Metagenomic Identification of Novel Eukaryotic Viruses with Small DNA Genomes in Pheasants

被引:2
|
作者
Kaszab, Eszter [1 ,2 ,3 ]
Bali, Krisztina [1 ,2 ]
Marton, Szilvia [1 ,2 ]
Ursu, Krisztina [4 ]
Farkas, Szilvia L. [5 ,6 ]
Feher, Eniko [1 ,2 ]
Doman, Marianna [1 ,2 ]
Martella, Vito [7 ]
Banyai, Krisztian [1 ,2 ,8 ]
机构
[1] HUN REN Vet Med Res Inst, H-1143 Budapest, Hungary
[2] Antimicrobial Resistance Vet Publ Hlth & Food Chai, Natl Lab Infect Anim Dis, H-1143 Budapest, Hungary
[3] Univ Debrecen, Hlth Inst 1, Fac Hlth Sci, H-4032 Debrecen, Hungary
[4] Natl Food Chain Safety Off, Vet Diagnost Directorate, H-1143 Budapest, Hungary
[5] Univ Vet Med, Dept Obstet, H-1078 Budapest, Hungary
[6] Univ Vet Med, Food Anim Med Clin, H-1078 Budapest, Hungary
[7] Univ Bari Aldo Moro, Dept Vet Med, I-70010 Valenzano, Italy
[8] Univ Vet Med, Dept Pharmacol & Toxicol, H-1078 Budapest, Hungary
来源
ANIMALS | 2024年 / 14卷 / 02期
关键词
virome; genome assembly; phylogenetic analysis; GYROVIRUS; PCR;
D O I
10.3390/ani14020237
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Simple Summary In this study, we report the diversity of viruses identified using metagenomics in the intestinal contents of dead pheasants. The study provides evidence for the presence of a heterogenous viral community, with an over-representation of viruses with small DNA genomes. This information will be useful for the development of diagnostic methods that can be used in routine health assessment and virus surveillance.Abstract A panel of intestinal samples collected from common pheasants (Phasianus colchicus) between 2008 and 2017 was used for metagenomic investigation using an unbiased enrichment protocol and different bioinformatic pipelines. The number of sequence reads in the metagenomic analysis ranged from 1,419,265 to 17,507,704 with a viral sequence read rate ranging from 0.01% to 59%. When considering the sequence reads of eukaryotic viruses, RNA and DNA viruses were identified in the samples, including but not limited to coronaviruses, reoviruses, parvoviruses, and CRESS DNA viruses (i.e., circular Rep-encoding single-stranded DNA viruses). Partial or nearly complete genome sequences were reconstructed of at least three different parvoviruses (dependoparvovirus, aveparvovirus and chaphamaparvovirus), as well as gyroviruses and diverse CRESS DNA viruses. Generating information of virus diversity will serve as a basis for developing specific diagnostic tools and for structured epidemiological investigations, useful to assess the impact of these novel viruses on animal health.
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页数:13
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