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Complete genome sequencing of tick-borne encephalitis virus directly from clinical samples : comparison of shotgun metagenomic and targeted amplicon-based sequencing
ID Zakotnik, Samo (Avtor), ID Knap, Nataša (Avtor), ID Bogovič, Petra (Avtor), ID Zorec, Tomaž Mark (Avtor), ID Poljak, Mario (Avtor), ID Strle, Franc (Avtor), ID Avšič-Županc, Tatjana (Avtor), ID Korva, Miša (Avtor)

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URLURL - Izvorni URL, za dostop obiščite https://www.mdpi.com/1999-4915/14/6/1267 Povezava se odpre v novem oknu

Izvleček
The clinical presentation of tick-borne encephalitis virus (TBEV) infection varies from asymptomatic to severe meningoencephalitis or meningoencephalomyelitis. The TBEV subtype has been suggested as one of the most important risk factors for disease severity, but TBEV genetic characterization is difficult. Infection is usually diagnosed in the post-viremic phase, and so relevant clinical samples of TBEV are extremely rare and, when present, are associated with low viral loads. To date, only two complete TBEV genomes sequenced directly from patient clinical samples are publicly available. The aim of this study was to develop novel protocols for the direct sequencing of the TBEV genome, enabling studies of viral genetic determinants that influence disease severity. We developed a novel oligonucleotide primer scheme for amplification of the complete TBEV genome. The primer set was tested on 21 clinical samples with various viral loads and collected over a 15-year period using the two most common sequencing platforms. The amplicon-based strategy was compared to direct shotgun sequencing. Using the novel primer set, we successfully obtained nearly complete TBEV genomes (>90% of genome) from all clinical samples, including those with extremely low viral loads. Comparison of consensus sequences of the TBEV genome generated using the novel amplicon-based strategy and shotgun sequencing showed no difference. We conclude that the novel primer set is a powerful tool for future studies on genetic determinants of TBEV that influence disease severity and will lead to a better understanding of TBE pathogenesis.

Jezik:Angleški jezik
Ključne besede:tick-borne encephalitis virus, whole genome sequencing, metagenomics, amplicons, next-generation sequencing, NGS, clinical samples
Vrsta gradiva:Članek v reviji
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:MF - Medicinska fakulteta
Status publikacije:Objavljeno
Različica publikacije:Objavljena publikacija
Leto izida:2022
Št. strani:16 str.
Številčenje:Vol. 14, iss. 6, art. 1267
PID:20.500.12556/RUL-145240 Povezava se odpre v novem oknu
UDK:616.9
ISSN pri članku:1999-4915
DOI:10.3390/v14061267 Povezava se odpre v novem oknu
COBISS.SI-ID:111682563 Povezava se odpre v novem oknu
Datum objave v RUL:13.04.2023
Število ogledov:823
Število prenosov:90
Metapodatki:XML DC-XML DC-RDF
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Gradivo je del revije

Naslov:Viruses
Skrajšan naslov:Viruses
Založnik:MDPI
ISSN:1999-4915
COBISS.SI-ID:517597977 Povezava se odpre v novem oknu

Licence

Licenca:CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.

Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:virus klopnega encefalitisa, sekvenciranje celotnega genoma, metagenomika

Projekti

Financer:Drugi - Drug financer ali več financerjev
Program financ.:University of Ljubljana, Faculty of Medicine, Institute of Microbiology and Immunology

Financer:ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:P3-0083
Naslov:Odnosi parazitskega obstajanja

Financer:ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:J3-2515
Naslov:Uporaba metagenomskega pristopa za odkrivanje povzročiteljev okužb osrednjega živčevja

Financer:EC - European Commission
Program financ.:H2020
Številka projekta:871029
Naslov:European Virus Archive GLOBAL
Akronim:EVA-GLOBAL

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