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Development of multiplexed bead arrays for the simultaneous detection of nucleic acid from multiple viruses in bat samples

Virus surveillance of wildlife populations is important for identifying, monitoring, and predicting the emergence of pathogens that pose a potential threat to animal and human health. Bats are identified as important wildlife hosts of many viruses capable of causing fatal human disease, including me...

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Autores principales: Boyd, Victoria, Smith, Ina, Crameri, Gary, Burroughs, Amy L., Durr, Peter A., White, John, Cowled, Christopher, Marsh, Glenn A., Wang, Lin-Fa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113788/
https://www.ncbi.nlm.nih.gov/pubmed/26190638
http://dx.doi.org/10.1016/j.jviromet.2015.07.004
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author Boyd, Victoria
Smith, Ina
Crameri, Gary
Burroughs, Amy L.
Durr, Peter A.
White, John
Cowled, Christopher
Marsh, Glenn A.
Wang, Lin-Fa
author_facet Boyd, Victoria
Smith, Ina
Crameri, Gary
Burroughs, Amy L.
Durr, Peter A.
White, John
Cowled, Christopher
Marsh, Glenn A.
Wang, Lin-Fa
author_sort Boyd, Victoria
collection PubMed
description Virus surveillance of wildlife populations is important for identifying, monitoring, and predicting the emergence of pathogens that pose a potential threat to animal and human health. Bats are identified as important wildlife hosts of many viruses capable of causing fatal human disease, including members of the henipaviruses, coronaviruses, rhabdoviruses and filoviruses. As global warming and habitat change are thought to impact upon pathogen transmission dynamics and increase the risk of spillover, virus surveillance in bat populations remains a significant component of efforts to improve the prediction and control of potential future disease outbreaks caused by bat-borne viruses. In this study we have developed two fluid bead array assays containing customized panels that target multiple bat-borne viruses. These assays detect up to 11 viral RNA's simultaneously in urine samples collected from wild bat populations in Australia and Bangladesh. The assays developed show high specificity for the target viruses and the analytical sensitivity compares favorably to qRT-PCR. These assays enhance the ability to monitor multi-pathogen dynamics and identify patterns of virus shedding from bat populations, thus informing key approaches to outbreak response and control.
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spelling pubmed-71137882020-04-02 Development of multiplexed bead arrays for the simultaneous detection of nucleic acid from multiple viruses in bat samples Boyd, Victoria Smith, Ina Crameri, Gary Burroughs, Amy L. Durr, Peter A. White, John Cowled, Christopher Marsh, Glenn A. Wang, Lin-Fa J Virol Methods Article Virus surveillance of wildlife populations is important for identifying, monitoring, and predicting the emergence of pathogens that pose a potential threat to animal and human health. Bats are identified as important wildlife hosts of many viruses capable of causing fatal human disease, including members of the henipaviruses, coronaviruses, rhabdoviruses and filoviruses. As global warming and habitat change are thought to impact upon pathogen transmission dynamics and increase the risk of spillover, virus surveillance in bat populations remains a significant component of efforts to improve the prediction and control of potential future disease outbreaks caused by bat-borne viruses. In this study we have developed two fluid bead array assays containing customized panels that target multiple bat-borne viruses. These assays detect up to 11 viral RNA's simultaneously in urine samples collected from wild bat populations in Australia and Bangladesh. The assays developed show high specificity for the target viruses and the analytical sensitivity compares favorably to qRT-PCR. These assays enhance the ability to monitor multi-pathogen dynamics and identify patterns of virus shedding from bat populations, thus informing key approaches to outbreak response and control. Elsevier B.V. 2015-10 2015-07-17 /pmc/articles/PMC7113788/ /pubmed/26190638 http://dx.doi.org/10.1016/j.jviromet.2015.07.004 Text en Copyright © 2015 Elsevier 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
Boyd, Victoria
Smith, Ina
Crameri, Gary
Burroughs, Amy L.
Durr, Peter A.
White, John
Cowled, Christopher
Marsh, Glenn A.
Wang, Lin-Fa
Development of multiplexed bead arrays for the simultaneous detection of nucleic acid from multiple viruses in bat samples
title Development of multiplexed bead arrays for the simultaneous detection of nucleic acid from multiple viruses in bat samples
title_full Development of multiplexed bead arrays for the simultaneous detection of nucleic acid from multiple viruses in bat samples
title_fullStr Development of multiplexed bead arrays for the simultaneous detection of nucleic acid from multiple viruses in bat samples
title_full_unstemmed Development of multiplexed bead arrays for the simultaneous detection of nucleic acid from multiple viruses in bat samples
title_short Development of multiplexed bead arrays for the simultaneous detection of nucleic acid from multiple viruses in bat samples
title_sort development of multiplexed bead arrays for the simultaneous detection of nucleic acid from multiple viruses in bat samples
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113788/
https://www.ncbi.nlm.nih.gov/pubmed/26190638
http://dx.doi.org/10.1016/j.jviromet.2015.07.004
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