Goodnight Karen Morgan, Tian Peng, Bissonnette Kaitlyn M
Purdue University, 311308, Botany and Plant Pathology, West Lafayette, Indiana, United States.
University of Missouri, 14716, Biological Sciences, Columbia, Missouri, United States;
Plant Dis. 2023 May 8. doi: 10.1094/PDIS-02-23-0385-PDN.
Charcoal rot, caused by , is abundantly present in the soil and has been reported as pathogenic to both soybean and corn, as well as numerous other hosts, including hemp grown for fiber, grain, and cannabinoids (Casano et al. 2018; Su et al. 2001). Hemp () production in Missouri was a relatively new addition to the 2021 growing season. Charcoal rot was reported in Reynolds, Knox, and Boone counties in Missouri from commercial and experimental fields. One of the fields in question experienced heavy disease pressure and had an uneven stand loss, but the total loss was estimated at approximately 60% of the field and was attributed to charcoal rot. Charcoal rot signs and symptoms, microsclerotia on the lower stem and root tissue, wilting and stem discoloration, were observed on a majority of the hemp plants received at the University of Missouri Plant Diagnostic Clinic in July and late Fall of 2021, including samples from Bradford Research Farm in Boone County and Greenley Research Center in Knox County. Root and crown tissue from the hemp plants from the Greenley Research Center were cultured onto acidified potato dextrose agar (APDA). and other fungi grew from the plated tissue after about three days of incubation at room temperature. was confirmed based on the presence of melanized hyphae and microsclerotia (Siddique et al. 2021). The microsclerotia were black, round to ovoid shaped and ranged from about 34-87 µm (average 64 µm) in length and 32-134 µm (average 65 µm) in width (n = 44). A single-hyphae isolation from a putative isolate was conducted to obtain a pure culture. The culture from the Greenley Research Center was used to complete Koch's postulates of charcoal rot on four hemp cultivars. Sterilized toothpicks were added to pure cultures of on APDA and incubated at room temperature for one week to allow for colonization and for use in greenhouse inoculation. Four hemp cultivars (Katani, Grandi, CFX-2, and CRS-1) were grown in a sterilized silt loam for three weeks in a greenhouse. About four plants per cultivar were grown for inoculation and one plant per cultivar was used as a control. The plants were inoculated with the colonized toothpicks that were gently rubbed onto stem tissue and subsequently inserted into the soil at the stem. For six weeks, the plants were kept in greenhouse conditions of 25°C with a 12-hour light and dark cycle and were watered when soil appeared dry. Plants were kept in a loosely sealed container constructed from wood and vinyl sheeting to minimize cross contamination with other plants grown in the same greenhouse. Plants were monitored weekly for charcoal rot symptoms. Symptoms that resembled charcoal rot, wilting and microsclerotia on the lower stem, were present on inoculated plants after about four weeks and symptoms were not present on the control plants. Isolates resembling in culture were recovered from symptomatic plants; therefore, Koch's postulates were successfully fulfilled and the fungus was recovered from the inoculated plants. DNA was extracted from the pure cultures of both the initial isolate and the isolate obtained from Koch's postulates using GeneJet Plant Genomic DNA Purification Kit (Thermo Scientific, California, USA) and the internal transcribed spacer (ITS) region of ribosomal DNA including ITS1, 5.8S, and ITS4 regions were amplified using universal primers ITS1 and ITS4 (White et al. 1990). The ITS region was sequenced and compared to reference sequences in GenBank by BLAST analysis. Recovered isolates (GenBank accession no. OQ455934.1) showed closest sequence similarity (100%) to accession number GU046909.1. Little is known about the life cycle, growth conditions, and possible inoculum buildup in the soil in hemp in Missouri. In addition, is a known pathogen of corn and soybean and effective management strategies are challenging for these crops as well due to the broad host range of the pathogen. Cultural management practices, such as crop rotations to reduce inoculum in the soil and closely monitoring for symptoms, may help reduce the severity of this disease.
由[病原菌名称未给出]引起的炭腐病在土壤中广泛存在,据报道,它对大豆、玉米以及许多其他寄主都具有致病性,包括用于生产纤维、谷物和大麻素的大麻(卡萨诺等人,2018年;苏等人,2001年)。密苏里州的大麻([大麻品种未给出])生产在2021年生长季是一个相对较新的产业。在密苏里州的雷诺兹县、诺克斯县和布恩县的商业和试验田中均有炭腐病的报道。其中一个受灾田块病害压力很大,植株损失不均,但估计该田块总损失约为60%,病因是炭腐病。2021年7月和深秋时节,密苏里大学植物诊断诊所收到的大多数大麻植株上都观察到了炭腐病的症状和体征,即下部茎和根组织上出现小菌核、萎蔫和茎变色,包括来自布恩县布拉德福德研究农场和诺克斯县格林利研究中心的样本。将来自格林利研究中心的大麻植株的根和冠组织接种到酸化马铃薯葡萄糖琼脂(APDA)上。在室温下培养约三天后,[病原菌名称未给出]和其他真菌从接种的组织中生长出来。根据黑化菌丝和小菌核的存在情况确认了[病原菌名称未给出](西迪克等人,2021年)。小菌核呈黑色,圆形至卵形,长度约为34 - 87微米(平均64微米),宽度为32 - 134微米(平均65微米)(n = 44)。从一个假定的[病原菌名称未给出]分离株进行单菌丝分离以获得纯培养物。来自格林利研究中心的[病原菌名称未给出]培养物用于在四个大麻品种上完成炭腐病的柯赫氏法则验证。将灭菌牙签添加到APDA上的[病原菌名称未给出]纯培养物中,在室温下培养一周,使其定殖,以便用于温室接种。四个大麻品种(卡塔尼、格兰迪、CFX - 2和CRS - 1)在温室中的灭菌粉质壤土中种植三周。每个品种大约种植四株用于接种,每个品种留一株作为对照。用定殖有[病原菌名称未给出]的牙签轻轻擦拭茎组织,然后插入茎部土壤中对接种植株进行接种。六周内保持植株处于25°C、12小时明暗周期的温室条件下,当土壤表面干燥时进行浇水。植株置于由木材和乙烯基薄板制成的松散密封容器中,以尽量减少与同一温室中其他植株的交叉污染。每周监测植株是否出现炭腐病症状。接种约四周后,接种植株出现了类似炭腐病的症状,如下部茎萎蔫和出现小菌核,而对照植株未出现症状。从有症状的植株中分离出了在培养特征上类似[病原菌名称未给出]的菌株;因此,成功完成了柯赫氏法则验证,并且从接种植株中重新分离出了该真菌。使用GeneJet植物基因组DNA纯化试剂盒(美国加利福尼亚州赛默飞世尔科技公司)从初始分离株和通过柯赫氏法则获得的分离株的纯培养物中提取DNA,并使用通用引物ITS1和ITS4扩增核糖体DNA的内部转录间隔区(ITS)区域,包括ITS1、5.8S和ITS4区域(怀特等人,1990年)。对ITS区域进行测序,并通过BLAST分析与GenBank中的参考序列进行比较。回收的分离株(GenBank登录号OQ455934.1)与登录号GU046909.1的[病原菌名称未给出]序列相似性最高(100%)。关于密苏里州大麻的生命周期、生长条件以及土壤中可能的接种体积累情况知之甚少。此外,[病原菌名称未给出]是玉米和大豆的已知病原菌,由于该病原菌寄主范围广泛,对这些作物实施有效的管理策略也具有挑战性。种植轮作等栽培管理措施,如减少土壤中的接种体以及密切监测症状,可能有助于减轻这种病害的严重程度。