Ottawa Research and Development Centre, Agriculture and Agri-Food Canada, Ottawa, Ontario, Canada.
Department of Plant Science, University of Manitoba, Winnipeg, Manitoba, Canada.
PLoS One. 2021 Jan 22;16(1):e0245333. doi: 10.1371/journal.pone.0245333. eCollection 2021.
The Goss's bacterial wilt pathogen, Clavibacter nebraskensis, of corn is a candidate A1 quarantine organism; and its recent re-emergence and spread in the USA and Canada is a potential biothreat to the crop. We developed and tested an amplicon-based Nanopore detection system for C. nebraskensis (Cn), targeting a purine permease gene. The sensitivity (1 pg) of this system in mock bacterial communities (MBCs) spiked with serially diluted DNA of C. nebraskensis NCPPB 2581T is comparable to that of real-time PCR. Average Nanopore reads increased exponentially from 125 (1pg) to about 6000 reads (1000 pg) after a 3-hr run-time, with 99.0% of the reads accurately assigned to C. nebraskensis. Three run-times were used to process control MBCs, Cn-spiked MBCs, diseased and healthy leaf samples. The mean Nanopore reads doubled as the run-time is increased from 3 to 6 hrs while from 6 to 12 hrs, a 20% increment was recorded in all treatments. Cn-spiked MBCs and diseased corn leaf samples averaged read counts of 5,100, 11,000 and 14,000 for the respective run-times, with 99.8% of the reads taxonomically identified as C. nebraskensis. The control MBCs and healthy leaf samples had 47 and 14 Nanopore reads, respectively. 16S rRNA bacteriomic profiles showed that Sphingomonas (22.7%) and Clavibacter (21.2%) were dominant in diseased samples while Pseudomonas had only 3.5% relative abundance. In non-symptomatic leaf samples, however, Pseudomonas (20.0%) was dominant with Clavibacter at 0.08% relative abundance. This discrepancy in Pseudomonas abundance in the samples was corroborated by qPCR using EvaGreen chemistry. Our work outlines a new useful tool for diagnosis of the Goss's bacterial wilt disease; and provides the first insight on Pseudomonas community dynamics in necrotic leaf lesions.
玉米戈斯氏细菌性萎蔫病原菌,即新田纳西棒杆菌,为玉米 A1 检疫性有害生物候选种;其近期在美国和加拿大重新出现和扩散,对农作物构成潜在生物威胁。我们开发并测试了一种基于扩增子的纳孔检测系统,用于检测新田纳西棒杆菌(Cn),该系统以嘌呤通透酶基因为靶标。在含有新田纳西棒杆菌 NCPPB 2581T 连续稀释 DNA 的模拟细菌群落(MBC)中,该系统的检测灵敏度(1pg)与实时 PCR 相当。在 3 小时的运行时间内,纳孔平均读数呈指数增长,从 125(1pg)增加到约 6000 个读数(1000pg),99.0%的读数准确分配给新田纳西棒杆菌。使用 3 种运行时间来处理对照 MBC、Cn 污染 MBC、患病和健康叶片样本。随着运行时间从 3 小时增加到 6 小时,纳孔读数平均增加一倍,而在 6 小时到 12 小时之间,所有处理的读数都增加了 20%。Cn 污染 MBC 和患病玉米叶片样本在相应运行时间的平均读数分别为 5100、11000 和 14000,99.8%的读数在分类学上被鉴定为新田纳西棒杆菌。对照 MBC 和健康叶片样本分别有 47 和 14 个纳孔读数。16S rRNA 细菌宏基因组分析表明,在患病样本中,鞘氨醇单胞菌(22.7%)和棒杆菌(21.2%)占主导地位,而假单胞菌的相对丰度仅为 3.5%。然而,在无症状叶片样本中,假单胞菌(20.0%)占主导地位,棒杆菌的相对丰度为 0.08%。在样本中假单胞菌丰度的这种差异通过 EvaGreen 化学法 qPCR 得到了证实。我们的工作概述了一种用于诊断戈斯氏细菌性萎蔫病的新有用工具;并提供了坏死叶片病变中假单胞菌群落动态的初步见解。