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在MinION便携式测序平台上对非洲猪瘟病毒和经典猪瘟病毒进行靶向全基因组测序。

Targeted Whole Genome Sequencing of African Swine Fever Virus and Classical Swine Fever Virus on the MinION Portable Sequencing Platform.

作者信息

McDowell Chester D, Kwon Taeyong, Assato Patricia, Mantlo Emily, Trujillo Jessie D, Gaudreault Natasha N, Caserta Leonardo C, Morozov Igor, Souza-Neto Jayme A, Pogranichniy Roman M, Diel Diego G, Richt Juergen A

机构信息

Department of Diagnostic Medicine/Pathobiology, College of Veterinary Medicine, Kansas State University, Manhattan, KS, USA.

Department of Population Medicine and Diagnostic Sciences, Cornell University College of Veterinary Medicine, Ithaca, NY, USA.

出版信息

bioRxiv. 2025 Jul 18:2025.07.16.665162. doi: 10.1101/2025.07.16.665162.

Abstract

African swine fever virus (ASFV) and classical swine fever virus (CSFV) are important transboundary animal diseases (TADs) affecting swine. ASFV is a large DNA virus with a genome size of 170-190 kilobases (kB) belonging to the family Asfarviridae, genus Asfivirus. CSFV is a single-stranded RNA virus with genome size of approximately 12 kB belonging to the family Flaviviridae, genus Pestivirus. Outbreaks involving either one of these viruses result in similar disease syndromes and significant economic impacts from: (i) high morbidity and mortality events; (ii) control measures which include culling and quarantine; and (iii) export restrictions of swine and pork products. Current detection methods during an outbreak provide minimal genetic information on the circulating virus strains/genotypes that are important for tracing and vaccine considerations. The increasing availability and reduced cost of next-generation sequencing (NGS), allows for the establishment of vital NGS protocols for the rapid identification and complete genetic characterization of outbreak strains during an investigation. NGS data provides a better understanding of viral spread and evolution facilitating the development of novel and effective control measures. In this study, panels of primers spanning the genomes of ASFV and CSFV were independently developed to generate approximately 10kB and 6kB amplicons, respectively. The primer panels consisted of 19 primer pairs for ASFV and 2 primer pairs for CSFV providing whole genome amplification of each pathogen. These primer pools were further optimized for batch pooling and thermocycling conditions, resulting in a total of 5 primer pools/reactions used for ASFV and 2 primer pairs/reactions for CSFV. The ASFV primer panel was tested on viral DNA extracted from blood collected from pigs experimentally infected with ASFV genotype I and genotype II viruses. The CSFV primer panel was tested on 11 different strains of CSFV representing the 3 known CSFV genotypes, and 21 clinical samples collected from pigs experimentally infected with 2 different genotype 1 viruses. ASFV and CSFV amplicons from optimized PCR reactions were subsequently sequenced on the Oxford Nanopore MinION platform. The targeted protocols for these viruses resulted in an average coverage greater than 1000X for ASFV with 99% of the genome covered, and 10,000X-20,000X for CSFV with 97% to 99% of the genomes covered. The ASFV targeted whole genome sequencing protocol has been optimized for genotype II ASF viruses that have been responsible for the more recent outbreaks outside of Africa. The CSFV targeted whole genome sequencing protocol has universal applications for the detection of all CSFV genotypes. Protocols developed and evaluated here will be essential complementary tools for early pathogen detection and differentiation as well as genetic characterization of these high consequence swine viruses, globally and within the United States, should an outbreak occur.

摘要

非洲猪瘟病毒(ASFV)和经典猪瘟病毒(CSFV)是影响猪的重要跨界动物疾病(TADs)。ASFV是一种大型DNA病毒,基因组大小为170 - 190千碱基(kb),属于非洲猪瘟病毒科、非洲猪瘟病毒属。CSFV是一种单链RNA病毒,基因组大小约为12 kb,属于黄病毒科、瘟病毒属。涉及这两种病毒之一的疫情会导致相似的疾病综合征,并产生重大经济影响,原因包括:(i)高发病率和死亡率事件;(ii)控制措施,包括扑杀和检疫;(iii)猪和猪肉产品的出口限制。疫情期间目前的检测方法提供的关于循环病毒株/基因型的遗传信息极少,而这些信息对于追踪和疫苗考量很重要。新一代测序(NGS)的可用性不断提高且成本降低,使得能够建立重要的NGS方案以在调查期间快速鉴定疫情毒株并对其进行完整的遗传特征分析。NGS数据能更好地了解病毒传播和进化,有助于制定新的有效控制措施。在本研究中, 分别独立开发了跨越ASFV和CSFV基因组的引物组,以分别产生约10kb和6kb的扩增子。ASFV引物组由19对引物组成, CSFV引物组由2对引物组成,可对每种病原体进行全基因组扩增。这些引物库针对批量混合和热循环条件进一步优化, 最终ASFV总共使用5个引物库/反应,CSFV使用2对引物/反应进行检测。ASFV引物组在从实验感染ASFV基因型I和基因型II病毒的猪采集的血液中提取的病毒DNA上进行了测试。CSFV引物组在代表3种已知CSFV基因型的11种不同CSFV毒株以及从实验感染两种不同基因型1病毒的猪采集的21份临床样本上进行了测试。优化的PCR反应产生的ASFV和CSFV扩增子随后在牛津纳米孔MinION平台上进行测序。针对这些病毒的目标方案使得ASFV平均覆盖度大于1000X,基因组覆盖度达99%,CSFV平均覆盖度为10000X - 20000X,基因组覆盖度为97%至99%。针对ASFV的全基因组测序方案已针对在非洲以外地区近期疫情中起作用的基因型II ASF病毒进行了优化。针对CSFV的全基因组测序方案可普遍应用于检测所有CSFV基因型。本文开发和评估的方案将成为全球以及美国境内早期病原体检测、鉴别以及这些高致病性猪病毒遗传特征分析的重要补充工具,以防疫情发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd07/12338688/a6255dc8f89b/nihpp-2025.07.16.665162v1-f0001.jpg

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