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Detection of swine-origin influenza A (H1N1) viruses using a localized surface plasmon coupled fluorescence fiber-optic biosensor

Identifieur interne : 001290 ( PascalFrancis/Checkpoint ); précédent : 001289; suivant : 001291

Detection of swine-origin influenza A (H1N1) viruses using a localized surface plasmon coupled fluorescence fiber-optic biosensor

Auteurs : Ying-Feng Chang [Taïwan] ; Sheng-Fan Wang [Taïwan] ; Jason C. Huang [Taïwan] ; Li-Chen Su [Taïwan] ; LING YAO [Taïwan] ; Ying-Chang Li [Taïwan] ; Suh-Chin Wu [Taïwan] ; Yi-Ming A. Chen [Taïwan] ; Jo-Ping Hsieh [Taïwan] ; CHIEN CHOU [Taïwan]

Source :

RBID : Pascal:11-0117774

Descripteurs français

English descriptors

Abstract

Swine-origin influenza A (H1N1) virus (S-OIV) was identified as a new reassortant strain of influenza A virus in April 2009 and led to an influenza pandemic. Accurate and timely diagnoses are crucial for the control of influenza disease. We developed a localized surface plasmon coupled fluorescence fiber-optic biosensor (LSPCF-FOB) which combines a sandwich immunoassay with the LSP technique using antibodies against the hemagglutinin (HA) proteins of S-OIVs. The detection limit of the LSPCF-FOB for recombinant S-OIV H1 protein detection was estimated at 13.9 pg/mL, which is 103-fold better than that of conventional capture ELISA when using the same capture antibodies. For clinical S-OIV isolates measurement, meanwhile, the detection limit of the LSPCF-FOB platform was calculated to be 8.25 x 104 copies/mL, compared with 2.06 x 106 copies/mL using conventional capture ELISA. Further-more, in comparison with the influenza A/B rapid test, the detection limit of the LSPCF-FOB for S-OIV was almost 50-fold in PBS solution and 25-fold lower in mimic solution, which used nasal mucosa from healthy donors as the diluent. The findings of this study therefore indicate that the high detection sensitivity and specificity of the LSPCF-FOB make it a potentially effective diagnostic tool for clinical S-OIV infection and this technique has the potential to be applied to the development of other clinical microbe detection platforms.


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Pascal:11-0117774

Le document en format XML

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<title xml:lang="en" level="a">Detection of swine-origin influenza A (H1N1) viruses using a localized surface plasmon coupled fluorescence fiber-optic biosensor</title>
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<s1>Institute ofBiophotonics, National Yang-Ming University</s1>
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<country>Taïwan</country>
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</affiliation>
<affiliation wicri:level="1">
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<s1>Graduate Institute of Electro-Optical Engineering, Chang Gung University</s1>
<s2>Taoyuan 333</s2>
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<sZ>1 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>6 aut.</sZ>
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<affiliation wicri:level="1">
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<s1>Department of Optics and Photonics, National Central University</s1>
<s2>Taoyuan 320</s2>
<s3>TWN</s3>
<sZ>4 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
</inist:fA14>
<country>Taïwan</country>
<wicri:noRegion>Taoyuan 320</wicri:noRegion>
</affiliation>
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</analytic>
<series>
<title level="j" type="main">Biosensors & bioelectronics</title>
<title level="j" type="abbreviated">Biosens. bioelectron.</title>
<idno type="ISSN">0956-5663</idno>
<imprint>
<date when="2010">2010</date>
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<title level="j" type="main">Biosensors & bioelectronics</title>
<title level="j" type="abbreviated">Biosens. bioelectron.</title>
<idno type="ISSN">0956-5663</idno>
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<term>Biosensor</term>
<term>Detection</term>
<term>Fluorescence</term>
<term>Gold</term>
<term>Influenza</term>
<term>Influenza A virus</term>
<term>Nanoparticle</term>
<term>Optical fiber</term>
<term>Pig</term>
<term>Surface plasmon</term>
<term>Swine</term>
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<term>Détection</term>
<term>Porc</term>
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<term>Plasmon surface</term>
<term>Virus grippal A</term>
<term>Fluorescence</term>
<term>Fibre optique</term>
<term>Biodétecteur</term>
<term>Or</term>
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<front>
<div type="abstract" xml:lang="en">Swine-origin influenza A (H1N1) virus (S-OIV) was identified as a new reassortant strain of influenza A virus in April 2009 and led to an influenza pandemic. Accurate and timely diagnoses are crucial for the control of influenza disease. We developed a localized surface plasmon coupled fluorescence fiber-optic biosensor (LSPCF-FOB) which combines a sandwich immunoassay with the LSP technique using antibodies against the hemagglutinin (HA) proteins of S-OIVs. The detection limit of the LSPCF-FOB for recombinant S-OIV H1 protein detection was estimated at 13.9 pg/mL, which is 10
<sup>3</sup>
-fold better than that of conventional capture ELISA when using the same capture antibodies. For clinical S-OIV isolates measurement, meanwhile, the detection limit of the LSPCF-FOB platform was calculated to be 8.25 x 10
<sup>4</sup>
copies/mL, compared with 2.06 x 10
<sup>6</sup>
copies/mL using conventional capture ELISA. Further-more, in comparison with the influenza A/B rapid test, the detection limit of the LSPCF-FOB for S-OIV was almost 50-fold in PBS solution and 25-fold lower in mimic solution, which used nasal mucosa from healthy donors as the diluent. The findings of this study therefore indicate that the high detection sensitivity and specificity of the LSPCF-FOB make it a potentially effective diagnostic tool for clinical S-OIV infection and this technique has the potential to be applied to the development of other clinical microbe detection platforms.</div>
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<s0>Swine-origin influenza A (H1N1) virus (S-OIV) was identified as a new reassortant strain of influenza A virus in April 2009 and led to an influenza pandemic. Accurate and timely diagnoses are crucial for the control of influenza disease. We developed a localized surface plasmon coupled fluorescence fiber-optic biosensor (LSPCF-FOB) which combines a sandwich immunoassay with the LSP technique using antibodies against the hemagglutinin (HA) proteins of S-OIVs. The detection limit of the LSPCF-FOB for recombinant S-OIV H1 protein detection was estimated at 13.9 pg/mL, which is 10
<sup>3</sup>
-fold better than that of conventional capture ELISA when using the same capture antibodies. For clinical S-OIV isolates measurement, meanwhile, the detection limit of the LSPCF-FOB platform was calculated to be 8.25 x 10
<sup>4</sup>
copies/mL, compared with 2.06 x 10
<sup>6</sup>
copies/mL using conventional capture ELISA. Further-more, in comparison with the influenza A/B rapid test, the detection limit of the LSPCF-FOB for S-OIV was almost 50-fold in PBS solution and 25-fold lower in mimic solution, which used nasal mucosa from healthy donors as the diluent. The findings of this study therefore indicate that the high detection sensitivity and specificity of the LSPCF-FOB make it a potentially effective diagnostic tool for clinical S-OIV infection and this technique has the potential to be applied to the development of other clinical microbe detection platforms.</s0>
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<name sortKey="Wang, Sheng Fan" sort="Wang, Sheng Fan" uniqKey="Wang S" first="Sheng-Fan" last="Wang">Sheng-Fan Wang</name>
<name sortKey="Wang, Sheng Fan" sort="Wang, Sheng Fan" uniqKey="Wang S" first="Sheng-Fan" last="Wang">Sheng-Fan Wang</name>
<name sortKey="Wu, Suh Chin" sort="Wu, Suh Chin" uniqKey="Wu S" first="Suh-Chin" last="Wu">Suh-Chin Wu</name>
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   |wiki=    Sante
   |area=    PandemieGrippaleV1
   |flux=    PascalFrancis
   |étape=   Checkpoint
   |type=    RBID
   |clé=     Pascal:11-0117774
   |texte=   Detection of swine-origin influenza A (H1N1) viruses using a localized surface plasmon coupled fluorescence fiber-optic biosensor
}}

Wicri

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Data generation: Wed Jun 10 11:04:28 2020. Site generation: Sun Mar 28 09:10:28 2021