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巴西首次报道由茄病镰刀菌复合种引起的番木瓜茎腐病

First Report of Stem Rot of Papaya Caused by Fusarium solani Species Complex in Brazil.

作者信息

Correia K C, Souza B O, Câmara M P S, Michereff S J

机构信息

Departamento de Agronomia, Universidade Federal Rural de Pernambuco, Recife, 52171-900, Pernambuco, Brazil.

出版信息

Plant Dis. 2013 Jan;97(1):140. doi: 10.1094/PDIS-06-12-0519-PDN.

Abstract

In October 2010, 2-year-old papaya (cv. Hawaii) trees with high incidence of stem rot were observed during a survey conducted in Rio Grande do Norte state, northeastern Brazil. Stems showing reddish brown-to-dark brown symptoms were collected and small pieces (4 to 5 mm) of necrotic tissues were surface sterilized for 1 min in 1.5% NaOCl, washed twice with sterile distilled water, and plated onto potato dextrose agar (PDA) amended with 0.5 g liter streptomycin sulfate. Plates were incubated at 25°C with a 12-h photopheriod for 4 days. Pure cultures with white, fluffy aerial mycelia were obtained by subculturing hyphal tips onto PDA. Identification was made using morphological characteristics and DNA based molecular techniques. Colonies grown on PDA and Spezieller Nährstoffarmer agar (SNA) for 10 days at 25°C with a 12-h photoperiod were used for morphological identification (3). The fungus produced cream sporodochia and two types of spores: microconidia were thin-walled, hyaline, ovoid, one-celled, and 6.8 to 14.6 × 2.3 to 4.2 μm; macroconidia were thick walled, hyaline, slightly curved, 3- to 5-celled, and 25.8 to 53.1 × 3.9 to 5.7 μm. Fifty spores of each type were measured. Rounded, thick-walled chlamydospores were produced, with two to four arranged together. On the basis of morphological characteristics (1), three fungal isolates (CMM-3825, CMM-3826, and CMM-3827) were identified as Fusarium solani (Mart.) Sacc. and were deposited in the Culture Collection of Phytopathogenic Fungi of the Universidade Federal Rural de Pernambuco (Recife, Brazil). Single-spore isolates were obtained and genomic DNA of the isolates was extracted and a portion of the translation elongation factor 1-alpha (EF1-α) gene of the isolates was amplified and sequenced (2). When compared with sequences available in the GenBank and Fusarium-ID databases, DNA sequences of the three isolates shared 99 to 100% sequence identity with F. solani species complex (GenBank Accession Nos. JF740784.1, DQ247523.1, and DQ247017.1). Representative sequences of the isolates were deposited in GenBank (Accession Nos. JQ808499, JQ808500, and JQ808501). Pathogenicity tests were conducted with four isolates on 3-month-old papaya (cv. Hawaii) seedlings. Mycelial plugs taken from the margin of actively growing colonies (PDA) of each isolate were applied in shallow wounds (0.4 cm in diameter) on the stem (center) of each plant. Inoculation wounds were wrapped with Parafilm. Control seedlings received sterile PDA plugs. Inoculated and control seedlings (10 each) were kept in a greenhouse at 25 to 30°C. After 2 weeks, all inoculated seedlings showed reddish brown necrotic lesions in the stems. No symptoms were observed in the control plants. The pathogen was successfully reisolated from symptomatic plants to fulfill Koch's postulates. To our knowledge, this is the first report of F. solani species complex causing papaya stem rot in Brazil. Papaya is an important fruit crop in the northeastern Brazil and the occurrence of this disease needs to be taken into account in papaya production. References: (1) C. Booth. Fusarium Laboratory Guide to the Identification of the Major Species. CMI, Kew, England, 1977. (2) D. M. Geiser et al. Eur. J. Plant Pathol. 110:473, 2004. (3) J. F. Leslie and B. A. Summerell. The Fusarium Laboratory Manual. Blackwell Publishing, Ames, IA, 2006.

摘要

2010年10月,在巴西东北部北里奥格兰德州进行的一项调查中,发现2岁的番木瓜(品种:夏威夷)树茎腐病发病率很高。采集表现出红棕色至深棕色症状的茎,将坏死组织的小块(4至5毫米)在1.5%次氯酸钠中进行表面消毒1分钟,用无菌蒸馏水冲洗两次,然后接种到添加了0.5克/升硫酸链霉素的马铃薯葡萄糖琼脂(PDA)上。平板在25°C、12小时光照周期下培养4天。通过将菌丝尖端转接至PDA上获得具有白色、蓬松气生菌丝体的纯培养物。使用形态学特征和基于DNA的分子技术进行鉴定。在25°C、12小时光照周期下,在PDA和特殊营养贫乏琼脂(SNA)上培养10天的菌落用于形态学鉴定(3)。该真菌产生奶油色分生孢子盘和两种类型的孢子:小分生孢子薄壁、透明、卵形、单细胞,大小为6.8至14.6×2.3至4.2微米;大分生孢子厚壁、透明、稍弯曲、3至5细胞,大小为25.8至53.1×3.9至5.7微米。每种类型测量50个孢子。产生圆形、厚壁的厚垣孢子,2至4个排列在一起。根据形态学特征(1),三个真菌分离株(CMM - 3825、CMM - 3826和CMM - 3827)被鉴定为茄腐镰刀菌(Mart.)Sacc.,并保存在伯南布哥联邦农村大学(巴西累西腓)植物病原真菌培养物保藏中心。获得单孢子分离株,提取分离株的基因组DNA,并扩增和测序分离株的翻译延伸因子1 - α(EF1 - α)基因的一部分(2)。与GenBank和镰刀菌鉴定数据库中可用的序列进行比较时,这三个分离株的DNA序列与茄腐镰刀菌种复合体共享99%至100%的序列同一性(GenBank登录号:JF740784.1、DQ247523.1和DQ247017.1)。分离株的代表性序列保存在GenBank(登录号:JQ808499、JQ808500和JQ808501)。用四个分离株对3个月大的番木瓜(品种:夏威夷)幼苗进行致病性测试。从每个分离株的活跃生长菌落(PDA)边缘取下的菌丝块接种到每株植物茎(中心)的浅伤口(直径0.4厘米)中。接种伤口用Parafilm包裹。对照幼苗接种无菌PDA块。接种和对照幼苗(各10株)保存在25至30°C的温室中。2周后,所有接种的幼苗在茎中出现红棕色坏死病变。对照植物未观察到症状。从有症状的植物中成功重新分离出病原体,以满足科赫法则。据我们所知,这是巴西首次报道茄腐镰刀菌种复合体引起番木瓜茎腐病。番木瓜是巴西东北部一种重要的水果作物,在番木瓜生产中需要考虑这种疾病的发生。参考文献:(1)C. Booth. Fusarium Laboratory Guide to the Identification of the Major Species. CMI, Kew, England, 1977.(2)D. M. Geiser等人。Eur. J. Plant Pathol. 110:473, 2004.(3)J. F. Leslie和B. A. Summerell. The Fusarium Laboratory Manual. Blackwell Publishing, Ames, IA, 2006.

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