小麦抗白粉病基因Pm21 的抑制基因

 小麦-簇毛麦6VS. 6AL 易位染色体含有抗白粉病基因Pm21,在我国的小麦育种中被广泛应用。近年来,一些含有Pm21 基因的小麦品种(系)开始感染白粉病。为探索含Pm21 的品种(系)感染白粉病的原因,本研究在6VS. 6AL 易位系与小麦品系(种)R14 和川农12 的杂交后代中利用分子标记CINAU17-1086 和CINAU18-723 辅助选择的遗传背景相对简单的F7 和F8 近等基因系为材料,研究了小麦抗白粉病基因Pm21 的抗病性表达。结果发现,在3 个含有6VS. 6AL 易位染色体的感病F6 植株繁殖的F7 近等基因系中发生了白粉病抗性的分离,分离比率符合13 感病︰ 3 抗病的理论值。在随机选取的F7 感病小麦单株所繁殖的F8 近等基因系中,有7 / 13 的株系一致地重感白粉病,有6 / 13 的株系发生了抗白粉病的分离,其中2 / 13 的株系分离比符合3 感病︰ 1 抗病、4 / 13 的株系分离比符合13 感病︰ 3 抗病的分离模式。这一结果指出,小麦株系中的抗白粉病基因Pm21 的抗性表达受小麦基因组中的一对显性抑制基因所控制,该基因来源于小麦品种(系)川农12或R14,建议命名为SuPm21。本研究指出,在把外源基因引入小麦的研究中,有利的外源基因与不含抑制基因的受体遗传资源同等重要。     

Mining wild barley for powdery mildew resistance

Powdery mildew, caused by Blumeria graminis f. sp. hordei (Bgh), is a worldwide disease problem on barley (Hordeum vulgare) with potentially severe impact on yield. Historically, resistance genes have been identified chiefly from cultivated lines and landraces; however, wild barley (H. vulgare subsp. spontaneum) accessions have proven to be extraordinarily rich sources of powdery mildew resistance. This study describes the characterization of a collection of 316 wild barley accessions, known as the Wild Barley Diversity Collection (WBDC), for resistance to powdery mildew and the genetic location of powdery mildew resistance loci. The WBDC was phenotyped for reaction to 40 different Bgh isolates at the seedling stage and genotyped with 10 508 molecular markers. Accessions resistant to all 40 isolates of Bgh were not found; however, three accessions (WBDC 053, 085 and 089) exhibited resistance to 38 of the isolates. Gene postulation analyses revealed that many accessions, while resistant, contained none of the 12 genes present in the Pallas near‐isogenic lines Mla1, Mla3, Mla6, Mla7, Mla9, Mla12, Mla13, Mlk1, MlLa, Mlg, Mlat and Ml(Ru2), suggesting that the accessions carry novel genes or gene combinations. A genome‐wide association study of powdery mildew resistance in the WBDC identified 21 significant marker‐trait associations that resolved into 15 quantitative trait loci. Seven of these loci have not been previously associated with powdery mildew resistance. Taken together, these results demonstrate that the WBDC is a rich source of powdery mildew resistance, and provide genetic tools for incorporating the resistance into barley breeding programmes.     

小麦新品系抗白粉病基因分析

 本文对6个小麦新品系所含的抗白粉病基因进行了遗传分析。将感病品种Liaochun10分别与SM 20121、SM 203390、SM 20125、SM 200332、SM 20126、SM 20005杂交和自交,并将这6个品系互配成半双列杂交组合。用小麦白粉菌15号小种的单孢堆菌系对各杂交组合的亲本、F₁、F₂代群体及F₃代家系进行了苗期抗病性鉴定。遗传分析表明,供试的6个品系对小麦白粉菌15号小种的抗性均由1对显性基因控制。等位性分析推断:SM 20121、SM 203390、SM 20125和SM 200332含有抗白粉病基因Pm12;SM 20126含有抗白粉病基因Pm21;SM 20005含有抗白粉病基因Pm16。建议将这6个品系作为优良抗病亲本利用。     

小麦抗白粉病基因Pm2的SSR标记筛选

为筛选与小麦抗白粉病基因Pm2紧密连锁的分子标记,将感病品种Chancellor与Pm2的近等基因系杂交,获得F1、F2分离群体,采用分离群体分组法对Pm2进行了微卫星(microsatellite,又称simple sequence repeats,SSR)标记分析.结果表明,定位于小麦5D染色体上的71对SSR引物中有12对引物能在Pm2的近等基因系、Chancellor间稳定地揭示出多态性差异,7对引物Xcfd189、Xcfd29、Xcfd8、Xcfd102、Xcfd7、Xcfd57和Xgwm190分别能在抗病、感病池间和F2分离群体的抗病、感病单株间稳定地扩增出特异性产物.7对引物所扩增的特异谱带分别为:Xcfd189360、Xcfd29190、Xcfd8160、Xcfd102250、Xcfd7200、Xcfd57245和Xgwm190210,它们与Pm2基因间的遗传距离分别为0、1.5、2.3、5.4、10.2、31.5和54.3 cM,其中标记Xcfd189360与Pm2共分离,标记Xcfd29190、Xcfd8160和Xcfd102250与Pm2紧密连锁,可用于Pm2的标记辅助选择.     

A comparative study of resistance to powdery mildew in wild emmer wheat in the seedling and adult plant stage

An isometric virus was isolated from cucumber plants growing in a plastic house in Crete and showing stunting and bright yellow mosaic of the leaves. Based on host range, properties in crude sap, behaviour during purification, electron microscopy and serology, the virus was identified as an isolate of artichoke yellow ringspot nepovirus. Ecological data corroborate transmission of the virus via the soil.Samenvatting Uit komkommerplanten in plastic-foliekassen op Kreta werd een bolvormig virus geïsoleerd; de aangetaste komkommerplanten vertoonden dwerggroei en helder geel mozaïek op de bladeren. Gebaseerd op de resultaten verkregen uit onderzoek met het virus naar de waardplantenreeks, de eigenschappen in perssap, zuivering, elektronen-microscopie en serologie kon het virus worden geïdentificeerd als een strain van het artichoke yellow ringspot nepovirus. Waarnemingen op het gebied van de ecologie wijzen op overdracht van het virus via de grond.     

Molecular characterization of a powdery mildew resistance gene in wheat cultivar suwon 92

ABSTRACT Powdery mildew, caused by Blumeria graminis f. sp tritici, is an important foliar disease of wheat worldwide. Pyramiding race-specific genes into a single cultivar and combining race-specific resistance genes with durable resistance genes are the preferred strategies to improve the durability of powdery mildew resistance. The objectives of this study were to characterize a powdery mildew resistance gene in Suwon 92 and identify gene-specific or tightly linked molecular markers for marker-assisted selection (MAS). A population of recombinant inbred lines (RILs) was derived by single seed descent from a cross between Suwon 92 and a susceptible cultivar, CI 13227. The RILs were screened for adult-plant infection type of powdery mildew and characterized with amplified fragment length polymorphism (AFLP) and simple sequence repeat (SSR) markers. The linked markers explained 41.3 to 69.2% of the phenotypic variances measured in 2 years. A morphological marker, hairy glume, was also associated with powdery mildew resistance in Suwon 92, and explained 43 to 51% of the phenotypic variance. The powdery mildew resistance gene in Suwon 92 was located on the short arm of chromosome 1A where Pm3 was located. Two gene-specific markers were developed based on the sequence of the cloned Pm3b gene. These two markers, which were mapped at the same locus in the peak region of the LOD score for the RIL population, explained most of the phenotypic variance for powdery mildew resistance in the RIL population. The powdery mildew resistance in Suwon 92 is most likely conditioned by the Pm3 locus. The gene markers developed herein can be directly used for MAS of some of the Pm3 alleles in breeding programs.     

Field assessment of resistance to powdery mildew in mature wheat plants

Rankit transformation of mildew scores was used in regression analyses to compare the times and methods of scoring resistance. This showed that time and method of assessment significantly altered the relative rank positions of different cultivars. Examination of 10 cultivars in detail showed that changes in rank were associated with differences in organ resistance.
Whole plot assessments based on a 0–9 scale provided a rapid and reliable means of ranking cultivars. Where possible, and particularly for breeders, at least two assessments are recommended, the first at or soon after flowering to estimate foliar infection, and the second 2 or 3 weeks later to estimate ear infection. For general comparisons of cultivars, sufficient information may be acquired from a single assessment when all plant organs are present and when the disease has had time to become well established.     

Quantitative trait Loci mapping for adult-plant resistance to powdery mildew in bread wheat

ABSTRACT Powdery mildew, caused by Blumeria graminis f. sp. tritici, is a major disease to wheat (Triticum aestivum) worldwide. Use of adult-plant resistance (APR) is an effective method to develop wheat cultivars with durable resistance to powdery mildew. In the present study, 432 molecular markers were used to map quantitative trait loci (QTL) for APR to powdery mildew in a doubled haploid (DH) population with 107 lines derived from the cross Fukuho-komugi x Oligoculm. Field trials were conducted in Beijing and Anyang, China during 2003-2004 and 2004-2005 cropping seasons, respectively. The DH lines were planted in a randomized complete block design with three replicates. Artificial inoculation was carried out in Beijing with highly virulent isolate E20 of B. graminis f. sp. tritici and the powdery mildew severity on penultimate leaf was evaluated four times, and the maximum disease severity (MDS) on penultimate leaf was investigated in Anyang under natural inoculation in May 2004 and 2005. The heritability of resistance to powdery mildew for MDS in 2 years and two locations ranged from 0.82 to 0.93, while the heritability for area under the disease progress curve was between 0.84 and 0.91. With the method of composite interval mapping, four QTL for APR to powdery mildew were detected on chromosomes 1AS, 2BL, 4BL, and 7DS, explaining 5.7 to 26.6% of the phenotypic variance. Three QTL on chromosomes 1AS, 2BL, and 7DS were derived from the female, Fukuho-komugi, while the one on chromosome 4BL was from the male, Oligoculm. The QTL on chromosome 1AS showed high genetic effect on powdery mildew resistance, accounting for 19.5 to 26.6% of phenotypic variance across two environments. The QTL on 7DS associated with the locus Lr34/Yr18, flanked by microsatellite Xgwm295.1 and Ltn (leaf tip necrosis). These results will benefit for improving powdery mildew resistance in wheat breeding programs.     

小麦慢白粉品种的抗性组分研究

 2003~2004年度和2004~2005年度在田间测定了16个小麦品种(系)对小麦白粉菌E20菌株的抗性组分,包括潜育期、侵染几率、产孢量、病斑扩展和传染期。结果表明,小麦慢白粉品种(系)与高感对照品种相比,表现为潜育期长、侵染几率低、产孢量低、病斑扩展慢的特点,且这4个抗性组分与对照的差异都达到了显著和极显著水平,但慢白粉品种的传染期变化无一定规律。参试慢白粉品种的抗性组分参数与病情曲线下面积(AUDPC)的相关分析表明,潜育期与AUDPC呈负相关,但相关性不显著;产孢量和病斑扩展与AUDPC呈正相关,两年数据相关性均达到显著水平;侵染几率与AUDPC呈正相关,但2003-2004年度相关性不显著,而2004~2005年度相关性显著;传染期与AUDPC相关关系不明显。由此可见,在慢白粉品种的病害流行中起主要作用的是产孢量、病斑扩展,而侵染几率、潜育期和传染期作用相对较小。     

三个小麦农家品种的苗期抗白粉病遗传分析

[目的]对3份小麦农家品种‘矮秆芒麦’、‘红头麦’和‘大红头’进行苗期抗性的遗传分析,研究它们的抗白粉病遗传特点,为其在抗病育种中的有效利用提供依据.[方法]将这3份小麦农家品种分别与感病品种‘铭贤169’正、反杂交,获得了F1和F2代.利用白粉菌E09菌株,分别对这3份农家品种、感病亲本‘铭贤169’以及各自的F1和F2代植株进行抗性鉴定.调查统计的数据经卡方测验分析其符合度.[结果]这3份农家品种对白粉菌E09菌株的抗性均由1对隐性核基因控制.[结论]3份农家品种对石家庄本地区的混合白粉病菌表现出良好的抗性,并且对E09的抗性均由1对隐性基因控制.可以进一步对它们进行分子标记及定位研究,为其作为抗源在小麦抗白粉病育种中的应用奠定基础.     

某些小麦品种抗白粉性遗传研究简报

 小麦白粉病近年在我省各地普遍发生,造成一定损失,研究明确主要品种抗白粉性的遗传行为,提高抗白粉小麦育种的效能,是一项急待开展的工作。本文简述了1983-1985年间我们对4个抗原品种在田间接种下进行抗白粉遗传研究的部分结果。     

甘肃小麦白粉病抗源材料的筛选及抗病基因库的组建

2002-2005年,对收集到的30份已知抗白粉病基因载体品种在甘肃省的不同生态区进行了抗病性监测,结果表明:Pm1、Pm3 a、Pm3 b、Pm3 c、Pm3 f、Pm4 a、Pm5、Pm6、Pm7、Pm8、Pm17在田间抗病性丧失,失去利用价值;Pm2、Pm19、Pm4+8、Pm4、Pm5+6、Pm13在田间抗病性较低,不宜单独作为亲本利用;Pm1+2+9、Pm2+6、Pm2+mld、Pm2+talent、Pm4+2 x、Pm4 b、Pm4 b+5、Pm20、Pm21、Pmxbd在田间抗性表现良好,在今后的育种工作中应充分加以利用。同时经过4年抗病性监测,从省内外2 638份小麦品种(系)材料中筛选出了抗病性强、综合农艺性状优良的92R137、贵农21等优异材料10余份,初步组建了抗白粉病基因库。文中还对抗病基因现状和利用及今后如何避免由于抗源单一化带来的白粉病流行进行了初步探讨。     

山西小麦品种和育种材料抗锈病、白粉病鉴定

2011—2015年,采用人工接菌方法,对25个育种单位的601份小麦品种和育种材料进行了小麦条锈病、叶锈病和白粉病的抗病性鉴定,筛选出对小麦条锈病抗性表现良好的品种材料36份,对小麦叶锈病抗性表现良好的品种材料16份,对小麦白粉病抗性表现良好的品种材料12份。     

小麦抗白粉病基因Pm6的微卫星标记鉴定

 Wheat powdery mildew, caused by Blumeria graminis f. sp. tritici, is a prevalent disease worldwide. Breeding and planting resistance cultivars have been proved effective and environmental friendly for control of the disease. To develop easily used PCR-based markers in marker assisted selection (MAS) for Pm6, a dominant powdery mildew resistance gene in wheat, 25 microsatellite markers on chromosome 2BL in wheat were screened between susceptible parent Yumai13 and resistance parent Timgalen carrying Pm6. F₂ population derived from Yumai13 and Timgalen was further analyzed by the marker Xgwm501. The results indicated that Xgwm501 was a co-dominant marker linked to Pm6 gene at a distance of 14.8 cM. 29 Pm-carrying varieties were tested by the marker Xgwm501 and only those carrying Pm6 showed 117 bp resistance specific band. This marker is proved to have high practicability and can be used in MAS of Pm6 gene in wheat breeding programs.     

Characterization and chromosomal location of powdery mildew resistance genes from wild barley PI282605

Journal of Plant Diseases and Protection - The objective of this work was to find the identity of three resistance genes against powdery mildew by mapping in an F2 population derived from a cross...     

354份小麦种质中抗白粉病基因Pm21和Pm13的分布研究

为了解本课题组现有种质资源中抗白粉病基因Pm21和Pm13的分布情况,本研究利用共分离分子标记SCAR1400和SCAR564,对收集于全国多个育种单位的354份小麦种质进行检测。结果表明:在检测的354份种质中,携带Pm21的有21份,分别为‘石H083-366’、‘BH50890-1-1’、‘06Y06’、‘南农02Y393’、‘09P80’、‘09P131’、‘09P283’、‘黔麦18号’、‘黔早麦15-3’、‘黔979-1’、‘黔9963-3’、‘黔9961-2’、‘YN06’、‘绵杂麦168’、‘MR168’、‘09品A6’、‘09品E6’、‘内麦836’、‘内麦9号’、‘绵阳39’和‘绵麦367’,检出率为5.9%,其中,8份来源于四川,来源于江苏和贵州的各有5份,河北、陕西和云南的材料中各有1份;仅有1份种质‘中大01’携带Pm13,来源于河南,检出率为0.28%。本研究结果可为抗白粉病基因资源的有效利用提供重要参考依据。     

甘肃省主要小麦生产品种及高代品系的抗白粉基因推导

［目的］ 采用基因推导法对目前甘肃省小麦主要生产品种及高代品系进行抗白粉基因分析,为甘肃省白粉病的抗病育种和品种使用及布局提供依据。［方法］ 利用21个小麦白粉菌株,结合品种系谱对甘肃14个小麦生产品种及28个高代品系进行抗白粉基因推导。［结果］ 14个生产品种中,1个含Pm8,1个含Pm4b,4个含未知抗病基因,其余8个对所有供试菌株全部表现感病;28个高代品系中,5个含Pm8〖STBZ〗,2个含Pm〖STBX〗3〖STBZ〗a,1个含Pm〖STBX〗4〖STBZ〗b,1个含Pm〖STBX〗30〖STBZ〗,5个含未知抗病基因,其余14个对所有供试菌株全部表现感病。［结论］ 目前甘肃小麦生产品种及高代品系中缺乏抗白粉病基因,一旦条件适宜,小麦白粉病在甘肃地区极易发生和流行,应该引起生产管理部门和育种专家的注意和重视。     

50个小麦生产及后备品种(系)的抗白粉病基因推导

为明确我国小麦品种(系)中抗白粉病基因的组成,利用25个不同毒性的小麦白粉菌菌株对50个小麦生产及后备品种(系)进行抗白粉病基因推导,结果表明,参试的50个小麦品种(系)中有8个小麦品种(系)对供试的25个菌株全部感病,5个品种含有抗病基因Pm8,2个品种含有Pm4a,9个品种含有Pm2+6,4个品种含有Pm2,22个品种(系)可能含有供试基因之外的其他抗性基因或新基因。此研究结果可为小麦抗病育种以及品种利用提供依据。     

两个陇南冬小麦品种苗期抗白粉病性遗传分析

2006-2009年,以甘肃陇南生产品种陇鉴9343、陇鉴9811作母本,铭贤169作父本进行杂交,F2代材料苗期分别接种白粉菌单孢菌系E05、E09进行抗性遗传分析,结果表明:对陇鉴9343组合,接种E05和E09,F2代植株抗感分离比分别为65:217和65:154,经卡方测验符合理论比1:3。对陇鉴9811组合,接种E05和E09,F2代植株抗感分离比分别为52:166和87:314,也符合理论1:3的比率。据此推知陇鉴9343、陇鉴9811对E05和E09的抗性均由1对隐性抗性基因控制。     

天水市小麦品种系抗白粉病性鉴定

1999～2001年,在抗病性观察圃,利用常规的抗病性鉴定方法,对29份大田主栽冬小麦品种进行抗白粉性鉴定。结果表明,不同小麦品种系对白粉病抗、感性存在明显差异。高抗、中抗、中感及高感的品种系分别占参试材料的13.8%、58.6%、10.3%及17.2%。其中中88375、中85130、蓝天3号、清山895等4个品种系对小麦白粉病连续2a以上表现出稳定的抗性。