Tan Choon Meng, Lin Yu-Chen, Li Jian-Rong, Chien Yuan-Yu, Wang Chien-Jui, Chou Lin, Wang Cheng-Wei, Chiu Yi-Ching, Kuo Chih-Horng, Yang Jun-Yi
Institute of Biochemistry, National Chung Hsing University, Taichung, Taiwan.
Institute of Plant and Microbial Biology, Academia Sinica, Taipei, Taiwan.
Front Microbiol. 2021 Nov 11;12:766221. doi: 10.3389/fmicb.2021.766221. eCollection 2021.
Phytoplasmas are uncultivated plant-pathogenic bacteria with agricultural importance. Those belonging to the 16SrII group, represented by ' P. aurantifolia', have a wide range of plant hosts and cause significant yield losses in valuable crops, such as pear, sweet potato, peanut, and soybean. In this study, a method that combines immunoprecipitation-based enrichment and MinION long-read DNA sequencing was developed to solve the challenge of phytoplasma genome studies. This approach produced long reads with high mapping rates and high genomic coverage that can be combined with Illumina reads to produce complete genome assemblies with high accuracy. We applied this method to strain NCHU2014 and determined its complete genome sequence, which consists of one circular chromosome with 635,584 bp and one plasmid with 4,224 bp. Although '. P. aurantifolia' NCHU2014 has a small chromosome with only 471 protein-coding genes, it contains 33 transporter genes and 27 putative effector genes, which may contribute to obtaining nutrients from hosts and manipulating host developments for their survival and multiplication. Two effectors, the homologs of SAP11 and SAP54/PHYL1 identified in '. P. aurantifolia' NCHU2014, have the biochemical activities in destabilizing host transcription factors, which can explain the disease symptoms observed in infected plants. Taken together, this study provides the first complete genome available for the 16SrII phytoplasmas and contributes to the understanding of phytoplasma pathogenicity.
植原体是一类具有农业重要性的未培养植物致病细菌。那些属于16SrII组的植原体,以“aurantifolia梨植原体”为代表,具有广泛的植物宿主,并在梨、甘薯、花生和大豆等重要作物中造成重大产量损失。在本研究中,开发了一种基于免疫沉淀富集和MinION长读长DNA测序相结合的方法,以解决植原体基因组研究的挑战。这种方法产生了具有高映射率和高基因组覆盖率的长读长,可与Illumina读长相结合,以产生高精度的完整基因组组装。我们将此方法应用于NCHU2014菌株,并确定了其完整基因组序列,该序列由一条635,584 bp的环状染色体和一条4,224 bp的质粒组成。尽管“aurantifolia梨植原体”NCHU2014的染色体较小,仅含有471个蛋白质编码基因,但它包含33个转运蛋白基因和27个假定效应蛋白基因,这可能有助于从宿主获取营养并操纵宿主发育以实现其生存和繁殖。在“aurantifolia梨植原体”NCHU2014中鉴定出的两个效应蛋白,即SAP11和SAP54/PHYL1的同源物,具有使宿主转录因子不稳定的生化活性,这可以解释在受感染植物中观察到的疾病症状。综上所述,本研究提供了首个可用于16SrII组植原体的完整基因组,并有助于理解植原体的致病性。