Abstract
We have isolated and characterized six chemically induced mutants of the filamentous fungusAspergillus nidulans that are resistant to the experimental fungicide 8-chloro-4-(2-chloro-4-fluoro-phenoxy)quinoline (LY214352). The mutants are 13- to 430-fold more resistant to LY214352 than the parental strain, and one of the mutant strains requires LY214352 for maximal growth. The resistance trait is governed by a single dominant or partially dominant gene in each mutant, and it is likely that all of the mutations are allelic. The LY214352-resistant mutants were not cross-resistant to other compounds that inhibit the growth ofA. nidulans. The implications of these findings on the potential for development of resistance to LY214352 are discussed.
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Literature Cited
Borck K, Braymer HD (1974) The genetic analysis of resistance to benomyl inNeurospora crassa. J Gen Microbiol 85:51–56
Coghlan MJ, Krumkalns EV, Caley BA, Hall HR, Arnold WA (1991) Synthesis and investigation of 4-phenoxyquino-lines as novel agents for the control of cereal and grape powdery mildew. In: Moberg WK (ed) The synthesis and chemistry of agrochemicals II. Washington, D.C.: ACS, pp 538–552
Davidse LC (1981) Resistance to acylalanine fungicides inPhytophthora megasperma f. sp.medicaginis. Neth J Plant Pathol 87:11–24
Davidse LC (1986) Benzimidazole fungicides: mechanism of action and biological impact. Annu Rev Phytopathol 24:43–65
Davidse LC, Hofman AE, Velthius GCM (1983) Specific interference of metalaxyl with endogenous RNA polymerase activity in isolated nuclei fromPhytophthora megasperma f. sp.medicaginis. Exp Mycol 7:344–361
Dekker J (1987) Development of resistance to modern fungicides and strategies for its avoidance. In: Lyr H (ed) Modern selective fungicides. New York: John Wiley and Sons, pp 39–52
De Waard MA, van Nistelrooy JGM (1980) An energy-dependent efflux mechanism for fenarimol in a wild-type strain and fenarimol-resistant mutants ofAspergillus nidulans. Pesticide Biochem Physiol 13:255–266
Dovas C, Skylakakis G, Georgopoulos SG (1976) The adaptability of the benomyl-resistant population ofCercospora beticola in Northern Greece. Phytopathology 66:1452–1456
Edlich W, Lyr H (1987) Mechanism of action of dicarboximide fungicides. In: Lyr H (ed) Modern selective fungicides. New York: John Wiley and Sons, pp 107–118
Elbein AD (1981) The tunicamycins—useful tools for studieson glycoproteins. Trends Biochem Sci 6:219–221
Georgopoulos SG, Chrysayi M, White GA (1975) Carboxin resistance in the haploid, the heterozygous diploid, and the plant-parasitic dicaryotic phase ofUstilago maydis. Pesticide Biochem Physiol 5:543–551
Henry MJ, Trivellas AE (1989) Laboratory-induced fungicide resistance to benzimidazole and azole fungicides inCercospora beticola. Pesticide Biochem Physiol 35:89–96
Hori M, Kakiki K, Misato T (1974) Interaction between polyoxin and the active center of chitin synthetase. Agr Biol Chem 38:699–705
Katan K, Shabi E, Gilpatrick JD (1983) Genetics of resistance to benomyl inVenturia inaequalis isolates from Israel and New York. Phytopathology 73:600–603
Kerridge D, Whelan WL (1984) The polyene macrolide antibiotics and 5-fluorocytosine: molecular actions and interactions. In: Trinci APJ, Ryley JF (eds) Mode of action of antifungal agents. New York: Cambridge University Press, pp 343–376
Kodama O, Akatsuka T (1982) Kitazin P and edifenphos, possible inhibitors of phosphatidylcholine biosynthesis. In: Muatsunaka S, Hutson DH, Murphy D (eds) Pesticide chemistry: human welfare and the environment, vol. 3. New York: Pergamon Press, pp 135–140
Leroux P, Fritz R (1984) Antifungal activity of dicarboximides and aromatic hydrocarbons and resistance to these fungicides. In: Trinci APJ, Ryley JF (eds) Mode of action of antifungal agents. New York: Cambridge University Press, pp 207–237
Lyr H (1987) Mechanism of action of aromatic hydrocarbon fungicides. In: Lyr H (ed) Modern selective fungicides. New York: John Wiley and Sons, pp 75–89
Misato T, Kakkiki K, Hori, M (1977) Mechanism of polyoxin resistance. Neth J Plant Pathol 83 (S1):253–260
Pontecorvo G, Rope JA, Hemmons LM, MacDonald KD, Bufton AWJ (1953) The genetics ofAspergillus nidulans. Adv Genet 5:141–238
Ryley JF, Wilson RG, Gravestock MB, Poyser JP (1981) Experimental approaches to antifungal chemotherapy. In: Garattini S, Goldin A, Hawking F, Kopin IJ (eds) Advances in pharmacology and chemotherapy, vol. 18. New York: Academic Press, pp 49–176
Sisler HD, Ragsdale NN (1984) Biochemical and cellular aspects of the antifungal action of ergosterol biosynthesis inhibitors. In: Trinci APJ, Ryley JF (eds) Mode of action of antifungal agents. New York: Cambridge University Press, pp 257–282
Taft CS, Selitrinnikoff CP (1988) LY121019 inhibitsNeurospora crassa growth and (1–3)-β-d-glucan synthase. J Antibiotics 41:697–701
Taga M, Waki T, Tsuda M, Ueyama A (1982) Fungicide sensitivity and genetics of IBP-resistant mutants ofPyricularia oryzae. Phytopathology 72:905–909
Uesugi Y (1982) Case study 3:Pyricularia oryzae of rice. In: Dekker J, Georgopoulos SG (eds) Fungicide resistance in crop protection. Wageningen: Pudoc, pp 207–218
Waldron C, Roberts CF (1974). Cold-sensitive mutants inAspergillus nidulans. I. Isolation and general characterisation. Mol Gen Genet 134:99–113
White GA, Thorn GD, Georgopoulos SG (1978)Oxathiin carboxamides highly active against carboxin-resistant succinic dehydrogenase complexes from carboxin-selected mutants ofUstilago maydis andAspergillus nidulans Pesticide Biochem Physiol 9:165–182
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Gustafson, G.D., Waldron, C. & Davis, G.E. Isolation, characterization, and genetic analysis ofAspergillus nidulans mutants resistant to the antifungal compound LY214352. Current Microbiology 23, 39–44 (1991). https://doi.org/10.1007/BF02092307
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DOI: https://doi.org/10.1007/BF02092307