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Journal of Biomedicine and Biotechnology
Volume 2009 (2009), Article ID 680160, 10 pages
http://dx.doi.org/10.1155/2009/680160
Review Article

The Venturia Apple Pathosystem: Pathogenicity Mechanisms and Plant Defense Responses

Biotechnology Division, Institute of Himalayan Bioresource Technology, Council of Scientific and Industrial Research, Palampur 176061, Himachal Pradesh, India

Received 27 March 2009; Revised 10 August 2009; Accepted 29 October 2009

Academic Editor: Sudhir Kumar Sopory

Copyright © 2009 Gopaljee Jha et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Venturia inaequalis is the causal agent of apple scab, a devastating disease of apple. We outline several unique features of this pathogen which are useful for molecular genetics studies intended to understand plant-pathogen interactions. The pathogenicity mechanisms of the pathogen and overview of apple defense responses, monogenic and polygenic resistance, and their utilization in scab resistance breeding programs are also reviewed.

1. Introduction

Apple scab also known as black spot, caused by Venturia inaequalis (Cke.) Wint. is one of the most serious diseases of apple reported from almost all apple producing countries and causes huge economic losses (up to 70% reduction in apple production) [1, 2]. Scab infection leads to deformation in shape and size of the fruits, premature leaf and fruit fall, and enhances susceptibility of tree to chilling and freezing injuries. The oldest available report of scab is in the year 1819 by a Swedish scientist, Fries, however, apples showing scab symptoms are depicted in paintings of sixteenth century, suggesting existence of the disease at that time [3]. The pathogen has been placed into genus Venturia by Winter in 1880. These historical accounts and its taxonomy have been reviewed by MacHardy [2]. V. inaequalis is a heterothallic fungus and contains seven haploid chromosomes [4]. Fusicladium dendriticum and Spilocaea pomi are its anamorphs. Alike other obligate parasites, it generally infects and lives in association with living tissues. However, an ability to be cultured on laboratory medium, possibility of in vitro mating, existence of extensive population diversity, uninucleate conidia, genetically uniform progenies, stability of genotype and phenotype of the progeny even after multiple rounds of subculturing, and availability of standardized protocol for genetic manipulation, and so forth, make it a useful model to study the pathogenesis of obligate fungal pathogens which are generally not culturable. The ease of isolation of ascospores produced by a single meiotic event and their presence in a specific order in which they are produced [4] are the useful features for segregation analysis, centromere mapping, and understanding the processes of fungal meiosis. Furthermore, V. inaequalis and Apple provide an interesting system to study the molecular interactions of a fungal pathogen and a woody host. During the course of co-evolution, V. inaequalis has accumulated various pathogenic attributes (genes) that play a crucial role in invasion without causing much damage to apple [3]. Similarly, apple has evolved mechanisms to prevent severity of the disease. In this review, we summarize the recent literature about the life cycle, pathogenicity mechanisms, nutritional requirements, and hypervariability amongst races of V. inaequalis. The apple defense/resistance mechanisms and their prospects in scab resistance breeding are also discussed.

1.1. V. inaequalis Life Cycle and Pathogenicity

V. inaequalis primarily causes disease on apple cultivars, however, it also infects Malus (Crabapple), Cotoneaster integerrima, Crataegus oxycantha (Hawthorn), Loquat, Pyracantha (Firethorn), Sarcocephalus esculantus, Sorbus (Mountain Ash), and Viburnum. The characteristic disease symptoms on apple include circular olive green velvety, necrotic or chlorotic lesions single or scattered on leaf surface, olivaceous spots on infected sepals and pedicels, and dark colored sharply bordered brown and corky lesions on young fruits while small black spots termed as “pin-point scab” on the matured fruits. The disease symptoms on the fruit and leaf are depicted in Figure 1. Light brown blisters surrounded by whitish rings constitute the symptoms on infected twigs. However, sometimes during severe infections peeling of bark from the twigs occurs which is known as grind or scurf.

fig1
Figure 1: Symptoms of Apple Scab disease. (a) The dark colored sharply bordered, brown, and corky lesions are apparent on the infected apple fruit. (b) Scattered, olivaceous green and velvety, chlorotic sporulating lesions are observed on the infected leaf.

V. inaequalis produces sexual and asexual spores, both capable of infecting apple. The pathogenic phase of disease starts with germination of ascospores (sexual spore) which serve as primary source of inoculum. Conidia, the asexual spores, are smooth, 0-1 septate, obpyriform to obclavate in structure, pale to mid-olivaceous brown in color, generally disseminated by wind or splashing rain, and serve as source of secondary infections [2]. Several cycles of conidia production and secondary infections take place within a single growing season of apple. At the beginning of winter, with the onset of leaf fall, the mycelium penetrates a bit deeper into leaf tissues and switches from vegetative to reproductive phase wherein the mycelia of two different mating types undergo sexual reproduction (mating). Following mating, a pseudothecium is produced which exhibits negative geotropism [5]. The asci of V. inaequalis are bitunicate, cylindrical, double walled, and loculus. The ascospore consists of two unequal sized cells having thin brittle outer wall and a thick elastic inner wall which assists persistence of the pathogen during winter [2]. The fungi primarily perenate on fallen leaves, however perenation on twigs and fruits is also reported but in such cases ascospores are not produced and the conidia serve as primary inoculum. The ascospores mature at the time of apple bud break during which host tissues are most susceptible. Once matured, the ascospores are released from the asci and get disseminated by rain and wind. Interestingly, the presence of light is required for optimal discharge of the ascospores [3, 6]. This and several other favorable pathogenic attributes of V. inaequalis are reviewed by MacHardy et al. [3].

In order to colonize and establish disease, the pathogen needs to adhere, germinate, and form infection structures to penetrate the host. The conidia/ascospores of V. inaequalis attach to wet hydrophobic surface of apple and germinate by producing germ tubes, generally formed from the apical end of conidia or any of the two cells of the ascospore. V. inaequalis enters the host through cuticle but not through stomata [2]. Upon contact with cuticle, germ tube gets differentiated into an appressorium and produces adhesive mucilaginous substances predicted to facilitate attachment to the host surface [7]. The mucilaginous substances are composed of proteins and carbohydrates such as -galactose and N-acetylglucosaminyl residues [8]. The presence of melanized ring at the base of growing appressorium is essential for successful pathogenesis [9]. However, Fitzgerald et al. [10] by silencing one of the melanin biosynthesis genes have observed that mutant exhibiting light brown phenotype is capable of infecting apple. Based upon the light brown phenotype associated with the mutant, it can be speculated that the mutant might still be producing melanin sufficient enough for successful pathogenesis. Application of mechanical pressure is not apparent during cuticle penetration [7]. It is hypothesized that the pathogen uses enzymatic hydrolysis to breach cuticle (Table 1). Extracellular cutinases are produced by germinating conidia and mycelium [11, 12]. The observations that treatment of a specific cutinase inhibitor could prevent subcuticular growth and penetration of cuticle by the pathogen further corroborate the role of cutinase in host entry [11]. Esterase-like activity has been reported transiently during germination of conidia, which possibly leads to softening of cutin making it easier for the pathogen to penetrate the cuticle [13]. After penetration, the infection hyphae get differentiated into primary hyphae which further grow to form subcuticular stroma giving rise to conidiophores which bear conidia that bulge out from the host cells by rupturing epidermis. The conidia and conidiophores, together, give a characteristic velvety appearance to the young lesions of scab. The conidia of Venturia are capable of adhesion and germination on nonhost plants such as Pyrus communis, however further development to establish infections occurs only on the host plants [14]. Kucheryava et al. [15] have observed that conidia can germinate, form appressorium and subcuticular hyphae-like structures when grown on a cellophane membrane placed over the PDA (Potato Dextrose Agar) plates, thus mimicking growth during infection process. The growth of Venturia on cellophane could be used to identify genes involved in fungal pathogenesis. By using this system, the authors could identify two genes (namely, Cin1 and Cin3, being cellophane induced) and further demonstrated that they are highly upregulated during apple infections. Studies are underway to establish the role of these genes during pathogenesis on apple.

tab1
Table 1: Factors predicted to govern pathogenicity and virulence of V. inaequalis.

Several mutants of V. inaequalis, defective in biochemical requirements isolated by UV or nitrogen mustard-mediated mutagenesis, demonstrated differential pathogenicity on apple. The mutants demonstrating reduced/non-pathogenicity (auxotrophs of arginine, choline, histidine, methionine, proline, purines, pyrimidines, and riboflavin) might be unable to obtain the particular biochemical from host, whereas the mutants capable of pathogenicity (auxotrophs of nicotinic acid, biotin, reduced sulfur, inositol, and pantothenic acid) could derive the nutrients from the host. Both the pathogenic and non-pathogenic biochemical mutants were capable of host penetration and disease establishment. However, the non pathogenic mutants exhibited very limited growth and were unable to sporulate with the choline mutant as an exception. The growth and sporulation deficiency of non pathogenic mutants (adenine mutant being exception) were restored if the particular biochemicals were supplied on the host surfaces.

The most enigmatic feature of V. inaequalis is that it forms subcuticular stroma without significant damage to host tissues. It is hypothesized to use cell wall-degrading enzymes (CWDEs) to breach plant cell wall to derive nutrients without forming haustorium. However, that fact that no obvious damage to the host tissues is observed until pathogen starts conidiating suggests a minor role of these enzymes in nutrient uptake. The cellulolytic, cutinolytic, pectinolytic, and -D-glucosidase activities have been detected from the culture supernatant ([2], Table 1). The endo-polygalacturonase (PG) and exo-PG like activities are reported during in vitro growth of the pathogen [22, 23]. It is speculated that the CWDEs of Venturia might be tightly attached with its cell wall and are released in a controlled manner to degrade the host cell wall to facilitate nutrient uptake. In other plant-pathosystems, the CWDEs serve as important virulence factors. However, their action in degrading plant cell walls also serves as a mark of infection and results in induction of plant defense response [2527]. The controlled release of CWDEs might be a strategy of Venturia to prevent induction of host defense response which if successfully mounted would prevent growth of the pathogen. The role of CWDEs during pathogenicity on apple and their ability to induce defense responses are yet to be established. Melanin (generally present as melanoprotein) produced by V. inaequalis is speculated to tether CWDEs and facilitates their slow release [24]. The melanoprotein further assists in diverting the solute flow towards the site of infections, probably by altering the membrane permeability and solute transport system of apple to facilitate availability of nutrients for pathogen growth and development [2].

1.2. Hypervariability of V. inaequalis

The isolates of V. inaequalis are hypervariable and exhibit differential pathogenicity on apple cultivars (known as differential hosts). Based upon such differences, the pathogen has been categorized into eight physiological races [2, 16, 20]. The salient features of these races are summarized in Table 2. However, some of the isolates of Venturia are capable of growing on two different differential hosts and hence it is difficult to classify them to particular race. Recently, Bus et al. [28] have proposed a new nomenclature by reconsidering the differential host used in previous studies. They propose to replace the previously used differential host containing more than one R genes with new accession/selection which carries only one R gene. This system of nomenclature is robust, as per international standard, and has a feature to update the differential host each time a new R gene is discovered [28].

tab2
Table 2: Physiological races of V. inaequalis.

The variations in sequences of internal transcribed spacer (ITS) region of the ribosomal DNA of V. inaequalis, presence of group one intron in this region [2932] and various molecular markers such as RAPD, PCR-RFLP [32, 33], AFLP [34, 35], and Microsatellites [32, 33, 35, 36] have been used to reveal genetic diversity amongst the isolates collected from different regions of the world. Gladieux et al. [35] using microsatellite markers have revealed maximum diversity amongst the isolates from Asia followed by Europe. The authors speculated that the pathogen might have originated in Asia and from there spread to Europe and recently to other apple growing countries. Hypervariability and evolution of strains that have overcome host resistance are attributed to the ability of Venturia to recombine its genetic material every year.

1.3. Apple Defense Responses

During the course of coevolution, apple has evolved mechanisms to prevent the severity of scab. The isolates of V. inaequalis provoke variable symptoms on different apple cultivars [2, 37, 38]. Based upon the extent of pathogen growth and nature of symptoms imparted by them on different apple cultivars, the responses are classified into class 0, 1, 2, 3a (syn. Class M), 3b (syn. Class3), and 4 (Table 3). The classes 0 to 3 are considered to be resistance responses while class 4 is a susceptible response. Several monogenic and polygenic loci capable of imparting scab resistance have been identified from wild cultivars of apple [2, 37, 39]. Interestingly, some of the susceptible cultivars also demonstrate variable extent of resistance against isolates of the pathogen [40]. The matured leaves of apple demonstrate ontogenic resistance because of which the pathogen growth is suppressed immediately after cuticle penetration and appearance of disease symptom gets delayed [2]. The strengthened cell wall and cuticular membrane along with sub-cuticular pH of such leaves are speculated to play a role in governing such resistance. A breakdown of ontogenic resistance revealed by restored growth of the pathogen is observed in the old senescing leaves of apple. Detailed studies are needed to elucidate the functionality of such resistance and understand its breakdown mechanism.

tab3
Table 3: List of apple R-genes imparting scab resistance.

Besides race specific and ontogenic resistance, apple employs diverse defense responses which provide resistance, albeit variable and suppress growth and spread of the pathogen. Ultrastructural studies have revealed that although conidia could germinate on apple leaves undergoing defense responses, formation of primary hyphae is delayed and growth of subcuticular stroma is suppressed resulting in reduced conidiation [2, 41]. Phenolics produced in response to V. inaequalis infections in apple are known to inhibit pathogen growth and are ascribed to be associated with defense mechanisms of scab resistant cultivars [2]. The inhibition of phenylalanine ammonia lyase (a key enzyme involved in the biosynthesis of phenolics) in scab resistant cultivar Sir Prize could render it susceptible to scab infections [42]. Phloridzin (a dihydrochalcone glycoside) produced by apple in response to Venturia, accumulated around the sites of infection, is postulated to get degraded into phloretin by pathogen and hinder its growth [2, 43]. Recently, efforts have been made to characterize genes involved in phloridzin biosynthesis in apple [44]. The treatment of yeast extract (a mimic of fungus infection) induces synthesis of six new compounds in the cell suspensions of apple cultivar Liberty but not in McIntosh [43]. The chemical structures of several of these compounds have been identified and they are speculated to function as phytoalexins [43, 45]. One of these compounds, named Malusfuran (2,4-methoxy-3-hydroxy-9-O- -D-glucosyloxydibenzofuran) and its aglycone and dibenzofuran derivatives can suppress the germination and growth of conidia/mycelium of V. inaequalis.

Several pathogenicity related (PR) proteins including -1,3-glucanase, chitinase, cysteine protease, osmotin-like protein, along with PR1 and thaumatin-like protein are constitutively expressed in the apoplast of resistant apple cultivar Remo and are induced by V. inaequalis in the susceptible cultivar Elstar [46]. Degenhardt et al. [47] have identified several defense-related genes and genes involved in cellular detoxification upregulated in the uninfected young leaves of Remo as compared to Elstar. The constitutive expression of these genes in Remo is speculated to constitute a part of apple defense response. Interestingly a large number of metallothioneins (involved in metal ion detoxifications) were constitutively expressed in Remo, while they get induced following V. inaequalis infections in Elster. The molecular basis of constitutive expression of these genes in the resistant cultivar and their pathogen inducibility in susceptible cultivar should be explored to fish out the key regulatory molecules. The identified key genes if used to raise transgenic apple under pathogen inducible promoters can upregulate defense-related genes upon contact with the pathogen and suppress disease. Two subclasses of PR-10 gene (APa and APb) are induced by acibenzolar-S-methyl, a salicylic acid (SA, a plant defense hormone) analog in apple leaves [48]. Significantly higher expression of APa is induced following Venturia infection during resistant interactions than during compatible interactions and the kinetics of its expression coincide with appearance of visible necrosis [49]. The transgenic apple expressing either the endo (ech42) or the exo (nag70) chitinase gene of Trichoderma harzianum (syn. T. atroviride) have been found to impart scab resistance in a susceptible cultivar McIntosh ([50, 51], Table 4). The transgenic lines containing both endo and exo-chitinase genes exhibit synergism in promoting scab resistance ([51], Table 4). The overexpression of these genes could impart resistance in another susceptible cultivar Galaxy and strengthen resistance in the Vf gene containing cultivar Ariane against race 6 ([52], Table 4). This study has initiated a direction to combine defense related genes along with resistance genes to enhance the durability and efficacy of apple resistance.

tab4
Table 4: Genes shown to impart scab resistance in apple.

Puroindoline B (PinB), a cysteine rich antifungal protein of wheat (Table 4), can suppress the growth of V. inaequalis [53]. The PinB gene when constitutively expressed in the cultivars Galaxy (susceptible to race 1) and Ariane could impart significant but variable resistance against race 6 of the pathogen in transgenic lines of both the cultivars, however, the transgenic Galaxy lines were still susceptible to race 1 [54]. This suggests that physiological differences between the strains can govern the PinB mediated resistance. Combining antifungal proteins along with resistance/defense-related genes can be a good strategy to enhance durability and efficiency of scab resistance in apple.

The NPR1 (Non-expressor of PR) protein plays a key role in systemic acquired resistance (SAR) in Arabidopsis thaliana [55]. Three AtNPR1 orthologs (MpNPR1-1, 2, and 3) have been identified from apple ([56], Table 4). The transgenic lines overexpressing MpNPR1-1 (considered as true apple orthog of AtNPR1) exhibit broad spectrum resistance against fungal (V. inaequalis and Gymnosporangium juniperi-virginianae, causative of cedar apple rust disease) and bacterial (Erwinia amylovora, causative of fire blight disease) pathogens, probably due to enhanced expression of PR proteins.

1.4. Gene-for-Gene Interactions

Plants have evolved a set of genes to detect and mount resistance responses against pathogens. Such genes are known as resistance (R) genes, and the pathogenic factors which are detected by the products of these genes are called Avirulence (avr) factors because their presence renders the pathogen avirulent [57]. This type of interaction, popularly known as gene-for-gene interaction, is followed by Venturia-Apple pathosystem [2, 17]. Several R gene containing loci have been isolated from apple cultivars [2, 37] and efforts have been made to characterize the avr genes of V. inaequalis (Table 1). According to a new nomenclature proposed by Bus et al. [28], apple scab resistance genes are named as Rvik (R refers to resistance gene, vi refers to Venturia inaequalis, and k refers to differential host) and the corresponding avr genes of the pathogen are named as avrRvik. The new and the old names of the apple resistance genes along with their differential host are mentioned in Table 3. The avrVf (avrRvi6) and avrVg (avrRvi1) have been isolated as two independently segregating factors which could render the pathogen avirulent on the Vf (Rvi6) and Vg (Rvi1) R gene containing apple cultivars, respectively [16]. The position of the avrVg (avrRvi1) has been determined using molecular markers [58] and several cosegregating and flanking (both sides) molecular markers have been isolated for this gene [59]. A contig of 330 kb spanning avrVg (avrRvi1) has been identified following chromosome walking on a BAC library of V. inaequalis [59]. Experiments involving multiple approaches are in progress to identify, clone, and sequence the gene and analyze its functionality [59]. AvrVm (AvrRvi5) like activity (inducing resistance on Vm containing apple) has been identified from culture supernatant of race 1 isolate [18]. The activity is narrowed down to three proteins having low molecular weight and low isoelectric points, however further work is needed to identify and characterize the protein [18].

1.4.1. Vf(Rvi6) Gene

Vf (Rvi6) gene, isolated from wild crab apple Malus floribunda 821, is the most studied R gene of apple [2, 37]. The Vf (Rvi6) gene has been extensively used for breeding scab resistance [2, 37, 60, 61]. Races 6 and 7 of V. inaequalis have evolved to breach the Vf (Rvi6) resistance [33, 62], however, they exhibit lack of genetic diversity and are clonally propagated due to founder effect [34].

Extensive research has been made to characterise the Vf (Rvi6) gene, cumulation of which has led to the isolation and full length cloning of the gene [37]. The gene HcrVf2 (Homologs to C. fulvus R genes of the Vf  region; syn. Vfa2) is considered to be the true Vf (Rvi6) gene which is constitutively expressed in apple [6871]. Its expression under CaMV35S promoter into a susceptible cultivar Gala [68] or under its native promoter into the susceptible cultivars Gala [71, 72] and Elstar [71] has been found to impart scab resistance comparable to that of Vf cultivars. Variations in the length of HcrVf native promoter could influence the gene expression and level of imparted resistance [71]. Alike Vf (Rvi6) gene, the resistance imparted by HcrVf2 demonstrates race specificity being susceptible to race 6 and 7 of the pathogen [73]. Effort has been initiated to understand the molecular cascades triggered by pathogen attack in HcrVf2 transgenic lines. In order to identify the genetic network involved in downstream signaling imparted by HcrVf2 in the transgenic apple cultivar Gala upon pathogen attack, a cDNA-AFLP protocol has been optimized by Paris et al. [74].

Beside HcrVf2, several Vf paralogs have been identified from apple, and gene duplication events seem to have played a role in their evolution [37]. These paralogs are thought to be reservoirs which apple might use following somatic recombination to develop resistance against rapidly evolving strains of the pathogen [76]. Recently, Malnoy et al. have raised transgenics of susceptible cultivars Galaxy and McIntosh expressing Vf (Rvi6) gene (Vfa2; syn. HcrVf2) and their paralogs Vfa1 (syn. HcrVf1) and Vfa4 under their respective promoters [77]. The Vfa1 and Vfa2 genes but not the Vfa4 gene imparted scab resistance in transgenic plants. The resistance imparted by Vfa2 expressed with its own promoter was less than that observed when the gene is expressed by CaMV35 or that exhibited by the Vf (Rvi6) cultivars obtained following classical breeding. The high level of expression by CaMV35 promoter and copresence of Vfa1 and Vfa2 genes in the Vf (Rvi6) introgressed cultivars are speculated to be a cause of observed variations. The cotransformation of Vfa1 and Vfa2 genes in apple should shed lights on synergism between them in imparting scab resistance.

1.5. Other Venturia Resistance Genes of Apple

Besides the Vf (Rvi6) gene, several R genes have been isolated which impart variable degrees of resistance ranging from class 0 to class 3b in apple. They are Va (Rvi10), Vb (Rvi12), Vbj (Rvi11), Vd (Rvi13), Vdg (Rvi9), Vfh (Rvi7), Vg (Rvi1), Vm(Rvi5), Vh2 (Rvi2), Vh3.1(Rvi3), Vh4 (Rvi4), Vh8 (Rvi8), Vr2 (Rvi15), and Rvi14 (Table 3). Recently, Vd3 resistance gene has been identified on LG1, close to Vf (Rvi6) locus between CH-Vf1 and 67105F17 markers [63]. Almost all the characterized plant R genes contain Leucine-rich repeats [57]. An apple Leucine-rich repeat (LRR) receptor-like protein kinase, LRPKm1, having domain architecture atypical of LRR receptor is speculated to be associated with apple defense against Venturia infection ([75], Table 4). The gene exhibits rapid and early induction during resistance interactions whereas a slow but steady increase even after 72 hours of infection is observed during susceptible interactions.

Beside monogenic R genes, several polygenic sources of scab resistance are known. Several quantitative trait loci (QTLs) imparting scab resistance and a number of resistance gene analogs (RGA; containing LRR and Nuclotide Binding Site domains) have been identified from different apple cultivars [37, 65]. Interestingly, quite a few of these R genes map to the same locus. The colocalization of the RGAs, QTLs, and R genes is a useful feature which should be utilized in apple breeding programs to cotransfer them into susceptible varieties. Since the pathogen has rendered several of the monogenic R genes ineffective, it will be useful to pyramid several such genes or there combination with other source of resistance for imparting effective and durable scab resistance as evolving resistance against the cocktail of these genes might be a difficult task for the pathogen. The availability of closely linked molecular markers for most of the known monogenic resistance genes and several other resistance related genes will facilitate work in this direction. In order to strategize breeding programmes, international effort “Monitoring of Venturia inaequalis virulences” has been initiated to analyse whether a particular apple R gene is breached by a particular race of pathogen and to what extent that race is spread ([64], http://www.vinquest.ch/). Furthermore, it has been proposed to standardize reporting of molecular markers associated in coupling with the new and previously reported R genes in relation with apple cultivars “Gala”, “Golden Delicious”, “Fiesta”, and “Prima” as standard.

2. Future Prospects

It might be evident from this review that V. inaequalis is an important plant pathogen because it causes huge economic losses and also has a very interesting lifestyle. It is an appropriate time to sequence whole genome of the pathogen. The availability of genome sequence will not only stimulate research in the field of Venturia-apple interactions and contribute to the basic understanding of this pathosystem but can also revolutionize the understanding of pathogenesis of other obligate pathogens. The genome sequence will help in identification of targets for development of new fungicides that are needed as the rapidly evolving pathogen has overcome most of the commonly used fungicides. Understanding the mechanisms of Venturia pathogenesis and intricacies of its interaction with apple should provide important insights for developing new strategies to combat the disease. The whole genome mutagenesis screen should be initiated to identify key virulence factors. The availability of standardized transformation methodologies in V. inaequalis will facilitate such efforts. The mechanism involved in break down of R gene mediated resistance by the pathogen should be explored. Understanding defense response associated signal transduction pathway of apple and characterizing key genes involved in imparting resistance will be very useful in engineering scab resistant apple. Availability of microarray platform for apple could trigger research to characterize the defense response associated transcriptome. The proteomics approach can be an alternative for this purpose. Pyramiding different resistance and defense related genes into a single cultivar seems to be helpful in imparting effective and durable resistance. Conventional breeding might take years to achieve the goal; however, using transgenic approach the goal can be achieved in a lesser span of time. Apple promoters that are induced upon Venturia infection should be identified to use them in a transgenic approach to express the key defense/resistance related genes. Expressing genes under apple promoters and generating marker-free plants can enhance the acceptability of the transgenic/cisgenic apple amongst the consumers.

Acknowledgments

Karnika Thakur and Priyanka Thakur are supported by a research fellowship from the Council of Scientific and Industrial Research (CSIR) and University Grant Commission (UGC), Government of India, respectively. The authors acknowledge the inputs and suggestions given by Dr PS Ahuja and Shammi Bhatti during manuscript preparation. The work has been supported by research funding from CSIR. They acknowledge that, due to space constraints, they have not been able to cite the valuable work of several researchers in this review. IHBT publication number: 0876.

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