Evidence map›Paper›PMID 38377039›Full record

ArticleMolecular plant-microbe interactions : MPMI2024

Comparing Methods for Detection and Quantification of Plasmodesmal Callose in

Amie F Sankoh, Joseph Adjei, Daniel M Roberts, Tessa M Burch-Smith

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Molecular plant-microbe interactions : MPMI, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

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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

4 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Amie F SankohDepartment of Biochemistry & Cellular and Molecular Biology, The University of Tennessee, Knoxville, TN 37996, U.S.A.
Joseph AdjeiDonald Danforth Plant Science Center, Saint Louis, MO 63132, U.S.A.
Daniel M RobertsDepartment of Biochemistry & Cellular and Molecular Biology, The University of Tennessee, Knoxville, TN 37996, U.S.A.
Tessa M Burch-SmithDonald Danforth Plant Science Center, Saint Louis, MO 63132, U.S.A.ORCID 0000-0002-5994-4343

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Callose, a β-(1,3)-d-glucan polymer, is essential for regulating intercellular trafficking via plasmodesmata (PD). Pathogens manipulate PD-localized proteins to enable intercellular trafficking by removing callose at PD or, conversely, by increasing callose accumulation at PD to limit intercellular trafficking during infection. Plant defense hormones like salicylic acid regulate PD-localized proteins to control PD and intercellular trafficking during immune defense responses such as systemic acquired resistance. Measuring callose deposition at PD in plants has therefore emerged as a popular parameter for assessing likely intercellular trafficking activity during plant immunity. Despite the popularity of this metric, there is no standard for how these measurements should be made. In this study, three commonly used methods for identifying and quantifying plasmodesmal callose by aniline blue staining were evaluated to determine the most effective in the

Indexed as

GlucansNicotianaPlant DiseasesPlant LeavesPlasmodesmataAniline CompoundsPlant ImmunityStaining and Labelinganiline blueAniline CompoundscalloseGlucansaniline bluecalloseimage analysisplasmodesmatasalicylic acid

Identifiers

What OpenQuestion holds

Textmetadata
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.