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1.
嘧霉胺对采后柑橘绿霉病的防治效果 总被引：1，自引：0，他引：1
在实验室和贮藏库条件下,对嘧霉胺单剂、嘧霉胺与抑霉唑或嘧霉胺和咪鲜胺混剂防治柑橘绿霉病的效果进行了评价。室内实验结果表明:采用500或1 000 mg/L嘧霉胺单剂、500 mg/L嘧霉胺+500 mg/L抑霉唑或500 mg/L嘧霉胺+500 mg/L咪鲜胺混剂在接种后12~18 h进行浸果处理,对由抑霉唑抗性或敏感菌株引起的绿霉病均有显著的防治效果,防效超过94%;500或1 000 mg/L 的抑霉唑对敏感菌株的防效在93%以上,但对抗性菌株的防效低于70%。贮藏库防效试验结果表明:在具抑霉唑抗性菌系的贮藏库中,上述质量浓度的嘧霉胺单剂、嘧霉胺与抑霉唑、或嘧霉胺与咪鲜胺混剂对绿霉病的防治效果明显优于抑霉唑单剂;而在不具抗抑霉唑菌系贮藏库中的防效则与抑霉唑相当。由此认为:嘧霉胺可作为抑霉唑的替代药剂应用于柑橘的采后处理,其推荐使用质量浓度为500~1 000 mg/L,可单独使用,也可与抑霉唑或咪鲜胺混合使用。 相似文献
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黑斑病是影响白术种植的主要病害之一,2015—2017年从浙江省磐安、天台、新昌和嵊州4地采集、分离得到137株白术黑斑病菌Alternaria alternata,采用菌丝生长速率法检测其对甲基硫菌灵和腐霉利的抗性。结果表明:供试的黑斑病菌群体 (n = 137) 对甲基硫菌灵的高水平抗性频率为77.4%,中等水平抗性频率为22.6%,未检测到敏感菌株;对腐霉利的抗性频率为20.4%,含21株低水平抗性菌株和7株中等水平抗性菌株。7种杀菌剂的室内毒力测定结果表明:咪鲜胺对白术黑斑病菌的活性最高,EC50值为0.15 mg/L。供试的137株白术黑斑病菌对咪鲜胺的EC50值分布在0.05~0.87 mg/L之间,平均EC50值为 (0.29 ± 0.11) mg/L,可作为敏感性基线。 相似文献
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为明确浙江省水稻恶苗病主要致病菌藤仓镰孢霉Fusarium fujikuroi对咪鲜胺的抗性现状,以1μg/mL为区分剂量,对2017和2018两年采自浙江省绍兴、嘉兴和金华3个地区稻田的共400株藤仓镰孢霉对咪鲜胺的抗性进行了检测,并测定了抗药性菌株的适合度及其对其他常用甾醇脱甲基抑制剂类(DMIs)杀菌剂的交互抗性。结果表明:两年的抗药性菌株频率分别为53.2%和46.7%;多数田间敏感菌株在产孢能力和孢子萌发能力上强于田间抗药性菌株,在菌丝生长速率和致病性方面则两者差异不大;就稻田藤仓镰孢霉而言,咪鲜胺与丙硫菌唑之间存在交互抗性,但咪鲜胺与戊唑醇、苯醚甲环唑、丙环唑、叶菌唑、己唑醇和三唑酮之间均不存在交互抗性。研究表明,浙江省稻田藤仓镰孢霉对咪鲜胺已经产生了严重的抗药性,需要轮换使用不同作用机制的杀菌剂进行防治。 相似文献
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为解析指状青霉Penicillium digitatum对抑霉唑和咪鲜胺的抗性机制和交互抗性机制,基于指状青霉甾醇14α-去甲基化酶（sterol 14α-demethylases,CYP51）CYP51A和CYP51B的氨基酸序列,采用同源建模的方法构建其三维结构,根据已报道的可能与抑霉唑抗性相关的突变位点CYP51A-Y308H及与咪鲜胺抗性相关的突变位点CYP51B-Y136H、CYP51B-Q309H和CYP51BF506I构建突变模型,采用分子对接法分析其突变前后与抑霉唑、咪鲜胺的结合模式,并进行氨基酸序列保守性分析。结果显示,抑霉唑和咪鲜胺与指状青霉CYP51的结合无特异性,两者均能与其CYP51A和CYP51B结合。指状青霉的CYP51A-Y308氨基酸残基及CYP51A-Y308H突变体氨基酸残基均不能与抑霉唑和咪鲜胺形成相互作用力,说明该突变与指状青霉对抑霉唑和咪鲜胺的抗性无关。指状青霉的CYP51B-Y136H突变导致其与咪鲜胺和抑霉唑的亲和力下降;指状青霉的CYP51B-Y136氨基酸位于CYP51B蛋白的保守区域,其产生的与咪鲜胺和抑霉唑抗性相关的随机突变在药剂... 相似文献
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Real-time PCR法定量检测柑橘绿霉病菌对抑霉唑的抗性频率 总被引：1，自引：0，他引：1
抑霉唑被广泛用来防治由指状青霉菌(Penicillium digitatum)引起的柑橘绿霉病。已有研究表明,柑橘绿霉病菌对抑霉唑的抗性由CYP51基因启动子区5个126-bp转录增强子的简单串联重复和126-bp转录增强子上199-bp的特异性片段插入所引起。基于这2种抗性分子机制,通过设计特异引物和优化条件,建立real-time PCR高通量分子检测技术,用于快速检测柑橘包装贮藏库中绿霉病菌群体对抑霉唑的抗性频率FR,指导科学用药。 相似文献
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9种杀菌剂对西瓜炭疽病菌的室内毒力测定及配比试验 总被引：3，自引：0，他引：3
为筛选防治西瓜炭疽病的高效低毒杀菌剂, 缓解和治理生产中病菌对药剂的抗性, 在室内离体条件下采用生长速率抑制法及孢子萌发抑制法测定了9种杀菌剂对西瓜炭疽病菌( Colletotrichum orbiculare )的毒力。结果表明, 嘧菌酯、咪鲜胺和甲基硫菌灵对病原菌菌丝生长的EC50在0.093 3~0.118 2 mg/L之间, 均小于1 mg/L, 表明西瓜炭疽病菌对上述杀菌剂比较敏感; 百菌清、烯肟菌酯和戊菌唑的EC50在2.310 1~5.925 9 mg/L, 病菌对药剂的敏感程度相对较低; 代森锰锌、恶霉灵和多菌灵的EC50分别为36.876 3、74.466 6和99.898 5 mg/L, 抑菌活性较差。孢子萌发试验中, 嘧菌酯、咪鲜胺和甲基硫菌灵对病菌孢子萌发的抑制活性最高, EC50在0.069 4~0.167 2 mg/L之间; 百菌清、烯肟菌酯、代森锰锌的抑制活性次之, EC50在1.853 0~9.503 9 mg/L之间; 多菌灵的抑制活性相对最低, EC50为99.335 3 mg/L。将两种不同作用机理的杀菌剂嘧菌酯与咪鲜胺按照2∶1的比例混配, 联合毒力测定和评价结果表明两者混配对抑制西瓜炭疽病菌具有增效作用。 相似文献
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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 (N)或丝氨酸Ser (S)。本研究表明樱桃采后灰霉病菌对甲基硫菌灵和腐霉利存在不同程度抗性,应在加强抗药性监测的同时与其他类型杀菌剂交替使用,延缓抗药性发展。 相似文献
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浙江衢州地区柑橘绿霉病菌对抑霉唑和多菌灵的抗性水平及其分子机制 总被引：2，自引：1，他引：1
研究了采自浙江衢州地区,包括柯城区、衢江区和开化县12个贮藏库的70个柑橘绿霉病菌Penicillium digitatum菌株对抑霉唑和多菌灵的抗性频率、抗性水平及其抗性分子机制。结果表明:柯城区和衢江区的抑霉唑抗性菌株(最低抑制浓度MIC≥0.5 μg/mL)的比例分别为77.1%和62.5%,两地抗性菌株的平均EC50值分别为2.07±1.04 μg/mL和2.35±0.73 μg/mL,分别是当地敏感菌株EC50值的41.4和47.0倍;而采自开化县的菌株均对抑霉唑敏感(MIC≤0.1 μg/mL),平均EC50值为0.04±0.02 μg/mL。柯城区和衢江区的多菌灵抗性菌株(MIC≥10 μg/mL) 的比例分别为54.3%和54.2%,而开化县的抗性菌株比例仅为9.1%。即来自柯城和衢江两个柑橘主产区的绿霉病菌群体对抑霉唑和多菌灵的抗性频率均远高于非柑橘主产区的开化县群体,说明抗药性群体的形成与药剂使用历史有关。进一步研究发现,衢州地区柑橘绿霉病菌对抑霉唑的抗性均属于IMZ-R3型,即与抑霉唑靶标基因 CYP51B 启动子区的插入突变有关,而对多菌灵的抗性则与 β-微管蛋白基因的992位核苷酸点突变(T→A)导致对应的200位点的氨基酸突变(F→Y)有关。 相似文献
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福建省玉米小斑病菌对丙环唑、烯唑醇和咪鲜胺的敏感性 总被引：4，自引：4，他引：0
为明确玉米小斑病菌对丙环唑、烯唑醇和咪鲜胺的敏感性,采用菌丝生长速率法测定了自福建省15个市、县分离的185株玉米小斑病菌对3种药剂的敏感性。结果显示:供试菌株对丙环唑、烯唑醇和咪鲜胺的EC50值分别在0.0186~7.779、0.0416~22.32和0.0053~7.930μg/mL之间。敏感性频率分布图显示,玉米小斑病菌群体中已出现对丙环唑、烯唑醇和咪鲜胺敏感性降低的亚群体。以连续单峰频次分布的大多数菌株群体的EC50平均值(0.5199±0.0284)、(0.4079±0.0204)和(0.3818±0.0202)μg/mL分别作为玉米小斑病菌对丙环唑、烯唑醇和咪鲜胺的相对敏感基线,发现各有15.14%、20.00%和17.30%的菌株对丙环唑、烯唑醇和咪鲜胺产生了抗性,抗性倍数最高分别为14.96、54.71和20.77。玉米小斑病菌对3种杀菌剂之间具有显著的交互抗性,而丙环唑和烯唑醇之间的交互抗性相关系数最高,为0.8662。本研究结果可为田间玉米小斑病防控杀菌剂的合理使用提供理论依据。 相似文献
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ABSTRACT Penicillium digitatum isolates (326), collected in California citrus groves and packinghouses, were assayed qualitatively for their sensitivity to imazalil, thiabendazole, and o-phenylphenol. Eighteen typical triple-resistant isolates, acquired in each of 3 years (1988, 1990, and 1994), were assayed quantitatively for their sensitivity to each of the three fungicides. No significant differences were found in the mean sensitivity of the isolates collected in different years. However, the proportion of isolates that were resistant to all three fungicides increased from 43% in 1988 to 77% in 1990 and 74% in 1994. Imazalil-resistant biotypes of P. digitatum were isolated frequently in California packinghouses, while resistant P. italicum was rare. No fungicide-resistant biotypes of either species were collected from citrus groves. Wild-type P. italicum was slightly less sensitive than wild-type P. digitatum to all three fungicides. The concentration of imazalil producing 50% growth inhibition (EC(50)) was three times greater when the age of the P. digitatum assay inoculum was increased from 12 to 24 h. Activity of imazalil increased with pH of the assay medium in the range pH 5.1 to 5.9, reflecting the greater concentration of dissociated imazalil at the higher pH value. 相似文献
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Metabolism of imazalil by wild-type and DMI-resistant isolates of Penicillium italicum 总被引：2，自引：0，他引：2
J. Guan L. Van Leemput M. A. Posthumus M. A. De Waard 《European journal of plant pathology / European Foundation for Plant Pathology》1992,98(3):161-168
Metabolism of imazalil (1-[2-(2,4-dichlorophenyl)-2-(2-propenyloxy)ethyl]-1H-imidazole) inPenicillium italicum isolates with a wild-type sensitivity and with various degrees of resistance to sterol demethylation inhibitors was studied in liquid cultures. The metabolite 1-[2(2,4-dichlorophenyl)-2-(2,3-dihydroxypropyloxy)ethyl]-1H-imidazole (R42243) was detected in the culture filtrate after prolonged incubation. The metabolism occurred in the propenyl side chain of imazalil probably through epoxidation and hydratation. This is the first report of such a conversion of imazalil in fungi. R42243 was much less toxic toP. italicum than imazalil. Therefore, the metabolism can be regarded as a detoxification step. Both wild-type and resistant isolates metabolized imazalil, but metabolism by resistant isolates was faster than by the wild-type isolate. This is probably caused by a relatively strong inhibition of growth of the wild-type isolate by the fungicide. Results indicate that the detoxification of imazalil does not operate as a mechanism of resistance. This conclusion was confirmed by the fact that resistant isolates showed cross-resistance to miconazole and R42243, which had a similar structure as imazalil except for the propenyl side chain. 相似文献
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Fusarium verticillioides reduces corn yield and contaminates infected kernels with the toxin fumonisin, which is harmful to humans and animals. Previous research has demonstrated that F. verticillioides can be controlled by the azole fungicide prochloraz. Currently, prochloraz is used as a foliar spray to control maize disease in China, which will increase the risk of resistance. Although F. verticillioides resistance to prochloraz has not been reported in the field, possible resistance risk and mechanisms resulting in prochloraz resistance were explored in the laboratory. Four prochloraz‐resistant strains of F. verticillioides were generated by successive selection on fungicide‐amended media. The mycelial growth rates of the mutants were inversely related to the level of resistance. All four mutants were cross‐resistant to the triazole fungicides triadimefon, tebuconazole and difenoconazole, but not to the multisite fungicide chlorothalonil or to the MAP/histidine‐kinase inhibitor fungicide fludioxonil. Based on the Y123H mutation in FvCYP51B, the four resistant mutants were subdivided into two genotypes: PCZ‐R1 mutants with wildtype FvCYP51B and PCZ‐R2 mutants with substitution Y123H in FvCYP51B. Wildtype FvCYP51B complemented the function of native ScCYP51 in Saccharomyces cerevisiae YUG37::erg11, whereas Y123H‐mutated FvCYP51B did not. For the PCZ‐R1 mutants, induced expression of FvCYP51A increased resistance to prochloraz. For the PCZ‐R2 mutants, disruption of FvCYP51B function by the Y123H substitution caused constitutive up‐regulation of FvCYP51A expression and thus resistance to prochloraz. 相似文献
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Séverine Fontaine Laëtitia Caddoux Florent Remuson Benoit Barrès 《Plant pathology》2022,71(4):785-792
In light of growing environmental concerns, surveys of fungicide resistance are needed to ensure efficient control of fungi and avoid unnecessary treatments. Investigations of fungicide resistance in Fusicoccum amygdali are scarce despite the economic impacts of this pathogen in peach and almond orchards. Thiophanate-methyl has been registered for more than 20 years to control F. amygdali but no resistance has been reported to date. This propesticide is metabolized by fungi into carbendazim, a β-tubulin inhibitor. Sensitivity to carbendazim of nine populations of F. amygdali from French orchards was assessed using germination bioassays. Also, resistance levels of 63 strains isolated from four populations were evaluated using mycelial growth assays. The underlying mechanism of resistance was investigated by sequencing the β-tubulin gene, the molecular target of thiophanate-methyl, in a set of isolates with different levels of sensitivity to carbendazim. Cross-resistance to thiophanate-methyl and to another β-tubulin inhibitor, diethofencarb, was also assessed in carbendazim-sensitive and -resistant strains. Isolates highly resistant to carbendazim were found in one of the nine orchards studied. Sequencing showed that resistant phenotypes carry a mutation in the β-tubulin gene leading to E198K substitution. Positive cross-resistance to thiophanate-methyl was confirmed and no negative cross-resistance to diethofencarb was identified in the phenotyped isolates, which were all resistant to this active substance. To our knowledge, this is the first report of resistance to thiophanate-methyl in F. amygdali. The high level of resistance of isolates sampled in one population is of concern, although the limited geographical scope of resistance suggests its recent emergence. 相似文献
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为明确江苏省小麦赤霉病菌群体对常用杀菌剂的抗药性情况,本研究于2017年-2021年连续5年分别从苏南、苏北及苏中小麦种植区采集病穗,分离培养获得赤霉病菌菌株共计4 055株,采用区分剂量法测定了供试菌株对4种杀菌剂(多菌灵、氰烯菌酯、戊唑醇和咪鲜胺)的抗性频率。结果表明:2017年-2021年江苏省田间小麦赤霉病菌对多菌灵的抗性频率分别为58.44%、56.30%、44.68%、48.28%、46.39%,呈逐年下降的趋势;不同地区小麦赤霉病菌对多菌灵的抗药性呈现地区差异性,苏北地区对多菌灵的抗性频率最高,其次是苏中地区,抗性频率最低的是苏南地区。2021年首次在田间采集到对氰烯菌酯、戊唑醇和咪鲜胺的抗性菌株,其抗性频率分别为0.45%、0.89%和0.09%,在以上的抗性菌株中同时具有多菌灵抗性的双重抗性菌株。表明江苏省小麦赤霉病菌对氰烯菌酯、戊唑醇和咪鲜胺产生了抗药性,虽抗性频率较低,仍需尽快制定田间抗性治理方案,延缓田间病菌对常用杀菌剂的抗性发展。 相似文献
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杀菌剂抗性分子检测技术的研究进展 总被引：1，自引：0，他引：1
靶标病菌基因突变是许多内吸性杀菌剂出现抗性的根本原因,检测与抗药性相关的靶标病菌基因突变对阐明抗药性发生的分子生物学机制及进行早期诊断具有重要意义。目前已成功用于检测靶标病菌抗药性菌株的分子检测技术有6种:等位基因特异性扩增、限制性片段长度多态性、等位基因特异性寡核苷酸杂交、单链构象多态性、实时定量PCR、变性高效液相色谱分析。这些技术能够快速、灵敏地检测田间早期出现的抗药性或抗药性种群的发展动态,在病害的可持续管理系统中科学使用杀菌剂方面发挥着重要作用。 相似文献
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H. Olvång 《European journal of plant pathology / European Foundation for Plant Pathology》1988,94(2):57-68
The sensitivity of 282 isolates ofSeptoria nodorum was tested on prochloraz, propiconazole and guazatine, and of 129 isolates ofDrechslera teres on prochloraz, propiconazole, imazalil and triadimefon. There was a great variation in sensitivity between isolates particularly at relatively low concentrations of the fungicides. However, none of the isolates was considered resistant towards the sterol biosynthesis inhibitors tested. Some isolates ofS. nodorum grew on concentrations of guazatine that may present difficulties in controlling them under practical conditions.Samenvatting Isolaten vanSeptoria nodorum (n=282) werden getoetst op gevoeligheid voor prochloraz, propiconazool en guazatine en vanDrechslera teres (n=129) voor prochloraz, propiconazool, imazalil en triadimefon. Er waren grote verschillen in de gevoeligheid van de isolaten, in het bijzonder bij lage concentraties van de fungiciden. Geen van de isolaten kan echter als resistent tegen sterolbiosynthese-remmers worden opgevat. Het feit, dat sommige van de isolaten vanS. nodorum zich ontwikkelden op media die hoge concentraties guazatine bevatten, kan echter duiden op moeilijkheden bij de bestrijding onder praktische omstandigheden. 相似文献