Gachango E, Kirk W, Hanson L, Rojas A, Tumbalam P, Shetty K
Department of Plant Pathology, Michigan State University, East Lansing.
Syngenta Crop Protection, Inc. Regional Headquarters, P.O. Box 18300, Greensboro, NC 27409.
Plant Dis. 2011 Feb;95(2):228. doi: 10.1094/PDIS-10-10-0737.
Fusarium dry rot of potato (Solanum tuberosum) is a postharvest disease caused by several Fusarium spp. Dry rot is managed primarily by reducing tuber bruising and promoting rapid wound healing. Dry rot symptomatic tubers were collected from Michigan seed lots in 2009 and 2010. The isolates may not have been exposed to fludioxonil because currently applications are restricted to seed not intended for seed production (3). Small sections were cut from the margins of necrotic regions with a scalpel, surface sterile in 10% sodium hypochlorite for 10 s, rinsed twice in sterile distilled water, and blotted with sterile filter paper. The tissue pieces were plated on half-strength potato dextrose agar (PDA) amended with 0.5 g/liter of streptomycin sulfate. The dishes were incubated at 23°C for 5 to 7 days. Cultures resembling Fusarium spp. were transferred onto water agar and hyphal tips from the margin of actively growing isolates were removed with a sterile probe and plated either on carnation leaf agar (CLA) or on half-strength PDA to generate pure cultures. Fusarium isolates were obtained and used for further studies. Among them, 54 were identified as Fusarium oxysporum and 23 as F. sambucinum. Identification was based on colony and conidial morphology on PDA and CLA, respectively. The identity was confirmed through DNA extraction followed by amplification and sequencing of the translation elongation factor (EF-1α) gene region. The Fusarium-ID v. (2) and the NCBI database were used to obtain the closest match to previously sequenced materials. Pathogenicity testing was done on disease-free potato tubers, cv. FL 1879. Tubers were surface sterilized for 10 min in 10% sodium hypochlorite and rinsed twice in distilled water. Three tubers per isolate were injected with 20 μl of a conidial suspension (10 conidia/ml) made from cultures grown on PDA for 7 days. Control tubers were injected with 20 μl of sterile distilled water. All tubers inoculated with F. sambucinum and F. oxysporum developed typical potato dry rot symptoms consisting of dry brown decay lesions. F. sambucinum and F. oxysporum were reisolated from all symptomatic tubers. An effective concentration for 50% reduction in growth (EC) was determined for each F. sambucinum and F. oxysporum isolate for thiabendazole (TBZ), fludioxonil, and difenoconazole using the spiral gradient endpoint method (1). Sensitive and resistant F. sambucinum and F. oxysporum isolates were reported. Fifteen isolates of F. sambucinum and thirty-four of F. oxysporum were resistant to fludioxonil with EC greater than 130 mg/liter. The remainder was sensitive to fludioxonil with EC ranging from 0.8 to 4.9 mg/liter. To our knowledge, this is the first report of resistance to fludioxonil in isolates of F. sambucinum and F. oxysporum in Michigan. Fusarium insensitivity in laboratory studies may not translate directly to commercial production. This disparity may result from interactions not experienced in mixed populations or within a living host. There has been no compelling evidence to suggest that fludioxonil has failed to perform because of insensitivity to Fusarium. The occurrence of such isolated strains necessitates the development and registration of partner chemistries that can preempt any future concerns on lack of performance of products in use. References: (1) H. Förster et al. Phytopathology 94:163, 2004. (2) D. Geiser et al. Eur. J. Plant Pathol. 110:473, 2004. (3) R. D. Peters et al. Plant Dis. 92:172, 2008.
马铃薯(Solanum tuberosum)镰刀菌干腐病是由几种镰刀菌引起的采后病害。干腐病主要通过减少块茎擦伤和促进伤口快速愈合来防治。2009年和2010年从密歇根州的种薯批次中采集了有干腐病症状的块茎。这些分离株可能未接触过咯菌腈,因为目前其应用仅限于非用于种子生产的种子(3)。用手术刀从坏死区域边缘切取小切片,在10%次氯酸钠中进行表面消毒10秒,在无菌蒸馏水中冲洗两次,并用无菌滤纸吸干。将组织块接种在添加了0.5克/升硫酸链霉素的半强度马铃薯葡萄糖琼脂(PDA)上。培养皿在23°C下培养5至7天。将类似镰刀菌属的培养物转移到水琼脂上,用无菌探针从活跃生长的分离株边缘取菌丝尖端,接种在香石竹叶琼脂(CLA)或半强度PDA上以获得纯培养物。获得了镰刀菌分离株并用于进一步研究。其中,54株被鉴定为尖孢镰刀菌,23株为接骨木镰刀菌。鉴定分别基于PDA和CLA上的菌落和分生孢子形态。通过DNA提取,随后对翻译延伸因子(EF - 1α)基因区域进行扩增和测序来确认其身份。使用Fusarium - ID v.(2)和NCBI数据库来获得与先前测序材料最接近的匹配。对无病马铃薯品种FL 1879的块茎进行致病性测试。块茎在10%次氯酸钠中表面消毒10分钟,在蒸馏水中冲洗两次。每个分离株用20微升由在PDA上培养7天的培养物制成的分生孢子悬浮液(10个分生孢子/毫升)注射到三个块茎中。对照块茎注射20微升无菌蒸馏水。所有接种接骨木镰刀菌和尖孢镰刀菌的块茎都出现了典型的马铃薯干腐病症状,包括干褐色腐烂病斑。从所有有症状的块茎中重新分离出接骨木镰刀菌和尖孢镰刀菌。使用螺旋梯度终点法(1)测定了每个接骨木镰刀菌和尖孢镰刀菌分离株对噻菌灵(TBZ)、咯菌腈和苯醚甲环唑的50%生长抑制有效浓度(EC)。报告了对接骨木镰刀菌和尖孢镰刀菌敏感和抗性的分离株。15株接骨木镰刀菌和34株尖孢镰刀菌分离株对咯菌腈耐药,EC大于每升130毫克。其余分离株对咯菌腈敏感,EC范围为0.8至4.9毫克/升。据我们所知,这是密歇根州接骨木镰刀菌和尖孢镰刀菌分离株对咯菌腈耐药的首次报道。实验室研究中镰刀菌的不敏感性可能无法直接转化为商业生产中的情况。这种差异可能是由于混合群体或活体宿主中未经历的相互作用导致的。没有确凿证据表明咯菌腈因对镰刀菌不敏感而失效。这些分离菌株的出现使得有必要开发和注册配套化学药剂,以避免未来对使用产品性能不佳的担忧。参考文献:(1)H. Förster等人,《植物病理学》94:163,2004年。(2)D. Geiser等人,《欧洲植物病理学杂志》110:473,2004年。(3)R. D. Peters等人,《植物病害》92:172,2008年。