Evidence map›Paper›PMID 30654746›Full record

ArticleBMC plant biology2019

CaLRR-RLK1, a novel RD receptor-like kinase from Capsicum annuum and transcriptionally activated by CaHDZ27, act as positive regulator in Ralstonia solanacearum resistance.

Shaoliang Mou, Feng Gao, Lei Shen, Sheng Yang, Weihong He, Wei Cheng, Yang Wu, Shuilin He

Open access · goldAbstract read
In one paragraph

Article in BMC plant biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
5.8field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 32 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Shaoliang MouCollege of Life Science, Fujian Agriculture and Forestry University, Fuzhou, Fujian, 350002, People's Republic of China.
Feng GaoCollege of Life Science, Fujian Agriculture and Forestry University, Fuzhou, Fujian, 350002, People's Republic of China.
Lei ShenKey Laboratory of Applied Genetics of Universities in Fujian Province, Fujian Agriculture and Forestry University, Fuzhou, Fujian, 350002, People's Republic of China.
Sheng YangKey Laboratory of Applied Genetics of Universities in Fujian Province, Fujian Agriculture and Forestry University, Fuzhou, Fujian, 350002, People's Republic of China.
Weihong HeCollege of Life Science, Fujian Agriculture and Forestry University, Fuzhou, Fujian, 350002, People's Republic of China.
Wei ChengKey Laboratory of Applied Genetics of Universities in Fujian Province, Fujian Agriculture and Forestry University, Fuzhou, Fujian, 350002, People's Republic of China.
Yang WuCollege of Life Science, Jinggangshan University, Ji'an, Jiangxi, 343000, People's Republic of China. 40770249@qq.com.
Shuilin HeKey Laboratory of Applied Genetics of Universities in Fujian Province, Fujian Agriculture and Forestry University, Fuzhou, Fujian, 350002, People's Republic of China. shlhe201304@aliyun.com.
Fujian Agriculture and Forestry University · CNJinggangshan University · CN

Funding

National Natural Science Foundation of China 31301254, 31372061, 31601761, 31401890, 31401312 and 31260482Natural Science Foundation of Fujian Province 2018J01616
6 · The paper itself

Abstract

backgroundBacterial wilt caused by Ralstonia solanacearum is one of the most important diseases in pepper worldwide, however, the molecular mechanism underlying pepper resistance to bacterial wilt remains poorly understood.

resultsHerein, a novel RD leucine-rich repeat receptor-like kinase, CaLRR-RLK1, was functionally characterized in immunity against R. solanacearum. CaLRR-RLK1 was targeted exclusively to plasma membrane and was up-regulated by R. solanacearum inoculation (RSI) as well as by the exogenous application of salicylic acid (SA), methyl jasmonate (MeJA) or ethephon (ETH). The silencing of CaLRR-RLK1 led to enhanced susceptibility of pepper plants to RSI, accompanied by down-regulation of immunity-related genes including CaACO1, CaHIR1, CaPR4 and CaPO2. In contrast, transient overexpression of CaLRR-RLK1 triggered hypersensitive response (HR)-like cell death and H2O2 accumulation in pepper leaves, manifested by darker trypan blue and DAB staining respectively. In addition, the ectopic overexpression of CaLRR-RLK1 in tobacco plants enhanced resistance R. solanacearum, accompanied with the immunity associated marker genes including NtPR2, NtPR2, NtHSR203 and NtHSR515. Furthermore, it was found that CaHDZ27, a positive regulator in pepper response to RSI in our previous study, transcriptionally activated CaLRR-RLK1 by direct targeting its promoter probably in a CAATTATTG dependent manner.

conclusionThe study revealed that CaLRR-RLK1 confers pepper resistance to R. solanacearum as the direct targeting of CaHDZ27.

Indexed as

CapsicumDisease ResistanceGene Expression Regulation, PlantHydrogen PeroxidePlant ImmunityPlant ProteinsRalstonia solanacearumHydrogen PeroxidePlant ProteinsCaHDZ27CaLRR-RLK1PepperPlant immunityRalstonia solanacearum

Identifiers

PMID30654746
PMCPMC6337819
OpenAlexW2910332328

What Socratic holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.