Evidence map›Paper›PMID 31829190›Full record

ArticleBMC genomics2019

Transcriptomic analyses reveal physiological changes in sweet orange roots affected by citrus blight.

Shimin Fu, Jonathan Shao, Avijit Roy, Ronald H Brlansky, Changyong Zhou, John S Hartung

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 22% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Whole-Genome DNA Methylation Analysis inFrontiers in plant science · 2022
    Article
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

6 authors at 4 institutions in 2 countries.

Shimin FuCitrus Research Institute, Southwest University, Chongqing, China.
Jonathan ShaoUnited States Department of Agriculture-Agricultural Research Service, Molecular Plant Pathology Laboratory, Beltsville, MD, USA.
Avijit RoyUSDA-APHIS-PPQ-S&T, Beltsville, MD, 20705, USA.
Ronald H BrlanskyCitrus Research and Education Center, University of Florida, Lake Alfred, FL, 33850, USA.
Changyong ZhouCitrus Research Institute, Southwest University, Chongqing, China. zhoucy@cric.cn.
John S HartungUnited States Department of Agriculture-Agricultural Research Service, Molecular Plant Pathology Laboratory, Beltsville, MD, USA. john.hartung@ars.usda.gov.ORCID http://orcid.org/0000-0001-6274-3481
Agricultural Research Service · USBeltsville Agricultural Research Center · USFlorida Department of Citrus · USSouthwest University · CN

Funding

Agricultural Research Service 801-8042-560Citrus Research and Development Foundation 14-921Fundamental Research Funds for the Central Universities XDJK2018C032
6 · The paper itself

Abstract

backgroundCitrus blight is a very important progressive decline disease of commercial citrus. The etiology is unknown, although the disease can be transmitted by root grafts, suggesting a viral etiology. Diagnosis is made by demonstrating physical blockage of xylem cells that prevents the movement of water. This test was used to identify symptomatic trees from four commercial groves in Florida. Total RNA extracts of phloem-enriched scaffold root tissues were prepared from seven trees that failed to take up water and from one healthy tree. These RNA extracts were used for transcriptomic analyses using paired end RNA-Seq from an Illumina 2500 system. The expression of transcripts annotated as polyprotein of citrus endogenous pararetrovirus were estimated by both RT-qPCR and RNA-Seq.

resultsTranscripts from seven RNA-Seq libraries from trees affected by citrus blight were compared to a control tree. 129-148 million RNA fragments (two paired-end reads/fragment) were generated per library and were mapped to the sweet orange reference genome. In response to citrus blight stress, genes encoding aquaporins, proteins with water channel activity and several cellulose synthase genes were down-regulated, whereas genes involved in lignin and glucosinolate biosynthesis were up-regulated. Transcripts encoding proteins in pathways of carbohydrate metabolism, nucleotide synthesis, signaling, hormone metabolism, secondary metabolism, transport, and biotic stress pathways were overwhelmingly down regulated in all libraries.

conclusionReduced water intake and xylem plugging were observed in the trees tested and the changes in their transcriptome were analyzed. Plants adapted to reduced water flow by regulating primary and secondary metabolism, nuclear transport and hormone associated pathways. The patterns of energy generation, transcription, translation and protein degradation were consistent with irreversible decline. The down regulation of cellulose synthase transcripts and up regulation of transcripts related to lignin production likely lead to an imbalance in the pathways leading to wood formation, and may lead to the blockage of the xylem vessels seen as the cardinal symptom of citrus blight. Transcripts of a pararetrovirus were elevated in the transcriptome of roots used in this study.

Indexed as

CitrusGene Expression ProfilingGene Expression Regulation, PlantGene LibraryPlant DiseasesPlant ProteinsPlant RootsSecondary MetabolismSequence Analysis, RNAWaterXylemPlant ProteinsWaterDrought responsePathogenesisPlant defenseWater transport

Identifiers

PMID31829190
PMCPMC6907255
OpenAlexW2996276375

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 OpenQuestion graph.