Chen F, Liu X, Chen S, Schnabel E, Schnabel G
College of Agriculture and Biotechnology, China Agricultural University, Beijing 100193, China.
College of Plant Science and Technology, Huazhong Agricultural University, Wuhan 430070, China.
Plant Dis. 2013 May;97(5):645-651. doi: 10.1094/PDIS-10-12-0924-RE.
In 2011 and 2012, significant brown rot disease caused by Monilinia fructicola was observed in a peach orchard in Spartanburg County, SC, despite preharvest fungicide applications of demethylation inhibitor (DMI), quinone outside inhibitor (QoI), and succinate dehydrogenase inhibitor (SDHI) fungicides. All 22 isolates obtained in 2011 from this orchard were sensitive to the QoI fungicide, azoxystrobin, and the methyl benzimidazole carbamate (MBC) fungicide, thiophanate-methyl. Five were resistant to the DMI fungicide, propiconazole, and were selected, together with five propiconazole-sensitive isolates, for further investigations. One of the 10 isolates was resistant to propiconazole but sensitive to the SDHI fungicide, boscalid (EC = 0.42 μg/ml), 3 were resistant to propiconazole with intermediate sensitivity to boscalid (EC 0.72 to 2.1 μg/ml); 2 were sensitive to propiconazole with intermediate sensitivity to boscalid; 3 were sensitive to propiconazole but resistant to boscalid (EC ≥ 2.1 μg/ml); and 1 (isolate MD22) was resistant to both propiconazole and boscalid. Disease incidence on detached fruit treated with formulated propiconazole or boscalid was significantly higher for MD22 compared to a sensitive control isolate. Continued monitoring of fungicide resistance in the same orchard in 2012 revealed an increase of isolates resistant to propiconazole from 22.7% in 2011 to 34.7%, and an increase of isolates resistant to both propiconazole and boscalid from 4.5% in 2011 to 18.4%. Propiconazole resistance was always associated with the presence of the 'Mona' mobile element located upstream of the sterol 14α-demethylase (MfCYP51) gene. To investigate whether mutations in the subunits of the succinate dehydrogenase enzyme were involved in boscalid resistance, significant portions of the M. fructicola SdhA, SdhB, SdhC, and SdhD genes were cloned and analyzed for 2 sensitive, 2 boscalid-resistant, and 6 dual-resistant isolates. Although sequence variation was found among the isolates, no single change correlated with resistance. Interestingly, analysis of isolates collected from orchards in 2001 and 2002, prior to the registration of boscalid, revealed a range of sensitivities to boscalid (EC 0.03 to 3.46 μg/ml) including boscalid-resistant isolates. The presence of boscalid-resistant isolates in the baseline population was unexpected and requires further investigation.
2011年和2012年,在南卡罗来纳州斯巴达堡县的一个桃园中,尽管在收获前使用了去甲基化抑制剂(DMI)、醌外抑制剂(QoI)和琥珀酸脱氢酶抑制剂(SDHI)类杀菌剂,仍观察到了由褐腐病菌(Monilinia fructicola)引起的严重褐腐病。2011年从该果园获得的所有22个分离株对QoI类杀菌剂嘧菌酯和甲基苯并咪唑氨基甲酸酯(MBC)类杀菌剂甲基硫菌灵敏感。有5个分离株对DMI类杀菌剂丙环唑耐药,从中选取这5个耐药分离株以及5个对丙环唑敏感的分离株进行进一步研究。10个分离株中的1个对丙环唑耐药,但对SDHI类杀菌剂啶酰菌胺敏感(EC = 0.42 μg/ml);3个对丙环唑耐药,对啶酰菌胺具有中等敏感性(EC 0.72至2.1 μg/ml);2个对丙环唑敏感,对啶酰菌胺具有中等敏感性;3个对丙环唑敏感,但对啶酰菌胺耐药(EC≥2.1 μg/ml);还有1个(分离株MD22)对丙环唑和啶酰菌胺均耐药。与敏感对照分离株相比,用制剂丙环唑或啶酰菌胺处理的离体果实上,MD22的发病率显著更高。2012年对同一果园杀菌剂耐药性的持续监测显示,对丙环唑耐药的分离株从2011年的22.7%增加到了34.7%,对丙环唑和啶酰菌胺均耐药的分离株从2011年的4.5%增加到了18.4%。丙环唑耐药性始终与位于甾醇14α-去甲基化酶(MfCYP51)基因上游的“Mona”移动元件的存在相关。为了研究琥珀酸脱氢酶亚基的突变是否与啶酰菌胺耐药性有关,对2个敏感、2个对啶酰菌胺耐药和6个双重耐药的褐腐病菌分离株的SdhA、SdhB、SdhC和SdhD基因的重要部分进行了克隆和分析。尽管在分离株之间发现了序列变异,但没有单一变化与耐药性相关。有趣的是,对2001年和2002年在啶酰菌胺登记之前从果园收集的分离株进行分析,发现它们对啶酰菌胺的敏感性范围较广(EC 0.03至3.46 μg/ml),包括对啶酰菌胺耐药的分离株。基线群体中存在对啶酰菌胺耐药的分离株出乎意料,需要进一步研究。