Cramer Robert A, Lawrence Christopher B
Department of Bioagricultural Sciences and Pest Management, Colorado State University, Fort Collins, CO, USA.
Fungal Genet Biol. 2004 Feb;41(2):115-28. doi: 10.1016/j.fgb.2003.10.009.
Alternaria brassicicola is a necrotrophic fungal pathogen that causes black spot disease on cruciferous plants including economically important Brassica species. The purpose of this study was to identify fungal genes expressed during infection of Arabidopsis. In order to identify candidate genes involved in pathogenicity, we employed suppression subtractive hybridization (SSH) between RNA isolated from A. brassicicola spores incubated in water and on the leaf surface of the Arabidopsis ecotype Landsberg. Two populations of cDNA were created from total RNA extracted after 24h when approximately 80% of the spores had germinated either on the leaf surface or in water. Following SSH, expression of clones was examined using dot-blot macro-arrays and virtual Northern blots. 47 cDNA clones differentially expressed between Alternaria infected Arabidopsis leaves and spore germination in water were selected for sequencing. Seventy-seven percent (36) of the cDNAs had significant homology to fungal sequences from databases examined, including available fungal genomes, while 13% (11) had no homology to sequences in the databases. All 36 genes had significant matches with genes of fungal origin, while 11 genes did not have significant hits in the databases examined. Five sequences were expressed on the plant leaf surface but not during spore germination in water according to virtual Northern blots. These five cDNAs were predicted to encode a cyanide hydratase, arsenic ATPase, formate dehydrogenase, major Alternaria allergen, and one unknown. RT-PCR was used to examine the expression of these five genes during infection of Brassica oleraceae var. capitata (cabbage), in vitro growth in nutrient rich media, and infection of Arabidopsis thaliana. Four of these genes are expressed in the nutrient rich medium, while the unknown gene P3F2 was only expressed during plant infection. The results of this study provide the first insight into genes expressed during A. brassicicola infection of Brassica species that may be involved in fungal pathogenesis.
链格孢菌是一种坏死性真菌病原体,可在包括具有重要经济价值的芸苔属物种在内的十字花科植物上引发黑斑病。本研究的目的是鉴定拟南芥感染过程中表达的真菌基因。为了鉴定参与致病性的候选基因,我们利用抑制性消减杂交(SSH)技术,对在水中培养以及在拟南芥生态型Landsberg叶片表面培养的链格孢菌孢子中分离出的RNA进行分析。当大约80%的孢子在叶片表面或水中萌发24小时后,从总RNA中创建了两个cDNA群体。经过SSH后,使用点杂交宏阵列和虚拟Northern印迹法检测克隆的表达。选择了47个在链格孢菌感染的拟南芥叶片和水中孢子萌发之间差异表达的cDNA克隆进行测序。77%(36个)的cDNA与所检测数据库中的真菌序列具有显著同源性,包括可用的真菌基因组,而13%(11个)与数据库中的序列无同源性。所有36个基因与真菌来源的基因有显著匹配,而11个基因在所检测的数据库中没有显著匹配。根据虚拟Northern印迹法,有五个序列在植物叶片表面表达,但在水中孢子萌发期间不表达。预计这五个cDNA分别编码氰化物水合酶、砷ATP酶、甲酸脱氢酶、主要链格孢过敏原和一个未知蛋白。利用RT-PCR检测这五个基因在甘蓝型油菜(卷心菜)感染过程、富营养培养基中的体外生长以及拟南芥感染过程中的表达情况。其中四个基因在富营养培养基中表达,而未知基因P3F2仅在植物感染期间表达。本研究结果首次揭示了链格孢菌感染芸苔属物种过程中可能参与真菌致病机制的基因表达情况。