Mackie Joanne, Kinoti Wycliff M, Chahal Sumit I, Lovelock David A, Campbell Paul R, Tran-Nguyen Lucy T T, Rodoni Brendan C, Constable Fiona E
School of Applied Systems Biology, La Trobe University, Melbourne, VIC 3083, Australia.
Agriculture Victoria Research, Department of Jobs, Precincts and Regions, AgriBio, Melbourne, VIC 3083, Australia.
Plants (Basel). 2022 Oct 14;11(20):2716. doi: 10.3390/plants11202716.
Rapid and reliable detection tools are essential for disease surveillance and outbreak management, and genomic data is essential to determining pathogen origin and monitoring of transmission pathways. Low virus copy number and poor RNA quality can present challenges for genomic sequencing of plant viruses, but this can be overcome by enrichment of target nucleic acid. A targeted whole genome sequencing (TWG-Seq) approach for the detection of cucumber green mottle mosaic virus (CGMMV) has been developed where overlapping amplicons generated using two multiplex RT-PCR assays are then sequenced using the Oxford Nanopore MinION. Near complete coding region sequences were assembled with ≥100× coverage for infected leaf tissue dilution samples with RT-qPCR cycle quantification (Cq) values from 11.8 to 38 and in seed dilution samples with Cq values 13.8 to 27. Consensus sequences assembled using this approach showed greater than 99% nucleotide similarity when compared to genomes produced using metagenomic sequencing. CGMMV could be confidently detected in historical seed isolates with degraded RNA. Whilst limited access to, and costs associated with second-generation sequencing platforms can influence diagnostic outputs, the portable Nanopore technology offers an affordable high throughput sequencing alternative when combined with TWG-Seq for low copy or degraded samples.
快速可靠的检测工具对于疾病监测和疫情管理至关重要,而基因组数据对于确定病原体来源和监测传播途径必不可少。低病毒拷贝数和较差的RNA质量可能给植物病毒的基因组测序带来挑战,但这可以通过富集目标核酸来克服。已开发出一种用于检测黄瓜绿斑驳花叶病毒(CGMMV)的靶向全基因组测序(TWG-Seq)方法,即使用两种多重RT-PCR检测法生成重叠扩增子,然后使用牛津纳米孔MinION进行测序。对于RT-qPCR循环定量(Cq)值为11.8至38的感染叶片组织稀释样品以及Cq值为13.8至27的种子稀释样品,组装出了覆盖度≥100×的近乎完整的编码区序列。与使用宏基因组测序产生的基因组相比,用这种方法组装的一致序列显示出大于99%的核苷酸相似性。在RNA降解的历史种子分离物中可以可靠地检测到CGMMV。虽然第二代测序平台的有限获取和相关成本可能影响诊断结果,但便携式纳米孔技术与TWG-Seq结合用于低拷贝或降解样品时,提供了一种经济实惠的高通量测序替代方案。