Bat white-nose syndrome (WNS), caused by the fungal pathogen Pseudogymnoascus destructans, has decimated North American hibernating bats since its emergence in 2006. Here, we utilize comparative genomics to examine the evolutionary history of this pathogen in comparison to six closely related nonpathogenic species. P. destructans displays a large reduction in carbohydrate-utilizing enzymes (CAZymes) and in the predicted secretome (~50%), and an increase in lineage-specific genes. The pathogen has lost a key enzyme, UVE1, in the alternate excision repair (AER) pathway, which is known to contribute to repair of DNA lesions induced by ultraviolet (UV) light. Consistent with a nonfunctional AER pathway, P. destructans is extremely sensitive to UV light, as well as the DNA alkylating agent methyl methanesulfonate (MMS). The differential susceptibility of P. destructans to UV light in comparison to other hibernacula-inhabiting fungi represents a potential “Achilles’ heel” of P. destructans that might be exploited for treatment of bats with WNS.
White-nose syndrome of bats (WNS) continues to decimate hibernating bat populations in North America. The fungal disease was first documented in 2006 in eastern North America (New York) and the fungus has advanced west across the continent, most recently being detected on the West coast of North America1. WNS can result in >90% mortality in local hibernating bat populations2 and is caused by the psychrophilic fungus Pseudogymnoascus destructans3,4. The fungus has a strict temperature growth range of ~4–20 °C and therefore can only infect bats during hibernation5. WNS is not a systemic infection, but rather is characterized by P. destructans colonization of the skin of hibernating bats, which manifests as cupping skin erosions based on histopathology6. Frequent arousal from hibernation, depletion of fat reserves, and dehydration appear to contribute to mortality in infected individuals7,8,9,10. P. destructans has been found throughout Eurasia and occasionally causes mild WNS symptoms; however, no mass mortality events have been observed in Eurasia11. P. destructans has spread in a “bulls eye” pattern in North America and has only been found in environments where WNS-infected bats are found, strongly suggesting that the fungus is not native to North America and represents a classic example of an introduced pathogen decimating a naïve population12,13. P. destructans is a member of the under-studied Pseudeurotiaceae family; while recent studies have resulted in several draft genome assemblies within this group, much of the biology of the fungal pathogen and its relatives remains unknown.
Here, we present functionally annotated genomes for P. destructans, as well as six closely related nonpathogenic Pseudogymnoascus species. Comparison of the pathogen with the nonpathogenic species provides an opportunity to obtain insight into the origins and adaptations of the fungal pathogen of WNS.
Sequencing, assembly, and annotation
Recent phylogenetic work that aimed at identification and resolution of closely related species to P. destructans resulted in moving this species from genus Geomyces to Pseudogymnoascus4. Moreover, sampling for fungal isolates from hibernacular soil resulted in identification of other closely related Pseudogymnoascus species that are not known to be pathogenic12. We previously described the hybrid genome assembly of P. destructans14; in addition, we chose six closely related species and sequenced these isolates using Illumina chemistry, resulting in ~×250 coverage for each genome (strains listed in Supplementary Table 1). All seven Pseudogymnoascus genomes were within the expected genome size for haploid ascomycetes (~30–36 MB) with ~50% GC content (Table 1). Genome annotation was completed using funannotate v0.1.8 (https://github.com/nextgenusfs/funannotate), resulting in 9335 protein-coding genome models for P. destructans and a range of 10,252–11,033 protein gene models for the nonpathogenic Pseudogymnoascus species (Table 1). Genome functional annotation (see “Methods” section) was added to each gene model; complete functional annotation is available in Supplementary Data 1–7.
Orthology and evolutionary phylogeny
Due to the importance of WNS, as well as interest in cold-tolerant fungi, there has recently been several draft genomes sequenced in the genus Pseudogymnoascus. To delineate relationships between these genomes, we acquired all Pseudogymnoascus genomes deposited in NCBI, as well as several outgroup species: Aspergillus nidulans, Botrytis cinerea, Fusarium fujikuroi, Penicillium chrysogenum, and Neurospora crassa (Supplementary Table 2). Single-copy BUSCO orthologs15 were extracted using Phyloma (https://github.com/nextgenusfs/phyloma) and were used to generate a maximum likelihood phylogeny in RAxML v8.29 (PROTGAMMALG; 1000 bootstrap replicates) from 822 concatenated gene models. To estimate time of evolutionary divergence, node calibrations from Beimforde et al.16 were used in r8s v1.8017; Leotiomycetes–Sordariomycetes 267–430 MYA, Eurotiomycetes 273–537 MYA, Sordariomycetes 207–339 MYA, and Pezizomycotina 400–583 MYA (Supplementary Data 8). This analysis illustrates that the nonpathogenic Pseudogymnoascus species sequenced here are among the closest known relatives of P. destructans (Fig. 1). Additionally, these data suggested that the last known common ancestor of P. destructans diverged approximately 23.5 MYA. The oldest known chiropteran species in the fossil record, Palaeochiropteryx, was estimated to have lived 50–40 MYA18,19, while the most recent adaptive speciation of Eurasian Myotis bat species occurred 9–6 MYA and the North American Myotis species emerged more recently at 6–3.2 MYA20. Thus, Eurasian Myotis species were present at the time when P. destructans diverged from its relatives, suggesting that it could have coevolved alongside modern-day Eurasian chiropteran species.
ProteinOrtho521 was used to identify 3949 single-copy orthologous groups between seven Pseudogymnoascus species used in this study, representing only 42.3% of the protein-coding genes in P. destructans. Relationships among these species were inferred from a maximum likelihood RAxML phylogeny based on the concatenated alignment of 500 orthologous proteins using Botrytis cinerea as an outgroup (Fig. 2). The orthologous proteome analysis identified 1934 unique proteins in P. destructans that were not found in any of the nonpathogenic Pseudogymnoascus species (Fig. 2 and Table 1), making P. destructans the species with the most unique proteins in our study. To identify orthologous proteins under positive selection, dN/dS ratios for all orthologous groups were calculated using the codeml M0 model from PAML22. Likelihood ratio tests comparing the M1/M2 models, as well as M7/M8 models with significance at <0.05 were calculated to validate the estimated dN/dS ratios greater than 1, ratios that suggest positive selection is occurring22. Forty-six orthologous groups displayed evidence of positive selection. Of those orthologous groups under positive selection, only 14 contained a protein from P. destructans (Supplementary Data 9). However, functional annotation for these orthologous groups did not provide sufficient information to predict a function for any of these orthologs.
Carbohydrate-activating enzymes (CAZymes) are a group of proteins involved in the breakdown and/or utilization of carbon. Genomes of fungi associated with plants, either plant pathogens or decomposers, generally harbor a greater number of CAZymes than those causing disease in animals23. The six nonpathogenic Pseudogymnoascus species on average harbored 493 CAZymes, ranging from 463 to 544; however, the genome of P. destructans contains only ~36% of the average number of CAZymes (179 in total) for the group (Fig. 2; Supplementary Data 10). The CAZymes can be further broken down into enzyme classes/modules. In comparison to the average of the nonpathogenic Pseudogymnoascus species, the genome of P. destructans harbors ~69% (22) of auxiliary activity (AA) enzymes, ~17% (4) of proteins containing carbohydrate-binding modules (CBM), ~20% (13) of the carbohydrate esterases (CE), ~30% (82) of the glycoside hydrolases (GH), ~10% (2) of the pectin lyases (PL), and ~95% (52) of the glycosyltransferases (GT). Moreover, there were no specific CAZy families that were expanded in P. destructans that would indicate enhanced ability to utilize certain carbohydrate sources. Due to the large decrease in CAZymes, we hypothesized that P. destructans would have limited growth on complex and/or different carbon sources in comparison to the nonpathogenic Pseudogymnoascus species. To test this hypothesis, we compared growth on 190 carbon sources using a modified Biolog Phenotype Array Platform. Consistent with the large reduction in CAZymes in its genome, P. destructans was unable to utilize many carbon sources that the nonpathogenic Pseudogymnoascus species could readily utilize (Fig. 3, Supplementary Data 11). These data are consistent with a recent report comparing growth characteristics of P. destructans to closely related soil fungi24. The reduced CAZyme repertoire is a shared characteristic of other fungal pathogens of animals, including the dermatophytes, the true fungal dimorphic pathogens, as well as skin-inhabiting yeasts23. Presumably, the reduction in CAZymes reflects a change in carbon availability/acquisition during the evolution from an ancestral saprobe to a bat pathogen, i.e., P. destructans may have shed CAZyme pathways necessary for living in soil/sediments but are not required for growth on hibernating bats.
A group of subtilisin serine endopeptidases (MEROPS family S08A) of P. destructans have previously been described as PdSP1, PdSP2,25 and one of them (PdSP2; destructin-1) was subsequently shown to degrade collagen, suggesting a potential role in colonization of bat skin26. Using the MEROPS protease database, 230 predicted proteases were identified from the P. destructans genome, which represents a 28% reduction compared to the average of the nonpathogenic Pseudogymnoascus species (average: 321; range: 308–330) (Fig. 2; Supplementary Data 12). The subtilisin proteases appear to be conserved in the Pseudogymnoascus species analyzed here and therefore is consistent with the observation from Vraný et al.27 that collagen-degrading enzymes are present in several nonpathogenic soil microorganisms. While proteases are likely to be involved in colonization of bat skin tissue by P. destructans, the previously identified subtilisin proteases (e.g., PdSP2; destructin-1) do not appear to have evolved specifically for this purpose. Moreover, PdSP2 has recently been shown to be more highly expressed in laboratory culture medium than during WNS28,29, indicating that it may not play a large role during pathogenesis.
Secreted proteins are generally important for fungi as digestion of nutrients using secreted enzymes occurs outside the fungal cell. Recently, fungal effectors have been described in plant pathogens (some of which can enter animal cells), an example of the intricate competitive arms race between pathogen and host (reviewed in refs. 30,31). The predicted secretome of P. destructans is also reduced by more than 50% in comparison to the nonpathogenic Pseudogymnoascus species (452 vs. average of 970 secreted proteins; range: 848–1033) (Fig. 2). The trend of fewer secreted proteins in fungal pathogens of animals has been previously described32,33, with one hypothesis being that losing unnecessary secreted proteins is an evolutionary strategy to evade vertebrate immune systems32. Previous reports indicate that fungal secretomes can be lineage specific, consistent with the observation that 56 of the 362 predicted soluble secreted proteins in P. destructans (~15%) do not have orthologs in the nonpathogenic Pseudogymnoascus species.
To visually depict the functional variation between species, we generated count data of InterProScan Domain and Pfam domains for each genome in our study (Supplementary Data 13–14). The resulting matrices were visualized using a nonmetric multidimensional scaling (NMDS) ordination, which consistently identified P. destructans as distinct from the nonpathogenic Pseudogymnoascus species (Supplementary Fig. 2). To identify functional groups and processes that were enriched (positively or negatively), which could help explain the shift in functional domains between P. destructans and the nonpathogenic Pseudogymnoascus species, we used a Gene Ontology (GO) term enrichment method. As expected and consistent with the ordinations, no enrichment of GO terms was found for any of the six nonpathogenic Pseudogymnoascus species. Two very broad biological processes (BP) were enriched in P. destructans: cellular processes (GO:0009987) and cellular metabolic processes (GO:00044327) (Supplementary Table 3). On the other hand, some more specific BP terms were underrepresented in P. destructans: transmembrane transport (GO:0055085), carbohydrate metabolic process (GO:005975), and oxidation–reduction process (GO:0055114). This is consistent with reductions in the secretome, as well as CAZymes using alternate methods as previously discussed. Additionally, the GO enrichment identified a trend in underrepresented BP terms related to transcription (GO:0006351, GO:0097659, and GO:0032774) (Supplementary Table 3). Generally, these data suggest that major genome-level differences between P. destructans and the nonpathogenic Pseudogymnoascus species are driven by the large differences in carbohydrate utilization enzymes, as well as a reduction in the putative secretome.
A hallmark of many ascomycete fungi is their ability to produce bioactive small molecules, such as the pharmaceuticals lovastatin and penicillin34. These small molecules are also known as secondary metabolites and many are produced by the coordinated effort of gene clusters (genes physically located in proximity to each other on a chromosome). Secondary metabolites have been hypothesized to be involved in niche exploitation by fungi, including evasion of vertebrate immune systems35. AntiSMASH v3.036 was used to predict secondary metabolite gene clusters from each genome. Based on antiSMASH prediction, P. destructans harbors 14 predicted secondary metabolite gene clusters, while the average for the nonpathogenic Pseudogymnoascus species was 27 gene clusters, with a range of 14–36 (Supplementary Table 4, Supplementary Data 15–21). Despite having fewer putative secondary metabolism clusters, the P. destructans genome encodes for the two non-ribosomal-polyketide synthetase enzymes required to produce the iron-scavenging siderophores that have previously been characterized chemically: ferrichrome and triacetylfusarinine C37 (Supplementary Data 15). Additionally, P. destructans harbors a putative melanin cluster that has been shown to be involved in pathogenicity in other fungi such as the opportunistic human pathogen Aspergillus fumigatus; four of the six nonpathogenic Pseudogymnoascus species also harbor a similar melanin-like cluster, which in A. fumigatus is physically located in the cell wall of spores of the fungus and has been hypothesized to function as protection from ultraviolet (UV) light and reactive oxygen species (ROS) damage38,39. The secondary metabolite arsenal of the Pseudeurotiacae fungi in this study is less than some other groups such as the Eurotiomycetes, which can have 70 or more secondary metabolism clusters. However, several of the secondary metabolites produced by P. destructans warrant future study as they could contribute to the development and persistence of WNS in bats.
An interesting characteristic of the P. destructans genome is that it contains a large expansion of repetitive DNA sequences, accounting for 38.17% of the genome, a significant expansion in comparison to the nonpathogenic Pseudogymnoascus species (Table 1). Coinciding with this repeat expansion is a reduction in total gene models, as well as a general trend toward a reduction in several gene families, driven largely by a massive reduction in CAZymes, secreted proteins, and proteases. At the same time, P. destructans contains more lineage- specific genes than the nonpathogenic Pseudogymnoascus species (Fig. 2). The observation of expanded repetitive elements and increasing numbers of lineage-specific genes is reminiscent of the lineage-specific regions/chromosomes in Fusarium oxysporum40. However, in contrast to F. oxysporum, analysis of the repetitive sequences across the P. destructans genome suggests a uniform distribution (Supplementary Fig. 2A) and lineage-specific genes were not colocalized with repetitive regions (Supplementary Fig. 2B). Similarly to fungal pathogens in the Onygenales, P. destructans lacks proteins containing the fungal cellulose-binding domain (CBM18)41; however, this does not seem to be tied to pathogenicity as 5 of the 6 nonpathogenic Pseudogymnoascus species also lack this functional domain. We were unable to identify protein families that were expanded in P. destructans, somewhat reminiscent of Coccidioides, which have very few expanded protein families41. This is in stark contrast to the amphibian chytrid pathogens (Batrachochytrium dendrobatidis and Batrachochytrium salamandrivorans), which have undergone an expansion of protease gene families, as well as their genomes en route to pathogenicity42. Given the evolutionary distance between the chytrids and ascomycete fungi, it is perhaps not surprising that these devastating fungal pathogens have different evolutionary trajectories.
Light and DNA repair pathways
Taken together, our data suggest that P. destructans has been a pathogen of bats for millions of years and thus has likely coevolved in the absence of light. Most organisms that have been found in the absence of light maintain the ability to repair DNA caused by UV light radiation, including most microbes that have been isolated from hibernacula43,44. Moreover, a metagenomics analysis of a cave ecosystem identified an overrepresentation of DNA repair enzymes, despite the absence of UV light45. We challenged the fungal species studied here with four different DNA-damaging agents that included UV, methyl methanesulfonate (MMS), 4-nitroquinoline (4-NQO), and camptothecin (CPT). While we observed slight differences in sensitivity among species (and even between isolates of P. destructans) with 4-NQO and CPT, the most dramatic differential sensitivity was seen with UV light and MMS (Fig. 4a). To further characterize the sensitivity to UV light, we employed a quantitative conidial survival assay and exposed the fungi to three different wavelengths of UV light and three different exposure levels (Fig. 4b). These data show that none of the fungi tested were sensitive to UV-A (366 nm) light at the dosage tested, while P. destructans is differentially sensitive to the higher-energy UV-B (312 nm) and UV-C (254 nm). Remarkably, a low dose of 5 mJ/cm2 exposure of UV-C light resulted in only ~15% survival, while a 10 mJ/cm2 UV-C exposure resulted in <1% survival of P. destructans (Fig. 4b).
UV light damages DNA by inducing the formation of pyrimidine dimers (cyclobutane dimers and 6-4 photoproducts), while MMS alkylates guanine and adenine nucleotides46. Damaged or modified nucleotides result in mispairing and/or replication fork blockage and therefore can result in mutations. Camptothecin’s mode of action is similar as it inhibits topoisomerase I function, which results in stalled replication forks; thus, lethal mutations can accumulate during S phase47. On the other hand, 4-NQO induces single base pair mutations with a bias toward guanine to thymine transversions48 and thus can cause direct mutagenesis. To combat DNA damage, organisms have employed several DNA repair pathways, including photoreactivation, base excision repair (BER), nucleotide excision repair (NER), double-strand break repair, mismatch repair, as well as alternate excision repair (AER) (reviewed in refs. 49,50,51). Using fission yeast (Schizosaccharomyces pombe) as a model organism, we extracted 169 proteins annotated as involved in DNA repair from www.pombase.org and queried them against the Pseudogymnoascus proteomes using BLAST (Supplementary Data 22). Six putative hits, UVE1, MAG1, MAG2, CENP-X, SWI5, and PIF1, were identified on the basis that they were absent in P. destructans but present in most of the six nonpathogenic Pseudogymnoascus. To validate that orthologous proteins were in fact missing as opposed to being misannotated, we queried the corresponding Pfam hidden Markov model (HMM) profiles from (http://www.pfam.org/) using an exhaustive HMM model search in Phyloma (https://github.com/nextgenusfs/phyloma), which can identify truncated and/or unannotated genes. These results indicated that MAG1, MAG2, and CENP-X orthologs were missing from all Pseudogymnoascus genomes (which is consistent with the low scores of the BLAST hits), while partial matches were found for SWI5 and PIF1, indicating either missed gene models during annotation or nonfunctional proteins. Finally, we were unable to find any trace of UVE1 in the P. destructans genome, despite finding clear homologs in the six nonpathogenic Pseudogymnoascus species, suggesting that UVE1 plays a large role in the repair of UV-damaged DNA in Pseudogymnoascus.
P. destructans harbors a putative DNA photolyase (VC83_00225); thus, photoreactivation could be a mechanism the fungus uses to repair UV-induced DNA lesions. However, DNA photolyases require light for function and therefore are unlikely to be a major contributor to DNA repair in hibernacula. Preliminary testing of survivability of P. destructans incubated in either light or dark indicated that light was insufficient to repair DNA lesions (Supplementary Fig. 3). There are several known classes of DNA photolyases in fungi, including the canonical CPD photolyase I family shown to directly repair cyclobutane dimers, as well as a cyr-DASH family shown to be involved in light-sensing phenotypes52,53. A maximum likelihood phylogeny shows that P. destructans VC83_00225 is a member of the cry-DASH family of DNA photolyases and is thus unlikely to contribute to direct photorepair of cyclobutane dimers (Fig. 5a). To be thorough, we tested photoreactivation in the laboratory and found no phenotype in P. destructans, while two of the nonpathogenic Pseudogymnoascus species that harbored at least one CPD photolyase I (P. verrucosus and P. sp. 24MN13) showed increased survival when exposed to UV-A (366 nm) light after DNA damage (Fig. 5b).
In fission yeast, UVE1 is a key component of the AER pathway; therefore, our data suggest that most UV-damaged DNA in Pseudogymnoascus is repaired through AER. A small percentage of repair can be attributed to photoreactivation in P. verrucosus and P. sp. 24MN13; however, this appears to not occur in P. destructans as it lacks a cyclobutane-dimer photorepair enzyme. The P. destructans genome harbors clear homologs for the major enzymes involved in NER pathway (Supplementary Data 22), and thus, more work is needed to determine why the general NER and BER pathways are unable to compensate for loss of AER in P. destructans. Nevertheless, the extreme sensitivity to UV-C light in P. destructans represents a genetic pathway that could be exploited for active management of WNS of bats. Currently, UV-A (366 nm) light is being used as a WNS noninvasive field diagnostic tool because the characteristic cupping skin lesions fluoresce under this wavelength54. While UV-A light tested under laboratory conditions had no effect on survival of P. destructans (Fig. 4), the use of UV-A as a diagnostic tool suggests that treating individual bats with a dosage of UV-C light is feasible. The relatively low dose (~10 mJ/cm2) of UV-C light required to kill P. destructans conidia could be applied to bats in a few seconds of exposure from a portable light source. More work is needed to understand the physiological effect of UV-C light on bats; however, it is encouraging that treatment of mammal fungal skin/nail infections with UV-C light has been used for dermatophyte fungi causing onychomycosis55, as well as wound infections caused by Candida albicans56.
WNS represents one of the most severe wildlife diseases ever recorded. Currently, there are no practical treatment options for containing the spread of WNS in North America and thus the fungus has moved rapidly across the continent. Survivor populations of affected bat species can still be found near the disease outbreak epicenter, so that there is hope that species extinction will be avoided, albeit with a prolonged recovery57. However, the long-term effects on ecosystems involving bats will not be understood for decades. Comparative genomics analyses presented here suggest that P. destructans is likely a true fungal pathogen of bats, evolving alongside Eurasian bat species for millions of years. The annotated genome of P. destructans in addition to several nonpathogenic closely related species provides a framework for understanding the pathobiology of WNS. The serendipitous discovery that P. destructans lacks a UVE1 homolog and is therefore extremely sensitive to pyrimidine dimer inducing DNA-damaging agents is a vulnerability that could be exploited for WNS management.
Growth conditions, DNA extraction, and sequencing
Fungal strains were grown in liquid-stationary culture58 for several days at 15 °C, mycelia were lyophilized, and subsequently genomic DNA (gDNA) was extracted as previously described59. High-molecular-weight gDNA was confirmed by gel electrophoresis. For sequencing on the Ion Torrent Personal Genome Machine (PGM), a random 400-bp size fractionated library was constructed using Ion Plus Fragment Library Kit (#4471257), templated using the Ion PGM Template OT2 400 Kit (#4479878), loaded on a 318v2 chip (#4484354, and sequenced using the Ion 400 bp Sequencing Kit (#4482002) (all kits were used according to the manufacturer’s recommendations). Library construction for sequencing using the Illumina GAx II and Illumina MiSeq was done using the NEBNext Library Prep Kit, purified using QIAQuick Cartridge Kit, and size fractionated using E-gel 2% size select gel electrophoresis system (ThermoFisher). For obtaining RNA-seq reads to assist with genome annotation, fungi were grown in liquid-shaking cultures at 15 °C for 3 days, mycelia were lyophilized, total RNA was extracted using TriZol (Invitrogen), and polyadenylated RNA was selected using the DynaBeads PolyA Cleanup Kit (Ambion). The poly-A RNA was then used to make libraries using the Ion RNA-seq Kit 2.0 and sequenced on the Ion Torrent PGM using Ion 200 bp Sequencing Kit (#4482006).
Initial attempts to build a high-quality assembly for P. destructans using paired-end MiSeq (2 × 250 bp) data resulted in heavily fragmented assemblies with several different assembly software (Discovar DeNovo, Abyss, Spades, CLC, etc.). We generated a highly contiguous assembly using a combination of PacBio reads, MiSeq, Roche 454 mate-pair reads, and Sanger end sequences from a 100-kb BAC library14. For five of the nonpathogenic Pseudogymnoascus species (UAMH10579, 03VT05, 05NY08, WSF3629, and 23342-1-I1), acceptable assemblies were generated using the de novo assembler in CLC Genomics Workbench 7.5 (Qiagen) using paired-end MiSeq reads (2 × 300 bp). For Pseudogymnoascussp. 24MN13, the paired-end Illumina (2 × 100 bp; GAIIx) data were found to have some bacterial contamination, thus, we generated a second sequencing library from a clean gDNA extraction for the Ion Torrent PGM, which was used for an initial assembly and scaffolding using the paired-end Illumina reads. Contamination was removed from the assemblies using DeconSeq60 and was subsequently error corrected using Pilon61. Small repetitive contigs from each assembly were identified using Mummer62 and were removed if they were 95% identical over 95% of their length with other contigs in the assembly (achieved using “funannotate clean” command).
Genome annotation and functional characterization
Detailed information on annotation and functional characterization is presented in Supplementary Methods.
Biolog phenotyptic microarray
Pseudogymnoascus species were tested for the ability to utilize 190 different carbon sources in the Biolog Phenotyptic Microarray platform (plates PM1 and PM2A). Fungal spores at a density of 1 × 104 spores were inoculated into 100 µl of carbon-free minimal medium (MM lacking glucose63) and then subsequently aliquoted into 96-well Biolog plates (PM1 and PM2A). Cultures were grown at 15 °C and the nonpathogenic Pseudogymnoascus species were incubated for 7 days, while P. destructans was incubated for 14 days. The plates were then photographed and growth was quantified using the Fiji/ImageJ plug-in ColonyArea 1.564. Relative growth was then normalized to growth on glucose and plotted in heatmap.2 from the gplots package in R65.
DNA damage assays
Conidia were harvested from fungal isolates from solid medium agar plates using sterile 0.01% Tween-80 water, purified by filtering over sterile miracloth (EMD Millipore #475855), and enumerated using a hemocytometer. For spot plate assays, conidia were serially diluted and 5 µl was pipetted onto the surface of glucose minimal agar medium63. Treatment with UV light was accomplished by exposing the spotted agar plate to 25 mJ/cm2 of UV-C (254 nm) light using a UV cross-linker (UVP CL-1000). Sensitivity to chemical DNA mutagens was done by preparing GMM agar medium that contained 25 µM CPT, 0.01% MMS, or 0.5 µg/ml of 4-nitroquinolone (4-NQO). Control and treated plates were incubated at 15 °C for 1 week prior to imaging. Colony-forming unit (CFU) assays were done by spread plating ~50 conidia on the surface of a GMM agar plate and were subsequently exposed to UV light in a UV cross-linker, and surviving colonies were counted after incubation at 15 °C for 1 week. Quantification of photoreactivation for each species was done using a very similar CFU assay comparing varying UV-C treatments followed by 1-h exposure to UV-A (366 nm) light in a UV cross-linker. Conidia were allowed to germinate for 24 h in the dark prior to UV-C (254 nm) treatments and subsequent UV-A (366 nm) treatment. Surviving colonies were counted after incubation in the dark at an appropriate temperature (15 °C for P. destructans and 25 °C for nonpathogenic Pseudogymnoascus species). All CFU assays were done in biological triplicates (n = 3) for each experimental condition.
Sequencing data and genome assemblies are available via NCBI under BioProject PRJNA276926 and SRA project SRP055906. All other relevant data supporting the findings of the study are available in this article and its Supplementary Information files, or from the corresponding author upon request.
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Funding was provided to J.M.P. and D.L.L. by the US Fish & Wildlife grant F14PG00132 and to K.P.D. and J.T.F. by US Fish & Wildlife grant F14AP00644. Additional funding and support for J.M.P. and D.L.L. were provided by the US Forest Service, Northern Research Station.
Electronic supplementary material
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