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Cell Microbiol. Author manuscript; available in PMC Dec 1, 2012.
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The role of effectors of biotrophic and hemibiotrophic fungi in infection


Biotrophic and hemibiotrophic fungi are successful groups of plant pathogens that require living plant tissue to survive and complete their life cycle. Members of these groups include the rust fungi and powdery mildews and species in the Ustilago, Cladosporium and Magnaporthe genera. Collectively, they represent some of the most destructive plant parasites, causing huge economic losses and threatening global food security. During plant infection, pathogens synthesise and secrete effector proteins, some of which are translocated into the plant cytosol where they can alter the host’s response to the invading pathogen. In a successful infection, pathogen effectors facilitate suppression of the plant’s immune system and orchestrate the reprogramming of the infected tissue so that it becomes a source of nutrients that are required by the pathogen to support its growth and development. This review summarizes our current understanding of the function of fungal effectors in infection.


During the co-evolution of fungal plant pathogens and their hosts there has been a seesawing interplay between pathogen virulence and host resistance. To date, there are more than 10,000 fungal species known to cause diseases on plants, compared with roughly 50 species that cause disease in humans (Agrios, 2005). This diversity is reflected by a wide variety of phytopathogen infection strategies. The parasite must penetrate pre-formed and induced physical barriers, such as the waxy cuticle on the leaf surface and the plant cell wall, and withstand pre-formed and induced anti-microbial chemicals. It must induce release of plant nutrients and acquire them for its own use. Throughout infection, the pathogen must overcome or avoid triggering the host immune system. Biotrophic fungi establish a close association with the host through the development of specialised infection hyphae or haustoria within living plant cells from which nutrients are taken up (Mendgen and Hahn, 2002). On the other hand, necrotrophic fungi secrete toxins and enzymes that kill host cells and then take up nutrients released from the dead tissue (Horbach et al., 2011). This latter strategy may limit the capacity of the host plant to mount a defense response including production of antifungal molecules. Hemibiotrophic fungi combine both strategies (Horbach et al., 2011). An initial biotrophic phase, during which the host’s immune system and cell death is actively suppressed, allows invasive hyphae to spread throughout the infected plant tissue. This is followed by a necrotrophic phase during which toxins are secreted by the pathogen to induce host cell death.

Until recently, the mechanisms biotrophic and hemibiotrophic fungi use to deal with the host immune system and to manipulate the living host cells were a mystery. However, in recent years it has become apparent that, like bacterial pathogens of plants and animals (Hann et al., 2010; Staskawicz et al., 2001), plant pathogenic fungi produce and secrete many so-called effector proteins that interact with the host and play an important role in virulence (Kamoun, 2009; Dodds et al., 2009). Since many of these fungal effectors were initially identified through their recognition by the plant immune system, in this review we will first briefly summarise plant immunity and then discuss the role of effectors from various model pathogenic fungi.

Multilayered plant immunity

Plants are able to recognise the presence of pathogens on different levels during infection (Jones and Dangl, 2006; Dodds and Rathjen, 2010). Initially, recognition of conserved pathogen associated molecular patterns (PAMPs) leads to PAMP-triggered immunity (PTI). The second layer of defense is activated when the host recognises specific pathogen effector proteins, which are produced to suppress PTI and facilitate infection, and is commonly referred to as effector triggered immunity (ETI).

Plants recognise common microbial patterns

PAMPs recognised by the plant immune system are generally molecules essential to the pathogen and cannot be modified without significant loss of viability. They include the abundant bacterial proteins, elongation factor Tu (EF-Tu) and flagellin, and the fungal cell wall polysaccharide, chitin (Zipfel, 2009). During infection, PAMPs present in the extracellular space (known as the apoplast) are recognised by transmembrane pattern recognition receptors (PRRs) present on the plant plasma membrane, a process that induces PTI (Zipfel, 2009). For instance, the Arabidopsis thaliana flagellin receptor, FLS2, recognises the highly conserved N-terminus of bacterial flagellin (flg22) and activates a MAP kinase pathway to induce expression of defense response genes (Gomez-Gomez and Boller, 2002). In addition, anti-microbial compounds and reactive oxygen species are produced and callose is deposited at the site of infection to strengthen the cell wall. Similarly the Arabidopsis CERK1 (Petutschnig et al., 2010) and rice CeBip receptors (Kaku et al., 2006) recognise chitin during fungal infection.

Plant pathogen effectors

In order to facilitate infection, plant pathogens secrete numerous effector proteins into the plant apoplast or cytosol. Most of our understanding of plant pathogen effectors comes from studies of prokaryotic pathogens, such as the bacterium Pseudomonas syringae which uses a type three secretion system (T3SS) to deliver about 30 effectors directly into the plant cytosol (Chang et al., 2005; Schechter et al., 2006). Many of these proteins target PRRs or their signalling partners, thereby interfering with defense signal transduction (Hann et al., 2010; Xiang et al., 2011; Axtell and Staskawicz, 2003; Gohre and Robatzek, 2008). One of the best characterised is P. syringae AvrPto. This small secreted protein inhibits PTI directly by interfering with flg22-induced FLS2 signalling inside the plant cell, allowing the bacteria to grow on A. thaliana (Xiang et al., 2008). Similar to a bacterial T3SS, plant pathogenic nematodes secrete effectors through their stylet, either into the apoplast or via feeding tubes directly into the cytosol of plant cells (Vieira et al., 2011; Vanholme et al., 2004). Less is known about effectors of filamentous pathogens, such as fungi and oomycetes, but it is now clear that these pathogens also secrete effectors into the plant apoplast or deliver them into host cells, where they may act to suppress defense responses or alter host metabolism (Kamoun, 2009; Panstruga and Dodds, 2009; Ellis et al., 2009).

Effector recognition by plant immune receptors

To counteract effector molecules, plants have developed an additional layer of immune recognition based on intracellular NB-LRR (nucleotide binding – leucine rich repeats) receptor proteins that can detect individual effectors either directlyor indirectly. These receptors are often referred to as resistance (R) proteins and the effectors they recognise as avirulence (Avr) proteins (Dodds and Rathjen, 2010; Jones and Dangl, 2006). Generally, the plant ETI response to R-protein-mediated recognition is more severe than PTI and frequently results in localised plant cell death, also known as the hypersensitive response (HR). This response is particularly effective against biotrophic pathogens which depend on living host cells for nutrition.

Effector function in biotrophic and hemibiotrophic fungi

The first fungal effectors were identified in attempts to clone Avr proteins recognised by host R proteins, and it became apparent that many were recognised within the host cell cytoplasm (Dodds et al., 2004; Jia et al., 2000). This implies delivery of the effectors into the plant cell during infection, and subsequent studies have directly visualised fungal effectors inside host cells (Kemen et al., 2005; Khang et al., 2010; Rafiqi et al., 2010). How do they get there? No system analogous to the bacterial T3SS has been identified in fungi. The fungal effectors contain canonical secretion signals and appear to be secreted through the standard endomembrane pathway. Some insight into the process of movement into the plant cell has come from the finding that oomycete pathogens, which have similar infection strategies to fungi but belong to the Stramenopile kingdom, secrete effector proteins with an N-terminal RxLR (Arg-x-Leu-Arg) host targeting signal (HTS) (Morgan and Kamoun, 2007). This signal, together with a downstream dEER (Asp-Glu-Glu-Arg) motif, is required for host cell entry of the Phytophthora infestans effector Avr3a (Whisson et al., 2007). Internalisation appears to be pathogen-independent (Dou et al., 2008). Kale et al (2010) suggested that the RxLR motif of several oomycete effectors binds to phosphatidyl inositol phosphates (PIPs) on the outer surface of the plant plasma membrane to mediate endocytosis. In contrast, Yaeno et al. (2011) found that PIP binding by these effectors was mediated by the C-terminal domain and not the RxLR region, arguing against a role in effector delivery.. Similar pathogen-independent uptake occurs with effectors from the biotrophic flax rust fungus, Melampsora lini (Rafiqi et al., 2010), but does not correlate with PIP binding (Gan et al., 2010a). However, unlike oomycete effectors, fungal effector proteins do not share a conserved HTS and it is not yet known how they are targeted to and enter the plant cell.

In contrast to the relatively small set of effectors produced by bacteria, recent advances through next-generation sequencing and large scale proteome analysis have now identified hundreds of proteins that are secreted by biotrophic and hemibiotrophic fungi (Dodds, 2010; Kamper et al., 2006; Spanu et al., 2010; Yoshida et al., 2009; Dean et al., 2005; Duplessis et al., 2011). Typically, these secreted proteins have low sequence homology to any known protein and there is little understanding of their function. Quite often all that is known is that they are recognised by cognate host R proteins, i.e., that they are Avr proteins (Stergiopoulos and de Wit, 2009; Gan et al., 2010b). Clarification of their role as effectors is hampered by apparent functional redundancy which often masks any obvious phenotype when individual genes are deleted or silenced (Lawrence et al., 2010; Mosquera et al., 2009; Muller et al., 2008). Nevertheless, recent research is beginning to reveal the function of increasing numbers of fungal effectors and the remainder of this review will focus on a selection of recently characterised effectors from biotrophic and hemibiotrophic fungi.

Cladosporium fulvum – a colonizer of the apoplast

C. fulvum is a biotrophic fungal pathogen which is the causal agent of leaf mould of tomato (Thomma et al., 2005). C. fulvum colonizes host leaves, where it grows in the extracellular spaces without penetrating host cells (Figure 1). The first characterised fungal effector was Avr9 from C. fulvum (Vandenackerveken et al., 1992). Avr9 is a small (28 amino acid), cysteine-rich secreted protein with yet unknown function that triggers HR in tomatoes containing the Cf-9 resistance gene. To avoid initial host recognition, C. fulvum employs a dual strategy to suppress PTI induced by chitin in its cell wall. The plant apoplast contains various plant-derived cell wall degrading enzymes, including chitinases. These can digest chitin in the fungal cell wall, which not only has a direct antifungal effect, but also releases chitin oligomers that are detected by PRRs and act as potent elicitors of PTI. During infection, C. fulvum secretes the effector, Ecp6, which contains a LysM chitin binding domain and which binds selectively to the chitin oligosaccharides, preventing their recognition by host PRRs (de Jonge et al., 2010). To limit the release of chitin oligosaccharides, C. fulvum also secretes the Avr4 effector which binds to chitin in the intact fungal cell wall, preventing its hydrolysis by host chitinases (van Esse et al., 2007; van den Burg et al., 2006).

Figure 1
Schematic diagram of fungal infection structures in and around an infected leaf cell. Four different fungal pathogens have different infection strategies, either invading the intercellular space (Cladosporium fulvum, C.f.), propagating hyphae within cells ...

In addition to chitin binding proteins, C. fulvum secretes the effector Avr2 which binds to and inhibits plant extracellular cysteine proteases required for basal defense (van Esse et al., 2008). Transgenic A. thaliana plants expressing Avr2 show enhanced susceptibility to the necrotrophic fungal pathogens of Arabidopsis, Botrytis cinerea and Plectosphaerella cucumerina. However, the transgenic Arabidopsis plants were not more susceptible to another necrotrophic fungus, Alternaria brassicicola nor to the biotrophic haustorium-forming oomycetes Phytophthora brassicae and Hyaloperonospora parasitica (van Esse et al., 2008).

The smut fungus, Ustilago maydis – clustering of putative effector genes

The maize pathogen U. maydis is a biotrophic fungus that penetrates the plant cell wall and forms invasive hyphae that are surrounded by the plant plasma membrane and are thought to be the main interface for nutrient uptake and signal exchange (Brefort et al., 2009). The relatively small genome (20.5 Mb) of U. maydis compared to other plant pathogenic fungi, encodes 429 predicted secreted proteins, 70% of which are of unknown function (Kamper et al., 2006). About 20% of these genes are organised into 12 clusters, most of which exhibit increased expression during infection. Targeted deletion of individual clusters of these putative effector genes revealed that four clusters contribute to virulence. By contrast, deletion of one of the other eight clusters led to hypervirulence, suggesting that fungal effectors may also limit pathogen growth. Despite their general up-regulation during infection, deletion of the other seven clusters did not alter virulence, possibly because of functional overlap of with proteins outside these domains.

A more recent study compared the genomes of U. maydis and Sporisorium reilianum, two closely related smut fungi that infect maize (Schirawski et al., 2010). The two genomes show extensive synteny, however, 43 regions in the U. maydis genome, including seven of the 12 clusters discussed above, displayed low sequence conservation. In these divergent clusters more than 60% of the genes are predicted to encode secreted proteins, more than five times higher than in the rest of the genome (Schirawski et al., 2010). Deletion of six randomly-picked U. maydis gene clusters out of the 43 regions with low sequence homology resulted in attenuated virulence in three cases, increased virulence in one case and wild-type virulence in two cases.

Although the precise roles of most of the predicted U. maydis effectors are unknown, the Pep1 effector has been characterised (Doehlemann et al., 2009). Pep1 is a small (178 amino acids) secreted protein that is required for successful invasion of epidermal cells of Zea mays. In vivo immunolocalisation studies have revealed the presence of Pep1 in apoplastic spaces in leaves as well as its accumulation at sites of cell-to-cell passage of U. maydis. Inoculation of leaves with deletion mutants of U. maydis lacking Pep1 (SG200Δpep1) led to the development of large necrotic patches and failure of the pathogen to establish a compatible interaction with the host. SG200Δpep1 mutants were still able to penetrate the plant cell wall and grow within the first invaded cell, but were unable to penetrate a second cell and plant cell death occurred soon after. Expression of Pep1 in this mutant strain under the control of an early infection stage-specific promoter, allowed infection of the second cell, but further infection was still inhibited, suggesting that this protein is required for cell-to-cell passage throughout infection.

Studies of U. maydis proteins involved in cell adhesion and surface coating, have identified two other putative effectors that play a role in infection, namely the secreted hydrophobin, Hum3, and the hydrophobic repetitive and secreted protein, Rsp1 (Muller et al., 2008). Although individual mutations in these genes did not alter U. maydis virulence, double mutants were unable to infect Z. mays successfully. The double mutants showed normal morphology in vitro, and development, mating and aerial hyphal growth were identical to the wild type strains. However, hyphal growth in maize leaves stopped soon after the first few plant cells were invaded and the infected leaves displayed local chlorosis and necrosis (Muller et al., 2008). Thus, these two proteins are specifically required for the infection process allowing the fungus to successfully proliferate in planta.

The rice blast fungus, Magnaporthe oryzae – the biotrophic interfacial complex

Magnaporthe oryzae (previously M. grisae), the rice blast fungus, is a hemibiotrophic filamentous ascomycete and the major fungal pathogen of rice (Oryza sativa) (Couch and Kohn, 2002). M. oryzae has a genome approximately 38 Mb in size (Dean et al., 2005) and, depending on the threshold used for protein minimum length, encodes between 739 (Dean et al., 2005) and 2,470 (Choi et al., 2010) putative secreted proteins.

After penetrating the leaf cuticle and outer epidermal cell wall, the M. oryzae appressorial penetration peg forms a filamentous primary hypha surrounded by the plant plasma membrane within the epidermal cell (Figure 1). As the primary hypha develops into a bulbous, specialised invasive hypha (IH), a lobed structure called the biotrophic interfacial complex (BIC) forms at the hyphal tip (Khang et al., 2010). Before being translocated into the plant cytosol, M. oryzae effector proteins accumulate in the BIC. During the first 12 hours after leaf inoculation, IH proliferate within the initially-penetrated epidermal cell, but subsequently IH grow into neighbouring cells (Kankanala et al., 2007). Upon entering the adjacent cell, a new BIC is formed and secretes effectors. Fluorescent tagging of two BIC-associated secreted effectors, BAS1 and PWL2, showed that these proteins move from the infected cell into neighbouring, uninfected cells prior to their invasion by IH. These effectors may thus function to somehow ‘prime’ neighbouring cells for fungal invasion. Two other BIC-associated proteins, BAS2 and BAS3, are highly up-regulated in IH, and are present at the sites at which hyphae cross the cell wall into an adjacent cell (Mosquera et al., 2009). In contrast, the BAS4 effector accumulates throughout the matrix between the IH and the extrainvasive hyphal membrane but not in the BIC, and was not detected in host cells, suggesting that that the BIC represents a specific interface for delivery of M. oryzae effectors. Individual knockout mutants of these genes did not display any phenotypic changes and their function remains to be determined.

AvrPiz-t, another M. oryzae secreted fungal effector, is recognised in the plant cytosol by the cognate R protein, Piz-t, and can suppress BAX-induced cell death in tobacco (Li et al., 2009) suggesting that AvrPiz-t is translocated into the plant cytosol where it interferes with induction of host cell death. The fungal metalloprotease, AvrPita1, which causes R-mediated cell death in rice cultivars containing the Pi-ta R gene (Jia et al., 2000), is a member of the AvrPita family present in most Magnaporthe species (Khang et al., 2008). AvrPita1 is mainly localised to the BIC and in the plant cytosol where it is thought to exert its function (Khang et al., 2010).

The powdery mildew pathogen, Blumeria graminis – massive amplification of effector genes

Blumeria graminis is an obligate biotrophic fungus and the causal agent of powdery mildew disease on important crops such as barley (B. graminis f.sp. hordei) and wheat (B. graminis f.sp. tritici). B. graminis grows as filamentous hyphae on the leaf surface, but after penetrating the wall of the underlying epidermal cells, forms specialised feeding structures known as haustoria surrounded by an intact plant plasma membrane (Figure 1). Because it is an obligate biotroph and cannot be grown in culture, the use of molecular genetic tools such as targeted gene knockouts to study effector function has been limited. The genome of the haploid B. graminis f.sp. hordei is estimated to be 120 Mb, about four times larger than that of other ascomycetes due to massive proliferation of retrotransposon-derived repetitive DNA (Spanu et al., 2010). Despite its size, the genome lacks key enzymes for primary and secondary metabolite production, transporters, enzymes for anaerobic fermentation as well as enzymes for inorganic nitrate and sulphate incorporation. The absence of these genes is likely to be associated with the pathogen’s inability to grow in vitro.

Spanu et al. (2010) found 248 candidate secreted effector proteins (CSEPs) in the B. graminis f.sp. hordei genome, defined as secreted proteins that lacked homologues outside the mildew family. In contrast to the situation in U. maydis, there was no obvious clustering of CSEP genes. Of the 248 CSEPs, 80% contained the N-terminal tripeptide motif Y/F/WxC, that was recently recognised in putative powdery mildew effector proteins, and predominantly occurs four amino acids after the signal peptide cleavage site (Godfrey et al., 2010). The conservation of this motif in powdery mildew effectors suggests a common functional role, possibly in effector delivery into the plant cytoplasm as observed for the oomycete RxLR motif. The CSEPs with an N-terminal Y/F/WxC motif are generally devoid of other cysteine residues except for a single conserved C-terminal cysteine, which may therefore constitute part of this motif, possibly forming a disulphide bond with the N-terminal cysteine.

These new CSEPs differ from the previously identified B. graminis effector candidates, AVRa10 and AVRk1, which do not contain a secretion signal peptide (Ridout et al., 2006). Transient expression of AVRa10 and AVRk1 in susceptible plant varieties enhanced infection while their expression in resistant plant varieties carrying the cognate, cytosolic R genes Mla10 or Mlk1, respectively, caused cell death (Ridout et al., 2006). These experiments suggest that although AVRa10 and AVRk1 lack a recognisable signal peptide, they are secreted by the fungus and are delivered into the host plant cytoplasm. AVRa10 and AVRk1 appear to be have evolved as fusions to TE1 retrotransposons and there are over a thousand paralogs in the B. graminis f. sp. hordei genome (Spanu et al., 2010). This linkage to retrotransposons could provide a mechanism for diversification and amplification during effector evolution. Evidence for the rapid evolution of effectors as compared to other genes also comes from comparison of the B. graminis genome with those of two related powdery mildew fungi, Erisyphe pisi and Golovinomyces orontii (Spanu et al., 2010). The effector complement in these three pathogens is highly diverse despite an otherwise well conserved genome.

The rust fungi – the role of haustoria in effector secretion

Rust fungi are a diverse group of plant pathogens with over 7,000 species known to cause diseases in plants (Maier et al., 2003). Similar to the powdery mildews, rust infection involves formation of haustoria that penetrate host cells, but rust hyphae proliferate within the leaf rather than on the leaf surface (Figure 1). The flax rust fungus (Melampsora lini) and its host plant flax (Linum usitatissiumum) have served as an important model for plant immunity since Flor’s early analysis of resistance and virulence provided the first genetic description (the ‘gene-for-gene’ model) of ETI (Flor, 1955). Numerous R genes have been cloned from flax and encode cytosolic receptors while the corresponding effectors recognised by several of these receptors encode secreted proteins that are expressed in haustoria (Lawrence et al., 2007). The first flax rust effector identified was AvrL567, a protein recognised by the L5, L6 and L7 R proteins (Dodds et al., 2004). AvrL567 has undergone diversifying selection, resulting in at least twelve variants, some of which have now escaped recognition by the cognate R proteins by altering surface exposed amino acid residues (Dodds et al., 2006; Wang et al., 2007). Screening of a haustorium-specific cDNA library, led to the identification of three other secreted rust effector proteins, AvrM, AvrP123 and AvrP4, (Catanzariti et al., 2006). Of these effectors, only AvrP123 shows homology to known proteins, since it contains a Kazal-like serine protease inhibitor motif, and their roles in infection are unknown. Silencing of AvrL567 in transgenic flax rust did not significantly affect rust infection (Lawrence et al., 2010), suggesting there may be redundancy of its effector function in M. lini. All of these secreted effectors are recognised inside the host cell by cytosolic R proteins, indicating that they are translocated into the host cytoplasm after their secretion from the pathogen. This was confirmed by immunolocalisation of AvrM, which was detected inside host cells containing haustoria (Rafiqi et al., 2010), as was also observed for the bean rust effector RTP1 (Kemen et al., 2005). AvrL567 and AvrM both appear to translocate autonomously into host cells as a result of cellular uptake signals located in the N-terminal regions of the proteins (Rafiqi et al., 2010), although the transport mechanism is not yet defined.

Melampsora larici-populina, the causal agent of poplar leaf rust, is a close relative of the flax rust fungus. As in B. graminis, massive proliferation of transposable elements has led to the expansion of the M. larici-populina genome (101.1 Mb), however, in poplar rust, this proliferation has not coincided with a dramatic reduction in gene content (Duplessis et al., 2011). Of the 16,841 predicted proteins, about 1,200 encode small secreted proteins (SSPs) and about 40% of these are expressed in M. larici-populina-infected leaves 96 hours post-inoculation. This corresponds to the stage of infection at which haustoria are formed in the infected leaves. The SSPs expressed at this time include homologs of flax rust AvrM, AvrL567, AvrP123 and AvrP4 effectors. Two thirds of the 1,200 SSPs can be organised in 169 families, each containing two to 111 members. The largest of these families contains SSPs that are cysteine-rich, a characteristic of many extracellular effectors (Dean et al., 2005; Mueller et al., 2008).

Genome expansion has also occurred in Puccinia graminis f. sp. tritici, the causal agent of wheat stem rust (Duplessis et al., 2011). Of 1,105 predicted SSPs in P. graminis f. sp. tritici, 29 are among the most highly transcriptionally up-regulated genes during infection. Recently, putative pathogenicity-related proteins were identified by proteome analysis of haustorium-enriched samples from infected plant tissue (Song et al., 2011) but no clear function in infection has been assigned.

Conclusion, future directions and challenges

Since Flor suggested the gene-for-gene model of plant immunity (Flor, 1955), we have come a long way in understanding the interplay between plant immunity and pathogen virulence mechanisms. However, important questions remain to be answered. The majority of fungal effectors that apparently function in the plant cytosol lack obvious translocation signals within their primary sequence, and it is not clear how the effectors are targeted to and taken across the plasma membrane into the host cell. The high level of diversity among fungal effectors and the low sequence homology to other proteins makes it difficult to predict their functions in disease. Although roles have been defined for some fungal effectors in suppressing immune responses, given the relatively long lasting biotrophic nature of some of these interactions, it is likely that other effectors may have roles in manipulating the host metabolism to increase nutrient availability to sustain the infection. With next generation sequencing we now have the tools to readily obtain whole genome information from most biotrophic and hemibiotrophic fungi, even though many are difficult to study in vitro. In many cases, this analysis has revealed that fungal genomes contain a large number of small secreted putative effectors that are rapidly evolving compared to the rest of the genome. This amplification and rapid evolution may be due to the strong selection pressure exerted by the plant’s immune recognition system and/or to host species-specific adaptation to different pathogenicity targets. To what extent have effectors in different fungal pathogens evolved to target the same proteins in different host plants? Many of the fungal pathogens that are currently the focus of scientific investigation are pathogens of crop plants, and much of their evolution may have been influenced by domestication of the crop and creation of new pathogenic niches. Have host-pathogen interactions on native hosts evolved differently to those on crop plants? Interestingly, two symbiotic fungi have recently been shown to also direct secreted effectors into host cells (Plett et al., 2011; Kloppholz et al., 2011). To what extent do mutualistic and pathogenic fungi share common host manipulating processes? To answer these and many other questions, we need to have a much better understanding of the functions of the diverse array of effector proteins in plant pathogens. Given the large numbers of putative effectors, this will be a challenging task. Nevertheless, the rapid development of genomic tools and advanced microscopic techniques for studies of protein localisations and interactions are providing unprecedented avenues for exploring the roles of pathogen effectors in the interplay between plants and their fungal pathogens.


This work was supported by the Australian Research Council (DP1093850), the Australian Grains Research and Development Corporation (CSP00099) and the US National Institutes of Health (GM074265-01A2). MK is supported by an Australian National University higher degree in research scholarship.


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