e, NIS1,
根据下文理解,NIS1貌似是一种PAMP分子,而不是效应子
e, NIS1,
根据下文理解,NIS1貌似是一种PAMP分子,而不是效应子
SGT1
SGT1(Suppressor of G2 allele of skp1)基因是拟南芥中一个重要的抗病基因,它参与了植物的免疫反应,并且还在植物的发育和生长中发挥作用。该基因编码一个小分子量蛋白,它具有多种功能,包括:
与HSP90结合,参与蛋白质的折叠和稳定; 与RPS2、RPS5等免疫受体结合,参与免疫信号的转导; 参与植物的激素信号通路,如赤霉素信号通路; 通过蛋白质降解途径调节免疫反应,如通过介导免疫受体的泛素化和蛋白酶体降解来调节免疫反应的强度。 SGT1的功能是通过与其他蛋白质相互作用来实现的,如与HSP90、免疫受体和泛素连接酶结合。此外,SGT1还可以形成复合物,如SGT1-SGT1B-HSP90复合物,来调节免疫反应的强度。
Deletion of NIS1 had little effect on the virulence of C. orbiculare against N. benthamiana,
说明病原菌PAMP分子引起cell death不一定与病原菌的virulence有关。病原菌的PAMP分子引起的cell death可能是由于植物的免疫系统对PAMP分子的强烈反应,导致非特异性的细胞死亡。这种细胞死亡被称为PAMP-triggered cell death (PTCD),通常是植物的免疫响应的一部分。PTCD可能会减缓病原菌的生长,但不一定会完全抵抗病原菌的入侵,因此不能直接说明病原菌的virulence。病原菌的virulence可能还受其他因素的影响,例如病原菌的毒力、侵染方式、菌丝生长速度等;
病原真菌的 virulence(致病性)主要与以下因素有关: 1. 分泌的效应蛋白:病原真菌通过分泌效应蛋白(effectors)进入植物细胞,从而抑制或激活植物的防御反应,进而导致病害。效应蛋白可以直接或间接地干扰宿主植物的代谢或信号传递途径,从而增强病原真菌的致病性。 2. 分泌的酶:病原真菌分泌各种酶,包括蛋白酶、纤维素酶、淀粉酶等,可以破坏植物细胞壁、膜和其他组织结构,从而使真菌更容易入侵和感染宿主。 3. 生长和发育:病原真菌的生长和发育对其致病性也有影响。例如,菌丝的生长速度和侵入性,分生孢子的数量和质量等都会影响其病害程度。 4. 与宿主的相互作用:病原真菌和宿主之间的相互作用也会影响其致病性。例如,病原真菌可以利用宿主的信号通路来调节其生长和发育,或者利用宿主的养分来增强其代谢活动。同时,宿主也会通过识别病原真菌的 PAMPs 或效应蛋白来启动防御反应,从而限制病原真菌的生长和侵染。
NIS1
根据下文理解,NIS1貌似是一种PAMP分子,而不是效应子
SGT1
SGT1(Suppressor of G2 allele of skp1)基因是拟南芥中一个重要的抗病基因,它参与了植物的免疫反应,并且还在植物的发育和生长中发挥作用。该基因编码一个小分子量蛋白,它具有多种功能,包括:
与HSP90结合,参与蛋白质的折叠和稳定; 与RPS2、RPS5等免疫受体结合,参与免疫信号的转导; 参与植物的激素信号通路,如赤霉素信号通路; 通过蛋白质降解途径调节免疫反应,如通过介导免疫受体的泛素化和蛋白酶体降解来调节免疫反应的强度。 SGT1的功能是通过与其他蛋白质相互作用来实现的,如与HSP90、免疫受体和泛素连接酶结合。此外,SGT1还可以形成复合物,如SGT1-SGT1B-HSP90复合物,来调节免疫反应的强度。
This suppression activity was specific for NLP1-induced cell death, since these effectors did not suppress INF1-induced necrosis.
炭疽菌对cell death的抑制属于PAMP-specific的
It is possible that the amount of translocated ChEC:mRFP fusion protein is below the detection limits of confocal microscopy and immunogold labelling.
在炭疽菌中没观测到BIC complex,说明炭疽菌效应子的转运在当时是个遗留问题
suggests wave one or two effectors (or their activities) may be recognized by these resistance proteins
说明早期表达的效应子即使没有进入拟南芥细胞,但也可能已经被拟南芥的抗病蛋白所识别
host-derived cell wall material is deposited beneath appressoria before any visible penetration or structural damage to the cuticle/cell wall,
宿主细胞壁成分主要沉积在炭疽菌丝对宿主细胞壁损伤处,说明拟南芥在炭疽菌进入宿主细胞时就已经感应到炭疽菌并作出相应的response
strong basipetal polarity associated with switch from radial (isometric) expansion to focused tip growth of the emerging penetration hypha
这句话描述了病原真菌侵染植物时的现象。在真菌侵染时,出现了从放射状(等轴性)生长转变为集中于顶端生长的强烈基向性现象。这种生长方式是由正在生长的侵染菌丝的细胞极性所决定的,细胞极性的改变导致了侵染菌丝的生长方向的改变。此时,侵染菌丝开始形成侵染孔(Appressorial penetration pores)以侵入植物细胞内部;
真菌的放射状生长是指菌丝在侵染过程中呈现出均匀生长的状态,而顶端集中生长则是指侵染过程中菌丝在生长的过程中逐渐形成一个朝向寄主细胞的极性生长状态。这个转变与多种因素、基因和分子机制有关。
首先,这种生长方式的转变与真菌侵染所处的环境有关。在寄主表面,真菌菌丝接触到的信号、化合物和力学特性等,都可能影响菌丝生长的方向和速度。
其次,这种转变也与真菌内部的基因和分子机制有关。例如,一些蛋白质可能在转变时起到关键作用,如Rho GTP酶、PIP2等。一些转录因子的调控也可能影响这种生长方式的转变,如STE20等。
总之,真菌从放射状生长转变为集中于顶端生长的强烈基向性现象是一个复杂的过程,受到多种因素、基因和分子机制的调控
在炭疽菌侵染宿主植物时,宿主植物会释放一系列信号分子来诱导炭疽菌丝的顶端集中生长。这些信号分子包括寄主识别分子、生长素、赤霉素、ABA等植物激素、以及一些钙离子调节因子等。这些信号分子可能通过感知菌丝末端与宿主接触前的孔道区域的方式诱导炭疽菌效应子基因的表达,从而调控菌丝顶端的集中生长,实现对宿主植物的侵染
this suggests that host-derived signals, rather than developmental cues, induce ChEC expression
说明炭疽菌侵染植物时,其菌丝的顶端集中生长主要是受到了宿主植物相关信号刺激,并且菌丝顶端集中生长可能与效应子的分泌有关;
ChEC3, ChEC3a or ChEC5 failed to suppress INF1-induced necrosis, whereas co-expression of Avr3aKI, a well-described suppressor of INF1-induced cell death [26], resulted in significant necrosis reduction in our assay
说明ChECs对cell death的抑制作用得看是哪个病原菌中的PAMP导致的cell death
last wave of effector genes, exemplified by ChNLP1 and ChToxB, is induced only during the switch to necrotrophy, suggesting that their toxic products contribute to terminating the biotrophic phase for subsequent necrotrophic growth
其余的效应子,ChNLP1和ChToxB在死体营养阶段高表达;ChNLP1注射本式烟6到8天后表现出necrosis,说明ChNLP1能导致细胞死亡;ChNLP1与ChEC3, ChEC3a, ChEC5,ChEC6 and CHEC34共注射之后,necrosis减少70 to 90%,但是ChNLP1与ChEC3, ChEC3a, ChEC5,ChEC6 and CHEC34不抑制INF1导致的细胞死亡;ChEC13, ChEC36 and ChEC89对necrosis和cell death的抑制不具有统计显著性;
In contrast, ChEC13, ChEC34, ChEC51, ChEC56, ChEC88 and ChEC89 are specifically induced during penetration and establishment of biotrophic hyphae (wave three)
六个ChEC13在活体营养阶段高表达;并且在the interface between the host plasma membrane and biotrophic hyphae部位大量聚集
unpenetrated appressoria in planta, exemplified by ChEC7 and ChEC9. Similarly, ChEC3, ChEC3a, ChEC4, ChEC6 and ChEC36
七个ChECs在最开始的unpennetrated appresoria阶段高表达;附着胞上的侵染钉(孔)表面被Beta-1,3-glucan组成的hypha wall包裹,而ChEC36定位于此处,并且附着胞可能通过highly polarized manner的方式将ChECs分泌出侵染钉(孔);说明ChECs先表达,再形成成熟蛋白聚集在侵染钉(孔),即宿主与病原菌接触位置
ChEC5 and ChEC91 were preferentially induced in saprotrophic mycelium. T
两个ChECs在菌丝阶段高表达,在侵染阶段低表达或不表达
Scientists have sequenced the entire transcriptome of Colletotrichum higginsianum, a fungal species that infects Arabidopsis and causes necrotrophic growth.
分析Ch的效应子如何操纵活体阶段宿主存活转换至死体阶段宿主细胞死亡
Colletotrichum gloeosporioides is a notable pathogen associated with > 470 different host species and is commercially significant as the major causal agent of post-harvest disease in fruits such as avocado, banana, mango, coffee and strawberries
Cg能侵染高达470多个宿主植物
whereas the necrotrophic stage of growth is characterized by upregulation of sequences encoding degradative enzymes
死体阶段高表达的主要是细胞壁降解酶
secondary metabolite synthesis genes were upregulated during initial stages of host colonization
此篇文章也支持部分次生代谢物合成酶基因在侵染早期的活体阶段高表达
Many studies on Colletotrichum are restricted to strains affecting single crop species
炭疽菌研究的局限在于只能单侵染单个物种
anthracnose diseases
炭疽病
Brassicaceae
十字花科
but tissue alkalinization was less pronounced in maize colonized by C. graminicola at this stage
暹罗炭疽和果生炭疽的定殖侵染是否会导致草莓茎基部的碱化作用
dicot cell walls are enriched with pectin (35% in dicots compared to 10% in maize), whereas the cell walls of grasses contain more hemicellulose (60% in grasses compared to 30% in dicots) and phenolics
双子叶植物的细胞壁富含pectin,但单子叶植物细胞壁富含hemicellulose和phenlics,而宿主细胞壁成分不同则会影响相应病原菌的细胞壁降解酶
Transcripts encoding a vast array of lytic enzymes are induced at the transition to necrotrophy
裂解酶在希金斯炭疽菌向死体营养阶段转换时高表达
ily to deliver protein effectors and secondary metabolites to the plant cell.
营养物质的trasporter在活体阶段并未有太多高表达,说明这些hyphae形成的主要作用应该是将effector和次生代谢物输出至宿主
These specialized hyphae morphologically resemble the haustoria of obligate biotrophs
希金斯炭疽菌在活体阶段从hyphae转变为haustoria,可能与effector的运输有关,也可能与碳源和氮源的营养物质有关
This suggests Colletotrichum requires a maximum capacity for host manipulation during intracellular colonization and that biotrophic hyphae provide a major interface for effector delivery to host cells.
CSEP在活体阶段大量高表达,可能与进入宿主细胞有关
Early during infection, the transcriptome of C. higginsianum was dominated by secondary metabolism genes, with 12 different secondary metabolism gene clusters being induced before penetration and during biotrophy
多个次生代谢物合成酶在希金斯炭疽菌在活体营养阶段高表达;由于是在活体阶段,这些次生代谢物可能是not toxin,可能与吸器和活体菌丝的形成有关
the majority (62%) of which are activated during necrotrophy
希金斯炭疽菌细胞壁降解酶在死体营养阶段高表达
C. graminicola and C. higginsianum belong to sister clades within the genus
暹罗炭疽和果生炭疽与希金斯炭疽分类关系如何?
Necrotrophy in C. higginsianum is associated with local alkalinization of Arabidopsis tissue, probably resulting from fungal ammonia secretion
在死体营养阶段,拟南芥宿主组织的碱化作用可能是由于病原菌的氨分泌导致
monocot and dicot plants
炭疽菌能侵染多种双子叶和单子叶植物