Targeted Disruption of Melanin Biosynthesis Genes in the Human Pathogenic Fungus Lomentospora prolificans and Its Consequences for Pathogen Survival

The dematiaceous (melanised) fungus Lomentospora (Scedosporium) prolificans is a life-threatening opportunistic pathogen of immunocompromised humans, resistant to anti-fungal drugs. Melanin has been shown to protect human pathogenic fungi against antifungal drugs, oxidative killing and environmental stresses. To determine the protective role of melanin in L. prolificans to oxidative killing (H2O2), UV radiation and the polyene anti-fungal drug amphotericin B, targeted gene disruption was used to generate mutants of the pathogen lacking the dihydroxynaphthalene (DHN)-melanin biosynthetic enzymes polyketide synthase (PKS1), tetrahydroxynapthalene reductase (4HNR) and scytalone dehydratase (SCD1). Infectious propagules (spores) of the wild-type strain 3.1 were black/brown, whereas spores of the PKS-deficient mutant ΔLppks1::hph were white. Complementation of the albino mutant ΔLppks1::hph restored the black-brown spore pigmentation, while the 4HNR-deficient mutant ΔLp4hnr::hph and SCD-deficient mutant ΔLpscd1::hph both produced orange-yellow spores. The mutants ΔLppks1::hph and ΔLp4hnr::hph showed significant reductions in spore survival following H2O2 treatment, while spores of ΔLpscd1::hph and the ΔLppks1::hph complemented strain ΔLppks1::hph:PKS showed spore survivals similar to strain 3.1. Spores of the mutants ΔLp4hnr::hph and ΔLpscd1::hph and complemented strain ΔLppks1::hph:PKS showed spore survivals similar to 3.1 following exposure to UV radiation, but survival of ΔLppks1::hph spores was significantly reduced compared to the wild-type strain. Strain 3.1 and mutants ΔLp4hnr::hph and ΔLppks1::hph:PKS were resistant to amphotericin B while, paradoxically, the PKS1- and SCD1-deficient mutants showed significant increases in growth in the presence of the antifungal drug. Taken together, these results show that while melanin plays a protective role in the survival of the pathogen to oxidative killing and UV radiation, melanin does not contribute to its resistance to amphotericin B.


Introduction
Lomentospora prolificans (formally Scedosporium prolificans) is a dematiaceous (melanised) fungus that has emerged over recent years as a serious and often life-threatening pathogen of immunocompromised individuals including those with AIDS, haematological malignancies and bone marrow and solid organ transplants [1][2][3][4][5][6][7][8]. In neutropenic patients, deep-seated infections disseminate rapidly with associated mortality rates of up to 80% [1,9]. Infections due to near-drowning were reported by the World Health Organisation after the Great Eastern Japan earthquake and tsunami in 2011 [10,11]. Recovery of L. prolificans from the sputum of cystic fibrosis patients has also been reported, but disease exacerbation due to the fungus has yet to be established [12]. tsunami in 2011 [10,11]. Recovery of L. prolificans from the sputum of cystic fibrosis patients has also been reported, but disease exacerbation due to the fungus has yet to be established [12].
In a previous study [38], we reported the generation of a monoclonal antibody specific to L. prolificans and identified its antigen through mass spectrometry and targeted gene disruption as the melanin biosynthetic enzyme 1,3,6,8-tetrahydroxynapthalene reductase [38]. As an extension to this study, we set out here to determine the role of this enzyme and two other enzymes involved in DHN-melanin production (scytalone dehydratase and polyketide synthase) in melanisation of L. prolificans and to investigate the consequences of enzyme loss for the survival of the pathogen. To this end, we use targeted disruption of polyketide synthase and scytalone dehydratase-encoding genes to generate enzyme-deficient mutants of the fungus and determine their sensitivities and that of the tetrahydroxynapthalene reductase-deficient mutant [38] to stresses incurred by UV radiation, oxidative killing and amphotericin B. Using this strategy, we show that melanin confers tolerance of the fungus to UV and oxidative killing, but does not contribute to its resistance to the polyene anti-fungal drug.    [38]. Scales bars in D-F = 1.5 cm; (G) Genomic DNA of wild-type strain 3.1 (lane 1) and putative ΔLppks1::hph transformants (lanes 2 to 7) were digested with the restriction enzyme HpaI, fractionated by gel electrophoresis and blotted onto Hybond-NX membrane. Lane L contains DNA size marker; (H) The membrane was probed with a 1.9-kb right flank fragment of the PKS1 ORF. presence of single 5.6-kb bands in lanes 5 and 7 (indicated by white asterisks), compared to the 6.5-kb band in lane 1 (indicated by black asterisk), indicates successful replacement of the PKS1 gene in these two strains; (I) Colony morphology of wild-type strain 3.  (E) Morphology of mutant ∆Lpscd1::hph after 2-weeks growth on OA at 30˝C showing abnormal beige pigmentation and comparison to the yellow-grey tetrahydroxynaphthalene reductase-deficient mutant ∆Lp4hnr::hph (F) developed previously [38]. Scales bars in D-F = 1.5 cm; (G) Genomic DNA of wild-type strain 3.1 (lane 1) and putative ∆Lppks1::hph transformants (lanes 2 to 7) were digested with the restriction enzyme HpaI, fractionated by gel electrophoresis and blotted onto Hybond-NX membrane. Lane L contains DNA size marker; (H) The membrane was probed with a 1.9-kb right flank fragment of the PKS1 ORF. The presence of single 5.6-kb bands in lanes 5 and 7 (indicated by white asterisks), compared to the single 6.5-kb band in lane 1 (indicated by black asterisk), indicates successful replacement of the PKS1 gene in these two strains; (I) Colony morphology of wild-type strain 3.

Targeted Disruption of L. prolificans Melanin Biosynthesis Genes and Recovery of Putative Mutants
In this study, we used targeted gene replacement to disrupt production of the enzymes polyketide synthase (PKS) and scytalone dehydratase (SCD) that catalyse steps [1] and [3] of DHN-melanin biosynthesis in L. prolificans as shown in Figure 1A. Production of a mutant strain (∆Lp4hnr::hph) deficient in the enzyme 1,3,6,8-tetrahydroxynapthalene reductase that catalyses step [2] of melanin biosynthesis in the fungus ( Figure 1A) was reported recently [38] and is included in this study for comparison to the newly developed mutants. Targeted gene disruptions were carried out following the split marker method [39]. For targeted replacement of the SCD-encoding gene SCD1, two rounds of PCR were required to complete the process. In the first round PCR, the left (upstream) (1.0-kb) and right (downstream) (0.9-kb) flanking regions of the SCD1 ORF were amplified using primer pairs Lpscd1-LFF/Lpscd1-LFR and Lpscd1-RFF/Lpscd1-RFR designed to include an extension complementary to the hygromycin phosphotransferase gene (HPH) conferring resistance to the antibiotic hygromycin B ( Table 1). The left and right fragments of the HPH gene were amplified from pCB1004 with primer pairs HY split/M13F and M13R/YG split, respectively. In a second round of PCR, the left flank was fused with one half of the hygromycin cassette (HY) (1.2-kb) and the right flank with the other half (YG) (0.8-kb). The second round PCR products LF+HY (2.1-kb) and RF+YG (1.7-kb) were used for protoplast transformation. Homologous recombination resulted in the replacement of the SCD1 ORF with the functional HPH gene. Putative ∆Lpscd1::hph mutants were selected based on resistance to the antibiotic hygromycin B (600 µg/mL). Table 1. Details of primer sequences used in this study.

Primer Name
Sequence Targeted replacement of the PKS1 gene was performed using a similar experimental strategy. Primer pairs Lppks1-LFF/Lppks1-LFR and Lppks1-RFF/Lppks1-RFR were used for amplification of 1.9-kb fragments from 5 1 and 3 1 flanks of the ORF respectively. The left and right fragments of the HPH gene were amplified as described. In a second round of PCR, the left flank was fused with one half of hygromycin cassette (HY) (1.2-kb) and the right flank with the other half of the hygromycin cassette (YG) (0.8-kb). The second round PCR products LF+HY (3.1-kb) and RF+YG (2.7-kb) were used for protoplast transformation. Homologous recombination resulted in the replacement of the PKS1 ORF with the functional HPH gene. Putative ∆Lppks1::hph mutants were similarly selected based on resistance to 600 µg/mL of the antibiotic hygromycin B.

Confirmation of Gene Disruptions by Southern Blotting and Abnormal Melanisation
Hygromycin B resistant mutants were investigated further by Southern blot analysis. A single putative ∆Lpscd1::hph mutant and six ∆Lppks1::hph putative mutants were analysed ( Figure 1). Genomic DNA from the putative ∆Lpscd1::hph mutant and the wild-type strain 3.1 were digested with the restriction enzyme BglII and the enzyme HpaI for putative ∆Lppks1::hph transformants and wild-type strain 3.1 control. The products were separated by agarose gel electrophoresis ( Figure 1B,G, respectively) and blotted onto Hybond-NX membranes ( Figure 1C,H, respectively). Respective membranes were probed with a 1.0-kb fragment upstream of the SCD1 ORF ( Figure 1C) or a 1.9-kb right flank fragment of the PKS1 ORF ( Figure 1H). The single putative ∆Lpscd1::hph mutant ( Figure 1C, lane 3) showed the correct fragment size of 6.9-kb compared to the 5.6-kb fragment of the wild-type strain ( Figure 1C, lane 1), while two ∆Lppks1::hph mutants ( Figure 1H, lanes 5 and 7 indicated by white asterisks) were identified with the correct fragment size of 5.6-kb compared to the 6.5-kb fragment of the wild-type strain ( Figure 1H, lane 1 indicated by black asterisk). Targeted disruption of the melanin biosynthesis gene SCD1 encoding the melanin biosynthesis enzyme scytalone dehydratase and PKS1 encoding the enzyme polyketide synthase resulted in abnormal pigmentation in the ∆Lpscd1::hph and ∆Lppks1::hph mutants when compared to the wild-type strain 3.1. The wild-type 3.1 strain is grey ( Figure 1D,I) in contrast to the beige colour of the ∆Lpscd1::hph mutant ( Figure 1E), while the tetrahydroxynaphthalene reductase-deficient mutant ∆Lp4hnr1::hph mutant ( Figure 1F), generated in a previous study [38], is yellow-grey. The two ∆Lppks1::hph mutants confirmed in Southern blots ( Figure 1H, lanes 5 and 7) were albino (white), exhibiting complete loss of pigmentation ( Figure 1J; the ∆Lppks1::hph mutant corresponding to lane 7 is panel H is shown) compared to the grey wild-type strain 3.1.

Complementation of the ∆Lppks1::hph Mutant and Restoration of Melanin Production
An albino ∆Lppks1::hph mutant ( Figure 1H, lane 7) was complemented by integration of a DNA fragment consisting of 3.0-kb of promoter region, 6.7-kb of the ORF and 0.6-kb terminator region of the PKS1 gene to restore gene functionality and concomitant melanin biosynthesis. The PKS1 fragment was amplified by PCR using the gene-specific primers Lppks-f1 and Lp-pksr1 (Table 1), designed to include 15-bp of sequence homologous to the ends of the linearized vector pCB1532. The vector pCB1532, which contains the sulfonylurea resistance allele of the Magnaporthe oryzae ILV1 gene [40], was linearized by digestion with the restriction enzymes BamHI and HindIII. The PCR product was ligated to linearized pCB1532 vector and used to transform competent E. coli cells, which were selected based on white-blue screening. Plasmid DNA was purified and sequenced to confirm the correct PKS1 insertion and the vector then transformed into the ∆Lppks1::hph mutant. Putative ∆Lppks1::hph:PKS complementation mutants were selected based on resistance to sulfonylurea. Genomic DNA of wild-type 3.1, ∆Lppks1::hph and putative complemented mutants was digested with the restriction enzyme BglII, fractionated by gel electrophoresis ( Figure 1K) and blotted onto a Hybond-NX membrane ( Figure 1L). The membrane was probed with a 0.8-kb fragment of the PKS1 ORF. The probe hybridized to a 7.3-kb fragment present in the wild-type 3.1 and complemented strains ( Figure 1L, lanes 1 and 4), which was absent in the two ∆Lppks1::hph mutants ( Figure 1L, lanes 2 and 3). Complementation of the polyketide synthase-deficient mutant restored melanin production ( Figure 1M), resulting in a grey phenotype in the ∆Lppks1::hph:PKS complementation mutant similar to the wild-type strain 3.1 ( Figure 1D,I).

Growth, Sporulation and Spore Pigmentation
Growth of the fungi on OA revealed no significant differences in growth rates compared to strain 3.1, with the exception of mutant ∆Sp4hnr::hph. With this mutant, there was a significant reduction in colony diameter by day 14 compared to the wild-type strain (Figure 2A), consistent with previous findings [38]. While spore production in the 14-day-old cultures was not significantly different between strain 3.1 and mutants ∆Lppks1::hph and ∆Lppks1::hph:PKS, production was significantly reduced in the mutant ∆Lp4hnr::hph and significantly increased in the mutant ∆Lpscd1::hph when compared to the wild-type strain ( Figure 2B). Spore suspensions prepared from the 14-day-old cultures showed marked differences in pigmentations. Spore suspensions from strain 3.1 were black-brown, whereas those from the albino mutant ∆Lppks1::hph were white ( Figure 2C). Spores of the complemented strain ∆Lppks1::hph:PKS were black-brown, showing that complementation had restored melanin biosynthesis resulting in a similar spore pigmentation to that of the wild-type strain. The mutant ∆Lpscd1::hph produced orange-yellow spore suspensions similar to that of the ∆Lp4hnr::hph generated previously [38].

Growth, Sporulation and Spore Pigmentation
Growth of the fungi on OA revealed no significant differences in growth rates compared to strain 3.1, with the exception of mutant ΔSp4hnr::hph. With this mutant, there was a significant reduction in colony diameter by day 14 compared to the wild-type strain (Figure 2A), consistent with previous findings [38]. While spore production in the 14-day-old cultures was not significantly different between strain 3.1 and mutants ΔLppks1::hph and ΔLppks1::hph:PKS, production was significantly reduced in the mutant ΔLp4hnr::hph and significantly increased in the mutant ΔLpscd1::hph when compared to the wild-type strain ( Figure 2B). Spore suspensions prepared from the 14-day-old cultures showed marked differences in pigmentations. Spore suspensions from strain 3.1 were black-brown, whereas those from the albino mutant ΔLppks1::hph were white ( Figure 2C). Spores of the complemented strain ΔLppks1::hph:PKS were black-brown, showing that complementation had restored melanin biosynthesis resulting in a similar spore pigmentation to that of the wild-type strain. The mutant ΔLpscd1::hph produced orange-yellow spore suspensions similar to that of the ΔLp4hnr::hph generated previously [38]. By day 14, the mutant ΔLp4hnr::hph had significantly reduced growth when compared to the wild-type strain (p < 0.05; Student's t-test). All other mutants showed growth comparable to strain 3.1 over the 14 day period. Each point is the mean of 3 replicates ± standard error; (B) Quantification of spore concentrations from 14-day-old OA plate cultures. Spore concentration of the mutant ΔLp4hnr::hph was significantly reduced (p < 0.05, analysis of variance (ANOVA)) when compared to strain 3.1 and the other mutants, whereas spore concentration was significantly increased in the mutant ΔLpscd1::hph when compared to the other strains. There were no significant differences in the spore concentrations of strains 3.1, ΔLppks1::hph and ΔLppks1::hph:PKS. Each bar is the mean of 3 replicates ± standard error and bars with similar letters indicate that differences in means are not statistically significant at p < 0.05 (ANOVA); (C) Colors of spore suspensions of L. prolificans 3.1 and the mutants ΔLppks1::hph, ΔLppks1::hph:PKS and ΔLpscd1::hph. By day 14, the mutant ∆Lp4hnr::hph had significantly reduced growth when compared to the wild-type strain (p < 0.05; Student's t-test). All other mutants showed growth comparable to strain 3.1 over the 14 day period. Each point is the mean of 3 replicates˘standard error; (B) Quantification of spore concentrations from 14-day-old OA plate cultures. Spore concentration of the mutant ∆Lp4hnr::hph was significantly reduced (p < 0.05, analysis of variance (ANOVA)) when compared to strain 3.1 and the other mutants, whereas spore concentration was significantly increased in the mutant ∆Lpscd1::hph when compared to the other strains. There were no significant differences in the spore concentrations of strains 3.1, ∆Lppks1::hph and ∆Lppks1::hph:PKS. Each bar is the mean of 3 replicates˘standard error and bars with similar letters indicate that differences in means are not statistically significant at p < 0.05 (ANOVA); (C) Colors of spore suspensions of L. prolificans 3.1 and the mutants ∆Lppks1::hph, ∆Lppks1::hph:PKS and ∆Lpscd1::hph.  Sensitivities of spores to oxidative killing by H2O2. Spores were exposed to 160 mM H2O2 or phosphate buffer only (control) for 60 min and then plated onto SDA. After incubation in the dark for 3 day at 30 °C, the number of colonies derived from germinated spores were counted and the % survival for each strain determined relative to matched controls (untreated spores). Each bar is the mean of 3 replicates ± standard error and bars with similar letters indicate that differences in means are not statistically significant at p < 0.05 (ANOVA). Under these conditions, ~50% of treated spores of the wild-type strain 3.1 survived compared to matched control spores. Compared to strain 3.1, there was a significant reduction in % survival of mutants ΔLppks1::hph and ΔLp4hnr::hph due to exposure to H2O2. There was no significant effect of H2O2 on the survival of mutant ΔLpscd1::hph or on the survival of ΔLppks1::hph:PKS compared to 3.1, showing that complementation of mutant ΔLppks1::hph had restored spore survival to wild-type levels; (B) Sensitivities of spores to UV light. Spores were exposed to a UV dose of 200 mJ/cm 2 and then plated onto SDA. After incubation in the dark for 3 days at 30 °C, the number of colonies derived from germinated spores were counted and the % survival for each strain determined relative to matched controls (untreated spores). Each bar is the mean of 3 replicates ± standard error and bars with similar letters indicate that differences in means are not statistically significant at p < 0.05 (ANOVA). Under these conditions, ~50% of treated spores of the wild-type strain 3.1 survived compared to matched control spores. Compared to strain 3.1, there was a significant reduction in % survival of mutant ΔLppks1::hph due to exposure to UV. There was no significant effect of UV exposure on the survival of mutants ΔLpscd1::hph and ΔLp4hnr::hph. Similarly, there was no significant difference in the % survival of ΔLppks1::hph:PKS spores compared to 3.1, showing that complementation of mutant ΔLppks1::hph had restored spore survival to wild-type levels; (C) Sensitivities of strains to the polyene antifungal drug amphotericin B. Each bar is the mean of 3 replicates ± standard error and bars with similar letters indicate that differences in means are not statistically significant at p < 0.05 (ANOVA).

Sensitivities to H 2 O 2
Exposure of spores of strain 3.1 to 160 mM H 2 O 2 for 60 min resulted in 50% survival relative to its matched control (non-treated spores) ( Figure 3A). When compared to the wild-type strain, the same treatment resulted in significant (p < 0.05) reductions in survival of the mutants ∆Lppks1::hph and ∆Lp4hnr::hph, with survival percentages relative to matched controls of 21% and 24% respectively. There was no significant difference in the effect of H 2 O 2 on survival of ∆Lppscd1::hph spores when compared to strain 3.1 with a percentage survival, relative to its matched control, of 45%. A similar result was found with the mutant ∆Lppks1::hph:PKS, with a percentage survival relative to its matched control of 46%, indicating that complementation had restored survival to wild-type levels.

Sensitivities to UV Radiation
A UV dose of 200 mJ/cm 2 resulted in 51% survival of strain 3.1 spores relative to non-irradiated control spores ( Figure 3B). Under the same treatment conditions, there was a significant (p < 0.05) decrease in percentage survival of the mutant ∆Lppks1::hph compared to the wild-type, with a percentage survival of 28%. There was no significant difference in effect of UV irradiation on the percentage survival of the mutants ∆Lpscd1::hph and ∆Lp4hnr::hph when compared to strain 3.1, with percentages of 40% and 42% respectively. A similar result was found with the mutant ∆Lppks1::hph:PKS, with a percentage survival relative to its matched control of 63%, indicating that complementation had restored survival to wild-type levels.

Sensitivities to Amphotericin B
All strains of L. prolificans tested to date are resistant to the broad-spectrum antifungal drug amphotericin B [14,15]. Here, we tested the susceptibility of the wild-type strain 3.1 and the melanin biosynthesis mutants to the drug and included, as a positive control, the drug-sensitive pathogen Aspergillus fumigatus (AF293). We chose a concentration of 32 µg/mL, having first established that strain 3.1 of the fungus is resistant to concentrations >16 µg/mL, consistent with other studies [13][14][15][16][17][18]. Growth (measured as dry weight of mycelium in mg) of the drug-resistant wild-type strain 3.1 and mutant ∆Lp4hnr1::hph was unaffected by the drug. Similarly, there was no significant difference in the growth of the complemented strain ∆Lppks1::hph:PKS in the presence and absence of the drug, showing that restoration of melanin biosynthesis re-established drug insensitivity of the fungus to wild-type levels. Unexpectedly, significant increases in growth were found in the albino mutant ∆Lppks1::hph and mutant ∆Lpscd1::hph in the presence of the drug, while the drug completely inhibited growth of the control pathogen Aspergillus fumigatus as expected.

Discussion
Lomentospora prolificans is a dematiaceous (melanised) fungus that causes life-threatening disseminated infections in immunocompromised humans and patients with underlying respiratory problems [1][2][3][4][5][6][7][8][9][10][11][12]. Disseminated infections known as scedosporiosis are caused by infectious propagules (spores) of the fungus that are inhaled, germinate and infect the lungs due to impaired respiratory immunity including loss of oxidative killing by macrophages and neutrophils. The pathogen displays inherent resistance to many of the mold-active antifungal drugs used in the clinical setting including the polyene amphotericin B [13][14][15][16][17][18]. The pigment melanin is an integral component of the fungal cell wall conferring protection to stresses that involve cell damage such as UV radiation and reactive oxygen species [22,[25][26][27][28][29][30]32,33] and which has been shown in other human pathogenic fungi to contribute to amphotericin B resistance [24,25,41]. In this study, we set out to investigate the role of melanin in resistance of L. prolificans to UV radiation, to oxidative killing by H 2 O 2 , and inhibition by amphotericin B. To do this, we used targeted disruption of melanin biosynthesis genes to generate mutants blocked at different stages in the DHN-melanin pathway.
In a previous study [38], we used targeted gene disruption to generate an L. prolificans mutant (∆Lp4hnr::hph) lacking the DHN-melanin enzyme tetrahydroxynaphthalene reductase (4HNR) which catalyzes the reduction of 1,3,6,8-THN to scytalone ( Figure 1A, step [2]). In this study, we used a similar process to generate additional mutants, ∆Lppks1::hph and ∆Lpscd1::hph, that lack polyketide synthase (PKS1) and scytalone dehydratase (SCD1) enzyme activities, respectively. Furthermore, we complemented the PKS-deficient mutant to restore melanin biosynthesis in the ∆Lppks1::hph mutant. The split marker technique of homologous recombination used here enables exchange of the open reading frame (ORF) of the enzyme-encoding gene with the hygromycin B phosphotransferase (HPH)-encoding gene, a selectable marker conferring resistance to the antibiotic hygromycin B. The procedure was carried out by amplification and fusion of linear DNA fragments to create the hygromycin-resistance cassette. A previous study had shown that the size of the sequences upstream and downstream of the ORF affects transformation efficiency [42] and so the lengths of flanking fragments used for homologous recombination were designed according to the size of each ORF. For the PKS-encoding gene, the flanks were approximately 1.9-kb (left flank) and 1.9-kb (right flank) owing to the large size of the PKS ORF (6.7-kb). In the case of the SCD-encoding gene, the flank sizes were shorter (approximately 1.0-kb and 0.9-kb for left and right flanks respectively), owing to the smaller size of the SCD ORF of approximately 0.7-kb.
Using this strategy, we were able to generate enzyme-deficient mutants that had abnormal pigmentation due to disruption of normal DHN-melanin biosynthesis. Previously, Ruiz-Diez and co-workers [43] used UV mutagenesis to generate melanin-deficient (mel´) mutants of L. prolificans that had unstable white phenotypes that reverted to the olive-grey to black characteristic of the wild-type strain, or mutants that had stable white phenotypes that varied in colony morphologies. Unlike UV mutagenesis, which is a random mutation process, targeted gene disruption allowed us to mutate individual enzyme-encoding genes involved in melanin biosynthesis in a highly specific way and to generate stable enzyme-deficient mutants. In the case of ∆Lpscd1::hph, colonies of the mutant were beige while its spore suspensions were orange-yellow. A similar spore pigmentation was shown in the ∆Lp4hnr::hph mutant developed previously that accumulated flaviolin as a shunt product [38]. Wang and co-workers [44] produced reddish-brown mutants lacking the corresponding SCD1 gene in the ascomycete Grosmannia clavigera and showed this color was due to accumulation of the intermediate scytalone. Targeted disruption of the L. prolificans PKS-encoding gene resulted in the production of albino (white) ∆Lppks1::hph mutants, similar to the white PKS-deficient mutants of Bipolaris oryzae and A. fumigatus developed elsewhere [45,46]. Complementation of the albino ∆Lppks1::hph mutant was successfully achieved, resulting in a mutant ∆Lppks1::hph:PKS with grey pigmentation similar to that of the wild-type strain.
Changes to normal melanin production in fungi can alter their morphology. Tseng and co-workers [47] showed that engineering the entomopathogen Metarhizium anisopliae to express DHN-melanin biosynthesis genes increased spore germination, hyphal branching and appressorium production. Mutants of the fungus Grosmannia clavigera with PKS and SCD gene disruptions had albino and reddish-brown phenotypes respectively, but had no marked differences in morphology, sporulation, or in vegetative growth compared to the wild-type strain. In the current study, vegetative growth and was significantly reduced in the 4HNR-deficient mutant ∆Lp4hnr::hph consistent with previous results [38], while growth was unaffected in the other two mutants and in the complemented strain ∆Lppks1::hph:PKS. Spore production was reduced in ∆Lp4hnr::hph and increased in ∆Lpscd1::hph.
Melanin is known to contribute to the stress tolerances of fungi, including both plant and human pathogens, conferring resistance to UV radiation [33] and to oxidation killing [22,[26][27][28][29]. Kheder and co-workers [48] showed that spore germination and radial growth was dramatically reduced in non-melanised strains of the plant pathogen Alternaria alternata compared to melanised strains as a consequence of UV exposure, while another study demonstrated resistance to UV light of melanised strains of the human pathogen Sporothrix schenckii compared to a melanin-deficient mutant [49]. In human pathogenic fungi, melanin acts as a free radical scavenger [50] and is associated with increased tolerance to H 2 O 2 in Cryptococcus neoformans, Aspergillus spp., S. schenckii and Fonsecaea pedrosoi [26][27][28][29][30]. In this study, the albino ∆Lppks1::hph mutant showed increased sensitivity to UV and H 2 O 2 in spore survival assays. Restoration of melanisation in the ∆Lppks1::hph:PKS complemented strain and increased survival of ∆Lppks1::hph:PKS spores to wild-type levels following UV and H 2 O 2 exposure, shows that melanin provides protection against UV damage and tolerance to oxidative killing in L. prolificans. In contrast, another study knocked down the polyketide synthase gene in Penicillium marneffei and found no difference between the wild-type and the mutant in rates of survival following exposure to UV light [51].
The resistance of L. prolificans to antifungal agents is well documented [13][14][15][16][17][18] and the contribution of melanin to antifungal drug resistance has been investigated in other human pathogenic fungi. Van Duin and co-workers [41] demonstrated the protective role of melanin in C. neoformans and Histoplasma capsulatum against amphotericin B, with non-melanised C. neoformans strains showing greater sensitivity to the drug than melanised strains [24]. Contrary to expectations, we found that the albino mutant of L. prolificans generated here (∆Lppks1::hph) showed significantly increased growth in the presence of amphotericin B, while complementation of the PKS gene in the mutant ∆Lppks1::hph:PKS bestowed insensitivity to the drug, similar to that of the wild-type strain 3.1. The unexpected increase in growth of the albino mutant in the presence of the drug, a phenomenon also found with the ∆Lpscd1::hph mutant, is difficult to explain. Paradoxical increases in growth of the human pathogens Candida albicans and Aspergillus fumigatus due to elevated concentrations of the anti-fungal echinocandin drug caspofungin have been reported [52,53], but increased resistance of fungi to a polyene anti-fungal drug as a consequence melanin deficiency has not previously been demonstrated. Indeed, melanin deficient (mel´) strains L. prolificans generated by UV mutagenesis [43] were shown to be as resistant to amphotericin B, nystatin and azoles as the wild-type parent. Despite this, amphotericin B has been shown to increase the melanin content of melanoma cells [54]. An alternative explanation for the increased growth of mutants ∆Lppks1::hph and ∆Lpscd1::hph might be compensation for DHN-melanin loss through alternative pathways of melanin biosynthesis. In addition to DHN-melanins, the ascomycete fungi Aspergillus fumigatus and A. nidulans are able to synthesize pyomelanin and DOPA-melanin [55]. Similar synthetic capabilities might also be present in L. prolificans. Notwithstanding this, we have shown that melanin does not contribute to the resistance of L. prolificans to amphotericin B, consistent with the findings of Ruiz-Diez and co-workers [43].
In conclusion, we have shown using targeted deletion of melanin biosynthesis genes that melanin confers L. prolificans with protection from oxidative killing by H 2 O 2 and protection from UV radiation, but is not involved in its resistance to the anti-fungal drug amphotericin B.

Genomic DNA Extraction
DNA extraction was carried out according to the procedures described in Alastruey-Izquierdo and co-workers [56]. Spores were harvested by flooding OA plate cultures with 20 mL sterile autoclaved Milli-Q water (MQ-H 2 O) and suspension with a sterile L-shaped spreader (Fisher Scientific UK Ltd., Loughborough, Leicestershire, UK). The suspension was filtered through sterile Miracloth (Calbiochem, San Diego, CA, USA) to remove hyphal tissue, centrifuged at 13,000ˆg to pellet spores and the spores re-suspended in sterile MQ-H 2 O. Sterile 75 cm 2 tissue culture flasks containing 100 mL of tissue culture medium (TCM; RPMI-1640 medium (R0883, Sigma) containing 10% fetal bovine serum (Labtech International Ltd., Uckfield, East Sussex, UK), 2 mM L-glutamine (G7513, Sigma), penicillin and streptomycin) were inoculated with spore suspension to give a final concentration of 10 4 spores/mL and incubated with shaking (35 rpm) in an Innova 4000 rotary incubator (Eppendorf UK Ltd., Stevenage, Hertfordshire, UK) for 48 h at 30˝C. Hyphal biomass was harvested by filtration through sterile Miracloth, washed with sterile MQ-H 2 O, blotted dry with paper towel (Kimberley-Clark Ltd., West Malling, Kent, UK) and stored at´80˝C until required. Frozen mycelium was ground to a fine powder in liquid N 2 using a mortar and pestle, the powder transferred to 1.5 mL micro-centrifuge tubes and 800 µL of extraction buffer (0.2 M Tris-HCl, 0.5 M NaCl, 10 mM EDTA, SDS 1%) added followed by 800 µL of phenol:chloroform:isoamyl alcohol mixture (25:24:1). The mixture was shaken gently for 30 s and then centrifuged at 14,000ˆg for 15 min at 4˝C. The upper layer was transferred to a fresh tube and mixed with an equal volume of phenol:chloroform:isoamyl alcohol mixture (25:24:1), vortexed for 30 s and centrifuged as described. The upper layer was combined with an equal volume of chloroform:isoamyl alcohol (24:1) and vortexed for 30 s. Following centrifugation for 5 min at 14,000ˆg, the upper layer was transferred to a fresh tube, the DNA precipitated by adding chilled isopropanol and pelleted by centrifugation at 4˝C for 15 min at 14,000ˆg. The pellet was washed with 70% ethanol and centrifuged for a further 10 min at 14,000ˆg. The pellet was dried for 15 min at 23˝C, re-suspended in 30 µL MQ-H 2 O containing RNAse and then incubated for 1 h at 37˝C. DNA quality and quantity was determined by both agarose gel electrophoresis and by using a Nanodrop spectrophotometer (Thermo Fisher Scientific, Waltham, MA, USA).

Digestion of Plasmid and Genomic DNA with Restriction Enzymes
Restriction enzymes were obtained from Promega UK Ltd. (Southampton, Hampshire, UK) or New England Biolabs (Ipswich, MA, USA). DNA (0.2-1.0 µg) was digested with 5 to 10 units of enzyme in a total volume of 30 µL. For Southern blot analysis, digestion was performed by incubating 50 µg of genomic DNA with 60 units of restriction enzyme in a total volume 50 µL. In both cases, the mixtures were incubated at 37˝C for 16 h.

L. prolificans Genome and Primer Design
The full genome sequence of L. prolificans strain 3.1 archived at Biosciences, University of Exeter [38] was used for primer design. Primers were constructed by using the online resource (http://depts.washington.edu/bakerpg/primertemp/primermelttemp.html) and for reverse complements (http://arep.med.harvard.edu/labgc/adnan/projects/Utilities/revcomp.html). The primers used in this study are shown in Table 1.

Polymerase Chain Reaction
Polymerase Chain Reaction (PCR) was used to amplify DNA fragments in an Applied Biosystems GeneAmp ® PCR System 2400 cycler (Applied Biosystems, Foster City, CA, USA). GoTaq ® Green Master Mix (Applied Biosystems, Foster City, CA, USA), Phusion High Fidelity DNA polymerase (New England Biolabs, Ipswich, MA, USA) or Long PCR enzyme mix (Thermo Fisher Scientific, Waltham, MA, USA) were used according to the manufacturer's instructions. For GoTaq, the reaction mixture contained 12.5 µL GoTaq Green Master Mix, 10 µM of forward and reverse primer, 50 ng of genomic DNA and nuclease free water to a total volume of 50 µL and PCR cycling conditions were an initial denaturation step at 98˝C for 3 min followed by 35 cycles at 98˝C for 1 min, 53.5-20˝C (depending on annealing temperature of primers) for 1 min and at 72˝C, followed by a final extension step at 72˝C for 10 min. Phusion High Fidelity DNA polymerase reaction mixture contained 5 µL of 5ˆPhusion HF buffer, 0.5 µL of 10 mM dNTPs, 0.25 µL Phusion, 10 µM of forward and reverse primer, 50 ng of genomic DNA and nuclease-free water to a final volume of 50 µL. PCR cycling conditions were an initial denaturation step at 98˝C for 30 s followed by 35 cycles of 98˝C for 10 s, 62˝C for 30 s and 72˝C for 45 s, with a final extension for 10 min at 72˝C. Long PCR enzyme mix was used for PKS1 gene amplification. The PCR reaction mixture contained 5 µL of 10ˆLong PCR buffer with 15 mM MgCl 2 , 1 µL of 10 mM dNTPs, 1 µL of 10 µM of forward and reverse primer, 50 ng of genomic DNA, Long PCR enzyme mix to a total volume of 50 µL with nuclease-free water. PCR cycling conditions were an initial denaturation step at 94˝C for 3 min, 10 cycles at 94˝C for 20 s, 50˝C for 30 s and 68˝C for 7 min, followed by 25 cycles of 94˝C for 20 s, 50˝C for 30 s, 68˝C for 7 min. The final extension step was at 68˝C for 1 min.

Electrophoresis and Purification of Genomic DNA and PCR Products
Agarose gel electrophoresis was used to fractionate digested DNA. The DNA was separated in 0.8% agarose gels and stained with ethidium bromide after mixing with loading dye (50 mL glycerol, 0.25 g bromophenol blue, 5 mL of 0.5 M EDTA (pH 8.0) and 45 mL MQ-H 2 O). Electrophoresis was carried out in 1ˆTris-borate EDTA buffer (TBE; 0.09 M Tris-borate, 0.002 M EDTA) for 1 h at 100 V. The DNA fragments were visualized using a UV transilluminator and fragment sizes was determined by comparison with a 1-kb ladder (Promega). Gel images were captured by using an Image Master VDS-CL gel documentation system (GE Healthcare Life Sciences, Little Chalfont, Buckinghampshire, UK) fitted with a Fujifilm FTI-500 Thermal Imaging system (GE Healthcare). DNA fragments were purified from agarose gels using Wizard ® SV gel and PCR Clean-Up Systems (Promega) according to the manufacturer's instructions. Purified DNA was stored at´20˝C until required.

DNA Ligation
Ligation of DNA fragments was carried out using the In-Fusion ® HD Cloning kit (Clontech Laboratories Inc., Mountain View, CA, USA) according to the manufacturer's instructions. The ligation reaction components were combined in a PCR tube in the following order: 2 µL 5ˆIn-Fusion HD enzyme premix, 50 ng linearized vector, 200 ng purified PCR fragment and MQ-H 2 O to a total volume of 10 µL. The cloning reaction was incubated at 50˝C for 15 min and then kept on ice until required.

Transformation of Competent Cells
Stellar competent Escherichia coli cells (Clontech) were thawed, placed on ice and mixed gently for even distribution. Fifty-µL of component cells were combined gently with 5 ng (2.5 µL) of In-Fusion cloning reaction. The tubes were incubated on ice for 30 min, heat-shocked at 42˝C for 45 s and then transferred to ice for 1-2 min. SOC medium (2% tryptone, 0.5% yeast extract, 10 mM NaCl, 2.5 mM KCl, 10 mM MgCl 2 , 20 mM glucose) preheated to 37˝C was added to a total volume of 500 µL. The tube was incubated for 1 h at 37˝C with shaking (200 rpm) in an Innova 4000 rotary incubator. One hundred-µL were streaked on LB agar plates (LB broth (tryptone, 10 g/L, yeast extract, 5 g/L, NaCl, 10 g/L, pH 7.5) containing 18 g/L agar) overlaid with X-Gal (40 µg/mL) and supplemented with 1 mL of 100 µg/mL ampicillin. Plates were inverted and incubated at 37˝C for 16 h. Colonies were selected based on white-blue screening.

Plasmid Isolation (Quick-Prep Method)
A single colony of transformed bacteria was used to inoculate 10 mL of LB broth containing 10 µL of 100 µg/mL ampicillin. The culture was incubated overnight at 37˝C with shaking (180 rpm) in an Innova 4000 rotary incubator (Eppendorf). A 1 mL aliquot of culture was transferred to a micro-centrifuge tube and, after centrifugation at 13,000ˆg for 1 min, the supernatant was discarded and the pellet re-suspended in 100 µL lysis solution (250 µL 1 M Tris-HCl (pH8.0), 200 µL 0.5 M EDTA, 170 µL, 60% sucrose, 2.4 mL MQ-H 2 O) and vortexed. Two hundred-µL of alkaline solution (100 µL 10 M NaOH, 500 µL 10% SDS, 4.4 mL MQ-H 2 O) was added and the samples were placed on ice for 10 min with occasional shaking. One hundred and fifty-µL of 3 M sodium acetate (pH 5.2) were added and the samples were incubated on ice for a further 10 min and then centrifuged (13,000ˆg) for 10 min at 4˝C. The supernatant was transferred to a fresh tube containing 1 mL of 100% ethanol and stored on ice for 10 min before centrifugation at 13,000ˆg for 10 min. This process was repeated with 70% ethanol, the pellet dried at 23˝C and then re-suspended in 30 µL of MQ-H 2 O containing 7 µL RNase (10 mg/mL). The DNA was stored at´20˝C until used.

Plasmid DNA Isolation (Midi-Prep Method)
High quality plasmid DNA was isolated using the PureYield™ Plasmid Midiprep System (Promega) according to the manufacturer's instructions. A single colony of bacterial cells was grown in 50 mL LB containing 1 mL of a 100 µg/mL ampicillin solution for 16 h at 37˝C with shaking (180 rpm) in an Innova 4000 rotary incubator (Eppendorf). The cells were centrifuged at 5,000ˆg for 10 min and the supernatant discarded. The pellet was re-suspended in 3 mL of cell re-suspension solution (50 mM Tris (pH 7.5), 10 mM EDTA, and 100 µg/mL of RNase). Three-mL of cell lysis solution (0.2 M NaOH, 1% (w/v) SDS) were added and the contents of the tube were mixed by inverting 3-2 times. After 3 min incubation at 23˝C, 5 mL of neutralization solution (4.09 M guanidine hydrochloride, 0.759 M potassium acetate, 2.12 M glacial acetic acid, pH 4.2) was added, the tube was inverted 5-20 times and the lysate centrifuged at 14,000ˆg for 15 min. The PureYield™ purification system was used to purify DNA according to the manufacturer's instructions and DNA stored at´20˝C until required.

Protoplast Transformation
Spores were harvested from 2-week-old OA cultures, inoculated into 100 mL TCM and incubated for 3 days at 30˝C with shaking (35 rpm) in an Innova 4000 rotary incubator. Hyphal biomass was harvested by filtration through Miracloth and washed and dried as described. The mycelium was transferred to a 50 mL Falcon tube containing 40 mL OM buffer/Glucanex (44 g MgSO 4¨7 H 2 O, 1.5 mL 10 mM NaPO 4 , 1.8 g of 5% Glucanex (Novo Nordisk, Copenhagen, Denmark), pH 5.6) and incubated at 30˝C with shaking (75 rpm) for 3 h. The contents of the tube were transferred to sterile polycarbonate Nalgene Oakridge tubes (Thermo Fisher) and the protoplasts were overlaid with chilled ST buffer (0.6 M Sorbitol and 0.1 M Tris-HCl (pH 7.0)). The protoplasts were centrifuged at 5000ˆg for 15 min at 4˝C using a swinging bucket rotor (Beckman JS-13.1, Beckman Coulter Inc., Brea, CA, USA) in a Beckman J2.MC centrifuge (Beckman Coulter). The protoplasts were recovered at the OM/ST interface and transferred to a sterile Oakridge tube, which was filled with cold STC buffer (1.2 M Sorbitol, 10 mM Tris-HCl (pH 7.5), 10 mM CaCl 2 ). Protoplasts were pelleted at 3000ˆg for 10 min at 4˝C and washed twice with 10 mL STC, with complete re-suspension each time. Protoplasts were re-suspended in 1 mL STC and numbers quantified using a haemocytometer. Protoplasts were combined with 3 µg DNA in a sterile micro-centrifuge tube in a final volume of 150 µL and incubated for 15 min at 23˝C. One-mL of PTC (60% PEG4000, 10 mM Tris-HCl (pH 7.5), 10 mM CaCl 2 ) was added and the contents were mixed by gentle inversion. The protoplasts were incubated at 23˝C for 15 min, added to 150 mL molten (45˝C) OCM agar (osmotically stabilized CM; 50 mL nitrate salt solution, 1 mL trace elements (22 mg/L zinc sulphate heptahydrate, 11 mg/L boric acid, 5 mg/L manganese(II) chloride tetrahydrate, 5 mg/L iron(II) sulphate heptahydrate, 1.7 mg/L cobalt(II) chloride hexahydrate, 1.6 mg/L copper(II) sulphate pentahydrate, 1.5 mg/L sodium molybdate dehydrate, 50 mg/L EDTA), 10 g glucose, 2 g peptone, 1 g yeast extract, 1 g casamino acids, 1 mL vitamin solution (0.001 g/L, biotin, 0.001 g/L, pyridoxine, 0.001 g/L, thiamine, 0.001 g/L riboflavin, 0.001 g/L, 0.001 g/L nicotinic acid), 273.84 g sucrose and 15 g agar in a final volume of 1 L, adjusted to pH 6.5 with 1 M NaOH) and the protoplast suspension poured into sterile 9 cm plastic culture dishes for incubation in the dark at 30˝C for 16 h. The plates were then overlaid with complete medium (CM; 10 g/L glucose, 2 g/L, peptone, 1 g/L, yeast extract (BD Biosciences UK, Oxford, Oxfordshire, UK), 1 g/L casamino acids, 0.1% trace elements, 0.1%, 0.1% vitamin solution, 6 g/L NaNO 3 , 0.5 g/L, KCl, 0.5 g/L, MgSO 4 , 1.5 g/L, KH 2 PO 4 , (pH to 6.5 with NaOH), 15 g/L agar) containing 600 µg/mL hygromycin B (Calbiochem) and were then incubated for 1 week in the dark at 30˝C. Colonies resistant to hygromycin B were sub-cultured on CM containing 200 µg/mL hygromycin B and finally onto OA. For selection of sulfonylurea-resistant transformants, CM was replaced with BDCM medium (yeast nitrogen base without amino acids and ammonium sulfate, agar 1.7 g/L, ammonium nitrate, 2 g/L, asparagine, 1 g/L, glucose, 10 g/L, sucrose, 0.8 M, pH 6.0) with chlorimuron ethyl at a concentration of 300 µg/mL in the overlay, chlorimuron ethyl at a concentration of 100 µg/mL in BDCM sub-cultures and finally growth on OA.

Southern Blotting
Southern blotting was carried out according to the protocol of Southern [57]. Thirty-µg of genomic DNA was digested overnight using an appropriate restriction enzyme. The products of digestion were separated on 0.8% agarose gels at 100 V for 3 h. Gels were immersed in 0.25 M HCl for 15 min, followed by 0.4 M NaOH for a further 15 min, for de-purination and neutralization respectively. Gel blots were carried out by placing gels onto Whatman 3 mm paper wetted with 0.4 M NaOH and supported by a Perspex sheet with the ends of the paper immersed in 0.4 M NaOH. Gels were covered with Hybond-NX membrane (GE Healthcare Life Sciences), two layers of Whatman 3 mm paper and paper towel (Kimberley Clark). Finally, a 500 g weight was placed on the blotted gel and the blot was incubated for 16 h at 23˝C. Transferred DNA was UV-cross linked to the membrane using a BioLink BLX crosslinker (Sigma-Aldrich).
DNA probes were amplified by using Phusion HF buffer and the appropriate primers shown in Table 1 and reaction mixtures labelled with PCR DIG labelling mix (Sigma-Aldrich). Membranes were incubated in Hybaid hybridization bottles (Thermo Fisher) in a hybridization oven (Thermo Fisher) with Southern hybridization buffer (500 mL 1 M NaPO 4 (pH 7.0), 350 mL 20% SDS and Seradest added to a final volume of 1 L) at 62˝C for 30 min. Probes were denatured by boiling for 10 min and then added to hybridization bottles containing the membranes. Following hybridization at 62˝C for 16 h, the membranes were washed twice (15 min each) at 62˝C with Southern wash buffer (100 mL 1 M NaPO 4 (pH 7.0), 50 mL 20% SDS and MQ-H 2 O to 1 L) and once at 23˝C using 20 mL DIG wash buffer 1 (6 mL Tween-20, 1.994 mL DIG buffer (maleic acid 0.1 M, NaCl 0.15 M, adjusted to pH 7.5 with 5 M NaOH) and with MQ-H 2 O added to 2 L) for 5 min. Membranes were submerged in 50 mL of blocking buffer (1 g semi-skimmed milk powder and 100 mL DIG buffer 1) for 30 min at 23˝C and then incubated with 50 mL of antibody solution (2.5 µL anti-digoxigenin-AP Fab fragments (Sigma-Aldrich) and 50 mL blocking buffer) under the same conditions. After two 15 min washes with DIG wash buffer and equilibriation with 20 mL DIG buffer 3 (200 mL of 1 M Tris-HCl, 40 mL of 5 M NaCl, 100 mL of 1 M MgCl 2 (pH 9.5) with MQ-H 2 O added to 2 L) for 5 min, membranes were incubated for 5 min with 2 mL CDP-star ® chemiluminescent substrate solution (Sigma-Aldrich) and dried completely. Finally, the membrane was exposed to X-ray film (Fuji Photo Film (UK) Ltd., Manchester, Cheshire, UK) placed in a film cassette and incubated at 37˝C for 15 min. Films were developed using an OPTIMA X-Ray Film Processor (Protec GmbH, Oberstenfield, Germany).

Hyphal Growth, Sporulation and Spore Pigmentation
Strains were inoculated centrally onto replicate OA plates and colony diameters were measured over a 2-week growth period at 30˝C, with spore production quantified after 14 day. Spores were suspended in 20 mL dH 2 O using plastic L-shaped spreaders, filtered through Miracloth, and spore concentrations determined using a haemocytometer. There were 3 replicates for each experiment and experiments were repeated 3 times.

Oxidative Killing by H 2 O 2
Preliminary investigations set out to establish the molarity and exposure time to H 2 O 2 that resulted in a 50% reduction in survival of the wild-type strain 3.1. Replicate spore suspensions with a concentration of 10 3 spores/mL were suspended in 100 mM phosphate buffer (pH 7.0) comprising a range of mM concentrations of H 2 O 2 . Following exposure, 300 µL of spore suspensions were spread on the surface of SDA plates and incubated for 3 day at 30˝C in the dark. The control consisted of untreated spores (suspended in buffer only) and percentage survival was determined from the numbers of colonies that developed from treated spores compared to the untreated control. Through this process it was determined that exposure of spores to 160 mM H 2 O 2 for 60 min resulted in 50% survival of treated spores of the wild-type compared to the matched untreated control. All subsequent experiments using mutant strains were conducted using this same treatment regime and percentage survival relative to matched controls determined as described. There were 3 replicates for each strain and experiments were conducted three times.

Sensitivity to UV Radiation
Preliminary investigations aimed to establish the UV dose at 254 nm that resulted in a 50% reduction in survival of the wild-type strain 3.1. Replicate spore suspensions with a concentration of 10 3 spores/mL were exposed to UV light generated by a HL-2000 HybriLinker Hybridization oven (UVP) with doses of 100, 200, 300, 400 and 500 mJ/cm 2 . Following exposure, 300 µL of spore suspensions were spread on the surface of SDA plates and incubated for 3 days at 30˝C in the dark. The control consisted of non-irradiated spores and percentage survival was determined from the numbers of colonies that developed from irradiated spores compared to the non-irradiated control. Through this process it was determined that a UV dose of 200 mJ/cm 2 resulted in 50% survival of irradiated spores of the wild-type compared to the matched non-irradiated control. All subsequent experiments using mutant strains were conducted at this dose and percentage survivals relative to matched controls determined as described. There were 3 replicates for each strain and experiments were conducted three times.

Sensitivity to Amphotericin B
The sensitivities of the mutants and strain 3.1 to the polyene amphotericin B (AmB; Sigma, A2942) were tested using a liquid culture method. Tissue culture medium was amended with a liquid formulation of AmB (Sigma; A2942) to give final concentration of 32 µg/mL and the control consisted of TCM amended with an equivalent volume of sterile MQ-H 2 O only. Tissue culture flasks (75 cm 2 ) containing AmB or control media were inoculated with spores of the L. prolificans strains, or the drug-sensitive pathogen Aspergillus fumigatus (strain AF293), to give a final concentration of 10 6 spores/mL. Flasks were incubated for 3 days at 30˝C with shaking (48 rpm) in an Innova 4000 rotary incubator and the mycelium was harvested, dried at 70˝C for 48 h and dry weights obtained. The experiment was repeated three times with three replicates for each strain and treatment.

Statistical Analysis
Unless otherwise stated, numerical data were analyzed using the statistical program Minitab (Minitab 16, Minitab ® , Coventry, UK). Analysis of variance (ANOVA) was used to compare means of more than two data sets and Post-hoc Tukey-Kramer analysis was then performed to distinguish which sets were significantly different from one another. For comparisons of percentages, data was transformed using the arcsin´1 function prior to statistical analysis.