Burnett A, Lalancette N, McFarland K
Department of Plant Biology and Pathology, Agricultural Research and Extension Center, Rutgers University, Bridgeton, NJ 08302-5919.
Plant Dis. 2010 Jan;94(1):126. doi: 10.1094/PDIS-94-1-0126A.
Reduced sensitivity and resistance of Monilinia fructicola to demethylation inhibitors (DMIs; fungicide group 3) have been previously found in stone fruit orchards in Georgia, South Carolina, Ohio, and New York (2). Resistance development is a major concern because of the importance of DMIs for brown rot management. Eleven single-spore isolates, originally collected during 2006 from separate commercial peach (Prunus persica) orchards in southern New Jersey, were removed from cold storage (5°C) in early 2008 and examined in vitro for resistance to the DMI propiconazole (Orbit 3.6EC; Syngenta Crop Protection, Inc., Greensboro, NC). After 19 months at 5°C, isolate 7 was inhibited 53.4% in growth on potato dextrose agar (PDA) amended at the discretionary dose of 0.3 μg/ml propiconazole; inhibition of the remaining isolates ranged from 81.4 to 100%. Inhibition values were based on two replications of eight colonies per isolate performed after incubation at 25°C for 4 days. Because of the previously reported relationship between duration of cold storage and propiconazole sensitivity, isolate 7 was tentatively deemed resistant (1). To confirm the in vitro results, isolates were grown at 25°C for 7 days on cellophane over PDA. Genomic DNA was isolated from mycelium with the DNeasy Plant Mini Kit (Qiagen, Inc., Valencia, CA). PCR with primers INS65-F and INS65-R was conducted on a GeneAmp thermal cycler (Applied Biosystems, Inc., Foster City, CA) as described previously to amplify a 65-bp region named 'Mona' associated with DMI resistance (2). PCR products were separated via electrophoresis on 0.8% agarose gel. The primers amplified a 376-bp fragment from isolate 7 and a 311-bp fragment from all other isolates, thus indicating the presence of Mona in isolate 7. Restriction fragment length polymorphism analysis using the BsrBI enzyme, specific to a single restriction site within Mona, was conducted on the amplified fragments from all isolates. Electrophoresis results showed digestion of the 376-bp fragment from isolate 7 into 140-bp and 236-bp fragments, thereby confirming the presence of Mona; none of the 311-bp fragments from the remaining isolates were cut by BsrBI. Although economic loss from brown rot has not been reported in New Jersey, these results show that propiconazole-resistant strains have been detected since 2006 and it is most likely that resistant strains of the pathogen are still present in commercial peach orchards. To combat this risk, current brown rot control recommendations are incorporating quinone outside inhibitors (QoIs; fungicide group 11) and carboxamides (fungicide group 7) into control programs as a resistance management strategy. More extensive sampling is planned to ascertain the prevalence and location of resistant strains. References: (1) K. D. Cox et al. Phytopathology 97:448, 2007. (2) C.-X. Luo et al. Plant Dis. 92:1099, 2008.
先前在佐治亚州、南卡罗来纳州、俄亥俄州和纽约州的核果类果园中发现,褐腐病菌(Monilinia fructicola)对脱甲基抑制剂(DMI,杀菌剂第3组)的敏感性降低和产生了抗性(2)。由于DMI对褐腐病防治至关重要,抗性的发展是一个主要问题。2006年从新泽西州南部不同商业桃园分别采集的11个单孢分离株,于2008年初从冷藏(5°C)中取出,在体外检测对DMI丙环唑(拿敌稳3.6EC;先正达作物保护公司,北卡罗来纳州格林斯伯勒)的抗性。在5°C下保存19个月后,分离株7在添加了0.3 μg/ml丙环唑的马铃薯葡萄糖琼脂(PDA)上生长受抑制53.4%;其余分离株的抑制率在81.4%至100%之间。抑制值基于每个分离株8个菌落的两次重复,在25°C下培养4天后进行测定。由于先前报道了冷藏时间与丙环唑敏感性之间的关系,分离株7初步被判定为抗性(1)。为了证实体外结果,将分离株在25°C下于PDA上的玻璃纸上培养7天。用DNeasy植物微量提取试剂盒(Qiagen公司,加利福尼亚州瓦伦西亚)从菌丝体中提取基因组DNA。如先前所述,在GeneAmp热循环仪(应用生物系统公司,加利福尼亚州福斯特城)上用引物INS65-F和INS65-R进行PCR,以扩增一个名为“Mona”的与DMI抗性相关的65-bp区域(2)。PCR产物通过在0.8%琼脂糖凝胶上电泳进行分离。引物从分离株7扩增出一个376-bp片段,从所有其他分离株扩增出一个311-bp片段,从而表明分离株7中存在Mona。对所有分离株的扩增片段进行限制性片段长度多态性分析,使用对Mona内单个限制性位点特异的BsrBI酶。电泳结果显示,分离株7的376-bp片段被切割成140-bp和236-bp片段,从而证实了Mona的存在;其余分离株的311-bp片段均未被BsrBI切割。尽管新泽西州尚未报道褐腐病造成的经济损失,但这些结果表明自2006年以来已检测到丙环唑抗性菌株,并且病原菌的抗性菌株很可能仍存在于商业桃园中。为应对这种风险,当前的褐腐病防治建议将醌外抑制剂(QoI,杀菌剂第11组)和甲酰胺类(杀菌剂第7组)纳入防治方案作为抗性管理策略。计划进行更广泛的采样以确定抗性菌株的流行情况和位置。参考文献:(1)K. D. Cox等人,《植物病理学》97:448,2007年。(2)C.-X. Luo等人,《植物病害》92:1099,2008年。