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引起马铃薯种薯块腐烂的镰刀菌属氟啶胺抗性分离株的首次报道。

First Report of Fludioxonil-Resistant Isolates of Fusarium spp. Causing Potato Seed-Piece Decay.

作者信息

Peters R D, Platt H W, Drake K A, Coffin R H, Moorehead S, Clark M M, Al-Mughrabi K I, Howard R J

机构信息

Agriculture and Agri-Food Canada, Charlottetown, PE Canada.

Cavendish Farms, Summerside, PE Canada.

出版信息

Plant Dis. 2008 Jan;92(1):172. doi: 10.1094/PDIS-92-1-0172A.

DOI:10.1094/PDIS-92-1-0172A
PMID:30786398
Abstract

Potato (Solanum tuberosum L.) diseases incited by Fusarium spp. include postharvest dry rot and seed-piece decay. Fusarium seed-piece decay is commonly controlled by preplant applications of chemical seed treatments. However, isolates of Fusarium spp. resistant to benzimidazole fungicides have been reported (2,4). In the spring of 2007, samples of cut seed tubers (cvs. Shepody and Russet Burbank) showing extensive symptoms of decay were received from three seedlots in Prince Edward Island (PE) and one seedlot in Saskatchewan (SK), Canada. All seed tubers had been treated with fludioxonil (Maxim Potato Seed Protectant [PSP], 0.5% fludioxonil) following cutting and then stored for 10 to 14 days prior to planting. Using standard isolation protocols (4), the 19 potato tuber pieces examined from PE and 2 from SK yielded 21 Fusarium isolates for further study. Five isolates (including both isolates from SK) were identified as Fusarium sambucinum Fuckel and the remaining 16 isolates were identified as F. coeruleum (Libert) Sacc. (3). To confirm identifications, isolates were compared with two known standards of each of F. sambucinum and F. coeruleum identified by K. Seifert (Agriculture and Agri-Food Canada, Ottawa, ON) by DNA sequencing of the partial β-tubulin gene or the translation elongation factor 1-α ( http://fusarium.cbio.psu.edu ; [1]). These standard isolates were also used as fludioxonil-sensitive controls in amended agar assays for chemical sensitivity. Agar plugs (5 mm in diameter) taken from the margins of 7-day-old cultures of the Fusarium isolates were transferred to petri dishes containing ½-strength potato dextrose agar amended with 0, 0.1, 1.0, 10.0, or 100.0 mg/liter of fludioxonil. Fludioxonil (Maxim PSP, 0.5% a.i.) was prepared as a stock solution in sterile distilled water and added to the molten agar after autoclaving. Culture incubation and mycelial growth measurements were performed as described previously (4). Measurements from four replicate petri dishes per concentration of fludioxonil were taken. Calculated EC values (fludioxonil concentration inhibiting pathogen growth by 50%) were obtained. The trial was repeated three times. The two standard isolates of F. sambucinum were sensitive to fludioxonil, with mean EC values of 0.002 (±0.002 standard error [SE]) and 0.005 (±0.002 SE) mg/liter. The two standard isolates of F. coeruleum were also sensitive to fludioxonil, with mean EC values of 0.17 (±0.005 SE) and 0.19 (± 0.005 SE) mg/liter. All other tested isolates of F. sambucinum and F. coeruleum were resistant to fludioxonil and showed no growth inhibition even at 100 mg of fludioxonil per liter. To our knowledge, this is the first report of resistance to fludioxonil in isolates of Fusarium spp. causing potato seed-piece decay. Since the isolates of F. sambucinum were also resistant to thiophanate-methyl and thiabendazole (data not shown), multiclass (benzimidazole and pyrrole) resistance was also documented. References: (1) D. M. Geiser et al. Eur. J. Plant Pathol. 110:473, 2004. (2) L. M. Kawchuk et al. Am. Potato J. 71:185, 1994. (3) P. E. Nelson et al. Fusarium Species: An Illustrated Manual for Identification. Pennsylvania State University Press, 1983. (4) R. D. Peters et al. Plant Dis. 85:1030, 2001.

摘要

由镰刀菌属(Fusarium spp.)引起的马铃薯(Solanum tuberosum L.)病害包括采后干腐病和种薯腐烂病。镰刀菌种薯腐烂病通常通过种植前施用化学种子处理剂来控制。然而,已有报道称镰刀菌属的一些分离株对苯并咪唑类杀菌剂具有抗性(2,4)。2007年春季,从加拿大爱德华王子岛(PE)的三个种薯批次和萨斯喀彻温省(SK)的一个种薯批次收到了表现出广泛腐烂症状的切块种薯(品种为Shepody和Russet Burbank)样本。所有种薯在切块后均用咯菌腈(适乐时马铃薯种子保护剂[PSP],0.5%咯菌腈)处理,然后在种植前储存10至14天。使用标准分离方法(4),从PE检查的19个马铃薯块茎切块和从SK检查的2个切块中获得了21个镰刀菌分离株用于进一步研究。5个分离株(包括来自SK的两个分离株)被鉴定为接骨木镰刀菌(Fusarium sambucinum Fuckel),其余16个分离株被鉴定为蓝色镰刀菌(F. coeruleum (Libert) Sacc.)(3)。为了确认鉴定结果,通过对部分β-微管蛋白基因或翻译延伸因子1-α进行DNA测序,将分离株与加拿大农业和农业食品部渥太华的K. Seifert鉴定的接骨木镰刀菌和蓝色镰刀菌的两个已知标准菌株进行比较(http://fusarium.cbio.psu.edu;[1])。这些标准菌株也用作改良琼脂试验中化学敏感性的咯菌腈敏感对照。从7日龄镰刀菌分离株培养物边缘取出的琼脂块(直径5毫米)转移到含有添加了0、0.1、1.0、10.0或100.0毫克/升咯菌腈的1/2强度马铃薯葡萄糖琼脂的培养皿中。咯菌腈(适乐时PSP,0.5%有效成分)在无菌蒸馏水中配制成储备溶液,并在高压灭菌后加入到熔化的琼脂中。培养物培养和菌丝生长测量如先前所述(4)进行。对每个咯菌腈浓度的四个重复培养皿进行测量。获得计算的EC值(抑制病原菌生长50%的咯菌腈浓度)。该试验重复三次。接骨木镰刀菌的两个标准菌株对咯菌腈敏感,平均EC值分别为0.002(±0.002标准误差[SE])和0.005(±0.002 SE)毫克/升。蓝色镰刀菌的两个标准菌株对咯菌腈也敏感,平均EC值分别为0.17(±0.005 SE)和0.19(±0.005 SE)毫克/升。所有其他测试的接骨木镰刀菌和蓝色镰刀菌分离株对咯菌腈具有抗性,即使每升含有100毫克咯菌腈也未表现出生长抑制。据我们所知,这是关于引起马铃薯种薯腐烂的镰刀菌属分离株对咯菌腈抗性的首次报道。由于接骨木镰刀菌的分离株对甲基硫菌灵和噻菌灵也具有抗性(数据未显示),因此也记录了多类(苯并咪唑和吡咯)抗性。参考文献:(1)D. M. Geiser等人,《欧洲植物病理学杂志》110:473,2004年。(2)L. M. Kawchuk等人,《美国马铃薯杂志》71:185,1994年。(3)P. E. Nelson等人,《镰刀菌物种:鉴定图解手册》。宾夕法尼亚州立大学出版社,1983年。(4)R. D. Peters等人,《植物病害》85:1030,2001年。

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