Cargando…

Cyclic Lipopeptides of Bacillus amyloliquefaciens DHA6 Are the Determinants to Suppress Watermelon Fusarium Wilt by Direct Antifungal Activity and Host Defense Modulation

Fusarium wilt, caused by Fusarium oxysporum f. sp. niveum (Fon), poses a serious threat to watermelon productivity. We previously characterized six antagonistic bacterial strains, including DHA6, capable of suppressing watermelon Fusarium wilt under greenhouse conditions. This study investigates the...

Descripción completa

Detalles Bibliográficos
Autores principales: Al-Mutar, Dhabyan Mutar Kareem, Noman, Muhammad, Abduljaleel Alzawar, Noor Salih, Azizullah, Li, Dayong, Song, Fengming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10301312/
https://www.ncbi.nlm.nih.gov/pubmed/37367623
http://dx.doi.org/10.3390/jof9060687
_version_ 1785064782106198016
author Al-Mutar, Dhabyan Mutar Kareem
Noman, Muhammad
Abduljaleel Alzawar, Noor Salih
Azizullah
Li, Dayong
Song, Fengming
author_facet Al-Mutar, Dhabyan Mutar Kareem
Noman, Muhammad
Abduljaleel Alzawar, Noor Salih
Azizullah
Li, Dayong
Song, Fengming
author_sort Al-Mutar, Dhabyan Mutar Kareem
collection PubMed
description Fusarium wilt, caused by Fusarium oxysporum f. sp. niveum (Fon), poses a serious threat to watermelon productivity. We previously characterized six antagonistic bacterial strains, including DHA6, capable of suppressing watermelon Fusarium wilt under greenhouse conditions. This study investigates the role of extracellular cyclic lipopeptides (CLPs) produced by strain DHA6 in Fusarium wilt suppression. Taxonomic analysis based on the 16S rRNA gene sequence categorized strain DHA6 as Bacillus amyloliquefaciens. MALDI-TOF mass spectrometry identified five families of CLPs, i.e., iturin, surfactin, bacillomycin, syringfactin, and pumilacidin, in the culture filtrate of B. amyloliquefaciens DHA6. These CLPs exhibited significant antifungal activity against Fon by inducing oxidative stress and disrupting structural integrity, inhibiting mycelial growth and spore germination. Furthermore, pretreatment with CLPs promoted plant growth and suppressed watermelon Fusarium wilt by activating antioxidant enzymes (e.g., catalase, superoxide dismutase, and peroxidase) and triggering genes involved in salicylic acid and jasmonic acid/ethylene signaling in watermelon plants. These results highlight the critical roles of CLPs as determinants for B. amyloliquefaciens DHA6 in suppressing Fusarium wilt through direct antifungal activity and modulation of plant defense responses. This study provides a foundation for developing B. amyloliquefaciens DHA6-based biopesticides, serving as both antimicrobial agents and resistance inducers, to effectively control Fusarium wilt in watermelon and other crops.
format Online
Article
Text
id pubmed-10301312
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-103013122023-06-29 Cyclic Lipopeptides of Bacillus amyloliquefaciens DHA6 Are the Determinants to Suppress Watermelon Fusarium Wilt by Direct Antifungal Activity and Host Defense Modulation Al-Mutar, Dhabyan Mutar Kareem Noman, Muhammad Abduljaleel Alzawar, Noor Salih Azizullah Li, Dayong Song, Fengming J Fungi (Basel) Article Fusarium wilt, caused by Fusarium oxysporum f. sp. niveum (Fon), poses a serious threat to watermelon productivity. We previously characterized six antagonistic bacterial strains, including DHA6, capable of suppressing watermelon Fusarium wilt under greenhouse conditions. This study investigates the role of extracellular cyclic lipopeptides (CLPs) produced by strain DHA6 in Fusarium wilt suppression. Taxonomic analysis based on the 16S rRNA gene sequence categorized strain DHA6 as Bacillus amyloliquefaciens. MALDI-TOF mass spectrometry identified five families of CLPs, i.e., iturin, surfactin, bacillomycin, syringfactin, and pumilacidin, in the culture filtrate of B. amyloliquefaciens DHA6. These CLPs exhibited significant antifungal activity against Fon by inducing oxidative stress and disrupting structural integrity, inhibiting mycelial growth and spore germination. Furthermore, pretreatment with CLPs promoted plant growth and suppressed watermelon Fusarium wilt by activating antioxidant enzymes (e.g., catalase, superoxide dismutase, and peroxidase) and triggering genes involved in salicylic acid and jasmonic acid/ethylene signaling in watermelon plants. These results highlight the critical roles of CLPs as determinants for B. amyloliquefaciens DHA6 in suppressing Fusarium wilt through direct antifungal activity and modulation of plant defense responses. This study provides a foundation for developing B. amyloliquefaciens DHA6-based biopesticides, serving as both antimicrobial agents and resistance inducers, to effectively control Fusarium wilt in watermelon and other crops. MDPI 2023-06-19 /pmc/articles/PMC10301312/ /pubmed/37367623 http://dx.doi.org/10.3390/jof9060687 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Al-Mutar, Dhabyan Mutar Kareem
Noman, Muhammad
Abduljaleel Alzawar, Noor Salih
Azizullah
Li, Dayong
Song, Fengming
Cyclic Lipopeptides of Bacillus amyloliquefaciens DHA6 Are the Determinants to Suppress Watermelon Fusarium Wilt by Direct Antifungal Activity and Host Defense Modulation
title Cyclic Lipopeptides of Bacillus amyloliquefaciens DHA6 Are the Determinants to Suppress Watermelon Fusarium Wilt by Direct Antifungal Activity and Host Defense Modulation
title_full Cyclic Lipopeptides of Bacillus amyloliquefaciens DHA6 Are the Determinants to Suppress Watermelon Fusarium Wilt by Direct Antifungal Activity and Host Defense Modulation
title_fullStr Cyclic Lipopeptides of Bacillus amyloliquefaciens DHA6 Are the Determinants to Suppress Watermelon Fusarium Wilt by Direct Antifungal Activity and Host Defense Modulation
title_full_unstemmed Cyclic Lipopeptides of Bacillus amyloliquefaciens DHA6 Are the Determinants to Suppress Watermelon Fusarium Wilt by Direct Antifungal Activity and Host Defense Modulation
title_short Cyclic Lipopeptides of Bacillus amyloliquefaciens DHA6 Are the Determinants to Suppress Watermelon Fusarium Wilt by Direct Antifungal Activity and Host Defense Modulation
title_sort cyclic lipopeptides of bacillus amyloliquefaciens dha6 are the determinants to suppress watermelon fusarium wilt by direct antifungal activity and host defense modulation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10301312/
https://www.ncbi.nlm.nih.gov/pubmed/37367623
http://dx.doi.org/10.3390/jof9060687
work_keys_str_mv AT almutardhabyanmutarkareem cycliclipopeptidesofbacillusamyloliquefaciensdha6arethedeterminantstosuppresswatermelonfusariumwiltbydirectantifungalactivityandhostdefensemodulation
AT nomanmuhammad cycliclipopeptidesofbacillusamyloliquefaciensdha6arethedeterminantstosuppresswatermelonfusariumwiltbydirectantifungalactivityandhostdefensemodulation
AT abduljaleelalzawarnoorsalih cycliclipopeptidesofbacillusamyloliquefaciensdha6arethedeterminantstosuppresswatermelonfusariumwiltbydirectantifungalactivityandhostdefensemodulation
AT azizullah cycliclipopeptidesofbacillusamyloliquefaciensdha6arethedeterminantstosuppresswatermelonfusariumwiltbydirectantifungalactivityandhostdefensemodulation
AT lidayong cycliclipopeptidesofbacillusamyloliquefaciensdha6arethedeterminantstosuppresswatermelonfusariumwiltbydirectantifungalactivityandhostdefensemodulation
AT songfengming cycliclipopeptidesofbacillusamyloliquefaciensdha6arethedeterminantstosuppresswatermelonfusariumwiltbydirectantifungalactivityandhostdefensemodulation