Evidence map›Paper›PMID 41351231›Full record

ArticleMolecular plant pathology2025

Experimental Coevolution Reveals That Ralstonia pseudosolanacearum PhcA Contributes to the Infection of Filamentous Phage RSCq.

Hailing Liang, Jiatian Chen, Yanan Xu, Shuqing Bin, Xiaotong Qin, Guimei Qin, Dehong Zheng

Abstract read
In one paragraph

Article in Molecular plant pathology, 2025. 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
–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

2 citing papers in PubMed.

  1. Article
  2. 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

7 authors.

Hailing LiangState Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, Guangxi Key Laboratory of Agro-Environment and Agro-Product Safety, College of Agriculture, Guangxi University, Nanning, China.
Jiatian ChenState Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, Guangxi Key Laboratory of Agro-Environment and Agro-Product Safety, College of Agriculture, Guangxi University, Nanning, China.
Yanan XuSchool of Pharmacy, Guangxi Medical University, Nanning, China.
Shuqing BinState Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, Guangxi Key Laboratory of Agro-Environment and Agro-Product Safety, College of Agriculture, Guangxi University, Nanning, China.
Xiaotong QinState Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, Guangxi Key Laboratory of Agro-Environment and Agro-Product Safety, College of Agriculture, Guangxi University, Nanning, China.
Guimei QinState Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, Guangxi Key Laboratory of Agro-Environment and Agro-Product Safety, College of Agriculture, Guangxi University, Nanning, China.
Dehong ZhengState Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, Guangxi Key Laboratory of Agro-Environment and Agro-Product Safety, College of Agriculture, Guangxi University, Nanning, China.ORCID 0000-0001-6339-2038

Funding

National Natural Science Foundation of China 32260713Natural Science Foundation of Guangxi Zhuang Autonomous Region 2023GXNSFBA026208Natural Science Foundation of Guangxi Zhuang Autonomous Region 2025GXNSFDA069039
6 · The paper itself

Abstract

The interaction between bacteria and filamentous phages, particularly in the context of bacterial pathogenesis, remains poorly understood compared with the well-documented interactions involving lytic phages. Here, we investigated the coevolutionary dynamics between Ralstonia pseudosolanacearum, the causative agent of plant bacterial wilt disease, and filamentous phages. Experimental coevolution revealed the critical role of the global virulence regulator PhcA in filamentous phage infection, demonstrating that its requirement for successful filamentous phage infection is independent of the type IV pili receptor. Notably, while PhcA deficiency conferred phage resistance, it did not impair filamentous phage genome replication or egress. Moreover, trade-offs between filamentous phage resistance and bacterial virulence were observed, highlighting the potential implications of filamentous phage for biocontrol strategies against R. pseudosolanacearum. Overall, our findings shed light on the intricate interplay between Ralstonia pathogens and filamentous phages, providing insights into the development of novel approaches for disease management.

Indexed as

Bacterial ProteinsInovirusRalstoniaPlant DiseasesVirulenceBacterial Proteinsexperimental coevolutionfilamentous phagephage resistancePhcARalstonia pseudosolanacearum

Identifiers

PMID41351231
PMCPMC12680784

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Registered trials

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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.