Evidence map›Paper›PMID 39639670›Full record

ArticleThe plant pathology journal2024

A Novel and Advanced Diagnostic Approach toward Paracidovorax citrulli Causing Bacterial Fruit Blotch in Watermelon by Direct SYBR Green Real-Time PCR Assay.

Hyeonheui Ham, Bang Wool Lee, Kyongnim Kim, Woohyung Lee, Yong Hwan Lee, Dong Suk Park

Abstract read
In one paragraph

Article in The plant pathology journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
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

6 authors.

Hyeonheui HamCrop Protection Division, National Institute of Agricultural Sciences, Rural Develop-ment Administration, Wanju 55365, Korea.
Bang Wool LeeCrop Protection Division, National Institute of Agricultural Sciences, Rural Develop-ment Administration, Wanju 55365, Korea.
Kyongnim KimCrop Protection Division, National Institute of Agricultural Sciences, Rural Develop-ment Administration, Wanju 55365, Korea.
Woohyung LeeCrop Protection Division, National Institute of Agricultural Sciences, Rural Develop-ment Administration, Wanju 55365, Korea.
Yong Hwan LeeCrop Protection Division, National Institute of Agricultural Sciences, Rural Develop-ment Administration, Wanju 55365, Korea.
Dong Suk ParkMicrobial Safety Division, National Institute of Agricultural Sciences, Rural Develop-ment Administration, Wanju 55365, Korea.

Funding

Rural Development Administration PJ01727101
6 · The paper itself

Abstract

Bacterial fruit blotch (BFB) caused by Paracidovorax citrulli is a devastating disease in cucurbit hosts such as watermelon. P. citrulli is a seed-borne pathogen, and contaminated seeds are the primary inoculum. Because it is difficult to control BFB after the emergence of the disease, it is essential to detect the pathogen and remove infected plant materials, including seeds, in the early stages. In this study, we developed a direct SYBR Green real-time polymerase chain reaction (PCR) method using a new species-specific marker for detecting P. citrulli with high specificity and sensitivity. The genome information of P. citrulli and related species was collected and compared to retrieve the P. citrulli-specific gene. The primer set RS01560-164 was designed based on the selected gene and tested for specificity and sensitivity using cloned DNA, genomic DNA, cell suspension, and suspensions obtained from infected watermelon cotyledons. Our primer set detected only P. citrulli from the closely related species with a detection limit of cloned DNA at 1.46 × 103 copies/µl, gDNA at 500 fg/µl, and cell suspension at 1.4 × 104 cfu/ml by real-time PCR. Our method also detected P. citrulli from diseased plants without the need for a DNA extraction phase. Therefore, the primer set and real-time PCR methods newly developed in this study could be applied for the specific detection of P. citrulli in plants or seeds with high sensitivity and robustness, providing the potential to manage BFB in cucurbits.

Indexed as

bio-PCRquantificationspecies-specific gene

Identifiers

PMID39639670
PMCPMC11626039

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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.