Caldo Rico A, Nettleton Dan, Wise Roger P
Department of Plant Pathology and Center for Plant Responses to Environmental Stresses, Iowa State University, Ames, Iowa 50011-1020, USA.
Plant Cell. 2004 Sep;16(9):2514-28. doi: 10.1105/tpc.104.023382. Epub 2004 Aug 19.
Plant recognition of pathogen-derived molecules influences attack and counterattack strategies that affect the outcome of host-microbe interactions. To ascertain the global framework of host gene expression during biotrophic pathogen invasion, we analyzed in parallel the mRNA abundance of 22,792 host genes throughout 36 (genotype x pathogen x time) interactions between barley (Hordeum vulgare) and Blumeria graminis f. sp hordei (Bgh), the causal agent of powdery mildew disease. A split-split-plot design was used to investigate near-isogenic barley lines with introgressed Mla6, Mla13, and Mla1 coiled-coil, nucleotide binding site, Leu-rich repeat resistance alleles challenged with Bgh isolates 5874 (AvrMla6 and AvrMla1) and K1 (AvrMla13 and AvrMla1). A linear mixed model analysis was employed to identify genes with significant differential expression (P value < 0.0001) in incompatible and compatible barley-Bgh interactions across six time points after pathogen challenge. Twenty-two host genes, of which five were of unknown function, exhibited highly similar patterns of upregulation among all incompatible and compatible interactions up to 16 h after inoculation (hai), coinciding with germination of Bgh conidiospores and formation of appressoria. By contrast, significant divergent expression was observed from 16 to 32 hai, during membrane-to-membrane contact between fungal haustoria and host epidermal cells, with notable suppression of most transcripts identified as differentially expressed in compatible interactions. These findings provide a link between the recognition of general and specific pathogen-associated molecules in gene-for-gene specified resistance and support the hypothesis that host-specific resistance evolved from the recognition and prevention of the pathogen's suppression of plant basal defense.
植物对病原体衍生分子的识别会影响攻击和反击策略,而这些策略会影响宿主 - 微生物相互作用的结果。为了确定活体营养型病原体入侵期间宿主基因表达的全局框架,我们在大麦(Hordeum vulgare)与白粉病病原体禾本科布氏白粉菌(Blumeria graminis f. sp hordei,Bgh)之间的36种(基因型×病原体×时间)相互作用中,并行分析了22,792个宿主基因的mRNA丰度。采用裂区裂区设计,研究了导入Mla6、Mla13和Mla1卷曲螺旋、核苷酸结合位点、富含亮氨酸重复序列抗性等位基因的近等基因大麦品系,用Bgh分离株5874(AvrMla6和AvrMla1)和K1(AvrMla13和AvrMla1)进行挑战。采用线性混合模型分析,以确定病原体攻击后六个时间点在不亲和和亲和大麦 - Bgh相互作用中具有显著差异表达(P值<0.0001)的基因。22个宿主基因,其中5个功能未知,在接种后长达16小时(hai)的所有不亲和和亲和相互作用中表现出高度相似的上调模式,这与Bgh分生孢子的萌发和附着胞的形成一致。相比之下,在接种后16至32小时(hai),在真菌吸器与宿主表皮细胞的膜对膜接触期间观察到显著的差异表达,在亲和相互作用中鉴定为差异表达的大多数转录本受到明显抑制。这些发现为基因对基因特异性抗性中一般和特定病原体相关分子的识别之间提供了联系,并支持宿主特异性抗性从识别和预防病原体对植物基础防御的抑制中进化而来的假设。