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Targeted Enrichment for Pathogen Detection and Characterization in Three Felid Species

Traditional diagnostic assays often lack sensitivity and can be difficult to multiplex across many pathogens. Next-generation sequencing (NGS) can overcome some of these problems but has limited application in the detection of low-copy-number pathogens in complex samples. Targeted genome capture (TG...

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Autores principales: Lee, Justin S., Mackie, Ryan S., Harrison, Thomas, Shariat, Basir, Kind, Trey, Kehl, Timo, Löchelt, Martin, Boucher, Christina, VandeWoude, Sue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5442522/
https://www.ncbi.nlm.nih.gov/pubmed/28330894
http://dx.doi.org/10.1128/JCM.01463-16
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author Lee, Justin S.
Mackie, Ryan S.
Harrison, Thomas
Shariat, Basir
Kind, Trey
Kehl, Timo
Löchelt, Martin
Boucher, Christina
VandeWoude, Sue
author_facet Lee, Justin S.
Mackie, Ryan S.
Harrison, Thomas
Shariat, Basir
Kind, Trey
Kehl, Timo
Löchelt, Martin
Boucher, Christina
VandeWoude, Sue
author_sort Lee, Justin S.
collection PubMed
description Traditional diagnostic assays often lack sensitivity and can be difficult to multiplex across many pathogens. Next-generation sequencing (NGS) can overcome some of these problems but has limited application in the detection of low-copy-number pathogens in complex samples. Targeted genome capture (TGC) utilizes oligonucleotide probes to enrich specific nucleic acids in heterogeneous extracts and can therefore increase the proportion of NGS reads for low-abundance targets. While earlier studies have demonstrated the utility of this technology for detection of novel pathogens in human clinical samples, the capacity and practicality of TGC-NGS in a veterinary diagnostic setting have not yet been evaluated. Here we report the use of TGC-NGS assays for the detection and characterization of diverse feline pathogen taxa. We detected 31 pathogens comprising nine pathogen taxa in 28 felid samples analyzed. This included 20 pathogens detected via traditional PCR and 11 additional pathogens that had not been previously detected in the same samples. Most of the pathogens detected were sequenced at sufficient breadth and depth to confidently classify them at the species or subspecies level. Target nucleic acids were enriched from a low of 58-fold to 56 million-fold relative to host nucleic acids. Despite the promising performance of these assays, a number of pathogens detected by conventional PCR or serology were not isolated by TGC-NGS, suggesting that further validation is required before this technology can be used in lieu of quality-controlled standard assays. We conclude that TGC-NGS offers great potential as a broad multiplex pathogen characterization assay in veterinary diagnostic and research settings.
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spelling pubmed-54425222017-06-08 Targeted Enrichment for Pathogen Detection and Characterization in Three Felid Species Lee, Justin S. Mackie, Ryan S. Harrison, Thomas Shariat, Basir Kind, Trey Kehl, Timo Löchelt, Martin Boucher, Christina VandeWoude, Sue J Clin Microbiol Clinical Veterinary Microbiology Traditional diagnostic assays often lack sensitivity and can be difficult to multiplex across many pathogens. Next-generation sequencing (NGS) can overcome some of these problems but has limited application in the detection of low-copy-number pathogens in complex samples. Targeted genome capture (TGC) utilizes oligonucleotide probes to enrich specific nucleic acids in heterogeneous extracts and can therefore increase the proportion of NGS reads for low-abundance targets. While earlier studies have demonstrated the utility of this technology for detection of novel pathogens in human clinical samples, the capacity and practicality of TGC-NGS in a veterinary diagnostic setting have not yet been evaluated. Here we report the use of TGC-NGS assays for the detection and characterization of diverse feline pathogen taxa. We detected 31 pathogens comprising nine pathogen taxa in 28 felid samples analyzed. This included 20 pathogens detected via traditional PCR and 11 additional pathogens that had not been previously detected in the same samples. Most of the pathogens detected were sequenced at sufficient breadth and depth to confidently classify them at the species or subspecies level. Target nucleic acids were enriched from a low of 58-fold to 56 million-fold relative to host nucleic acids. Despite the promising performance of these assays, a number of pathogens detected by conventional PCR or serology were not isolated by TGC-NGS, suggesting that further validation is required before this technology can be used in lieu of quality-controlled standard assays. We conclude that TGC-NGS offers great potential as a broad multiplex pathogen characterization assay in veterinary diagnostic and research settings. American Society for Microbiology 2017-05-23 2017-06 /pmc/articles/PMC5442522/ /pubmed/28330894 http://dx.doi.org/10.1128/JCM.01463-16 Text en Copyright © 2017 Lee et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Clinical Veterinary Microbiology
Lee, Justin S.
Mackie, Ryan S.
Harrison, Thomas
Shariat, Basir
Kind, Trey
Kehl, Timo
Löchelt, Martin
Boucher, Christina
VandeWoude, Sue
Targeted Enrichment for Pathogen Detection and Characterization in Three Felid Species
title Targeted Enrichment for Pathogen Detection and Characterization in Three Felid Species
title_full Targeted Enrichment for Pathogen Detection and Characterization in Three Felid Species
title_fullStr Targeted Enrichment for Pathogen Detection and Characterization in Three Felid Species
title_full_unstemmed Targeted Enrichment for Pathogen Detection and Characterization in Three Felid Species
title_short Targeted Enrichment for Pathogen Detection and Characterization in Three Felid Species
title_sort targeted enrichment for pathogen detection and characterization in three felid species
topic Clinical Veterinary Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5442522/
https://www.ncbi.nlm.nih.gov/pubmed/28330894
http://dx.doi.org/10.1128/JCM.01463-16
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