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Rapid multiserotype detection of human rhinoviruses on optically coated silicon surfaces

Background: More than 100 immunologically distinct serotypes of human rhinoviruses (HRV) have been discovered, making detection of surface exposed capsid antigens impractical. However, the non-structural protein 3C protease (3Cpro) is essential for viral replication and is relatively highly conserve...

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Autores principales: Ostroff, Rachel, Ettinger, Anna, La, Helen, Rihanek, Marynette, Zalman, Leora, Meador, James, Patick, Amy K, Worland, Steve, Polisky, Barry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science B.V. 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7128216/
https://www.ncbi.nlm.nih.gov/pubmed/11378491
http://dx.doi.org/10.1016/S1386-6532(01)00150-0
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author Ostroff, Rachel
Ettinger, Anna
La, Helen
Rihanek, Marynette
Zalman, Leora
Meador, James
Patick, Amy K
Worland, Steve
Polisky, Barry
author_facet Ostroff, Rachel
Ettinger, Anna
La, Helen
Rihanek, Marynette
Zalman, Leora
Meador, James
Patick, Amy K
Worland, Steve
Polisky, Barry
author_sort Ostroff, Rachel
collection PubMed
description Background: More than 100 immunologically distinct serotypes of human rhinoviruses (HRV) have been discovered, making detection of surface exposed capsid antigens impractical. However, the non-structural protein 3C protease (3Cpro) is essential for viral replication and is relatively highly conserved among serotypes, making it a potential target for diagnostic testing. The thin film biosensor is an assay platform that can be formatted into a sensitive immunoassay for viral proteins in clinical specimens. The technology utilizes an optically coated silicon surface to convert specific molecular binding events into visual color changes by altering the reflective properties of light through molecular thin films. Objective: To develop a rapid test for detection of HRV by developing broadly serotype reactive antibodies to 3Cpro and utilizing them in the thin film biosensor format. Study design: Polyclonal antibodies to 3Cpro were purified and incorporated into the thin film assay. The in vitro sensitivity, specificity and multiserotype cross-reactivity of the 3Cpro assay were tested. Nasal washes from naturally infected individuals were also tested to verify that 3Cpro was detectable in clinical specimens. Results: The 3Cpro assay is a 28-min, non-instrumented room temperature test with a visual limit of detection of 12 pM (picomolar) 3Cpro. In terms of viral titer, as few as 1000 TCID(50) equivalents of HRV2 were detectable. The assay detected 45/52 (87%) of the HRV serotypes tested but showed no cross-reactivity to common respiratory viruses or bacteria. The thin film assay detected 3Cpro in HRV-infected cell culture supernatants coincident with first appearance of cytopathic effect. Data are also presented demonstrating 3Cpro detection from clinical samples collected from HRV-infected individuals. The assay detected 3Cpro in expelled nasal secretions from a symptomatic individual on the first day of illness. In addition, 9/11 (82%) concentrated nasal wash specimens from HRV infected children were positive in the 3Cpro test. Conclusion: We have described a novel, sensitive thin film biosensor for rapid detection of HRV 3Cpro. This test may be suitable for the point of care setting, where rapid HRV diagnostic test results could contribute to clinical decisions regarding appropriate antibiotic or antiviral therapy.
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spelling pubmed-71282162020-04-08 Rapid multiserotype detection of human rhinoviruses on optically coated silicon surfaces Ostroff, Rachel Ettinger, Anna La, Helen Rihanek, Marynette Zalman, Leora Meador, James Patick, Amy K Worland, Steve Polisky, Barry J Clin Virol Article Background: More than 100 immunologically distinct serotypes of human rhinoviruses (HRV) have been discovered, making detection of surface exposed capsid antigens impractical. However, the non-structural protein 3C protease (3Cpro) is essential for viral replication and is relatively highly conserved among serotypes, making it a potential target for diagnostic testing. The thin film biosensor is an assay platform that can be formatted into a sensitive immunoassay for viral proteins in clinical specimens. The technology utilizes an optically coated silicon surface to convert specific molecular binding events into visual color changes by altering the reflective properties of light through molecular thin films. Objective: To develop a rapid test for detection of HRV by developing broadly serotype reactive antibodies to 3Cpro and utilizing them in the thin film biosensor format. Study design: Polyclonal antibodies to 3Cpro were purified and incorporated into the thin film assay. The in vitro sensitivity, specificity and multiserotype cross-reactivity of the 3Cpro assay were tested. Nasal washes from naturally infected individuals were also tested to verify that 3Cpro was detectable in clinical specimens. Results: The 3Cpro assay is a 28-min, non-instrumented room temperature test with a visual limit of detection of 12 pM (picomolar) 3Cpro. In terms of viral titer, as few as 1000 TCID(50) equivalents of HRV2 were detectable. The assay detected 45/52 (87%) of the HRV serotypes tested but showed no cross-reactivity to common respiratory viruses or bacteria. The thin film assay detected 3Cpro in HRV-infected cell culture supernatants coincident with first appearance of cytopathic effect. Data are also presented demonstrating 3Cpro detection from clinical samples collected from HRV-infected individuals. The assay detected 3Cpro in expelled nasal secretions from a symptomatic individual on the first day of illness. In addition, 9/11 (82%) concentrated nasal wash specimens from HRV infected children were positive in the 3Cpro test. Conclusion: We have described a novel, sensitive thin film biosensor for rapid detection of HRV 3Cpro. This test may be suitable for the point of care setting, where rapid HRV diagnostic test results could contribute to clinical decisions regarding appropriate antibiotic or antiviral therapy. Elsevier Science B.V. 2001-05 2001-05-22 /pmc/articles/PMC7128216/ /pubmed/11378491 http://dx.doi.org/10.1016/S1386-6532(01)00150-0 Text en Copyright © 2001 Elsevier Science B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Ostroff, Rachel
Ettinger, Anna
La, Helen
Rihanek, Marynette
Zalman, Leora
Meador, James
Patick, Amy K
Worland, Steve
Polisky, Barry
Rapid multiserotype detection of human rhinoviruses on optically coated silicon surfaces
title Rapid multiserotype detection of human rhinoviruses on optically coated silicon surfaces
title_full Rapid multiserotype detection of human rhinoviruses on optically coated silicon surfaces
title_fullStr Rapid multiserotype detection of human rhinoviruses on optically coated silicon surfaces
title_full_unstemmed Rapid multiserotype detection of human rhinoviruses on optically coated silicon surfaces
title_short Rapid multiserotype detection of human rhinoviruses on optically coated silicon surfaces
title_sort rapid multiserotype detection of human rhinoviruses on optically coated silicon surfaces
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7128216/
https://www.ncbi.nlm.nih.gov/pubmed/11378491
http://dx.doi.org/10.1016/S1386-6532(01)00150-0
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