Abstract:Phytophthora infestans causes the severe late blight disease of potato. During its infection process, P. infestans delivers hundreds of RXLR (Arg-x-Leu-Arg, x behalf of any one amino acid) effectors to manipulate processes in its hosts, creating a suitable environment for invasion and proliferation. Several effectors interact with host proteins to suppress host immunity and inhibit plant growth. However, little is known about how P. infestans regulates the host transcriptome. Here, we identified an RXLR effect… Show more
“…Droplets (10 µl) were pipetted onto the surface of detached leaves, placed in sealed boxes with moist tissue to maintain humidity, and kept in weak light. Lesions were measured 3–5 days post‐inoculation (dpi) and scored as described previously (Wang et al , ). Disease indexes were analysed with about 30 leaves from 10 potato plants for each treatment.…”
Section: Methodsmentioning
confidence: 99%
“…The biomass level analysis was performed as described by Wang et al (). The leaves were harvested at 3–5 dpi and total DNA was extracted with cetyltrimethylammonium bromide solution.…”
Copper‐based antimicrobial compounds are widely and historically used to control plant diseases, such as late blight caused by Phytophthora infestans, which seriously affects the yield and quality of potato. We previously identified that copper ion (Cu2+) acts as an extremely sensitive elicitor to induce ethylene (ET)‐dependent immunity in Arabidopsis. Here, we found that Cu2+ induces the defence response to P. infestans in potato. Cu2+ suppresses the transcription of the abscisic acid (ABA) biosynthetic genes StABA1 and StNCED1, resulting in decreased ABA content. Treatment with ABA or inhibitor fluridone made potato more susceptible or resistance to late blight, respectively. In addition, potato with knockdown of StABA1 or StNCED1 showed greater resistance to late blight, suggesting that ABA negatively regulates potato resistance to P. infestans. Cu2+ also promotes the rapid biosynthesis of ET. Potato plants treated with 1‐aminocyclopropane‐1‐carboxylate showed enhanced resistance to late blight. Repressed expression of StEIN2 or StEIN3 resulted in enhanced transcription of StABA1 and StNCED1, accumulation of ABA and susceptibility to P. infestans. Consistently, StEIN3 directly binds to the promoter regions of StABA1 and StNCED1. Overall, we concluded that Cu2+ triggers the defence response to potato late blight by activating ET biosynthesis to inhibit the biosynthesis of ABA.
“…Droplets (10 µl) were pipetted onto the surface of detached leaves, placed in sealed boxes with moist tissue to maintain humidity, and kept in weak light. Lesions were measured 3–5 days post‐inoculation (dpi) and scored as described previously (Wang et al , ). Disease indexes were analysed with about 30 leaves from 10 potato plants for each treatment.…”
Section: Methodsmentioning
confidence: 99%
“…The biomass level analysis was performed as described by Wang et al (). The leaves were harvested at 3–5 dpi and total DNA was extracted with cetyltrimethylammonium bromide solution.…”
Copper‐based antimicrobial compounds are widely and historically used to control plant diseases, such as late blight caused by Phytophthora infestans, which seriously affects the yield and quality of potato. We previously identified that copper ion (Cu2+) acts as an extremely sensitive elicitor to induce ethylene (ET)‐dependent immunity in Arabidopsis. Here, we found that Cu2+ induces the defence response to P. infestans in potato. Cu2+ suppresses the transcription of the abscisic acid (ABA) biosynthetic genes StABA1 and StNCED1, resulting in decreased ABA content. Treatment with ABA or inhibitor fluridone made potato more susceptible or resistance to late blight, respectively. In addition, potato with knockdown of StABA1 or StNCED1 showed greater resistance to late blight, suggesting that ABA negatively regulates potato resistance to P. infestans. Cu2+ also promotes the rapid biosynthesis of ET. Potato plants treated with 1‐aminocyclopropane‐1‐carboxylate showed enhanced resistance to late blight. Repressed expression of StEIN2 or StEIN3 resulted in enhanced transcription of StABA1 and StNCED1, accumulation of ABA and susceptibility to P. infestans. Consistently, StEIN3 directly binds to the promoter regions of StABA1 and StNCED1. Overall, we concluded that Cu2+ triggers the defence response to potato late blight by activating ET biosynthesis to inhibit the biosynthesis of ABA.
“…For drop inoculation, the surfaces of detached leaves were inoculated with 15 μl of P. infestans zoospore suspension and then placed at 18°C in sealed boxes with 100% RH environment, and kept in weak light. The diameters of lesions were measured at 5 dpi and scored as described by Wang et al (2019). The biomass of P. infestans was also analysed.…”
Potato (Solanum tuberosum) is one of the most important food and economic crops in the world. However, similar to other plants, potato yield and quality are severely impaired by various microbial pathogens during the life cycle. Phytophthora infestans, the causal agent of late blight, is a major threat to potato production. Late blight can occur at any time of the growing season, causing serious economic and output losses for field-grown potato. Given its lethality, wide host range, and broad geographical distribution, the pathogen is considered one of the most destructive pathogens in agricultural systems (Kamoun et al., 2015; Nowicki et al., 2012). Plants have evolved an effective innate immune system to fight pathogens. Generally, the system includes two types: microbe-or pathogen-associated molecular pattern (PAMP)-triggered immunity (PTI) and effector-triggered immunity (ETI) (Dodds and Rathjen, 2010;
“…The P. infestans isolate HLJ, a strongly pathogenic oomycete, was conserved at the State Key Laboratory of Shandong Agricultural University, Tai’an, Shandong, China ( Wang et al, 2019 ). P. infestans HLJ was grown in Petri dishes with Rye A for 2 weeks at 18°C.…”
Long non-coding RNA (lncRNA) is a crucial regulatory mechanism in the plant response to biotic and abiotic stress. However, their roles in potato (Solanum tuberosum L.) resistance to Phytophthora infestans (P. infestans) largely remain unknown. In this study, we identify 2857 lncRNAs and 33,150 mRNAs of the potato from large-scale published RNA sequencing data. Characteristic analysis indicates a similar distribution pattern of lncRNAs and mRNAs on the potato chromosomes, and the mRNAs were longer and had more exons than lncRNAs. Identification of alternative splicing (AS) shows that there were a total of 2491 lncRNAs generated from AS and the highest frequency (46.49%) of alternative acceptors (AA). We performed R package TCseq to cluster 133 specific differentially expressed lncRNAs from resistance lines and found that the lncRNAs of cluster 2 were upregulated. The lncRNA targets were subject to KEGG pathway enrichment analysis, and the interactive network between lncRNAs and mRNAs was constructed by using GENIE3, a random forest machine learning algorithm. Transient overexpression of StLNC0004 in Nicotiana benthamiana significantly suppresses P. infestans growth compared with a control, and the expression of extensin (NbEXT), the ortholog of the StLNC0004 target gene, was significantly upregulated in the overexpression line. Together, these results suggest that lncRNAs play potential functional roles in the potato response to P. infestans infection.
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