Department of Veterinary Pathobiology, College of Veterinary Medicine, Oklahoma State University (OSU), Stillwater, OK 74078, USA.
Laboratório de Virologia, Faculdade de Veterinária, Universidade Federal do Rio Grande do Sul (UFRGS), Rio Grande do Sul, Porto Alegre 90040-060, Brazil.
Viruses. 2021 Dec 3;13(12):2425. doi: 10.3390/v13122425.
Bovine 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 (, , and ) 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 (), double-stranded DNA ( and ), single-stranded RNA (, , and ), and double-stranded RNA () 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.
牛血清已被广泛用作培养基和其他应用的通用补充物,包括生物制品的制造和合成肉的生产。目前,商业牛血清按照地区指南测试可能存在的病毒污染物。监管机构制定的测试侧重于检测选定的动物源性病毒,基于病毒分离、免疫荧光和血球吸附测定。然而,这些测试可能无法检测生物制品中的新出现或新兴病毒。高通量测序是一种强大的选择,因为不需要事先了解病毒靶标。在本研究中,我们使用特定的混合样本制备和富集方法,使用 Illumina 平台对来自墨西哥(一批)、新西兰(两批)和美国(四批)的七批商业牛血清进行病毒组学评估。鉴定出多种环状复制酶编码单链 (CRESS) DNA 家族(、、和)。此外,在 85%的测试批次中发现了与粪便污染相关的新近发现的噬菌体 CrAssphage。此外,还鉴定出了代表单链 DNA (), 双链 DNA (和), 单链 RNA (、、和) 和双链 RNA () 的病毒家族的序列。这些结果表明,与病毒富集相关的高通量测序是一种强大的工具,在测试混合生物制品以检测当前测试方案遗漏的病毒污染物时,应被视为额外的安全层。