Identification and analysis of Phytophthora cactorum genes up-regulated during cyst germination and strawberry infection

• Published in: Current genetics 2011-10, Vol.57 (5), p.297-315
• Main Authors: Chen, Xiaoren, Klemsdal, Sonja Sletner, Brurberg, May Bente
• Format: Article
• Language: English
• Subjects: Biochemistry; Biomedical and Life Sciences; cDNA libraries; Cell Biology; complementary DNA; crown rot; Developmental stages; Economic importance; Expressed Sequence Tags; Fragaria - microbiology; Fruits; gene expression regulation; Gene Library; genes; germination; Host plants; Life Sciences; Microbial Genetics and Genomics; Microbiology; Molecular Sequence Data; new methods; Nucleic Acid Hybridization - methods; Pathogens; Phytophthora - genetics; Phytophthora - pathogenicity; Phytophthora cactorum; Plant Diseases - microbiology; Plant Sciences; Proteomics; Research Article; Reverse Transcriptase Polymerase Chain Reaction; strawberries; suppression subtractive hybridization; Up-Regulation
• ISSN: 0172-8083; 1432-0983
• DOI: 10.1007/s00294-011-0348-0

The oomycete Phytophthora cactorum can cause economically important diseases on numerous host plants worldwide, such as crown rot on strawberry. To explore the molecular mechanisms underlying the pathogenicity of P. cactorum on strawberry, transcriptional analysis of P. cactorum during strawberry infection and cyst germination was performed by applying suppression subtractive hybridization (SSH) and effector-specific differential display (ESDD) techniques. Two SSH cDNA libraries were generated, enriched for P. cactorum genes expressed during infection or during cyst germination, respectively, and 137 unique differentially expressed genes were identified. To specifically select RxLR effector genes from P. cactorum, ESDD was performed using RxLR and EER motif-based degenerate primers. Eight RxLR effector candidate genes as well as 67 other genes were identified out of 124 selected fragments. The expression levels of 20 putatively up-regulated genes were further analyzed using real-time RT-PCR, showing that, indeed 19 of these 20 genes were up-regulated during at least one of the studied developmental stages or during strawberry crown invasion, relative to the mycelium. This study provides a first overview of P. cactorum genes that are up-regulated immediately prior to or during strawberry infection and also provides a novel method for selecting RxLR effector genes from the unsequenced genome of P. cactorum.