Evidence map›Paper›PMID 37878074›Full record

ArticleArchives of microbiology2023

Transcriptomic analysis of Ralstonia solanacearum in response to antibacterial volatiles of Bacillus velezensis FZB42.

Hafiz Abdul Samad Tahir, Qurban Ali, Faheem Uddin Rajer, Qaisar Shakeel, Waqqas Gillani, Rana Binyamin, Hafiz Muhammad Abdullah Tayyab, Abdur Rashid Khan, Qin Gu, Xuewen Gao and 1 more

Abstract read
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Article in Archives of microbiology, 2023. 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
3.6field-weighted citation impact, top 8% 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

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, 9 citations in OpenAlex.

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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 at 6 institutions in 2 countries.

Hafiz Abdul Samad TahirKey Laboratory of Integrated Management of Crop Diseases and Pests, Ministry of Education, Department of Plant Pathology, College of Plant Protection, Nanjing Agricultural University, Nanjing, 210095, People's Republic of China.
Qurban AliKey Laboratory of Integrated Management of Crop Diseases and Pests, Ministry of Education, Department of Plant Pathology, College of Plant Protection, Nanjing Agricultural University, Nanjing, 210095, People's Republic of China.
Faheem Uddin RajerDepartment of Plant Pathology, Faculty of Crop Protection, Sindh Agriculture University, Tandojam, 70060, Pakistan.
Qaisar ShakeelDepartment of Plant Pathology, The Islamia University of Bahawalpur, Bahawalpur, Punjab, Pakistan.
Waqqas GillaniPakistan Tobacco Board, Ministry of National Food Security and Research, Peshawar, Pakistan.
Rana BinyaminMuhammad Nawaz Sharif University of Agriculture, Multan, Pakistan.
Hafiz Muhammad Abdullah TayyabDepartment of Plant Pathology, University of Agriculture, Faisalabad, Punjab, Pakistan.
Abdur Rashid KhanKey Laboratory of Integrated Management of Crop Diseases and Pests, Ministry of Education, Department of Plant Pathology, College of Plant Protection, Nanjing Agricultural University, Nanjing, 210095, People's Republic of China.
Qin GuKey Laboratory of Integrated Management of Crop Diseases and Pests, Ministry of Education, Department of Plant Pathology, College of Plant Protection, Nanjing Agricultural University, Nanjing, 210095, People's Republic of China.
Xuewen GaoKey Laboratory of Integrated Management of Crop Diseases and Pests, Ministry of Education, Department of Plant Pathology, College of Plant Protection, Nanjing Agricultural University, Nanjing, 210095, People's Republic of China.
Huijun WuKey Laboratory of Integrated Management of Crop Diseases and Pests, Ministry of Education, Department of Plant Pathology, College of Plant Protection, Nanjing Agricultural University, Nanjing, 210095, People's Republic of China. hjwu@njau.edu.cn.
Nanjing Agricultural University · CNGovernment of Pakistan · PKIslamia University of Bahawalpur · PKMuhammad Nawaz Shareef University of Agriculture · PKSindh Agriculture University · PKUniversity of Agriculture Faisalabad · PK

Funding

National Natural Science Foundation of China (31972325, 32172490),Natural Science Foundation for Excellent Youth Scholars of Jiangsu Province, China (BK20200078).This work was supported by National Key R&D Plan Intergovernmental International Science and Technology Innovation Cooperation Project (2022YFE0121800)
6 · The paper itself

Abstract

Volatile organic compounds (VOCs), produced by a variety of microbial species and used as biological agents, have been demonstrated to play a significant role in controlling phytopathogens. In continuation of our previous studies, we aim to elucidate the underlying mechanisms and pathways involved in interactions between pathogens and microbial VOCs. In the current study, we tested how VOCs produced by Bacillus velezensis FZB42 affect the growth of Ralstonia solanacearum TBBS1 in vitro.Query The result showed that the colony growth of R. solanacearum was reduced with an inhibition rate of 0.83 ± 0.043 as compared to the control 1.7 ± 0.076, respectively. The number of viable cells of R. solanacearum was significantly decreased to 7.68 CFU/mL as compared to the control (9.02 CFU/mL). In addition, transcriptomic analysis of R. solanacearum in response to VOCs produced by FZB42 was performed to better understand the effect of VOCs on R. solanacearum. The transcriptional response of R. solanacearum to FZB42-VOCs was determined using an Illumina RNA-seq approach. The results revealed significant changes in the expression of 2094 R. solanacearum genes, including 593 upregulated and 1501 downregulated genes. To validate the RNA-seq results, the expression of 10 genes was quantified using RT-qPCR. Furthermore, Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) databases were used to functionally annotate differentially expressed genes. Significant changes were observed in genes directly or indirectly related to virulence, including those related to bacterial invasion, motility, chemotaxis, and secretion systems. Overall, RNA-seq profiling provides new insights into the possible fundamental molecular mechanisms that are responsible for the reduction in growth and virulence of R. solanacearum upon application of FZB42-VOC.

Indexed as

Ralstonia solanacearumVolatile Organic CompoundsAnti-Bacterial AgentsBacillusGene Expression ProfilingTranscriptomeAnti-Bacterial AgentsVolatile Organic CompoundsBacillus velezensisRalstonia solanacearumRNA-seq analysisVolatile Organic Compounds

Identifiers

PMID37878074
OpenAlexW4387931298

What OpenQuestion holds

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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.