Peng X D, Huang S L, Lin S H
School of Life Science and Technology, Nanyang Normal University, 473061 Nanyang, China.
Sugarcane Research Institute, Guangxi Academy of Agricultural Sciences, 530007 Nanning, China.
Plant Dis. 2015 Jan;99(1):159. doi: 10.1094/PDIS-08-14-0814-PDN.
In October 2012, a brown spot disease was found on corn kernels during a field survey in Nanyang city (33°01' N, 112°29' E), China. The incidences of affected ears and kernels were 2 to 10% (n = 600) and 0.08 to 0.4% (n = 25,000), respectively. Symptoms first appeared as circular or irregular brown spots on the endosperm. These spots subsequently enlarged or coalesced, resulting in the formation of a large light-brown or light-yellow irregular speckle commonly surrounded by a dark-brown edge. Pure fungal cultures with similar morphological characteristics were obtained from surface-disinfected symptomatic kernels using a conventional method for isolation of culturable microbes. The isolated fungal cultures were purified by single-spore isolation (3). A representative isolate F1 was randomly selected, used for pathogenicity tests, and identified using morphological and molecular methods. Colonies on PDA were circular with abundant villiform aerial mycelia. The color of colonies was white-gray at first and turned to light yellow or became ochraceous after 3 days of incubation at 28°C. Hyphae were hyaline and less septate, with rectangular branches. Sporangiophores were erect and unbranched or branched, with globose sporangia formed on their tips. Sporangiospores were elliptical to round, 3.6 to 7.3 × 1.6 to 3.7 μm (n = 100) in size. Two gene regions were amplified for multilocus sequence typing. The D1/D2 region of the nuclear large subunit ribosomal RNA gene (nucLSU) was amplified with primers NL1 and NL4 and the rDNA internal transcribed spacer (ITS) with primers ITS1 and ITS4. PCR products were purified using an Axygen nucleic acid purification kit for sequencing. Both rDNA D1/D2 and rDNA-ITS sequences were submitted to GenBank with accession numbers KM093834 and KM203872, respectively. The isolate F1 showed 98% identity with two isolates of Mucor irregularis (KC524427 and KC461926) in rDNA-ITS sequences and 99% identity with multiple isolates (JX976221, JX976203, and JX976219) of M. irregularis in rDNA D1/D2 sequences. Pathogenicity tests of isolate F1 were conducted based on Koch's postulates. Thirty kernels of fresh ears (milk stage) were pricked by sterilized toothpicks and separately inoculated with a sporangiospore suspension (1 × 10 spores/ml) and 5-day-old mycelial plugs (5 × 5 mm) of isolate F1. Kernels on ears that were inoculated with sterilized water and pure PDA plugs were separately used as controls. After 7 days of incubation, brown spot symptoms developed on the F1-inoculated kernels, which were similar to those observed on the naturally infected ears from the field samples. The control ears remained symptomless during the inoculation tests. Fungal cultures showing the same morphological characteristics as those of isolate F1 were consistently recovered from the diseased cobs inoculated by isolate F1, indicating that M. irregularis was responsible for corn kernel brown spot disease. M. irregularis was reported as a pathogen causing human skin diseases in China (5), America (1), and India (2) and as a phytopathogen causing fruit rot on durian (4). This is the first report of M. irregularis causing corn kernel brown spot disease in China. References: (1) M. M. Abuali et al. J. Clin. Microbiol. 47:4176, 2009. (2) B. M. Hemashettar et al. J. Clin. Microbiol. 49:2372, 2011. (3) S. L. Huang and K. Kohmoto. Bull. Fac. Agric., Tottori Univ. 44:1, 1991. (4) W. F. Wang et al. Plant Quarant. l23:60, 2009. (5) Y. Zhao et al. Mycopathologia 168:243, 2009.
2012年10月,在中国南阳市(北纬33°01′,东经112°29′)进行田间调查时,在玉米粒上发现了一种褐色斑点病。受影响的果穗和籽粒发病率分别为2%至10%(n = 600)和0.08%至0.4%(n = 25,000)。症状最初表现为胚乳上出现圆形或不规则褐色斑点。这些斑点随后扩大或融合,形成一个大的浅褐色或浅黄色不规则斑纹,通常被深褐色边缘包围。使用传统的可培养微生物分离方法,从表面消毒的有症状籽粒中获得了具有相似形态特征的纯真菌培养物。分离得到的真菌培养物通过单孢分离法进行纯化(3)。随机选择一个代表性分离株F1,用于致病性测试,并采用形态学和分子方法进行鉴定。在PDA上的菌落呈圆形,有丰富的绒毛状气生菌丝。菌落颜色起初为灰白色,在28°C培养3天后变为浅黄色或赭色。菌丝透明,隔膜较少,有矩形分支。孢囊梗直立,不分枝或分枝,顶端形成球形孢子囊。孢子囊孢子椭圆形至圆形,大小为3.6至7.3×1.6至3.7μm(n = 100)。扩增两个基因区域用于多位点序列分型。使用引物NL1和NL4扩增核糖体RNA基因大亚基(nucLSU)的D1/D2区域,使用引物ITS1和ITS4扩增rDNA内部转录间隔区(ITS)。PCR产物使用Axygen核酸纯化试剂盒进行纯化以便测序。rDNA D1/D2和rDNA-ITS序列均已提交至GenBank,登录号分别为KM093834和KM203872。分离株F1在rDNA-ITS序列上与不规则毛霉的两个分离株(KC524427和KC461926)有98%的同一性,在rDNA D1/D2序列上与不规则毛霉的多个分离株(JX976221、JX976203和JX976219)有99%的同一性。基于科赫法则对分离株F1进行致病性测试。用灭菌牙签刺破30个新鲜果穗(乳熟期)的籽粒,分别接种分离株F1的孢子囊孢子悬液(1×10个孢子/ml)和5日龄菌丝块(5×5mm)。接种灭菌水和纯PDA菌块的果穗上的籽粒分别用作对照。培养7天后,接种F1的籽粒上出现褐色斑点症状,与田间样品中自然感染果穗上观察到的症状相似。在接种测试期间,对照果穗无症状。从接种分离株F1的病穗上始终能分离出与分离株F1形态特征相同的真菌培养物,表明不规则毛霉是玉米粒褐色斑点病的病原菌。在中国(5)、美国(1)和印度(2),不规则毛霉被报道为引起人类皮肤疾病的病原菌,在泰国(4)被报道为引起榴莲果实腐烂的植物病原菌。这是中国关于不规则毛霉引起玉米粒褐色斑点病的首次报道。参考文献:(1)M. M. Abuali等人,《临床微生物学杂志》47:4176,2009年。(2)B. M. Hemashettar等人,《临床微生物学杂志》49:2372,2011年。(3)S. L. Huang和K. Kohmoto,《鸟取大学农学院学报》44:1,1991年。(4)W. F. Wang等人,《植物检疫》123:60,2009年。(5)Y. Zhao等人,《真菌病理学》168:243,2009年。