Fungal pathogens-a sweet and sour treat for toll-like receptors.

Hundred-thousands of fungal species are present in our environment, including normal colonizers that constitute part of the human microbiota. The homeostasis of host-fungus interactions encompasses efficient fungal sensing, tolerance at mucosal surfaces, as well as antifungal defenses. Decrease in host immune fitness or increase in fungal burden may favor pathologies, ranging from superficial mucocutaneous diseases to invasive life-threatening fungal infections. Toll-like receptors (TLRs) are essential players in this balance, due to their ability to control both inflammatory and anti-inflammatory processes upon recognition of fungal-specific pathogen-associated molecular patterns (PAMPs). Certain members of the TLR family participate to the initial recognition of fungal PAMPs on the cell surface, as well as inside phagosomes of innate immune cells. Active signaling cascades in phagocytes ultimately enable fungus clearance and the release of cytokines that shape and instruct other innate immune cells and the adaptive immune system. Some TLRs cooperate with other pattern recognition receptors (PRRs) (e.g., C-type lectins and Galectins), thus allowing for a tailored immune response. The spatio-temporal and physiological contributions of individual TLRs in fungal infections remains ill-defined, although in humans, TLR gene polymorphisms have been linked to increased susceptibility to fungal infections. This review focuses entirely on the role of TLRs that control the host susceptibility to environmental fungi (e.g., Aspergillus, Cryptoccocus, and Coccidoides), as well as to the most frequent human fungal pathogens represented by the commensal Candida species. The emerging roles of TLRs in modulating host tolerance to fungi, and the strategies that evolved in some of these fungi to evade or use TLR recognition to their advantage will also be discussed, as well as their potential suitability as targets in vaccine therapies.

Introduction

An estimated 1.5 million fungal species are present in the environment (Hube, 2009). Some of them have evolved as commensal colonizers of cutaneous and mucosal surfaces in humans. While only a few fungal microbes are actually true pathogens for healthy individuals, in Western societies opportunistic fungi can cause life-threatening infections in immunosuppressed individuals, ranging from superficial mucocutaneous disease to invasive deep-seated infections. In developing countries, fungal infections affect not only immunocompromised but also immunocompetent healthy individuals in region of endemic mycoses (Brown et al., 2012), with Cryptococcus species (spp.) representing the major human fungal pathogen (Del Poeta and Chaturvedi, 2012). The main fungal pathogens affecting humans comprise those ubiquitously present in the environmental fungi, Aspergillus fumigatus, Cryptoccocus neoformans and more recently Cryptoccocus gatii, Histoplasma capsulatum, Coccidoides posadasii, Pneumocystis jirovecii and the commensal P. jiroveci or the Candida spp. The rising incidence in fungal infections observed in the last decades correlates with increases in invasive medical interventions, long-term hospitalization and with large numbers of immunosuppressed patients due to acquired- (e.g., HIV infection) or treatment-induced immunodeficiency such as transplantation or anticancer therapy (Pfaller and Diekema, 2007, 2010). No obvious clinical symptoms distinguish invasive fungal infections from other microbial infections. Furthermore, clinical diagnoses pose a huge challenge, since current methods are not always reliable, speedy, accurate, or specific, in particular when speciation is required for efficient antifungal therapy. Thus, anti-fungal treatments are often delayed or inappropriately applied. Consequently, fungi stand out as the fourth main cause of hospital acquired infections in “at-risk” populations, despite availability of efficient but costly antifungal therapies (Perlin, 2011; Pfaller, 2012).

Several particularities distinguish fungal from viral or bacterial microbes in their interaction with host immune cells. For instance, many fungal pathogens are dimorphic and able to undergo morphogenesis upon environmental or host stimuli, which facilitates immune evasion or dissemination and niche occupancy in the host. Morphogenesis is hence considered a major virulence trait (Gow et al., 2012). Further, all fungal eukaryotes are protected by the cell wall, a highly complex and flexible meshwork of carbohydrate polymers such as mannans, β-glucans, and chitin interwoven in a protein matrix (Gow and Hube, 2012). Due to its physical properties and its plasticity, this unique structure confers strong protection against all kinds of environmental stresses, including immune cell attack. It also is a major source of fungal pathogen-associated molecular patterns (PAMPs) that mediate host-fungi interaction during recognition by immune cells (Levitz, 2010).

The major class of pattern recognition receptors (PRRs) known to be involved in sensing and recognition of fungal PAMPs comprise the C-type lectin receptor family recognizing glucan and mannan (such as Dectin-1, Dectin-2, Mincle, SIGNR, and mannose receptor), the scavenger receptors (such as CD5 and CD36), Galectin-3, and the Toll-like receptor (TLR) family (Romani, 2011). This review addresses TLRs recognizing fungal pathogens on hematopoietic and non-hematopoietic cells, recapitulating the most recent advances in the field. We shall reiterate the emerging concept of TLRs in shaping host-fungal relationships. Importantly, we will also discuss fundamental differences of TLR function in mouse and humans, since there is increasing evidence not only for cell-type specific responses, but also for species-specific distinct roles of TLRs in fungal immunity or tolerance.

Fungal sensing by toll-like receptors

Recognition of fungal PAMPs by surface and phagosomal TLRs

The precise molecular nature of fungal PAMPs that active specific TLRs is difficult to pin down due to the often collaborative mechanism of TLR recognition and the plasticity of the fungal cell wall. Whereas fungal PAMPs are clearly recognized by a number of TLRs (i.e., TLR2/1, TLR4, TLR3, TLR2/6, TLR7, and TLR9), they are not the primary receptors driving pathogen engulfment. Fungal PAMPs for cell-surface TLRs have been mainly characterized for Candida albicans, but they remain mostly unknown for other fungi. For C. albicans, mutants with specific cell wall defects have facilitated the identification of PAMPs. Because cell-wall mutations often attenuate virulence or induce compensatory alteration of the cell wall composition (Murciano et al., 2011), altered immune responses to such mutants should be interpreted with caution. Nonetheless these studies have proven useful in identifying cell wall components activating TLRs (Figure 1). For example, TLR2 recognizes fungal β-glucans of several fungal species (Viriyakosol et al., 2005; Netea et al., 2006; Sorgi et al., 2009). In addition, it also specifically interacts with phospholipo-mannans (PLMs), linear beta-1,2-oligomannoside structures that are unique to C. albicans (Jouault et al., 2003). TLR2 is also stimulated by as yet unidentified ligands present on conidia and hyphae forms of A. fumigatus (Netea et al., 2003). TLR2/TLR1 and TLR2/TLR6 heterodimers are receptors for the glucuronoxylomannan (GXM) component of Cryptococcus neoformans (Fonseca et al., 2010). Notably, A. fumigatus activates mouse but not human TLR2/6 heterodimers, whereas TLR2/1 heterodimers recognize A. fumigatus both in human and mice (Rubino et al., 2012). This is a striking example of differences between human and mice in fungal recognition. TLR4 is activated upon ligation of C. albicans O-linked mannans (Netea et al., 2006), as well as C. neoformans GXM (Shoham et al., 2001). Ligands for TLR4 are present as well on A. fumigatus conidia but not hyphae (Netea et al., 2003).

Figure 1

TLR signaling induced in host cells upon interaction with fungal pathogens. Surface Toll-like receptors (TLRs), as well as endosomal TLRs participate to the recognition of fungal PAMPs [e.g., O- and N-linked mannans, phospholipo-mannan (PLM), glucuronoxylomannan (GXM), α-mannosides, β-glucans, DNA, and RNA]. Activation of surface TLRs involves their homo- (TLR4) or hetero-dimerisation (TLR2/TLR1 or TLR6). The diversity of signaling pathways is increased by the involvement of co-receptors of the C-type lectin family (e.g., SIGNR1 and Dectin-1) or Galectin-3. Confirmed physical interactions between PRRs are represented by double-head arrows. The integration of simultaneously activated signaling pathways occurs at the level of intracellular adaptors and transcription factors shared between overlapping pathways. The resulting cytokine responses shape the activation of the adaptive response and ultimately modulate the outcome for the host. This figure was adapted from Bourgeois et al. (2010) by including newly published data from Biondo et al. (2012) and Takahara et al. (2012), and as reviewed in Romani (2011) and Leibundgut-Landmann et al. (2012). A. fumigatus, Aspergillus fumigatus; C. albicans, Candida albicans; Candida spp, Candida species; C. neoformans; Cryptococcus neoformans; M. furfur, Malassesia furfur.

In addition, to cell surface PAMPs, nucleic acids liberated from fungi within the phagosome also stimulate or modulate the dynamic host response during infection. TLR3 is activated by double-stranded RNA from A. fumigatus conidia in lung epithelial cells (Beisswenger et al., 2012). Single-stranded RNA from Candida spp. are ligands for TLR7 in mouse bone-marrow dendritic cells (BM-DCs) (Biondo et al., 2011). TLR9-mediated sensing of fungal genomic DNA (gDNA) appears conserved across fungal species (Nakamura et al., 2008; Ramirez-Ortiz et al., 2008; Miyazato et al., 2009; Biondo et al., 2011) and the recruitment of TLR9 to fungi-containing phagosome is observed with several fungal species (Kasperkovitz et al., 2011). Recognition of gDNA from A. fumigatus and C. neoformans occurs at unmethylated CpG motifs (Nakamura et al., 2008; Ramirez-Ortiz et al., 2008; Tanaka et al., 2011). By contrast, TLR9 detection of Candida gDNA does not seem to be restricted to these motifs (Miyazato et al., 2009).

TLRs and modulation of immunity to fungi

Hematopoietic stem cells

Recent advances in hematopoietic stem cell (HSC) research suggest that commensal microbes, including fungi, “shape” the steady-state hematopoiesis through their interaction with TLRs (Boiko and Borghesi, 2012). Ligation of TLRs on mouse or human HSCs by microbial PAMPs affects both proliferation and differentiation (Baldridge et al., 2011; Boiko and Borghesi, 2012). At steady state, bone marrow from mice lacking TLR4, TLR9, or MyD88 exhibit enhanced reconstitution activity (Massberg and Von Andrian, 2009). Furthermore, in Drosophila, mutations in the Toll/cactus pathway cause a deregulated hematopoiesis (Qiu et al., 1998). Thus, TLR signaling in HSCs may serve two purposes: (1) it participates in the maintenance of basal hematopoietic homeostasis in the absence of triggers, and (2) it activates emergency hematopoiesis upon microbial infections. In a mouse model of systemic infection, C. albicans stimulates both proliferation and differentiation of HSCs and committed progenitors, driving enhanced granulopoiesis independently of G-CSF (Basu et al., 2000) but in a MyD88/TLR2-dependent fashion (Yanez et al., 2009, 2010, 2011). Notably, TLR2 promotes the differentiation of HSCs into macrophages and monocyte-derived DCs upon interaction with Candida spp. (Yanez et al., 2010, 2011).

Innate, adaptive and non-hematopoietic effector cells

Professional phagocytes such as neutrophils, monocyte/macrophages, and dendritic cells, are rapidly recruited at the site of infection upon fungal challenge (Lionakis et al., 2010, 2012; Majer et al., 2012; Wuthrich et al., 2012b). Notably, the lack of TLR2 impairs the early recruitment as well as killing capacity of neutrophils against A. fumigatus (Meier et al., 2003; Bellocchio et al., 2004a). Similarly, fewer neutrophil/monocytes are recruited in TLR2−/− mice in comparison to wild-type animals at day 1 after post-peritoneal infection with live C. albicans (Tessarolli et al., 2010). Interestingly, upon intraperitoneal challenge with heat-killed C. albicans, TLR2 defficiency has no effect on early (4 h) phagocyte recruitment, but results in an enhanced macrophage recruitment in mutant versus control mice at day 3 after infection (Netea et al., 2004). These results suggest that TLR2 differentially modulates phagocyte recruitment during the course of candidiasis. Additionally, the use of live versus heat-killed Candida cells may affect both kinetics and nature of recruited phagocytes. Phagocytes emerging at day 1 of post-peritoneal infection with live Candida exhibit impaired nitric-oxide release, myeloperoxidase activity, chemokine, and cytokine production, as well as neutrophil survival in the absence of TLR2 (Tessarolli et al., 2010). Thyoglycolate-elicited TLR2−/− neutrophils and macrophages show reduced phagocytic activity toward C. albicans than their wild-type counterparts (Tessarolli et al., 2010). Notably, no significant effects of TLR2 on phagocytosis by similar cells has also been reported (Netea et al., 2004), perhaps due to distinct experimental conditions used in the phagocyte preparations.

By contrast, the absence of TLR4 diminishes neutrophil effector functions against both A. fumigatus and C. albicans (Meier et al., 2003; Bellocchio et al., 2004b; Gasparoto et al., 2010), whereas TLR9 deficiency enhances the fungicidal capacity of neutrophils as well as macrophages (Bellocchio et al., 2004b; Kasperkovitz et al., 2011). Lack of TLRs also modulates the cytokine response in macrophages and dendritic cells upon fungal encounters (for review see, Romani, 2011) (Figure 1). In BM-DCs, but not in bone-marrow derived-macrophages, both TLR7 and TLR9 trigger the release of IFN-β in response to Candida (Biondo et al., 2011, 2012; Bourgeois et al., 2011). Notably, IL-12 p70 release is also dependent on both TLR7 and TLR9 in these cells (Biondo et al., 2012).

Th1 and Th17 are the principal Th subsets that contribute to a protective adaptive response to fungal pathogens (for review see, Hernandez-Santos and Gaffen, 2012; Leibundgut-Landmann et al., 2012; Wuthrich et al., 2012a). However, IL-17 and Th17 cells have been reported to be detrimental in certain mouse models of fungal infection (Zelante et al., 2009). In humans, by contrast, a defect in IL-17 signaling is linked to increased susceptibility to mucocutaneous Candida infection (Puel et al., 2011). Regulatory T-cells (Tregs) modulate the Th1/Th17 balance either by preventing expansion of the Th17 subset or by minimizing host damage (Loures et al., 2009). However, Tregs may also enhance the Th17 response and promote fungal clearance (Pandiyan et al., 2011). TLRs could influence the adaptive response either indirectly via activation of antigen presenting cells (APCs) or, by acting as co-receptors for TCRs directly on T-cells (for review see Jin et al., 2012). It is generally accepted that TLRs mediate the development of antifungal Th1 response. Notably, MyD88 is dispensable for the CD4+ T-cell priming against and trafficking during Aspergillus airway infections (Rivera et al., 2006), but it is required for the differentiation of fungi-specific CD4+ T-cells into IFN-γ-producing cells in lungs. TLR2, however, may promote T-reg differentiation. Indeed, TLR2−/− mice have reduced levels of natural Tregs in comparison with wild-type mice, suggesting that TLR2 also regulates Treg homeostasis. In a Paracoccidoides brasiliensis intratracheal infection model, TLR2 promotes Treg expansion, thereby limiting Th17 cell differentiation and tissue pathology (Loures et al., 2009). By contrast, in a systemic infection model of candidiasis, TLR2-mediated recognition of Candida triggers IL-10 production and decreases Th1 polarisation (Netea et al., 2004). Recent studies suggest that TLRs may also play a direct role in the induction of a Th17 antifungal response: TLR6 exerts protective effects in a model of chronic Aspergillus-induced asthma, by promoting IL-23 release and a subsequent Th17 response (Moreira et al., 2011). In a skin-resident DC subset, Langerhans cells, MyD88 is required for their full activation and function in response to C. albicans infection, including the development of a Th17 response (Haley et al., 2012). Similarly, in a Blastomyces dermatidis-specific TCR mouse model, MyD88 but not dectin-1 is required for the development of a vaccine-induced Th17 subset and resistance to infection, which is consistent with the involvement of TLRs in DC activation (Wuthrich et al., 2011). Furthermore, TLR3-defficient mice fail to activate protective memory-CD8+ T cells following vaccination by A. fumigatus (Carvalho et al., 2012b). Thus, some TLRs expressed in APCs may be good candidates to stimulate DCs for antifungal vaccination strategies both as danger signals and to condition professional APCs to induce the appropriate class of protective adaptive immunity (for review see, Iannitti et al., 2012; Roy and Klein, 2012).

Terminally differentiated epithelial cells also take an active part in antifungal defense and immune surveillance (for review see, Naglik and Moyes, 2011; Weindl et al., 2011). The TLR expression levels are altered in these cells upon fungal infection, and their cytokine response is, at least in part, TLR-dependent. In mice, TLR4 is required for protection of epithelial cells from fungal invasion in the presence of polymorphonuclear leucocytes (PMNs) (Weindl et al., 2007). Similarly, TRIF−/−epithelial cells are more susceptible to A. fumigatus due to over activation of Th17 cytokines and down-regulation of Th1-Tregs (De Luca et al., 2010). Thus, TLR signaling in epithelial cells may modulate the inter-cellular communication and cooperation between hematopoietic and non-hematopoietic cells. Deregulation of underlying processes can enhance immunopathology and impair clearance (De Luca et al., 2010). Notably, TLRs also modulate the ability of epithelial cells and innate immune cells to sense and respond to danger signals others than established TLR ligands, including host or fungal proteases or other host “damage-associated molecular patterns” (DAMPs) (Moretti et al., 2008; Sorci et al., 2011).

Mechanisms modulating toll-like receptor signaling during fungal recognition

Because microbial pathogens usually carry multiple classes of PAMPs, their recognition may involve the simultaneous or sequential activation of several PRRs from different families. Collaboration between PRRs and/or cross talk between their signaling pathways can enhance the specificity and coverage of PAMP recognition and enables a tailored host response (Van De Veerdonk et al., 2008a) (Figure 1). TLR2 transduces signals as a heterodimer recruiting either, TLR1 or TLR6 (Ozinsky et al., 2000). However, the functional consequences of these TLR cooperations for fungal recognition remain ill-defined. In addition, several molecules including C-type lectins or other carbohydrate-binding proteins have been identified as TLR2 co-receptors (e.g., Dectin-1, SIGNR1, and Galectin-3). Interestingly, depending on the co-receptor involved, co-ligation of TLR2 may either enhance a TLR2-dependent response (Smeekens et al., 2010; Takahara et al., 2012) or modulate its PAMPs specificity (Jouault et al., 2006). Dectin-1 has also been shown to synergies with TLR4 signaling (Ferwerda et al., 2008).

The molecular basis of signaling pathway crosstalk is just beginning to be investigated (reviewed in Hontelez et al., 2012). Dectin-1 signaling requires its clustering and the formation of a phagocytic synapse (Goodridge et al., 2011). No physical interaction between TLR2 and Dectin-1 have been reported so far, but TLR2 co-immunoprecipitates with Galectin-3 following stimulation with C. albicans (Jouault et al., 2006). Interestingly, Galectin-3 also co-immunoprecipitates with Dectin-1 (Esteban et al., 2011), suggesting that Galectin-3 may mediate the cooperation between TLR2 and Dectin-1 signaling. TLR2 also co-immunoprecipitates with SIGNR1 (Takahara et al., 2012). Thus, the dynamic clustering and/or exclusion of PRRs from the phagocytic synapse may control and modulate signaling cross talks during the initial immune response to surface PAMPs. Subsequent liberation of fungal PAMPs such as nucleic acids, through fungal pathogen degradation in the course of phagosome maturation may promote further recruitment of PRRs (Stuart and Ezekowitz, 2005; Kasperkovitz et al., 2010).

In addition to microbial PAMPs, host DAMPs arising from tissue damage such as S100B proteins are also released at the site of inflammation during infection. In a TLR2-dependent fashion, low doses of S100B proteins promote fungal clearance and protect against inflammation-induced epithelial damage in lungs of mice with A. fumigatus intranasal infections. By contrast, the TLR3/TRIF axis may reduce over-production of S100B proteins, thereby preventing exacerbation of the inflammation reaction to promote its resolution (Sorci et al., 2011). Thus, host DAMPs may collaborate with PAMP-activated TLRs to control the outcome of the inflammatory response.

C. albicans is uniquely recognized by TLR2 after antifungal treatment that targets and alters the cell wall (Roeder et al., 2004). Similarly, pretreatment of C. albicans or A. fumigatus with anti-fungal drugs enhance their ability to stimulate TLR expression in human PMNs (Salvenmoser et al., 2010). These results suggest that beside their direct fungicidal properties, antimycotics may also facilitate pathogen detection by the host and thereby, facilitate clearance.

Fungal strategies to escape or subvert detection by toll-like receptors

Many fungal pathogens have developed strategies to escape or subvert host immune recognition systems, including sensing by TLRs or other PRRs (for review see, Collette and Lorenz, 2011). Cell wall remodeling upon environmental stress or during hyphae formation may change PAMP composition and alter accessibility for TLRs as observed for many species (Hohl et al., 2005; Collette and Lorenz, 2011). Furthermore, formation of large cellular structures either by germination and filamentation in dimorphic fungi, or by nuclear replication without fission in Cryptococcus, can hamper phagocytosis (Okagaki et al., 2010; Zaragoza et al., 2010) and thereby, is likely to prevent activation of the intra-phagosomal recognition processes.

Cryptococcus spp. and several other fungi secrete polysaccharides and protein cargos through dedicated exosomes upon host interaction. Supernatant of C. neoformans cultures inhibit TLR9 activation by C. neoformans DNA (Yamamoto et al., 2011). Similarly, A. fumigatus cell wall components differentially modulate TLR2 and TLR4 signaling (Chai et al., 2011).

Activation of endosomal TLR7-9 is controlled by their timely recruitment to the phagosome and proteolytic processing upon ligand binding (Ewald and Barton, 2011). Thus, modulation of intracellular protein trafficking and phagosome maturation, are likely to influence the recognition of fungal pathogens by endosomal TLRs. Candida spp. as well as H. capsulatum prevent phagosomal maturation and acidification (Eissenberg et al., 1993; Marcil et al., 2008; Fernandez-Arenas et al., 2009; Garcia-Rodas et al., 2011; Seider et al., 2011). C. neoformans and C. albicans share the ability to escape the phagosome, although using entirely distinct mechanisms (Collette and Lorenz, 2011). Paradoxically, the rapid recruitment of TLR9 to the fungus-containing phagosomes favors persistence, suggesting that this receptor may be exploited as an immune evasion strategy by several fungal species (Kasperkovitz et al., 2010, 2011).

TLR-signaling and inborn susceptibility to fungal infections

Mouse models of fungal infections

Mice lacking MyD88, the signaling adaptor shared by several surface and endosomal receptors, but also by the IL-1, IL-18, and IL-33 receptors, are hypersensitive to systemic C. albicans infections (Bellocchio et al., 2004a; Villamon et al., 2004), as well as to intraperitoneal and intranasal C. neoformans infections (Yauch et al., 2004; Biondo et al., 2005). Fungal clearance is impaired in MyD88−/− mice during systemic and intra-gastric candidiasis, pulmonary, as well as corneal aspergillosis, and during C. neoformans infections (Bellocchio et al., 2004a; Yauch et al., 2004; Biondo et al., 2005; De Luca, 2007; Leal et al., 2010). Consistently, expression of Th1 and inflammatory cytokines during C. neoformans infections is lower in mice lacking MyD88 when compared to wild-type mice (Biondo et al., 2005).

In corneal aspergillosis, TRIF-deficient mice do not exhibit a fungal killing defect (Leal et al., 2010). However, in intra-gastric infection models, TRIF−/− mice fail to prevent spreading of C. albicans to peripheral organs (De Luca, 2007). In pulmonary aspergillosis, TRIF−/− mice as well as TLR3−/− mice are highly susceptible to infection and develop pathogen-induced inflammation (De Luca et al., 2010; Carvalho et al., 2012b). Thus, these data suggest that TLR signaling adaptors drive pathways with distinct effector functions in fungal pathogenesis. TRIF pathways appear to promote tolerance, whereas MyD88 is required for fungicidal activity (Romani, 2011).

Mice lacking TLR2 exhibit an intrinsic defect in the number of CD4+CD25+Treg subset that maintains peripheral tolerance, but may also dampen the immune response to infection (Netea et al., 2004). Upon intravenous Candida infection, absence of Tregs results in improved fungal clearance 7 days after infection and better survival of TLR2−/− mice when compared to wild-type mice (Bellocchio et al., 2004a; Netea et al., 2004). By contrast, in an intraperitoneal model of candidiasis, clearance is impaired 1 day afterinfection in the absence of TLR2 (Tessarolli et al., 2010). TLR2-deficient mice infected with P. jirovecii display intenser severity in symptoms, as well as increased fungal burden and decreased TNFα and nitric oxide release in the lungs (Wang et al., 2008).

Immunosuppressed TLR2−/− mice (neutropenic and treated with antibiotics) have an increased susceptibility to A. fumigatus following intratracheal infection and increased fungal burden in the lung in comparison to wild-type immunosuppressed animals (Balloy et al., 2005). By contrast, cyclophosphamide-treated TLR2−/−mice are equally susceptible to intranasal Aspergillus infections than control mice, although untreated mutant mice have higher lung fungal burden (Bellocchio et al., 2004a). In a model of chronic fungal asthma, TLR2−/− mice show impaired airway hyper-responsiveness to A. fumigatus and reduced fungal clearance at early infection stages. As a result of fungal persistence, but also perhaps due to the deficiency in the Treg subset, airway hyper-responsiveness increases during the adaptive phase of this disease model (Buckland et al., 2008). In a model of mouse corneal inflammation, TLR2-deficiency does not affect immune cell infiltration or fungal clearance (Leal et al., 2010). Conversely, Aspergillus-induced corneal inflammation in rats is decreased following application of TLR2 siRNA when compared to non-specific siRNA and fungal clearance, as well as the outcome of fungal disease, are improved (Guo et al., 2012).

TLR2−/− mice are also more susceptible to intranasal or intraperitoneal cryptococcal infections and exhibit higher fungal burden (Yauch et al., 2004; Biondo et al., 2005), as well as decreased inflammatory cytokines (Biondo et al., 2005). By contrast, in a model of Cryptococcus intratracheal infections, TLR2−/− mice show no changes in survival in comparison to control mice (Nakamura et al., 2006). Thus, in most mouse models of fungal airway infection, TLR2 appears to contribute to fungal clearance, perhaps by modulating the induction of inflammatory cytokines. However, depending on the airway infection model, the disease outcome itself may vary from unaffected to increased susceptibility. Conversely, in systemic or corneal infection models, T-regs may hinder fungal clearance and worsen the outcome of fungal disease.

Mice lacking TLR4 are either hyperresistant, hypersensitive or equally susceptible to fungal challenges than wild-type mice, depending on the C. albicans or the mouse strains used or the infection route. The recently described variable recognition of different C. albicans strains by TLR4 may account for some of these apparent discrepancies (Netea et al., 2010). TLR4 recognition may be required to elicit host defense only against strains inducing proinflammatory cytokines in a TLR4-dependent fashion. Interestingly, C. albicans mutants lacking particular glycosylation patterns such as O-glycosylation, are specifically recognized by TLR4, and lead to enhanced activation of macrophages (Lewis et al., 2012). Hence, intraspecies variability in cell wall glycosylation can determine the nature of the interaction between TLR4 and C. albicans strains, and thereby the type and intensity of the host immune response. A similar mechanism may be operating in flies, since Toll-signaling in Drosophila can distinguish virulent from avirulent Candida strains (Glittenberg et al., 2011).

Lack of TLR4 exacerbates the host inflammatory response to P. jirovecii in mice, though without affecting pathogen clearance (Ding et al., 2005). However, the course of intranasal, tracheal, intravenous, or intraperitoneal infections with C. neoformans remains unaffected in these mutant mice in comparison with control mice (Yauch et al., 2004; Biondo et al., 2005; Nakamura et al., 2006). In a model of pulmonary fungal infection with C. posadasii, lack of TLR4 improved fungal clearance (Awasthi, 2010). By contrast, Aspergillus killing is impaired in TLR4−/− mice in a model of corneal inflammation, although immune cell infiltration is unaffected (Leal et al., 2010). Whether intraspecies variabilities in cell wall composition can determine the nature of interactions between TLR4 and other fungal species than Candida remains open.

TLR3-defficient mice fail to activate protective memory-CD8+ T cells following Aspergillus vaccination (Carvalho et al., 2012b). Mice deficient in TLR7 are more susceptible to systemic infections by low doses of C. albicans than their WT wild-type littermates. However, when challenged with higher doses, the mutant mice are equally susceptible to infection than the control mice (Biondo et al., 2012).

A lack of TLR9 impairs clearance and decreases survival to C. neoformans challenge in an intranasal infection model (Nakamura et al., 2008; Wang et al., 2011). In this model, TLR9 contributes to the early induction of CCL7 and IFN-γ, thereby promoting recruitment and activation of DCs and other effector cells. Similarly, a lack of TLR9 during intratracheal C. neoformans infections results in impaired clearance during the adaptive phase, decreased recruitment of lymphocyte and macrophages, as well as alternative activation of macrophages (Zhang et al., 2010). By contrast, TLR9−/− mice depleted from neutrophils/inflammatory monocytes prior to tracheal infection with A. fumigatus, exhibit delayed mortality in comparison to depleted control mice (Ramaprakash et al., 2009). Notably, although TLR9-deficiency in immunosuppressed mice has no effect on survival to A. fumigatus after intranasal infections, it improves clearance (Bellocchio et al., 2004a).

Using high dose challenges, TLR9−/− mice show no significant alterations in survival to clinical isolates of C. albicans (Van De Veerdonk et al., 2008b; Miyazato et al., 2009; Biondo et al., 2012), and even enhanced clearance when infected with an avirulent strain (Bellocchio et al., 2004a). However, a lower fungal dose leads to increased susceptibility to systemic candidiasis and impaired fungal clearance in TLR9−/− mice (Biondo et al., 2012), indicating that the fungal load may determine the role of TLR9 during infection. In summary, TLR9 signaling appears to mediate clearance of Cryptococcus and low doses of C. albicans. However, TLR9 may be exploited for immune evasion by C. albicans at higher doses or A. fumigatus. Interestingly, endosomal TLR7, TLR8, and TLR9 show inhibitory cooperations or interactions (Wang et al., 2006). Notably, autoimmune models have been instrumental for a better understanding of regulatory interactions between endosomal TLRs, indicating a modulatory role of TLR9 on TLR7 signaling (Ewald and Barton, 2011). Thus, the improved clearance observed in TLR9−/− phagocytes may result from hyperactivated TLR7 signaling in absence of TLR9 (Nickerson et al., 2010).

Thus, contrary to the strong impact of MyD88 deficiency on fungal clearance and disease susceptibility, data from animal models with single TLR defects are more difficult to interpret or often even conflicting. This may result, at least in part, from the central role of MyD88 as adapter protein not only for most TLRs but also for cytokine receptors recognizing IL-1, IL-18, and IL33. IL-1R signaling for instance has an essential function in the defense against C. albicans but not all fungal species (Bellocchio et al., 2004a; Leal et al., 2010; Wang et al., 2011). Hence, the contribution of individual TLRs to protection against infection appears to greatly vary depending on the fungal strain and/or species, infection model, infection dose as well as the genetics of mouse strains.

Furthermore, unchanged susceptibility of some TLR-deficient mouse strains may be due to a possible dual role of TLRs on pathogen clearance but also host tolerance (Ayres and Schneider, 2008; Carvalho et al., 2012a; Medzhitov et al., 2012). In this scenario, lack of a given TLR may impair fungicidal mechanisms, but also improve host tolerance to infection such that the final outcome of disease appears unaffected by the TLR absence. The notion that tolerance to infections is as crucial for resolution of infections as it is for resistance to the pathogen is a relatively recent conceptual idea in mammalian infection biology (Schneider and Ayres, 2008; Carvalho et al., 2012a; Medzhitov et al., 2012). Consequently, experimental approaches that enable identification and quantification of trade-offs between tolerance and resistance may help to better characterize and understand the roles and contributions of TLRs to microbial infections in general.

In humans

By sharp contrast to mice, humans with MyD88 signaling defects do not have increased incidence of fungal infections (Von Bernuth et al., 2008). This may relate to the fact that Candida spp. are commensal colonizers of humans but not of mice (Savage and Dubos, 1967), but also that significant differences exist between human and mouse TLR signaling (Rehli, 2002). However, some TLR single nucleotide polymorphisms (SNPs) in TLR genes significantly augment the risk of contracting fungal infection in humans (summarized in Table 1). TLR1 SNPs are associated with higher susceptibility to candidemia in humans. In agreement, cytokine release by blood monocytes in response to C. albicans is impaired in these patients (Plantinga et al., 2012). Invasive aspergillosis is one of the most important nosocomial infections after HSC transplantations (Cunha et al., 2011; Lamoth et al., 2011). Recipients of allogeneic HSC transplants carrying the TLR1 Arg80Thr or both TLR1 Asn248Ser and TLR6 Ser249Pro SNPs are more prone to Aspergillus infections (Kesh et al., 2005). Increased susceptibility to aspergillosis is also observed in this “at-risk” group in patients carrying a TLR3 +95C/A, but not a TLR3 L412F, SNP (Carvalho et al., 2012b). As a result of the TLR3 +95C/A SNP, activation of a memory-protective CD8+ T-cell responses against Aspergillus is impaired (Carvalho et al., 2012b). By contrast, TLR3 L412F SNP is associated with increased prevalence of cutaneous candidiasis and impaired TLR3 signaling (Nahum et al., 2011, 2012).

Table 1

TLR polymorphisms associated with increased susceptibility to fungal diseases.

Gene	SNPs or haplotypes	Effect	Disease	Outcome	References
TLR1	R80T, N248S, I602S	Reduced cytokine production by PBMCs in vitro	Invasive aspergillosis, C. albicans systemic infections	Susceptibility	Kesh et al., 2005; Plantinga et al., 2012
TLR3	+95C/A	Failure to activate CD8+ T-cell response	Invasive aspergillosis	Susceptibility	Carvalho et al., 2012b
	L412F	Decreased TLR3 functionality	Chronic mucocutaneous candidiasis	Susceptibility	Nahum et al., 2011
TLR4	D299G/T399I	Predicted to impair ligand binding	Invasive aspergillosis, A. fumigatus, CCPA, C. albicans systemic infections	Susceptibility	Van Der Graaf et al., 2006; Bochud et al., 2008; Carvalho et al., 2008; De Boer et al., 2011
TLR6	S249P	Unknown	Invasive aspergillosis	Susceptibility	Kesh et al., 2005
TLR9	T-1237C	Increased NF-κB binding affinity	ABPA	Susceptibility	Carvalho et al., 2008

ABPA, allergic bronchopulmonaryaspergillosis; CCPA, chronic cavitary pulmonary aspergillosis; C. albicans, Candida albicans; A. fumigatus, Aspergillus fumigatus. Modified from Romani, (2011)

An enhanced risk of chronic pulmonary aspergillosis has been linked to allele G on TLR4 Asp299Gly (Carvalho et al., 2008). The prevalence of this SNP in association with TLR4 Thr399Ile was also higher in a patient cohort suffering from Candida blood-stream infection in comparison to the control group (Van Der Graaf et al., 2006). Peripheral blood mononuclear cells (PBMCs) from patients carrying both polymorphisms exhibited enhanced IL-10 release upon C. albicans challenge (Van Der Graaf et al., 2006) but not PBMCs from patients carrying only the TLR4 Asp299Gly (Van Der Graaf et al., 2005). Finally, allele C on TLR9 T-1237C has been linked to a higher susceptibility to allergic bronchopulmonary aspergillosis (Carvalho et al., 2008). Hence, a growing body of evidence indicates that TLRs are actively involved in Candida and Aspergillus recognition in humans and most likely in recognition of other fungal pathogens as well. The challenges associated with such studies are the low number of patients/groups and the relative low risk of infection in people carrying these SNPs, perhaps due to genetic redundancy in certain components (Netea et al., 2012) or because of TLR dual roles in shaping both resistance and tolerance to fungi. The consequences of SNPs may become more obvious in individuals with a weakened immune system. The continuous identification of new SNPs and the characterization of their effects at the molecular and cellular level will help a further uncovering of TLR roles in the antifungal immune response in humans. The identification of functional SNPs may also serve to detect “at-risk” patients and design efficient prophilaxy when necessary. Interestingly, age-related alterations in the host response to fungi may also occur, as recent data indicate that neutrophils from elderly individuals express lower levels of TLR2 than younger patients (Gasparoto et al., 2012).

Conclusions and perspectives

Historically, TLRs were the first described specific PRRs for fungal pathogens. The past 12 years of research on host immune response to fungi have delineated the roles of several TLRs in mediating cytokine response upon fungal interaction. Importantly, mouse survival studies have uncovered somewhat contradictory (protective or detrimental) or even non-conclusive (without effect) data on the role of TLRs in the murine antifungal response. Similarly, humans lacking MyD88, an ubiquitous signaling adaptor for TLRs, fail to show increased incidences of fungal infections. To date, no genetic defects in human TLRs have been associated with a primary immune deficiency conferring increased susceptibility to either mucocutaneous or invasive fungal infections (reviewed in Lilic, 2012). However, certain TLR SNPs are clearly associated with increased susceptibility to fungal disease in specific “at-risk” populations, suggesting that TLRs are involved in fine-tuning the outcome of various host-fungus interactions (e.g., commensalism, symbiosis, latency, infection, and dissemination). In agreement, at the cellular levels, most TLRs appear not to be required for the primary step of sensing and engulfment of fungal microbes by innate immune cells. However, TLRs are recruited to sites of host cell-microbe recognition and modulate the subsequent host-fungi interplay in maturing phagosomes. Furthermore, certain TLRs mediate specific protective adaptive responses. Thus, such TLRs may be suitable targets for activating DCs in efforts to generate fungal vaccines (Iannitti et al., 2012; Roy and Klein, 2012).

The outcome of a host response is determined by several phases, including activation of inflammatory defenses aimed at eliminating pathogens. However, uncontrolled host inflammatory responses promote sepsis and can be fatal for the host (Lionakis et al., 2012; Majer et al., 2012). Thus, the ability of the host to (1) control the inflammatory response in a timely manner and (2) to activate tissue repair mechanisms to resolve organ damages are critical components of a proper host immune response (Medzhitov et al., 2012). In this prospect, new findings suggest that TLRs and other PRRs may be involved in epithelial resistance to fungi (Weindl et al., 2011; Iliev et al., 2012). Whether TLR signaling also modulates the activity of professional phagocytes that promote the resolution of inflammation and repair processes during fungal infection (Sica and Mantovani, 2012), remains to be established.

Finally, exciting recent advances in the molecular mechanisms driving an immune memory of innate origin (Netea et al., 2011), open new fields concerning possible roles of TLRs in host-fungus interactions. Indeed, fungal β-glucans acting through Dectin-1 are clearly able to prime mouse and human monocytes to elicit a stronger inflammatory response upon restimulation with C. albicans or other PAMPs, and this by inducing chromatin remodeling (Quintin et al., 2012). The effect of β-glucans, reminiscent of the LPS-mediated priming of some TLR4-induced genes through chromatin modifications (Foster and Medzhitov, 2009), raises the question whether other fungal PAMPs, such as nucleic acids, may also induce monocyte priming in a TLR-dependent fashion. These data also suggest new ways by which PRRs in innate cells, including TLRs, exploit host chromatin remodeling to shape the host immune response to fungi at steady-state and during dynamics of infections (Tierney et al., 2012).

Funding

This work was funded by the Christian Doppler Research Society and by a grant from the FWF-DACH programme to Karl Kuchler (FWF-Project API-746-B11). Christelle Bourgeois was also supported by the EC Marie Curie Training Network “CanTrain” (CT-2004-512481).

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.