Melanin is not required for turgor generation but enhances cell-wall rigidity in appressoria of the corn pathogen Colletotrichum graminicola

• Published in: Molecular plant-microbe interactions Vol. 27; no. 4; pp. 315 - 327
• Main Authors: Ludwig, Nancy, Löhrer, Marco, Hempel, Marcus, Mathea, Sebastian, Schliebner, Ivo, Menzel, Matthias, Kiesow, Andreas, Schaffrath, Ulrich, Deising, Holger B, Horbach, Ralf
• Format: Journal Article
• Language: English
• Published: United States The American Phytopathological Society 01.04.2014
• Subjects: Ascomycetes; Cell Wall - physiology; Colletotrichum - physiology; Colletotrichum graminicola; DNA, Fungal - genetics; Gene Expression Regulation, Fungal - physiology; Melanins - biosynthesis; Melanins - genetics; Microscopy, Atomic Force; Molecular Sequence Data; Plant Diseases - microbiology; Zea mays; Zea mays - microbiology
• DOI: 10.1094/MPMI-09-13-0267-R
• ISSN: 0894-0282

The ascomycete and causative agent of maize anthracnose and stem rot, Colletotrichum graminicola, differentiates melanized infection cells called appressoria that are indispensable for breaching the plant cell wall. High concentrations of osmolytes accumulate within the appressorium, and the internal turgor pressure of up to 5.4 MPa provides sufficient force to penetrate the leaf epidermis directly. In order to assess the function of melanin in C. graminicola appressoria, we identified and characterized the polyketide synthase 1 (CgPKS1) gene which displayed high similarity to fungal polyketide synthases (PKS) involved in synthesis of 1,3,6,8-tetrahydronaphthalene, the first intermediate in melanin biosynthesis. Cgpks1 albino mutants created by targeted gene disruption were unable to penetrate intact leaves and ruptured frequently but, surprisingly, were able to penetrate ultrathin polytetrafluoroethylene membranes mimicking the plant surface. Nonmelanized Cgpks1 appressoria were sensitive to externally applied cell-wall-degrading enzymes whereas melanized appressoria were not affected. Expression studies using a truncated CgPKS1 fused to green fluorescent protein revealed fluorescence in immature appressoria and in setae, which is in agreement with transcript data obtained by RNA-Seq and quantitative polymerase chain reaction. Unexpectedly, surface scans of mutant and wild-type appressoria revealed considerable differences in cell-wall morphology. Melanization of appressoria is indispensable for successful infection of intact leaves. However, cell collapse experiments and analysis of the appressorial osmolyte content by Mach-Zehnder interferometry convincingly showed that melanin is not required for solute accumulation and turgor generation, thus questioning the role of melanin as a barrier for osmolytes in appressoria of C. graminicola.