Ghuffar Salman, Ahmed Muhammad Zeshan, Irshad Gulshan, Zeshan Muhamamd Ahmad, Qadir Abdul, Anwaar Hafiz Arslan, Mansha Muhammad Zeeshan, Asadullah Hafiz Muhammad, Abdullah Ahsan, Farooq Usman
University of Arid Agriculture, 72599, Plant pathology, Department of plant pathology PMAS Arid agriculture university Rawalpindi, Rawalpindi, Pakistan, 46000.
University of Arid Agriculture, 72599, plant pathology, Department of plant pathology PMAS Arid agriculture university Rawalpindi, Rawalpindi, Pakistan, 46000;
Plant Dis. 2020 Oct 13. doi: 10.1094/PDIS-06-20-1390-PDN.
In June 2015 & 2016, a postharvest survey of table grapes (Vitis vinifera) cv. King's Ruby, was carried out in five different commercial fruit markets of Rawalpindi (33°38'19.2″N, 73°01'45.0″E) district, Punjab Province. Symptoms appeared as brownish lesions with black sporulation on grapes berries. The incidence of these symptoms on bunches ranged from 12 to 17% at all sites. Symptomatic tissue pieces were surface-sterilized with 0.1% sodium hypochlorite (NaOCl) for 30 seconds, rinsed three times with sterile distilled water, dried on filter paper for 45 seconds, and incubated on potato dextrose agar (PDA) at 25°C. After 3 days, dark brown to black mycelium were formed on PDA media. A total of 24 isolates were examined morphologically. The apex of the conidiophore was observed to be radiate. Vesicles were found to be spherical and covered with irregular metulae and phialides. Conidia were globose or subglobose measured (3.14 μm ± 2.24 in averaged diameter: n=50), dark brown to black, with roughened cell walls. The conidiophores were also smooth-walled, hyaline, and became melanized toward the vesicle. These characteristics of the fungus were similar to those described for Aspergillus niger van Tiegh (de Hoog et al. 2000). For molecular identification, the internal transcribed spacer (ITS) region, beta-tubulin (Bt) gene and partial RNA polymerase II largest subunit (RPB2) gene of representative isolate (Asp.n02) was amplified using primers ITS1/ITS4, BT2a/BT2b and RPB2-6F/RPB2-7R respectively (White et al., 1990; Glass & Donaldson, 1995; Liu et al. 1999). Sequences were deposited in GenBank (ITS, MN658871; Bt2, MT117924; and RPB2, MT318289). Based on BLAST analysis, sequences of the ITS region, Bt2 genes, and RPB2 gene showed 99 to 100% similarity of isolate Asp.n02 to Aspergillus niger (Accession Nos. MK307680.1, MN195121.1, MF078661.1 for ITS gene, MN567299.1, MK451029.1, MK451020.1 for Bt2 gene, and MK450788.1, MK450790.1 for RPB2 gene). To complete Koch's postulates, 10-µl aliquots of spore suspensions (106 spores/ml) of isolate: Asp.n 02 was pipetted onto three non-wounded and four wounded (5 mm diam) asymptomatic grape berries cv. King's Ruby (seven berries per isolate), Sterile distilled water was applied to asymptomatic berries similaries to serve as a negative control (Ghuffar et al. 2018; Jayawardena et al. 2018). Berries were incubated at 25 ± 2°C in sterile moisture chambers, and the experiment was conducted twice. Brownish lesions leading to black sporulation similar to the original symptoms were observed on both wounded and non-wounded inoculated berries after 3 days, whereas no symptoms were recorded on the negative control. The morphology of the fungus that was re-isolated from each of the inoculated berries was identical to that of the original cultures. Aspergillus niger was reported previously in Europe and Israel causing mycotoxin (Ochratoxin A) OTA production on Table grapes (Bau et al. 2006). To our knowledge, this is the first report of Aspergillus niger causing black rot of grapes in Pakistan. This finding will help to plan effective disease management strategies against the black rot of grapes in Pakistan.
2015年6月和2016年,在旁遮普省拉瓦尔品第(北纬33°38'19.2″,东经73°01'45.0″)的五个不同商业水果市场,对鲜食葡萄(欧亚种葡萄)品种“国王红宝石”进行了采后调查。葡萄浆果上出现褐色病斑并伴有黑色孢子形成的症状。在所有地点,这些症状在果穗上的发生率为12%至17%。将有症状的组织块用0.1%次氯酸钠(NaOCl)表面消毒30秒,用无菌蒸馏水冲洗三次,在滤纸上干燥45秒,然后在25°C的马铃薯葡萄糖琼脂(PDA)上培养。3天后,PDA培养基上形成深褐色至黑色的菌丝体。共对24个分离株进行了形态学检查。观察到分生孢子梗顶端呈辐射状。发现囊泡呈球形,覆盖着不规则的小梗和瓶梗。分生孢子呈球形或近球形(平均直径3.14μm±2.24,n = 50),深褐色至黑色,细胞壁粗糙。分生孢子梗壁也光滑、透明,向囊泡方向变黑。该真菌的这些特征与黑曲霉(de Hoog等人,2000年)描述的特征相似。为了进行分子鉴定,分别使用引物ITS1/ITS4、BT2a/BT2b和RPB2 - 6F/RPB2 - 7R扩增代表性分离株(Asp.n02)的内部转录间隔区(ITS)、β - 微管蛋白(Bt)基因和部分RNA聚合酶II最大亚基(RPB2)基因(White等人;Glass和Donaldson,1995年;Liu等人,1999年)。序列已存入GenBank(ITS,MN658871;Bt2,MT117924;和RPB2,MT318289)。基于BLAST分析,ITS区域、Bt2基因和RPB2基因的序列显示分离株Asp.n02与黑曲霉的相似性为99%至100%(ITS基因登录号为MK307680.1、MN195121.1、MF078661.1;Bt2基因登录号为MN567299.1、MK451029.1、MK451020.1;RPB2基因登录号为MK450788.1、MK450790.1)。为了完成柯赫氏法则,将分离株Asp.n 02的孢子悬浮液(106个孢子/ml)10μl等分吸取到三个未受伤和四个受伤(直径5mm)的无症状“国王红宝石”葡萄浆果上(每个分离株接种七个浆果),将无菌蒸馏水类似地施用于无症状浆果作为阴性对照(Ghuffar等人,2018年;Jayawardena等人,2018年)。浆果在25±2°C的无菌保湿箱中培养,实验进行了两次。三天后,在受伤和未受伤的接种浆果上均观察到导致黑色孢子形成的褐色病斑,类似于原始症状,而阴性对照未记录到症状。从每个接种浆果上重新分离出的真菌形态与原始培养物相同。此前在欧洲和以色列报道过黑曲霉在鲜食葡萄上产生霉菌毒素(赭曲霉毒素A)OTA。据我们所知,这是巴基斯坦关于黑曲霉引起葡萄黑腐病的首次报道。这一发现将有助于制定针对巴基斯坦葡萄黑腐病的有效病害管理策略。