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Review

Purine Acquisition and Synthesis by Human Fungal Pathogens

by
Jessica L. Chitty
1,2 and
James A. Fraser
1,*
1
Australian Infectious Diseases Research Centre, School of Chemistry & Molecular Biosciences, the University of Queensland, St Lucia, Queensland 4072, Australia
2
Institute for Molecular Bioscience, the University of Queensland, St Lucia, Queensland 4072, Australia
*
Author to whom correspondence should be addressed.
Microorganisms 2017, 5(2), 33; https://doi.org/10.3390/microorganisms5020033
Submission received: 31 May 2017 / Revised: 6 June 2017 / Accepted: 6 June 2017 / Published: 8 June 2017
(This article belongs to the Special Issue Fungal Nutrition Assimilation Strategies and Pathogenicity)
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Abstract

:
While members of the Kingdom Fungi are found across many of the world’s most hostile environments, only a limited number of species can thrive within the human host. The causative agents of the most common invasive fungal infections are Candida albicans, Aspergillus fumigatus, and Cryptococcus neoformans. During the infection process, these fungi must not only combat the host immune system while adapting to dramatic changes in temperature and pH, but also acquire sufficient nutrients to enable growth and dissemination in the host. One class of nutrients required by fungi, which is found in varying concentrations in their environmental niches and the human host, is the purines. These nitrogen-containing heterocycles are one of the most abundant organic molecules in nature and are required for roles as diverse as signal transduction, energy metabolism and DNA synthesis. The most common life-threatening fungal pathogens can degrade, salvage and synthesize de novo purines through a number of enzymatic steps that are conserved. While these enable them to adapt to the changing purine availability in the environment, only de novo purine biosynthesis is essential during infection and therefore an attractive antimycotic target.

1. The Diversity of Fungi and the Environments They Inhabit

Federico Cesi, founder of the Accademia dei Lincei and a keen observer of his local environment, first attempted the scientific classification of organisms. “Imperfect” plants, particularly fungi, fascinated Cesi; his colleague Galileo Galilei constructed a microscope to help him observe these organisms in great detail, and Cesi commissioned hundreds of drawings of mushroom species collected from Rome and southern Umbria until his death in 1630 [1]. The Italian priest and botanist Pier Antonio Micheli later continued Cesi’s classification. His most notable work Nova Plantarum Genera documented 1400 new “plant” species collected from around Europe, of which 900 were fungi or lichens and included the first documented human fungal pathogen [2]. A few decades later, Swedish botanist and zoologist Carl Linné made a significant contribution to modern taxonomy by classifying organisms from around the globe in his seminal work Systema Naturae, although fungal species were poorly addressed in this publication [3]. Almost 100 years later, mycologists Christian Hendrik Persoon and Elias Magnus Fries addressed these shortcomings by classifying fungi sent by leading scientists from around the world [4,5,6]. Combined, these extensive works that took place over four centuries identified thousands of fungi that expanded well beyond Cesi’s Italian mushrooms to include more diverse species inhabiting a wide range of environments. However, it was not until 1969 that the Fungi were classified as their own kingdom and not a subset of plants [7,8]. With the aid of genomic sequencing, the number of species identified now numbers over one million and these are believed to be just the tip of the iceberg, accounting for an estimated 5–7% of species with many environments largely unsampled [9,10].
Species from the kingdom Fungi differ greatly in habitat, morphology and nutrient requirements. As heterotrophs, these organisms digest organic molecules such as proteins, polysaccharides and nucleotides, and are often found in nutrient rich environments. In contrast, many fungi can survive in extreme conditions. Aspergillus sydowii inhabits deep-sea hydrothermal vents more than 700 meters below sea level where temperatures reach almost boiling point [11]. Penicillium chrysogenum can be found in the Atacama Desert, where it has been hyper arid for at least three million years [12]. Nadsoniella nigra var. hesuelica survives periodic freezing and thawing in Antarctica [13]. Other species survive in a very different extreme environment—the human host —where fungal pathogens must be heat tolerant, resilient to immune defenses and scavenge nutrients that can be difficult to acquire [14].
Of the fungal pathogens affecting humans, three pose the most consistent major threat worldwide: Aspergillus fumigatus, Candida albicans and Cryptococcus neoformans, causing aspergillosis, candidiasis and cryptococcosis, respectively. Even with the best available antifungal treatment in developed countries, low efficacy, toxicity and resistance is a major contributor to the high mortality associated with these invasive fungal infections [15,16]. Each preferentially infects specific sites in patients, from the lung in pulmonary aspergillosis to the brain in cryptococcal meningoencephalitis and the blood stream in systemic candidiasis, yet all employ similar mechanisms to acquire sufficient nutrients to survive and establish an infection [17,18,19].
Unlike C. neoformans and A. fumigatus, which are often found in soil, guano and decaying matter [20,21,22,23], C. albicans is a commensal species, commonly found in the gastrointestinal tract and on mucocutaneous surfaces [24,25]. While these environments are vastly different, one important class of biological compounds consistently present are the purines.
To expel excess nitrogen, bird excreta contains high concentrations of the insoluble hetrocyclic compound uric acid, a strategy that reduces water loss compared to the mammalian excretion of nitrogen as its soluble derivative urea [26]. Fresh plant matter such as cauliflower has a purine content of approximately 0.4 mg/g [27]; when living organisms, such as plants, decompose, purines become enriched in soil and so are available to fungi such as C. neoformans and A. fumigatus [28]. Furthermore, the different tissues of the live human host also vary significantly in the context of purines. The concentrations of purines in the gastrointestinal tract inhabited by C. albicans are dependent on the host’s diet, whereas the cerebral spinal fluid to which C. neoformans disseminates is a particularly purine-poor environment [29,30,31].

2. Purines and Their Role in the Cell

Purine, a term coined by Emil Fisher in 1884 after he synthesized a novel compound from “pure urine”, is a molecule composed of one six and one five-membered nitrogen-containing ring fused together. The addition of at least one phosphate to this molecule makes it a nucleotide, a biochemically important component of the cell [32]. These molecules are essential to DNA and RNA biosynthesis, energy metabolism and signal transduction, and are the most widely occurring nitrogen-containing heterocycle in nature [33]. Purines are also predicted to have been amongst the first organic compounds synthesized by abiotic chemistry on the early earth; adenine, the nucleobase of adenosine triphosphate (ATP), is proposed to have been formed during the prebiotic era by the condensation of five hydrogen cyanide molecules [34,35].

3. Purines as a Nitrogen Source

Defects in the degradation of purines for the excretion of excess nitrogen were first implicated to play a role in disease in 1848 by Alfred Garrod. However, the biochemical process in a microbe of degrading purines to acquire nitrogen required for growth was not studied until 1853 when Friedrich Wohler investigated this process in an unidentified yeast species. Nitrogen is a major component of a number of molecules, including amino acids, pyrimidines, and purines, and is essential for life. Fungi are known for their ability to use a wide range of nitrogen sources via a range of catabolic enzymes [36,37].
The process of utilizing purines as a nitrogen source proceeds via the degradation of xanthine to uric acid by xanthine oxidase. Uric acid can then be sequentially degraded by a further five enzymatic activities to produce ammonia (Figure 1). Depending on the fungal species, the entry point for this degradation pathway varies. For example, during its evolution into a facultative anaerobe Saccharomyces cerevisiae lost oxygen-dependent urate oxidase, but it can still use allantoin or allantoate as a nitrogen source. In contrast, the fungal pathogen C. neoformans can utilize uric acid as a sole nitrogen source [38,39,40].
The importance of maintaining a fully functional degradation pathway is not true for all fungi; some plant colonizing species of fungi such as Piriformospora indica lack this ability [41]. The Pneumocystis pneumonia-causing fungus Pneumocystis jirovecii also lacks the catabolic enzymes required for the degradation of purines, although this is the only human fungal pathogen known to do so [42].

4. Salvaging Purines

As well as breaking down the purines obtained from the environment to serve as a nitrogen source, fungi also scavenge these essential nutrients for metabolic processes. Small molecules such as nucleotides are detected by plasma membrane-localized sensors to be transported across the plasma membrane to be used in nucleotide biosynthesis [43]. A number of proteins have been identified in fungi that transport purines. Three distinct nucleobase-specific transporter classes exist: nucleobase-ascorbate transporter (NAT) families 1 and 2, the nucleobase cation symporter family 1 (NCS1) and the AzgA-like family. These are all secondary active transporters as they catalyze the transport of two chemical species, a purine and a proton, in the same direction [44], Once scavenged nucleotides are transported into the cell via these dedicated transporters, they are available for incorporation into the salvage pathway. The principal enzymes responsible for the interconversion of purines are hypoxanthine xanthine guanine phosphoribosyltransferase (HXGPT) and adenine phosphoribosyltransferase, enzymes that transfer a 5-phosphoribosyl group to a purine to create the corresponding nucleotide.

5. Synthesizing Purines

Fungi may not always be able to salvage sufficient purines from the environment; in many cases nucleotides must be synthesized de novo from precursor molecules. Acquiring purines from the environment is energetically favorable compared to de novo biosynthesis, which requires 14 enzymatic activities and a number of cofactors for the magnesium-dependent generation of either ATP or guanosine triphosphate (GTP) from phosphoribosyl pyrophosphate. Inosine monophosphate (IMP) biosynthesis requires the acquisition of ammonia from two molecules of l-glutamine, ligation of l-aspartate, and hydrolysis of four ATP molecules, with two 10-formyl-THF formyl donors. For the synthesis of ATP from IMP (Figure 2), an additional l-aspartate molecule is ligated, and one GTP and two ATP molecules are hydrolyzed. The synthesis of GTP from IMP (Figure 2) requires an additional molecule of one l-glutamine, hydrolysis of three ATPs and the hydride transfer from one nicotinamide adenine dinucleotide (NAD+) molecule. In total, in order for de novo synthesis to occur, 10 molecules of ATP are hydrolyzed per molecule of AMP synthesized, and 11 for GMP [45,46]. It is estimated that 107 ATP molecules are used per second per S. cerevisiae cell; therefore, the steady supply of purine nucleotides is essential for survival. While scavenging these purines is the most energy efficient strategy, having an intact de novo purine synthesis pathway is highly advantageous to fungi that inhabit environments with varying concentrations of purines [46].
Some species of fungi have lost the ability to synthesize purines and rely solely on the salvage of nucleotides from their environment. The Microsporidia have lost a number of enzymatic activities required for the de novo synthesis of purines, meaning the complete process is no longer possible in these obligate parasites [47,48]. However, the high expression of nucleoside diphosphate kinase required for the phosphorylation of adenosine and guanosine suggests that aspects of purine biosynthesis still play an important role in the metabolism of these parasites [47].

6. Purine Metabolism in Candida Albicans

While records detailing the symptoms of oral candidiasis date back to 400 B.C., for many centuries, these were thought to originate from the host rather than an infectious agent [49,50]. In 1771, Rosen von Rosenstein identified an invasive fungal pathogen as the causative agent of this disease, and, in 1847, the French mycologist Charles Philippe Robin classified it as Oidium albicans [51,52]. Almost a century later, Christine Marie Berkhout reclassified it under the current genus Candida [52].
The commensal pathogen C. albicans is a frequent member of the gut microbiota; in healthy individuals, it is observed in approximately 40% of the population [25]. For those that do not have an intact immune system, this pathogen poses a major threat and is the leading cause of hospital-acquired bloodstream infections, with those in intensive care units being most at risk [53]. The switch from unicellular commensal yeast to pleiomorphic invasive pathogen is driven by multiple environmental cues. In vitro, this can be induced by changes in pH, temperature, CO2 concentration, serum and many other factors [54,55,56,57].
The yeast form of C. albicans commonly found in the gastrointestinal tract has plentiful access to nutrients, including proteins, carbohydrates, fats and nucleotides such as purines. The concentration of available purines varies depending on the diet of the host (Table 1) with foods high in purines such as seaweed containing millimolar concentrations, and foods low in purines such as carrots containing nanomolar concentrations [58]. Prior to purine absorption by the host in the small intestine—in particular, in the mucosa of the duodenum—these purines are available to be scavenged by the gut microbiota [59]. In its pathogenic form, C. albicans is found in the bloodstream where it causes candidemia; the available purines in the blood are in the micromolar concentration range (Table 1) [60].
Enzymes required for the degradation of purines into ammonia have not been well characterized in C. albicans. BLASTp analyses using C. neoformans orthologs revealed that genes predicted to encode the majority of purine degradation components are present in C. albicans. Six enzymes required for the sequential breakdown of xanthine to ammonium were identified: xanthine oxidase (C2_00180C) for the conversion of xanthine to uric acid, 5-hydroxyisourate (HIU) hydrolase (C2_08460C) for the conversion HIU to 2-oxo-4-hydroxy-4-carboxy-5-ureidoimidazoline (OHCU), OHCU decarboxylase (C3_01620W) for the conversion of OHCU to (S)-allantoin, allantoinase (C3_00180C) for the conversion of allantoin to allantoate, and allantoicase (C2_00630C) converting allantoate to urea. For the final step of hydrolyzing urea to ammonia, C. albicans encodes a urea amidolyase (C1_04660W) that carries out two steps: carboxylation of urea to urea-1-carboxylate, followed by hydrolysis to two molecules of ammonia. In addition, a zinc cluster transcription factor exclusively found in fungi has been identified as playing a role in purine catabolism in C. albicans. Ppr1 regulates uracil degradation in S. cerevisiae but plays a different role in C. albicans, where it is involved in the regulation of allantoin degradation [64].
Salvage of nitrogenous compounds by C. albicans from the environment is essential in the production of virulence factors such as adherence to the host tissue, hyphal morphogenesis, and release of ammonia to counteract acidification of the phagolysosome [65]. UV microscopy has shown that, in vitro, C. albicans actively takes up the purines guanine and adenine within a few hours from the growth medium. The concentrations of purines within the vacuole of the cell became supersaturated, suggesting that when purines are available, the fungus scavenges all it can [66]. The consumption of extracellular nucleotides in C. albicans occurs via their hydrolysis to nucleosides by ecto-enzymes attached to the cell membrane that actively import purines into the cell [67].
While the enzymes of the purine salvage pathway have not been characterized in this species, BLASTp analyses using C. neoformans orthologs revealed the presence of a gene predicted to encode adenine phosphoribosyl transferase (C2_01430W), suggesting that C. albicans can covert adenine to AMP. A likely member of the phosphoribosyl transferase family (C2_02740C) responsible for the conversion of one or more of hypoxanthine, xanthine and/or guanine into their respective phosphorylated nucleotides is also present. Other enzymes involved in the interconversion of purines are anticipated in C. albicans; a BLASTp analysis using S. cerevisiae orthologs identified genes predicted to encoded adenine deaminase (C2_03360W) and guanine deaminase (C7_00670W) for the conversion of adenine to hypoxanthine and guanine to xanthine.
While only a few of the genes required for de novo purine biosynthesis have been characterized in C. albicans, BLASTp analysis using C. neoformans orthologs reveals genes thought to encode the ten enzymatic activities required for the conversion of phosphoribosyl pyrophosphate to IMP: PRP transferase (C1_07710C), GAR synthetase/AIR synthetase (C1_07890C), GAR transformlyase (C2_03090C), FGAM synthetase (CR_04740C), AIR carboxylase (C3_04520C), SAICAR synthetase (CR_06150C), ADS lyase (CR_06150C) and AICAR transformylase/inosine cyclohydrolase (ATIC) (CR_04090C). Additionally, the four enzymatic activities for synthesis of ATP from IMP (ADS synthetase (C1_09640W), ADS lyase (CR_06150C), adenylate kinase (C6_01910W) and nucleotide diphosphate kinase (C5_02890W)) and the four activities for GTP synthesis from IMP (IMP dehydrogenase (C2_06390C), GMP synthase (C1_09490C), guanylate kinase (C503790W), and nucleoside diphosphate kinase (C5_02890W)) are also predicted to be encoded by genes identified in C. albicans.
Mutation and deletion studies of some of the genes encoding the enzymatic activities required for de novo purine biosynthesis have been carried out in C. albicans. Mutants found to produce red pigmentation were hypothesized to encode AIR carboxylase and SAICAR synthetase based on S. cerevisiae studies identifying the pigmentation as a result of the accumulation of oxidized and polymerized AIR in the vacuole [68]. Subsequent targeted gene disruption of the ade2 gene encoding AIR carboxylase in C. albicans results in reduced virulence in a murine candidiasis model [69]. The strain was unable to proliferate in human serum unless supplemented with exogenous adenine, and, although not completely avirulent, exhibited a 100-fold attenuation of virulence [69].
The deletion of genes encoding two other enzymes of the de novo purine biosynthesis pathway in C. albicans has also been performed. The genes ADE8 and GUA1 encoding the enzymes GAR transformylase and GMP synthase have been deleted and in vivo growth assays for both strains showed they were unable to grow on media without supplementation of exogenous purines; adenine was required for the ade8 mutant and guanine was required for the gua1 mutant [70,71,72]. Both of these deletion strains were hypersensitive to the purine biosynthesis inhibitors methotrexate and 6-azauracil [71]. In a candidiasis model of infection, the gua1 strain is avirulent [70].

7. Purine Metabolism in Aspergillus Fumigatus

Historically, the Aspergillus molds have been recognized as a genus since 1729 [2]. They have been attributed to infection since the French revolution, and the species fumigatus known to frequently cause aspergillosis since the early 1900s [73,74]. More recently A. fumigatus has become recognized as the most prevalent airborne fungal pathogen, commonly causing severe or fatal infections in immunocompromised individuals [75,76,77].
The asexual conidia of A. fumigatus are produced in abundance and inhaled by animals and humans on a regular basis. In healthy individuals, these are cleared by the innate immune system; however, in an immunodeficient individual, they pose a significant risk. Invasive aspergillosis is frequently observed in cancer and transplant patients, accounting for 10–25% of life-threatening opportunistic infections in leukemia treatment centers and 15–25% in transplant units [77,78,79,80,81,82,83].
Like many decomposers, A. fumigatus is commonly found in soil where organic matter provides plentiful nutrients. Purine availability varies considerably in this niche depending on a number of factors. Investigation of purine composition of soil has identified that humic acids (the principle component of soil humus) are richer in the purines guanine and adenine than the pyrimidines cytosine, thymine and uracil. The concentration of purines in dry soils have been shown to range from 21 to 138 μg per gram and the concentration distribution is consistent within soils: guanine is the most abundant, followed by cytosine, adenine, thymine and the least abundant, uracil [63]. Purine concentrations also vary greatly in plant life that will eventually become part of the diet of saprobes; the legume Alysicarpus vaginalis and the Jujube fruiting tree species Ziziphus jujube and Ziziphus mauritiana have been determined to have average purine concentrations of 0.005 to 2.6 μg/mL of guanine and 0.002 to 1.2 μg/mL of adenine (Table 1) [61,62].
Compared to this, the lung of an infected individual is a vastly different environment. The small size of the conidia of A. fumigatus (2–3 μm) allows them to enter the respiratory tract, descend to the aveoli and bind to surfactant proteins to be endocytosed by epithelial cells [78,84,85]. In the lungs, host-produced extracellular ATP plays a role as an endogenous signaling molecule involved in inflammation [86]. Once in the bloodstream, A. fumigatus encounters guanine at a concentration of 97 μM and adenine at 0.2 μM (Table 1).
While purine metabolism has not been well characterized in A. fumigatus, more extensive characterization of the pathway in Aspergillus species has been carried out in Aspergillus nidulans, with all enzyme-encoding genes believed to be associated with degradation, salvage, and de novo biosynthesis of purines identified in this species [87,88,89,90]. BLASTp analysis using A. nidulans orthologs revealed that the majority of purine degradation components are also likely present in A. fumigatus. A. nidulans encodes a second enzyme, xanthine α ketoglutarate dependent dioxygenase, for the conversion of xanthine to uric acid; this was not identified in A. fumigatus by BLASTp analysis but the alternative enzyme xanthine oxidase (Afu2g10520) (which is also present in A. nidulans) was identified.
BLASTp analyses using A. nidulans orthologs revealed the genes predicted to encode enzymes of the salvage pathway in A. fumigatus, including hypoxanthine xanthine guanine phosphoribosyl transferase (Afu4g04550) and adenine phosphoribosyl transferase (Afu7g02310), suggesting that A. fumigatus can convert hypoxanthine to IMP, xanthine to XMP, guanine to GMP, and adenine to AMP, respectively. In addition to phosphoribosyl transferase enzymes, A. fumigatus is predicted to encode adenine deaminase (Afu8g02860) and xanthine dehydrogenase (Afu4g11220) for the conversion of adenine to hypoxanthine and hypoxanthine to xanthine. The adenine deaminase enzyme encoded by the nadA gene is involved in the conversion of AMP to IMP and can be considered as a degradation or a salvage enzyme. In A. nidulans, adenine deaminase is essential for the utilisation of adenine as a sole nitrogen source, and, unlike other enzymes required for purine degradation, its expression is not supressed by ammonium, perhaps reflecting an increase in purine interconversion when grown in favourable conditions [91].
BLASTp analyses of the characterized genes of de novo purine biosynthesis from A. nidulans predicted genes encoding the ten enzymatic activities required for the conversion of phosphoribosyl pyrophosphate to IMP to be present in A. fumigatus, as are the four enzymatic activities for synthesis of ATP from IMP and the four activities for synthesis of GTP from IMP. The deletion of the purine biosynthesis GMP synthase-encoding guaA gene in A. fumigatus has shown that the strain is unable to grow on media lacking exogenous guanine, and, in a murine model of infection, the guaA deletion mutant was avirulent [70]. Computational modeling has supported the hypothesis that these purine biosynthesis enzymes could serve as potential drug targets in A. fumigatus and the related species Aspergillus niger [92].

8. Purine Metabolism in Cryptococcus Neoformans

The basidiomycete yeast Cryptococcus neoformans was first identified in 1894 by Sanfelice in peach juice and associated with disease shortly after, identified from lesions from the tibia in a 31-year-old patient [93,94]. The division of higher fungi or Basidiomycota is important for the effective breakdown of organic compounds in the environment. Their coevolution with woody plants for over 350 million years has given rise to many species possessing ligno-cellulytic enzymes that digest plant cell walls. This digestive process is essential in the formation of soil humus [95,96,97]. The soil humus contains varying levels of purines, highly dependent on the flora of the area (Table 1).
As well as soil, C. neoformans is commonly associated with bird guano. Unlike mammals, some species require excess nitrogen to be converted to uric acid for its excretion rather than urea; the uric acid cycle requires more energy but conserves water, which, for many organisms such as birds, is more important [98,99]. Bird excreta, or guano, has long been valued for its fertilizing properties. Ancient South American civilizations added this fertilizer to enrich soil and improve crops, risking their lives to sail 21 km off the coast of Pisco to the guano-rich Chincha Islands [100]. This ancient tradition reached Europe through the exploration of Alexander von Humboldt, leading to a time that became known as the guano boom [101]. Chemists such as Gustav Magnus analyzed the nitrogen content to determine the prices that guano should be sold. He reported an acid precipitation on the guano material and found a novel compound now known as guanine to be in high concentrations [102]. Bird guano is also high in uric acid, the ingredient responsible for the bird guano-associated damage of buildings, particularly limestone. Since the identification of guanine from guano, no quantitative analysis has been done to identify the specific concentration of purines in this substrate.
C. neoformans has been associated with bird guano since the 1960s and has since been identified worldwide from bird droppings in a range of locations [21,22]. Pigeon guano medium supports the growth of C. neoformans and the production of a key virulence factor, melanin. In addition, C. neoformans is able to undergo its sexual cycle on pigeon guano, supporting the theory that pigeon guano is the ecological niche of this fungal pathogen, as it can complete its life cycle solely in this environment [103].
Unlike Aspergillus species that can use a wide range of nitrogen sources, C. neoformans is more limited and restricted to ammonium, amino acids and purines [37]. All genes encoding the predicted enzymes of the purine degradation pathway in C. neoformans have been characterized. Six enzymatic reactions are required for the breakdown of xanthine to ammonium and are as follows: urate oxidase for oxidation of urate to HIU (CNAG_04307, URO1), HIU hydrolase (CNAG_06694, URO2) hydrolyzing HIU to OHCU, OHCU decarboxylase (CNAG_00639, URO3) converting OHCU to (S) allantoin, allantoinase (CNAG_00934, DAL1) hydrolyzing allantoin to allantoate, allantoicase (CNAG_01108, DAL2) converting allantoate to urea, and finally urease (CNAG_05540, URE1) hydrolyzing urea to ammonium [104]. Each of the genes identified to encode these enzymes has been sequentially deleted and characterized [104]. None of these deleted genes affected production of the virulence factors capsule or melanin, nor initiation of the C. neoformans sexual cycle [104]. In a murine inhalation model of cryptococcosis, only urease, the final enzyme of the pathway for the hydrolysis of urea to ammonia, is required for pathogenesis [105,106,107].
The salvage pathway in C. neoformans consists of a number of enzymes that can interconvert purine intermediates. The nucleoside hydrolases are required for the hydrolysis of nucleotides to nucleosides; hypoxanthine-xanthine-guanine phosphoribosyltransferase (CNAG_02546, HPT1) (HXGPRT) and adenine phosphoribosyltransferase (CNAG_01390, APH1) phosphorylate the nucleotides hypoxanthine, xanthine, guanine, and adenine to IMP, XMP, GMP and ATP, respectively [108,109]. The phosphoribosyltransferases have been studied in this organism, and the deletion of the genes encoding these enzymes did not result in any phenotypic differences from the wild-type, nor affect virulence in a murine model of cryptococcosis suggesting purine salvage is not important during the infection process [108,109].
Like C. albicans and A. fumigatus, C. neoformans encodes ten enzymatic activities for the conversion of phosphoribosylpyrophosphate to IMP. Additionally, four enzymatic activities are required for IMP to be converted to GMP and four enzymatic activities for its conversion to AMP. Deletion of the gene encoding AIR carboxylase (CNAG_02294, ADE2) showed the identical phenotype to C. albicans and S. cerevisiae of red pigmentation produced and similarly led to the pathway’s investigation as a potential antifungal drug target. The ade2Δ mutant in a murine inhalation model and rabbit cryptococcal meningitis model was avirulent [110,111]. Enzyme kinetic assays using recombinantly purified protein revealed differences in activity between C. neoformans and Gallus gallus AIR carboxylase, suggesting that this could be a novel target of inhibition against the fungal pathogen [112].
Analysis of the enzymes from the IMP branchpoint to either adenine or guanine synthesis has been carried out for four enzymes in C. neoformans: adenylosuccinate synthetase (ADSS) (CNAG_02858, ADE12), adenylosuccinate lyase (ADSL) (CNAG_03270, ADE13), inosine monophosphate dehydrogenase (IMPDH) (CNAG_00441, IMD1) and guanine monophosphate synthase (GMP synthase) (CNAG_01877, GUA1) [108,109,113,114]. Deletion of the genes encoding these enzymes leads to strains that are purine auxotrophs, are attenuated for virulence factor production and are avirulent in a murine inhalation model, contrasting starkly with the salvage mutants and highlighting the importance of de novo purine biosynthesis during infection [108,109,113,114]. Biochemical and structural analyses have determined potential differences between these fungal enzymes and their human counterparts that may be exploited in the development of fungal-specific therapeutics [108,109,111,112,113,114].

9. Purine Biosynthesis as an Antifungal Drug Target

Since the 1940s, the synthesis of purines has been an important biochemical pathway in the discovery of novel drugs [80,115,116]. The enzymatic activities of the purine biosynthesis pathway have been particularly useful targets in the development or discovery of antibiotic, anticancer and immunosuppressive agents, such as hadacidin, mercaptopurine, and mycophenolic acid (MPA) [117,118,119,120,121,122].
MPA, an inhibitor of the rate-limiting enzyme IMPDH in de novo synthesis of guanosine nucleotides, has been shown to have activity against C. albicans, A. fumigatus and C. neoformans [70,108,123,124]. Mode of action studies have determined that MPA binds to the site of the mobile flap of IMPDH and prevents formation of the closed enzyme conformation [125]. Studies of C. neoformans IMPDH have shown that, while it is inhibited by MPA, unlike mammalian IMPDH, this drug is able to bind to all conformations of the fungal IMPDH and not exclusively to the open conformation [108]. Interestingly, only limited inhibition of A. fumigatus IMPDH by MPA occurs, which is perhaps unsurprising given that MPA is produced by several Penicillium species commonly found in the same environments, and A. fumigatus, therefore, may have developed some resistance to the compound produced by competing species in its environmental niche [126]. Unfortunately, MPA itself cannot be used as an antifungal agent in the clinic against opportunistic pathogens due to its immunosuppressive activity; however, investigating this drug for activity against fungal enzymes is proof of principle that the enzyme of these pathways can be targeted by inhibitors of purine biosynthesis and may be a starting point for fungal specific inhibitor development.
The l-aspartate analog hadacidin has been identified as an antibiotic and anticancer agent that targets ADS synthetase [117,127]. First isolated from Penicillium frequentans, this compound exhibits 100% inhibition against Eschrichia coli as well as excellent clinical activity against human adenocarcinoma [128]. However, in fungi, this compound does not show antifungal activity against C. neoformans or A. fumigatus, and whilst there is some inhibition of C. albicans growth, this is limited [109]. In enzyme kinetics assays, hadacidin cannot fully inhibit C. neoformans ADS synthetase, but, again, this compound could serve as a basis for the development of antimycotics that act via ADS synthetase [109]. While little, if anything, is known about the antifungal activity of other purine biosynthesis inhibitors such as mercaptopurine (which closely resembles hypoxanthine and adenine and targets the HGPRT enzyme), the known activities of MPA and hadacidin along with the available crystal structures of their targets suggests that purine biosynthesis has the potential to be a valuable target for future antimycotic development.

10. Conclusions

While the salvage of environmental purines, the synthesis of de novo purine nucleotides and the breakdown of purines to their simplest form, ammonia, are common to the fungi that pose the most consistent major threat to humans, these processes are not all essential during the infection process. Scavenging purines from their environmental niche likely confers a selective advantage to A. fumigatus, C. albicans and C. neoformans. However, during infection, the de novo biosynthesis pathway is essential, likely due to pressures such as rapid proliferation, host immune defenses, and differences in purine availability. Deletion or disruption of enzymes from the de novo purine pathway in all three species are associated with either avirulence or reduced virulence of strains, making these an attractive antifungal drug target.

Acknowledgments

Jessica L. Chitty is a recipient of a Queensland Medical Research Scholarship. James A. Fraser received funding from the National Health and Medical Research Council, Grant APP1049716.

Author Contributions

Jessica L. Chitty and James A. Fraser wrote the paper.

Conflicts of Interest

The authors declare no conflict of interest.

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Microorganisms 05 00033 g001 550
Figure 1. Blue represents enzymes found in C. albicans, A. fumigatus, and C. neoformans. Pink represents an enzyme found in both C. albicans and A. fumigatus. Green represents an enzyme found in A. fumigatus only. Abbreviated enzyme names: PRP (Phosphoribosylpyrophosphate) amidotransferase, GAR (glycinamide ribotide) synthetase, GAR (phosphoribosyl-glycinamide) transformylase, FGAM (formylglycinamidine-ribonucleotide) synthetase, AIR aminoimidazole ribotide) synthetase, AIR (Phosphoribosylaminoimidazole) carboxylase, SAICAR (N-succinyl-5-aminoimidazole-4-carboxamide ribotide) synthetase, ADS (adenylosuccinate) lyase, AICAR (5-aminoimidazole-4-carboxamide ribonucleotide) transformylase, IMP (inosine monophosphate) cyclohydrolase, ADS (adenylosuccinate) synthetase, IMP (inosine monophosphate) dehydrogenase, GMP (guanine monophosphate) synthase.
Figure 1. Blue represents enzymes found in C. albicans, A. fumigatus, and C. neoformans. Pink represents an enzyme found in both C. albicans and A. fumigatus. Green represents an enzyme found in A. fumigatus only. Abbreviated enzyme names: PRP (Phosphoribosylpyrophosphate) amidotransferase, GAR (glycinamide ribotide) synthetase, GAR (phosphoribosyl-glycinamide) transformylase, FGAM (formylglycinamidine-ribonucleotide) synthetase, AIR aminoimidazole ribotide) synthetase, AIR (Phosphoribosylaminoimidazole) carboxylase, SAICAR (N-succinyl-5-aminoimidazole-4-carboxamide ribotide) synthetase, ADS (adenylosuccinate) lyase, AICAR (5-aminoimidazole-4-carboxamide ribonucleotide) transformylase, IMP (inosine monophosphate) cyclohydrolase, ADS (adenylosuccinate) synthetase, IMP (inosine monophosphate) dehydrogenase, GMP (guanine monophosphate) synthase.
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Figure 2. Structures of the key intermediates involved in de novo and salvage pathways containing a purine ring (blue) and the resultant non-purine breakdown product urea.
Figure 2. Structures of the key intermediates involved in de novo and salvage pathways containing a purine ring (blue) and the resultant non-purine breakdown product urea.
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Table
Table 1. Concentration of purines (μM unless indicated) from the habitats of C. albicans, A. fumigatus and C. neoformans.
Table 1. Concentration of purines (μM unless indicated) from the habitats of C. albicans, A. fumigatus and C. neoformans.
Source of purineAdenineGuanineXanthineHypoxanthineInosineReference
Average meal 1 (per gram)0.91.01.80.02ND[58]
Human Blood serum0.49720172168[60]
Human Cerebral spinal fluid0.20.52.43.90.6[29,30]
Human Intracellular1.597ND370211[60]
Plant matter average 20.4 μg/mL1.3 μg/mL0.8 μg/mL1.0 μg/mL1.2 μg/mL[61,62]
Soil average 319 M %19 M %NDNDND[63]
ND for no data. 1 Average meal defined as 100g rice, 75g carrot, 75g peas, 100g chicken [58]. 2 Average plant matter concentration from of A. vaginalis, Z. jujuba, Z. jujuba var. spinosa and Z. mauritiana plants [61,62]. 3 An average soil concentration was determined as proportion of purine relative to the g of air-dried soil from different locations [63].

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Chitty, J.L.; Fraser, J.A. Purine Acquisition and Synthesis by Human Fungal Pathogens. Microorganisms 2017, 5, 33. https://doi.org/10.3390/microorganisms5020033

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Chitty JL, Fraser JA. Purine Acquisition and Synthesis by Human Fungal Pathogens. Microorganisms. 2017; 5(2):33. https://doi.org/10.3390/microorganisms5020033

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Chitty, Jessica L., and James A. Fraser. 2017. "Purine Acquisition and Synthesis by Human Fungal Pathogens" Microorganisms 5, no. 2: 33. https://doi.org/10.3390/microorganisms5020033

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