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美澳型核果褐腐病菌对甲基硫菌灵和啶酰菌胺的敏感性 总被引：4，自引：1，他引：3
采用传统检测方法测定了我国北方地区美澳型核果褐腐病菌对常用杀菌剂甲基硫菌灵和新药剂啶酰菌胺的敏感性,并采用12条ISSR引物对不同抗性水平的菌株进行了分析.结果显示:74株菌株中检测出5株对甲基硫菌灵表现高抗、2株表现低抗的菌株;我国抗性菌株的突变位点与美国加州抗性菌株的突变位点相同;啶酰菌胺对来自我国和美国、新西兰、法国的45株美澳型核果褐腐病菌的EC50分布频率呈单峰曲线,EC50在0.059～0.320 μg/mL之间,平均值为0.174±0.064μg/mL;基于ISSR分析得到的UPGMA聚类组与菌株的来源地及对甲基硫菌灵的抗性无相关性. 相似文献
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贵州省烟草赤星病菌对啶酰菌胺的敏感性基线 总被引：1，自引：0，他引：1
对2014—2015年采自贵州省田间未使用过琥珀酸脱氢酶抑制剂 (SDHIs) 的烟草赤星病病样进行了病原菌分离和鉴定,并采用菌丝生长速率法建立了烟草赤星病菌群体对啶酰菌胺的敏感性基线。结果表明:虽然烟草赤星病菌不同菌株在菌落、孢子形态和致病性上有较大差异,但均属于交链格孢Alternaria alternata。啶酰菌胺抑制赤星病菌群体 (n = 102) 菌丝生长的EC50值在0.186~5.818 μg/mL之间,平均EC50值为 (2.157 ± 1.112) μg/mL,不同敏感性菌株频率分布为连续的单峰曲线,该平均EC50值可以作为烟草赤星病菌对啶酰菌胺的敏感性基线。进一步研究表明,贵州省烟草赤星病菌的Sdh B基因在第209位、277位和224位等密码子存在核苷酸多样性,但未发现这种多样性与烟草赤星病菌对啶酰菌胺的敏感性之间存在关联。 相似文献
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采用菌丝生长速率法测定了樱桃黑斑病菌交链格孢Alternaria alternata群体(n=103)对新型琥珀酸脱氢酶抑制剂(SDHI)氟唑菌酰羟胺的敏感性，评价了该药剂对A. alternata菌株孢子萌发的抑制活性及其对樱桃黑斑病的保护和治疗作用。结果表明：氟唑菌酰羟胺对103株A. alternata菌株群体的EC50值在0.027～1.175μg/m L之间，平均EC50值为(0.236±0.101)μg/m L，敏感性频率分布呈现单峰曲线，该平均EC50值可作为樱桃A. alternata菌株对氟唑菌酰羟胺的敏感性基线；进一步分析发现，琥珀酸脱氢酶中的铁硫蛋白(SDHB)和两个嵌膜蛋白(SDHC和SDHD)亚基未发现与敏感性差异有关的氨基酸突变。氟唑菌酰羟胺对樱桃A. alternata的孢子萌发也有较强的抑制活性，并且对樱桃黑斑病的保护作用防治效果强于治疗作用防治效果。这些结果可为氟唑菌酰羟胺在樱桃黑斑病及其他病害管理上的推广和科学用药提供依据。 相似文献
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为明确中国福建省番茄灰霉病菌对氟啶胺的敏感性及其与不同杀菌剂的交互抗性,采用菌丝生长速率法测定了106株采自福建省主要番茄产区的番茄灰霉病菌对氟啶胺的敏感性。结果表明,氟啶胺对福建省番茄灰霉病菌菌丝生长的EC50值在0.0037～0.0452 μg/mL之间,平均值为（0.0221 ±0.0098）μg/mL,其敏感性频率分布呈连续单峰曲线,符合正态分布,因此可将该EC50平均值（0.0221±0.0098）μg/mL作为福建省番茄灰霉病菌对氟啶胺的敏感基线,用于其田间抗药性监测。从106株菌株中选择15株对氟啶胺敏感性不同的菌株,测定了其对嘧霉胺、异菌脲、腐霉利和啶氧菌酯的敏感性。结果表明,供试5种杀菌剂对15株番茄灰霉病菌菌丝生长的平均抑制活性依次为氟啶胺 >异菌脲 >腐霉利 >啶氧菌酯 >嘧霉胺,氟啶胺与异菌脲、腐霉利、啶氧菌酯和嘧霉胺之间均不存在交互抗性。 相似文献
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为评价西瓜蔓枯病菌对啶酰菌胺的抗性风险,了解其抗性机理,室内通过药剂驯化方法获得2株啶酰菌胺的抗性突变体XF21-3和YC60-1,测定了抗性突变体的生物学特性,并通过对Sdh B基因片段的测序比对,分析了西瓜蔓枯病菌对啶酰菌胺的抗性机理。生物测定结果表明:啶酰菌胺对2株抗性突变体的EC50值分别为108和124 μg/mL,抗性倍数（RR）分别为1 007和1 347,均为高抗菌株;抗性突变体的菌丝生长速率和产孢量均大于亲本菌株,但其致病性与亲本菌株无显著差异,对外界环境渗透压的敏感性低于亲本菌株;此外,啶酰菌胺与萎锈灵、戊唑醇、乙霉威及醚菌酯之间均不存在交互抗性,但与噻呋酰胺之间存在交互抗性。Sdh B基因片段测序及比对结果表明,高抗性突变体中Sdh B亚基277位上的氨基酸所对应的碱基由CAC突变为TAC,即由组氨酸（His）突变为酪氨酸（Tyr）。研究表明,西瓜蔓枯病菌在药剂选择压力下容易形成啶酰菌胺的抗性群体,且抗性突变体的离体适合度高于亲本菌株,此外,啶酰菌胺与同类型杀菌剂噻呋酰胺之间存在交互抗性,因此认为西瓜蔓枯病菌对啶酰菌胺具有中等抗性风险;同时进一步验证了Sdh B亚基277位上的氨基酸突变（His→Tyr,CAC→TAC）是西瓜蔓枯病菌对啶酰菌胺产生抗性的原因。 相似文献
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不同机制杀菌剂对小麦白粉病的敏感性及与三唑酮的交互抗性 总被引：7，自引：2，他引：5
为明确三唑酮和氟环唑、吡唑醚菌酯、啶酰菌胺、嘧菌环胺、乙嘧酚5种不同作用机制的杀菌剂对小麦白粉病的敏感性及交互抗性,采用田间小区试验和室内喷雾离体叶段法测定了不同杀菌剂对小麦白粉病的防治效果。结果表明,5种不同作用机制杀菌剂对小麦白粉病的防治效果可达90%以上,而三唑酮最高的防治效果仅为72.17%;小麦白粉病菌群体对氟环唑、吡唑醚菌酯、啶酰菌胺、嘧菌环胺、乙嘧酚的敏感性EC50分别在0.087~1.901、0.058~1.402、0.186~3.014、0.222~6.005、0.006~1.742μg/mL之间,5种不同作用机制杀菌剂的敏感性均呈连续单峰曲线,可作为小麦白粉病菌对5种不同作用机制杀菌剂的敏感基线。研究表明,三唑酮与氟环唑、吡唑醚菌酯、啶酰菌胺、嘧菌环胺、乙嘧酚之间不存在交互抗性。 相似文献
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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 总被引：1，自引：0，他引：1
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。 相似文献
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由立枯病丝核菌引起的烟草立枯病是我国烟草苗床上危害最严重的病害之一。本研究评价了5种杀菌剂 (嘧菌酯、啶酰菌胺、氟啶胺、丙环唑和嘧霉胺) 对立枯丝核菌菌丝生长、菌核形成和萌发的影响,以及其对烟草立枯病的防治效果。结果表明:立枯丝核菌菌丝对氟啶胺和嘧菌酯的敏感性高于丙环唑和啶酰菌胺,而对嘧霉胺的敏感性较低;嘧菌酯对菌核形成的抑制作用强于丙环唑、氟啶胺、啶酰菌胺和嘧霉胺;5种杀菌剂对立枯丝核菌菌核萌发均无抑制作用。在离体烟叶的保护活性方面,12.5和50 mg/L的嘧菌酯和啶酰菌胺对立枯病的保护作用优于氟啶胺、丙环唑和嘧霉胺;在治疗活性方面,50和200 mg/L的嘧菌酯的治疗作用优于其他4种杀菌剂。因此,供试的5种杀菌剂中嘧菌酯最适合用于烟草立枯病的防治。 相似文献
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Anastasios A. Malandrakis Zoi A. Apostolidou Dimitra Louka Anastasios Markoglou Fotini Flouri 《European journal of plant pathology / European Foundation for Plant Pathology》2018,152(1):199-211
Field isolates of Alternaria alternata collected from tomato processors were characterized for sensitivity to respiration inhibitors using in vitro mycelial growth assays. Pyraclostrobin (QoI), boscalid, fluopyram and isopyrazam (SDHIs) mean EC50 values were 0.32, 1.43, 2.21, and 3.53 μg/ml respectively. Of the 42 isolates, 36 were sensitive to all respiration inhibiting fungicides tested whereas three isolates were less sensitive to boscalid, one to pyraclostrobin and two were simultaneously resistant to both inhibitors and isopyrazam. Correlation analysis between fungicide sensitivities revealed a positive cross-resistance between pyraclostrobin and tebuconazole, and between cyprodinil and mancozeb. There was no cross-resistance between QoIs, SHDIs or any other mode of action. Sequencing of the QoI and SDHI targets revealed the G143A cytochrome b resistance mutation in all pyraclostrobin-resistant isolates while analysis of the succinate dehydrogenase coding gene revealed point mutations in two of three of the gene subunits analyzed in boscalid-resistant isolates. Specifically, two isolates carried the H277Y and three the H133Q resistance mutations located in the sdhB and sdhD subunits of the respiration complex II, respectively. Isolates bearing the H277Y mutation also carried the G143A cytochrome b resistance mutation. Boscalid and pyraclostrobin-resistant isolates exhibited greater pathogenicity and sporulation compared to sensitive isolates, respectively. Isolates with cross-resistance exhibited greater pathogenicity and sporulation but slower mycelial growth compared to sensitive isolates. This is the first report of field isolates of A. alternata with single or double resistance to QoIs and SDHIs in Greece and should be considered in planning and implementing effective anti-resistance strategies. 相似文献
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BACKGROUND: Recently in Japan, isolates resistant to boscalid, a succinate dehydrogenase inhibitor (SDHI), have been detected in Corynespora cassiicola (Burk. & Curt.) Wei and Podosphaera xanthii (Castaggne) Braun & Shishkoff, the pathogens causing Corynespora leaf spot and powdery mildew disease on cucumber, respectively. Resistant isolates of C. cassiicola are widely distributed and represent a serious problem in disease control at present. Novel SDHI fungicides, including fluopyram, are now under development. RESULTS: The growth of very highly boscalid‐resistant, highly resistant and sensitive isolates of C. cassiicola was strongly suppressed on fluopyram‐amended YBA agar medium. Although boscalid and another SDHI, penthiopyrad, hardly controlled Corynespora leaf spot and powdery mildew on cucumber plants when very highly or highly boscalid‐resistant isolates were employed for inoculation, fluopyram still exhibited excellent control efficacy against these resistant isolates as well as sensitive isolates of C. cassiicola and P. xanthii. CONCLUSION: Differential sensitivity to boscalid, penthiopyrad and fluopyram, clearly found in these two important pathogens of cucumber, may indicate involvement of a slightly distinct site of action for fluopyram from the two other SDHIs. This finding may lead to the discovery of unique SDHIs in the future. Copyright © 2011 Society of Chemical Industry 相似文献
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BACKGROUND: Didymella bryoniae has a history of developing resistance to single‐site fungicides. A recent example is with the succinate‐dehydrogenase‐inhibiting fungicide (SDHI) boscalid. In laboratory assays, out of 103 isolates of this fungus, 82 and seven were found to be very highly resistant (BVHR) and highly resistant (BHR) to boscalid respectively. Cross‐resistance studies with the new SDHI penthiopyrad showed that the BVHR isolates were only highly resistant to penthiopyrad (BVHR‐PHR), while the BHR isolates appeared sensitive to penthiopyrad (BHR‐PS). In this study, the molecular mechanism of resistance in these two phenotypes (BVHR‐PHR and BHR‐PS) was elucidated, and their sensitivity to the new SDHI fluopyram was assessed. RESULTS: A 456 bp cDNA amplified fragment of the succinate dehydrogenase iron sulfur gene (DbSDHB) was initially cloned and sequenced from two sensitive (BS‐PS), two BVHR‐PHR and one BHR‐PS isolate of D. bryoniae. Comparative analysis of the DbSDHB protein revealed that a highly conserved histidine residue involved in the binding of SDHIs and present in wild‐type isolates was replaced by tyrosine (H277Y) or arginine (H277R) in the BVHR‐PHR and BHR‐PS variants respectively. Further examination of the role and extent of these alterations showed that the H/Y and H/R substitutions were present in the remaining BVHR‐PHR and BHR‐PS variants respectively. Analysis of the sensitivity to fluopyram of representative isolates showed that both SDHB mutants were sensitive to this fungicide as the wild‐type isolates. CONCLUSION: The genotype‐specific cross‐resistance relationships between the SDHIs boscalid and penthiopyrad and the lack of cross‐resistance between these fungicides and fluopyram should be taken into account when selecting SDHIs for gummy stem blight management. Copyright © 2011 Society of Chemical Industry 相似文献
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The molecular basis of resistance to the fungicide boscalid in 25 Alternaria alternata field mutants exhibiting resistance to boscalid and previously tested negative for AaSDHB mutations conferring boscalid resistance was investigated by cloning and sequencing the A. alternata SDHC ( AaSDHC ) and SDHD ( AaSDHD ) genes from a boscalid-sensitive isolate. The SDHB and SDHC/SDHD genes encode the iron sulphur and two membrane-anchored subunits of succinate:ubiquinone oxidoreductase (SQR) that constitute the boscalid fungicide molecular targets. The deduced amino acid sequences exhibited low similarities with SDHC and SDHD peptides from other organisms, but residues essential to form the ubiquinone binding site or important in SQR assembly were particularly conserved. Sequence comparisons of the AaSDHC and AaSDHD genes between resistant mutants and wild-type isolates revealed that two highly conserved histidine residues implicated in the heme b ligation and located at codon 134 in AaSDHC (22 mutants) and codon 133 in AaSDHD (two mutants) were replaced by arginine residues (H134R and H133R). In another mutant, a substitution of an aspartate by a glutamic acid occurred at amino acid position 123 (D123E) in AaSDHD. Additional tests revealed that mycelial growth of boscalid-resistant isolates was reduced when isolates were subjected to oxidative stress. The identified mutations were confirmed using PCR-RFLP assays. This is apparently the first report of mutations located in the heme b ligands of the cytochrome II gene associated with carboxamide resistance. 相似文献
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由多主棒孢Corynespora cassiicola引起的黄瓜棒孢叶斑病是黄瓜上的重要病害。本研究测定了对啶酰菌胺不同抗性类型多主棒孢的生物学特性差异和环境适合度,旨在为探明多主棒孢对啶酰菌胺的抗性变化机制提供生物学研究基础。随机选取不同地区24株对啶酰菌胺具有不同抗性类型的多主棒孢,分析了7种类型抗性突变体对几种不同琥珀酸脱氢酶抑制剂类 (SDHIs) 杀菌剂的交互抗性、不同抗性类型多主棒孢在无药剂选择压力下的抗性遗传稳定性,以及抗性突变体在不同碳源、氮源、温度等环境条件下的生物学特性及适合度。结果表明:除突变类型SdhB-H278Y及SdhB-H278R对啶酰菌胺与氟吡菌酰胺之间存在负交互抗性外,其他突变类型对啶酰菌胺与吡噻菌胺、氟吡菌酰胺及萎锈灵之间均表现为正交互抗性;所有突变类型菌株的抗药性均能稳定遗传;不同突变类型菌株之间致病性存在差异,其中SdhD-D95E突变体的致病力最强;利于所有突变类型菌株生长的碳源是麦芽糖,氮源种类则对突变体的生长影响不显著;各突变类型菌株的最适生长温度范围为25~30 ℃,其中突变体SdhD-D95E在高于30 ℃条件下菌丝生长速率大于其他突变体;耐热性研究中,抗性突变体经65 ℃高温处理45 min后无法存活,同时发现,60 ℃条件下突变体能正常生长,而敏感菌株不能生长;各质量浓度NaCl处理下,SdhD-D95E突变菌株菌丝生长速率快于其他突变菌株,而SdhB-H278Y突变菌株慢于其他突变菌株;葡萄糖对SdhB-H278R突变菌株的生长较为重要。研究表明,对啶酰菌胺不同抗性类型多主棒孢突变菌株的生物学特性及适合度存在差异,SdhD-D95E突变菌株适合度有所提高,表明该突变类型多主棒孢在田间具有较强的竞争力,容易形成优势种群。 相似文献
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从浙江省5地采集了112株西 (甜) 瓜蔓枯病菌Stagonosporppsis citrulli,采用区分剂量法检测其对苯并咪唑类杀菌剂甲基硫菌灵 (以下简称Ben) 和琥珀酸脱氢酶抑制剂类 (SDHIs) 杀菌剂啶酰菌胺 (简称Bos) 的抗性。结果显示:112株西 (甜) 瓜蔓枯病菌对Ben和Bos的抗药性频率分别为100%和28.6%,其中对甲基硫菌灵产生高水平抗性 (BenHR) 的菌株达100%,对啶酰菌胺产生低水平抗性 (BosLR) 和高水平抗性 (BosHR) 的菌株分别为18.8%和9.8%。抗药性分子机制研究表明:BenHR菌株中β-tubulin的第198位氨基酸由Glu (E) 突变成了Ala (A);BosHR菌株中Sdh B的第277位氨基酸由His (H) 突变成了Tyr (Y),但BosLR的抗性机制还需进一步研究。研究结果表明,浙江省西 (甜) 瓜蔓枯病菌对苯并咪唑类杀菌剂甲基硫菌灵的抗性已十分严重,尽管大多数菌株对啶酰菌胺仍表现敏感,但在一些地区已存在高水平抗性菌株,应在加强抗药性监测的同时,注意SDHIs类杀菌剂的科学使用。 相似文献
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Non‐target site SDHI resistance is present as standing genetic variation in field populations of Zymoseptoria tritici 
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A new generation of more active succinate dehydrogenase (Sdh) inhibitors (SDHIs) is currently widely used to control Septoria leaf blotch in northwest Europe. Detailed studies were conducted on Zymoseptoria tritici field isolates with reduced sensitivity to fluopyram and isofetamid; SDHIs which have only just or not been introduced for cereal disease control, respectively.RESULTS
Strong cross‐resistance between fluopyram and isofetamid, but not with other SDHIs, was confirmed through sensitivity tests using laboratory mutants and field isolates with and without Sdh mutations. The sensitivity profiles of most field isolates resistant to fluopyram and isofetamid were very similar to a lab mutant carrying SdhC‐A84V, but no alterations were found in SdhB, C and D. Inhibition of mitochondrial Sdh enzyme activity and control efficacy in planta for those isolates was severely impaired by fluopyram and isofetamid, but not by bixafen. Isolates with similar phenotypes were not only detected in northwest Europe but also in New Zealand before the widely use of SDHIs.CONCLUSION
This is the first report of SDHI‐specific non‐target site resistance in Z. tritici. Monitoring studies show that this resistance mechanism is present and can be selected from standing genetic variation in field populations. © 2017 The Authors. Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry. 相似文献18.
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. 相似文献
19.
Field isolates of Alternaria solani, which causes early blight of potato in Idaho, USA were evaluated in vitro for their sensitivity towards the succinate dehydrogenase inhibitor (SDHI) fungicides boscalid, fluopyram and penthiopyrad. A total of 20 isolates were collected from foliar‐infected tissue in 2009, 26 in 2010 and 49 in 2011. Fungicide sensitivity was tested using the spiral‐gradient end point dilution method. The frequency of boscalid‐resistant isolates (>50% relative growth when using a spiral dilution gradient starting at 507 mg L?1) drastically increased over the duration of this study (15% in 2009, 62% in 2010 and 80% in 2011). Increasing resistance to fluopyram and penthiopyrad was observed. However, cross‐resistance was only observed between boscalid and penthiopyrad. The target site of this fungicide class is the succinate dehydrogenase (SDH) enzyme complex, which is vital for fungal respiration. Sequence analysis of the SDH complex revealed mutations in the subunits B and D that were correlated with the emergence of boscalid resistance in potato fields in Idaho. In particular, H277R and H133R were identified in SDH subunits B and D, respectively. The presence of restriction sites in the gene sequences allowed the development of a rapid PCR‐RFLP method to assess boscalid sensitivity in A. solani populations. 相似文献
20.
Mutations in sdh genes in field isolates of Zymoseptoria tritici and impact on the sensitivity to various succinate dehydrogenase inhibitors 下载免费PDF全文
下载免费PDF全文 Zymoseptoria tritici is the causal agent of septoria tritici blotch (STB), a foliar wheat disease important worldwide. Succinate dehydrogenase inhibitors (SDHIs) have been used in cereals for effective control of STB for several years, but resistance towards SDHIs has been reported in several phytopathogenic fungi. Resistance mechanisms are target‐site mutations in the genes coding for subunits B, C and D of the succinate dehydrogenase (SDH) enzyme. Previous monitoring data in Europe indicated the presence of single isolates of Z. tritici with reduced SDHI sensitivity. These isolates carried mutations leading to amino acid exchanges: C‐T79N, C‐W80S in 2012; C‐N86S in 2013; B‐N225T and C‐T79N in 2014; and C‐V166M, B‐T268I, C‐N86S, C‐T79N and C‐H152R in 2015. The current study provides results from microtitre and greenhouse experiments to give an insight into the impact of different mutations in field isolates on various SDHIs. In microtitre tests, the highest EC50 values for all tested SDHIs were obtained with mutants carrying C‐H152R. Curative greenhouse tests with various SDHIs confirmed the findings of microtitre tests that isolates with C‐H152R are, in general, controlled with lower efficacy than isolates carrying B‐T268I, C‐T79N and C‐N86S. SDHI‐resistant isolates of Z. tritici found in the field were shown to have cross‐resistance towards all SDHIs tested. So far, SDHI‐resistant isolates of Z. tritici have been found in low frequencies in Europe. Therefore, FRAC recommendations for resistance management in cereals, including a limited number of applications, alternation and combination with other MOAs, should be followed to prolong SDHI field efficacy. 相似文献