Marques M W, Lima N B, Michereff S J, Câmara M P S, Souza C R B
Departamento de Agronomia, Universidade Federal Rural de Pernambuco, Recife, 52171-900, Pernambuco, Brazil.
Instituto de Ciências Biológicas, Universidade Federal do Pará, Belém, 66017-070, Pará, Brazil.
Plant Dis. 2012 Jan;96(1):144. doi: 10.1094/PDIS-05-11-0425.
From September to December 2010, mango (Mangifera indica L.) stems showing dieback symptoms were collected during a survey conducted in São Francisco Valley, northeastern Brazil. 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 in the dark for 14 to 21 days and colonies that were morphologically similar to species of Botryosphaeriaceae were transferred to PDA. Colonies developed a compact mycelium that was initially white, but becoming gray dark after 4 to 6 days of incubation at 25°C in darkness. Identification was made using morphological characteristics and DNA based molecular techniques. Pycnidia were obtained on 2% water agar with sterilized pine needles as substratum after 3 weeks of incubation at 25°C under near-UV light. Pycnidia were large, multilocular, eustromatic, covered with hyphae; locule totally embedded without ostioles, locule walls consisting of a dark brown textura angularis, becoming thinner and hyaline toward the conidiogenous region. Conidia were hyaline, thin to slightly thickened walled, aseptate, with granular contents, bacilliform, straight to slightly curved, apex and base both bluntly rounded or just blunt, 15.6 to 25.0 (20.8) μm long, and 2.7 to 7.9 (5.2) μm wide, length/width = 4.00. According to these morphological characteristics, three isolates (CMM1364, CMM1365, and CMM1450) were identified as Pseudofusicoccum stromaticum (1,3,4). PCR amplification by universal primers (ITS4/ITS5) and DNA sequencing of the internal transcribed spacer (ITS1-5.8S-ITS2 rRNA gene cluster) were conducted to confirm the identifications through BLAST searches in GenBank. The isolates were 100% homologous with P. stromaticum (3) (GenBank Accession Nos. AY693974 and DQ436935). Representative sequences of the isolates were deposited in GenBank (Accession Nos. JF896432, JF966392, and JF966393). Pathogenicity tests were conducted with the P. stromaticum strains on 5-month-old mango seedlings (cv. Tommy Atkins). 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 (five each) were kept in a greenhouse at 25 to 30°C. After 5 weeks, all inoculated seedlings showed leaf wilting, drying out of the branches, and necrotic lesions in the stems. No symptoms were observed in the control plants. P. stromaticum was successfully reisolated from symptomatic plants to fulfill Koch's postulates. P. stromaticum was described from Acacia, Eucalyptus, and Pinus trees in Venezuela (3,4), and there are no reports of this fungus in other hosts (2). To our knowledge, this is the first report of P. stromaticum causing mango dieback in Brazil and worldwide. References: (1) P. W. Crous et al. Stud. Mycol. 55:235, 2006. (2) D. F. Farr and A. Y. Rossman. Fungal Databases. Systematic Mycology and Microbiology Laboratory, ARS, USDA. Retrieved from http://nt.ars-grin.gov/fungaldatabases/ , 18 May 2011. (3) S. Mohali et al. Mycol. Res. 110:405, 2006. (4) S. R. Mohali et al. Fungal Divers. 25:103, 2007.
2010年9月至12月期间,在巴西东北部圣弗朗西斯科谷地进行的一项调查中,采集了表现出枝枯症状的芒果(Mangifera indica L.)茎段。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黑暗条件下培养14至21天,将形态上与葡萄座腔菌科物种相似的菌落转移到PDA上。菌落在25°C黑暗中培养4至6天后,形成紧密的菌丝体,最初为白色,之后变为暗灰色。使用形态学特征和基于DNA的分子技术进行鉴定。在25°C近紫外光下培养3周后,在以灭菌松针为基质的2%水琼脂上获得了分生孢子器。分生孢子器大,多腔,具真子座,被菌丝覆盖;腔室完全埋生,无孔口,腔室壁由暗褐色角状组织构成,向产孢区域变薄且透明。分生孢子透明,壁薄至稍厚,无隔膜,具颗粒状内含物,杆状,直或稍弯曲,顶端和基部均钝圆或仅为钝形, 长15.6至25.0(20.8)μm,宽2.7至7.9(5.2)μm,长宽比 = 4.00。根据这些形态学特征,三个分离株(CMM1364、CMM1365和CMM1450)被鉴定为基质拟隐孢壳菌(1,3,4)。通过通用引物(ITS4/ITS5)进行PCR扩增,并对内部转录间隔区(ITS1-5.8S-ITS2 rRNA基因簇)进行DNA测序,通过在GenBank中进行BLAST搜索来确认鉴定结果。这些分离株与基质拟隐孢壳菌(3)(GenBank登录号AY693974和DQ436935)具有100%的同源性。分离株的代表性序列保存在GenBank(登录号JF896432、JF966392和JF966393)中。用基质拟隐孢壳菌菌株对5月龄芒果幼苗(品种Tommy Atkins)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干(中部)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5株)置于25至30°C的温室中。5周后, 所有接种的幼苗均出现叶片萎蔫、枝条干枯和茎干坏死病斑。对照植株未观察到症状。从有症状的植株中成功重新分离出基质拟隐孢壳菌,从而证实了柯赫氏法则。基质拟隐孢壳菌在委内瑞拉的金合欢、桉树和松树中被描述过(3,4),在其他寄主中没有该真菌的报道(2)。据我们所知,这是基质拟隐孢壳菌在巴西和全球范围内引起芒果枝枯病的首次报道。参考文献:(1)P. W. Crous等人,《Stud. Mycol.》55:235,2006年。(2)D. F. Farr和A. Y. Rossman,《真菌数据库》。系统真菌学和微生物学实验室,美国农业部农业研究局。从http://nt.ars-grin.gov/fungaldatabases/获取,2011年5月18日。(3)S. Mohali等人,《Mycol. Res.》110:405,2006年。(4)S. R. Mohali等人,《Fungal Divers.》25:103,2007年。