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A Bead-Based Multiplex Assay for the Detection of DNA Viruses Infecting Laboratory Rodents
The Federation of European Laboratory Animal Science Association (FELASA) recommends screening of laboratory rodents and biological materials for a broad variety of bacterial agents, viruses, and parasites. Methods commonly used to date for pathogen detection are neither cost-effective nor time- and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4023972/ https://www.ncbi.nlm.nih.gov/pubmed/24835244 http://dx.doi.org/10.1371/journal.pone.0097525 |
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author | Höfler, Daniela Nicklas, Werner Mauter, Petra Pawlita, Michael Schmitt, Markus |
author_facet | Höfler, Daniela Nicklas, Werner Mauter, Petra Pawlita, Michael Schmitt, Markus |
author_sort | Höfler, Daniela |
collection | PubMed |
description | The Federation of European Laboratory Animal Science Association (FELASA) recommends screening of laboratory rodents and biological materials for a broad variety of bacterial agents, viruses, and parasites. Methods commonly used to date for pathogen detection are neither cost-effective nor time- and animal-efficient or uniform. However, an infection even if silent alters experimental results through changing the animals’ physiology and increases inter-individual variability. As a consequence higher numbers of animals and experiments are needed for valid and significant results. We developed a novel high-throughput multiplex assay, called rodent DNA virus finder (rDVF) for the simultaneous identification of 24 DNA viruses infecting mice and rats. We detected all 24 DNA viruses with high specificity and reproducibility. Detection limits for the different DNA viruses varied between 10 and 1000 copies per PCR. The validation of rDVF was done with DNA isolated from homogenised organs amplified by pathogen specific primers in one multiplex PCR. The biotinylated amplicons were detected via hybridisation to specific oligonucleotide probes coupled to spectrally distinct sets of fluorescent Luminex beads. In conclusion, rDVF may have the potential to replace conventional testing and may simplify and improve routine detection of DNA viruses infecting rodents. |
format | Online Article Text |
id | pubmed-4023972 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-40239722014-05-21 A Bead-Based Multiplex Assay for the Detection of DNA Viruses Infecting Laboratory Rodents Höfler, Daniela Nicklas, Werner Mauter, Petra Pawlita, Michael Schmitt, Markus PLoS One Research Article The Federation of European Laboratory Animal Science Association (FELASA) recommends screening of laboratory rodents and biological materials for a broad variety of bacterial agents, viruses, and parasites. Methods commonly used to date for pathogen detection are neither cost-effective nor time- and animal-efficient or uniform. However, an infection even if silent alters experimental results through changing the animals’ physiology and increases inter-individual variability. As a consequence higher numbers of animals and experiments are needed for valid and significant results. We developed a novel high-throughput multiplex assay, called rodent DNA virus finder (rDVF) for the simultaneous identification of 24 DNA viruses infecting mice and rats. We detected all 24 DNA viruses with high specificity and reproducibility. Detection limits for the different DNA viruses varied between 10 and 1000 copies per PCR. The validation of rDVF was done with DNA isolated from homogenised organs amplified by pathogen specific primers in one multiplex PCR. The biotinylated amplicons were detected via hybridisation to specific oligonucleotide probes coupled to spectrally distinct sets of fluorescent Luminex beads. In conclusion, rDVF may have the potential to replace conventional testing and may simplify and improve routine detection of DNA viruses infecting rodents. Public Library of Science 2014-05-16 /pmc/articles/PMC4023972/ /pubmed/24835244 http://dx.doi.org/10.1371/journal.pone.0097525 Text en © 2014 Höfler et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Höfler, Daniela Nicklas, Werner Mauter, Petra Pawlita, Michael Schmitt, Markus A Bead-Based Multiplex Assay for the Detection of DNA Viruses Infecting Laboratory Rodents |
title | A Bead-Based Multiplex Assay for the Detection of DNA Viruses Infecting Laboratory Rodents |
title_full | A Bead-Based Multiplex Assay for the Detection of DNA Viruses Infecting Laboratory Rodents |
title_fullStr | A Bead-Based Multiplex Assay for the Detection of DNA Viruses Infecting Laboratory Rodents |
title_full_unstemmed | A Bead-Based Multiplex Assay for the Detection of DNA Viruses Infecting Laboratory Rodents |
title_short | A Bead-Based Multiplex Assay for the Detection of DNA Viruses Infecting Laboratory Rodents |
title_sort | bead-based multiplex assay for the detection of dna viruses infecting laboratory rodents |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4023972/ https://www.ncbi.nlm.nih.gov/pubmed/24835244 http://dx.doi.org/10.1371/journal.pone.0097525 |
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