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A novel Phytophthora infestans haustorium-specific membrane protein is required for infection of potato

机译:马铃薯感染需要新颖的疫霉疫霉菌特异性吸膜

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摘要

Phytophthora infestans causes late-blight, a devastating and re-emerging disease of potato crops. During the early stages of infection, P. infestans differentiates infection-specific structures such as appressoria for host epidermal cell penetration, followed by infection vesicles, and haustoria to establish a biotrophic phase of interaction. Here we report the cloning, from a suppression subtractive hybridization library, of a P. infestans gene called Pihmp1 encoding a putative glycosylated protein with four closely spaced trans-membrane helices. Pihmp1 expression is upregulated in germinating cysts and in germinating cysts with appressoria, and significantly upregulated throughout infection of potato. Transient gene silencing of Pihmp1 led to loss of pathogenicity and indicated involvement of this gene in the penetration and early infection processes of P. infestans. P. infestans transformants expressing a Pihmp1::monomeric red fluorescent protein (mRFP) fusion demonstrated that Pihmp1 was translated in germinating sporangia, germinating cysts and appressoria, accumulated in the appressorium, and was located at the haustorial membrane during infection. Furthermore, we discovered that haustorial structures are formed over a 3 h period, maturing for up to 12 h, and that their formation is initiated only at sites on the surface of intercellular hyphae where Pihmp1::mRFP is localized. We propose that Pihmp1 is an integral membrane protein that provides physical stability to the plasma membrane of P. infestans infection structures. We have provided the first evidence that the surface of oomycete haustoria possess proteins specific to these biotrophic structures, and that formation of biotrophic structures (infection vesicles and haustoria) is essential to successful host colonization by P. infestans.
机译:疫霉疫霉导致晚疫病,是马铃薯作物的毁灭性和新出现的疾病。在感染的早期阶段,致病疫霉可区分感染特异性结构,例如用于宿主表皮细胞渗透的压感器,随后是感染囊泡和吸管,以建立相互作用的生物营养阶段。在这里,我们从抑制消减杂交文库中报告了一种名为Pihmp1的致病疫霉基因的克隆,该基因编码具有四个紧密间隔的跨膜螺旋的假定糖基化蛋白。 Pihmp1表达在发芽的囊肿和伴有发芽的囊肿中上调,并且在整个马铃薯感染过程中均显着上调。 Pihmp1的瞬时基因沉默导致致病性丧失,并表明该基因参与了感染晚疫病菌的侵袭和早期感染过程。表达Pihmp1 ::单体红色荧光蛋白(mRFP)融合体的P. infestans转化子表明Pihmp1在发芽的孢子囊,发芽的囊肿和Appressoria中翻译,积累在Appressorium中,并在感染期间位于子宫膜上。此外,我们发现,排尿结构在3小时内形成,成熟期长达12小时,并且它们的形成仅在Pihmp1 :: mRFP定位于细胞间菌丝表面的位点开始。我们建议Pihmp1是一种不可或缺的膜蛋白,可为感染后无疫杆菌的质膜提供物理稳定性。我们提供了第一个证据,卵菌卵菌表面具有对这些生物营养结构具有特异性的蛋白质,并且生物营养结构(感染囊泡和尿道)的形成对于成功感染致病疫霉的宿主定殖至关重要。

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