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April 24, 2026ACS Omega0 citationsOpen Access

Sustainable Biocontrol of Agave Vascular Wilt Using an Inactivated Mycelial Formulation from the Mangrove Endophyte Talaromyces islandicus M31

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APAlbert D. PatiñoJPJavier PlasenciaSDSandip Das

Key Points

  • The research aims to evaluate the potential of Talaromyces islandicus M31 for biocontrol of Fusarium-induced vascular wilt in agave.
  • Isolated compounds from solid-state fermentation of Talaromyces islandicus M31.
  • Conducted in vitro growth-inhibitory assays and in vivo tests using inactivated fungal mycelium.
  • Assessed membrane integrity disruption through macromolecule leakage and microscopy.
  • (–)-luteoskyrin showed the strongest growth inhibition against Fusarium species over two months.
  • The inactivated mycelial formulation effectively reduced Fusarium infection in agave.
  • Disruption of membrane integrity was demonstrated via macromolecule leakage assays.

Abstract

The genus Fusarium comprises several plant pathogenic species, some of which are etiological agents of vascular wilt in agave plants, inducing systemic necrosis across the roots, caudex (cone), and foliar tissues. Such disease compromises host vigor and biomass productivity, ultimately reducing the organoleptic quality of fermented and distilled derivatives, including mezcal, tequila, and other distillates. Thus, as part of our ongoing bioprospecting efforts in unexplored areas of Mexico, the chemical study of the organic extract from a solid-state fermentation culture of the manglicolous endophyte fungus Talaromyces islandicus M31, isolated in the Punta Sur Ecological Park in Cozumel Island Biosphere Reserve, Mexico, led to the separation of eight anthraquinone derivatives active against the agave pathogens Fusarium incarnatum (CRT-153 and CRT-197), Fusarium proliferatum (CRT-142), and Fusarium oxysporum (CRT-098 and CRT-214). Among the molecules tested, the bisdihydroanthraquinone (–)-luteoskyrin (6) exhibited the strongest growth-inhibitory activity, which was also measured over a two-month span. Through macromolecule leakage assay and scanning electron microscopy, we found that (–)-luteoskyrin (6) disrupted membrane integrity in F. incarnatum. Furthermore, a simple formulation consisting of inactivated T. islandicus M31 mycelium was tested in vivo to control Fusarium infection in agave. The results suggest that (–)-luteoskyrin (6) acts synergistically with other components, resulting in remarkable anti-Fusarium activity and demonstrating its efficacy and advantages for pest management.

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Cite This Study

Patiño et al. (2026) studied this question.

synapsesocial.com/papers/69eb084f553a5433e34b368ahttps://doi.org/10.1021/acsomega.6c01311
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