Departamento de Protección de Cultivos, Instituto de Agricultura Sostenible, Consejo Superior de Investigaciones Científicas (CSIC), Córdoba, Spain.
PLoS One. 2012;7(11):e48646. doi: 10.1371/journal.pone.0048646. Epub 2012 Nov 7.
Knowledge on the genetic basis underlying interactions between beneficial bacteria and woody plants is still very limited, and totally absent in the case of olive. We aimed to elucidate genetic responses taking place during the colonization of olive roots by the native endophyte Pseudomonas fluorescens PICF7, an effective biocontrol agent against Verticillium wilt of olive. Roots of olive plants grown under non-gnotobiotic conditions were collected at different time points after PICF7 inoculation. A Suppression Subtractive Hybridization cDNA library enriched in induced genes was generated. Quantitative real time PCR (qRT-PCR) analysis validated the induction of selected olive genes. Computational analysis of 445 olive ESTs showed that plant defence and response to different stresses represented nearly 45% of genes induced in PICF7-colonized olive roots. Moreover, quantitative real-time PCR (qRT-PCR) analysis confirmed induction of lipoxygenase, phenylpropanoid, terpenoids and plant hormones biosynthesis transcripts. Different classes of transcription factors (i.e., bHLH, WRKYs, GRAS1) were also induced. This work highlights for the first time the ability of an endophytic Pseudomonas spp. strain to mount a wide array of defence responses in an economically-relevant woody crop such as olive, helping to explain its biocontrol activity.
关于有益细菌与木本植物相互作用的遗传基础的知识仍然非常有限,而在橄榄中则完全不存在。我们旨在阐明橄榄根被本地内生菌荧光假单胞菌 PICF7 定殖时发生的遗传反应,PICF7 是一种防治橄榄黄萎病的有效生防剂。在非无菌条件下生长的橄榄植物的根在 PICF7 接种后不同时间点收集。生成了一个富含诱导基因的抑制性消减杂交 cDNA 文库。定量实时 PCR(qRT-PCR)分析验证了所选橄榄基因的诱导。对 445 个橄榄 EST 的计算分析表明,植物防御和对不同胁迫的反应代表了在 PICF7 定殖橄榄根中诱导的基因的近 45%。此外,定量实时 PCR(qRT-PCR)分析证实了脂氧合酶、苯丙烷、萜类和植物激素生物合成转录物的诱导。不同类别的转录因子(即 bHLH、WRKYs、GRAS1)也被诱导。这项工作首次强调了一种内生假单胞菌菌株在一种经济上相关的木本作物(如橄榄)中引发广泛防御反应的能力,有助于解释其生防活性。