四川猕猴桃灰霉病菌对4种杀菌剂的抗药性检测

为明确猕猴桃灰霉病菌对常见杀菌剂的抗药性状况, 本试验于2016年-2018年调查统计了四川猕猴桃生产中防控灰霉病所用的药剂种类和施药频次, 并从四川8个猕猴桃主产区采集病叶?病花和病果, 经单孢分离获得122个灰葡萄孢 Botrytis cinerea 菌株, 采用最低抑制浓度法(MIC)测定其对4种化学药剂嘧霉胺?咯菌腈?腐霉利和异菌脲的抗药性?结果表明:用于四川猕猴桃灰霉病防控的药剂主要有8种, 其中嘧霉胺?异菌脲和腐霉利3种药剂施用频次最高; 猕猴桃灰霉病菌对嘧霉胺?咯菌腈?腐霉利和异菌脲的抗性频率分别达95.08%?86.07%?80.33%和5.74%, 且不同产区的灰霉病菌对药剂的抗药性频率不同; 所测菌株对4种杀菌剂的敏感性类型共有8种, 其中以Pyr RFlu RPcm RIpr S(对嘧霉胺?咯菌腈?腐霉利表现抗性, 对异菌脲表现敏感)类型为主, 该类型的菌株占65.57%, 对4种杀菌剂均表现抗性的菌株为7株?表明四川省猕猴桃灰霉病菌对嘧霉胺?咯菌腈?腐霉利和异菌脲已经产生了抗药性, 对异菌脲抗药性较低, 迫切需要筛选新的杀菌剂防治猕猴桃灰霉病?     

蔬菜灰霉病菌对腐霉利抗药性变异及其治理

蔬菜灰霉病菌（Botrytis cinerea）分生孢子经紫外光灯照射，可获得10^-4～10^-5频率的腐霉利抗药性突变体。获得的13个抗性突变体的抗性水平平均EC50值为18.45ug/ml,EC90值为305.17ug/ml。抗性突变体的可溶性蛋白谱带比其亲本敏感菌株多2～4条，其中Rf=0.38的蛋白谱带是抗性菌株所拥有而敏感菌株所共同缺乏的。抗性菌株对腐霉利抗药性稳定遗传，具有与亲本菌株相同的致病性。苗期抗、感测定结果表明，灰霉克杀菌剂对腐霉利突变体具有明显的克抗作用。田间抗性菌治理使用灰霉克400～800倍对大棚番茄灰霉病平均防效为95.93%～75.8%,优于腐霉剂600倍的平均防效(61.32%)。     

番茄灰霉病菌对腐霉利的抗药性检测及生物学性状研究

采用区分剂量法,检测了来自福建省、上海市、辽宁省和内蒙古自治区不同采样点的番茄灰霉病菌Botrytis cinerea对腐霉利的抗性频率;选取未施药地区的敏感菌株,建立了灰霉病菌对腐霉利的敏感基线;比较了常年施药地区与未施药地区灰霉病菌的抗性频率差异,测定了施药10年以上地区番茄灰霉病菌的抗性指数;研究比较了抗、感菌株的生物学性状。结果表明:腐霉利对127株敏感菌株的平均EC50值为(0.31±0.08) μg/mL;供试4省市灰霉病菌对腐霉利均表现出了很高的抗性频率,其中内蒙古自治区和辽宁省采样点的抗性菌株频率高于90%;在施药历史超过10年的215株田间菌株中,抗性水平最高的菌株来自辽宁省,抗性指数为44.3;施药地区灰霉病菌的抗性频率均高于未施药地区;抗性菌株的抗药性可稳定遗传;供试11株抗性和敏感菌株在产孢量和孢子萌发率、菌丝生长速率、活体致病力等生物学性状方面的差异与其抗性水平之间无明显相关性。     

河南省番茄灰霉病菌对3种杀菌剂的抗药性检测

为了明确河南省番茄灰霉病菌对苯并咪唑类杀菌剂多菌灵、二甲酰亚胺类杀菌剂腐霉利和氨基甲酸酯类杀菌剂乙霉威的抗药性状况,2013年从河南省不同保护地中采集番茄灰霉病病果或病叶,经单孢分离共获得番茄灰霉病菌菌株139株。采用最低抑制浓度法（MIC）测定了其对多菌灵、腐霉利和乙霉威的抗药性。结果显示：番茄灰霉病菌对多菌灵、腐霉利和乙霉威产生抗性菌株的频率分别为81. 29%、80.58%和93.53%; 所测菌株对3类杀菌剂的抗性类型有BenRDicSNPCS、BenRDicRNPCS、BenRDicSNPCR、BenSDicRNPCR、BenSDicSNPCR和BenRDicRNPCR 6种,所占比例分别为2. 88%、3.60%、3.60%、5.04%、13.67%和71. 22%。表明河南省番茄灰霉病菌已对多菌灵、腐霉利和乙霉威产生抗药性,迫切需要筛选新的杀菌剂防治番茄灰霉病。     

北京地区番茄灰霉病菌的多重抗药性检测

2009年12月-2010年5月,在北京12个郊区县采集番茄病标样150份,分离纯化得到109个灰葡萄孢（Botrytis cinerea）单孢菌株,用最低抑制浓度法（MIC）测定了其对苯并咪唑类（多菌灵）、二甲酰亚胺类（腐霉利）和氨基甲酸酯类（乙霉威）杀菌剂的抗药性。结果表明：番茄灰霉病菌对多菌灵、腐霉利和乙霉威产生抗性菌株的频率分别为96.3%、80.7% 和58.7%;所测菌株对3类杀菌剂的抗性类型有BenRDicSNPCS、BenSDicSNPCR、BenRDicRNPCS和BenRDicRNPCR 4种,所占比例分别是19.3%、3.7%、21.1%和56.0%,表明北京地区番茄灰霉病菌对苯并咪唑类、二甲酰亚胺类和氨基甲酸酯类三类杀菌剂的抗药性严重,在生产中需慎用,应选择一些替代的新型杀菌剂和生物农药。     

樱桃采后灰霉病菌对甲基硫菌灵、乙霉威和腐霉利的抗性

本文采用单孢分离法对四川汉源和山东烟台等地采集的樱桃果实进行了采后灰霉病的病原菌分离和鉴定;采用区分剂量法分别测定了菌株对苯并咪唑类杀菌剂甲基硫菌灵、乙霉威和二甲酰亚胺类杀菌剂腐霉利的敏感性,并进一步分析了抗药性菌株的分子机制。结果表明,分离得到的54株樱桃采后灰霉病菌均为灰葡萄孢Botrytis cinerea,对甲基硫菌灵的总抗性频率高达79.6%,其中甲基硫菌灵抗性-乙霉威敏感(BEN R1)菌株频率为25.9%;甲基硫菌灵-乙霉威双重抗性菌株(BEN R2)频率为53.7%;检测到腐霉利抗性菌株(DCF R) 9株,频率为16.7%。甲基硫菌灵抗性菌株在β-tubulin基因上的突变共有2种类型：BEN R1抗性菌株中,第198位密码子发生点突变(GAG→GCG),编码氨基酸由Glu (E)突变成缬氨酸Ala (A);在BEN R2抗性菌株中,第198位密码子发生点突变(GAG→GTG),编码氨基酸由Glu (E)突变成缬氨酸Val (V)。DCF R菌株在BcOS1的第365位密码子由ATC突变成AAC或AGC,导致编码的氨基酸由异亮氨酸Ile (I)突变成天冬酰胺Asn (...     

紫外光诱导哈茨木霉产生腐霉利抗性菌株的研究

通过紫外光照射结合使用含药培养基培养得到了 3个哈茨木霉腐霉利抗性突变菌株。抗性菌株与亲本菌株相比较 ,其抗药性提高 1 0 0倍以上 ,与异菌脲、菌核净和甲基立枯磷存在交互抗性。抗性菌株在无药培养基上连续转移培养 8次 ,抗性程度未见下降。在适合度上 ,抗性菌株的菌丝生长速率有所下降 ,而在产孢能力、活体抑菌能力上有的抗性菌株要高于亲本菌株。 3个抗性菌株均保持了对灰霉病菌的拮抗能力     

莘县地区灰霉病菌对腐霉利的抗药性研究

本研究检测了聊城莘县地区的燕塔街道、张鲁镇、古城镇、燕店镇、董杜庄镇、王奉镇、大王寨乡、俎店乡八个乡镇的芸豆、樱桃西红柿、番茄、茄子和辣椒五种作物的56株灰霉病菌对腐霉利抗药性。以1μg/m L为标准[7],灰霉病菌对腐霉利的抗性频率高达98. 21%,其中8. 93%的菌株为高抗菌株,51. 78%的菌株为低抗菌株。不同乡镇、不同作物的灰霉病菌对腐霉利的抗药性也存在着明显的差异,燕塔街道和大王寨乡出现了高抗菌株,张鲁镇和俎店乡也出现了较大比例的中抗菌株,董杜庄镇和王奉镇的灰霉菌株仍处于较低的抗药性水平。     

湖南省草莓灰霉病菌对4种杀菌剂的抗药性检测

为明确湖南省草莓灰霉病菌菌株的抗药性状况,2013-2015年从湖南省不同地区草莓灰霉病病果或病叶上经单孢分离获得草莓灰霉病菌454株,采用最小抑制浓度法(MIC)检测不同地区草莓灰霉病菌株对多菌灵、腐霉利、异菌脲、嘧霉胺的抗药性。结果表明:草莓灰霉病菌对多菌灵、腐霉利、异菌脲、嘧霉胺的抗性频率分别为55.73%,77.31%、3.52%和77.31%;所测菌株对4种杀菌剂的敏感性类型有Cbz~RPcm~RIpd~RPmt~R、CbzSPcm~RIpd~RPmt~R、Cbz~RPcm~RIpdSPmt~R、Cbz~SPcm~RIpdSPmt~S、Cbz~RPcm~SIpd~SPmt~R、Cbz~SPcm~RIpd~SPmt ~R等6种,其所占比例分别为33.26%、5.07%、41.41%、4.63%、3.96%、11.67%,未发现对4种杀菌剂均敏感的类型,表明湖南省草莓灰霉病菌已对多菌灵、腐霉利和嘧霉胺产生抗药性,对异菌脲的抗药性较低。     

灰霉病菌对三种杀菌剂的抗性表现型分布及稳定性测定

采用最低抑制浓度法(MIC)和菌落直径法,对采自山西晋中、晋南、晋东南和晋北4个地区的188个灰霉病菌株对3种杀菌剂的抗性表现型和稳定性进行了测定,旨在了解灰霉病菌的抗药性状况和预测其抗性发展趋势。结果表明:对多菌灵的抗性表现型可分为敏感(S)、低抗或中抗(RM)和高抗(R),对腐霉利和乙霉威可分为敏感(S)和抗性(R)。以对多菌灵、腐霉利和乙霉威的抗性为序,检测出8种不同类型的抗性表现型,即RRR、RRS、RSR、RSS、RMRS、RMSR、RMSS 和SSR。各表现型的分布频率随各地区用药历史和水平的不同而变化,并与抗性监测结果相一致。对55个不同抗性表现型的单孢菌株的稳定性测定结果表明:继代无药培养10代后,以RRR和RSS型表现最稳定,而其余类型菌株均不同程度发生了变异,尤其是RMSS和RMRS型菌株100%发生了变异,抗性表现型不稳定的菌株占52.7%。对多菌灵的抗性变化趋势是由敏感向低抗、再向高抗发展;对腐霉利的抗性变化主要是由抗性转变为敏感;而对乙霉威的抗性则相对比较稳定。     

Genotyping of benzimidazole-resistant and dicarboximide-resistant mutations in Botrytis cinerea using real-time polymerase chain reaction assays

Botrytis cinerea, an economically important gray mold pathogen, frequently exhibits multiple fungicide resistance. A fluorescence resonance energy transfer-based real-time polymerase chain reaction assay has been developed to detect benzimidazole- and dicarboximide-resistant mutations. Three benzimidazole-resistant mutations-(198)Glu to Ala (E198A), F200Y, and E198K-in beta-tubulin BenA were detected using a single set of fluorescence-labeled sensor and anchor probes by melting curve analysis. Similarly, three dicarboximide-resistant mutations-I365S, V368F plus Q369H, and Q369P-in the histidine kinase BcOS1 were successfully distinguished. Unassigned melting profiles in BenA genotyping assay resulted in the identification of a new benzimidazole-resistant BenA E198V mutation. This mutation conferred resistance to carbendazim as do E198A and E198K mutations. The isolates with BenA E198V mutation showed a negative cross-resistance to diethofencarb, but to a lesser extent than the E198A mutants. A survey of 210 B. cinerea field isolates revealed that most of benzimidazole-resistant isolates possessed the E198V or E198A mutation in the BenA gene, and the I365S mutation in the BcOS1 gene was also frequently observed in Japanese isolates. However, benzimidazole-resistant isolates with BenA F200Y or E198K mutations, which confer the diethofencarb-insensitive phenotype, were rare. Our BenA and BcOS1 genotyping is a rapid and reliable method that is suitable for monitoring the fungicide-resistant field population.     

上海地区草莓灰霉病菌对啶酰菌胺的敏感性检测及抗性机制分析

为明确上海地区草莓灰霉病菌Botrytis cinerea Pers. 对主要防治药剂啶酰菌胺的敏感性水平及抗性机制,采用平皿法检测了采自上海市6个区县的195株草莓灰霉病菌株对啶酰菌胺的敏感性,并分析了其中20株不同敏感型菌株的琥珀酸脱氢酶基因序列。结果显示:啶酰菌胺对上海地区草莓灰霉病菌菌丝生长的EC₅₀最小值为0.15 μg/mL,最大值大于110 μg/mL;对孢子萌发的EC₅₀最小值为0.19 μg/mL,最大值大于50 μg/mL。上海地区草莓灰霉病菌对啶酰菌胺的抗性频率为29.74% (抗性水平大于10),高抗频率为20.51% (抗性水平大于100)。该抗性的产生与琥珀酸脱氢酶SdhB亚基发生H272R或P225F突变有关,其中H272R突变发生较为普遍。研究表明,上海地区草莓灰霉病菌对啶酰菌胺的抗性水平及抗性频率较高,主要抗性机制为病原菌琥珀酸脱氢酶SdhB亚基上的H272R突变。     

速克灵抗性灰霉病菌菌株性质的研究

研究结果表明,灰霉菌对二甲酰亚胺类与苯并咪唑类药剂之间不存在交互抗药性,与传统的保护性杀菌剂之间也不存在交互抗药性。杀菌剂福美双、克菌丹、百菌清对二甲酰亚胺类抗性菌抑菌效果较好。高抗二甲酰亚胺类药剂的某些菌株产孢能力大于敏感菌株。抗性菌单孢分离后代仍保留抗性。大棚草莓连续9次喷撒速克灵,每次间隔10—14天,未发现速克灵抗性菌株的产生。盆栽草莓试验表明,无药条件下,抗性菌株的致病力明显低于敏感菌;正常用药条件下,速克灵对抗性菌株的防治效果明显低于敏感菌株。     

Sequence variation in the two-component histidine kinase gene of Botrytis cinerea associated with resistance to dicarboximide fungicides

The complete two-component histidine kinase gene (Bos1) was sequenced from eight dicarboximide-resistant (D^R) and six-sensitive (D^S) field isolates of Botrytis cinerea. Comparisons in the predicted amino acid sequences of Bos1 showed that each two D^R isolates had a single point mutation at amino acid position 365 from an isoleucine to serine (I365S) or to an asparagine (I365N). Three D^R isolates were characterized with a change from glutamine to proline at position 369 (Q369P) as well as an asparagine to serine at the position 373 (N373S). These mutations located within the 90-amino-acid repeats of Bos1 have been reported previously. One new mutation, however, was found in the D^R isolate 65-E8. In this isolate, a null mutation at the amino acid position 1040 in the Bos1 was detected. Inoculation tests showed that this isolate was nearly nonpathogenic to cucumber. After the Bos1 gene from the sensitive isolate 38B1 was transferred into the resistant isolate 65-E8, all transformants tested were sensitive to iprodione and capable of infecting cucumber. DNA fingerprint generated by micro-satellite primed-PCR showed that isolates were not clustered based on their sensitivity to iprodione. Results from this study indicate that mutations in the Bos1 gene associated with dicarboximide resistance are diverse in B. cinerea, and the Bos1 gene is associated with virulence of B. cinerea.     

浙江省果蔬灰霉病菌对嘧菌酯的抗药性研究

采用菌丝生长速率法,连续监测了2010—2012年间浙江省果蔬灰霉病菌对QoI类杀菌剂嘧菌酯的敏感性变化。 结果表明:病菌群体中的低敏感性亚群体的比例明显上升,EC50值>5 mg/L 菌株的比例分别为12.5%、15.8%和28.3%;在菌丝生长阶段和孢子萌发阶段,旁路氧化在灰霉病菌对嘧菌酯敏感性中的平均相对贡献值(F)分别为2.91±0.89和5.72±2.82;嘧菌酯抗药性菌株的菌丝生长速率、产孢量、产菌核数和致病力与敏感菌株相比无显著差异。抗药性分子机制研究表明,灰霉病菌中存在2种类型的cyt b基因:Ⅰ型cyt b基因在第143位密码子后紧跟内含子;Ⅱ型cyt b基因在第143位密码子后没有紧跟内含子。大多数的灰霉病菌菌株属于Ⅱ型。Ⅰ型菌株均为嘧菌酯敏感菌株,Ⅱ型菌株为嘧菌酯敏感菌株或抗性菌株。抗性菌株的cyt b 基因的第143位密码子由甘氨酸(GGC)突变为了丙氨酸(GCC),抗药性机制为G143A。     

Molecular characterization of boscalid resistance in field isolates of Botrytis cinerea from apple

Botrytis cinerea isolates obtained from apple orchards were screened for resistance to boscalid. Boscalid-resistant (BosR) isolates were classified into four phenotypes based on the levels of the concentration that inhibited fungal growth by 50% relative to control. Of the 220 isolates tested, 42 were resistant to boscalid, with resistant phenotypes ranging from low to very high resistance. There was cross resistance between boscalid and carboxin. Analysis of partial sequences of the iron-sulfur subunit of succinate dehydrogenase gene in B. cinerea (BcSdhB) from 13 BosR and 9 boscalid-sensitive (BosS) isolates showed that point mutations in BcSdhB leading to amino acid substitutions at the codon position 272 from histidine to either tyrosine (H272Y) or arginine (H272R) were correlated with boscalid resistance. Allele-specific polymerase chain reaction (PCR) analysis of 66 BosR isolates (including 24 additional isolates obtained from decayed apple fruit) showed that 19 carried the point mutation H272Y and 46 had the point mutation H272R, but 1 BosR isolate gave no amplification product. Analysis of the BcSdhB sequence of this isolate revealed a different point mutation at codon 225, resulting in a substitution of proline (P) by phenylalanine (F) (P225F). The results indicated that H272R/Y in BcSdhB were the dominant genotypes of mutants in field BosR isolates from apple. A multiplex allele-specific PCR assay was developed to detect point mutations H272R/Y in a single PCR amplification. Levels of boscalid resistance ranged from low to very high within isolates carrying either the H272R or H272Y mutation, indicating that, among BosR isolates, different BosR phenotypes (levels of resistance) were not associated with particular types of point mutations (H272R versus H272Y) in BcSdhB. Analysis of genetic relationships between 39 BosR and 56 BosS isolates based on three microsatellite markers showed that 39 BosR isolates and 30 BosS isolates were clustered into two groups, and the third group consisted of only BosS isolates, suggesting that the development of resistance to boscalid in B. cinerea likely is not totally random, and resistant populations may come from specific genetic groups.