小麦抗源兴资9104抗条锈性遗传研究初报

采用常规杂交和基因推导法相结合,在苗期和成株期对小麦优良抗病种质兴资9104进行抗条锈性遗传研究。结果表明,兴资9104至少含有1对显性全生育期抗条锈病基因和1对成株抗条锈病基因,分别控制对条锈菌生理小种条中17号的全生育期抗性和对条中32号的成株期抗性。兴资9104可能携带有YrSK基因。建议在小麦抗病育种中     

水稻分子育种亲本材料在东北地区的稻瘟病抗性评价

对212份分子育种亲本在稻瘟病重发区自然鉴定圃进行田间抗性鉴定,发现分别有117个和39个品种对叶瘟和穗颈瘟表现抗性,19个品种对叶瘟和穗颈瘟均表现中抗以上抗性,叶瘟与穗颈瘟发病严重度存在显著相关性.进一步利用辽宁和黑龙江的混合菌株在水稻苗期,对田间苗期和成株期均表现抗病的19个品种进行人工接种鉴定,分别筛选出对辽宁东...     

玉米自交系及杂交种苗期抗青枯病鉴定

1987～1990年,全国育种攻关单位提供588份玉米杂交种,自交系进行成株期抗病性鉴定,对其中表现成株期抗病的232份材料进行苗期接种鉴定,苗期仍表现抗病的66份,占28.4%;人工接种苗期发病均重于成株期,用苗期鉴定基本可替代成株期抗病性鉴定。     

水稻对白叶枯病的成株抗性

有些水稻品种对白叶枯病(Xanthomonas campestris pv.oryzae)的侵染表现出成株期抗性,其植株在苗期感病,随着植株成长由感病转为抗病。13个有成株抗性的品种中,有些能抗供试的4个菲律宾小种,而另一些只对1或2个小种有成株抗性。菌系与品种间互作较强,表明有些水稻品种对白叶枯病的成株抗性似乎属“小种专化”。抗性转变的情况多种多样,有些品种从苗期到孕穗期逐渐由感病转为抗病,另一些品种从感病转向抗病的界限非常明显。不同品种对同一菌系的转抗叶位不同,同一品种对不同菌株的转抗叶位也不一样。具有 Xa-6基因的品种的成株抗性仍表现稳定。高温对感病品种和成株抗性品种在转抗以前的感病阶段的病情发展有促进作用。具有 xa-5基因的 IR1545-339在高温下仍然有其鉴别抗性反应,对其有致病力的小种4的病情类似TNI。     

玉米矮花叶病的抗性遗传分析

以玉米自交系X178和B73杂交培育的183个重组自交系为试验材料,采用人工接种的方法,在苗期、拔节期、抽雄期和成株期进行了玉米矮花叶病的抗性鉴定.结果表明,183份重组自交系之间对玉米矮花叶病的抗性存在着较大的差异,在抽雄期和成株期各有3个高抗的超亲分离;苗期和拔节期的病株率均呈现正态分布,抽雄期和成株期则表现为感病家系较多的偏态分布,且家系病株率的变异系数随生长发育变得越来越小,但抗性遗传力则越来越大.说明对玉米矮花叶病的抗性鉴定在成株期较准,苗期受环境影响较大;成株期的抗性由2～3对主基因控制,同时存在多基因修饰或互作;抗性基因之间以加性效应为主.     

云南小麦品种（系）锈病和赤霉病抗性功能基因的KASP标记检测

利用5个锈病成株期抗性基因的KASP标记Sr2_ger9 3p、Lr34jagger、CSTM4_67G、Lr68-2、VPM_SNP和抗赤霉病基因Fhb1的KASP标记TaHRC-KASP,对云南省育成的42个小麦品种（系）进行检测,旨在筛选出含有目标基因的优异小麦种质,为云南省持久抗病小麦新品种（系）的选育提供材料。结果表明,4个材料含兼抗型成株抗锈病基因Lr34/Yr18/Sr57,频率为9.52%;6个品种（系）含兼抗型成株抗锈病基因Lr67/Yr46/Sr55,频率为14.29%;7个材料含抗慢叶锈病基因Lr68,频率为16.67%;含兼抗型成株抗锈病基因Sr2/Yr30和成株抗叶锈基因Lr37的材料各有1个,频率均为2.38%;未检测出含抗赤霉病基因Fhb1的品种（系）。云麦69、云麦75、云麦56、宜麦1号和宜麦3号等兼有2个成株期抗锈病基因,可作为今后云南持久抗锈病育种的抗源材料。     

不同黄瓜材料对枯萎病的抗性评价

以危害我国黄瓜的优势枯萎病生理小种4为供试菌源,运用室内苗期人工接种和田间成株期病圃检测2种方法对43份黄瓜材料进行了枯萎病的抗性评价,苗期接种筛选出抗病材料7份,中抗材料16份,感病和高感材料20份。其中抗(含中抗)材料占53.5%,感病材料占46.5%。欧洲血缘的抗病(中抗以上)材料占39.5%;华北和日本血缘的抗和中抗材料占13.9%。成株期田间病圃的鉴定结果与苗期接种基本一致,符合率达86.7%。说明苗期接种结果准确,接种方法可靠。同时还表明了黄瓜种质资源中蕴藏着对改良枯萎病抗性有利用价值的基因资源,其中欧洲黄瓜抗源较丰富,华北和日本类型的黄瓜枯萎病抗源相对匮乏。     

78份四川小麦育成品种(系)条锈病抗性鉴定与抗条锈病基因分子检测

四川省是小麦条锈菌新小种产生的重要地区之一,了解2016年以来四川小麦育成品种(系)对当前流行的条锈菌生理小种和致病类型的抗性水平以及明确其抗条锈病基因的分布状况,可为四川育种防控小麦抗条锈病和品种布局提供理论依据。本研究选择2个小种CYR32和CYR34对78份四川小麦育成品种(系)进行苗期鉴定,利用当前小麦条锈菌优势小种CYR32、CYR33、CYR34,以及贵22-14、贵农致病类群等混合菌进行成株期人工接种鉴定,并利用19个抗条锈病QTL和基因QYr.nwafu-4BL、Yr5、Yr10、Yr15、Yr17、Yr18、Yr26、Yr28、Yr29、Yr30、Yr36、Yr39、Yr41、Yr48、Yr65、Yr67、Yr78、Yr80和Yr81的分子标记对供试材料进行抗条锈病基因检测。结果表明,在78份供试材料的苗期鉴定中,对CYR32表现出抗性的有60份,占76.92%;对CYR34表现出抗性的有40份,占51.28%;同时对CYR32和CYR34表现抗性的有36份,占46.15%。78份小麦品种(系)在成株期均表现抗条锈病,其中绵麦835、蜀麦1743、蜀麦1829和蜀麦1868表现为免疫。苗期和成株期抗病性鉴定结果表明,成株期抗性材料有42份,占53.85%;全生育期抗性材料有36份,占46.15%。分子检测结果表明,可能携带QYr.nwafu-4BL、Yr15、Yr17、Yr18、Yr26、Yr28、Yr29、Yr30、Yr39、Yr41、Yr65、Yr67、Yr78、Yr80和Yr81的材料分别有5、5、45、2、30、5、30、39、3、2、22、8、23、6和24份。同时携带2~6个抗条锈病基因的聚合材料分别有24、22、11、14和3份,占94.87%。所有供试品种(系)均未检测到Yr5、Yr10、Yr36和Yr48,仅西科麦18未检测到上述19个抗条锈病基因,可能携带其他已知或新的条锈病抗性基因。本研究鉴定了78份四川小麦育成品种(系)对条锈病抗性水平整体较好,明确了其携带的抗条锈病基因,为利用其培育持久抗性小麦品种提供了科学依据。     

小麦品种贵农21,贵农22抗病性研究

采用温室苗期测定和成株期人工诱发接种鉴定方法研究了簇毛麦——硬粒小麦杂种后代贵农21、22的抗病性。苗期抗性测定表明,贵农21、22对国外15个小麦条锈菌生理小种表现为免疫至近免疫反应,仅对具有毒性基因Yr10的菌系82E16表现出中度感病,对供试的国内14个主要条锈菌菌系呈观免疫至近免疫反应。田间成株期抗性试验结果显示,贵农21、22对小麦条锈病、白粉病免疫,高抗秆锈病,中抗叶锈病。小麦品种贵农21、22可作为抗病资源和生产品种加以推广应用。     

水稻抗稻瘟病基因Pi-ta和Pi-b多重PCR体系的构建与应用

稻瘟病是我国水稻主产区的重要病害之一, 其主效抗性基因Pi-ta和Pi-b在我国很多稻区表现广谱持久的稻瘟病抗性, 被广泛应用于我国的水稻育种和生产。本研究选用稻瘟病抗性基因Pi-ta和Pi-b及其等位基因的功能标记, 在对22份分别已知抗病基因Pi-ta和Pi-b以及感病基因pi-ta与pi-b组成的水稻品种检测验证基础上, 建立了2套稻瘟病基因多重PCR体系: 体系I同时检测抗病基因Pi-ta与Pi-b, 体系II 同时检测感病基因pi-ta与pi-b, 并利用2套体系对336份高世代育种材料进行检测, 与单标记检测结果比较, 表现稳定可靠, 重复性好。本研究构建的抗稻瘟病基因分子标记多重PCR体系可用于水稻种质资源的快速评价和抗稻瘟病分子标记辅助育种。     

苗期及灌浆期抗Bipolaris sorokiniana叶枯病小麦品种（系）鉴定及相关性分析

叶枯病对小麦生产危害严重,麦根腐平脐蠕孢菌（Bipolaris sorokiniana）是小麦叶枯病的主要致病菌。为筛选抗B. sorokiniana叶枯病小麦种质,采用“孢子液喷洒、套袋（罩）保湿”接菌鉴定的方法,于2019-2020年对130个小麦品种（系）进行苗期及灌浆期叶枯病抗性鉴定,同时分析了小麦苗期与灌浆期对B. sorokiniana叶枯病抗性的相关性。结果表明,130个小麦品种（系）中,苗期抗病材料占32.3%,其中高抗与中抗材料分别为1.5%与30.8%,无免疫材料;感病材料占67.7%,其中中感与高感材料分别为20.8%与46.9%;灌浆期抗、感叶枯病材料分别占11.5%与88.5%,无高抗材料;小麦苗期与灌浆期对B. sorokiniana叶枯病抗性呈显著正相关关系（r = 0.72）。此结果为抗B. sorokiniana叶枯病的遗传育种与抗病机理研究提供了优异的种质资源;基于苗期抗性与灌浆期抗性的显著相关性,可以通过室内快速准确的苗期叶枯病抗性鉴定预测大田条件下小麦灌浆期的抗性,节省时间,减轻大田鉴定繁重的工作量,并降低环境因素对鉴定结果的影响。     

14个小麦品种(系)抗叶锈性分析

选用16个小麦叶锈菌菌系对14个小麦品种(系)进行抗叶锈性鉴定和苗期抗叶锈基因推导,初步分析这些品种(系)的抗性和携带的抗病基因;进一步利用21个与Lr基因紧密连锁或共分离的分子标记,对这14个品种(系)中可能含的抗叶锈基因进行鉴定。结果表明,s98351-2-2-2-1可能含Lr3a、Lr28和Lr50;9629-03A-4-1-1可能含Lr37;97167-1-2-1-1-2-1、919-20-2c2、9589、免中438、9916-8-6和9916-8-18含Lr26;96104-1-5-1c2可能含Lr28;00-55-3-1-1含Lr1;1R13可能含Lr24、Lr37和Lr38;1R17可能含Lr24和Lr38;1R35含Lr10和Lr34,还可能含Lr3a和Lr50;9524-1-2-2-1含未知抗叶锈基因或本试验使用的已知抗病基因以外的抗叶锈基因。所有品种(系)均不含Lr9、Lr19、Lr20、Lr21、Lr29、Lr35、Lr42和Lr47基因。测试的14个品种(系)中有比较丰富的抗叶锈病基因,可为育种提供丰富的抗源。     

从美国引进的小麦抗锈品种的抗锈性测定和我国及美国小麦叶锈菌的毒性比较研究

1981年在河北农业大学温室分别用中国小麦叶锈菌4个小种360、376、377和60对从美国引进的13个抗锈品种进行了抗叶锈性测定,在河北省植保所田间进行了成株期对叶、条锈的抗性测定.1982年在美国堪萨斯州立大学温室分别用美国的小麦叶绣菌培养物PRTUS1、3、4、5、6、7、8、9、10、11、13和19对13个品种中的9个进行了抗叶锈性测定.苗期测定结果指出,其中3个品种Kans 63324,STW 646407和II-11996-4R-SM-1R对所测的中国小种都表现抵抗,但对美国的培养物大多数抵抗,而在所测的9个品种中没有对所有美国培养物都抵抗的.在对比两国之间中国小麦叶锈菌小种和美国小麦叶锈菌培养物的毒性时进一步指出,有些品种犹如LA1415,STW597725和STW597947对美国的少数培养物抵抗,而对所有的中国小种感染.田间试验用小麦条锈菌小种19和21接种指出品种NB61975、NB66523和STW597944对条锈是免疫的,NB61977和II-119966-4R-SM-1R是高抗的.     

小麦抗病基因同源序列(RGAs)的克隆与分析

RGA(抗性基因同源序列)法是克隆植物抗性基因的一种经济有效的方法,成为近年来的研究热点。本实验综合分析了拟南芥,西红柿,水稻,烟草等植物已克隆的抗性基因,并以这些抗性基因的NBS(核酸结合位点),LRR(富含亮氨酸重复),STK(丝氨酸/苏氨酸激酶)保守结构域设计并合成了几十对RGA引物,对小麦抗条锈病材料进行PCR扩增,获得以Xal-NBS为引物的R88RGA片段,经克隆和序列比对分析,发现该片段与逆境条件下植物抗病信号传导相关,与蛋白激酶同源性达到96%。此项研究对抗病机理的研究和基因的发掘有重要的指导意义。     

源于长穗偃麦草的小麦新品系CH7034抗白粉病基因的染色体定位

CH7034是一个兼抗小麦白粉病和条锈病的新种质材料,通过普通小麦与八倍体小偃麦"小偃7430"杂交、回交选育而成.为明确其白粉病抗性的遗传机制及抗性基因的染色体位置,用小麦高感品系"SY95-71"与CH7034杂交,所获F1、F2及其双亲在温室用白粉病E09菌系的15号小种接种,对CH7034的白粉病抗性进行鉴定和遗传分析.结果表明,无论是苗期还是成株期,CH7034对白粉病菌均表现为免疫,且具有与其抗性供体小偃7430及野生亲本长穗偃麦草相似的白粉病抗性,F1代抗病反应型为O或O'级,F2代抗感分离比符合R:S=3:1,说明CH7034抗性受显性单基因控制.用307对小麦微卫星引物对一个148株的F2群体进行分析,发现小麦微卫星标记xgwm311与抗病基因连锁,遗传距离为12.4 cM.用中国春缺-四体和双端体材料进一步验证与抗病相关的片段位于2A染色体的长臂上,进而将CH7034所含的抗白粉病基因定位于小麦的2AL上.     

Characterization of the durable resistance to yellow rust in old winter wheat cultivars in the Netherlands

Summary Winter wheat cultivars released in the Netherlands before 1930 carried durable resistance to yellow rust. Cultivars released in the period between 1930 and 1950 often were durably resistant while recent cultivars infrequently showed durable resistance. This durable resistance was not difficult to transfer to new cultivars. Twenty nine older cultivars with durable resistance and eight recent non-durably resistant cultivars were tested in the seedling stage and in the adult plant stage against 12 West-European yellow rust races and against some non-European races in the seedling stage only. The adult plant tests were carried out in race nursery tests in the Flevopolder. Per race nursery all 37 cultivars, planted in hills of about 20 plants on both sides of the highly susceptible cv. Michigan Amber, were exposed to one race.The infection type of each cultivar-race combination was scored on 0 to 9 scale once in the seedling stage and twice in the adult plant stage. In the race nurseries the percentage leaf area affected was evaluated three times to be used to calculate the area under the disease progress curve (AUDPC). This AUDPC multiplied with the mean infection type in the field gave the susceptibility index (SI).The infection types were classified into resistant (R), intermediate (I) or susceptible (S) when the infection types were 0 to 3, 4 to 6 or 7 to 9, respectively. Four categories of resistance were discerned on the basis of the three infection type scores: 1) RRR, overall resistance; complete or near-complete resistant at all stages. 2) SRR, adult plant resistance, complete- or near-complete resistant at the adult plant stage only. 3) SRS and SSR, temperature sensitive resistance, the resistance changed from the one evaluation data to the other. 4) SSS and an SI lower than that of Michigan Amber, partial resistance.The frequencies of overall, adult plant and temperature sensitive resistance were 1.4, 52 and 54% in the older cultivars and 40, 62 and 22% in the recent ones, respectively. Among the older cultivars all had a fair to high level of partial resistance, the SI being on average only 20% of that of Michigan Amber, while most cultivars also seemed to carry temperature sensitive resistance. The partial resistance of the recent cultivars was of a much lower level with a mean SI compared to that of Michigan Amber of 61%. Partial resistance was highly correlated (r = –0.94) with the mean resistance scores from the Dutch Recommended Cultivars Lists. It was concluded that partial resistance and temperature sensitive resistance were the major components of the durable resistance in the older cultivars.     

Level and Nature of the Resistance to the Cereal Aphid, Sitobion avenae (F.), in Thirteen Winter Wheat Cultivars

Thirteen winter wheat cultivars were tested under field and greenhouse conditions for resistance to the cereal aphid, Sitobion avenae (F.). Marked differences were recorded between cultivars in nonpreference (anti-xenosis), antibiosis and tolerance to aphids. Nonpreference was significantly (P < 0.001) correlated with antibiosis measured in terms of the biomass of aphids on naturally and nonsignificantly (P > 0.1) on artificially infested ears (criterion for cultivar antibiosis). Over all the cultivars, there was no correlation between nonpreference and tolerance and between antibiosis and tolerance to aphids.
Five cultivars expressed high level of resistance to S. avenae . The high resistance of three cultivars was due to high nonpreference and antibiosis, and only in two cultivars all three mechanisms contributed to resistance.     

山西省小麦主栽品种抗叶锈病研究

选用14个具有不同毒性基因组合的叶锈菌系，推导分析了来自山西省6个育种单位和种子部门的24个重要小麦品种所携带的抗叶锈病基因状况。在供试的44个已知抗叶锈病基因(或基因组合)中，推导出了Lr1，Lr3，Lr13，Lr23，Lr26，Lr30等6个抗叶锈病基因，以单基因或基因组合形式分别分布在19个小麦品种中，其中Lr1，Lr3，Lr26是供试材料的主要已知抗叶锈病基因。成株期抗病性鉴定结果表明，在24个供试品种中，仅有晋麦62号和鲁麦14号两个品种表现出对叶锈病良好的抗性，晋麦31号、晋麦56号和晋麦61号3个品种表现为中抗至中感(杂合类型)，晋春9号、晋春13号、晋偃746—9等12个品种具有慢叶锈病特征。     

New sources of resistance for stripe rust in barley

Eight spring barley accessions from the gene bank in Gatersleben, Germany, and 10 cultivars were tested for stripe rust resistance. Tests were performed at the seedling stage in the growth chamber and as adult plants in the field. All accessions and six cultivars were scored as resistant against race 24 under all test conditions, with very few plants as exceptions, while the susceptible control cultivars ‘Karat’ and ‘Certina’, and four other cultivars were attacked in all cases. Differences between accessions and between cultivars were detected after infection with isolates from ‘Trumpf’ and ‘Bigo’ (seedling tests only). Infection structures within seedling leaves without pustules and for the first time within leaves of adult plants from the field were analysed by fluorescence microscopy. With this method additional genetic Differences in the resistance reaction could be detected which could not to be seen in the resistance test. Crosses between the accessions and the susceptible cultivar ‘Karat’ led to segregating F₂ progenies. The percentage of resistant plants varied between the accessions. This also indicates a different genetic basis of resistance in the accessions. The infection structures observed by fluorescence microscopy stopped earlier in leaves of the two accessions HOR 8979 and HOR 8991 than in leaves of other accessions in all the tests. These accessions were the only ones with more than 50% resistant plants in all F₂ tests. In general, the accessions from the gene bank can be used as new resistance sources against stripe rust.     

Seedling and adult plant resistance to yellow rust in Iranian bread wheats

In order to evaluate wheat response to yellow rust, 25 advanced, promising and commercial bread wheat cultivars were tested as seedlings in greenhouse conditions in Karaj, Iran, and as adult plants in field conditions at four locations. Five pathotypes of yellow rust, 14E176A⁺, 134E142A+, 6E210A+, 4E128A- and 64E146A+ prevailing in field test locations, were used in the seedling tests. The results showed that some of the cultivars have seedling or overall resistance to the pathotypes and some have adult plant resistance. Cultivars M-70-4 and MV17 were resistant to all pathotypes as seedlings and showed good adult plant resistance. This revised version was published online in August 2006 with corrections to the Cover Date.