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在美国,栎生葡萄座腔菌导致活栎(弗吉尼亚栎)枝条枯死和枝干溃疡的首次报道

First Report of Diplodia quercivora Causing Shoot Dieback and Branch Cankers on Live Oak (Quercus virginiana) in the United States.

作者信息

Dreaden T J, Black A W, Mullerin S, Smith J A

机构信息

School of Forest Resources and Conservation, University of Florida, Gainesville 32611.

出版信息

Plant Dis. 2014 Feb;98(2):282. doi: 10.1094/PDIS-07-13-0736-PDN.

Abstract

In September 2010, live oak (Quercus virginiana Mill.) trees in an Alachua County, FL, shopping center parking lot were observed with shoot dieback and cankers on small branches. Isolations were made from canker margins by surface sterilizing tissue in 2.5% sodium hypochlorite and plating on potato dextrose agar (PDA) and incubating at 23°C. Fungi morphologically similar to Diplodia quercivora Linaldeddu & A.J.L. Phillips (mycelium initially velvety and white and later turning pale to dark olivaceous and grayish in reverse) were consistently isolated from symptomatic tissue (2). The two loci used by Linaldeddu et al. (2) in the description of D. quercivora were sequenced to identify a representative isolate (PL1345) as D. quercivora. The internal transcribed spacer (ITS) (GenBank Accession No. KF386635) and translation factor 1-alpha (EF-1α) (KF386636) regions were amplified and sequenced using primers ITS1F/ITS4 (3) and EF1-728F/EF1-986R (1). BLASTn searches of the two sequences resulted in 99% (467 of 469 and 257 of 259, respectively) homology with D. quercivora CBS 133852, confirming the fungal isolates' identity as D. quercivora. In October 2011, Koch's postulates were verified by inoculating, repeated twice, three Q. virginiana saplings (stem diameters, 12 to 14 mm; at inoculation sites approximately 50 mm above soil line) with isolate PL1345. Agar plugs (3 × 3 mm) taken from the margin of a 12-day-old culture on PDA were inserted into flaps in the stems made by a sterile blade with the mycelia facing the cambial tissue. One negative control tree was mock inoculated with a sterile PDA plug. All inoculation sites were sealed with Parafilm and maintained in a greenhouse (19 to 29°C). Trees were assessed for symptoms 90 days after inoculation. External bleeding was noted on all but one tree, and all flaps became necrotic. Pycnidia were observed on the outer surface of the flap on one inoculated tree. Negative controls showed no bleeding and their tissue flaps remained alive. Vertical length of phloem necrosis and percent of stem girdling were measured after removing the bark. Mean necrotic length and percent girdling for inoculated saplings were 48 mm (standard error [SE] = 10.6) and 26.6% (SE = 5.7) for the first inoculation and 46 mm (SE = 17) and 25% (SE = 5) for the second, respectively. Controls showed no internal necrosis and all produced healthy callus tissue at inoculation sites. Two of the pathogen-inoculated trees per inoculation were sampled and the pathogen was re-isolated from each. Recovered fungal isolates were confirmed as D. quercivora based on morphology and 100% ITS sequence homology to PL1345. D. quercivora was first described as causing shoot dieback and cankers on Q. canariensis in Tunisia and was found to be pathogenic to three additional Mediterranean oak species, Q. ilex, Q. pubescens, and Q. suber (2). To our knowledge, this is the first report of D. quercivora causing cankers on Q. virginiana and the first report of the fungus outside of Tunisia. Given the damage this pathogen has caused there, efforts to monitor the spread of this disease would seem warranted. More research is needed to assess the risk this pathogen poses to North American oaks, however. References: (1) I. Carbone et al. Mycologia 91:553, 1999. (2) B. T. Linaldeddu et al. Mycologia 105:1266, 2013. (3) T. J. White et al. PCR Protocols: A Guide to Methods and Applications. Academic Press, San Diego, 1990.

摘要

2010年9月,在佛罗里达州阿拉楚阿县一个购物中心停车场的活栎树(弗吉尼亚栎,Quercus virginiana Mill.)上,观察到小枝出现梢枯和溃疡症状。通过将组织在2.5%次氯酸钠中进行表面消毒,然后接种到马铃薯葡萄糖琼脂(PDA)上,并在23°C下培养,从溃疡边缘进行分离。从有症状的组织中持续分离出形态上与栎双极毛盘孢菌(Diplodia quercivora Linaldeddu & A.J.L. Phillips,菌丝体最初为天鹅绒状白色,后来反面变为浅至深橄榄色和灰色)相似的真菌(2)。对Linaldeddu等人(2)在描述栎双极毛盘孢菌时使用的两个基因座进行测序,以鉴定一个代表性分离株(PL1345)为栎双极毛盘孢菌。使用引物ITS1F/ITS4(3)和EF1-728F/EF1-986R(1)扩增并测序内部转录间隔区(ITS)(GenBank登录号KF386635)和翻译因子1-α(EF-1α)(KF386636)区域。对这两个序列进行BLASTn搜索,结果显示与栎双极毛盘孢菌CBS 133852具有99%的同源性(分别为469个碱基中的467个和259个碱基中的257个),从而确认真菌分离株为栎双极毛盘孢菌。2011年10月,通过用分离株PL1345对接种三次的三株弗吉尼亚栎树苗(茎直径12至14毫米;接种部位在土壤线以上约50毫米处)进行接种,重复两次,验证了柯赫氏法则。从PDA上12日龄培养物的边缘取下琼脂块(3×3毫米),用无菌刀片在茎上切出切口,将琼脂块插入切口中,使菌丝体面向形成层组织,并对一株阴性对照树用无菌PDA块进行模拟接种。所有接种部位用Parafilm密封,并置于温室(19至29°C)中。接种90天后对树木进行症状评估。除一株树外,所有树木均出现外部流胶现象且所有切口均坏死。在一株接种树上,在切口的外表面观察到分生孢子器。阴性对照无流胶现象,其组织切口保持存活。去除树皮后,测量韧皮部坏死的垂直长度和茎环割的百分比。第一次接种的接种树苗的平均坏死长度和环割百分比分别为48毫米(标准误差[SE]=10.6)和26.6%(SE=5.7),第二次接种分别为46毫米(SE=17)和25%(SE=5)。对照无内部坏死现象,且在接种部位均产生健康的愈伤组织。每次接种的两株接种病原体的树进行采样,并从每株树中重新分离出病原体。根据形态学以及与PL1345的ITS序列100%同源性,确认回收的真菌分离株为栎双极毛盘孢菌。栎双极毛盘孢菌最初被描述为在突尼斯导致加那利栎的梢枯和溃疡,并且被发现对另外三种地中海栎树,即冬青栎、柔毛栎和栓皮栎具有致病性(2)。据我们所知,这是栎双极毛盘孢菌在弗吉尼亚栎上导致溃疡的首次报道,也是该真菌在突尼斯以外地区的首次报道。鉴于这种病原体在那里造成的损害,似乎有必要努力监测这种疾病的传播。然而,需要更多研究来评估这种病原体对北美栎树构成的风险。参考文献:(1)I. Carbone等人,《真菌学》91:553,1999年。(2)B.T. Linaldeddu等人,《真菌学》1:1266,2013年。(3)T.J. White等人,《PCR实验方案:方法与应用指南》。学术出版社,圣地亚哥,1990年。

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