Diseases caused by fungi and oomycetes currently cause important economic losses in crops (^{Meng et al., 2009}). On the other hand, the world population increase demands greater amounts and quality of agricultural products, and consequently, a greater use of pesticides to fight diseases (^{Lahlali et al., 2022}). However, in recent years, consumers have become more aware of the side effects of the use of pesticides such as chemical fungicides on human health and the environment (^{Hou and Wu, 2010}). One of the alternatives to reduce dependence on pesticides is biological control (^{Compant et al., 2005}; ^{Barratt et al., 2018}), which is defined, in general terms, as any living microorganism (including viruses) used to fight a pathogen or pest by parasitism, antibiosis, competition for space or resources (^{Eilenberg et al., 2001}; ^{Stenberg et al., 2021}). In this regard, several species of basidiomycete mycoparasites have been reported as potential biocontrol agents (^{White and Traquair, 2006}; ^{Pineda-Suazo et al., 2021}). Mycoparasitism is a lifestyle in which the fungus establishes parasitic interactions with other fungi (^{Karlsson et al., 2017}). Mycoparasitic fungi are enzyme producers with the ability to degrade the cell walls of fungi, allowing them to penetrate into other fungi to extract nutrients for their development (^{Cao et al., 2009}). In this sense, the fungus Irpex lacteus is characterized by its saprophytic habit, although it has been proven to have a mycoparasitic behavior under certain conditions, implying interactions in which

• ^{Meng et al., 2009}
  Common processes in pathogenesis by fungal and oomycete plant pathogens, described with gene ontology terms

  BMC Microbiology, 2009
  Meng, S Torto-Alalibo, T Chibucos, MC Tyler, BM Dean, RA (2009). Common processes in pathogenesis by fungal and oomycete plant pathogens, described with gene ontology terms. BMC Microbiology 9 (Suppl 1):S7. 10.1186/1471-2180-9-S1-S7
• ^{Lahlali et al., 2022}
  Biological control of plant pathogens: a global perspective

  Microorganisms, 2022
  Lahlali, R Ezrari, S Radouane, N Kenfaoui, J Esmaeel, Q El Hamss, H Belabess, Z Barka, EA (2022). Biological control of plant pathogens: a global perspective. Microorganisms 10(3):596. 10.3390/microorganisms10030596
• ^{Hou and Wu, 2010}
  Safety impact and farmer awareness of pesticide residues

  Food and Agricultural Immunology, 2010
  Hou, B Wu, L (2010). Safety impact and farmer awareness of pesticide residues. Food and Agricultural Immunology 21(3):191-200. 10.1080/09540105.2010.484858
• ^{Compant et al., 2005}
  Use of plant growth-promoting bacteria for biocontrol of plant diseases: principles, mechanisms of action, and future prospects

  Applied and Environmental Microbiology, 2005
  Compant, S Duffy, B Nowak, J Clément, C Barka, EA (2005). Use of plant growth-promoting bacteria for biocontrol of plant diseases: principles, mechanisms of action, and future prospects. Applied and Environmental Microbiology 71. 10.1128/AEM.71.9.4951-4959.2005
• ^{Barratt et al., 2018}
  The status of biological control and recommendations for improving uptake for the future

  BioControl, 2018
  Barratt, BIP Moran, VC Bigler, F Van Lenteren, JC (2018). The status of biological control and recommendations for improving uptake for the future. BioControl 63:155-167. 10.1007/s10526-017-9831-y
• ^{Eilenberg et al., 2001}
  Suggestions for unifying the terminology in biological control

  BioControl, 2001
  Eilenberg, J Hajek, A Lomer, C (2001). Suggestions for unifying the terminology in biological control. BioControl 46: 387-400. 10.1023/A:1014193329979
• ^{Stenberg et al., 2021}
  When is it biological control? A framework of definitions, mechanisms, and classifications

  Journal of Pest Science, 2021
  Stenberg, JA Sundh, I Becher, PG Bjorkman, C Dubey, M Egan, PA Friberg, H Gil, JF Jensen, DF Jonsson, M Karlsson, M Khalil, S Ninkovic, V Rehermann, G Vetukuri, RR Viketoft, M (2021). When is it biological control? A framework of definitions, mechanisms, and classifications. Journal of Pest Science 94:665-676. 10.1007/s10340-021-01354-7
• ^{White and Traquair, 2006}
  Necrotrophic mycoparasitism of Botrytis cinerea by cellulolytic and ligninocellulolytic Basidiomycetes

  Canadian Journal of Microbiology, 2006
  Necrotrophic mycoparasitism of Botrytis cinerea by cellulolytic and ligninocellulolytic Basidiomycetes
• ^{Pineda-Suazo et al., 2021}
  Growth inhibition of phytopathogenic fungi and oomycetes by Basidiomycete Irpex lacteus and identification of its antimicrobial extracellular metabolites

  Polish Journal of Microbiology, 2021
  Growth inhibition of phytopathogenic fungi and oomycetes by Basidiomycete Irpex lacteus and identification of its antimicrobial extracellular metabolites
• ^{Karlsson et al., 2017}
  Necrotrophic mycoparasites and their genomes

  Microbiology Spectrum, 2017
  Karlsson, M Atanasova, L Jensen, DF Zeilinger, S (2017). Necrotrophic mycoparasites and their genomes. Microbiology Spectrum 5(2):FUNK-0016-2016. 10.1128/microbiolspec.funk-0016-2016
• ^{Cao et al., 2009}
  Mycoparasitism of endophytic fungi isolated from reed on soilborne phytopathogenic fungi and production of cell wall-degrading enzymes in vitro

  Current Microbiology, 2009
  Cao, R Liu, X Gao, K Mendgen, K Kang, Z Gao, J Dai, Y Wang, X (2009). Mycoparasitism of endophytic fungi isolated from reed on soilborne phytopathogenic fungi and production of cell wall-degrading enzymes in vitro. Current Microbiology. 10.1007/s00284-009-9477-9

I. lacteus colonizes and obtains nutrients from other fungi by secreting diverse hydrolytic enzymes (Metreveli et al., 2014; ^{Mezule a d Civzele, 2020}; ^{Gafforov et al., 2023}). The mycoparasitic abilities I. lacteus suggest possible applications in the biological control of phytopathogens in the agricultural context (^{White and Traquair, 2006}; ^{Sivanandhan et al., 2017}; ^{Yin et al., 2021}). Due to this, the aim of this investigation was to evaluate the fungus I. lacteus (isolate P7B) in vitro with a dual confrontation against 22 fungi and one oomycete.

• ^{Mezule a d Civzele, 2020}
  Bioprospecting white-rot Basidiomycete Irpex lacteus for improved extraction of lignocellulose-degrading enzymes and their further application

  Journal of Fungi (Basel), 2020
  Mezule, L Civzele, A (2020). Bioprospecting white-rot Basidiomycete Irpex lacteus for improved extraction of lignocellulose-degrading enzymes and their further application. Journal of Fungi (Basel) 6(4):256. 10.3390/jof6040256
• ^{Gafforov et al., 2023}
  Irpex lacteus (Fr.) Fr. - IRPICACEAE

  Ethnobiology of Uzbekistan. Ethnobiology., 2023
  Gafforov, Y Deshmukh, SK Tomšovský, M Yarasheva, M Wang, M Rapior, S (2023). Irpex lacteus (Fr.) Fr. - IRPICACEAE. Ethnobiology of Uzbekistan. Ethnobiology. Springer, Cham, Suiza. 1203-2217. 10.1007/978-3-031-23031-8_114
• ^{White and Traquair, 2006}
  Necrotrophic mycoparasitism of Botrytis cinerea by cellulolytic and ligninocellulolytic Basidiomycetes

  Canadian Journal of Microbiology, 2006
  Necrotrophic mycoparasitism of Botrytis cinerea by cellulolytic and ligninocellulolytic Basidiomycetes
• ^{Sivanandhan et al., 2017}
  Biocontrol properties of Basidiomycetes: An Overview

  Journal of Fungi, 2017
  Sivanandhan, S Khusro, A Paulraj, MG Ignacimuthu, S AL-Dhabi, NA (2017). Biocontrol properties of Basidiomycetes: An Overview. Journal of Fungi 3(1):2. 10.3390/jof3010002
• ^{Yin et al., 2021}
  Antifeedant and antiphytopathogenic metabolites from co-culture of endophyte Irpex lacteus, phytopathogen Nigrospora oryzae, and entomopathogen Beauveria bassiana

  Fitoterapia, 2021
  Antifeedant and antiphytopathogenic metabolites from co-culture of endophyte Irpex lacteus, phytopathogen Nigrospora oryzae, and entomopathogen Beauveria bassiana

This work was conducted in the Plant Physiology and Biotechnology Laboratory of the Facultad de Ciencias Agropecuarias y Ambientales of the Universidad Autónoma de Guerrero (FCAA-UAGro), located in Iguala de la Independencia, Guerrero, México.

For this study, isolate P7B was taken from an endophytic mycoparasitic fungus, which was isolated from the asymptomatic area of the Cedrus sp. rhizosphere, identified molecularly by DNA extraction, and for this purpose, the internal transcribed spacer (ITS) region of the ribosomal DNA as amplified by PCR using the ITS1/ITS4 primers (^{White et al., 1990}). DNA extraction, PCR, and sequencing were performed by the sequencing service of the Macrogen company (Macrogen, Inc., Seoul, Korea). The sequences obtained were edited and aligned using the MEGA X^® program, and a consensus sequence was obtained, which was compared with those available in the GenBank.

• ^{White et al., 1990}
  Amplification and Direct sequencing of fungal ribosomal RNA genes for phylogenetics

  PCR Protocols. A Guide to Methods and Applications, 1990
  White, TJ Bruns, T Lee, S Taylor, J (1990). Amplification and Direct sequencing of fungal ribosomal RNA genes for phylogenetics. PCR Protocols. A Guide to Methods and Applications. Academic Press, CA, USA, 315-322.

Isolate I. lacteus P7B underwent a dual confrontation against 22 fungi and one oomycete associated to diverse diseases (Table 1), belonging to the collection of phytopathogenic fungi of the Plant Physiology and Biotechnology Laboratory of the FCAA-UAGro. Strains of phytopathogenic fungi and the mycoparasitic agent (P7B) aged 12 days, developed in a PDA medium. For the confrontation, a disk, 0.5 cm in diameter and with mycelia, was placed 1.0 cm from the edge of the Petri dish and each isolation was placed on the opposite side of the dish, equidistantly. Three repetitions were used for each fungus or oomycete, along with control treatments, which consisted in placing a mycelium disk from each microorganism on one side of the Petri dish. The culture media were placed at a temperature of 28 °C, and the area of inhibition was recorded using a millimeter ruler when the control treatments covered the entire surface of the Petri dish with a PDA medium, which occurred approximately 14 days after cultured. Exceptionally, the treatments confronted with Rhizopus spp. were incubated for approximately 23 days, since a slow mycoparasitism was observed for I. lacteus P7B for this genus. Photographs were taken of the advancement of the dual confrontation every 24 hours (Sony camera, Vario-Tessar^®). Additionally, the area of interaction between microorganisms was analyzed against the antagonistic fungus I. lacteus P7B, in order to observe possible damages in the structures of the parasitized microorganisms, using a compound microscope (LABOMED^®).

Based on the values registered of the confrontations between microorganisms and the fungus I. lacteus P7B, the percentage of inhibition was estimated using the formula = (D1-D2)/D1*100.

where:

D1= Mycelial diameter of the control

D2= Mycelial diameter of the confronted microorganism

The analysis of the consensus sequence in the GenBank with the BLAST tool showed that isolate P7B had a percentage of identity of 99.85% with Irpex lacteus (accession number JX290579). The consensus sequence derived from this study was deposited in the GenBank with accession number PP922180.

In the in vitro evaluation of 22 fungi and one oomycete against I. lacteus P7B (Table 1), approximately 14 days later, it displayed 100% mycoparasitism on all the microorganisms it was confronted with (Figure 1), except for the genus Rhizopus (23 days). Figure 2 shows some representative examples of the confrontation between I. lacteus P7B against fungi and one oomycete, in which a clear gradual mycelial invasion was observed. By the end of the experiment, it was determined that the fungus I. lacteus P7B induced an inhibition of 100% in all confrontations (Figure 1, 2).

On the other hand, the fungi and an oomycete confronted with I. lacteus P7B all presented degradation of their structures when observed under the microscope. For example, Macrophomina sp. (isolate C4), in the zone of interaction, displayed degradation of sclerotia and hyphae (Figure 3B); Alternaria sp. (isolate AL1), it presented degraded conidia and hyphae (Figure 3D); for Rhizopus sp. (isolate RIZOPAP), degradation of sporangia was observed (Figure 3F); in control treatments, structures displayed no apparent damage (Figure 3A, C and E).

This work showed the mycoparasitic ability of I. lacteus P7B against 22 fungi and one oomycete associated to diverse phytosanitary problems. Literature on the potential of I. lacteus as a biocontrol agent is scarce. The fungus I. lacteus has the ability to produce diverse hydrolytic enzymes such as chitinases and glucanases, which degrade the cell walls of other fungi, facilitating the acquisition of nutrients (^{Qin et al., 2018}; Roncero and Vázquez de Aldana, 2019). In a study carried out by ^{White and Traquair (2006}), by confronting I. lacteus against Botrytis cinerea in vitro, they proved that I. lacteus was able to parasite B. cinerea by degrading its structures such as conidiophores and conidia and parasiting its sclerotia, and reported a percentage of mycoparasitism of 100%, similar results reported in this study. On the other hand, in Mexico, I. lacteus has been evaluated against Fusarium pseudocircinatum, F. mexicanum, Colletotrichum coccodes, C. gloeosporioides, Phytophthora capsici and P. cinnamomi with a percentage of inhibition between 16.7 and 46.3% (^{Pineda-Suazo et al., 2021}). In this investigation, I. lacteus P7B displayed a greater capacity for mycoparasiting diverse fungi and an oomycete, possibly due to the type of isolation. In addition, I. lacteus has been reported to belong to the group of necrotrophic mycoparasites, which are characterized for being highly destructive, scarcely specialized (^{Viterbo et al., 2007}) and generally presenting a high range of hosts, including phytopathogens and extend to diverse taxonomic groups (Viterbo and Horwitz et al., 2010), as in this study, where I. lacteus parasite fungi and an oomycete of the divisions Ascomycota, Zygomycota and Oomycota. Additionally, compounds, derived from I. lacteus such as terpenes and aldehydes, have been detected which have an antifungal potential (Pineda- Suazo et al., 2021; ^{Wang et al., 2021}).

• ^{Qin et al., 2018}
  Dye-decolorizing peroxidases in Irpex lacteus combining the catalytic properties of heme peroxidases and laccase play important roles in ligninolytic system

  Biotechnology for Biofuels, 2018
  Dye-decolorizing peroxidases in Irpex lacteus combining the catalytic properties of heme peroxidases and laccase play important roles in ligninolytic system
• ^{White and Traquair (2006}
  Necrotrophic mycoparasitism of Botrytis cinerea by cellulolytic and ligninocellulolytic Basidiomycetes

  Canadian Journal of Microbiology, 2006
  Necrotrophic mycoparasitism of Botrytis cinerea by cellulolytic and ligninocellulolytic Basidiomycetes
• ^{Pineda-Suazo et al., 2021}
  Growth inhibition of phytopathogenic fungi and oomycetes by Basidiomycete Irpex lacteus and identification of its antimicrobial extracellular metabolites

  Polish Journal of Microbiology, 2021
  Growth inhibition of phytopathogenic fungi and oomycetes by Basidiomycete Irpex lacteus and identification of its antimicrobial extracellular metabolites
• ^{Viterbo et al., 2007}
  Plant disease biocontrol and induced resistance via fungal mycoparasites

  The Mycota, vol. IV, 2007
  Viterbo, A Inbar, J Hadar, Y Chet, I (2007). Plant disease biocontrol and induced resistance via fungal mycoparasites. The Mycota, vol. IV. Springer, Berlin, Germany, 127-146. 10.1007/978-3-540-71840-6_8
• ^{Wang et al., 2021}
  The selective anti-fungal metabolites from Irpex lacteus and applications in the chemical interaction of Gastrodia elata, Armillaria sp., and endophytes

  Fitoterapia, 2021
  The selective anti-fungal metabolites from Irpex lacteus and applications in the chemical interaction of Gastrodia elata, Armillaria sp., and endophytes

The fungus I. lacteus mycoparasited 100% in vitro 22 fungi and one oomycete evaluated in this study. Future investigations may focus on evaluating the antagonistic activity of I. lacteus under field conditions for the control of phytopathogens, as well as on the evaluation and determination of antifungal compounds derived from I. lacteus P7B.