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1.
为明确看麦娘Alopecurus aequalis抗性种群YL的靶标抗性机制,采用基因克隆法对看麦娘抗性和敏感种群间乙酰辅酶A羧化酶(ACCase)和乙酰乳酸合成酶(ALS)基因序列进行扩增、克隆和测序,比对二者ACCase和ALS基因序列的差异,探寻其产生抗药性突变的基因位点,同时测定该突变型抗性种群YL对不同ACCase和ALS抑制剂类除草剂的交互抗性。结果显示,与看麦娘敏感种群TL相比,抗性种群YL的ACCase基因CT区域第2 041位氨基酸由异亮氨酸(ATT)突变为天冬酰胺酸(AAT),ALS基因Domain A区域第197位氨基酸由脯氨酸(CCC)突变为精氨酸(CGC)。看麦娘抗性种群YL对ACCase抑制剂炔草酯产生了高水平抗性,抗性倍数为43.96,对高效氟吡甲禾灵和精喹禾灵产生了中等水平抗性,抗性倍数分别为18.33和15.87,对唑啉草酯、烯草酮和烯禾啶较敏感;对ALS抑制剂氟唑磺隆产生了低水平抗性,抗性倍数为8.39,对啶磺草胺和咪唑乙烟酸较敏感。表明ACCase基因第2 041位和ALS基因第197位氨基酸突变是导致看麦娘抗性种群YL对精噁唑禾草灵和甲基二磺隆同时产生抗性的重要原因之一。  相似文献   

2.
看麦娘是中国长江中下游地区稻茬麦田的主要恶性杂草之一,甲基二磺隆是防治小麦田看麦娘等禾本科杂草的重要除草剂.该研究团队前期在安徽省凤台县小麦田采集到疑似抗性种群看麦娘(AHFT-01),为明确其对甲基二磺隆的抗性发生情况及潜在的抗性机制,采用温室盆栽法在整株水平上测定了该种群对甲基二磺隆及其他乙酰乳酸合成酶(ALS)抑...  相似文献   

3.
为明确荠菜种群对苯磺隆的抗性水平及其靶标抗性产生的分子机制,采用整株水平测定法测定了荠菜对苯磺隆及其他5种乙酰乳酸合成酶(ALS)抑制剂类除草剂的抗性水平,同时扩增和比对了荠菜抗性和敏感种群之间ALS基因的差异。结果显示:与敏感种群15-ZMD-1相比,抗性种群15-ZMD-5对苯磺隆产生了高水平抗性,抗性倍数为219.6;15-ZMD-5种群不同单株中共存在3种突变方式,分别为ALS基因197位点脯氨酸(CCT)突变为亮氨酸(CTT)、574位点色氨酸(TGG)突变为亮氨酸(TTG)以及单株同时发生上述197和574位点的氨基酸突变。15-ZMD-5抗苯磺隆种群对嘧草硫醚、啶磺草胺和氟唑磺隆均产生了高水平的交互抗性,抗性倍数分别为41.2、79.3和87.8;对双氟磺草胺和咪唑乙烟酸产生了低水平的交互抗性,抗性倍数分别为8.5和5.6。分析表明,荠菜抗性种群ALS基因发生的氨基酸突变可能是导致其对ALS抑制剂类除草剂产生抗性的重要原因之一。  相似文献   

4.
野慈姑是我国稻田危害最严重的杂草之一。以黑龙江稻田采集的野慈姑(Sagittaria trifolia Linn.)为研究对象,通过室内生物测定和分子克隆技术,对野慈姑的吡嘧磺隆抗性水平进行检测,并从靶标位点突变的角度解释抗性产生原因。结果表明,采自哈尔滨稻田的2个野慈姑种群N03及N06均为高抗种群,抗性达到4倍剂量以上。经比对2个抗性种群的靶标酶ALS基因发现,Pro197的脯氨酸分别被亮氨酸、丝氨酸取代,该位点的突变可能是野慈姑种群对磺酰脲类除草剂产生抗药性的主要原因。  相似文献   

5.
河南省麦田荠菜对苯磺隆的抗性及其交互抗性   总被引:1,自引:0,他引:1  
为明确河南省荠菜Capsella bursa-pastoris种群对苯磺隆的抗性水平及其可能存在的抗性机理,应用整株法测定了采自驻马店及南阳等6个荠菜发生严重市的10个荠菜种群对苯磺隆的抗性,扩增和比对了荠菜苯磺隆抗性种群及敏感种群之间靶标酶乙酰乳酸合成酶基因ALS的差异,并使用单剂量法测定了以上种群对双氟磺草胺、啶磺草胺及氟唑磺隆等ALS抑制剂类除草剂的交互抗性。结果表明,驻马店市的汝南县冯湾村(ZMD-1)及平舆县五里路村(ZMD-3)荠菜种群对苯磺隆的抗性倍数分别为3.1和2.5,表现出低水平抗性;驻马店市汝南县赖楼村(ZMD-2)和周口市川汇区文庄村(ZK-1)荠菜种群对苯磺隆的抗性倍数分别为21.7和57.8,表现出高水平抗性;南阳市唐河县上屯村(NY-2)荠菜种群对苯磺隆的抗性倍数为116.5,表现出极高水平抗性,其它种群对苯磺隆仍然较敏感。NY-2、ZMD-2和ZK-1种群的ALS基因第197位氨基酸由脯氨酸(CCT)分别突变为丝氨酸(TCT)、丙氨酸(GCT)和亮氨酸(CTT),其它种群中均未发现有突变产生;这3个种群在氟唑磺隆推荐剂量处理下,死亡率仅为18.9%、23.3%和11.1%,说明已对氟唑磺隆产生了较高水平的交互抗性,其中NY-2种群对双氟磺草胺和啶磺草胺产生了低水平交互抗性,推荐剂量下死亡率分别为82.2%和83.1%。表明ALS基因突变很可能是导致荠菜种群对苯磺隆等ALS抑制剂类除草剂产生抗性的重要原因。  相似文献   

6.
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)...  相似文献   

7.
通过整株盆栽法研究黑龙江省佳木斯市汤原县(种群R1)、856农场(种群R2)、密山市(种群R3)3个水稻田野慈姑种群对丙嗪嘧磺隆的抗性水平,采用分子生物学技术分析3个野慈姑种群在靶标酶基因上的差异,确定3个野慈姑种群对丙嗪嘧磺隆和苄嘧磺隆是否存在交互抗性。结果显示,黑龙江R1、R2、R3种群抗性指数(RI)分别为11.92、22.68、35.99。与敏感的七台河种群S相比,R1、R2、R3的ALS基因均在Pro_(197)位发生不同突变。R1种群为Thr_(197)取代了Pro_(197);R2、R3种群为Ser_(197)取代了Pro_(197),ALS基因的突变是其产生抗性的主要原因。3个野慈姑种群对丙嗪嘧磺隆和苄嘧磺隆存在交互抗性。  相似文献   

8.
为了明确宁夏稻区稗草对五氟磺草胺抗性水平及抗性机制。采用整株生物测定法测定了宁夏地区6个稗的原变种Echinochloa crus-galli var.crus-galli种群对五氟磺草胺的抗性水平,并测定了每个种群的乙酰乳酸合酶基因(ALS)序列和ALS酶离体活性,以及P450抑制剂马拉硫磷对稗草种群抗性水平的影响。结果显示,与敏感种群相比,5个疑似抗性种群对五氟磺草胺表现出不同程度的抗性(10.18倍~32.71倍),其中抗性种群N14,N22,N27和N51的ALS 574位色氨酸突变为亮氨酸,N53的197位脯氨酸突变为亮氨酸,敏感种群N43没有发现突变位点,五氟磺草胺对抗性种群ALS酶的IC50均明显高于敏感种群,马拉硫磷对五氟磺草胺有增效作用,可提高稗草种群对五氟磺草胺的敏感性。综上所述,稗草种群对五氟磺草胺产生抗性是由于靶标基因ALS突变,同时稗草种群对五氟磺草胺的抗性也可能与细胞色素P450介导的代谢增强有关。  相似文献   

9.
杂草对AHAS抑制剂的抗药性分子机理研究进展   总被引:3,自引:1,他引:2  
除草剂在田间的重复及不合理使用,导致了杂草抗药性的发生和发展。其中AHAS抑制剂由于靶标单一,抗性发展十分迅速。截至2009年,已有103种杂草对AHAS抑制剂产生了抗药性,占19类化学除草剂总抗药性杂草生物型的近1/3。从AHAS基因突变位点及种类与杂草抗药性水平的关系、AHAS基因突变与AHAS酶活性的关系、AHAS基因拷贝数与杂草抗药性的关系以及AHAS酶与除草剂结合前后的三维结构等方面,综述了杂草对AHAS抑制剂产生抗药性的机理,旨在为AHAS抑制剂抗性研究提供参考。并对自然种群目标基因的等位基因检测技术(ECOTILLING)和衍生型酶切扩增多态性序列(dCAPS)两种通过检测等位基因多态性的手段快速诊断抗药性杂草的新技术进行了介绍,讨论了延缓杂草抗药性发生和发展的策略。  相似文献   

10.
为明确河南省部分地区麦田荠菜Capsella bursa-pastoris对苯磺隆的抗性水平及抗性靶标分子机制,采用整株生物法测定了12个荠菜种群的抗性水平,并对乙酰乳酸合成酶(acetolactate synthase,ALS)离体活性和ALS基因突变进行了测定分析。结果表明,商丘市民权县花园村(MQ)、周口市西华县小于楼村(XH)、平顶山市叶县穆寨村(YX)、许昌市长葛市董庄村(CG)采集的荠菜种群对苯磺隆产生了较高的抗性,GR_(50)分别为129.14、110.67、62.91和85.29 g/hm~2,抗性倍数分别为215.23、184.45、104.85和142.15倍;ALS离体活性测定所得I_(50)分别为5.85、4.87、1.38和3.83μmol/L,抗性倍数分别为83.57、69.57、19.71和54.71倍;其余8个种群的GR_(50)在0.60~2.86 g/hm~2之间,抗性倍数在1.00~4.77之间;I_(50)在0.07~0.37μmol/L之间,抗性倍数在1.00~5.29之间。荠菜种群MQ、XH的ALS基因Domain A区域第197位脯氨酸(CCT)均突变为丝氨酸(TCT),荠菜种群CG的第197位脯氨酸(CCT)突变为亮氨酸(CTT),表明靶标ALS基因突变是荠菜对苯磺隆产生抗性的重要原因之一,但荠菜种群YX的ALS基因保守区内暂未发现突变位点,其抗药性可能由其它原因造成。  相似文献   

11.
Yu Q  Han H  Powles SB 《Pest management science》2008,64(12):1229-1236
BACKGROUND: In the important grass weed Lolium rigidum (Gaud.), resistance to ALS‐inhibiting herbicides has evolved widely in Australia. The authors have previously characterised the biochemical basis of ALS herbicide resistance in a number of L. rigidum biotypes and established that resistance can be due to a resistant ALS and/or enhanced herbicide metabolism. The purpose of this study was to identify specific resistance‐endowing ALS gene mutation(s) in four resistant populations and to develop PCR‐based molecular markers. RESULTS: Six resistance‐conferring ALS mutations were identified: Pro‐197‐Ala, Pro‐197‐Arg, Pro‐197‐Gln, Pro‐197‐Leu, Pro‐197‐Ser and Trp‐574‐Leu. All six mutations were found in one population (WLR1). Each Pro‐197 mutation conferred resistance to the sulfonylurea (SU) herbicide sulfometuron, whereas the Trp‐574‐Leu mutation conferred resistance to both sulfometuron and the imidazolinone (IMS) herbicide imazapyr. A derived cleaved amplified polymorphic sequences (dCAPS) marker was developed for detecting resistance mutations at Pro‐197. Furthermore, cleaved amplified polymorphic sequences (CAPS) markers were developed for detecting each of the six mutant resistant alleles. Using these markers, the authors revealed diverse ALS‐resistant alleles and genotypes in these populations and related them directly to phenotypic resistance to ALS‐inhibiting herbicides. CONCLUSION: This study established the existence of a diversity of ALS gene mutations endowing resistance in L. rigidum populations: 1–6 different mutations were found within single populations. At field herbicide rates, resistance profiles were determined more by the specific mutation than by whether plants were homo‐ or heterozygous for the mutation. Copyright © 2008 Society of Chemical Industry  相似文献   

12.
Lolium species (ryegrasses) are genetically highly variable plants that are both forage crops and major weeds across the globe. As weeds, they rapidly evolve resistance under the selective pressure of acetolactate-synthase (ALS) inhibitors, the most resistance-prone herbicide group. Quick and accurate diagnosis is therefore of importance to prevent resistance spread in ryegrass. To develop proactive molecular tools for the detection of mutant, resistant ALS alleles, we assessed variation in the ryegrass ALS gene. Sequencing the full 1929-bp ALS coding sequence in 59 plants from six distant locations revealed a total of 208 polymorphic nucleotide positions (one every 9.3 nucleotides). The heterogeneous distribution of synonymous and non-synonymous substitutions along the ALS coding sequence suggested that nucleotide variation of ALS is shaped by purifying and background selection. Using regions of the ALS coding sequence with a low number of polymorphic nucleotide sites, five derived cleaved amplified polymorphic sequence (dCAPS) assays were developed targeting codons crucial for herbicide sensitivity. These enabled the first detection in ryegrass of a Pro-197-Thr substitution that confers herbicide resistance. Most assays could also be used to genotype Festuca and Vulpia plants. These dCAPS assays should prove powerful tools for both resistance diagnosis and population genetics studies.  相似文献   

13.
Acetolactate synthase (ALS) inhibitors are the most resistance‐prone herbicide group. Rapid resistance diagnosis is thus of importance for their optimal use. We formulate rules to use the derived cleaved amplified polymorphic sequence method to develop molecular tools detecting a change at a given codon, the nature of which is unknown. We applied them to Alopecurus myosuroides (black grass) to develop assays targeting ALS codons A122, P197, A205, W574 and S653 that are crucial for herbicide sensitivity. These assays detected W574L or P197T, or both substitutions, in most plants analysed from a field where ALS inhibitors failed after 3 years of use. Similar assays can easily be set up for any species. Given the rapidity of selection for resistance to ALS inhibitors, these assays should be very useful in proactive herbicide resistance diagnosis.  相似文献   

14.
为明确河南省部分地区的多花黑麦草Lolium multiflorum种群对乙酰辅酶A羧化酶(acetylCoA carboxylase,ACCase)和乙酰乳酸合成酶(acetolactate synthase,ALS)抑制剂类除草剂的抗性水平和抗性机理,采用整株生物测定法测定采自新乡市和驻马店市的多花黑麦草种群对ACCase抑制剂类除草剂精噁唑禾草灵、炔草酯、唑啉草酯和ALS抑制剂类除草剂甲基二磺隆、氟唑磺隆、啶磺草胺的抗性水平,并对多花黑麦草ACCase和ALS靶标酶编码基因进行克隆及氨基酸序列比对,分析其靶标抗性机理。结果显示,与多花黑麦草敏感种群HNXX01相比,HNZMD04和HNXX05种群对6种除草剂均产生了抗性,HNZMD04种群对精噁唑禾草灵和啶磺草胺的相对抗性倍数分别为44.65和40.31,对炔草酯和氟唑磺隆的相对抗性倍数分别为11.91和11.93;HNXX05种群对精噁唑禾草灵和氟唑磺隆的相对抗性倍数分别为27.70和25.67。HNZMD04和HNXX05抗性种群的ACCase基因均发生了D2078G突变,2个种群的突变率分别为55%和70%;HNZMD04...  相似文献   

15.
R MARSHALL  S R MOSS 《Weed Research》2008,48(5):439-447
Several UK populations of the grass weed Alopecurus myosuroides were identified where high proportions of individuals showed resistance to the acetolactate synthase (ALS)‐inhibiting herbicides, mesosulfuron‐methyl + iodosulfuron‐methyl sodium mixture and sulfometuron‐methyl. Screening with sulfometuron, followed by DNA sequencing of the ALS gene from resistant and susceptible individuals, led to the identification of eight populations where a single point mutation segregated with resistance to sulfometuron. All highly resistant individuals from seven of eight populations showed a single‐nucleotide polymorphism (SNP) in the first position of the Pro197 codon of an A. myosuroides ALS gene, conferring a predicted proline to threonine target‐site change. One population showed resistant individuals with single‐nucleotide polymorphism in the second position of the Trp574 codon, conferring a predicted tryptophan to leucine substitution. No other mutations segregating with resistance were found. Enzyme assays confirmed that resistance was due to an altered form of ALS enzyme, which was less susceptible to inhibition by sulfonylureas, making this one of the first fully characterised cases of ALS target‐site resistance in a European grass weed. Increased information regarding the nature and distribution of ALS target‐site mutation may help support sustainable management strategies, allowing continued use of mesosulfuron + iodosulfuron against this weed in the UK.  相似文献   

16.
Schoenoplectiella juncoides is a noxious sedge weed in rice paddy fields that has evolved resistance to sulfonylurea (SU) herbicides. The molecular basis of resistance is amino acid substitutions at Pro197, Trp574 or Asp376 in the acetolactate synthase (ALS) enzyme, which is the target of SUs. Schoenoplectiella juncoides has two ALS genes and resistant plants have point mutations that cause amino acid substitutions in either encoded protein. Single‐nucleotide substitutions at the codon for Pro197 in the ALS genes can cause six types of amino acid substitutions and all of these substitutions have been found in both ALS genes among Japanese SU‐resistant biotypes. Whole‐plant herbicide responses differ among the amino acid substitution types. Furthermore, analyses of ALS activity in plant extracts show that the extracts’ responses to herbicides differ, depending on which ALS gene is mutated. The activity responses of the ALS extracts to the SU, imazosulfuron, showed double‐sigmoid curves with plateaus of ~30% inhibition for Pro197 substitutions in ALS1 and ~70% for Pro197 substitutions in ALS2. This indicates that ALS1 and ALS2 contribute to the responses with a proportion of 7:3. The double‐sigmoid curves can be reconstructed to show the responses of the resistant and susceptible enzymes separately by regression analysis. The resistance levels of the separate ALS1 or ALS2 mutated enzyme are highly correlated with the whole‐plant responses, with a relationship that the former is the square of the latter. This could provide a quantitative insight into the physiological basis of resistance.  相似文献   

17.
BACKGROUND: The increasing use of ACCase‐inhibiting herbicides has resulted in evolved resistance in key grass weeds infesting cereal cropping systems worldwide. Here, a thorough and systematic approach is proposed to elucidate the basis of resistance to three ACCase herbicides in a Lolium multiflorum Lam. (Italian rye grass) population from the United Kingdom (UK24). RESULTS: Resistance to sethoxydim and pinoxaden was always associated with a dominant D2078G (Alopecurus myosuroides Huds. equivalent) target‐site mutation in UK24. Conversely, whole‐plant herbicide assays on predetermined ACCase genotypes showed very high levels of resistance to diclofop‐methyl for all three wild DD2078 and mutant DG2078 and GG2078 ACCase genotypes from the mixed resistant population UK24. This indicates the presence of other diclofop‐methyl‐specific resistance mechanism(s) yet to be determined in this population. The D2078G mutation could be detected using an unambiguous DNA‐based dCAPS procedure that proved very transferable to A. myosuroides, Avena fatua L., Setaria viridis (L.) Beauv. and Phalaris minor Retz. CONCLUSION: This study provides further understanding of the molecular basis of resistance to ACCase inhibitor herbicides in a Lolium population and a widely applicable PCR‐based method for monitoring the D2078G target‐site resistance mutation in five major grass weed species. Copyright © 2010 Society of Chemical Industry  相似文献   

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