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Fusarium oxysporum Casein Kinase 1, a Negative Regulator of the Plasma Membrane H(+)-ATPase Pma1, Is Required for Development and Pathogenicity

Like many hemibiotrophic plant pathogens, the root-infecting vascular wilt fungus Fusarium oxysporum induces an increase in the pH of the surrounding host tissue. How alkalinization promotes fungal infection is not fully understood, but recent studies point towards the role of cytosolic pH (pH(c)) a...

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Detalles Bibliográficos
Autores principales: Mariscal, Melani, Miguel-Rojas, Cristina, Hera, Concepción, Fernandes, Tânia R., Di Pietro, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9786551/
https://www.ncbi.nlm.nih.gov/pubmed/36547634
http://dx.doi.org/10.3390/jof8121300
Descripción
Sumario:Like many hemibiotrophic plant pathogens, the root-infecting vascular wilt fungus Fusarium oxysporum induces an increase in the pH of the surrounding host tissue. How alkalinization promotes fungal infection is not fully understood, but recent studies point towards the role of cytosolic pH (pH(c)) and mitogen-activated protein kinase (MAPK) signaling. In fungi, pH(c) is mainly controlled by the essential plasma membrane H(+)-ATPase Pma1. Here we created mutants of F. oxysporum lacking casein kinase 1 (Ck1), a known negative regulator of Pma1. We found that the ck1Δ mutants have constitutively high Pma1 activity and exhibit reduced alkalinization of the surrounding medium as well as decreased hyphal growth and conidiation. Importantly, the ck1Δ mutants exhibit defects in hyphal chemotropism towards plant roots and in pathogenicity on tomato plants. Thus, Ck1 is a key regulator of the development and virulence of F. oxysporum.