The MAD1 Adhesin of Metarhizium anisopliae Links Adhesion with Blastospore Production and Virulence to Insects, and the MAD2 Adhesin Enables Attachment to Plants

ABSTRACT Metarhizium anisopliae is a fungus of considerable metabolic and ecological versatility, being a potent insect pathogen that can also colonize plant roots. The mechanistic details of these interactions are unresolved. We provide evidence that M. anisopliae adheres to insects and plants using two different proteins, MAD1 and MAD2, that are differentially induced in insect hemolymph and plant root exudates, respectively, and produce regional localization of adhesive conidial surfaces. Expression of Mad1 in Saccharomyces cerevisiae allowed this yeast to adhere to insect cuticle. Expression of Mad2 caused yeast cells to adhere to a plant surface. Our study demonstrated that as well as allowing adhesion to insects, MAD1 at the surface of M. anisopliae conidia or blastospores is required to orientate the cytoskeleton and stimulate the expression of genes involved in the cell cycle. Consequently, the disruption of Mad1 in M. anisopliae delayed germination, suppressed blastospore formation, and greatly reduced virulence to caterpillars. The disruption of Mad2 blocked the adhesion of M. anisopliae to plant epidermis but had no effects on fungal differentiation and entomopathogenicity. Thus, regulation, localization, and specificity control the functional distinction between Mad1 and Mad2 and enable M. anisopliae cells to adapt their adhesive properties to different habitats.

[1]  Y. Ohya,et al.  Involvement of actin and polarisome in morphological change during spore germination of Saccharomyces cerevisiae , 2005, Yeast.

[2]  Mason Zhang,et al.  Functional and Structural Diversity in the Als Protein Family of Candida albicans* , 2004, Journal of Biological Chemistry.

[3]  S. Palumbi,et al.  Molecular genetics of ecological diversification: duplication and rapid evolution of toxin genes of the venomous gastropod Conus. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[4]  R. S. St. Leger,et al.  Construction of an improved mycoinsecticide overexpressing a toxic protease. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[5]  Chengshu Wang,et al.  A collagenous protective coat enables Metarhizium anisopliae to evade insect immune responses. , 2006, Proceedings of the National Academy of Sciences of the United States of America.

[6]  C. Walker,et al.  CIRCADIAN RHYTHMS IN MICROORGANISMS : New Complexities , 2006 .

[7]  B. Kerry Rhizosphere Interactions and the Exploitation of Microbial Agents for the Biological Control of Plant-Parasitic Nematodes. , 2000, Annual review of phytopathology.

[8]  H. Wösten,et al.  Hydrophobins: multipurpose proteins. , 2001, Annual review of microbiology.

[9]  G. Fink,et al.  A Saccharomyces gene family involved in invasive growth, cell-cell adhesion, and mating. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[10]  D. Sim,et al.  Fungal Pathogen Reduces Potential for Malaria Transmission , 2005, Science.

[11]  K. Tatchell,et al.  Role of the septin ring in the asymmetric localization of proteins at the mother-bud neck in Saccharomyces cerevisiae. , 2005, Molecular biology of the cell.

[12]  Yee-Chun Chen,et al.  Candida albicans Als1p: an adhesin that is a downstream effector of the EFG1 filamentation pathway , 2002, Molecular microbiology.

[13]  S. Prasertphon,et al.  The formation and circulation, in Galleria, of hyphal bodies of entomophtoraceous fungi☆ , 1968 .

[14]  Chengshu Wang,et al.  Differential gene expression by Metarhizium anisopliae growing in root exudate and host (Manduca sexta) cuticle or hemolymph reveals mechanisms of physiological adaptation. , 2005, Fungal genetics and biology : FG & B.

[15]  J. Berman,et al.  Candida albicans INT1-Induced Filamentation in Saccharomyces cerevisiae Depends on Sla2p , 2001, Molecular and Cellular Biology.

[16]  Bateman,et al.  The role of destruxins in the pathogenicity of metarhizium anisopliae for three species of insect , 1999, Journal of invertebrate pathology.

[17]  L. Hoyer,et al.  The ALS gene family of Candida albicans. , 2001, Trends in microbiology.

[18]  S. Klotz,et al.  Accessibility of the peptide backbone of protein ligands is a key specificity determinant in Candida albicans SRS adherence. , 2004, Microbiology.

[19]  F. Eisenhaber,et al.  A sensitive predictor for potential GPI lipid modification sites in fungal protein sequences and its application to genome-wide studies for Aspergillus nidulans, Candida albicans, Neurospora crassa, Saccharomyces cerevisiae and Schizosaccharomyces pombe. , 2004, Journal of molecular biology.

[20]  W. Lo,et al.  The cell surface flocculin Flo11 is required for pseudohyphae formation and invasion by Saccharomyces cerevisiae. , 1998, Molecular biology of the cell.

[21]  J. Berman,et al.  Linkage of adhesion, filamentous growth, and virulence in Candida albicans to a single gene, INT1. , 1998, Science.

[22]  P. Sundstrom Adhesion in Candida spp , 2002, Cellular microbiology.

[23]  J. Jiménez,et al.  Role of the Septin Cdc10 in the Virulence of Candida albicans , 2006, Microbiology and immunology.

[24]  N. Keyhani,et al.  Adhesion of the Entomopathogenic Fungus Beauveria (Cordyceps) bassiana to Substrata , 2005, Applied and Environmental Microbiology.

[25]  R. S. St. Leger,et al.  Metarhizium spp., cosmopolitan insect-pathogenic fungi: mycological aspects. , 2004, Advances in applied microbiology.

[26]  R. S. St. Leger,et al.  Field Studies Using a Recombinant Mycoinsecticide (Metarhizium anisopliae) Reveal that It Is Rhizosphere Competent , 2002, Applied and Environmental Microbiology.

[27]  Heinz Schwarz,et al.  Septin-dependent compartmentalization of the endoplasmic reticulum during yeast polarized growth , 2005, The Journal of cell biology.

[28]  J. W. Taylor Molecular Phylogenetic classification of fungi. , 1995, Archives of medical research.

[29]  D. Sim,et al.  Transmission Fungal Pathogen Reduces Potential for Malaria , 2009 .

[30]  M. Momany,et al.  Aspergillus nidulans septin AspB plays pre- and postmitotic roles in septum, branch, and conidiophore development. , 2002, Molecular biology of the cell.

[31]  M. Longtine,et al.  Candida albicans Int1p interacts with the septin ring in yeast and hyphal cells. , 2001, Molecular biology of the cell.

[32]  Amy S. Gladfelter,et al.  Interplay between septin organization, cell cycle and cell shape in yeast , 2005, Journal of Cell Science.

[33]  C. Norden,et al.  Dissection of septin actin interactions using actin overexpression in Saccharomyces cerevisiae , 2004, Molecular microbiology.

[34]  P. Kahn,et al.  Threonine-Rich Repeats Increase Fibronectin Binding in the Candida albicans Adhesin Als5p , 2006, Eukaryotic Cell.

[35]  J. Konopka,et al.  Septin Function in Yeast Model Systems and Pathogenic Fungi , 2005, Eukaryotic Cell.