2021
DOI: 10.3390/microorganisms9071426
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Genomic Diversity of CRESS DNA Viruses in the Eukaryotic Virome of Swine Feces

Abstract: 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 to… Show more

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Cited by 8 publications
(13 citation statements)
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“…The Rep of the BitternCV and Bee-eaterCV contained conserved motifs controlling the RCR processes of eukaryotic CRESS DNA viruses, including the probable N-terminal RCR (I–III) and C-terminal superfamily 3 helicase (Walker-A Walker-B, and C) motifs, as well as an arginine finger ( Table 2 ). These motifs showed the highest similarity with that of typical for circo- and cycloviruses and imply similar course of replication for all these viruses [ 2 , 22 , 27 , 28 ].…”
Section: Resultsmentioning
confidence: 92%
“…The Rep of the BitternCV and Bee-eaterCV contained conserved motifs controlling the RCR processes of eukaryotic CRESS DNA viruses, including the probable N-terminal RCR (I–III) and C-terminal superfamily 3 helicase (Walker-A Walker-B, and C) motifs, as well as an arginine finger ( Table 2 ). These motifs showed the highest similarity with that of typical for circo- and cycloviruses and imply similar course of replication for all these viruses [ 2 , 22 , 27 , 28 ].…”
Section: Resultsmentioning
confidence: 92%
“…The complete genomes of the PCV2 strains were evaluated for recombination events using the RDP4 program with default parameters, and were considered as recombinants if supported by two, or >two detection methods (3Seq, BOOTSCAN, CHIMAERA, GENECONV, MAXCHI, RDP, and SISCAN) with a highest acceptable p-value of p < 0.01 with Bonferroni's correction, as described previously [38,39,42]. Phylogenetic analyses of PCV2 were carried out by both maximum-likelihood (ML) and neighbor-joining (NJ) methods using the MEGA7 software, with the Kimura 2-parameter model of substitution and 1000 bootstrap replicates, whereas phylogenetic analysis of CRESSV2/ENG22 was performed by the ML method, supported with 1000 bootstrap replicates and the LG + F + G + I model of substitution, as described in previous studies [8,15,38].…”
Section: Sequence Analysismentioning
confidence: 99%
“…Since the pigeon circovirus-like sequence was detected in a fecal sample, we could not determine whether the virus infected pigs, or was of dietary origin (consumption of avian feces). The partial rep sequence in ENG22 shared maximum homology with unclassified CRESS DNA viral sequences from porcine feces [8] and was eventually characterized for the complete genome.…”
Section: Identification Of a Pigeon Circovirus-like Sequence And Comp...mentioning
confidence: 99%
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