Potential Utility of Bacillus amyloliquefaciens SFB-1 as a Biocontrol Agent for Sweetpotato Black Rot Caused by Ceratocystis fimbriata

<b>Background/Objectives</b>: Sweetpotato black rot, caused by <i>Ceratocystis fimbriata</i>, is a severe fungal disease in sweetpotato production. Biological control strategies represent a promising, environmentally sustainable approach to managing this disease. This study investigates the biocontrol potential of <i>Bacillus amyloliquefaciens</i> SFB-1 against <i>C. fimbriata</i>. <b>Methods</b>: The antagonistic activities of strain SFB-1 on <i>C. fimbriata</i> were assessed through <i>in vitro</i> assays, including evaluations of mycelial inhibition, spore germination, and mycelial morphology. Pathogenicity assays on harvested sweetpotato roots assessed lesion diameter and depth. A transcriptomic analysis of <i>C. fimbriata</i> exposed to strain SFB-1 was performed to explore the underlying antifungal mechanism of SFB-1 on <i>C. fimbriata</i>. The qRT-PCR was employed to validate the RNA-seq results. <b>Results</b>: <i>In vitro</i> assays demonstrated that strain SFB-1 inhibited <i>C. fimbriata</i> mycelial growth by up to 81.01%, caused mycelial swelling, and completely suppressed spore germination at 10<sup>8</sup> CFU/mL. The cell-free supernatant of strain SFB-1 also suppressed <i>C. fimbriata</i> growth. Pathogenicity assays revealed that strain SFB-1 treatments reduced lesion diameter and depth on harvested sweetpotato roots by over 50% compared to untreated controls. Transcriptomic analysis of <i>C. fimbriata</i> treated with strain SFB-1 identified 1164 differentially expressed genes, with significant alterations in genes associated with cell wall integrity, cell membrane stability, spore germination, detoxification, and antioxidant responses. The qRT-PCR validation of 16 genes confirmed the consistency with the RNA-seq results. <b>Conclusions</b>: <i>B. amyloliquefaciens</i> SFB-1 demonstrates significant biocontrol efficacy against <i>C. fimbriata</i> through multiple mechanisms, positioning it as a promising solution for the sustainable management of sweetpotato black rot.

Authors

Institutions

Publication Details

Journal
Genes
Published
2024-11-28
DOI
https://doi.org/10.3390/genes15121540
Citations
4
Primary Topic
Plant-Microbe Interactions and Immunity
Type
article
Field-Weighted Citation Impact
2.40
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Potential Utility of Bacillus amyloliquefaciens SFB-1 as a Biocontrol Agent for Sweetpotato Black Rot Caused by Ceratocystis fimbriata

Chengling Zhang, Xiaosi Zhou, Veronica Tshogofatso Kgosi, Fangyuan Gao et al.
4 citations
Genes
Plant-Microbe Interactions and Immunity
2.40
article

Potential Utility of Bacillus amyloliquefaciens SFB-1 as a Biocontrol Agent for Sweetpotato Black Rot Caused by Ceratocystis fimbriata

Chengling Zhang, Xiaosi Zhou, Veronica Tshogofatso Kgosi, Fangyuan Gao, Houjun Sun, Jingwei Chen, Dongjing Yang, Zhao Liang, Wei Tang, Jukui Ma
article en
4 citations

Abstract

<b>Background/Objectives</b>: Sweetpotato black rot, caused by <i>Ceratocystis fimbriata</i>, is a severe fungal disease in sweetpotato production. Biological control strategies represent a promising, environmentally sustainable approach to managing this disease. This study investigates the biocontrol potential of <i>Bacillus amyloliquefaciens</i> SFB-1 against <i>C. fimbriata</i>. <b>Methods</b>: The antagonistic activities of strain SFB-1 on <i>C. fimbriata</i> were assessed through <i>in vitro</i> assays, including evaluations of mycelial inhibition, spore germination, and mycelial morphology. Pathogenicity assays on harvested sweetpotato roots assessed lesion diameter and depth. A transcriptomic analysis of <i>C. fimbriata</i> exposed to strain SFB-1 was performed to explore the underlying antifungal mechanism of SFB-1 on <i>C. fimbriata</i>. The qRT-PCR was employed to validate the RNA-seq results. <b>Results</b>: <i>In vitro</i> assays demonstrated that strain SFB-1 inhibited <i>C. fimbriata</i> mycelial growth by up to 81.01%, caused mycelial swelling, and completely suppressed spore germination at 10<sup>8</sup> CFU/mL. The cell-free supernatant of strain SFB-1 also suppressed <i>C. fimbriata</i> growth. Pathogenicity assays revealed that strain SFB-1 treatments reduced lesion diameter and depth on harvested sweetpotato roots by over 50% compared to untreated controls. Transcriptomic analysis of <i>C. fimbriata</i> treated with strain SFB-1 identified 1164 differentially expressed genes, with significant alterations in genes associated with cell wall integrity, cell membrane stability, spore germination, detoxification, and antioxidant responses. The qRT-PCR validation of 16 genes confirmed the consistency with the RNA-seq results. <b>Conclusions</b>: <i>B. amyloliquefaciens</i> SFB-1 demonstrates significant biocontrol efficacy against <i>C. fimbriata</i> through multiple mechanisms, positioning it as a promising solution for the sustainable management of sweetpotato black rot.

GenesVol. 15(12)
Nanjing Agricultural University (CN), Sweet Potato Research Institute (CN)
Responsible consumption and production
Openalex Percentile: Top 10%
Plant-Microbe Interactions and Immunity
2.40
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.