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The inheritance and durability of scab resistance in apple progenies
Published August 12, 2005

In order to select the appropriate parent cultivars and maintain the durability of resistance, it is important to clarify the mechanisms of inheritance of scab resistance depending on the parents. It has been known that the progeny segregation ratios based on scab-resistance do not depend only on the genotype of the resistance locus but also on... the genetical makeup of the donor and recipient parents as well as on the susceptible parent.

The aim of this study has been to demonstrate what factors in the Vf, Vr and VA scab-resistant cultivars — combined with susceptible and resistant parents — affect the inheritance and durability of resistance in seedlings in their first 4 year's growing four years' growth. After inoculating apple seedlings sown in 2001 with the suspension of Venturia inaequalis (Cke.) Wint. in the greenhouse, we studied the segregation ratios of the progenies into reaction classes. Seedlings showing resistance in the greenhouse were also evaluated for scab-resistance after they had been moved to the field and had naturally been infected with the pathogen in 2002 and 2004.

The majority of our results obtained in the greenhouse test, similarly to earlier experiences, have not justified monogenic inheritance at the phenotypic level. The effect of susceptible parent cultivars on the segregation ratio of progenies have become apparent again. The high infection rate of seedlings in the field trials, which had previously exhibited varying degrees of resistance in the greenhouse test, has raised concern. Our data has raised further doubts, concerning the durability of Vf resistance in Hungary. It is assumed that the composition of natural field populations of Venturia inaequalis in Szigetcsép has changed. The complexity of Vf resistance has been confirmed. The high infection rate in the progenies derived from Vf resistant cultivars draws the attention to the importance of utilizing additional sources of resistance.

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Scab resistance in Malus sp. progenies - inheritance and resistance stability
Published April 14, 2003

Susceptibility of progenies of some Ma/us species to apple scab was evaluated. Susceptibility of hybrid families was observed first in greenhouse after artificial inoculations by the suspension of the pathogen, Venturia inaequalis (Cooke) Wint., then in open field. The Hungarian type of Malus floribunda, which proved be scab resistant in our examinations, has a positive effect on the segregation of progenies to resistant and susceptible individuals as a male parent, not depending on the rate of susceptibility of the other parent. However, the German type of Malus floribunda and Malus prunifolia act as dominant, highly susceptible parents.

Malus x purpurea and Malus baccata, which proved to be highly susceptible to apple scab in open field and in artificial inoculations, transmits its susceptibility only slightly to its progenies as a male parent.

According to our experiments, the inheritance of scab resistance of Malus floribunda cannot be considered as monogenic, as published by other authors.

Scab susceptibility of parents influences the segregation of progenies to resistant or susceptible individuals. The moderately scab susceptible `Idared' as female parent has a statistically proved positive effect on the segregation of its progenies.

More factors indicate the appearance of a new race of Venturia inaequalis (Cke.) Wint.: change of the symptoms in the greenhouse; considerable increase of susceptible individuals after greenhouse inoculation in 1997; more and more progenies of the male parent Malus floribunda became susceptible to scab in open field.

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The genetic background of resistance to common bacterial blight in newly identified common bean lines on the basis of inheritance studies
Published February 23, 2000

Common bacterial blight (CBB), caused by Xanthomonas campestris pv. phaseoli (Xcp). is a major disease problem of common bean (Phaseolus vulgaris L.). The inheritance of resistance in Xrl and Xr2 lines to two isolates of Xcp was studied in the F2 and F3 popu­lations from the crosses between these lines and the Masay ...variety (susceptible to Xcp). Segregation patterns indicated that different single recessive genes presumably in coupling phase linkage determined the resistance to the HUN and EK-1 1 strains of Xcp in both lines. The presence of some minor, modifying genes beside the monogenic genetic background of resistance was also observed. Xrl and Xr2 lines represent valuable new monogenic genetic sources in resistance breeding to CBB.

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Inheritance of male sterility in apricot
Published September 11, 2001

Progenies (total of 1,114 seedlings) from crosses representing all possible genotypic combinations between 4 male-fertile and 1 male-sterile apricot parents were scored for the male sterility trait. Crosses between putative heterozygous normal cultivars yielded 25% of male-sterile seedlings, which supports a previous hypothesis that male steril...ity is controlled by a recessive allele of one nuclear locus. Crosses between those parents and putative homozygous normal cultivars did not produce any male-sterile tree. Finally, the proportion of male-sterile progeny in crosses between a male-sterile and two male-fertile cultivars depended on the genotype of the male parent. When it was heterozygous approximately 50% of the progeny was sterile, whereas when a homozygous fertile parent was used, no male-sterile progeny was obtained. These results confirm a previously proposed model, in which the male sterility trait in apricot is controlled by a single recessive gene.

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Inheritance of blooming time in walnut, with regard to the property of reproductional autoregulation of species
Published February 23, 2000

A great number of crosses have been made with Hungarian and foreign varieties as partners to breed improved varieties. This species shows a particular trait, namely the autoregulation of fruit set, which affects considerably the productivity of commercial orchards. Thus the inheritance of the blooming time of the male and female flowers has bee...n explored for several years in the progenies.

It has been stated that

- the feature of the partners does not turn up predictably in the progeny,

- it is most important to take into consideration the blooming time class of both, male and female flowers in planning associations of varieties for commercial orchards.

- in years of irregular spring weather the stability of the blooming time of the variety or in other words the deviation of the actual blooming time of variety from its characteristic blooming-time class is also very important.


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Inheritance of fruit colour and of shoot's pigmentation in the case of interspecific raspberry hybrids
Published May 18, 2005

In our research, fruit colour and the shoot's red pigmentation were evaluated in the hybrids of Rubus idaeus and Rubus parvifolius crossings. Y and Ys genes beside the T genes determine the fruit colour of interspecific hybrids, which is characteristic for raspberry. For the explanation of the significantly higher results of s...egregation then expected at the yellow fruit colour hybrids, we have supposed the presence of a second yellow gene (Y2). In the yellow colour, a lot of different shade colours can be identified from light yellow to the apricot colour. In the regulation of the production of yellow and red colour, several other genes can participate also. Identification of these genes would require more additional research. The C gene determines the shoot colour of raspberry and in the case of wild raspberries we have revealed the role of a dominant Pr gene. The Y and Pr genes are descended linked. The value of crossing over is approximately 15%. The anthocyanin production inhibitory effect of the Y gene extends only for fruit. At the shoots of yellow fruit plants, strong anthocyanin production was observed.

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General defense system in the plant kingdom III.
Published October 16, 2002

Our observations regarding the symptoms not fitting into, significantly differing from the hypersensitive defense system, which we noticed during the judgment of several plant species, symptoms provoked on several million plants have constituted a unified entity. They have provided evidence for the existence of a different plant defense system.... We called this so far unknown basic response of plants to biotic effects as general defense system. This system defends them from the attack of numerous microbe species in the environment.

The evolutionary intermediate phase between the general and the specific, the two defense systems is the susceptible host—pathogen relation. The vertical resistance system of plants escaping from the susceptible host—pathogen relation, based on specific hypersensitive reaction also suggested the existence of a more original, general defense system and the susceptible host—pathogen relation developed as a result of the collapse of that system.

The evolutionary relation of the two defense systems is proved by the only recessive inheritance of the older general defense system and in the majority of cases dominant hereditary course of the specific defense system. In our experiences, the modifying genes of the recessive general defense system, in most cases, are behind the specific defense systems, which are known to have monogenic dominant hereditary course and react with hypersensitive tissue destruction. This seemingly striking genetic fact is explained by the following: the general defense system less dependent on environmental effects regulates much faster pathophysiological reaction than the specific resistance genes strongly dependant on environmental effects coding dominant hypersensitive reaction.

The general and specific defense reactions, the processes excluding the microbes attacking plants with compacting of cell growth and tissue destruction, which mean two opposite strategies, building on and regulating each other constitute the entity of resistance to plant disease.

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General defense system in the plant kingdom
Published March 21, 2001

The goal of plant breeders is to improve the resistance of crops against virus, bacterium and fungus pathogens was easiest to achieve by selection for phenotypes displaying the hypersensitive reaction. The resistant plant of that type keeps its health by preventing or delaying the systemization of the pathogen by destruction of cells a...nd tissues of variable size or amputation of the contaminated organs. The faster the reaction of the host plant is the more efficient and economical is the defense, since the extent of tissue destruction decreases proportionally with the speed of reaction.

During a breeding program for resistance carried out on several plant species, mainly vegetables over thirty years, also an alternative defense reaction has been experienced, which fundamentally differs from the hypersensitive reaction. In that reaction the cells and tissues of the host plant being exposed to the pathogen do not die, on the contrary they hinder systemization of the pathogen by tissue thickening. An additional significant difference is that on the contrary to hypersensitive reaction this reaction is less host- or pathogen-specific and works excellently even at high temperature (over 40 °C).

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Inheritance of the characters related to flower formation, blooming and fertilisation in apple
Published September 13, 1999

On the base of observations performed during a period of 20 years the blooming characters-of apple varieties and their progenies the following statements are actual.

In blooming dynamics there was no difference between paternal and maternal effects. In the assignment to blooming time groups, the paternal effect prevailed wher...eas in the tendency of flower initiation on long shoots maternal parent was more decisive. Varieties as 'Golden Delicious'. 'Jonathan', 'Red Delicious', 'Rome Beauty' and 'Staymared' and their respective, naturally raised mutants did not differ in blooming characters.

The possibility of predicting the relation to blooming time groups of early (July, August) ripening individuals is low, whereas late (September. October) ripening ones have a good chance to be medium late in blooming time.


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