A Group III histidine kinase (mhk1) upstream of high-osmolarity glycerol pathway regulates sporulation, multi-stress tolerance and virulence of Metarhizium robertsii, a fungal entomopathogen.

The role of Metarhizium robertsii Group III histidine kinase (mhk1) in regulating various phenotypes of the fungal entomopathogen and the transcripts of 25 downstream genes likely associated with the phenotypes were probed by constructing Δmhk1 and Δmhk1/mhk1 mutants. All examined Δmhk1 phenotypes except unchanged sensitivity to fungicide (dimethachlon) differed significantly from those of wild type and Δmhk1/mhk1, which were similar to each other. Significant phenotypic changes in Δmhk1 included increased conidial yields on two media, increased tolerance to H(2)O(2) , decreased tolerance to menadione, increased tolerance to hyperosmolarity, increased conidial thermotolerance, decreased conidial UV-B resistance and reduced virulence to Tenebrio molitor larvae. The mhk1 disruption elevated the transcripts of nine genes, including two associated with conidiation (flbC and hymA) and three encoding catalases but decreased seven other gene transcripts, including three for superoxide dismultases, under normal conditions. The high-osmolarity glycerol pathway MAPK phosphorylation level in Δmhk1 culture was increased 1.0- to 1.8-fold by KCl, sucrose and menadione stresses but reduced drastically by H(2)O(2) or heat (40°C) stress, accompanied with different transcript patterns of all examined genes under the stresses. Our results confirmed the crucial role of mhk1 in regulating the expression of the downstream genes and associated phenotypes important for the fungal biocontrol potential.