Broad-Spectrum Activity of Volatile Organic Compounds from Three Yeast-like Fungi of the Galactomyces Genus Against Diverse Plant Pathogens

References

• Spadaro D, Droby S. Development of biocontrol products for postharvest diseases of fruit: the importance of elucidating the mechanisms of action of yeast antagonists. Trends Food Sci Technol. 2016;47:39–49.
   Web of Science ®Google Scholar
• Carmona-Hernandez S, Reyes-Pérez JJ, Chiquito-Contreras RG, et al. Biocontrol of postharvest fruit fungal diseases by bacterial antagonists: a review. Agronomy. 2019;9:121.
   Google Scholar
• Freimoser FM, Rueda-Mejia MP, Tilocca B, et al. Biocontrol yeasts: mechanisms and applications. World J Microbiol Biotechnol. 2019;35:154.
   PubMed Web of Science ®Google Scholar
• Morath SU, Hung R, Bennett JW. Fungal volatile organic compounds: a review with emphasis on their biotechnological potential. Fungal Biol Rev. 2012;26:73–83.
   Google Scholar
• Minerdi D, Bossi S, Gullino ML, et al. Volatile organic compounds: a potential direct long-distance mechanism for antagonistic action of Fusarium oxysporum strain MSA 35. Environ Microbiol. 2009;11:844–854.
   PubMed Web of Science ®Google Scholar
• Cernava T, Aschenbrenner IA, Grube M, et al. A novel assay for the detection of bioactive volatiles evaluated by screening of lichen-associated bacteria. Front Microbiol. 2015;6:398.
   Web of Science ®Google Scholar
• Irtwange SV. Application of biological control agents in pre- and postharvest operations. Int J Agric Eng. 2006;8:1–12.
   Google Scholar
• Eayre CG, Skaria M, Bull CT, et al. An avirulent Galactomyces species that controls green mold of citrus caused by Penicillium digitatum. Subtrop Plant Sci. 2003;55:46–50.
   Google Scholar
• McKay AH, Förster H, Adaskaveg JE. Toxicity and resistance potential of selected fungicides to Galactomyces and Penicillium spp. causing postharvest fruit decays of citrus and other crops. Plant Dis. 2012;96:87–96.
   Web of Science ®Google Scholar
• Schisler DA, Janisiewicz WJ, Boekhout T, et al. Agriculturally important yeasts: biological control of field and postharvest diseases using yeast antagonists, and yeasts as pathogens of plants. In: Kurtzman CP, Fell JW, Boekhout T, editors. The yeasts. 4th ed. Amsterdam (The Netherlands): Elsevier; 2011. p. 45–52.
   Google Scholar
• Chen PH, Chen RY, Chou JY. Screening and evaluation of yeast antagonists for biological control of Botrytis cinerea on strawberry fruits. Mycobiology. 2018;46:33–46.
   PubMed Web of Science ®Google Scholar
• Zhang L, Khabbaz SE, Wang A, et al. Detection and characterization of broad-spectrum antipathogen activity of novel rhizobacterial isolates and suppression of Fusarium crown and root rot disease of tomato. J Appl Microbiol. 2015;118:685–703.
   PubMed Web of Science ®Google Scholar
• Silva JCP, Campos VP, Barros AF, et al. Plant volatiles reduce the viability of the root-knot nematode Meloidogyne incognita either directly or when retained in water. Plant Dis. 2018;102:2170–2179.
   Web of Science ®Google Scholar
• Freire ES, Campos VP, Pinho RSC, et al. Volatile substances produced by Fusarium oxysporum from coffee rhizosphere and other microbes affect Meloidogyne incognita and Arthrobotrys conoides. J Nematol. 2012;44:321–328.
   PubMed Web of Science ®Google Scholar
• Riedel RM. Interactions of plant-parasitic nematodes with soil-borne plant pathogens. Agric Ecosyst Environ. 1988;24:281–292.
   Web of Science ®Google Scholar
• Akhtar M, Malik A. Roles of organic soil amendments and soil organisms in the biological control of plant-parasitic nematodes: a review. Bioresour Technol. 2000;74:35–47.
   Web of Science ®Google Scholar
• Oka Y, Koltai H, Bar‐Eyal M, et al. New strategies for the control of plant‐parasitic nematodes. Pest Manag Sci. 2000;56:983–988.
   Web of Science ®Google Scholar
• McSorley R. Overview of organic amendments for management of plant-parasitic nematodes, with case studies from Florida. J Nematol. 2011;43:69–81.
   PubMed Web of Science ®Google Scholar
• Fuhrich DG, Lessey BA, Savaris RF. Comparison of HSCORE assessment of endometrial beta3 integrin subunit expression with digital HSCORE using computerized image analysis *(ImageJ). Anal Quant Cytopathol Histpathol. 2013;35:210–216.
   PubMedGoogle Scholar
• Michereff SJ, Silveira NSS, Reis A, et al. Epiphytic bacteria antagonistic to Curvularia leaf spot of yam. Microb Ecol. 1994;28:101–110.
   PubMed Web of Science ®Google Scholar
• Huang R, Li GQ, Zhang J, et al. Control of postharvest Botrytis fruit rot of strawberry by volatile organic compounds of Candida intermedia. Phytopathology. 2011;101:859–869.
   PubMed Web of Science ®Google Scholar
• R Core Team. R: a language and environment for statistical computing. Vienna (Austria): R Foundation for Statistical Computing; 2019. Available from: https://www.r-project.org/
   Google Scholar
• Knudsen GR, Dandurand LMC. Ecological complexity and the success of fungal biological control agents. Adv Agric. 2014;2014:1–11.
   Google Scholar
• Sacristán N, González L, Castro JM, et al. Technological characterization of Geotrichum candidum strains isolated from a traditional Spanish goats' milk cheese. Food Microbiol. 2012;30:260–266.
   Web of Science ®Google Scholar
• Grondin E, Sing ASC, James S, et al. Flavour production by Saprochaete and Geotrichum yeasts and their close relatives. Food Chem. 2017;237:677–684.
   Web of Science ®Google Scholar
• Pretscher J, Fischkal T, Branscheidt S, et al. Yeasts from different habitats and their potential as biocontrol agents. Fermentation. 2018;4:31.
   Google Scholar
• Frézal L, Jacqua G, Neema C. Adaptation of a fungal pathogen to host quantitative resistance. Front Plant Sci. 2018;9:1554.
   Web of Science ®Google Scholar
• Le May C, Montarry J, Morris CE, et al. Editorial: plant pathogen life-history traits and adaptation to environmental constraints. Front Plant Sci. 2020;10:1730.
   Web of Science ®Google Scholar
• Gubler WD, Feliciano CJ, Bordas AC, et al. X. fragariae and C. cladosporioides cause strawberry blossom blight. Calif Agr. 1999;53:26–28.
   Google Scholar
• Nam MH, Park MS, Kim HS, et al. Cladosporium cladosporioides and C. tenuissimum cause blossom blight in strawberry in Korea. Mycobiology. 2015;43:354–359.
   PubMed Web of Science ®Google Scholar
• Robles-Yerena L, Ayala-Escobar V, Leyva-Mir SG, et al. First report of Cladosporium cladosporioides causing leaf spot on tomato in Mexico. J Plant Pathol. 2019;101:759–759.
   Web of Science ®Google Scholar
• Wang X, Radwan MM, Taráwneh AH, et al. Antifungal activity against plant pathogens of metabolites from the endophytic fungus Cladosporium cladosporioides. J Agric Food Chem. 2013;61:4551–4555.
   PubMed Web of Science ®Google Scholar
• Paynter Q, Hennecke B. Competition between two biological control agents, Neurostrota gunniella and Phloeospora mimosae-pigrae, and their impact on the invasive tropical shrub Mimosa pigra. Biocontrol Sci Technol. 2001;11:575–582.
   Web of Science ®Google Scholar
• Osemwegie OO, Oghenekaro AO, Owolo LO. Effects of pulverized Ganoderma spp., on Sclerotium rolfsii Sacc and post-harvest tomato (Lycopersicon esculentum Mill.) fruits preservation. J Appl Sci Res. 2010;6:1794–1800.
   Google Scholar
• Jia XH, Fu JF, Wang WH, et al. First report of Athelia bombacina causing postharvest fruit rot on pear. J Integr Agric. 2018;17:2596–2599.
   Web of Science ®Google Scholar
• Dodd SL, Hill RA, Stewart A. Control of Athelia rolfsii disease on lentil seedlings using 6-pentyl-α-pyrone. Soil Biol Biochem. 2000;32:1033–1034.
   Web of Science ®Google Scholar
• El-Hasan A, Walker F, Schöne J, et al. Antagonistic effect of 6-pentyl-alpha-pyrone produced by Trichoderma harzianum toward Fusarium moniliforme. J Plant Dis Prot. 2007;114:62–68.
   Web of Science ®Google Scholar
• Riga E. The effects of Brassica green manures on plant parasitic and free living nematodes used in combination with reduced rates of synthetic nematicides. J Nematol. 2011;43:119–121.
   Web of Science ®Google Scholar
• Casas-Flores S, Herrera-Estrella A. Antagonism of plant parasitic nematodes by fungi. In: Kubicek CP, Druzhinina IS, editors. Environmental and microbial relationships. The Mycota. Vol. 4. Heidelberg: Springer; 2007. p. 147–157.
   Google Scholar
• Moosavi MR, Zare R. Fungi as biological control agents of plant-parasitic nematodes. In: Mérillon J, Ramawat K, editors. Plant defence: biological control. Progress in biological control. Vol. 12. Dordrecht: Springer; 2012. p. 67–107.
   Google Scholar
• Favre-Bonvin J, Ponchet M, Djian C, et al. Acetic acid: a selective nematicidal metabolite from culture filtrates of Paecilomyces lilacinus (Thom) Samson and Trichoderma longibrachiatum Rifai. Nematology. 1991;37:101–112.
   Google Scholar
• Kwok OCH, Plattner R, Weisleder D, et al. A nematicidal toxin from Pleurotus ostreatus NRRL 3526. J Chem Ecol. 1992;18:127–136.
   PubMed Web of Science ®Google Scholar
• Hallmann J, Sikora RA. Occurrence of plant parasitic nematodes and non‐pathogenic species of Fusarium in tomato plants in Kenya and their role as mutualistic synergists for biological control of root‐knot nematodes. Int J Pest Manage. 1994;40:321–325.
   Web of Science ®Google Scholar