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dc.contributor.authorPaim, Willian Pintopt_BR
dc.contributor.authorMaggioli, Mayara Fernandapt_BR
dc.contributor.authorFalkenberg, Shollie M.pt_BR
dc.contributor.authorRamachandran, Akhileshpt_BR
dc.contributor.authorWeber, Matheus Nunespt_BR
dc.contributor.authorCanal, Cláudio Wageckpt_BR
dc.contributor.authorBauermann, Fernando Vicosapt_BR
dc.date.accessioned2022-01-19T04:36:44Zpt_BR
dc.date.issued2021pt_BR
dc.identifier.issn1999-4915pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/234194pt_BR
dc.description.abstractBovine serum has been widely used as a universal supplement in culture media and other applications, including the manufacture of biological products and the production of synthetic meat. Currently, commercial bovine serum is tested for possible viral contaminants following regional guidelines. Regulatory agencies’ established tests focused on detecting selected animal origin viruses and are based on virus isolation, immunofluorescence, and hemadsorption assays. However, these tests may fail to detect new or emerging viruses in biological products. High-throughput sequencing is a powerful option since no prior knowledge of the viral targets is required. In the present study, we evaluate the virome of seven commercial batches of bovine serum from Mexico (one batch), New Zealand (two batches), and the United States (four batches) using a specific preparation and enrichment method for pooled samples and sequencing using an Illumina platform. A variety of circular replicase-encoding single-stranded (CRESS) DNA families (Genomoviridae, Circoviridae, and Smacoviridae) was identified. Additionally, CrAssphage, a recently discovered group of bacteriophage correlated with fecal contamination, was identified in 85% of the tested batches. Furthermore, sequences representing viral families with single-stranded DNA (Parvoviridae), double-stranded DNA (Polyomaviridae and Adenoviridae), single-stranded RNA (Flaviviridae, Picornaviridae, and Retroviridae), and double-stranded RNA (Reoviridae) were identified. These results support that high-throughput sequencing associated with viral enrichment is a robust tool and should be considered an additional layer of safety when testing pooled biologicals to detect viral contaminants overlooked by the current testing protocols.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofViruses. Basel. Vol. 13, no. 12 (Dec. 2021), 2425, 14 p.pt_BR
dc.rightsOpen Accessen
dc.subjectViral metagenomicsen
dc.subjectViromapt_BR
dc.subjectBovine serumen
dc.subjectSoro bovinopt_BR
dc.subjectDiagnosticen
dc.subjectProdutos biológicospt_BR
dc.subjectEstados Unidospt_BR
dc.subjectSurveillanceen
dc.subjectMéxicopt_BR
dc.subjectNova Zelândiapt_BR
dc.subjectSequenciamento de nucleotídeos em larga escalapt_BR
dc.titleVirome characterization in commercial bovine serum batches : a potentially needed testing strategy for biological productspt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb001136082pt_BR
dc.type.originEstrangeiropt_BR


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