Perspectives on the utilization of resistance mechanisms from host and nonhost plants for durable protection of Brassica crops against Alternaria blight

Survey methodology

Several search engines, including PubMed, Web of Science advanced search, and Google Scholar, as well as specific journal websites, were used, and the search was performed based on key words specifically chosen for the topic. Literature was retrieved and sorted based on the relevance of the topic. The literature was then mined to extract data, and relevant articles published from 1960 to 2018 were used to support and elaborate the hypothesis of this review. Various citations from these articles were back-referred to obtain further detailed information. Together, the compiled information was processed by the authors to prepare the manuscript. Perspectives on the relevant concepts were incorporated based on the authors’ expertise in this field of research.

Symptoms and epidemiology

Alternaria blight disease symptoms occur in the leaves, petiole, inflorescence, stem, pods, and seeds (Verma & Saharan, 1994). The initial symptoms of blight appear on the older leaves of the plant, as discrete pinpoint spots, which later enlarge and become surrounded by a distinct yellow halo with concentric rings (Kumar et al., 2014). These spots ultimately coalesce, forming large patches of chlorotic and necrotic foliar blight lesions, resulting in defoliation. The pathogen resides in the center of the lesions, which is surrounded by yellow halos, the zone created by the diffusion of fungal metabolites (Tewari, 1983; Agarwal et al., 1997). Symptoms produced by all three species of Alternaria are similar. However, the spots formed by A. brassicae are greyish in color (Kumar et al., 2014). On the stems, the spots are elongated, while they appear round and blackish on the pods. Infection on the leaves and pods reduces photosynthetic potential, which not only results in reduced seed development and weight but also in reduced oil content and quality and poor germination efficiency (Kolte, 1996; Meena et al., 2010). In severely infected plants, the entire pod gets covered with numerous black spots, ultimately causing significant yield loss due to premature shattering.

In field conditions, disease development and spread are generally favored under temperatures ranging from 12 °C to 27 °C and a relative humidity of 70%, while on pods, infection occurs at a daily temperature range of 20–30 °C, together with more than 9 h of sunshine and leaf wetness (Awasthi & Kolte, 1994). Frequent rains are favorable for disease initiation and spread on the leaves of Brassica, particularly during the rosette to flowering stages. Furthermore, the frequency of infection is the highest during the flowering and pod stages (Prasad, Saxena & Chandra, 2003). According to a report by Awasthi & Kolte (1994), the susceptibility of the plants increases with age 30 days after sowing. Plants less than 30 days old do not show any symptoms, but they are highly susceptible 60–90 days after sowing.

Resistance mechanisms operating in wild and tolerant species of Brassica

Various studies have been carried out to analyze the effect of Alternaria blight infection on host plant physiology and metabolism, but reports on host–pathogen interactions at the genetic and molecular level are still limited. A recent study has indicated that Arabidopsis can be a used as an efficient model system for deciphering the genetic and molecular mechanisms involved during interaction with A. brassicae (Mandal, Rajarammohan & Kaur, 2018).

Studies on the mechanisms of resistance to Alternaria blight have implicated polygenes (Tripathi et al., 1980; Medhi, 1985; Zhang, Xu & Takahata, 1996; Krishnia, Saharan & Singh, 2000), while some studies have attributed it to dominant nuclear genes (Tripathi et al., 1978; Subudhi & Raut, 1994; Zhang et al., 1997). Thus far, different sources of resistance to A. brassicae have been identified from host germplasm, including wild and tolerant species of Brassica. The resistance in the host germplasm has different components, which mainly include structural components such as epicuticular waxes, as well as biochemical components like phenols and phytoalexins. Epicuticular waxes form a direct physical barrier in the plant, providing resistance to Alternaria (Conn, 1986; Conn & Tewari, 1989). High deposits of epicuticular wax, forming a protective hydrophobic coating on the leaf surface, reduce the adherence of inoculum, conidia germination, and germ tube formation in the plant (Saharan, 1992). Some Brassicaceae members, including B. napus, B. carinata, and Sinapis alba, have been reported to have higher epicuticular wax compared to B. rapa and B. juncea, and therefore, the former are less susceptible to Alternaria blight infection (Conn, Tewari & Hadziyev, 1984; Tewari, 1986). High quantities of epicuticular wax have been observed in the progeny of interspecific crosses between B. napus and B. juncea (Singh, Singh & Srivastava, 1999).

Alternaria blight-resistant varieties accumulate high amounts of biochemical compounds such as phenols. After infection, blight-tolerant species of Brassica such as B. carinata and B. napus have been observed to accumulate a higher amount of total phenols compared to the susceptible species B. juncea and B. rapa (Gupta et al., 1990; Gupta, Gupta & Kaushik, 1995; Gupta & Kaushik, 2002). Meanwhile, the levels of soluble and reducing sugars and soluble nitrogen have been found to be lower in resistant species. In another study, resistance to the disease was reported to be associated with increased levels of antioxidant enzymes of the phenolic pathway, such as polyphenol oxidase, peroxidase, and catalase (Singh et al., 2009). Furthermore, phytoalexin accumulation in response to pathogen infection and its role in disease resistance have been well studied in Brassica. Phytoalexins are low-molecular-weight antimicrobial compounds produced by plants after pathogen infection. Cultivars of both resistant (B. napus, Camelina sativa, Eruca sativa) and susceptible (B. rapa) species show the elicitation of phytoalexins (Tewari, Conn & Dahiya, 1987; Tewari, Conn & Dahiya, 1988; Conn, Tewari & Dahiya, 1988; Conn et al., 1991). The highly resistant C. sativa produces a large number of phytoalexins that are involved in regulating resistance to A. brassicae (Tewari, 1991). Rapid accumulation of phytoalexins in C. sativa after pathogen infection has been found to inhibit fungal growth on the leaf surface (Jejelowo, Conn & Tewari, 1991).

The Alternaria pathogen has also been found to secrete both host-specific and nonhost-specific toxic metabolites, enabling a wide range of infection symptoms (Nishimura & Kohmoto, 1983; Kohmoto, Otani & Tsuge, 1995; Agrios, 2005). These toxins have been shown to alter the permeability and functioning of the cell membrane and organelles, thereby inhibiting various physiological processes of the host plant (Mathur & Chand, 1991). Destruxin B, a host-specific Alternaria phytotoxin acts as a pathogenicity factor responsible for its aggressiveness and for the susceptibility of the host plant. The Alternaria- tolerant species S. alba detoxifies destruxin B, and this is followed by simultaneous phytoalexin formation and elicitation. Together, these processes constitute the resistance mechanism of S. alba against A. brassicae (Pedras & Smith, 1997; Pedras et al., 2001). Some compounds related to camalexin and 6-methoxycamalex have also been found to confer toxicity to A. brassicae (Dzurilla et al., 1998).

Exploiting the resistance mechanisms from host germplasm for developing blight-resistant brassicas

Several attempts have been made to exploit resistance sources from the wild relatives of Brassica and transfer them into cultivated Brassica (Aneja & Agnihotri, 2013). Efforts have been made in screening blight-resistant cultivars; however, high levels of resistance to A. brassicae have not been observed among cultivated Brassica species. The species show varying degrees of resistance responses against Alternaria blight, and accordingly, B. rapa and B. juncea are classified as being more susceptible to the disease than B. napus and B. carinata (Skoropad & Tewari, 1977). Of late, studies aimed at identifying blight-tolerant oilseed Brassica germplasm have been increasing. Table S1 enlists the sources of resistance, including the related wild species or weedy varieties of Brassica against Alternaria blight. These related wild species have been found to harbor genes conferring resistance to Alternaria blight that can be used for resistance breeding (Ghose et al., 2008; Chatterjee, Mazumder & Basu, 2013).

In the past few decades, various conventional and modern approaches have been used to develop blight-resistant cultivars by exploiting resistance sources from host germplasm. Conventional approaches involve the screening of germplasm for blight-resistant plant materials, followed by the transfer of resistance traits from tolerant species into susceptible cultivars by hybridization combined with multiple crosses. Inter- and intraspecific crosses of B. juncea and B. carinata were established to understand the inheritance pattern of resistance to Alternaria blight (Krishnia, Saharan & Singh, 2000), which showed that dominant and additive genes govern the inheritance of resistance to Alternaria blight. Thus, a successful breeding method should utilize both the gene effects. However, there is a limitation in such breeding approaches owing to the low availability of suitable resistance sources/genes within the available germplasm of cultivated Brassica and insurmountable self-incompatibility barriers in combining the resistance traits from distantly related wild Brassica species. Modern biotechnological interventions involving tissue culture and genetic transformation approaches have also been established for the development of improved varieties. In vitro ovary culture and ovule culture have been attempted for transferring resistance traits from S. alba cv. Carine to B. napus cv. Brutor (Chevre et al., 1994) and Erucastrum cardaminoides to B. oleracea var. alboglabra (Mohanty et al., 2009). Intergeneric hybrids of B. campestris and B. spinescens have also been developed (Agnihotri et al., 1991). Moreover, the somatic hybridization technique has been applied for transferring the resistance traits from blight-tolerant species to susceptible ones, for example, S. alba to B. napus (Primard et al., 1988), B. carinata to B. juncea (Sharma & Singh, 1992), and B. nigra and B. oleracea (Jourdan & Salazar, 1993). Attempts have also been made for the introduction of somaclonal variations for the incorporation of disease resistance/tolerance to Alternaria blight through mutagenesis using gamma rays, ethyl methanesulfonate, and ethyl nitrosourea (Verma & Rai, 1980; Agnihotri et al., 2009). In addition, the defense response might be activated by treatment with biotic and abiotic agents for combating A. brassicae infection in oilseed brassicas. Vishwanath et al. (1999) showed that resistance in a susceptible cultivar of B. juncea against the extremely virulent A. brassicae isolate A and reasonably virulent isolate C, both from B. carinata, was induced after inoculating the plants with the avirulent A. brassicae isolate D. As another example, the application of β-aminobutyric acid on the leaves of B. carinata was found to induce resistance to A. brassicae (Chavan, Bhargava & Kamble, 2013). In future, the activation of the defense response without gene manipulation may act as a better substitute for the conventional use of fungicides. Unfortunately, till date, none of the conventional or modern biotechnological methods have been found to be feasible or stable in developing blight-resistant Brassica species. Under such circumstances, it is pragmatic to use novel sources of resistance from plant species that are not hosts to the pathogen. The transfer of genes from nonhost plants conferring resistance to the pathogen is a promising strategy in parallel to the current efforts towards the development of oilseed Brassica varieties resistant to Alternaria blight.

Exploiting nonhost disease resistance mechanisms

NHR is expressed by all the members of a plant species to a particular pathogen (Nurnberger & Lipka, 2005). Exploiting NHR has been suggested as an option for developing broad-spectrum disease resistance in plants (Ellis, 2006; Lee et al., 2017). In recent years, considerable progress has been made in understanding the interaction of several host species and A. brassicae, but there are few and indirect reports on studies examining the NHR mechanisms involved during the interaction of A. brassicae with nonhost plants. Understanding the mechanisms and identifying the genes involved in NHR to A. brassicae may provide an opportunity to engineer transgenic Brassica plants that provide durable resistance to A. brassicae. For example, in recent years, some success in genetic transformation involving the transfer of resistance genes from nonhost plants into oilseed Brassicas has been reported. Mondal et al. (2003) found that the overexpression of tobacco chitinase conferred resistance to Alternaria leaf spot in transgenic Brassica, as demonstrated by the inhibitory effect of the transgenics on the hyphal growth of A. brassicae. They further reported the development of transgenic B. juncea (cv. RLM 198) constitutively expressing a class I basic glucanase of tomato, which arrested the hyphal growth of A. brassicae by 15–54% (Mondal et al., 2007). Moreover, the introduction of the chitin-binding lectin hevein from rubber plants into B. juncea led to resistance to A. brassicae (Kanrar et al., 2002). Such studies highlight the necessity to dissect the mechanisms and reveal the genes involved in NHR for the development of resistant cultivars.

For this, the first step is to identify potential nonhost plants that can reveal robust and exploitable mechanisms for suitable transfer to a host plant for imparting broad-spectrum resistance. Besides, the nonhost plant should be distinct from the non-adapted plant, where, for example, the fungal spores fail to adhere, deposit, and remain on the leaf surface for germination (Niks & Rubiales, 2002). Here, we discuss some of the nonhost plants for A. brassicae based on the available literature and the intercropping systems followed in different parts of world. In many intercropping systems, species of the Brassicaceae family are cultivated with certain other plant species in the same field for many decades (Singh, Kumar & Singh, 2010; Shekhawat et al., 2012; Ao & Saud, 2016; Ebrahimi et al., 2016; Jeromela et al., 2017). In the same field, A. brassicae infects Brassica plants but cannot infect the other plant species (http://www.plantwise.org/KnowledgeBank). The Plantwise Knowledge Bank database (http://www.plantwise.org/KnowledgeBank) lists the plant species infected by A. brassicae in different parts of world. Through this database, we ensured that the identified nonhost plants have not been reported to be infected by A. brassicae. Hence, those species can act as potential nonhost plants against this pathogen. Curiously, in the course of evolution, the pathogen gets enough opportunities to infect these nonhost plants, but they are unable to overcome the NHR. A few examples of such nonhost plants, which are intercropped with host plants such as mustard (B. juncea), are chickpea (Cicer arietinum and C. kabulium), lentil (Lens culinaris), cowpea (Vigna unguiculata), barley (Hordeum vulgare), sugarcane (Saccharum officinarum), and potato (Solanum tuberosum) (Table 1). It would be interesting to determine the factors that dictate the failure of A. brassicae to infect these nonhost plants. The NHR of these plants to A. brassicae may involve multiple layers of defense that could be distinct for each plant species.

Possible NHR mechanisms in nonhost plants to A. brassicae

NHR to fungi is highly conserved among different plant species and seems to involve multiple layers of resistance (Heath, 2000). NHR mainly comprises pre-invasion and post-invasion defenses (Lee et al., 2017; Fonseca & Mysore, 2018). Based on the current understanding of the NHR mechanisms in other related nonhost plant–pathosystems such as Arabidopsis and powdery mildew fungus, barley and powdery mildew fungus, and Medicago and the rust fungal pathogen (Collins et al., 2003; Lipka et al., 2005; Jafary et al., 2008; Douchkov et al., 2014a; Douchkov et al., 2014b; Ishiga et al., 2015), we have proposed the possible NHR mechanisms in a nonhost plant against A. brassicae (Fig. 1). The NHR mechanisms operating at the pre-invasion level mainly involve both pre-formed and inducible defense responses. The germination of A. brassicae spores requires host stimuli, high humidity, and surface water to increase wetness on the leaf surface (Verma & Saharan, 1994). Pre-formed defenses may involve structural features such as the abundance of leaf trichomes, which reduces leaf wettability, as well as the lack of stimuli from the nonhost plant, which eventually causes irregular spore germination or a complete lack thereof (Niks & Rubiales, 2002). Pre-formed barriers also include chemical compounds present on the leaf surface, for example, antimicrobial enzymes and secondary metabolites, which might inhibit spore germination (Heath, 1997a; Heath, 1997b; Morrisey & Osbourn, 1999; Heath, 2000). The ability of A. brassicae spores to germinate on nonhost tomato and wheat plants was tested by McRoberts & Lennard (1996). They found that the spores were able to germinate with the same efficiency on the nonhost and host plants. These spores may have overcome the pre-formed chemical barriers, thereby being able to germinate on the leaf surface. Furthermore, the entry of germinated A. brassicae spores inside the plants is achieved either by targeting the stomata, which is a more predominant mode for entry, or directly through the cuticle (Changsri & Weber, 1960; Tsuneda & Skoropad, 1978). Stomatal recognition by a pathogen requires specific plant topographical cues, which allow germ tube development and eventually facilitate the penetration inside the plant (Hoch et al., 1987; Heath, 1997a; Staples & Hoch, 1997; Niks & Rubiales, 2002). A study on tomato and wheat plants showed that germ tube development of A. brassicae was not affected, but the pathogens failed to enter the stomata of the nonhost plants, unlike in the host plants (McRoberts & Lennard, 1996). It is possible that in the nonhost plants, stomata are not accurately recognized by the pathogen because the surface topography may significantly differ from that of the host leaf. The lack of stomatal recognition by the pathogen may lead to the development of the germ tube, albeit away from the location of the stomatal opening. This sort of disruption in the orientation of the germ tube may not allow the pathogen to enter inside the leaf tissue. Another pre-formed structural barrier includes cuticular waxes, which retard pathogen entry into the leaf tissues (Tewari & Skoropad, 1976; Skoropad & Tewari, 1977; Conn, 1986; Serrano et al., 2015). For example, barley has excessive cuticular wax, consisting of approximately 54% long-chain β-diketones, 20% hydroxylated β-diketones, and other hydrocarbons (Wettstein-Knowles & Netting, 1976; Simpson & Von Wettstein-Knowles, 1980). Together, these form thick cuticular layers that occlude the stomatal features involved in germ tube penetration inside the leaf tissue (Uppalapati et al., 2012). Besides, Alternaria, being a necrotrophic pathogen, sometimes directly enters the host plant through the cuticle by enzymatically digesting cutin waxes by means of cutinolytic enzymes (Tewari, 1986; Conn & Tewari, 1989). For a few tolerant host species, a high content of cuticular waxes acts as a physical barrier that provides resistance to A. brassicae (Tewari & Skoropad, 1976; Skoropad & Tewari, 1977; Conn & Tewari, 1989). We propound that nonhost plants may have appreciably high amounts of cuticular waxes, which may restrict pathogens from penetrating inside the plant. The penetration attempts by the pathogen on the nonhost plant may trigger inducible defense responses in the plant. The nonhost plant can induce stomatal closure, prevent the entry of A. brassicae, and mount an inducible chemical barrier involving the rapid formation of phytoalexins—antimicrobial compounds inhibiting hyphal development and differentiation (Grayer & Harborne, 1994; Mert-Turk, 2002; Iriti & Faoro, 2007). The differentiation of hyphae is important for penetration through intercellular spaces, and certain nutrients are essential for hyphal development and differentiation (Giri et al., 2013). Thus, in a nonhost plant, the lack of nutrients and presence of antimicrobial compounds in the apoplast may inhibit the development of hyphae into mycelium. Moreover, the defense responses also involve the formation of a structural barrier to arrest fungal growth and penetration in the cell wall (Underwood, 2007; Voigt, 2015). For example, A. brassicae fails to penetrate the cell wall in tomato and wheat plants, and callose-containing papilla formation is observed in the cell wall regions where the pathogen attempts to penetrate such plants(McRoberts & Lennard, 1996). The pathogen also produces nonhost-specific or general toxins that can damage the plant cells, which eventually leads to necrosis (Buchwaldt & Green, 1992; Bains, Tewari & Ayer, 1993; Parada et al., 2007). To avoid this, a nonhost plant may recognize these toxins and employ defense mechanisms to detoxify these toxins (Pedras et al., 2001). Some NHR mechanisms operate at the post-invasion level, which might restrict the pathogen from invading the epidermal cells in the nonhost plant. These defense responses mainly involve ROS accumulation and defense-induced cell death, which do not allow the mycelium to ramify through and between the cells. Eventually, fungal proliferation might be restricted by rapid HR (McRoberts & Lennard, 1996; Gilchrist, 1998).

Understanding the molecular events in NHR to other Alternaria species

Defense responses are evoked in both host and nonhost infections; however, the NHR involves not only earlier induction but also a robust defense response compared to the host plant. Both A. brassicicola and A. brassicae affect almost the same cruciferous crops and generally exhibit similar symptoms (Saharan, Mehta & Meena, 2016; Meena et al., 2016). However, the literature indicates that Arabidopsis and S. alba, which belong to the same family (Brassicaceae) show NHR to A. brassicicola (Thomma et al., 1999; Pedras et al., 2001) but act as hosts for A. brassicae (Hansen & Earle, 1997; Sharma et al., 2002). A recent study showed Arabidopsis accession Gre-0 to be highly susceptible to A. brassicae (Mandal, Rajarammohan & Kaur, 2018). Therefore, understanding the NHR mechanisms in these plants against A. brassicicola will indirectly illustrate the resistance mechanisms operating during the interaction of A. brassicae with nonhost plants or absent during the interaction with these susceptible host plants. Hence, this section covers the molecular mechanisms of NHR to A. brassicicola.

In A. thaliana and S. alba, early and high-level induction of defense-related genes, namely, pathogenesis-related-1 (PR1), β-1,3 glucanase (PR2), and chitinase (PR3), occurs compared to B. juncea after infection with A. brassicae or A. brassicicola (Narusaka et al., 2003; Van Wees et al., 2003; Ghose et al., 2008; Nayanakantha et al., 2016; Mandal, Rajarammohan & Kaur, 2018). Moreover, the expression of PR3, encoding chitinase, remained undetected in B. juncea after pathogen infection, but its expression was highly induced in S. alba (Nayanakantha et al., 2016). However, both A. thaliana and S. alba actively secrete chitinase enzymes, which hydrolyze the fungal cell wall and release chitin fragments (Narusaka et al., 2003; Chatterjee, Mazumder & Basu, 2013). These chitin fragments are recognized by some receptors that activate effective defense responses against the pathogens (Wan et al., 2008). This suggests that the defense-related genes are activated earlier in nonhost plants than in host plants as a part of the NHR strategy, and the chitinase capable of degrading fungal cell walls plays an important role in restricting pathogen growth at early stages of infection. Furthermore, the receptors involved in chitin recognition in Arabidopsis, e.g., CERK 1 or LysM receptor-like kinase (LysM-RLK) and phytosulfokine receptor kinase (PSK), were found to be induced after A. brassicicola infection (Wan et al., 2008; Loivamaki et al., 2010). Wan et al. (2008) also showed that a mutation in the LysM-RLK gene inhibits the induction of all chitin-responsive defense genes and compromises the NHR to A. brassicicola. Similarly, Arabidopsis homologs for RLK receptors were identified in S. alba, and their expression was highly induced after infection with A. brassicicola; the genes were downregulated in B. juncea (Ghose et al., 2008). This indicates that chitin digestion from the fungal cell wall and its perception by the plant may play an essential role during defense signaling in nonhost plants. The NHR response involves the stimulation of a signal transduction cascade after the perception of a pathogen by the plant cell, which initiates the activation of protein kinases and members of MAP kinases and subsequently leads to defense gene activation in nonhost plants (Lawrence et al., 2008). MAPK6 expression was found to be highly induced for a longer duration in S. alba plants infected with A. brassicicola, but it was downregulated in B. juncea (Taj et al., 2010). These findings lead us to speculate that MAPK6 might be involved in imparting NHR and targeting many downstream components that are involved in effective defense response.

Salicylic acid (SA), jasmonic acid (JA), and abscisic acid (ABA) are the key modulators involved in phytohormone signaling during plant defense. JA-mediated signaling is predominantly involved in general defense against necrotrophic pathogens (Glazebrook, 2005). In Arabidopsis, JA-mediated activation of the defense response occurs against A. brassicicola (Thomma et al., 1998; Van Wees et al., 2003), while S. alba challenged with the same pathogen induces ABA-mediated and JA-mediated defense responses (Mazumder et al., 2013). In contrast, susceptible B. juncea plants induce SA-mediated defense signaling pathways (Thomma et al., 1998; Van Wees et al., 2003; Mazumder et al., 2013). It is likely that there is a significant amount of crosstalk between phytohormones and a convergence of two or more signaling pathways, which play a role in deciding whether disease progression will occur or the defense pathways will overcome the pathogen. Considering these studies together, we surmise that early signaling events in nonhost plants has a major role in imparting NHR to A. brassicicola.

Possible strategies for developing durable Alternaria blight-resistant Brassica crops by using genomic tools

Based on a literature survey on intercropping systems, we have shortlisted the nonhost plants for A. brassicae (Table 1) that can be chosen for dissecting the NHR mechanisms. As discussed earlier, the NHR to A. brassicae may involve four different phases based on fungal invasion and penetration events (Fig. 1). Prior to any specific study, it is important to classify the nonhost plants based on these four phases by using pathological assays. This will provide a clear idea about whether the NHR operates at the pre-invasion or post-invasion level. Now, we outline the five major strategies for working towards the ultimate goal of developing durable Alternaria blight-resistant Brassica crops.

Inter or intra-specific introgression of candidate genes from nonhost plants to Brassica crops

The first strategy involves the identification of genes conferring NHR by utilizing conventional or molecular breeding approaches, followed by the introgression of candidate genes from nonhost plants to Brassica crops. This can be achieved in two ways. First, where possible, interspecific crosses of the host with a nonhost may be performed to transfer resistance traits from the nonhost plant to a host plant. The unwanted background in the progeny can be removed by crossing it with wild-type host plants and selecting for the targeted traits only. Then, the progeny can be screened for response to A. brassicae. Plants showing resistance to the pathogen can be subsequently subjected to QTL mapping to identify the genes involved in NHR. Once the genes are identified, they can be successfully introgressed into the desired varieties to provide resistance to A. brassicae. The major limitation with this approach, however, is that the progeny generally suffers from sterility and abnormal segregation, which can hinder the identification of genes involved in resistance. To our knowledge, the only available example of an interspecific cross made between a host and nonhost plant is that of Lactuca and Bremia (Jeuken et al., 2008).

The second approach is to cross two different varieties of nonhost plants (intraspecific cross: completely resistant genotype × moderately resistant genotype) that differ in the degree of resistance towards A. brassicae. This will allow the inheritance of NHR-specific QTL of the resistant donor into the moderately susceptible genotypes of the same species of the nonhost plant (Jafary et al., 2008; Niks & Marcel, 2009). The progeny obtained can be similarly studied as described above for identifying the genes involved in NHR and transferring them into target crops. However, if the nonhost plant does not have significant variation in the degree of resistance towards the pathogen, the inheritance of NHR-specific genes might be difficult (Fig. 2).

Conclusion and future perspectives

Selection from within the existing germplasm and the utilization of these sources to incorporate resistance in cultivated varieties through conventional breeding techniques have embodied the basic approaches for generating disease-resistant varieties. However, the exploitation of resistance mechanisms from host germplasm sources has shown limited success in the development of disease-resistant crop varieties. Meanwhile, when genes are introduced from related genera or families, the durability of resistance might be questionable, particularly when a single gene regulating one pathway for defense is employed. Therefore, it is essential to conduct parallel research based on the exploitation of NHR sources or genes against the pathogen over the course of developing varieties resistant to Alternaria blight. Compared to other forms of resistance, NHR governs defense responses to a broad range of pathogens. It is a stable, durable, and robust form of resistance that relies on multiple defense components. Sustainable and broad-spectrum resistance under field conditions makes NHR a promising resource for crop improvement. We speculate that the strategies proposed for exploiting NHR by applying the latest molecular biology techniques involving transcriptomic approaches and genomic tools such as VIGS, TIGS, and mutagenesis will be useful in identifying novel sources of NHR and developing Brassica crops with durable disease resistance. The utilization of model plants can be pivotal in identifying the genes and deciphering the pathways operational during NHR. A model plant can serve as a promising tool to enable plant breeders to transfer the knowledge obtained from it into crop plants for developing disease-resistant crops. However, the utilization of NHR sources for effective crop improvement is beset by several limitations, the major one being that one sole NHR mechanism cannot be exploited to combat all the pathogens of a crop. NHR is a more complex form of defense due to the involvement of multiple pathways; hence, it is less feasible in crop breeding applications. Furthermore, pathogens having a rapid evolutionary rate in nature tend to overcome the NHR mechanisms operating in the nonhost plants.