value, although the change was less than ten times, suggesting no significant difference in the clinical effectiveness. A small number .of isolates showed mutation in the T and/or B cell epitope region of NA.
No mutation that affected the IC50 value or effectiveness of NAIs was detected. Antigenic mutations of NA, which influence the selection of epidemic strains, were not determined. Continuous observation will be necessary to further clarify the genetic features of NA.</description><identifier>ISSN: 0016-254X</identifier><identifier>PMID: 25942938</identifier><language>jpn</language><publisher>Japan</publisher><subject>Antigens, Viral - genetics ; Antigens, Viral - immunology ; Antiviral Agents - pharmacology ; B-Lymphocytes - immunology ; Humans ; Influenza A Virus, H3N2 Subtype - drug effects ; Influenza A Virus, H3N2 Subtype - enzymology ; Influenza A Virus, H3N2 Subtype - genetics ; Influenza A Virus, H3N2 Subtype - isolation & purification ; Influenza, Human - virology ; Japan ; Neuraminidase - genetics ; Real-Time Polymerase Chain Reaction ; T-Lymphocytes - immunology</subject><ispartof>Fukuoka igaku zasshi = Hukuoka acta medica, 2015-01, Vol.106 (1), p.16-22</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25942938$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ikematsu, Hideyuki</creatorcontrib><creatorcontrib>Chong, Yong</creatorcontrib><creatorcontrib>Shirane, Kenjiro</creatorcontrib><creatorcontrib>Toh, Hidehiro</creatorcontrib><creatorcontrib>Sasaki, Hiroyuki</creatorcontrib><creatorcontrib>Koga, Yui</creatorcontrib><creatorcontrib>Urata, Michiyo</creatorcontrib><creatorcontrib>Hotta, Taeko</creatorcontrib><creatorcontrib>Uchiumi, Takeshi</creatorcontrib><creatorcontrib>Kang, Donchon</creatorcontrib><title>Analysis of influenza A/H3N2 neuraminidase genes obtained from influenza patients in the 2011/12 and 2012/13 seasons in Japan</title><title>Fukuoka igaku zasshi = Hukuoka acta medica</title><addtitle>Fukuoka Igaku Zasshi</addtitle><description>Influenza virus has neuraminidase (NA), a surface protein with enzymatic activity that is essential for virus replication. Mutation may affect the effectiveness of NA inhibitors that are used for the treatment of influenza patients. In this study, we determined the NA gene sequences from the clinical isolates of influenza patients to examine the chronological genetic changes and the relation to drug susceptibility.
For 96 A/H3N2 virus isolates the 50% inhibitory concentration (IC50) (48 each from the 2011-12 and 12-13 influenza seasons) was measured. RT-PCR was done with extracted viral RNA, followed by nucleotide sequencing.
One putative amino acid mutation, D151N, was found in an NA activity-related cite in five of ninety-six tested isolate. The mutation did not affect the IC50 value. The mutations identified at amino acid positions 387 and 400 were statistically correlated with an increased IC50 value, although the change was less than ten times, suggesting no significant difference in the clinical effectiveness. A small number .of isolates showed mutation in the T and/or B cell epitope region of NA.
No mutation that affected the IC50 value or effectiveness of NAIs was detected. Antigenic mutations of NA, which influence the selection of epidemic strains, were not determined. Continuous observation will be necessary to further clarify the genetic features of NA.</description><subject>Antigens, Viral - genetics</subject><subject>Antigens, Viral - immunology</subject><subject>Antiviral Agents - pharmacology</subject><subject>B-Lymphocytes - immunology</subject><subject>Humans</subject><subject>Influenza A Virus, H3N2 Subtype - drug effects</subject><subject>Influenza A Virus, H3N2 Subtype - enzymology</subject><subject>Influenza A Virus, H3N2 Subtype - genetics</subject><subject>Influenza A Virus, H3N2 Subtype - isolation & purification</subject><subject>Influenza, Human - virology</subject><subject>Japan</subject><subject>Neuraminidase - genetics</subject><subject>Real-Time Polymerase Chain Reaction</subject><subject>T-Lymphocytes - immunology</subject><issn>0016-254X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkDFPwzAUhD2AaFX6F5BHlqj2c-w4Y1UBBSFYQGKLXupnsJQ4IU6GIvHfKVAkpjudvrvhTthcCGky0PnLjC1TCrUQALIEac_YDHSZQ6nsnH2uIzb7FBLvPA_RNxPFD-Tr1VY9AI80DdiGGBwm4q8U6cDVI4ZIjvuha_9VehwDxTEdIj6-EQch5UoCx-i-Payk4okwdfEHucMe4zk79dgkWh51wZ6vr5422-z-8eZ2s77PeglmzMpaIOR5rV3pnZYFFIBKGCOFL2xhtdOFJFGiQ-dqaxR5bcnnmvKdF2QKtWCXv7v90L1PlMaqDWlHTYORuilV0lghS6GMOqAXR3SqW3JVP4QWh331d5n6AkneZew</recordid><startdate>201501</startdate><enddate>201501</enddate><creator>Ikematsu, Hideyuki</creator><creator>Chong, Yong</creator><creator>Shirane, Kenjiro</creator><creator>Toh, Hidehiro</creator><creator>Sasaki, Hiroyuki</creator><creator>Koga, Yui</creator><creator>Urata, Michiyo</creator><creator>Hotta, Taeko</creator><creator>Uchiumi, Takeshi</creator><creator>Kang, Donchon</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>201501</creationdate><title>Analysis of influenza A/H3N2 neuraminidase genes obtained from influenza patients in the 2011/12 and 2012/13 seasons in Japan</title><author>Ikematsu, Hideyuki ; Chong, Yong ; Shirane, Kenjiro ; Toh, Hidehiro ; Sasaki, Hiroyuki ; Koga, Yui ; Urata, Michiyo ; Hotta, Taeko ; Uchiumi, Takeshi ; Kang, Donchon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p126t-9b0a244b5d9fd517272a306610f78785d571e09adaddb863ef58ef45e4cf0e673</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>jpn</language><creationdate>2015</creationdate><topic>Antigens, Viral - genetics</topic><topic>Antigens, Viral - immunology</topic><topic>Antiviral Agents - pharmacology</topic><topic>B-Lymphocytes - immunology</topic><topic>Humans</topic><topic>Influenza A Virus, H3N2 Subtype - drug effects</topic><topic>Influenza A Virus, H3N2 Subtype - enzymology</topic><topic>Influenza A Virus, H3N2 Subtype - genetics</topic><topic>Influenza A Virus, H3N2 Subtype - isolation & purification</topic><topic>Influenza, Human - virology</topic><topic>Japan</topic><topic>Neuraminidase - genetics</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>T-Lymphocytes - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ikematsu, Hideyuki</creatorcontrib><creatorcontrib>Chong, Yong</creatorcontrib><creatorcontrib>Shirane, Kenjiro</creatorcontrib><creatorcontrib>Toh, Hidehiro</creatorcontrib><creatorcontrib>Sasaki, Hiroyuki</creatorcontrib><creatorcontrib>Koga, Yui</creatorcontrib><creatorcontrib>Urata, Michiyo</creatorcontrib><creatorcontrib>Hotta, Taeko</creatorcontrib><creatorcontrib>Uchiumi, Takeshi</creatorcontrib><creatorcontrib>Kang, Donchon</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Fukuoka igaku zasshi = Hukuoka acta medica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ikematsu, Hideyuki</au><au>Chong, Yong</au><au>Shirane, Kenjiro</au><au>Toh, Hidehiro</au><au>Sasaki, Hiroyuki</au><au>Koga, Yui</au><au>Urata, Michiyo</au><au>Hotta, Taeko</au><au>Uchiumi, Takeshi</au><au>Kang, Donchon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analysis of influenza A/H3N2 neuraminidase genes obtained from influenza patients in the 2011/12 and 2012/13 seasons in Japan</atitle><jtitle>Fukuoka igaku zasshi = Hukuoka acta medica</jtitle><addtitle>Fukuoka Igaku Zasshi</addtitle><date>2015-01</date><risdate>2015</risdate><volume>106</volume><issue>1</issue><spage>16</spage><epage>22</epage><pages>16-22</pages><issn>0016-254X</issn><abstract>Influenza virus has neuraminidase (NA), a surface protein with enzymatic activity that is essential for virus replication. Mutation may affect the effectiveness of NA inhibitors that are used for the treatment of influenza patients. In this study, we determined the NA gene sequences from the clinical isolates of influenza patients to examine the chronological genetic changes and the relation to drug susceptibility.
For 96 A/H3N2 virus isolates the 50% inhibitory concentration (IC50) (48 each from the 2011-12 and 12-13 influenza seasons) was measured. RT-PCR was done with extracted viral RNA, followed by nucleotide sequencing.
One putative amino acid mutation, D151N, was found in an NA activity-related cite in five of ninety-six tested isolate. The mutation did not affect the IC50 value. The mutations identified at amino acid positions 387 and 400 were statistically correlated with an increased IC50 value, although the change was less than ten times, suggesting no significant difference in the clinical effectiveness. A small number .of isolates showed mutation in the T and/or B cell epitope region of NA.
No mutation that affected the IC50 value or effectiveness of NAIs was detected. Antigenic mutations of NA, which influence the selection of epidemic strains, were not determined. Continuous observation will be necessary to further clarify the genetic features of NA.</abstract><cop>Japan</cop><pmid>25942938</pmid><tpages>7</tpages></addata></record> |
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subjects | Antigens, Viral - genetics Antigens, Viral - immunology Antiviral Agents - pharmacology B-Lymphocytes - immunology Humans Influenza A Virus, H3N2 Subtype - drug effects Influenza A Virus, H3N2 Subtype - enzymology Influenza A Virus, H3N2 Subtype - genetics Influenza A Virus, H3N2 Subtype - isolation & purification Influenza, Human - virology Japan Neuraminidase - genetics Real-Time Polymerase Chain Reaction T-Lymphocytes - immunology |
title | Analysis of influenza A/H3N2 neuraminidase genes obtained from influenza patients in the 2011/12 and 2012/13 seasons in Japan |
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