Evidence map›Paper›PMID 41366299›Full record

ArticleBMC plant biology2025

Integrated multi-omics reveals terpenoid-driven metabolic and transcriptional regulation underlying sweetpotato resistance to black rot disease.

Fei Zhang, Fangfang Mu, Qiguo Hu, Houjun Sun, Mengjiao Lan, Yu Li, Hang Yang, Mingku Zhu, Jukui Ma, Huijun Zhang and 1 more

Abstract read
In one paragraph

Article in BMC plant biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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

3 citing papers in PubMed.

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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

11 authors.

Fei ZhangInstitute of Integrative Plant Biology, School of Life Sciences, Jiangsu Normal University, Xuzhou, Jiangsu Province, 221116, People's Republic of China.
Fangfang MuInstitute of Integrative Plant Biology, School of Life Sciences, Jiangsu Normal University, Xuzhou, Jiangsu Province, 221116, People's Republic of China.
Qiguo HuInstitute of Integrative Plant Biology, School of Life Sciences, Jiangsu Normal University, Xuzhou, Jiangsu Province, 221116, People's Republic of China.
Houjun SunInstitute of Integrative Plant Biology, School of Life Sciences, Jiangsu Normal University, Xuzhou, Jiangsu Province, 221116, People's Republic of China.
Mengjiao LanInstitute of Integrative Plant Biology, School of Life Sciences, Jiangsu Normal University, Xuzhou, Jiangsu Province, 221116, People's Republic of China.
Yu LiSchool of Life Sciences, Huaibei Normal University, Huaibei, Anhui Province, 235000, People's Republic of China.
Hang YangInstitute of Integrative Plant Biology, School of Life Sciences, Jiangsu Normal University, Xuzhou, Jiangsu Province, 221116, People's Republic of China.
Mingku ZhuInstitute of Integrative Plant Biology, School of Life Sciences, Jiangsu Normal University, Xuzhou, Jiangsu Province, 221116, People's Republic of China.
Jukui MaInstitute of Integrative Plant Biology, School of Life Sciences, Jiangsu Normal University, Xuzhou, Jiangsu Province, 221116, People's Republic of China.
Huijun ZhangSchool of Life Sciences, Huaibei Normal University, Huaibei, Anhui Province, 235000, People's Republic of China. zhhuijun@126.com.
Zongyun LiInstitute of Integrative Plant Biology, School of Life Sciences, Jiangsu Normal University, Xuzhou, Jiangsu Province, 221116, People's Republic of China. zongyunli@jsnu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sweetpotato black rot, caused by the fungus Ceratocystis fimbriata, adversely affects yield and postharvest quality. We applied integrated transcriptomic and metabolomic profiling to elucidate resistance mechanisms in the black rot-resistant cultivar SS23 versus the susceptible cultivar GS08. Phenotypically, SS23 developed substantially milder symptoms and smaller lesions, whereas GS08 suffered extensive root damage. Multi-omics integration revealed that SS23 mounted a rapid defense response characterized by the upregulation of defense-related genes (e.g., peroxidase, chitinase) and a coordinated metabolic reprogramming that increased levels of resistance-associated compounds, including the amino acids leucine and proline and sesquiterpenoids such as plumericin. By contrast, GS08 exhibited a delayed transcriptional response and suppression of amino acid metabolic pathways. Our analyses highlight the central role of terpenoid biosynthesis in resistance: SS23 activated terpene synthases (IbTPS) together with cytochrome P450s to promote production of antifungal terpenoids, whereas GS08 primarily upregulated the upstream mevalonate pathway enzyme HMG-CoA reductase (IbHMGR) without corresponding downstream specialization. Volatile profiling detected 13 terpenoids in SS23 following infection (including isoterpinolene) versus 6 in GS08. To the best of our knowledge, we are the first to report the identification of specific antifungal terpenoids, such as isoterpinolene, being induced in sweetpotato roots in response to black rot. Tightly interconnected gene-metabolite networks in SS23 appear to constrain pathogen progression, whereas metabolic dysregulation in GS08 strongly correlated with susceptibility. These findings emphasize terpenoid-pathway manipulation as a promising strategy for developing black rot-resistant sweetpotato and nominate several core genes as candidate molecular markers for precision breeding.

Indexed as

AscomycotaDisease ResistanceIpomoea batatasPlant DiseasesTerpenesGene Expression ProfilingGene Expression Regulation, PlantMetabolomicsMultiomicsTranscriptomeTerpenesBlack rot diseaseDisease resistanceMetabolomicSweetpotatoTerpenoidTranscriptomic

Identifiers

PMID41366299
PMCPMC12690883

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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.