Evidence map›Paper›PMID 36494781›Full record

ArticleBMC plant biology2022

Analysis of proteomic changes in cassava cv. Kasetsart 50 caused by Sri Lankan cassava mosaic virus infection.

Wanwisa Siriwan, Nuannapa Hemniam, Nattachai Vannatim, Srihunsa Malichan, Somruthai Chaowongdee, Sittiruk Roytrakul, Sawanya Charoenlappanit, Aroonothai Sawwa

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Article in BMC plant biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

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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

5 citing papers in PubMed, 8 citations in OpenAlex.

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4 · The record

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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 3 institutions in 1 country.

Wanwisa SiriwanDepartment of Plant Pathology, Faculty of Agriculture, Kasetsart University, Bangkok, 10900, Thailand. wanwisa.si@ku.th.
Nuannapa HemniamDepartment of Plant Pathology, Faculty of Agriculture, Kasetsart University, Bangkok, 10900, Thailand.
Nattachai VannatimDepartment of Plant Pathology, Faculty of Agriculture, Kasetsart University, Bangkok, 10900, Thailand.
Srihunsa MalichanDepartment of Plant Pathology, Faculty of Agriculture, Kasetsart University, Bangkok, 10900, Thailand.
Somruthai ChaowongdeeCenter of Excellence On Agricultural Biotechnology (AG-BIO/MHESI), Bangkok, 10900, Thailand.
Sittiruk RoytrakulNational Center for Genetic and Engineering and Biotechnology (BIOTECH), National Science and Technology Development Agency, Pathumthani, 12100, Thailand.
Sawanya CharoenlappanitNational Center for Genetic and Engineering and Biotechnology (BIOTECH), National Science and Technology Development Agency, Pathumthani, 12100, Thailand.
Aroonothai SawwaBiotechnology Research and Development Office, Department of Agriculture, Thanyaburi, Pathumthani, 12110, Thailand.
Kasetsart University · THNational Center for Genetic Engineering and Biotechnology · THEastern Asia University · TH

Funding

Kasetsart University Research and Development Institute FF(KU)18.65
6 · The paper itself

Abstract

backgroundSri Lankan cassava mosaic virus (SLCMV) is a plant virus causing significant economic losses throughout Southeast Asia. While proteomics has the potential to identify molecular markers that could assist the breeding of virus resistant cultivars, the effects of SLCMV infection in cassava have not been previously explored in detail.

resultsLiquid Chromatography-Tandem Mass Spectrometry (LC/MS-MS) was used to identify differentially expressed proteins in SLCMV infected leaves, and qPCR was used to confirm changes at mRNA levels. LC/MS-MS identified 1,813 proteins, including 479 and 408 proteins that were upregulated in SLCMV-infected and healthy cassava plants respectively, while 109 proteins were detected in both samples. Most of the identified proteins were involved in biosynthetic processes (29.8%), cellular processes (20.9%), and metabolism (18.4%). Transport proteins, stress response molecules, and proteins involved in signal transduction, plant defense responses, photosynthesis, and cellular respiration, although present, only represented a relatively small subset of the detected differences. RT-qPCR confirmed the upregulation of WRKY 77 (A0A140H8T1), WRKY 83 (A0A140H8T7), NAC 6 (A0A0M4G3M4), NAC 35 (A0A0M5JAB4), NAC 22 (A0A0M5J8Q6), NAC 54 (A0A0M4FSG8), NAC 70 (A0A0M4FEU9), MYB (A0A2C9VER9 and A0A2C9VME6), bHLH (A0A2C9UNL9 and A0A2C9WBZ1) transcription factors. Additional upregulated transcripts included receptors, such as receptor-like serine/threonine-protein kinase (RSTK) (A0A2C9UPE4), Toll/interleukin-1 receptor (TIR) (A0A2C9V5Q3), leucine rich repeat N-terminal domain (LRRNT_2) (A0A2C9VHG8), and cupin (A0A199UBY6). These molecules participate in innate immunity, plant defense mechanisms, and responses to biotic stress and to phytohormones.

conclusionsWe detected 1,813 differentially expressed proteins infected cassava plants, of which 479 were selectively upregulated. These could be classified into three main biological functional groups, with roles in gene regulation, plant defense mechanisms, and stress responses. These results will help identify key proteins affected by SLCMV infection in cassava plants.

Indexed as

ManihotBegomovirusPlant BreedingPlant DiseasesProteomicsCassava cv. Kasetsart 50Geminivius and Sri Lankan cassava mosaic virusProteomic profiling

Identifiers

PMID36494781
PMCPMC9737768
OpenAlexW4311677384

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.