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引起加利福尼亚州英国核桃嫁接结合部死亡的柠檬色葡萄座腔菌和半知新座壳孢的首次报道

First Report of Lasiodiplodia citricola and Neoscytalidium dimidiatum Causing Death of Graft Union of English Walnut in California.

作者信息

Chen S F, Fichtner E, Morgan D P, Michailides T J

机构信息

Department of Plant Pathology, University of California Davis, Kearney Agricultural and Extension Center (KARE), Parlier, 93648.

University of California Cooperative Extension, Tulare, 93274.

出版信息

Plant Dis. 2013 Jul;97(7):993. doi: 10.1094/PDIS-10-12-1000-PDN.

DOI:10.1094/PDIS-10-12-1000-PDN
PMID:30722540
Abstract

California produces 99% of the English walnuts (Juglans regia) in the USA. In August 2012 in Tulare County, about 5,000 out of 90,000 trees were killed in a walnut nursery by a distinct black canker that developed around the graft union. The cankers appeared to be initiated at the heading cut on the rootstock, and expanded down to the rootstock and through the budded union up to the scion, resulting in mortality of scion. The walnut nursery was located adjacent to a mature walnut orchard. The fungi isolated from the cankers were identified as Lasiodiplodia citricola and Neoscytalidium dimidiatum based on morphological characteristics and DNA sequence comparisons. L. citricola was isolated from one of the 10 graft unions, while N. dimidiatum from the other nine. L. citricola isolates were characterized by white, aerial mycelium on potato dextrose agar that turned gray after 4 days and produced ellipsoidal to ovoid hyaline one-celled conidia that became 2-celled and brown with thick walls and longitudinal striations in the wall (1). N. dimidiatum isolates were characterized by ellipsoid to ovoid, hyaline conidia with a truncate base and an acutely rounded apex, initially 1-celled, and some becoming brown and 2-celled at maturity; no muriform conidia were produced (3). These identifications were confirmed by analyses of the ITS, BT2, and TEF-1α gene regions. The three gene regions were amplified by using the primers and methods described in (4). For L. citricola (isolates 7E78 to 7E80), a DNA sequence BLASTn at GenBank showed 100% identity with accessions GU945354 (ITS) and GU945340 (TEF-1α) of the ex-type specimen (CBS124707, BT2 sequencing data was not available) (3). For N. dimidiatum (isolates 7E61 to 7E63), a BLASTn search showed a high identify (ITS, 100%; BT2, 99%; TEF-1α, 99%) with reference sequence of N. dimidiatum (ITS, GQ330903; BT2, GU251768; TEF-1α, GU251240). Sequences of the studied DNA regions were deposited to GenBank as KC357298 to KC357303 (ITS); KC357304 to KC357309 (BT2); and, KC357310 to KC357315 (TEF-1α). The pathogenicity of L. citricola in comparison with N. dimidiatum in J. regia cvs. Chandler, Tulare, and Vina was evaluated in an orchard at KARE, by using two isolates each of L. citricola (7E78, 7E80) and N. dimidiatum (7E61, 7E63). Pathogenicity tests were performed by inoculating ten 2-year-old branches per isolate in late September 2012 by the method described in (2). After 3 weeks, the average lesion lengths caused by L. citricola on Chandler, Tulare, and Vina were 152, 156, and 188 mm, respectively, and 32, 38, and 34 mm, respectively, caused by N. dimidiatum. The lesion length averages produced on the three cultivars by the four isolates were all significantly (P < 0.05) longer than their respective controls (average length 10 mm on all cultivars). L. citricola, but not N. dimidiatum, killed branches of Chandler, Tulare, and Vina in 10 days. Both L. citricola and N. dimidiatum were reisolated from the inoculated branches and no fungus was isolated from the control, confirming Koch's postulates. These results confirmed that the walnut graft union canker was caused by either L. citricola or N. dimidiatum. To our knowledge, this is the first report of death of newly grafted walnut trees caused by L. citricola and N. dimidiatum worldwide, and also the first report of L. citricola infecting walnut worldwide. References: (1) J. Abdollahzadeh et al. Persoonia. 25:1, 2010. (2) S. F. Chen et al. Plant Dis. 97:994, 2013. (3) D. Pavlic et al. Mycologia. 106:851, 2008. (4) B. Slippers et al. Mycologia. 96:83, 2004.

摘要

美国99%的英国核桃(胡桃)产自加利福尼亚。2012年8月,在图莱里县,一个核桃苗圃中9万棵树里约有5000棵被一种明显的黑色溃疡病害致死,这种病害在嫁接处周围出现。溃疡似乎始于砧木的截头切口,向下扩展至砧木,并通过芽接处向上蔓延至接穗,导致接穗死亡。该核桃苗圃毗邻一个成熟的核桃果园。根据形态特征和DNA序列比较,从溃疡处分离出的真菌被鉴定为柠檬色刺盘孢和半知盘多毛孢。从10个嫁接处中的1个分离出了柠檬色刺盘孢,从另外9个分离出了半知盘多毛孢。柠檬色刺盘孢分离株在马铃薯葡萄糖琼脂上的特征是具有白色气生菌丝体,4天后变为灰色,并产生椭圆形至卵形的透明单细胞分生孢子,这些分生孢子变为2细胞,褐色,壁增厚且有纵向条纹(1)。半知盘多毛孢分离株的特征是椭圆形至卵形、透明的分生孢子,基部截形,顶端锐圆,最初为1细胞,有些在成熟时变为褐色且2细胞;不产生砖格状分生孢子(3)。通过对ITS、BT2和TEF - 1α基因区域的分析证实了这些鉴定结果。使用(4)中所述的引物和方法扩增这三个基因区域。对于柠檬色刺盘孢(分离株7E78至7E80),在GenBank上进行的DNA序列BLASTn显示与模式标本(CBS124707,无法获得BT2测序数据)的登录号GU945354(ITS)和GU945340(TEF - 1α)具有100%的同一性(3)。对于半知盘多毛孢(分离株7E61至7E63),BLASTn搜索显示与半知盘多毛孢的参考序列(ITS,GQ330903;BT2,GU251768;TEF - 1α,GU251240)具有高度同一性(ITS,100%;BT2,99%;TEF - 1α,99%)。所研究DNA区域的序列已作为KC357298至KC357303(ITS);KC357304至KC357309(BT2);以及KC357310至KC357315(TEF - 1α)存入GenBank。在KARE的一个果园中,使用柠檬色刺盘孢(7E78、7E80)和半知盘多毛孢(7E6