Bouzidi Mohamed Fouad, Parlange Francis, Nicolas Paul, Mouzeyar Said
UMR 1095 INRA-UBP "Amélioration et Santé des Plantes", Université Blaise Pascal, 24, Avenue des Landais 63177 Aubière Cedex, France.
BMC Microbiol. 2007 Dec 6;7:110. doi: 10.1186/1471-2180-7-110.
Sunflower downy mildew is a major disease caused by the obligatory biotrophic oomycete Plasmopara halstedii. Little is known about the molecular mechanisms underlying its pathogenicity. In this study we used a genomics approach to gain a first insight into the transcriptome of P. halstedii.
To identify genes from the obligatory biotrophic oomycete Plasmopara halstedii that are expressed during infection in sunflower (Helianthus annuus L.) we employed the suppression subtraction hybridization (SSH) method from sunflower seedlings infected by P. halstedii. Using this method and random sequencing of clones, a total of 602 expressed sequence tags (ESTs) corresponding to 230 unique sequence sets were identified. To determine the origin of the unisequences, PCR primers were designed to amplify these gene fragments from genomic DNA isolated either from P. halstedii sporangia or from Helianthus annuus. Only 145 nonredundant ESTs which correspond to a total of 373 ESTs (67.7%) proved to be derived from P. halstedii genes and that are expressed during infection in sunflower. A set of 87 nonredundant sequences were identified as showing matches to sequences deposited in public databases. Nevertheless, about 7% of the ESTs seem to be unique to P. halstedii without any homolog in any public database.
A summary of the assignment of nonredundant ESTs to functional categories as well as their relative abundance is listed and discussed. Annotation of the ESTs revealed a number of genes that could function in virulence. We provide a first glimpse into the gene content of P. halstedii. These resources should accelerate research on this important pathogen.
向日葵霜霉病是由专性活体营养卵菌寄生霜霉引起的一种主要病害。关于其致病的分子机制知之甚少。在本研究中,我们采用基因组学方法首次深入了解寄生霜霉的转录组。
为了鉴定专性活体营养卵菌寄生霜霉在向日葵(Helianthus annuus L.)感染过程中表达的基因,我们采用抑制性消减杂交(SSH)方法,以被寄生霜霉感染的向日葵幼苗为材料。利用该方法和克隆的随机测序,共鉴定出602个表达序列标签(EST),对应230个独特序列集。为了确定单序列的来源,设计了PCR引物,从寄生霜霉孢子囊或向日葵中分离的基因组DNA中扩增这些基因片段。只有145个非冗余EST(共373个EST,占67.7%)被证明来源于寄生霜霉基因,且在向日葵感染过程中表达。一组87个非冗余序列被鉴定为与公共数据库中存储的序列匹配。然而,约7%的EST似乎是寄生霜霉特有的,在任何公共数据库中都没有任何同源物。
列出并讨论了非冗余EST在功能类别上的分配总结及其相对丰度。EST的注释揭示了一些可能在毒力中起作用的基因。我们首次初步了解了寄生霜霉的基因内容。这些资源应能加速对这种重要病原体的研究。