麦田抗性生物型荠菜对苯磺隆的抗性机制研究

为明确抗性生物型荠菜对苯磺隆的抗性机制,分别测定了苯磺隆对抗性和敏感生物型荠菜体内乙酰乳酸合成酶(ALS)、谷胱甘肽-S-转移酶(GSTs)、超氧化物歧化酶(SOD)、过氧化物酶(POD)和过氧化氢酶(CAT)的影响。结果表明:离体条件下,抗性生物型荠菜体内ALS对苯磺隆的敏感性明显降低,苯磺隆对荠菜抗性和敏感生物型ALS的抑制中浓度(I50)分别为0.722 8和0.052 1 μmol/L,抗性与敏感生物型I50的比值为13.87;活体条件下,施用苯磺隆后,抗性和敏感生物型荠菜ALS活性均受到一定程度的抑制,但抗性生物型ALS活性受到抑制后能逐渐恢复,而敏感生物型则不能恢复;经苯磺隆处理后,抗性生物型GSTs相对活力明显高于敏感生物型,而抗性和敏感生物型体内POD、SOD和CAT相对活力无明显差异。研究表明,抗性生物型荠菜体内ALS对苯磺隆敏感性降低是其抗药性产生的原因之一,而GSTs对苯磺隆代谢能力的差异也可能与荠菜对苯磺隆的抗性有关。     

麦田不同杂草对苯磺隆敏感性差异的分子机制

为了探讨麦田常见杂草对苯磺隆敏感性差异的分子机制,测定了苯磺隆对4种杂草活性及对杂草体内靶标酶(ALS)和代谢酶(GSTs)的影响差异。结果表明,泽漆对苯磺隆的敏感性最低,IC50为123.16gai/hm2;猪殃殃和荠菜次之,分别为8.47、1.07gai/hm2;播娘蒿最敏感,为0.29gai/hm2。离体条件下,苯磺隆对播娘蒿、泽漆ALS的IC50值分别为6.40、54.90mgai/L。活体条件下,苯磺隆处理后,播娘蒿体内ALS活力低于对照,第9天降为对照的31.20%,而敏感性低的泽漆处理后1～2天ALS活力虽略有下降,但第3天明显提高,第4天达到峰值,为对照的2.90倍,此后逐渐恢复至对照水平。4种杂草本身所含GSTs活性存在较大差异,泽漆GSTs活性最高。经苯磺隆处理后,泽漆与猪殃殃GSTs活性明显提高,第4天时达到峰值,相对活性分别为1.23和1.25,并持续在较高水平;而荠菜、播娘蒿GSTs活性虽分别在第3、5天达到峰值,但多数时间相对活性低于1。结果表明,麦田不同杂草体内ALS的敏感性差异和GSTs的代谢差异是对苯磺隆敏感性不同的两个重要原因。     

山东省部分市县麦田杂草麦家公Lithospermum arvense对苯磺隆的抗药性

采用温室盆栽法和培养皿法测定了山东省部分市县冬小麦田杂草麦家公Lithospermum arvense L.对苯磺隆的抗药性水平,以及其抗药性生物型乙酰乳酸合成酶(ALS)对苯磺隆的敏感性。温室盆栽结果显示,供试杂草对苯磺隆产生了不同程度的抗药性,其中胶州麦家公生物型抗性水平最高,抗性倍数为12.8倍;培养皿法测定结果也显示胶州麦家公生物型抗性水平最高,但抗性倍数为3.89倍。交互抗性测定结果表明,胶州抗性麦家公生物型对其他ALS抑制剂噻吩磺隆和苄嘧磺隆已产生不同程度的交互抗性,其中对噻吩磺隆的抗性倍数达到3.11倍。离体条件下,与敏感生物型ALS活力的抑制中浓度(IC50)相比较,胶州抗性麦家公生物型的IC50值是敏感麦家公的 2.65倍。表明ALS敏感性降低可能是山东部分市县麦家公对苯磺隆产生抗药性的重要原因之一。     

中国北方部分地区麦田荠菜对苯磺隆的抗性水平

为明确北方地区冬小麦田荠菜对苯磺隆的抗性水平,运用培养皿法和温室盆栽法分别测定了山东、山西、河南、河北、陕西5省13个地区采集点麦田潜在抗药性生物型对苯磺隆的抗性水平,并分别测定了驻马店梁祝镇采集点荠菜潜在抗药性生物型和敏感生物型乙酰乳酸合成酶(ALS)对苯磺隆的敏感性。培养皿法测定结果表明:驻马店梁祝镇采集点荠菜抗药性生物型对苯磺隆的抗性水平最高,抗性倍数为6.17倍,其他采集点荠菜抗性倍数在0.94～2.04倍之间,仍处于较为敏感状态。温室盆栽法测定结果表明:驻马店梁祝镇采集点荠菜抗性倍数仍为最高,达到233倍, 其他地区采集点荠菜抗性倍数在1.23～3.73倍之间,尚未产生明显的抗药性。离体条件下,苯磺隆对荠菜抗药性和敏感生物型ALS的抑制中浓度(IC50)分别为0.664 μmol/L和0.053 3 μmol/L,抗药性生物型的抗性倍数达12.5倍。结果表明,驻马店梁祝镇采集点荠菜已对苯磺隆产生了较高水平的抗药性,而其体内ALS敏感性降低可能是抗药性产生的原因之一。     

小麦田麦家公对苯磺隆的抗性机理

为明确麦田阔叶杂草麦家公Lithospermum arvense L.对苯磺隆的抗性机理，以苯磺隆抗性和敏感型麦家公为材料，比较分析这2个生物型麦家公靶标酶乙酰乳酸合成酶（acetolactate synthase，ALS）、解毒酶谷胱甘肽-S-转移酶（glutathione-S-transferase，GST）以及保护酶过氧化物酶（peroxidase，POD）、超氧化物歧化酶（superoxide dismutase，SOD）和过氧化氢酶（catalase，CAT）对苯磺隆的响应差异性。结果表明，抗性麦家公ALS对苯磺隆的敏感性较敏感型麦家公显著下降，苯磺隆的抑制中浓度分别为0.187、0.036 μmol/L。苯磺隆胁迫后，抗性和敏感型麦家公ALS活性都出现下降，但抗性麦家公ALS活性可恢复，而敏感型麦家公ALS活性则不能恢复；2个生物型麦家公GST活性都能被苯磺隆诱导，但抗性麦家公GST累计活性为29.31 U，高于敏感型麦家公（25.90 U）；抗性麦家公SOD累计活性为24.49 U，较敏感型麦家公（19.31 U）高，且具有较强的恢复能力；抗性麦家公POD和CAT累计活性分别为126.92~550.68 U和41.41~77.19 U，也高于敏感型麦家公的93.75~271.04 U、42.17~57.28 U。因此，靶标酶ALS对苯磺隆敏感性减弱是麦家公产生抗性的一个重要原因，解毒酶GST、SOD、POD和CAT活性升高可能与抗性有关。     

中国北方部分冬麦区猪殃殃对苯磺隆的抗性水平

采用温室盆栽法和培养皿法分别测定7省14个县市14块麦田的猪殃殃潜在抗药性生物型和临近非耕地敏感生物型对苯磺隆的抗性水平。温室盆栽法试验结果表明,除河北省石家庄、山西省太原、陕西省周至、山东省泰安采集点麦田猪殃殃生物型对苯磺隆仍处于敏感状态外,其它地区麦田猪殃殃均产生了不同程度的抗药性,抗性倍数在1.6～4.3之间,其中河南省许昌采集点抗药性最高,达4.3倍,安徽省太和、陕西省华县采集点抗药性最低,抗性倍数均为1.6;培养皿法试验结果表明,河南省许昌采集点抗药性较高,抗性倍数为2.2,而安徽省太和、陕西省华县采集点抗药性较低,抗性倍数分别为1.9和1.7。两种方法的抗性趋势基本一致。     

山东省冬小麦田猪殃殃抗药性水平及ASL靶标抗性机理分析

为明确山东省冬小麦田猪殃殃Galium aparine对常规除草剂氯氟吡氧乙酸、苯磺隆及双氟磺草胺的抗性水平和抗性种群的乙酰乳酸合成酶(acetolactate synthase,ALS)靶标抗性机理,在温室内采用整株生物测定法测定21个猪殃殃种群对氯氟吡氧乙酸、苯磺隆和双氟磺草胺的抗性水平,同时根据猪殃殃ALS基因序列设计引物,提取猪殃殃高抗种群单株基因组DNA进行测序,并与拟南芥Arabidopsis thaliana敏感型ALS基因进行比对,查找突变位点分析其抗性机理。结果表明,21个猪殃殃种群对氯氟吡氧乙酸均敏感,尚未产生抗性;90.48%的猪殃殃种群已对苯磺隆产生了抗性,其中低抗、中抗和高抗种群分别占总种群数的23.81%、23.81%和42.86%,相对抗性指数最高为1 134.82;71.43%的猪殃殃种群已对双氟磺草胺产生了抗性,其中低抗、中抗和高抗种群分别占总种群数的19.05%、9.52%和38.10%,相对抗性指数最高为87.05。高抗苯磺隆种群XZ-1和LW均发生了ALS基因第197位氨基酸功能位点的突变,其中XZ-1种群发生了CCC(脯氨酸)到TCC(丝氨酸)...     

麦田猪殃殃对苯磺隆抗药性的快速检测

以采自山东、河南、安徽、陕西等地麦田及非农田的10个猪殃殃Galium aparine生物型为试材,运用单剂量甄别技术对不同生物型对苯磺隆的抗药性进行了检测,并以温室盆栽法及皿内抗性水平测定法验证其可靠性和可行性。结果表明:在甄别剂量(有效成分)85 mg/L下,猪殃殃不同生物型萌发率存在显著性差异,可以较好区分猪殃殃抗、感生物型;温室盆栽法及皿内抗性水平测定法结果一致,除采自山东泰安和陕西周至的麦田猪殃殃对苯磺隆仍处于敏感状态外,其他3个地区麦田猪殃殃均产生了不同程度的抗药性,且均与皿内单剂量甄别法结果一致,表明皿内单剂量甄别法具有可靠性和可行性。     

江苏省不同地区猪殃殃种群对常用除草剂的敏感性差异

采用整株生测法测定采自江苏省不同地区的20个猪殃殃种群对麦田常用除草剂苯磺隆、苄嘧磺隆、二甲四氯钠、氯氟吡氧乙酸、唑草酮的敏感性差异。结果表明,苯磺隆处理后,20个种群中有12个种群的ED50值超过推荐剂量,对苯磺隆产生明显的抗性;12个抗苯磺隆种群中有10个种群对苄嘧磺隆产生交互抗性,4个种群对二甲四氯钠产生多抗性,但对氯氟吡氧乙酸、唑草酮敏感;抗乙酰乳酸合酶(ALS)抑制剂类除草剂的猪殃殃种群比例呈现苏南到苏北逐渐增加的趋势,苯磺隆和苄嘧磺隆间存在交互抗性,部分抗ALS种群对二甲四氯钠具有多抗性,但抗性种群均对氯氟吡氧乙酸、唑草酮敏感。     

抗绿磺隆地肤生物型对磺酰脲类和其它除草剂的反应

生长在工业区的地肤连续几年施用绿磺隆,地肤对该种及其它几种抑制乙酰乳酸合成酶(ALS)的除草剂明显产生抗性。在室内用抑制幼苗干重积累50％的药剂剂量比率(GR 50R/s)计:抗性植株对5种磺酰脲类除草剂和一种咪唑啉酮类除草剂的抗性是敏感植株的2～180倍以上。同样,ALS酶活性分析表明,抑制抗性植株ALS酶所需药量是敏感植株的3～30多倍。ALS酶活性分析还表明,抗性地肤对甲磺隆、醚苯磺隆和噻磺隆的抗性极其相似,但对苯磺隆的抗性是对噻磺隆的2.5倍。然而生长在春小麦地中的抗性地肤对除草剂的反应却与ALS酶分析的结果不一致。在田间,每公顷使用32g噻磺隆,对抗性地肤几乎不起作用,相反,用甲磺隆、醚苯磺隆、苯磺隆各8克/公顷处理时,地肤幼苗密度虽不减少,但其生长十分缓慢,药后2个月,不施药处理区地肤幼苗生物量是施药区的4倍。其它几种作用方式的除草剂,如氟草烟、溴苯睛/二甲四氯、2,4—D丙酸/2,4D酯以及2,4D酯对田间抗性地肤有较好防效。二氯喹啉酸虽不降低地肤密度,但残存植株的生长发育受到阻碍。为延缓和控制对ALS酶抑制剂产生抗性的地肤种群的发展,可以轮换或混合使用以上几种不同作用方式 的除草剂。     

Conyza albida: a new biotype with ALS inhibitor resistance

Summary A biotype of Conyza albida resistant to imazapyr was discovered on a farm in the province of Seville, Spain, on land that had been continuously treated with this herbicide. This is the first reported occurrence of target site resistance to acetolactate synthase (ALS)-inhibiting herbicides in C. albida . In order to characterize this resistant biotype, dose–response experiments, absorption and translocation assays, metabolism studies, ALS activity assays and control with alternative herbicides were performed. Dose–response experiments revealed a marked difference between resistant (R) and susceptible (S) biotypes with a resistance factor [ED₅₀(R)/ED₅₀(S)] of 300. Cross-resistance existed with amidosulfuron, imazethapyr and nicosulfuron. Control of both biotypes using alternative herbicides was good using chlorsulfuron, triasulfuron, diuron, simazine, glyphosate and glufosinate. The rest of the herbicides tested did not provide good control for either biotype. There were no differences in absorption and translocation between the two biotypes, the maximum absorption reached about 15%, and most of the radioactivity taken up remained in the treated leaf. The metabolism pattern was similar and revealed that both biotypes may form polar metabolites with similar retention time (R_f). The effect of several ALS inhibitors on ALS (target site) activity measured in leaf extracts from both biotypes was investigated. Only with imazapyr and imazethapyr did the R biotype show a higher level of resistance than the S biotype [I₅₀ (R)/I₅₀(S) value of 4.0 and 3.7 respectively]. These data suggest that the resistance to imazapyr found in the R biotype of C. albida results primarily from an altered target site.     

湖南省部分地区棉田牛筋草(Eleusine indica)对精喹禾灵的抗性

采用整株法测定了湖南省部分地区棉田牛筋草(Eleusine indica)对精喹禾灵的抗性水平,还测定了精喹禾灵对牛筋草抗(R)、感(S)种群体内GSTs及SOD、POD、CAT影响的差异。整株法测定结果显示,相对于敏感的南县种群,其他地区棉田牛筋草对精喹禾灵的抗性指数在1.6~9.7之间,其中湘阴种群最高为9.7,澧县种群最低为1.6;精喹禾灵处理2d后,R种群GSTs活性急剧上升,在第3天达到最高,随后急剧下降,5d之后趋于平缓。S种群GSTs活性在施药后先上升后下降。药剂处理后,R种群的SOD和POD活性在中期显著低于S种群,R、S种群的CAT活性在药后第9天有明显差异。结果表明,R种群对精喹禾灵产生抗性的原因可能是GSTs对精喹禾灵的代谢作用加强,抗氧化酶系活性的变化可能与抗性相关。     

Herbicide resistance in Aster squamatus conferred by a less sensitive form of acetolactate synthase

A biotype of Aster squamatus (Sprengel) Hieronymus with suspected resistance to the ALS-inhibiting herbicide imazapyr was detected in a chicken farm in the province of Seville, Spain, which had been treated once a year with imazapyr for 10 years. Resistance to imazapyr in this biotype was studied using dose-response experiments, absorption and translocation assays, metabolism studies and ALS activity assays. The rate of imazapyr required to inhibit A squamatus growth by 50% (ED50) was 15 times higher for the R (resistant) than for the S (susceptible) biotype. Cross-resistance existed for the ALS-inhibitors imazamox, imazethapyr, amidosulfuron, nicosulfuron, rimsulfuron, triasulfuron and tribenuron, but not for bensulfuron. Control of A squamatus using alternative herbicides was poor with clopyralid, intermediate with quinclorac, amitrole and MCPA, and excellent with 2,4-D, glufosinate and glyphosate. Absorption of [14C]imazapyr increased over time for both the R and S biotypes, and translocation from the treated leaf to shoots and roots was similar in both biotypes, with most of the radioactivity remaining in the treated leaf. No metabolites of imazapyr were detected in either biotype. Sensitivity of the ALS enzyme (target site) to imazapyr was lower for the R biotype (I50(R) = 4.28 x I50(S)). The mechanism of imazapyr resistance in this R biotype appears to be an altered ALS conferring decreased sensitivity to imazapyr at the whole-plant level.     

Assessment of two biotypes of Solanum ptycanthum that differ in resistance levels to imazamox

Glasshouse and laboratory experiments were conducted on acetolactate synthase (ALS) homozygous resistant Solanum ptycanthum biotypes from Illinois (IL‐R) and Indiana (IN‐R), and homozygous susceptible biotypes from Illinois (IL‐S) and Indiana (IN‐S). Genetic similarity of biotypes was assessed by random amplified polymorphic DNA (RAPD) markers, which determined that the Illinois biotypes are more similar to each other than to the IN‐R biotype. ALS enzyme activity from the IL‐R and IN‐R biotypes had I₅₀ values of 362 and 352 μM imazamox respectively. Dose–response experiments using three‐ to four‐leaf‐stage plants of the IL‐R and IN‐R biotypes had GR₅₀ values of 242 and 69 g ae ha⁻¹ imazamox respectively. Whole‐plant and ALS enzyme results are different than previously reported values in the literature, which was attributed in the current study to the original IN‐R population having individuals that were segregating for ALS resistance. Metabolism studies showed no difference in percentage [¹⁴C]imazamox remaining between the IL‐R and IN‐R biotypes up to 72 h after treatment. The IL‐S biotype metabolised [¹⁴C]imazamox approximately two times faster than the IL‐R and IN‐R biotypes and this trait was heritable. Response of F₃ plants containing homozygous ALS‐resistant alleles from the IL‐R biotype in a genetic background of 50% Illinois and 50% Indiana biotypes suggests that genetic factors other than an altered target site or metabolism may also contribute to the magnitude of resistance at the whole‐plant level in resistant biotypes.     

Mechanism of resistance to bensulfuron-methyl in Alisma plantago-aquatica biotypes from Portuguese rice paddy fields

Two Alisma plantago‐aquatica biotypes resistant to bensulfuron‐methyl were detected in rice paddy fields in Portugal’s Mondego (biotype T) and Tagus and Sorraia (biotype Q) River valleys. The fields had been treated with bensulfuron‐methyl‐based herbicide mixtures for 4–6 years. In order to characterize the resistant (R) biotypes, dose–response experiments, absorption and translocation assays, metabolism studies and acetolactate synthase (ALS) activity assays were performed. There were marked differences between R and susceptible (S) biotypes, with a resistance index (ED₅₀R/S) of 500 and 6.25 for biotypes Q and T respectively. Cross‐resistance to azimsulfuron, cinosulfuron and ethoxysulfuron, but not to metsulfuron‐methyl, imazethapyr, bentazone, propanil and MCPA was demonstrated. No differences in the absorption and translocation of ¹⁴C‐bensulfuron‐methyl were found between the biotypes studied. Maximum absorption attained 1.12, 2.02 and 2.56 nmol g⁻¹ dry weight after 96 h incubation with herbicide, for S, Q and T biotypes respectively. Most of the radioactivity taken up by the roots was translocated to shoots. Bensulfuron‐methyl metabolism in shoots was similar in all biotypes. The R biotypes displayed a higher level of ALS activity than the S biotype, both in the presence and absence of herbicide and the resistance indices (IC₅₀R/S) were 20 197 and 10 for biotypes Q and T respectively. These data confirm for the first time that resistance to bensulfuron‐methyl in A. plantago‐aquatica is target‐site‐based. In practice, to control target site R biotypes, it would be preferable to use mixtures of ALS inhibitors with herbicides with other modes of action.     

黑龙江省大豆田反枝苋对氟磺胺草醚的抗药性机制研究

为明确反枝苋抗性种群对氟磺胺草醚的抗性机制,分别测定了氟磺胺草醚对反枝苋抗性和敏感种群体内原卟啉原氧化酶(PPO)、谷胱甘肽S-转移酶(GSTs)、超氧化物歧化酶(SOD)、过氧化物酶(POD)和过氧化氢酶(CAT)活性的影响。结果表明:氟磺胺草醚处理后,抗性和敏感反枝苋种群PPO活性均受到一定程度的抑制,但抗性种群活性受到抑制后能逐渐恢复,而敏感种群则不能恢复;施用氟磺胺草醚后,抗性和敏感反枝苋种群GSTs和SOD活性变化无明显差异,抗性和敏感反枝苋种群POD和CAT活性均受到一定程度的抑制,但抗性种群活性受到抑制后能逐渐恢复,而敏感种群则不能恢复。研究表明,反枝苋抗性种群体内PPO对氟磺胺草醚敏感性降低是其产生抗药性的原因之一,反枝苋POD和CAT对活性氧的抵御能力差异也可能与反枝苋对氟磺胺草醚的抗性有关。     

Sulfonylurea herbicide resistance in Sonchus asper biotypes in Alberta, Canada

Summary Two Sonchus asper (spiny annual sow-thistle) biotypes, suspected of being resistant to the sulfonylurea herbicide metsulfuron-methyl, were collected in 1996 from two barley ( Hordeum vulgare ) fields in central Alberta, Canada. Both fields had received at least six applications of acetolactate synthase (ALS)-inhibiting herbicide(s). The responses of the two resistant (R) biotypes and two susceptible (S) biotypes to several sulfonylurea herbicides, and to herbicides and herbicide mixtures with other mechanisms of action, were compared. Both R biotypes were highly resistant to all sulfonylurea herbicides, but their control with other herbicides and mixtures was effective and comparable to that of the S biotypes. ALS extracted from an R biotype was about 440 times more resistant to metsulfuron-methyl than that of an S biotype, indicating that resistance was conferred by an ALS enzyme that was less sensitive to inhibition by the herbicide. Competitiveness and seed production of S. asper varied among biotypes, but the differences were probably the result of ecotype differences rather than resistance or susceptibility to sulfonylurea herbicides. This is the first reported occurrence of target site-based S. asper resistance to ALS-inhibiting herbicides.