A simple screening assay for receptor switching of avian influenza viruses
Identifieur interne : 001969 ( PascalFrancis/Corpus ); précédent : 001968; suivant : 001970A simple screening assay for receptor switching of avian influenza viruses
Auteurs : Ompreya Suptawiwat ; Alita Kongchanagul ; Wisoot Chan-It ; Arunee Thitithanyanont ; Witawat Wiriyarat ; Krisada Chaichuen ; Taweesak Songserm ; Yasuo Suzuki ; Pilaipan Puthavathana ; Prasert AuewarakulSource :
- Journal of clinical virology [ 1386-6532 ] ; 2008.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
Abstract
Background: Adaptation of the receptor-binding preference from a2,3- to a2,6-linked sialic acid is an essential step for an avian influenza virus to transmit efficiently in human population and become a pandemic virus. The currently available assays for receptor-binding preference are complex and not widely available. Objectives: A simple high-throughput screening assay will facilitate early detection of a potential pandemic virus, which is crucial for the prevention and control of the possible pandemic. We wanted to develop a simple assay to differentiate influenza viruses with α2,3- or α2,6-linked receptor-binding preference. Study design: The assay employs a specific sialidase (from Salmonella thyphimurium) that can eliminate α2,3-linked sialic acid from red blood cells. A reduction of hemagglutination titer indicates α2,3-linked receptor preference in this assay. Results: Using a panel of H5N1 avian influenza isolates and H1/H3 human influenza isolates, as well as mutated H5 reverse genetics virus, the assay could accurately differentiate the viruses according to their receptor-binding preference. Furthermore, the assay was sufficiently sensitive to detect a minor variant with a2,6-linkage-specificity in a background of a2,3-linkage-specific virus. Conclusions: We have developed a simple screening assay capable of detecting avian influenza viruses that have switched their receptor-binding preference. © 2008 Elsevier B.V. All rights reserved.
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Pour connaître la documentation sur le format Inist Standard.
pA |
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Format Inist (serveur)
NO : | PASCAL 08-0322956 INIST |
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ET : | A simple screening assay for receptor switching of avian influenza viruses |
AU : | SUPTAWIWAT (Ompreya); KONGCHANAGUL (Alita); CHAN-IT (Wisoot); THITITHANYANONT (Arunee); WIRIYARAT (Witawat); CHAICHUEN (Krisada); SONGSERM (Taweesak); SUZUKI (Yasuo); PUTHAVATHANA (Pilaipan); AUEWARAKUL (Prasert) |
AF : | Faculty of Medicine, Siriraj Hospital, Mahidol University/Bangkok/Thaïlande (1 aut., 2 aut., 3 aut., 9 aut., 10 aut.); Faculty of Science, Mahidol University/Bangkok/Thaïlande (4 aut.); Faculty of Veterinary Science, Mahidol University/Bangkok/Thaïlande (5 aut., 6 aut.); Faculty of Veterinary Medicine, Kasetsart University/Kampangsaen/Thaïlande (7 aut.); College of Life and Health Sciences, Chubu University/Kasugai/Japon (8 aut.) |
DT : | Publication en série; Courte communication, note brève; Niveau analytique |
SO : | Journal of clinical virology; ISSN 1386-6532; Pays-Bas; Da. 2008; Vol. 42; No. 2; Pp. 186-189; Bibl. 1/4 p. |
LA : | Anglais |
EA : | Background: Adaptation of the receptor-binding preference from a2,3- to a2,6-linked sialic acid is an essential step for an avian influenza virus to transmit efficiently in human population and become a pandemic virus. The currently available assays for receptor-binding preference are complex and not widely available. Objectives: A simple high-throughput screening assay will facilitate early detection of a potential pandemic virus, which is crucial for the prevention and control of the possible pandemic. We wanted to develop a simple assay to differentiate influenza viruses with α2,3- or α2,6-linked receptor-binding preference. Study design: The assay employs a specific sialidase (from Salmonella thyphimurium) that can eliminate α2,3-linked sialic acid from red blood cells. A reduction of hemagglutination titer indicates α2,3-linked receptor preference in this assay. Results: Using a panel of H5N1 avian influenza isolates and H1/H3 human influenza isolates, as well as mutated H5 reverse genetics virus, the assay could accurately differentiate the viruses according to their receptor-binding preference. Furthermore, the assay was sufficiently sensitive to detect a minor variant with a2,6-linkage-specificity in a background of a2,3-linkage-specific virus. Conclusions: We have developed a simple screening assay capable of detecting avian influenza viruses that have switched their receptor-binding preference. © 2008 Elsevier B.V. All rights reserved. |
CC : | 002A05C10; 002B05C02J |
FD : | Influenzavirus aviaire; Acide sialique; Exo-α-sialidase; Erythrocyte; Microbiologie; Virologie; Grippe aviaire |
FG : | Influenzavirus A; Orthomyxoviridae; Virus; Glycosidases; Glycosylases; Hydrolases; Enzyme; Zoopathogène; Virose; Infection; Cellule sanguine |
ED : | Avian influenzavirus; Sialic acid; Exo-α-sialidase; Red blood cell; Microbiology; Virology; Avian influenza |
EG : | Influenzavirus A; Orthomyxoviridae; Virus; Glycosidases; Glycosylases; Hydrolases; Enzyme; Zoopathogen; Viral disease; Infection; Blood cell |
SD : | Avian influenzavirus; Siálico ácido; Exo-α-sialidase; Eritrocito; Microbiología; Virología; Gripe aviar |
LO : | INIST-26272.354000197837120140 |
ID : | 08-0322956 |
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Pascal:08-0322956Le document en format XML
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<term>Sialic acid</term>
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<front><div type="abstract" xml:lang="en">Background: Adaptation of the receptor-binding preference from a2,3- to a2,6-linked sialic acid is an essential step for an avian influenza virus to transmit efficiently in human population and become a pandemic virus. The currently available assays for receptor-binding preference are complex and not widely available. Objectives: A simple high-throughput screening assay will facilitate early detection of a potential pandemic virus, which is crucial for the prevention and control of the possible pandemic. We wanted to develop a simple assay to differentiate influenza viruses with α2,3- or α2,6-linked receptor-binding preference. Study design: The assay employs a specific sialidase (from Salmonella thyphimurium) that can eliminate α2,3-linked sialic acid from red blood cells. A reduction of hemagglutination titer indicates α2,3-linked receptor preference in this assay. Results: Using a panel of H5N1 avian influenza isolates and H1/H3 human influenza isolates, as well as mutated H5 reverse genetics virus, the assay could accurately differentiate the viruses according to their receptor-binding preference. Furthermore, the assay was sufficiently sensitive to detect a minor variant with a2,6-linkage-specificity in a background of a2,3-linkage-specific virus. Conclusions: We have developed a simple screening assay capable of detecting avian influenza viruses that have switched their receptor-binding preference. © 2008 Elsevier B.V. All rights reserved.</div>
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<fC03 i1="02" i2="X" l="ENG"><s0>Sialic acid</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>05</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA"><s0>Siálico ácido</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>05</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE"><s0>Exo-α-sialidase</s0>
<s2>FE</s2>
<s5>06</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG"><s0>Exo-α-sialidase</s0>
<s2>FE</s2>
<s5>06</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA"><s0>Exo-α-sialidase</s0>
<s2>FE</s2>
<s5>06</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE"><s0>Erythrocyte</s0>
<s5>07</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG"><s0>Red blood cell</s0>
<s5>07</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA"><s0>Eritrocito</s0>
<s5>07</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE"><s0>Microbiologie</s0>
<s5>08</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG"><s0>Microbiology</s0>
<s5>08</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA"><s0>Microbiología</s0>
<s5>08</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE"><s0>Virologie</s0>
<s5>09</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG"><s0>Virology</s0>
<s5>09</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA"><s0>Virología</s0>
<s5>09</s5>
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<fC03 i1="07" i2="X" l="FRE"><s0>Grippe aviaire</s0>
<s2>NM</s2>
<s5>14</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG"><s0>Avian influenza</s0>
<s2>NM</s2>
<s5>14</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA"><s0>Gripe aviar</s0>
<s2>NM</s2>
<s5>14</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE"><s0>Influenzavirus A</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="01" i2="X" l="ENG"><s0>Influenzavirus A</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="01" i2="X" l="SPA"><s0>Influenzavirus A</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="02" i2="X" l="FRE"><s0>Orthomyxoviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="02" i2="X" l="ENG"><s0>Orthomyxoviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="02" i2="X" l="SPA"><s0>Orthomyxoviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="03" i2="X" l="FRE"><s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="03" i2="X" l="ENG"><s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="03" i2="X" l="SPA"><s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="04" i2="X" l="FRE"><s0>Glycosidases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="04" i2="X" l="ENG"><s0>Glycosidases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="04" i2="X" l="SPA"><s0>Glycosidases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="05" i2="X" l="FRE"><s0>Glycosylases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="05" i2="X" l="ENG"><s0>Glycosylases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="05" i2="X" l="SPA"><s0>Glycosylases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="06" i2="X" l="FRE"><s0>Hydrolases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="06" i2="X" l="ENG"><s0>Hydrolases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="06" i2="X" l="SPA"><s0>Hydrolases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="07" i2="X" l="FRE"><s0>Enzyme</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="07" i2="X" l="ENG"><s0>Enzyme</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="07" i2="X" l="SPA"><s0>Enzima</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="08" i2="X" l="FRE"><s0>Zoopathogène</s0>
<s5>13</s5>
</fC07>
<fC07 i1="08" i2="X" l="ENG"><s0>Zoopathogen</s0>
<s5>13</s5>
</fC07>
<fC07 i1="08" i2="X" l="SPA"><s0>Zoopatógeno</s0>
<s5>13</s5>
</fC07>
<fC07 i1="09" i2="X" l="FRE"><s0>Virose</s0>
</fC07>
<fC07 i1="09" i2="X" l="ENG"><s0>Viral disease</s0>
</fC07>
<fC07 i1="09" i2="X" l="SPA"><s0>Virosis</s0>
</fC07>
<fC07 i1="10" i2="X" l="FRE"><s0>Infection</s0>
</fC07>
<fC07 i1="10" i2="X" l="ENG"><s0>Infection</s0>
</fC07>
<fC07 i1="10" i2="X" l="SPA"><s0>Infección</s0>
</fC07>
<fC07 i1="11" i2="X" l="FRE"><s0>Cellule sanguine</s0>
<s5>18</s5>
</fC07>
<fC07 i1="11" i2="X" l="ENG"><s0>Blood cell</s0>
<s5>18</s5>
</fC07>
<fC07 i1="11" i2="X" l="SPA"><s0>Célula sanguínea</s0>
<s5>18</s5>
</fC07>
<fN21><s1>203</s1>
</fN21>
<fN44 i1="01"><s1>OTO</s1>
</fN44>
<fN82><s1>OTO</s1>
</fN82>
</pA>
</standard>
<server><NO>PASCAL 08-0322956 INIST</NO>
<ET>A simple screening assay for receptor switching of avian influenza viruses</ET>
<AU>SUPTAWIWAT (Ompreya); KONGCHANAGUL (Alita); CHAN-IT (Wisoot); THITITHANYANONT (Arunee); WIRIYARAT (Witawat); CHAICHUEN (Krisada); SONGSERM (Taweesak); SUZUKI (Yasuo); PUTHAVATHANA (Pilaipan); AUEWARAKUL (Prasert)</AU>
<AF>Faculty of Medicine, Siriraj Hospital, Mahidol University/Bangkok/Thaïlande (1 aut., 2 aut., 3 aut., 9 aut., 10 aut.); Faculty of Science, Mahidol University/Bangkok/Thaïlande (4 aut.); Faculty of Veterinary Science, Mahidol University/Bangkok/Thaïlande (5 aut., 6 aut.); Faculty of Veterinary Medicine, Kasetsart University/Kampangsaen/Thaïlande (7 aut.); College of Life and Health Sciences, Chubu University/Kasugai/Japon (8 aut.)</AF>
<DT>Publication en série; Courte communication, note brève; Niveau analytique</DT>
<SO>Journal of clinical virology; ISSN 1386-6532; Pays-Bas; Da. 2008; Vol. 42; No. 2; Pp. 186-189; Bibl. 1/4 p.</SO>
<LA>Anglais</LA>
<EA>Background: Adaptation of the receptor-binding preference from a2,3- to a2,6-linked sialic acid is an essential step for an avian influenza virus to transmit efficiently in human population and become a pandemic virus. The currently available assays for receptor-binding preference are complex and not widely available. Objectives: A simple high-throughput screening assay will facilitate early detection of a potential pandemic virus, which is crucial for the prevention and control of the possible pandemic. We wanted to develop a simple assay to differentiate influenza viruses with α2,3- or α2,6-linked receptor-binding preference. Study design: The assay employs a specific sialidase (from Salmonella thyphimurium) that can eliminate α2,3-linked sialic acid from red blood cells. A reduction of hemagglutination titer indicates α2,3-linked receptor preference in this assay. Results: Using a panel of H5N1 avian influenza isolates and H1/H3 human influenza isolates, as well as mutated H5 reverse genetics virus, the assay could accurately differentiate the viruses according to their receptor-binding preference. Furthermore, the assay was sufficiently sensitive to detect a minor variant with a2,6-linkage-specificity in a background of a2,3-linkage-specific virus. Conclusions: We have developed a simple screening assay capable of detecting avian influenza viruses that have switched their receptor-binding preference. © 2008 Elsevier B.V. All rights reserved.</EA>
<CC>002A05C10; 002B05C02J</CC>
<FD>Influenzavirus aviaire; Acide sialique; Exo-α-sialidase; Erythrocyte; Microbiologie; Virologie; Grippe aviaire</FD>
<FG>Influenzavirus A; Orthomyxoviridae; Virus; Glycosidases; Glycosylases; Hydrolases; Enzyme; Zoopathogène; Virose; Infection; Cellule sanguine</FG>
<ED>Avian influenzavirus; Sialic acid; Exo-α-sialidase; Red blood cell; Microbiology; Virology; Avian influenza</ED>
<EG>Influenzavirus A; Orthomyxoviridae; Virus; Glycosidases; Glycosylases; Hydrolases; Enzyme; Zoopathogen; Viral disease; Infection; Blood cell</EG>
<SD>Avian influenzavirus; Siálico ácido; Exo-α-sialidase; Eritrocito; Microbiología; Virología; Gripe aviar</SD>
<LO>INIST-26272.354000197837120140</LO>
<ID>08-0322956</ID>
</server>
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