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关于棒孢叶斑病菌引起的棉花靶斑病在佐治亚州的首次报道

First Report of Target Spot Caused by Corynespora cassiicola on Cotton in Georgia.

作者信息

Fulmer A M, Walls J T, Dutta B, Parkunan V, Brock J, Kemerait R C

机构信息

Department of Plant Pathology, University of Georgia, Coastal Plain Experiment Station, Tifton, GA 31793.

出版信息

Plant Dis. 2012 Jul;96(7):1066. doi: 10.1094/PDIS-01-12-0035-PDN.

Abstract

In 2005, crop consultants in southwestern Georgia reported an unusual occurrence of leaf spot in cotton (Gossypium hirsutum L.). Initial symptoms first developed as brick red dots that led to the formation of irregular to circular lesions with tan-to-light brown centers. Lesions further enlarged and often demonstrated a targetlike appearance formed from concentric rings within the spot. Observations included estimates of premature defoliation up to 70%, abundant characteristic spots on the leaves and bracts, and losses of several hundred kg of lint/ha. When symptomatic leaves were submitted to the University of Georgia Tifton Plant Disease Clinic in Tifton, GA, for identification in 2008, the causal agent was tentatively diagnosed as Corynespora cassiicola (Berk. & M.A. Curtis) C.T. Wei on the basis of similar symptoms and signs previously reported on cotton (3). In September 2011, symptomatic leaves were obtained from diseased cotton within a field (var. DP 1048B2RF) near Attapulgus, GA. Symptomatic tissue from diseased leaves was surface disinfested in 0.5% sodium hypochlorite for 1 min and plated on potato dextrose agar (PDA). Ten isolates were incubated at 21.1°C for 2 weeks with a 12/12 h light/dark cycle using fluorescent light located approximately 70 cm above the cultures. After 1 week, two isolates were transferred to quarter strength PDA for enhanced sporulation and were grown under the same conditions. Conidiophores from the isolated fungus were simple, erect, intermittently branching and septate, and gave rise to single, subhyaline conidia. Conidia had 4 to 17 pseudosepta and were 50 to 197 μm long and 7 to 16 μm wide, straight to curved, and obclavate to cylindrical. Pathogenicity tests were conducted by spraying 10 cotton seedlings (DP 555BR and DP 1048B2RF, two to four true leaf stage) until runoff with a blended suspension from a 2-week-old pure culture of the fungus diluted with 100 mL of sterile water. Five plants were sprayed with sterile water as noninoculated controls. Cotton seedlings were then incubated in a moist chamber at 21.1°C for 48 h. Within 1 week, all inoculated plants showed symptoms similar to those of diseased field plants. Symptoms were not observed on noninoculated control plants. The fungus was reisolated five times from symptomatic leaves and grown in pure culture. Conidia and conidiophores were identical to the morphology of the original isolates, and were similar to descriptions of C. cassiicola (2). To confirm the identity of the pathogen, DNA was extracted from a week-old culture and amplified with specific primers for loci "ga4" and "rDNA ITS" (1). DNA sequences obtained with the Applied Biosystems 3730xl 96-capillary DNA Analyzer showed 99% identity to C. cassiicola from BLAST analysis in GenBank. The resulting sequence was deposited into GenBank (Accession No. JQ717069). To our knowledge, this is the first report of this pathogen in Georgia. Given the increasing prevalence of this disease in southwestern Georgia, its confirmation is a significant step toward management recommendations for growers. Because foliar diseases caused by C. cassiicola are commonly referred to as "target spot" in other crops (e.g., soybeans), it is proposed that Corynespora leaf spot of cotton be known as "target spot of cotton." References: (1) L. J. Dixon et al. Phytopathology 99:1015, 2009. (2) M. B. Ellis and P. Holliday. CMI Description of Pathogenic Fungi and Bacteria, 303, 1971. (3) J. P. Jones. Phytopathology 51:305, 1961.

摘要

2005年,佐治亚州西南部的作物顾问报告称棉花(陆地棉)出现了异常的叶斑病。最初症状表现为砖红色斑点,随后发展为不规则至圆形病斑,病斑中心呈棕褐色至浅褐色。病斑进一步扩大,通常呈现出由斑点内同心环形成的靶状外观。观察结果包括估计高达70%的过早落叶、叶片和苞叶上大量典型病斑,以及每公顷数百公斤皮棉的损失。2008年,有症状的叶片被送往佐治亚大学蒂夫顿植物病害诊所(位于佐治亚州蒂夫顿)进行鉴定,根据此前棉花上报道的类似症状和体征,暂定致病病原体为多主棒孢(Corynespora cassiicola (Berk. & M.A. Curtis) C.T. Wei)(3)。2011年9月,从佐治亚州阿塔普尔格斯附近一块田地(品种DP 1048B2RF)中患病棉花上获取有症状的叶片。将患病叶片上的有症状组织在0.5%次氯酸钠中进行表面消毒1分钟,然后接种到马铃薯葡萄糖琼脂(PDA)上。十个分离菌株在21.1°C下,使用距离培养物约70厘米的荧光灯,以12/12小时光/暗循环培养2周。1周后,将两个分离菌株转移到四分之一强度的PDA上以促进产孢,并在相同条件下培养。分离出的真菌的分生孢子梗简单、直立、间歇性分枝且有隔膜,产生单个、近无色的分生孢子。分生孢子有4至17个假隔膜,长50至197μm,宽7至16μm,直或弯曲,倒棍棒形至圆柱形。通过用100毫升无菌水稀释的真菌2周龄纯培养物的混合悬浮液喷洒10株棉苗(DP 555BR和DP

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