Larrea-Sarmiento Adriana E, Olmedo-Velarde Alejandro, Wang Xupeng, Borth Wayne, Domingo Ryan, Matsumoto Tracie K, Suzuki Jon Y, Wall Marisa M, Melzer Michael J, Hu John
Department of Plant and Environmental Protection Sciences, University of Hawaii, Honolulu, HI 96822, USA.
United States Department of Agriculture, Agricultural Research Service, Daniel K. Inouye U. S. Pacific Basin Agricultural Research Center, Hilo, HI 96720, USA.
Pathogens. 2022 Dec 5;11(12):1470. doi: 10.3390/pathogens11121470.
Pineapple ( L. [Merr.]) accessions from the U.S. Tropical Plant Genetic Resources and Disease Research (TPGRDR) in Hilo, Hawaii were subjected to RNA-sequencing to study the occurrence of viral populations associated with this vegetatively propagated crop. Analysis of high-throughput sequencing data obtained from 24 germplasm accessions and public domain transcriptome shotgun assembly (TSA) data identified two novel sadwaviruses, putatively named "pineapple secovirus C" (PSV-C) and "pineapple secovirus D" (PSV-D). They shared low amino acid sequence identity (from 34.8 to 41.3%) compared with their homologs in the Pro-pol region of the previously reported PSV-A and PSV-B. The complete genome (7485 bp) corresponding to a previously reported partial sequence of the badnavirus, pineapple bacilliform ER virus (PBERV), was retrieved from one of the datasets. Overall, we discovered a total of 69 viral sequences representing ten members within the , , and genera. Genetic diversity and recombination events were found in members of the pineapple mealybug wilt-associated virus (PMWaV) complex as well as PSVs. PMWaV-1, -3, and -6 presented recombination events across the quintuple gene block, while no recombination events were found for PMWaV-2. High recombination frequency of the RNA1 and RNA2 molecules from PSV-A and PSV-B were congruent with the diversity found by phylogenetic analyses. Here, we also report the development and improvement of RT-PCR diagnostic protocols for the specific identification and detection of viruses infecting pineapple based on the diverse viral populations characterized in this study. Given the high occurrence of recombination events, diversity, and discovery of viruses found in germplasm, the reported and validated RT-PCR assays represent an important advance for surveillance of viral infections of pineapple.
对来自美国夏威夷希洛热带植物遗传资源与疾病研究中心(TPGRDR)的菠萝(L. [Merr.])种质进行RNA测序,以研究与这种无性繁殖作物相关的病毒群体的发生情况。对从24个种质中获得的高通量测序数据以及公共领域转录组鸟枪法组装(TSA)数据进行分析,鉴定出两种新型萨德瓦病毒,暂命名为“菠萝赛柯病毒C”(PSV-C)和“菠萝赛柯病毒D”(PSV-D)。与先前报道的PSV-A和PSV-B的Pro-pol区域中的同源物相比,它们的氨基酸序列同一性较低(从34.8%到41.3%)。从其中一个数据集中检索到了与先前报道的杆状DNA病毒——菠萝杆状内质网病毒(PBERV)的部分序列相对应的完整基因组(7485 bp)。总体而言,我们共发现了69个病毒序列,代表了 、 和 属中的10个成员。在菠萝粉蚧萎蔫相关病毒(PMWaV)复合体成员以及PSV中发现了遗传多样性和重组事件。PMWaV-1、-3和-6在五重基因块中出现了重组事件,而PMWaV-2未发现重组事件。PSV-A和PSV-B的RNA1和RNA2分子的高重组频率与系统发育分析发现的多样性一致。在此,我们还报告了基于本研究中鉴定的不同病毒群体,开发和改进用于特异性鉴定和检测感染菠萝的病毒的RT-PCR诊断方案。鉴于在种质中发现的重组事件发生率高、多样性以及病毒的发现,所报道和验证的RT-PCR检测方法代表了菠萝病毒感染监测的一项重要进展。