Zheng Sujiao, Ke Xiwang, Yin Lihua, Cui Dongmei, Zhang Haitao, Tai Lianmei, Zuo Yuhu
Wei Sheng Wu Xue Bao. 2015 Apr 4;55(4):425-32.
The aim of the study is to identify the pathogen causing adzuki bean (Phaseolus angularis) rust in Daqing, Heilongjiang province.
Adzuki bean rust leaves were collected from Daqing, Heilongjiang province, China. A pure culture of rust isolate ZXL01 was obtained by single pustule isolation. Its taxonomic status was determined by observing the number of germ pores of urediniospores, germ pore location and the wall thickness of teliopores, and sequencing ribosomal DNA internal transcribed spacer (rDNA-ITS).
Morphological studies showed that most of the urediospores of ZXL01 had two germ pores that were far from spores' equator area. The wall thickness of teliopores ranged from 2.9 to 3. 3 microm. The rDNA-ITS sequence of ZXL01 was clustered in one clade with 2 reference isolates of Uromyces vignae (GenBank accession numbers AB115718 and AB115731) at 99% bootstrap levels in the phylogenetic tree. A 500 bp amplified product was obtained by the specific primers UV-ITSF/R, which was specific for U. Vignae.
The morphological features and ITS analysis indicated that the rust fungus ZXL01 occurred on leaves of adzuki bean in Daqing was U. Vignae, and the accession number of GenBank was KM461700.
本研究旨在鉴定黑龙江省大庆市引起赤豆锈病的病原菌。
从中国黑龙江省大庆市采集赤豆锈病叶片。通过单疱分离获得锈菌分离株ZXL01的纯培养物。通过观察夏孢子的芽孔数量、芽孔位置和冬孢子的壁厚,并对核糖体DNA内部转录间隔区(rDNA-ITS)进行测序来确定其分类地位。
形态学研究表明,ZXL01的大多数夏孢子有两个远离孢子赤道区域的芽孔。冬孢子的壁厚在2.9至3.3微米之间。在系统发育树中,ZXL01的rDNA-ITS序列在99%的自展水平下与2个菜豆单胞锈菌参考分离株(GenBank登录号AB115718和AB115731)聚类在一个分支中。用菜豆单胞锈菌特异性引物UV-ITSF/R扩增得到500bp的产物。
形态学特征和ITS分析表明,大庆市赤豆叶片上发生的锈菌ZXL01为菜豆单胞锈菌,GenBank登录号为KM461700。