Mitogen activated protein kinases SakAHOG1 and MpkC collaborate for Aspergillus fumigatus virulence
Summary Here, we investigated which stress responses were influenced by the MpkC and SakA mitogen‐activated protein kinases of the high‐osmolarity glycerol (HOG) pathway in the fungal pathogen Aspergillus fumigatus. The ΔsakA and the double ΔmpkC ΔsakA mutants were more sensitive to osmotic and oxid...
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Published in | Molecular microbiology Vol. 100; no. 5; pp. 841 - 859 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford
Blackwell Publishing Ltd
01.06.2016
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Online Access | Get full text |
ISSN | 0950-382X 1365-2958 |
DOI | 10.1111/mmi.13354 |
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Abstract | Summary
Here, we investigated which stress responses were influenced by the MpkC and SakA mitogen‐activated protein kinases of the high‐osmolarity glycerol (HOG) pathway in the fungal pathogen Aspergillus fumigatus. The ΔsakA and the double ΔmpkC ΔsakA mutants were more sensitive to osmotic and oxidative stresses, and to cell wall damaging agents. Both MpkC::GFP and SakA::GFP translocated to the nucleus upon osmotic stress and cell wall damage, with SakA::GFP showing a quicker response. The phosphorylation state of MpkA was determined post exposure to high concentrations of congo red and Sorbitol. In the wild‐type strain, MpkA phosphorylation levels progressively increased in both treatments. In contrast, the ΔsakA mutant had reduced MpkA phosphorylation, and surprisingly, the double ΔmpkC ΔsakA had no detectable MpkA phosphorylation. A. fumigatus ΔsakA and ΔmpkC were virulent in mouse survival experiments, but they had a 40% reduction in fungal burden. In contrast, the ΔmpkC ΔsakA double mutant showed highly attenuated virulence, with approximately 50% mice surviving and a 75% reduction in fungal burden. We propose that both cell wall integrity (CWI) and HOG pathways collaborate, and that MpkC could act by modulating SakA activity upon exposure to several types of stresses and during CW biosynthesis.
We investigated which stress responses were influenced by the MpkC and SakA mitogen‐activated protein (MAP) kinases of the high‐osmolarity glycerol (HOG) pathway in the fungal pathogen Aspergillus fumigatus. The ΔsakA and the double ΔmpkC ΔsakA mutants were more sensitive to osmotic and oxidative stresses, and to cell wall damaging agents. A. fumigatus ΔsakA and ΔmpkC were virulent in mouse survival experiments. In contrast, the ΔmpkC ΔsakA double mutant showed highly attenuated virulence. We propose that both Cell Wall Integrity (CWI) and HOG pathways collaborate, and that MpkC could act by modulating SakA activity upon exposure to several types of stresses and during cell wall biosynthesis. |
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AbstractList | Summary Here, we investigated which stress responses were influenced by the MpkC and SakA mitogen-activated protein kinases of the high-osmolarity glycerol (HOG) pathway in the fungal pathogen Aspergillus fumigatus. The [Delta]sakA and the double [Delta]mpkC [Delta]sakA mutants were more sensitive to osmotic and oxidative stresses, and to cell wall damaging agents. Both MpkC::GFP and SakA::GFP translocated to the nucleus upon osmotic stress and cell wall damage, with SakA::GFP showing a quicker response. The phosphorylation state of MpkA was determined post exposure to high concentrations of congo red and Sorbitol. In the wild-type strain, MpkA phosphorylation levels progressively increased in both treatments. In contrast, the [Delta]sakA mutant had reduced MpkA phosphorylation, and surprisingly, the double [Delta]mpkC [Delta]sakA had no detectable MpkA phosphorylation. A. fumigatus [Delta]sakA and [Delta]mpkC were virulent in mouse survival experiments, but they had a 40% reduction in fungal burden. In contrast, the [Delta]mpkC [Delta]sakA double mutant showed highly attenuated virulence, with approximately 50% mice surviving and a 75% reduction in fungal burden. We propose that both cell wall integrity (CWI) and HOG pathways collaborate, and that MpkC could act by modulating SakA activity upon exposure to several types of stresses and during CW biosynthesis. Summary Here, we investigated which stress responses were influenced by the MpkC and SakA mitogen‐activated protein kinases of the high‐osmolarity glycerol (HOG) pathway in the fungal pathogen Aspergillus fumigatus. The ΔsakA and the double ΔmpkC ΔsakA mutants were more sensitive to osmotic and oxidative stresses, and to cell wall damaging agents. Both MpkC::GFP and SakA::GFP translocated to the nucleus upon osmotic stress and cell wall damage, with SakA::GFP showing a quicker response. The phosphorylation state of MpkA was determined post exposure to high concentrations of congo red and Sorbitol. In the wild‐type strain, MpkA phosphorylation levels progressively increased in both treatments. In contrast, the ΔsakA mutant had reduced MpkA phosphorylation, and surprisingly, the double ΔmpkC ΔsakA had no detectable MpkA phosphorylation. A. fumigatus ΔsakA and ΔmpkC were virulent in mouse survival experiments, but they had a 40% reduction in fungal burden. In contrast, the ΔmpkC ΔsakA double mutant showed highly attenuated virulence, with approximately 50% mice surviving and a 75% reduction in fungal burden. We propose that both cell wall integrity (CWI) and HOG pathways collaborate, and that MpkC could act by modulating SakA activity upon exposure to several types of stresses and during CW biosynthesis. We investigated which stress responses were influenced by the MpkC and SakA mitogen‐activated protein (MAP) kinases of the high‐osmolarity glycerol (HOG) pathway in the fungal pathogen Aspergillus fumigatus. The ΔsakA and the double ΔmpkC ΔsakA mutants were more sensitive to osmotic and oxidative stresses, and to cell wall damaging agents. A. fumigatus ΔsakA and ΔmpkC were virulent in mouse survival experiments. In contrast, the ΔmpkC ΔsakA double mutant showed highly attenuated virulence. We propose that both Cell Wall Integrity (CWI) and HOG pathways collaborate, and that MpkC could act by modulating SakA activity upon exposure to several types of stresses and during cell wall biosynthesis. |
Author | Hagiwara, Daisuke de Castro, Patrícia Alves Brown, Neil Andrew Valiante, Vito Brakhage, Axel A. de Assis, Leandro José Hori, Juliana I. Rocha, Marina Campos dos Reis, Thaila Fernanda Bruder Nascimento, Ariane Cristina Mendes de Oliveira Bom, Vinícius Leite Pedro Goldman, Gustavo H. Malavazi, Iran Ramalho, Leandra Naira Zambelli |
Author_xml | – sequence: 1 givenname: Ariane Cristina Mendes de Oliveira surname: Bruder Nascimento fullname: Bruder Nascimento, Ariane Cristina Mendes de Oliveira organization: Universidade de São Paulo – sequence: 2 givenname: Thaila Fernanda surname: dos Reis fullname: dos Reis, Thaila Fernanda organization: Universidade de São Paulo – sequence: 3 givenname: Patrícia Alves surname: de Castro fullname: de Castro, Patrícia Alves organization: Universidade de São Paulo – sequence: 4 givenname: Juliana I. surname: Hori fullname: Hori, Juliana I. organization: Universidade de São Paulo – sequence: 5 givenname: Vinícius Leite Pedro surname: Bom fullname: Bom, Vinícius Leite Pedro organization: Universidade de São Paulo – sequence: 6 givenname: Leandro José surname: de Assis fullname: de Assis, Leandro José organization: Universidade de São Paulo – sequence: 7 givenname: Leandra Naira Zambelli surname: Ramalho fullname: Ramalho, Leandra Naira Zambelli organization: Universidade de São Paulo – sequence: 8 givenname: Marina Campos surname: Rocha fullname: Rocha, Marina Campos organization: Universidade Federal de São Carlos – sequence: 9 givenname: Iran surname: Malavazi fullname: Malavazi, Iran organization: Universidade Federal de São Carlos – sequence: 10 givenname: Neil Andrew surname: Brown fullname: Brown, Neil Andrew organization: Plant Science and Crop Biology, Rothamsted Research – sequence: 11 givenname: Vito surname: Valiante fullname: Valiante, Vito organization: Leibniz Institute for Natural Product Research and Infection Biology‐Hans Knöll Institute – sequence: 12 givenname: Axel A. surname: Brakhage fullname: Brakhage, Axel A. organization: Leibniz Institute for Natural Product Research and Infection Biology (HKI), Jena, Germany; Institute for Microbiology, Friedrich Schiller University – sequence: 13 givenname: Daisuke surname: Hagiwara fullname: Hagiwara, Daisuke organization: Chiba University – sequence: 14 givenname: Gustavo H. surname: Goldman fullname: Goldman, Gustavo H. organization: Universidade de São Paulo |
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publication-title: Mol Microbiol |
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Here, we investigated which stress responses were influenced by the MpkC and SakA mitogen‐activated protein kinases of the high‐osmolarity glycerol... Summary Here, we investigated which stress responses were influenced by the MpkC and SakA mitogen-activated protein kinases of the high-osmolarity glycerol... |
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SubjectTerms | Biosynthesis Collaboration Kinases Oxidative stress Phosphorylation |
Title | Mitogen activated protein kinases SakAHOG1 and MpkC collaborate for Aspergillus fumigatus virulence |
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