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墨西哥索诺拉州西瓜根腐病由角担菌属引起的首次报道

First Report of Root Rot of Watermelon Caused by Ceratobasidium sp. in Sonora, Mexico.

作者信息

Meza-Moller A, Rentería-Martínez M E, Guerra-Camacho M A, Romo-Tamayo F, Ochoa-Meza A, Moreno-Salazar S F

机构信息

Universidad Estatal de Sonora, Unidad Académica Hermosillo, Ley Federal del Trabajo y Perimetral S/N, Hermosillo, Sonora, Mexico.

Laboratorio de Biología Molecular, Departamento de Agricultura y Ganadería de la Universidad de Sonora, Carretera a Bahía de Kino Km. 21, Hermosillo, Sonora, Mexico.

出版信息

Plant Dis. 2014 Jun;98(6):847. doi: 10.1094/PDIS-09-13-0974-PDN.

Abstract

Watermelon is one of the major crops grown in Mexico and represents 4% of the total cultivated area with fruits in this country. In 2013, Sonora State was ranked second in the production of watermelon at a national level. Fungal and oomycete diseases are among the main biotic factors affecting watermelon production, particularly those caused by species of the genera Fusarium, Phytophthora, Pythium, and Rhizoctonia. During the spring of 2013, wilting or death symptoms were confirmed in approximately 50% of ungrafted watermelon plants grown in four sampled fields along the coast of Hermosillo and Guaymas Valley in Sonora, Mexico. On both roots and stems of infected plants, localized lesions were found that were 0.2 to 2.0 cm long, reddish brown, and slightly sunken on the stem base. In some cases, the discolorations encompassed nearly 90% of the root system. One-centimeter pieces from the edge of lesions on stems and roots were superficially disinfected with 1% sodium hypochlorite, then rinsed with sterile distilled water, placed onto petri dishes containing potato dextrose agar (PDA), and incubated at 25°C for 3 days. Fungal colonies were white initially, then turned brown, and septate hyphae were 3.7 to 4.3 μm in diameter and branched at right angles with a constriction at the origin of the branch point. These characteristics are typical of the genus Rhizoctonia. Binucleate cells from five isolates were observed using a lactophenol aniline blue solution stain, according to Ceratobasidium morphological descriptions. Mycelia from five isolates grown on PDA was used for DNA extraction. The rDNA-ITS region was amplified using PCR with the universal fungal primers ITS1 and ITS4 (3). The purified products were separately sequenced in both directions using the same primer pair. The sequences obtained were 99% similar to those of Ceratobasidium sp. AG-F and AG-Fa isolates (accessions KC193238.1 on Tagetes erecta, HQ168370.1 on Musa spp., and JX913821.1 on soy-rice-weeds, respectively) from GenBank (2,4). The pathogenicity of the fungus was tested under growth chamber conditions. Sets of seven healthy watermelon seedlings of the Sugar red variety were inoculated with five isolates of Ceratobasidium. Three disks (8 mm in diameter) of mycelia grown on PDA were placed around the roots of each plantlet. The pots were maintained at 27 ± 0.1°C for 14 days with a photoperiod of 12 h. Seven uninoculated seedlings were used as a control. Initial symptoms showing water-soaked lesions developed on all inoculated seedlings within 6 to 7 days, while typical disease symptoms appeared after 10 to 14 days after inoculation. Seedlings without inoculum were free from infection. The fungus was re-isolated from the inoculated seedlings on PDA, and identified as Ceratobasidium sp., confirmed using morphological characteristics. A similar disease has been reported recently in Italy and Arizona (1); however, this report is the first description of a Ceratobasidium sp. causing root rot of watermelon in Sonora, Mexico. Agricultural areas where the study was carried represent 90% of the total area cultivated with watermelon in this state, so it is necessary to evaluate the impact of this pathogen in the crop. References: (1) C. Nischwitz et al. APS joint meeting, 2013. (2) A. Saroj et al. Plant Dis. 97:1251, 2013. (3) T. J. White et al. PCR Protocols: A Guide to Methods and Applications. Academic Press, San Diego, CA, 1990. (4) J. Yin et al. Plant Dis. 95:490, 2011.

摘要

西瓜是墨西哥种植的主要作物之一,占该国水果种植总面积的4%。2013年,索诺拉州在全国西瓜产量中排名第二。真菌和卵菌病害是影响西瓜生产的主要生物因素,尤其是由镰刀菌属、疫霉属、腐霉属和丝核菌属的物种引起的病害。2013年春季,在墨西哥索诺拉州埃莫西约和瓜伊马斯山谷沿岸四个抽样田块中种植的约50%未嫁接西瓜植株上,确认出现了萎蔫或死亡症状。在受感染植株的根和茎上,发现了局部病斑,病斑长0.2至2.0厘米,红棕色,茎基部略有凹陷。在某些情况下,变色几乎覆盖了90%的根系。将茎和根上病斑边缘的1厘米片段用1%次氯酸钠进行表面消毒,然后用无菌蒸馏水冲洗,置于含有马铃薯葡萄糖琼脂(PDA)的培养皿中,在25°C下培养3天。真菌菌落最初为白色,然后变为棕色,分隔菌丝直径为3.7至4.3μm,以直角分支,分支点起始处有缢缩。这些特征是丝核菌属的典型特征。根据角担菌属的形态学描述,使用乳酸酚苯胺蓝溶液染色观察了五个分离株的双核细胞。使用在PDA上生长的五个分离株的菌丝体进行DNA提取。使用通用真菌引物ITS1和ITS4通过PCR扩增rDNA-ITS区域(3)。使用相同引物对分别对纯化产物进行双向测序。获得的序列与来自GenBank的角担菌属AG-F和AG-Fa分离株(分别在万寿菊上的登录号为KC193238.1、在香蕉属植物上的登录号为HQ168370.1、在大豆-水稻-杂草上的登录号为JX913821.1)的序列相似度为99%(2,4)。在生长室条件下测试了该真菌的致病性。用五个角担菌分离株接种了七株健康的糖红品种西瓜幼苗。在每株幼苗的根周围放置三个在PDA上生长的直径8毫米的菌丝圆盘。花盆在27±0.1°C下保持14天,光周期为12小时。七株未接种的幼苗用作对照。所有接种的幼苗在6至7天内出现了最初的水浸状病斑症状,而典型的病害症状在接种后10至14天出现。未接种接种物的幼苗未感染。从接种的幼苗上在PDA上重新分离出该真菌,并根据形态特征鉴定为角担菌属。最近在意大利和亚利桑那州也报道了类似病害(1);然而,本报告是首次描述在墨西哥索诺拉州引起西瓜根腐病的角担菌属。进行该研究的农业区域占该州西瓜种植总面积的90%,因此有必要评估这种病原体对作物的影响。参考文献:(1)C. Nischwitz等人,2013年APS联合会议。(2)A. Saroj等人,《植物病害》97:1251,2013年。(3)T. J. White等人,《PCR协议:方法与应用指南》。学术出版社,加利福尼亚州圣地亚哥,1990年。(4)J. Yin等人,《植物病害》95:490,2011年。

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