Genomic Diversity of CRESS DNA Viruses in the Eukaryotic Virome of Swine Feces

Replication-associated protein (Rep)-encoding single-stranded DNA (CRESS DNA) viruses are a diverse group of viruses, and their persistence in the environment has been studied for over a decade. However, the persistence of CRESS DNA viruses in herds of domestic animals has, in some cases, serious economic consequence. In this study, we describe the diversity of CRESS DNA viruses identified during the metagenomics analysis of fecal samples collected from a single swine herd with apparently healthy animals. A total of nine genome sequences were assembled and classified into two different groups (CRESSV1 and CRESSV2) of the Cirlivirales order (Cressdnaviricota phylum). The novel CRESS DNA viral sequences shared 85.8–96.8% and 38.1–94.3% amino acid sequence identities for the Rep and putative capsid protein sequences compared to their respective counterparts with extant GenBank record. Data presented here show evidence for simultaneous infection of swine herds with multiple novel CRESS DNA viruses, including po-circo-like viruses and fur seal feces-associated circular DNA viruses. Given that viral genomes with similar sequence and structure have been detected in swine fecal viromes from independent studies, investigation of the association between presence of CRESS DNA viruses and swine health conditions seems to be justified

Recombination Events Shape the Genomic Evolution of Infectious Bronchitis Virus in Europe

Infectious bronchitis of chicken is a high morbidity and mortality viral disease affecting the poultry industry worldwide; therefore, a better understanding of this pathogen is of utmost importance. The primary aim of this study was to obtain a deeper insight into the genomic diversity of field infectious bronchitis virus (IBV) strains using phylogenetic and recombination analysis. We sequenced the genome of 20 randomly selected strains from seven European countries. After sequencing, we created a genome sequence data set that contained 36 European origin field isolates and 33 vaccine strains. When analyzing these 69 IBV genome sequences, we identified 215 recombination events highlighting that some strains had multiple recombination breaking points. Recombination hot spots were identified mostly in the regions coding for non-structural proteins, and multiple recombination hot spots were identified in the nsp2, nsp3, nsp8, and nsp12 coding regions. Recombination occurred among different IBV genotypes and involved both field and vaccine IBV strains. Ninety percent of field strains and nearly half of vaccine strains showed evidence of recombination. Despite the low number and the scattered geographical and temporal origin of whole-genome sequence data collected from European Gammacoronaviruses, this study underlines the importance of recombination as a major evolutionary mechanism of IBVs

Novel Parvovirus Related to Primate Bufaviruses in Dogs

A novel protoparvovirus species, related genetically to human bufaviruses, was identified in dogs with respiratory signs. The canine bufavirus was distantly related to the well-known canine protoparvovirus, canine parvovirus type 2, sharing low amino acid identities in the nonstructural protein 1 (40.6%) and in the capsid protein 1 (33.4%). By screening collections of fecal, nasal, and oropharyngeal samples obtained from juvenile dogs (<1 year of age), canine bufavirus DNA appeared as a common component of canine virome. The virus was common in the stool samples of dogs with or without enteric disease and in the nasal and oropharyngeal swab samples of dogs with respiratory signs. However, the virus was not detected in nasal and oropharyngeal swab samples from animals without clinical signs

Genomic Epidemiology and Evolution of Duck Hepatitis A Virus

Duck hepatitis A virus (DHAV), an avian picornavirus, causes high-mortality acute disease in ducklings. Among the three serotypes, DHAV-1 is globally distributed, whereas DHAV-2 and DHAV-3 serotypes are chiefly restricted to Southeast Asia. In this study, we analyzed the genomic evolution of DHAV-1 strains using extant GenBank records and genomic sequences of 10 DHAV-1 strains originating from a large disease outbreak in 2004–2005, in Hungary. Recombination analysis revealed intragenotype recombination within DHAV-1 as well as intergenotype recombination events involving DHAV-1 and DHAV-3 strains. The intergenotype recombination occurred in the VP0 region. Diversifying selection seems to act at sites of certain genomic regions. Calculations estimated slightly lower rates of evolution of DHAV-1 (mean rates for individual protein coding regions, 5.6286 × 10−4 to 1.1147 × 10−3 substitutions per site per year) compared to other picornaviruses. The observed evolutionary mechanisms indicate that whole-genome-based analysis of DHAV strains is needed to better understand the emergence of novel strains and their geographical dispersal

Madarak polyomavírusainak és CRESS DNS vírusainak összehasonlító genomvizsgálata

Viruses with small circular DNA genomes comprise also members of Cressdnaviricota phylum (including Circoviridae family) with single-stranded genome, and viruses of the Polyomaviridae family with double-stranded genome. In this study cloacal swab samples, collected from wild bird species living at various aquatic sites in Hungary, were examined to reveal the presence of circoviruses, cycloviruses or other circular replication-associated protein encoding single-stranded (CRESS) DNA viruses. The samples were collected for compulsory seasonal influenza virus surveillance

Characterization of the genomic sequence of a novel CRESS DNAvirus identified in Eurasian jay (Garrulus glandarius)

Abstract Circular replication associated protein (Rep)-encoding ssDNA (CRESS DNA) viruses have diversegenomic architecture and are widely distributed in differentecosystems. In this study we characterized the completegenomic sequence of a novel circovirus-like virus, Garrulusglandarius associated circular virus-1 (GgaCV-1). Thegenome size (1971 nt) and other features (the nonanucleotide,rolling circle replication motif and SF3 helicase motif)are also reminiscent of circoviruses. Similar genomeswith uni-directionally localized and overlapping rep andcap genes are typical of type V CRESS DNA viruses thatwere identified in invertebrates and environmental samplesof aquatic ecosystems. GgaCV-1 showed the highestaa identity with partial rep sequences detected in bat feces(77%) and with the rep (54%) and cap (42%) of LakeSarah-associated circular virus-23 of New Zealand freshwatermussel origin. A dietary origin for GgaCV-1 couldnot be excluded as the virus was detected in the cloacalswab specimen of an Eurasian jay. Further studies may helpto reveal the linkage among variable organisms regardingvirus transmissio