Differential sensitivity of Ustilago maydis to fungal antibiotics on simple and complex media

We have observed that the basidiomycete Ustilago maydis can be partially or completely resistant to antibiotics when grown in defined growth media. In synthetic medium based on the fully defined mixture of simple organic compounds and salts U. maydis displays near wild-type growth at concentrations of hygromycin that effectively kill cells in complex nutrient media. The antibiotics geneticin, nourseothricin and phleomycin had similar effects. In contrast, the fungicide carboxin was equally effective in all growth media tested. Our observations could guide selection of growth media for genetic transformation of Ustilago and other fungi when sensitivity to common antibiotics is used as a selectable marker. Creative Commons License This work is licensed under a Creative Commons Attribution-Share Alike 4.0 License. This regular paper is available in Fungal Genetics Reports: http://newprairiepress.org/fgr/vol62/iss1/3 8 Differential sensitivity of Ustilago maydis to fungal antibiotics on simple and complex media Anju Verma, Tamas Kapros, and Jakob H. Waterborg * 1 Division of Plant Sciences and Bond Life Sciences Center, University of Missouri-Columbia, Columbia, MO 65211, USA; 2 Division of Cell Biology and Biophysics, School of Biological Sciences, University of Missouri-Kansas City, Kansas City, MO 64110, USA. * Corresponding author Fungal Genetics Reports 62:813 We have observed that the basidiomycete Ustilago maydis can be partially or completely resistant to antibiotics when grown in defined growth media. In synthetic medium based on the fully defined mixture of simple organic compounds and salts U. maydis displays near wild-type growth at concentrations of hygromycin that effectively kill cells in complex nutrient media. The antibiotics geneticin, nourseothricin and phleomycin had similar effects. In contrast, the fungicide carboxin was equally effective in all growth media tested. Our observations could guide selection of growth media for genetic transformation of Ustilago and other fungi when sensitivity to common antibiotics is used as a selectable marker. Introduction Like many other laboratories we have successfully used the fungicide carboxin as a selectable marker in gene transformation (Brachmann et al., 2004; Brachmann et al., 2001; Fernandez-Alvarez et al., 2009; Kojic and Holloman, 2000; Topp et al., 2002) to knock-out variant-specifically histone H3 isotype loci (Verma et al., 2011). After transformation, transformants were cultured under continued selection until stable, non-heterokaryon clones could be isolated (Verma et al., 2011). These cultures were maintained on synthetic minimal media consisting of yeast nitrogen base (YNB), a standard mixture of small organic compounds and salts, with glucose (SD). When attempting to use other standard antibiotic selectable markers such as hygromycin, geneticin, nourseothricin and phleomycin (Brachmann et al., 2004; Kamper, 2004; Kojic and Holloman, 2000), selection was not observed. Other laboratories have used these markers extensively in generating genetic transformants of Ustilago, but they used chemically complex media, primarily based on mixtures of yeast extract and bactopeptone supplemented with glucose (YPD) or sucrose (YPS) (Berndt et al., 2010; Brachmann et al., 2004; Brachmann et al., 2001; Lovely et al., 2011; Tsukuda et al., 1988), but also Complete Medium (Garcia-Pedrajas et al., 2008; Holliday, 1974; Lee et al., 1999) or Potato Dextrose (Brachmann et al., 2004; Heidenreich et al., 2008; Zameitat et al., 2007). In our hands too, these complex media, in particular YPS, can be used effectively for antibiotic selection. However, we report here that in simple SD medium aminoglycoside and glycopeptide antibiotics, all larger and more hydrophilic than carboxin, are largely or completely ineffective. We speculate that uptake of these antibiotics depends on Ustilago cell membrane transport mechanisms that are absent in the simple SD medium. This observation poses an impediment if one wants to create auxotrophic mutants, e.g. for essential amino acids like leucine (Fotheringham and Holloman, 1990) or nucleotide bases like adenine (Verma et al., 2016) in YNB-based synthetic minimal media. Materials and Methods Simple, synthetic-defined media SD and SS consisted of 6.7 g yeast nitrogen base (YNB) without amino acids (Fisher Scientific, BD Difco) with 20 g dextrose (glucose) or sucrose (Sigma-Aldrich), respectively, in 1 L water. pH-buffered SD medium (SDS) was prepared by including 50 mM succinic acid and Published by New Prairie Press, 2017 9 adjustment of the pH to 7 with NaOH. Semi-defined, complex growth media YPD and YPS2 contained 10 g yeast extract (BD Difco), 20 g bactopeptone (BD Difco) with 20 g glucose or sucrose, respectively, in 1 L water. In addition to this rich complex medium (Tsukuda et al., 1988), we also tested the poorer formulation YPS1 with only 4 g yeast extract and 4 g bactopeptone per L (Brachmann et al., 2004). Ustilago growth rates and antibiotic effects were indistinguishable between YPS1 and YPS2. For plate cultures, media were supplemented with 15 g agar (Fisher Scientific) per L. Unless specified, media were autoclaved without adjusting the pH of approximately 6.5. Aliquots of stock solutions of antibiotics were added to the desired final concentrations into autoclaved simple or complex agar media, after cooling to approximately 55 C. Filter-sterilized hygromycin (SigmaAldrich) and geneticin (G418, Gibco BRL) stocks were 50 mg/mL water; nourseothricin (NTC, Jena Bioscience, Germany) was 100 mg/mL water; phleomycin (InVivogen) was 20 mg/mL stock as purchased. Carboxin (5,6-dihydro-2-methyl-1,4-oxathi-ine-3-carboxanilide; Vitavax) was 10 mg/mL methanol, diluted from a 34% suspension in methanol, a kind gift from S. Gold (Athens, GA) and used at 3 μg/mL (Verma et al., 2011). Wildtype U. maydis 521 haploid strain FGSC 9021 (Verma et al, 2011) was revived from –70 C storage in 50% glycerol, grown on SD plates at 30 C and single colonies were grown overnight in 50 mL SD or YPD at 30 C at 150 rpm in 125 mL flasks. Multiple samples of 250 cells in 10 microliter medium, after volume adjustment based on hematocytometer counting, were spotted on 100 mm diameter Petri dishes with 40 ml agar medium, allowed to dry, and incubated in the dark at 30 C for at least 1 week. Note that initial inoculum sizes increased as colonies grew, spreading across the agar surface (Fig. 1). Figure 1. Examples of U. maydis growth on solid media. Multiple aliquots of 10 μL of Ustilago suspension culture containing 250 cells were spotted on agar plates with complex or simple nutrient media and with sucrose or glucose (see Legend of Table 1) and grown in the dark at 30 C for 3 (A, F) or 6 days (B-E, G-S). A-J: complex media; K-S: simple media. Table 1 scores are indicated between square brackets. A. control, YPS1 [+++]; B. hygromycin, 200 μg/mL, YPS1 [NO]; C. geneticin, 200 μg/mL, YPS1 [NO]; D. nourseothricin, 150 μg/mL, YPS1 [NO]; E. phleomycin, 50 μg/mL, YPS1 [NO]; F. control, YPS2 [+++]; G. hygromycin, 300 μg/mL, YPS1 [NO]; H. geneticin, 250 μg/mL, YPS2 [NO]; I. nourseothricin, 300 μg/mL, YPS2 [NO]; J. phleomycin, 20 μg/mL, YPS2 [NO]; K. control, SD [+++]; L. hygromycin, 150 μg/mL, SD [++]; M. geneticin, 100 μg/mL, SD [+++]; N. nourseothricin, 150 μg/mL, SD [++]; O. phleomycin, 15 μg/mL, SD [+++]; P. hygromycin, 250 μg/mL, SD [+]; Q. geneticin, 300 μg/mL, SD [+++]; R. nourseothricin, 300 μg/mL, SD [+]; S. phleomycin, 50 μg/mL, SD [++]. Note the somewhat variable size of the 10 μL spots applied on plates like A where large colonies grow in only 3 days and plates like B, where the application spots remain faintly visible but microscopic colonies are never detected. http://newprairiepress.org/fgr/vol62/iss1/3 DOI: 10.4148/1941-4765.1002 10 Results and Discussion In our research to create selective knock-outs for the two single locus histone H3 variants in Ustilago, successful transformation at single loci was achieved using the selectable marker carboxin on simple defined (SD) growth media based on yeast nitrogen base (YNB) and glucose (Verma et al., 2011). The mutant succinate dehydrogenase cassette (Brachmann et al., 2004) which confers resistance to carboxin (Keon et al., 1991) was stably integrated in the Ustilago genome at the knock-out locus. To study the single remaining histone H3 variant function, we wished to replace its promoter by that of the inactivated gene, switching between the cell-cycle regulated H3 promoter and the constitutive H3 promoter (Verma et al., 2011). In the search for a second usable selectable marker, we were surprised by abundant growth on SD plates with hygromycin, geneticin (G418), nourseothricin (NTC) and phleomycin (Fig. 1) at antibiotic concentrations that were described as effective by other laboratories using Ustilago (Berndt et al., 2010; Brachmann et al., 2004; Brachmann et al., 2001; Garcia-Pedrajas et al., 2008; Heidenreich et al., 2008; Kamper, 2004; Kojic and Holloman, 2000; Lee et al., 1999; Lovely et al., 2011; Tsukuda et al., 1988; Zameitat et al., 2007). Reviewing growth media used by these laboratories, none had used simple media like our YNB-based one with glucose. We confirmed that indeed these antibiotics were effective against wild type Ustilago strains when yeast extractand bactopeptone-based media were used (Fig. 1) at the effective concentrations described (Table 1). We explored some of the possible factors involved to find conditions that would allow use of these antibiotics as selectable markers in simple media during the development of auxotrophic markers, such as the ade2 knockout (Verma et al., 2016). The effects of the composition of growth media during genetic transformation and selection of Ustilago has been recognized by others. For instance, the inclusion of high concentrations of sorbitol in protoplast transformation of Ustilago is required for the stabilization of the protoplasts but it