RESUMO
Powdery mildews are phytopathogens whose growth and reproduction are entirely dependent on living plant cells. The molecular basis of this life-style, obligate biotrophy, remains unknown. We present the genome analysis of barley powdery mildew, Blumeria graminis f.sp. hordei (Blumeria), as well as a comparison with the analysis of two powdery mildews pathogenic on dicotyledonous plants. These genomes display massive retrotransposon proliferation, genome-size expansion, and gene losses. The missing genes encode enzymes of primary and secondary metabolism, carbohydrate-active enzymes, and transporters, probably reflecting their redundancy in an exclusively biotrophic life-style. Among the 248 candidate effectors of pathogenesis identified in the Blumeria genome, very few (less than 10) define a core set conserved in all three mildews, suggesting that most effectors represent species-specific adaptations.
Assuntos
Ascomicetos/genética , Deleção de Genes , Genes Fúngicos , Genoma Fúngico , Hordeum/microbiologia , Doenças das Plantas/microbiologia , Adaptação Fisiológica , Ascomicetos/crescimento & desenvolvimento , Ascomicetos/metabolismo , Ascomicetos/patogenicidade , Metabolismo dos Carboidratos , Proteínas de Transporte/genética , Proteínas de Transporte/metabolismo , Enzimas/genética , Enzimas/metabolismo , Evolução Molecular , Proteínas Fúngicas/química , Proteínas Fúngicas/genética , Proteínas Fúngicas/metabolismo , Interações Hospedeiro-Patógeno/genética , Redes e Vias Metabólicas/genética , Anotação de Sequência Molecular , Retroelementos , Análise de Sequência de DNA , Especificidade da EspécieRESUMO
cDNA microarrays of Blumeria graminis f sp hordei transcript profiles during the asexual development cycle reveal the dynamics of global gene expression as the fungus germinates, penetrates, feeds on its host, and produces masses of conidia for dispersal. The expression profiles of genes encoding enzymes involved in primary metabolism show that there is a striking degree of coordinate regulation of some of the genes in the same pathway. In one example, genes encoding several glycolytic enzymes are significantly upregulated as mature appressoria form and also in infected epidermis, which contain fungal haustoria. In another example, mRNAs for lipid degrading enzymes are initially expressed at high levels in the conidia and the early germination stages and decrease significantly later. We discuss these results and draw inferences on the metabolic status of this obligate biotrophic fungus as it infects its host and completes its life cycle.
Assuntos
Ascomicetos/enzimologia , Metabolismo Energético/genética , Proteínas Fúngicas/genética , Regulação Enzimológica da Expressão Gênica/genética , Regulação Fúngica da Expressão Gênica/genética , Ascomicetos/genética , Metabolismo dos Carboidratos , Germinação/genética , Glicólise/genética , Metabolismo dos Lipídeos , Doenças das Plantas/genética , Doenças das Plantas/microbiologia , Plantas/microbiologiaRESUMO
High-density cDNA microarrays (2,027 unigenes) were used to analyze transcript profiles of the plant-pathogenic fungus Blumeria graminis f. sp. hordei throughout its asexual life cycle and development of infection. RNA was obtained from four stages preceding penetration and four stages after penetration of the host cells. The microarray data was validated by comparing the expression of a plasma membrane H+-ATPase and fructose-1,6-bis phosphatase with the data obtained from a quantitative polymerase chain reaction (PCR) assay. The results showed that there was a global switch in expression between the pre- and postpenetrative stages. This was largely due to accumulation of RNA encoding protein biosynthesis genes in the late stages. Other functional clusters, such as virulence-related genes and sterol metabolism genes, are up-regulated in pre- and postpenetration stages, respectively. A group of RNAs whose abundance correlated with the expression of cap20, a gene known to be required for virulence in Colletotrichum gloeosporioides, identified genes that are strong candidates for pathogenicity factors in B. graminis.