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1.
Summary Horizontal, uniform, race-non-specific or stable resistance can be discerned according to Van der Plank, from vertical, differential, race-specific or unstable resistance by a test in which a number of host genotypes (cultivars or clones) are tested against a number of pathogen genetypes traces of isolatest. If the total non-environmental variance in levels of resistance is due to main effects only differences between cultivars and differences between isolates) the resistance and the pathogen many (in the broad sense) are horizontal in nature. Vertical resistance and pathogenicity are characterized by the interaction between host and pathogen showing up as a variance compenent in this test due to interaction between cultivars and isolates.A host and pathogen model was made in which resistance and pathogenicity are governed by live polygenic loci. Within the host the resistance genes show additivity. Two models were investigated in model I resistance and pathogenicity genes operate in an additive way as envisaged by Van der Plank in his horizontal resistance. Model II is characterized by a gene-for-gene action between the polygenes of the host and those of the pathogen.The cultivar isolate test in model I showed only main effect variance. Surprisingly, the variance in model II was also largely due to main effects. The contribution of the interaction to the variance uppeared so small, that it would be difficult to discern it from a normal error variance.So-called horizontal resistance can therefore be explained by a polygenic resistance, where the individual genes are vertical and operating on a gene-for-gene basis with virulence genes in the pathogen. The data reported so far support the idea that model II rather than model I is the realistic one.The two models also revealed that populations with a polygenic resistance based on the gene-for-gene action have an increased level of resistance compared with the addition model, while its stability as far as mutability of the pathogen is concerned, is higher compared to those with an additive gene action. Mathematical studies of Mode too support the gene-for-gene concept.The operation of all resistance and virulence genes in a natural population is therefore seen as one integrated system. All genes for true resistance in the host population, whether they are major or minor genes are considered to interact in a gene-for-gene way with virulence genes either major or minor, in the pathogen population.The models revealed other important aspects. Populations with a polygenic resistance based on a gene-for-gene action have an increased level of resistance compared to populations following the addition model. The stability, as far as mutability of the pathogen is concerned, is higher in the interaction model than in the addition model.The effect of a resistance gene on the level of resistance of the population consists of its effect on a single plant times its gene frequency in the population. Due to the adaptive forces in both the host and the pathogen population and the gene-for-gene nature of the gene action an equilibrium develops that allows all resistance genes to remain effective although their corresponding virulence genes are present. The frequencies of the resistance and virulence genes are such that the effective frequencies of resistance genes tend to be negatively related to the magnitude of the gene effect. This explains why major genes often occur at low frequencies, while minor genes appear to be frequent. It is in this way that the host and the pathogen, both as extremely variable and vigorous populations, can co-exist.Horizontal and vertical resistance as meant by Van der Plank therefore do not represent different kinds of resistances, they represent merely polygenic and oligogenic resistances resp. In both situations the individual host genes interact specifically with virulence genes in the pathogen. Van der Plank's test for horizontal resistance appears to be a simple and sound way to test for polygenic inheritance of resistance.The practical considerations have been discussed. The agro-ecosystems should be made as diverse as possible. Multilines, polygenic resistance, tolerance, gene deployment and other measures should be employed, if possible in combination. 相似文献
2.
H. T. Wiersema 《Euphytica》1955,4(3):197-205
Summary Scorch is a soilborne disease of flax which as far as known only occurs in the Netherlands, Belgium and Northern France. Due to the publication of Marchal (1900) the fungus Asterocystis radicis
de Wild had for a long time been considered as the causal organism. In later years, however, Dutch investigators (v. d. Meer, 1928, and Diddens, 1931) proved that the disease is caused by the fungus Pythium megalacanthum
de Bary and that Asterocystis is quite harmless to flax.The only way of controlling the disease has been the breeding of resistant varieties. As early as 1888 Prof. L. Broekema established that resistance occurs and attempted to raise scorch-resistant varieties. In later years also other investigators and breeders worked on the same problem.The breeding for flax scorch resistance forms part of the working programme of the S.V.P. (Foundation for Agricultural Plant Breeding). Though different isolates of the scorch-fungus were tested by the author, no physiological specialization was found. He evolved a laboratory method for investigating flax scorch resistance and studies the heredity of the resistance. On page 204 the resistance of some varieties is expressed n relative figures.It is attempted to promote breeding work of Dutch private breeders by providing them with resistant populations and lines.Vlasbrand is een bodemziekte welke, voor zoverre bekend, alleen voorkomt in Nederland, België en Noord-Frankrijk. Op grond van de publicatie van Marchal (1900) werd de schimmel Asterocystis radicis
de Wild lange tijd als de veroorzaker van deze ziekte beschouwd. In latere jaren bewezen Nederlandse onderzoeksters (v. d. Meer, 1928 en Diddens, 1931) echter dat de ziekte door de schimmel Pythium megalacanthum
de Bary veroorzaakt wordt en dat Asterocystis ongevaarlijk is voor vlas.Het kweken van resistente rassen vormt de enige mogelijkheid de ziekte te bestrijden. Prof. L. Broekema stelde reeds in 1888 vast, dat resistentie voorkomt en trachtte vlasbrand resistente rassen te kweken. In latere jaren legden ook anderen zich hierop toe.Het kweken op vlasbrand resistentie vormt een onderdeel van het werkprogramma van de S.V.P. Hoewel verschillende isolaties door de schrijver onderzocht zijn, werd geen physiologische specialisatie aangetroffen. Hij werkte een laboratoriummethode uit voor onderzoek op vlasbrandresistentie en bestudeert de erfelijkheid van de resistentie. Op blz. 204 is de resistentie van enige rassen in verhoudingscijfets uitgedrukt.Door de Nederlandse kwekers te voorzien met resistente populaties wordt getracht de kweekarbeid te bevorderen. 相似文献
3.
E. C. Roumen 《Euphytica》1992,64(1-2):143-148
Summary Six rice genotypes, differing in partial resistance, were exposed to three isolates of the blast pathogen. Of the variance due to host and pathogen genotypes, 39% was due to host genotype effects, 60% was due to isolate effects, and only 1% was due to host genotype × isolate interactions. Although small, this interaction variance was highly significant and mainly due to the IR50 × W6-1 and IR37704 × JMB8401-1 combinations. Although behaving largely as race-non-specific (large main effects only), the partial resistance cannot be classified as race-non-specific. The results suggest that minor genes for partial resistance operate in a gene for gene relationship with minor genes in the pathogen. 相似文献
4.
Breeding for resistance to lentil Ascochyta blight 总被引：1，自引：0，他引：1
Ascochyta blight, caused by Ascochyta lentis, is one of the most globally important diseases of lentil. Breeding for host resistance has been suggested as an efficient means to control this disease. This paper summarizes existing studies of the characteristics and control of Ascochyta blight in lentil, genetics of resistance to Ascochyta blight and genetic variations among pathogen populations (isolates). Breeding methods for control of the disease are discussed. Six pathotypes of A. lentis have been reported. Many resistant cultivars/lines have been identified in both cultivated and wild lentil. Resistance to Ascochyta blight in lentil is mainly under the control of major genes, but minor genes also play a role. Current breeding programmes are based on crossing resistant and high‐yielding cultivars and multilocation testing. Gene pyramiding, exploring slow blighting and partial resistance, and using genes present in wild relatives will be the methods used in the future. Identification of more sources of resistance genes, good characterization of the host‐pathogen system, and identification of molecular markers tightly linked to resistance genes are suggested as the key areas for future study. 相似文献
5.
6.
Pre-emptive breeding to control wheat rusts 总被引：1，自引：0，他引：1
R. A. McIntosh 《Euphytica》1992,63(1-2):103-113
Summary Pre-emptive or anticipatory breeding for resistance is breeding for resistance to future pathotypes. It is assumed that these will be derivatives of currently frequent pathotypes that need to mutate with respect to single host resistance genes in order to attack widely-grown cultivars. Success in this approach depends on relevant knowledge of the pathogenicity phenotypes and host resistance genes that occur throughout the wheat-growing areas. Because durability of resistance cannot be assumed, resistance breeding strategies are usually supported with the maintenance of genetic diversity to provide buffering against extreme crop losses in the event of significant pathogenic changes. 相似文献
7.
Summary It has been reported why resistance is needed in crop plants, how it has been searched for, and how long the resistance could be maintained in the host varieties. Uniform and differential resistance have been discussed and integrated within one genetic system. The possible evolution of both polygenes and major genes for resistance is discussed. Polygenes probably are older and produce the materials necessary for a host to show resistance, major genes acting as switching genes. Breeding for disease resistance has been briefly debated in connection with the discussion on host resistance. 相似文献
8.
Summary Resistance to parasites can be distinguished into true resistance and pseudo or escape resistance. In the former resistance mechanisms operate after intimate contact between the host tissue and the parasite has been established. The resistance is expressed by a reduced growth of the parasite in or on the host tissue. Escape resistances operate before the parasite has made contact with the host tissue and is expressed by a reduced chance of such contacts. True resistance genes are assumed to act in a gene-for-gene way with virulence genes in the parasite. Genes governing escape resistances are supposed to function independently from genes in the parasite (no gene-for-gene action). It is deduced, that escape resistances and polygenic true resistances both are of a horizontal nature. Vertical resistance is to be found in the category of monogenic true resistances. 相似文献
9.
稻瘟病菌无毒基因研究进展 总被引：2，自引：0，他引：2
水稻与稻瘟菌间存在广泛而特异的相互作用,是研究寄主与病原物互作的重要模式系统。无毒基因是病原物遗传因子,能诱发寄主植物产生抗病性,是稻瘟菌与水稻互作最重要的激发子。为寻求稻瘟病防治的新策略,本研究概述了研究稻瘟病菌无毒基因的意义,归纳了抗性基因与无毒基因互作的3种模式,总结了国内外稻瘟病菌无毒基因的克隆及功能研究,探讨了无毒基因在生产上病害流行预测中的应用,指出利用抗性基因与无毒基因的关系对稻瘟菌分类将会更为科学和实用,应进一步加快稻瘟病菌无毒基因的克隆。 相似文献
10.
David A.C. Pink 《Euphytica》2002,124(2):227-236
Strategies to deploy non-durable `major' or `R' genes for resistance to plant diseases are reviewed. The reasons for continuation
of deployment of R genes singly despite its obvious failure are discussed. Alternative deployment strategies are described
and the potential impact of plant biotechnology on the deployment of resistance genes is discussed. A strategy focusing on
the crop phenotype, taking into account production practices, the nature of the pathogen and alternative control measures
to determine the most appropriate deployment of host resistance genes is advocated.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
11.
Genes which confer partial resistance to the rusts in wheat figure prominently in discussions of potential durable resistance strategies. The positional cloning of the first of these genes, Lr34/Yr18 and Yr36, has revealed different protein structures, suggesting that the category of partial resistance genes, as defined by phenotype, likely groups together suites of functionally heterogenous genes. With the number of mapped partial rust resistance genes increasing rapidly as a result of ongoing advances in marker and sequencing technologies, breeding programs needing to select and prioritize genes for deployment confront a fundamental question: which genes or gene combinations are more likely to provide durable protection against these evolving pathogens? We argue that a refined classification of partial rust resistance genes is required to start answering this question, one based not merely on disease phenotype but also on gene cloning, molecular functional characterization, and interactions with other host and pathogen proteins. Combined with accurate and detailed disease phenotyping and standard genetic studies, an integrated wheat-rust interactome promises to provide the basis for a functional classification of partial resistance genes and thus a conceptual framework for their rational deployment. 相似文献
12.
Sources of Resistance to Powdery Mildew in Barley Lines Derived from Hordeum spontaneum Collected in Israel 总被引：1，自引：0，他引：1
Fourty two barley lines direved from the F7 of crosses between barley cultivars and different accessions of Hordeum spontaneum collected in Israel and 30 lines or varieties with known genes for resistance to powdery mildew were included m this study. Eleven European and three Israeli powdery mildew cultures, possessing virulence genes corresponding to known resistance genes, were used to make comparisons between the varieties with known resistance genes and H. spontaneum derived lines. The reaction pattern of 39 H. spontaneum derived lines was clearly different from the reaction pattern o; any of the known genes for mildew resistance included in this study. Only two cases were observed in which the reaction pattern of H. spontaneum derived lines agreed with reaction patterns of known genes for mildew resistance viz. Ml-a9 and Ml-p. Trie Mildew resistance of one line apparently traces back to uncontrolled outcrossing with a Ml-a.6+Ml-g resistant cultivar. Since the majority of the 42 host genotypes tested showed distinctive variation in resistant reaction types against different mildew cultures, this study docs not support the assumption that differences in resistant infection types against distinct mildew cultures are sufficient to indicate the presence of supplementary genes for resistance in a given genotype of the host. The results justify the conclusion that the natural population of H. spontaneum in Israel forms a large gene pool for mildew resistance which is not yet used m cultivated barley. 相似文献
13.
M. S. Hovmøller 《Plant Breeding》1989,103(3):228-234
Race specific powdery mildew resistance in 23 winter wheat cultivars, eight spring wheat cultivars, and 14 lines/cultivars possessing known powdery mildew resistance genes, has been studied by analyzing host/pathogen interactions. The cultivars were tested as intact seedlings, and as detached primary leaf segments on water agar; both methods revealed reproducible and concordant results. The 45 cultivars/lines were divided into 24 resistance spectra according to the patterns of reaction to the powdery mildew isolates used. Of the 31 cultivars investigated, eight did not possess any of the resistance genes detected, and the remaining 23 were divided in 16 resistance spectra. The race specific resistance of nine cultivars was conferred by the single resistance genes Pm2, Pm4b, Pm5/Ml-i: or Pm6, while the race specific resistance of 14 cultivars was conferred by 2, 3, 4 or 5 genes in combination. 相似文献
14.
寄主诱导的基因沉默(host-induced gene silencing,HIGS)以病原菌生长发育、产孢繁殖、侵染或致病过程中的关键基因作为靶点,在寄主植物中表达针对靶基因的RNAi构建体,在病原菌侵染植物的过程中,摄入相应的ds RNA或si RNA分子,通过识别、结合特异核苷酸序列,干扰病菌靶基因表达,从而抑制病菌侵染和扩展,使植物表现抗病。这项技术为培育基于病原菌特异序列的植物抗病性奠定了基础,显示了巨大的应用潜力。本文综述了利用HIGS技术提高植物真菌病抗性的最新研究进展,总结了国内外利用这项技术改良植物真菌病害抗性的主要策略、技术路线,展望了发展应用前景。 相似文献
15.
胡麻木酚素含量的全基因组关联分析 总被引：1，自引：0，他引：1
为了挖掘胡麻木酚素含量相关基因,本研究用269份胡麻种质的基因型数据和木酚素含量数据进行全基因组关联分析研究。呼和浩特、集宁、锡盟和新疆等4个环境下木酚素含量的统计分析表明:新疆伊犁地区种的269份胡麻种质平均木酚素含量为最大,变异系数依次排序为锡盟<呼和浩特<集宁<新疆,广义遗传力为60.67%。4个环境下胡麻种质木酚素含量均呈现正太分布的趋势。全基因组关联分析获得了13个显著SNP位点和21个候选基因,为胡麻分子标记辅助育种以及高木酚素含量新品种选育提供科学依据。 相似文献
16.
重要胡麻栽培品种的抗旱性综合评价及指标筛选 总被引：13，自引：0，他引：13
以15份国内胡麻栽培品种为材料, 设自然降雨和正常灌水2个处理, 考察与抗旱性相关的7个农艺性状、8个生理生化指标及产量指标, 采用综合抗旱系数、因子分析、隶属函数、聚类分析和灰色关联度分析相结合的方法, 对其抗旱性进行综合评价、抗旱型划分和评价指标筛选。结果显示, 相关性状指标对干旱胁迫的反应及关联程度各异, 可优先选择与抗旱性关系密切的产量及其相关性状、光合作用因子、叶片抗氧化因子等相关生理生化性状;因子分析表明, 6个公因子可代表胡麻抗旱性90.89%的原始数据信息量。基于抗旱性度量值(drought resistance comprehensive evaluation values, D值)和加权抗旱系数(weight drought resistance coefficient, WDC值)的各品种抗旱性排序相近, 位居前6位的抗旱品种相同。各品种D值与综合抗旱系数(comprehensive drought resistance coefficient, CDC值)、WDC值、产量抗旱系数(yield drought resistance coefficient, Y值)之间均呈极显著正相关, 而各品种Y值与CDC、WDC值间极显著正相关;据D值将供试品种划分为5个抗旱级别, 可较好地反映品种的选育条件及适应地区。试验结果说明以D值为主要参数, 以WDC为辅助评价参数, 评价以产量为主要考量目标的胡麻抗旱性是适宜且准确的;以抗旱性综合评价方法进行胡麻抗旱性综合评价、抗旱型划分、评价指标筛选是准确的。 相似文献
17.
Present status of genetics of rust resistance in flax 总被引：5，自引：0，他引：5
Summary Present knowledge of host genes conferring resistance to rust in flax and their genetics are reviewed. There are at least 34 genes conferring resistance to rust occurring in seven groups, namely, K, L, M, N, P, D and Q. Expression of these host genes is affected by temperature, genetic background and by the inhibitor gene present in certain rust strains. Recombination analysis indicates that genes within each of the M and N groups are probably closely linked and that of the L group are genetically complex. When testcross progeny between two genes of the L group were screened, susceptible and modified recombinants were recovered. Some of these susceptible recombinants yielded rare resistant revertants in their progeny. Mechanism of such reversion is not defined but appears to follow a definite pattern. It is also indicated that some of the recombinants represent new specificity. A molecular approach of cloning host genes in flax is described. 相似文献
18.
Durability of resistance against fungal, bacterial and viral pathogens; present situation 总被引：8，自引：0，他引：8
Jan E. Parlevliet 《Euphytica》2002,124(2):147-156
In evolutionary sense no resistance lasts forever. The durability of a resistance can be seen as a quantitative trait; resistances
may range from not durable at all (ephemeral, or transient) to highly durable. Ephemeral resistance occurs against fungi and
bacteria with a narrow host range, specialists. It is characterised by a hypersensitive reaction (HR), major gene inheritance and many resistance genes, which often occur
in multiple allelic series and/or complex loci. These resistance genes (alleles) interact in a gene-for-gene way with a virulence
genes (alleles) in the pathogen to give an incompatible reaction. The pathogen neutralises the effect of the resistance gene
by a loss mutation in the corresponding avirulence allele. The incompatible reaction is not elicited any more and the pathogenicity
is restored. The pathogens can afford the loss of many avirulences without loss of fitness. Durable resistance against specialised
fungi and bacteria is often quantitative and based upon the additive effects of some to several genes, the resulting resistance
being of another nature than the hypersensitive reaction. This quantitative resistance is present to nearly all pathogens
at low to fair levels in most commercial cultivars. Durable resistance of a monogenic nature occurs too and is usually of
a non-HR type. Resistance against fungi and bacteria with a wide host range, generalists, is usually quantitative and durable. Resistances against viruses are often fairly durable, even if these are based on monogenic,
race-specific, HR resistances. The level of specialisation does not seem to be associated with the durability of resistance.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
19.
Downy mildew on lettuce is currently controlled using host resistance genes (Dm genes) that confer race-specific resistance in seedlings. Field resistance (FR) that is active in adult plants but not seedlings was identified in the cvs. Grand Rapids and Iceberg. The goal of our study was to evaluate the utility of Grand Rapids as a source of novel Bremia resistance alleles, particularly in comparison with Iceberg. To measure FR, downy mildew symptoms were evaluated following natural infection in field experiments. The responses of Grand Rapids and Iceberg were similar in many respects. Although both cultivars had a small percentage of plants exhibiting disease symptoms, the average disease ratings were as low as for cultivars with effective Dm genes. We observed no evidence for race specificity. FR was effective over 3 years of our study, despite documented variation within pathogen populations. Both cultivars lacked all known seedling resistance genes except Dm13, which was not responsible for the resistance observed in field experiments. Similar segregation of FR was observed in F2 populations for both Grand Rapids and Iceberg. The presence of highly susceptible families within Grand Rapids × Iceberg populations suggested the presence of at least one unique resistance allele in each cultivar. Preliminary genetic analysis of FR from Grand Rapids revealed a high estimate of narrow-sense heritability that suggested simple inheritance, but single gene models did not fit the observed data. Our results suggest that Grand Rapids may represent an underutilized resource for controlling downy mildew in lettuce. 相似文献
20.
Aphis glycines Matsumura, the soybean aphid, first arrived in North America in 2000 and has since become the most important insect pest of domestic soybean, causing significant yield loss and increasing production costs annually in many parts of the USA soybean belt. Research to identify sources of resistance to the pest began shortly after it was found and several sources were quickly identified in the USDA soybean germplasm collection. Characterization of resistance expression and mapping of resistance genes in resistant germplasm accessions resulted in the identification of six named soybean aphid resistance genes: Rag1, rag1c, Rag2, Rag3, rag4, and Rag5 (proposed). Simple sequence repeat markers flanking the resistance genes were identified, facilitating efforts to use marker-assisted selection to develop resistant commercial cultivars. Saturation or fine-mapping with single nucleotide polymorphism markers narrowed the genomic regions containing Rag1 and Rag2 genes. Two potential NBS-LRR candidate genes for Rag1 and one NBS-LRR gene for Rag2 were found within the regions. Years before the release of the first resistant soybean cultivar with Rag1 in 2009, a soybean aphid biotype, named biotype 2, was found that could overcome the resistance gene. Later in 2010, biotype 3 was characterized for its ability to colonize plants with Rag2 and other resistance genes. At present, three biotypes have been reported that can be distinguished by their virulence on Rag1 and Rag2 resistance genes. Frequency and geographic distribution of soybean aphid biotypes are unknown. Research is in progress to determine the inheritance of virulence and develop DNA markers tagging virulence genes to facilitate monitoring of biotypes. With these research findings and the availability of host lines with different resistance genes and biotypes, the soybean aphid-soybean pest-host system has become an important model system for advanced research into the interaction of an aphid with its plant host, and also the tritrophic interaction that includes aphid endosymbionts. 相似文献