Stanghellini M E, Mohammadi M, Mathews D M, Adkins S
Department of Plant Pathology and Microbiology, University of California, Riverside 92521.
USDA-ARS, Fort Pierce, FL 34945.
Plant Dis. 2014 Jun;98(6):852. doi: 10.1094/PDIS-11-13-1123-PDN.
In late May 2013, collapse of mature watermelon plants (Citrullus lanatus L.) at first harvest occurred in several drip-irrigated commercial fields in the Coachella Valley, California. Above-ground symptoms consisted of chlorosis, wilting, and death of leaves starting at the crown and progressing rapidly towards the tip of vines. Structural roots of collapsed plants appeared healthy but feeder roots exhibited a brownish discoloration. Microscopic examination revealed that almost all epidermal cells of feeder roots contained either sporangia or resting spores of a fungus tentatively identified, based upon morphological characteristics, as Olpidium bornovanus (Sahtiy.) Karling. No other fungi or fungal-like organisms were microscopically observed in or isolated from structural roots, feeder roots, or vascular tissue of collapsed plants. Leaf, root, and peduncle samples from collapsed plants were tested for Melon necrotic spot virus (MNSV), a virus known to be transmitted by O. bornovanus, and Squash vein yellowing virus (SqVYV), a whitefly-transmitted ipomovirus known to cause watermelon vine decline (1). No MNSV was detected using previously described methods (3). No SqVYV was detected by testing total RNA from symptomatic plants (RNeasy Plant Mini Kit, Qiagen, Valencia, CA) with reverse transcription-PCR using previously described primers and methods (1,2). Genomic DNA was extracted from zoospores of the fungus which were obtained from a single-sporangial isolate maintained on watermelon seedlings. Analysis of ITS 1 and 2 gene sequences and a subsequent search in NCBI GenBank revealed a 99% identity to nucleotide sequences for O. bornovanus (Accession Nos. AB205215 and AB665758). To confirm Koch's postulates, roots of three 5-day-old watermelon seedlings were inoculated by exposure to zoospores (~1 × 10) in a beaker for 2 min and then transplanted into pots containing vermiculite. Pots were irrigated daily and incubated in a growth chamber (25°C, 12-h photoperiod). Controls consisted of non-inoculated watermelon seedlings. The experiment was repeated twice. Within 15 days of inoculation, all inoculated plants were stunted, and roots of stunted plants were brown and most root epidermal cells were filled with either sporangia or resting spores of O. bornovanus. Within 30 days of inoculation, 40 to 60% of the inoculated plants died in all three experiments. No other microorganisms were microscopically observed in or isolated from necrotic roots. Control plants remained symptomless over the duration of the study. Although O. bornovanus has been reported as a root pathogen of melons in greenhouse conditions (3), this is the first worldwide report of the fungus as a root pathogen of watermelons and its association with a late season vine decline in the field. Near-saturated soil conditions resulting from a daily irrigation regime during the latter part of the growing season apparently favored extensive root colonization by this indigenous and opportunistic zoosporic fungus, suggesting that growers should exercise care regarding the duration and frequency of irrigation events. References: (1) S. Adkins et al. Phytopathology 97:145, 2007. (2) S. Adkins et al. Plant Dis. 1119, 2008. (3) M. E. Stanghellini et al. Plant Dis. 94:163, 2010.
2013年5月下旬,加利福尼亚州科切拉谷的几个滴灌商业种植田中,头茬成熟西瓜植株(西瓜)出现萎蔫。地上症状包括褪绿、萎蔫,叶片从叶冠开始发黄,并迅速向藤蔓尖端发展。萎蔫植株的结构根看起来健康,但须根呈现褐色。显微镜检查显示,须根的几乎所有表皮细胞都含有孢子囊或一种真菌的休眠孢子,根据形态特征初步鉴定为甜瓜根囊霉(Sahtiy.)Karling。在萎蔫植株的结构根、须根或维管组织中,未在显微镜下观察到或分离出其他真菌或类真菌生物。对萎蔫植株的叶片、根和果梗样本进行了甜瓜坏死斑病毒(MNSV)检测,已知该病毒由甜瓜根囊霉传播,还检测了南瓜叶脉黄化病毒(SqVYV),这是一种由粉虱传播的甘薯褪绿病毒,已知可导致西瓜藤蔓衰退(1)。采用先前描述的方法(3)未检测到MNSV。通过使用先前描述的引物和方法(1,2),对有症状植株的总RNA(RNeasy Plant Mini Kit,Qiagen,加利福尼亚州瓦伦西亚)进行逆转录PCR检测,未检测到SqVYV。从保存在西瓜幼苗上的单孢子囊分离物获得的真菌游动孢子中提取基因组DNA。对ITS 1和2基因序列进行分析,并随后在NCBI GenBank中搜索,结果显示与甜瓜根囊霉的核苷酸序列有99%的同一性(登录号:AB205215和AB665758)。为了证实科赫法则,将三株5日龄西瓜幼苗的根在烧杯中暴露于游动孢子(约1×10)2分钟进行接种,然后移植到装有蛭石的花盆中。花盆每天浇水,并在生长室(25°C,12小时光照周期)中培养。对照组为未接种的西瓜幼苗。该实验重复了两次。接种后15天内,所有接种植株生长受阻,生长受阻植株的根呈褐色,大多数根表皮细胞充满甜瓜根囊霉的孢子囊或休眠孢子。接种后30天内,在所有三个实验中,40%至60%的接种植株死亡。在坏死根中未在显微镜下观察到或分离出其他微生物。在研究期间,对照植株一直无症状。尽管甜瓜根囊霉在温室条件下已被报道为甜瓜的根部病原菌(3),但这是该真菌作为西瓜根部病原菌及其与田间后期藤蔓衰退相关性的首次全球报道。生长季节后期每日灌溉制度导致土壤接近饱和状态,显然有利于这种本地兼机会性游动孢子真菌广泛侵染根部,这表明种植者应注意灌溉事件的持续时间和频率。参考文献:(1)S. Adkins等人,《植物病理学》97:145,2007年。(2)S. Adkins等人,《植物病害》1119,2008年。(3)M. E. Stanghellini等人,《植物病害》94:163,2010年。