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1.
河南省番茄灰霉病菌对3种杀菌剂的抗药性检测   总被引：2，自引：0，他引：2  
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。  相似文献   

2.
设施蔬菜灰霉病菌对不同类型杀菌剂的抗性检测   总被引：14，自引：8，他引：14  
为了明确设施蔬菜灰霉病菌Botryotinia fuckeliana的抗药性现状,采用菌丝生长速率法检测了20052006年采自浙江、江苏、山东和辽宁4省的144个菌株对6种常用防治药剂的敏感性。结果表明,灰霉病菌对百菌清已经产生了低水平的抗性,频率为5.56%,其对多菌灵的抗性非常严重,总的抗性频率为43.05%,高抗(HR)频率为27.08%;乙霉威的EC50值在0.137728.9μg/mL之间,平均为40.06μg/mL。其中多菌灵-乙霉威双抗频率为36.11%,且首次检测到了两种新的双抗类型。二甲酰亚胺类杀菌剂在生产上已经应用近20年,但灰霉病菌对异菌脲和腐霉利只有频率为20%左右的低水平抗性,没有检测到高抗菌株;苯胺嘧啶类杀菌剂嘧霉胺虽然只应用几年时间,但已经产生了抗性,其抗性菌株频率为4.16%。研究表明,设施蔬菜灰霉病菌对常用的6种防治药剂均产生了不同程度的抗性。  相似文献   

3.
番茄叶霉病菌异菌脲抗药性突变体的诱导与生物学性状   总被引：2，自引：1，他引：1  
测定了苯并咪唑类杀菌剂敏感-乙霉威抗性(BenS-DieR)、苯并咪唑类杀菌剂抗性-乙霉威敏感(BenR-DieS)和苯并咪唑类杀菌剂抗性-乙霉威抗性(BenR-DieR)3种类型的番茄叶霉病菌Cladosporium fulvum菌株对不同类型药剂的敏感性。结果表明,蕃茄叶霉病菌对供试药剂的敏感性与其对苯并咪唑类杀菌剂及乙霉威的敏感性无关。根据药剂对3类菌株EC50值的平均值, 16种杀菌剂抑制菌丝生长的活性依次为腐霉利＞乙烯菌核利＞异菌脲＞戊唑醇＞百菌清＞嘧霉胺＞醚菌酯＞代森锰锌＞8-羟基喹啉铜＞丙环唑＞苯醚甲环唑＞嘧菌酯＞灭锈胺＞烯酰吗啉＞烟酰胺＞三唑酮;抑制孢子萌发的活性依次为醚菌酯＞腐霉利＞百菌清＞乙烯菌核利＞灭锈胺＞8-羟基喹啉铜＞异菌脲＞代森锰锌＞嘧菌酯＞烟酰胺＞嘧霉胺＞戊唑醇＞丙环唑＞苯醚甲环唑＞三唑酮＞烯酰吗啉。通过紫外诱变共获得17株抗异菌脲突变体,突变频率为4.5×10-7。其中低抗、中抗和高抗菌株分别占 17.65%、70.59%和11.75%。这些突变体对腐霉利和乙烯菌核利表现交互抗性,对苯并咪唑类、脱甲基抑制剂(DMIs)、QoIs等药剂的敏感性与亲本菌株之间没有显著性差异,与亲本菌株在生长、产孢、致病能力等方面也无显著差异,但对渗透胁迫的敏感性要显著高于亲本。  相似文献   

4.
番茄叶霉病菌对多菌灵、乙霉威及代森锰锌抗性检测   总被引：11，自引：4，他引：11       下载免费PDF全文
报道了番茄叶霉病菌Fulvia fulva对多菌灵、乙霉威及代森锰锌的敏感性基线,以及抗性频率和抗性水平。离体条件下,多菌灵、乙霉威及代森锰锌对番茄叶霉病菌敏感菌株的平均EC50值分别为0.101、2.475、9.067 μg/mL;最低抑制浓度(MIC)值分别为0.5、5、50 μg/mL 。山西晋南地区番茄叶霉病菌对3种杀菌剂的抗性频率最高,分别达到97.4%、70.5%、98.7%;山西吕梁地区与太原地区相对较低,但该病菌对3种杀菌剂的抗性频率也都超过了30%。辽宁沈阳、山东寿光、河北保定番茄叶霉病菌对多菌灵的抗性频率均为100%;对乙霉威的抗性频率前两地为100%,保定为10%;对代森锰锌的抗性频率都超过90%。所有抗性菌株对多菌灵均属于高抗类型,抗性指数超过5000,测不出MIC值;对乙霉威有50%的高抗菌株,抗性指数在100以上;对代森锰锌各地均未发现高抗菌株,低抗和中抗菌株所占比例较大,其抗性指数集中在50左右。对多菌灵与乙霉威具有双重抗性的菌株占测试菌株总数的49.9%,并且首次在田间发现了对3种杀菌剂都具有抗性的番茄叶霉病菌多抗菌株。  相似文献   

5.
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   

6.
番茄灰霉病菌对腐霉利的抗药性检测及生物学性状研究   总被引：6，自引：2，他引：4  
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。  相似文献   

7.
湖南省草莓灰霉病菌对4种杀菌剂的抗药性检测   总被引：2，自引：0，他引：2  
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。  相似文献   

8.
褐腐病菌Monilinia fructicola是引起多种果树褐腐病的重要病原菌,前期研究发现该病原菌对甲基硫菌灵的抗性与Tub2蛋白的多个氨基酸变异有关。为明确不同类型菌株的温度适应性及乙霉威是否对所有抗性类型菌株均具有抑菌活性,本研究测定了敏感型菌株S及3种抗性类型包括R(E198A)、R(E198Q)及R(F200Y)型菌株的温度敏感性及其对甲基硫菌灵、多菌灵和乙霉威的敏感性差异,同时分析了不同突变类型菌株对苯并咪唑类药剂和乙霉威的交互抗性。结果表明,4种类型菌株的最适生长温度为21~22 ℃,其中R(E198Q)型菌株的最适生长温度最低,且其在低温13 ℃和高温28 ℃条件下,生长速率显著低于其他3类菌株,而S、R(E198A)及R(F200Y)型菌株在所有温度条件下的生长速率均无显著差异。3种抗性类型菌株对甲基硫菌灵的敏感性有所差异,其中R(E198Q)型表现较为敏感,R(F200Y)型在低浓度下与R(E198A)型无明显差异,但在高浓度下对甲基硫菌灵表现较为敏感;对多菌灵的敏感性差异与甲基硫菌灵相似;只是R(E198Q) 和R(F200Y)型菌株对多菌灵比甲基硫菌灵更为敏感。乙霉威的敏感性测定结果表明,R(E198A)型菌株表现敏感,S类型表现为不敏感性,R(E198Q)及 R(F200Y)两种类型均表现为抗性,且抗性水平差别不大。线性相关分析结果表明,仅R(E198A)型菌株和S型菌株对苯并咪唑类杀菌剂和乙霉威敏感性存在显著负相关性 (甲基硫菌灵和乙霉威:r = ?0.992,p = 0.000;多菌灵和乙霉威:r = ?0.982,p = 0.001)。综合分析结果表明,在3类抗性菌株中,仅R(E198A)型菌株对苯并咪唑类杀菌剂和乙霉威存在负交互抗性。  相似文献   

9.
选择对多菌灵、乙霉威和苯酰菌胺具有不同敏感性的胶孢炭疽菌 Colletotrichum gloeosporioides、辣椒疫霉菌 Phytophthora capsici 及恶疫霉菌 P.cactorum,采用菌丝生长速率抑制法及氨基酸序列比对法分析了其 β-微管蛋白氨基酸突变与敏感性的关系。结果表明,胶孢炭疽菌对苯酰菌胺、多菌灵和乙霉威的敏感性与 β-微管蛋白198位或200位氨基酸突变有关:对多菌灵敏感、对苯酰菌胺和乙霉威不敏感的胶孢炭疽菌 β-微管蛋白氨基酸198位为谷氨酸(E),200位为苯丙氨酸(F);对多菌灵已产生抗性而对苯酰菌胺和乙霉威不敏感的菌株,其 β-微管蛋白氨基酸200位由苯丙氨酸(F)突变为了酪氨酸(Y);对多菌灵高抗、对苯酰菌胺和乙霉威敏感的菌株其 β-微管蛋白氨基酸198位由谷氨酸(E)突变为了丙氨酸(A)。辣椒疫霉菌和恶疫霉菌对苯酰菌胺敏感,对多菌灵和乙霉威均不敏感。检测疫霉菌菌株 β-微管蛋白未发现氨基酸突变,但发现其 β-微管蛋白氨基酸在196~200位与胶孢炭疽菌差异较大,这可能是导致苯酰菌胺仅对疫霉菌有抑制效果的原因。  相似文献   

10.
大麦云纹斑病菌对杀菌剂的抗性检测及同工酶谱类型   总被引：2，自引：0，他引：2  
1993～1994年大麦云纹斑病菌(Rhynchosporium secalis)对杀菌剂多菌灵、三唑醇的抗药性监测表明,该菌对两种杀菌剂的敏感程度发生了变化,并且首次在田间发现了大麦云纹斑病菌的多抗菌株。这类菌株对多菌灵、乙霉威及三唑醇都具有抗药性,且抗性程度很高。与1990～1991年得到的资料相比,随着杀菌剂选择压力的增加,大田群体中三唑醇高抗菌株比例逐年增加。对该菌同工酶分析结果表明,α—酯酶有7种表现型,磷酸葡萄糖变位酶有2种表现型,过氧化氢酶有3种表现型,无论对去甲基抑制剂类(DMI)表现抗性或敏感菌株,无论调节酶还是非调节酶,其酶谱表现型的变异基本相似。这表明大麦云纹斑病菌对DMI类抗药性突变存在于多个菌系的基因型背景群体中,而不是只起源于单一的广泛分布的菌系。  相似文献   

11.
From 2003 to 2006, a total of 426 single-conidial isolates of B. cinerea collected from greenhouse vegetables in China were characterized for resistance to benzimidazole fungicides and diethofencarb according to inhibition of mycelial growth. Rapid development of double-resistance to benzimidazoles and diethofencarb was observed. Three types of benzimidazole-resistant isolates, Ben R1, Ben R2 and Ben R3 were detected. A new phenotype, Ben R3, which showed low level of resistance to benzimidazole fungicides and resistance to diethofencarb, was detected with frequencies of 6.8%, 10.0%, 13.2% and 12.4% from 2003 to 2006, respectively. Further studies indicated that Ben R3 was caused by a point mutation from GAG in sensitive(S) isolates to GTG at codon 198 in the β-tubulin gene, predicted to cause a change from glutamic acid to valine. Ben R3 isolates had comparable growth, sporulation and pathogenicity ability as isolates of other phenotypes but were more sensitive at lower temperatures.  相似文献   

12.
 Laboratory mutants of Cochliobolus heterostrophus resistant to iprodione were obtained after chemical mutageneses. All the mutants were able to grow on the medium amended with iprodione 100 μg/ml. They showed positive cross-resistance to procymidone and fludioxonil and were sensitive to high osmolarity. Crosses between the mutant and a wild-type strain revealed that the fungicide resistance and osmotic sensitivity traits were inherited by their offspring in a 1 : 1 mutant/wild type ratio, indicating that the mutant phenotypes in these strains were due to alteration at a single gene locus. Results from allelism tests indicated that three genes (Dic1, Dic2, Dic3) conferred the mutant phenotypes. Among them, Dic1 mutant strains were classified into three types on the basis of their phenotypes. The first type was moderately resistant to the fungicides and less sensitive to osmotic stress than the other Dic1 mutant strains. The second type showed moderate fungicide resistance, but growth was inhibited under lower osmotic stress (50 mM KCl). The other Dic1 mutant strains grew well on medium containing iprodione and fludioxonil even at a concentration of 100 μg/ml and were highly sensitive to osmotic stress. The Dic2 and Dic3 mutant strains had moderate resistance to the fungicides with low-level osmotic sensitivity. The Dic1 gene was epistatic to Dic2 and Dic3 for fungicide resistance and hypostatic to them for osmotic sensitivity. These results suggest that the osmoregulatory system is involved in fungicide resistance in laboratory mutants of C. heterostrophus. Received: March 14, 2002 / Accepted: August 13, 2002  相似文献   

13.
北京地区番茄灰霉病菌的多重抗药性检测   总被引：5，自引：0，他引：5  
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。  相似文献   

14.
From 2005 to 2009, a total of 479 single-conidial isolates of Phomopsis obscurans were collected from strawberry. The isolates were characterized for their resistance to benzimidazole fungicides, diethofencarb, and sterol demethylation inhibitors (DMIs). Low-level DMI resistant isolates (DMI-LR) and two types of benzimidazole-resistant (Ben R) isolates, Ben R1 (benzimidazole-resistant and diethofencarb -sensitive) and Ben R2 (benzimidazole-resistant and diethofencarb -resistant), were detected. Both Ben R and DMI-LR isolates exhibited comparable growth, sporulation, and pathogenicity with the sensitive isolates. No significant difference in growth at low temperature was observed between Ben R and benzimidazole-sensitive (Ben S) isolates. Ben R1 was caused by a point mutation from GAG to GTG at codon 198 in the β-tubulin gene in Ben S isolates, predicted to cause a change from glutamic acid to valine. Ben R2 was induced by a point mutation from TTC to TAC at codon 200 in the β-tubulin gene in Ben S isolates.  相似文献   

15.
Anthracnose, caused by Colletotrichum gloeosporioides, is one of the most important diseases in grape-growing regions worldwide. In Jiangsu Province of China, quinone-outside inhibitor fungicides (QoIs) have been extensively sprayed as disease control for more than 10 years. A spore germination assay of 64 isolates obtained from 32 commercial vineyards was used to assess isolate sensitivity to azoxystrobin and 62 were found to be resistant to azoxystrobin. The biological fitness of QoI-resistant (QoIR) isolates was significantly lower than the sensitive isolates (QoIS) in terms of mycelial growth and conidiation. Nucleotide sequence alignment of CgCytb genes from the QoIR and QoIS isolates revealed that two point mutations (F129L and G143A) are involved in the QoI resistance. Isolates with the G143A mutation expressed high resistance to azoxystrobin, whereas isolates carrying the F129L mutation exhibited moderate resistance. Positive cross-resistance was observed between azoxystrobin and kersoxim-methyl, pyraclostrobin, or benzothiostrobin, but not with fluazinam. This study provides important information for management of QoIR populations of C. gloeosporioides in the field.  相似文献   

16.
Field strains of Botrytis cinerea Pers ex Fr, the causal agent of grey mould diseases, were collected from French vineyards between 1993 and 2000. Several phenotypes have been characterized according to the inhibitory effects of fungicides towards germ-tube elongation and mycelial growth. Two types of benzimidazole-resistant strains (Ben R1 and Ben R2) could be detected; negative cross-resistance to phenylcarbamates (e.g. diethofencarb) was only found in Ben R1. Benzimidazole resistance was related to point mutations at codon 198 (Ben R1) or 200 (Ben R2) of the beta-tubulin gene. Most dicarboximide-resistant strains were also weakly resistant to aromatic hydrocarbon fungicides (e.g. dicloran) but remained sensitive to phenylpyrroles (e.g. fludioxonil). These resistant field strains (Imi R1) contained a single base pair mutation at position 365 in a two-component histidine kinase gene, probably involved in the fungal osmoregulation. Three anilinopyrimidine-resistant phenotypes have been identified. In the most resistant one (Ani R1), resistance was restricted to anilinopyrimidines, but no differences were observed in the amino-acid sequences of cystathionine beta-lyase (the potential target site of these fungicides) from Ani R1 or wild-type strains. In the two other phenotypes (Ani R2 and Ani R3), resistance extended to various other groups of fungicide, including dicarboximides, phenylpyrroles and sterol biosynthesis inhibitors. This multi-drug resistance was probably determined by over-production of ATP-binding cassette transporters. The hydroxyanilide fenhexamid is a novel botryticide whose primary target site is the 3-keto reductase involved in sterol C-4 demethylations. Apart from the multi-drug-resistant strain Ani R3, three other fenhexamid-resistant phenotypes have been recognized. For two of them (Hyd R1 and Hyd R2) fenhexamid-resistance seemed to result from P450-mediated detoxification. Reduced sensitivity of the target site could be the putative resistance mechanism operating in the third resistant phenotype (Hyd R3). Increased sensitivity to inhibitors of sterol 14 alpha-demethylase recorded in Hyd R1 strains was related to two amino-acid changes at positions 15 and 105 of this enzyme.  相似文献   

17.
Field isolates ofBotryotinia fuckeliana were collected from naturally infected plants. Their responses to the multisite fungicide dichlofluanid in mycelium growth test fell into three phenotypic classes, characterized by the following EC50 (and MIC) values ing ml–1: sensitivity, 1–3 (6–10); low resistance, 3–10 (> 100); high resistance, 10–30 (> 100). The corresponding values obtained for these classes in a spore germination test were respectively: 0.05 (0.2), 0.05–0.1 (0.5), 0.5–1 (0.9–1.5). Resistant isolates were crossed with two sensitive and two resistant strains of appropriate mating type to determine the genetic basis of resistance. Distribution of resistance phenotypes in ascospore progeny indicated that a gene, namedDic1, was probably responsible for the low or high resistance of 14 mutants selectively collected from experimental plots of greenhouse-grown gerbera sprayed several times with dichlofluanid or tolyfluanid. A second gene, namedDic2, was probably responsible for the low resistance displayed by two isolates (from grapevine and from carnation) maintained in the laboratory collection. As a result of the investigation, the use of dichlofluanid in integrated management programmes against grey mould is discussed.  相似文献   

18.
Isolates ofVenturia inaequalis and ofV. pirina sensitive (S) or resistant (R) to benomyl were examined in vitro on media amended with two phenylcarbamate fungicides. There was a negatively correlated cross-resistance (NCCR) to both methyl N-(3,5-dichlorophenyl) carbamate (MDPC) and isopropyl N-(3,4-diethoxyphenyl) carbamate (NPC) in some benomylresistant isolates. InV. inaequalis, isolates with low benomyl resistance (LR) did not show NCCR to MDPC, whereas isolates with medium (MR), high (HR) and very high (VHR) resistance to benomyl were more sensitive to MDPC than were the benomyl-sensitive isolates. To NPC, MR and VHR isolates showed NCCR whereas LR and HR isolates reacted similarly as sensitive isolates. InV. pirina only HR and VHR isolates showed NCCR to MDPC. The VHR isolates were sensitive to NPC, whereas the reactions of S, LR, MR and HR to NPC were similar.Crosses between benomyl-sensitive and benomyl-resistantV. pirina as well as between different resistant isolates showed that NCCR is inheritable and controlled by a single Mendelian gene.Samenvatting Benomyl-gevoelige en-resistente isolaten vanVenturia inaequalis enV. pirina werden in vitro onderzocht op media met de fungiciden methyl N-(3,5-dichlorophenyl) carbamate (MDPC) en isopropyl N-(3,4-dichlorophenyl) carbamate (NPC). Een aantal benomyl-resistente isolaten van deze pathogeen bleken een negatief gecorreleerde kruisresistentie (NCCR) te vertonen ten opzichte van MDPC en NPC.Isolaten vanV. inaequalis met matige (MR), hoge (HR) en zeer hoge (VHR) benomyl-resistentie vertoonden NCCR. Ten opzichte van NPC vertoonden alleen MR en VHR isolaten NCCR, en niet de LR en HR isolaten. InV. pirina vertoonden HR en VHR isolaten NCCR ten opzichte van MDPC, maar alleen de VHR isolaten ten opzichte van NPC.Kruisingen tussen benomyl-gevoelige en-resistenteV. pririna, en tussen verschillende benomyl-resistente isolaten onderling, toonden aan dat NCCR erfelijk is en berust op een enkel gen.Contribution No. 1712-E, 1986 series, from the ARO.  相似文献   

19.
ABSTRACT Stability of phenotypes of isolates of Botrytis cinerea that were sensitive or resistant to benzimidazole and dicarboximide fungicides was examined in the absence of fungicides in laboratory and growth room experiments. Twelve greenhouse isolates of B. cinerea were subcultured on potato dextrose agar (PDA) for 20 generations and on geranium seedlings for 15 generations. Three isolates of each of the following four phenotypes were used: sensitive to the fungicides thiophanate-methy1 (a benzimidazole) and vinclozolin (a dicarboximide) (S(T)S(V)), resistant to both fungicides (R(T)R(V)), resistant to thiophanate-methy1 and sensitive to vinclozolin (R(T)S(V)), and sensitive to thiophanate-methy1 and resistant to vinclozolin (S(T)R(V)). In three trials on PDA, 36 populations were subcultured; 8 populations changed phenotypes by the end of 20 generations, as determined by conidium germination on fungicide-amended medium. Five of the eight initially were S(T)R(V); the resulting phenotypes were S(T)S(V), R(T)S(V), and R(T)R(V). Populations from eight other isolates exhibited temporary changes in phenotype during intermediate generations on PDA but reverted to initial phenotypes by the twentieth generation; five of these populations changed to phenotype R(T)R(V). In two geranium seedling trials, each of the 12 greenhouse isolates was inoculated onto a set of three seedlings for each generation, and diseased tissue that developed was used to initiate the next generation. Therefore, a total of 72 populations of B. cinerea were subcultured in the two trials; 5 of these populations changed phenotype at the end of 15 generations. Three of the five initially were S(T)R(V); these changed to phenotypes S(T)S(V) or R(T)R(V). In each of the two trials on geranium seedlings, a population subcultured from one S(T)S(V) isolate changed phenotype one to phenotype R(T)R(V) and one to phenotype R(T)S(V). In all trials, no population resistant to thiophanate-methy1 changed to a thiophanate-methy1-sensitive phenotype, and no population changed to phenotype S(T)R(V). Random amplified polymorphic DNA (RAPD) fingerprints were generated with the 12 initial isolates and 49 isolates subcultured on PDA or geranium seedlings. Cluster analyses of RAPD markers showed that subcultured isolates exhibiting the same phenotype clustered together and that subcultured isolates derived from a common greenhouse isolate but with different phenotypes were in different clusters. Some populations that did not change phenotype exhibited considerable differences in RAPD marker patterns. The results of this study indicate that, in the absence of fungicides, sensitive populations of B. cinerea can develop resistance to thiophanate-methy1 and vinclozolin, and this resistance can be maintained in populations through multiple generations. Populations resistant only to vinclozolin (S(T)R(V)) exhibited a high frequency of phenotype change, and populations resistant to both fungicides (R(T)R(V)) were stable.  相似文献   

20.
A total of 568 B. cinerea isolates were collected from diseased sweet basil plants and the air in 10 sweet basil greenhouses. Mycelial growth tests were used to evaluate the sensitivity of these isolates to benomyl, fenhexamid, iprodione, polyoxin AL and pyrimethanil. EC50 values for polyoxin, the main botryticide on sweet basil in Israel, ranged from 0.4 to 6.5 μg ml?1 and had a bimodal distribution; the EC50 values for sensitive isolates ranged from 0.4 to 1.5 μg ml?1 and the EC50 values for low-level resistant isolates ranged from 4 to 6.5 μg ml?1. Among populations that had not been exposed to polyoxin treatments, 20 to 35 % of the collected isolates were low-level resistant for polyoxin. Polyoxin treatments in an experimental greenhouse shifted the equilibrium in favour of low-level resistant isolates, and the change occurred rapidly: from a frequency of 20 % low-level resistant isolates in the population that had never been treated with polyoxin to a frequency of 72 % after a few treatments over two seasons. Prolonged use of polyoxin in Israeli basil crops (in some sites for more than 10 years) does not appear to have led to the development of high-level resistance, but low-level resistant isolates were found in commercial greenhouses with the frequency of up to 73 %. High-level resistance to benzimidazoles was common (60 to 80 % of isolates) in greenhouses with a history of benzimidazole treatments; whereas 15–25 % of the isolates from greenhouses in which fungicides were not used were resistant. Low-level resistance to dicarboximides was fairly widespread (frequency of 30 to 80 % depending on the greenhouse) and a few cases of moderate resistance to dicarboximides were also noted (frequency of 0 to 9 %). Neither high- nor low-level resistance to anilinopyrimidines was common in sweet basil commercial greenhouses (0 to 7 %). However, 34 % of the isolates were strongly resistant in the experimental greenhouse, following a few treatments with anilinopyrimidine fungicides during the previous season. Before those treatments, the proportion of anilinopyrimidines resistant isolates had been 1 %. About 3 % of the isolates exhibited low-level resistance to fenhexamid and no isolates were found to be strongly resistant to fenhexamid. Low-level resistance to one fungicide was often associated with low-level resistances to other fungicides. Thirty-two phenotypes exhibiting resistance to one or more of the tested fungicides were noted among B. cinerea isolates. Resistant isolates showed similar or reduced fitness parameters in comparison to wild-type isolates.  相似文献   

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