A Deep-Sequencing Workflow for the Fast and Efficient Generation of High-Quality African Swine Fever Virus Whole-Genome Sequences

被引:50
作者
Forth, Jan H. [1 ]
Forth, Leonie F. [1 ]
King, Jacqueline [1 ]
Groza, Oxana [2 ]
Huebner, Alexandra [1 ]
Olesen, Ann Sofie [3 ]
Hoeper, Dirk [1 ]
Dixon, Linda K. [4 ]
Netherton, Christopher L. [4 ]
Rasmussen, Thomas Bruun [5 ,6 ]
Blome, Sandra [1 ]
Pohlmann, Anne [1 ]
Beer, Martin [1 ]
机构
[1] Friedrich Loeffler Inst, Fed Res Inst Anim Hlth, Sudufer 10, D-17493 Greifswald, Germany
[2] Republican Ctr Vet Diagnost, Anim Hlth Diagnost Lab, Str Murelor 3, MD-2051 Mun Chisinau, Moldova
[3] Univ Copenhagen, Fac Hlth & Med Sci, Dept Vet & Anim Sci, DK-1870 Frederiksberg C, Denmark
[4] Pirbright Inst, Ash Rd, Woking GU24 0NF, Surrey, England
[5] Tech Univ Denmark, DTU Natl Vet Inst, DK-4771 Lindholm, Kalvehave, Denmark
[6] Statens Serum Inst, Dept Virus & Microbiol Special Diagnost, DK-2300 Copenhagen S, Denmark
来源
VIRUSES-BASEL | 2019年 / 11卷 / 09期
基金
英国生物技术与生命科学研究理事会; 欧盟地平线“2020”;
关键词
African swine fever virus (ASFV); next-generation sequencing (NGS); whole-genome sequencing; Nanopore sequencing; target enrichment; NEXT-GENERATION; REPLICATION; DNA; EPIDEMIOLOGY; DIVERSITY; INFECTION; VIRULENCE; DISEASE; EASTERN; RUSSIA;
D O I
10.3390/v11090846
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
African swine fever (ASF) is a severe disease of suids caused by African swine fever virus (ASFV). Its dsDNA genome (170-194 kbp) is scattered with homopolymers and repeats as well as inverted-terminal-repeats (ITR), which hamper whole-genome sequencing. To date, only a few genome sequences have been published and only for some are data on sequence quality available enabling in-depth investigations. Especially in Europe and Asia, where ASFV has continuously spread since its introduction into Georgia in 2007, a very low genetic variability of the circulating ASFV-strains was reported. Therefore, only whole-genome sequences can serve as a basis for detailed virus comparisons. Here, we report an effective workflow, combining target enrichment, Illumina and Nanopore sequencing for ASFV whole-genome sequencing. Following this approach, we generated an improved high-quality ASFV Georgia 2007/1 whole-genome sequence leading to the correction of 71 sequencing errors and the addition of 956 and 231 bp at the respective ITRs. This genome, derived from the primary outbreak in 2007, can now serve as a reference for future whole-genome analyses of related ASFV strains and molecular approaches. Using both workflow and the reference genome, we generated the first ASFV-whole-genome sequence from Moldova, expanding the sequence knowledge from Eastern Europe.
引用
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页数:18
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