Characterization of three mitogen-activated protein kinase kinase-like proteins in Beauveria bassiana.

Pbs2, Mkk1 and Ste7 orthologs are three mitogen-activated protein kinase (MAPK) kinases (MAPKKs) acting as checkpoints of the Hog1, Slt2 and Fus3 MAPK cascades that constitute major parts of fungal signaling network. Here, we show that three other MAPKK-like proteins (Mkk4/5/6) exist in Beauveria bassiana and other entomopathogenic or non-entomopathogenic fungi but lack in yeasts and aspergilli, and elucidate how they function in the fungal insect pathogen. Based on phenotypic defects of single-, double- and triple-deletion mutants, Mkk4, Mkk5 and Mkk6 played collaborative or independent roles in sustaining radial growth on various media, conidiation capacity, conidial germination, conidial UV-B resistance, and/or virulence. In stress assays, three single-deletion Δmkk mutants showed increased tolerance to cell wall stress but null response to a 3-h heat shock at 40 °C during normal incubation. Only did Δmkk6 exhibit increased sensitivity to either menadione or H2 O2 oxidation. Intriguingly, Δmkk5 and Δmkk6 displayed a remarkable increase in cellular sensitivity to a high osmolarity of NaCl or KCl instead of non-salt sorbitol, suggesting a link of their increased sensitivity to the toxicity of a high Na+ /K+ concentration rather than to the plausible osmotic stress of either salt. However, all of the deletion mutants showed no resistance to fludioxonil, a phenylpyrrole-type fungicide. A discussion is provided on whether Mkk4, Mkk5 and Mkk6 could be likely associated with or without the MAPK cascades in B. bassiana.