The Study of Viral RNA Diversity in Bird Samples Using De Novo Designed Multiplex Genus-Specific Primer Panels

Advances in the next generation sequencing (NGS) technologies have significantly increased our ability to detect new viral pathogens and systematically determine the spectrum of viruses prevalent in various biological samples. In addition, this approach has also helped in establishing the associatio...

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Main Authors: Andrey A. Ayginin, Ekaterina V. Pimkina, Alina D. Matsvay, Anna S. Speranskaya, Marina V. Safonova, Ekaterina A. Blinova, Ilya V. Artyushin, Vladimir G. Dedkov, German A. Shipulin, Kamil Khafizov
Format: Article
Language:English
Published: Hindawi Limited 2018-01-01
Series:Advances in Virology
Online Access:http://dx.doi.org/10.1155/2018/3248285
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spelling doaj-3363cc522a944a3d853ee1c58ac1da5a2021-07-02T17:53:02ZengHindawi LimitedAdvances in Virology1687-86391687-86472018-01-01201810.1155/2018/32482853248285The Study of Viral RNA Diversity in Bird Samples Using De Novo Designed Multiplex Genus-Specific Primer PanelsAndrey A. Ayginin0Ekaterina V. Pimkina1Alina D. Matsvay2Anna S. Speranskaya3Marina V. Safonova4Ekaterina A. Blinova5Ilya V. Artyushin6Vladimir G. Dedkov7German A. Shipulin8Kamil Khafizov9Central Research Institute of Epidemiology, Moscow 111123, RussiaCentral Research Institute of Epidemiology, Moscow 111123, RussiaCentral Research Institute of Epidemiology, Moscow 111123, RussiaCentral Research Institute of Epidemiology, Moscow 111123, RussiaCentral Research Institute of Epidemiology, Moscow 111123, RussiaCentral Research Institute of Epidemiology, Moscow 111123, RussiaLomonosov Moscow State University, Moscow 119991, RussiaCentral Research Institute of Epidemiology, Moscow 111123, RussiaCentral Research Institute of Epidemiology, Moscow 111123, RussiaCentral Research Institute of Epidemiology, Moscow 111123, RussiaAdvances in the next generation sequencing (NGS) technologies have significantly increased our ability to detect new viral pathogens and systematically determine the spectrum of viruses prevalent in various biological samples. In addition, this approach has also helped in establishing the associations of viromes with many diseases. However, unlike the metagenomic studies using 16S rRNA for the detection of bacteria, it is impossible to create universal oligonucleotides to target all known and novel viruses, owing to their genomic diversity and variability. On the other hand, sequencing the entire genome is still expensive and has relatively low sensitivity for such applications. The existing approaches for the design of oligonucleotides for targeted enrichment are usually involved in the development of primers for the PCR-based detection of particular viral species or genera, but not for families or higher taxonomic orders. In this study, we have developed a computational pipeline for designing the oligonucleotides capable of covering a significant number of known viruses within various taxonomic orders, as well as their novel variants. We have subsequently designed a genus-specific oligonucleotide panel for targeted enrichment of viral nucleic acids in biological material and demonstrated the possibility of its application for virus detection in bird samples. We have tested our panel using a number of collected samples and have observed superior efficiency in the detection and identification of viral pathogens. Since a reliable, bioinformatics-based analytical method for the rapid identification of the sequences was crucial, an NGS-based data analysis module was developed in this study, and its functionality in the detection of novel viruses and analysis of virome diversity was demonstrated.http://dx.doi.org/10.1155/2018/3248285
collection DOAJ
language English
format Article
sources DOAJ
author Andrey A. Ayginin
Ekaterina V. Pimkina
Alina D. Matsvay
Anna S. Speranskaya
Marina V. Safonova
Ekaterina A. Blinova
Ilya V. Artyushin
Vladimir G. Dedkov
German A. Shipulin
Kamil Khafizov
spellingShingle Andrey A. Ayginin
Ekaterina V. Pimkina
Alina D. Matsvay
Anna S. Speranskaya
Marina V. Safonova
Ekaterina A. Blinova
Ilya V. Artyushin
Vladimir G. Dedkov
German A. Shipulin
Kamil Khafizov
The Study of Viral RNA Diversity in Bird Samples Using De Novo Designed Multiplex Genus-Specific Primer Panels
Advances in Virology
author_facet Andrey A. Ayginin
Ekaterina V. Pimkina
Alina D. Matsvay
Anna S. Speranskaya
Marina V. Safonova
Ekaterina A. Blinova
Ilya V. Artyushin
Vladimir G. Dedkov
German A. Shipulin
Kamil Khafizov
author_sort Andrey A. Ayginin
title The Study of Viral RNA Diversity in Bird Samples Using De Novo Designed Multiplex Genus-Specific Primer Panels
title_short The Study of Viral RNA Diversity in Bird Samples Using De Novo Designed Multiplex Genus-Specific Primer Panels
title_full The Study of Viral RNA Diversity in Bird Samples Using De Novo Designed Multiplex Genus-Specific Primer Panels
title_fullStr The Study of Viral RNA Diversity in Bird Samples Using De Novo Designed Multiplex Genus-Specific Primer Panels
title_full_unstemmed The Study of Viral RNA Diversity in Bird Samples Using De Novo Designed Multiplex Genus-Specific Primer Panels
title_sort study of viral rna diversity in bird samples using de novo designed multiplex genus-specific primer panels
publisher Hindawi Limited
series Advances in Virology
issn 1687-8639
1687-8647
publishDate 2018-01-01
description Advances in the next generation sequencing (NGS) technologies have significantly increased our ability to detect new viral pathogens and systematically determine the spectrum of viruses prevalent in various biological samples. In addition, this approach has also helped in establishing the associations of viromes with many diseases. However, unlike the metagenomic studies using 16S rRNA for the detection of bacteria, it is impossible to create universal oligonucleotides to target all known and novel viruses, owing to their genomic diversity and variability. On the other hand, sequencing the entire genome is still expensive and has relatively low sensitivity for such applications. The existing approaches for the design of oligonucleotides for targeted enrichment are usually involved in the development of primers for the PCR-based detection of particular viral species or genera, but not for families or higher taxonomic orders. In this study, we have developed a computational pipeline for designing the oligonucleotides capable of covering a significant number of known viruses within various taxonomic orders, as well as their novel variants. We have subsequently designed a genus-specific oligonucleotide panel for targeted enrichment of viral nucleic acids in biological material and demonstrated the possibility of its application for virus detection in bird samples. We have tested our panel using a number of collected samples and have observed superior efficiency in the detection and identification of viral pathogens. Since a reliable, bioinformatics-based analytical method for the rapid identification of the sequences was crucial, an NGS-based data analysis module was developed in this study, and its functionality in the detection of novel viruses and analysis of virome diversity was demonstrated.
url http://dx.doi.org/10.1155/2018/3248285
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