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  1. KRISHI Publication and Data Inventory Repository
  2. Natural Resource Management A8
  3. ICAR-Central Soil Salinity Research Institute M1
  4. NRM-CSSRI-Publication
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Please use this identifier to cite or link to this item: http://krishi.icar.gov.in/jspui/handle/123456789/50210
Title: Biological Management of Banana Fusarium Wilt Caused by Fusarium oxysporum f. sp. cubenseTropical Race 4 Using Antagonistic Fungal Isolate CSR-T-3 (Trichoderma reesei)
Other Titles: Not Available
Authors: Thukkaram Damodaran
Shailendra Rajan
Kavita Yadav
Vinay K. Mishra
Ram Gopal
Nidhi Kumari
Muthukumar Manoharan
Sunil K. Jha
Sandeep Kumar
Israr Ahmad
ICAR Data Use Licennce: http://krishi.icar.gov.in/PDF/ICAR_Data_Use_Licence.pdf
Author's Affiliated institute: ICAR::Central Soil Salinity Research Institute,Regional Research Station, Lucknow India
ICAR- Central Institute for Subtropical Horticulture,Lucknow, India
Published/ Complete Date: 2020-12-16
Project Code: Not Available
Keywords: Trichoderma reesei, banana, Fusarium wilt TR4, antifungal, LC-MS, gene expression, field evaluation
Publisher: Frontiers in Microbiology
Citation: Not Available
Series/Report no.: Not Available;
Abstract/Description: Fusarium wilt in bananas is one of the most devastating diseases that poses a serious threat to the banana industry globally. With no effective control measures available to date, biological control has been explored to restrict the spread and manage the outbreak. We studied the effective biological control potential of different Trichoderma spp. in the management of Fusarium oxysporum f. sp. cubense tropical race 4 (Foc TR4). Expression of the defense related genes and metabolites in banana plants inoculated with Foc TR4 and treated with effective Trichoderma sp interactions were also studied. The in vitro growth inhibition of Foc TR4 by Trichoderma reesei isolate CSR-T-3 was 85.19% indicating a higher antagonistic potential than other Trichoderma isolates used in the study. Further, in in vivo assays, the banana plants treated with the isolate CSR-T-3 T. reesei had a significant reduction in the disease severity index (0.75) and also had increased phenological indices with respect to Foc TR4 treated plants. Enhanced activity of defense enzymes, such as β-1, 3-glucanase, peroxidase, chitinase, polyphenol oxidase, and phenylalanine ammonia lyase with higher phenol contents were found in the Trichoderma isolate CSR-T-3 treated banana plants challenge-inoculated with Foc TR4. Fusarium toxins, such as fusaristatin A, fusarin C, chlamydosporal, and beauveric acid were identified by LC-MS in Foc TR4-infected banana plants while high intensity production of antifungal compounds, such as ß-caryophyllene, catechin-o-gallate, soyasapogenol rhamnosyl glucoronide, peptaibols, fenigycin, iturin C19, anthocyanin, and gallocatechin-o-gallate were detected in T. reesei isolate CSR-T-3 treated plant previously inoculated with Foc TR4. Gene expression analysis indicated the upregulation of TrCBH1/TrCBH2, TrXYL1, TrEGL1, TrTMK1, TrTGA1, and TrVEL1 genes in CSR-T-3 treatment. LC-MS and gene expression analysis could ascertain the upregulation of genes involved in mycoparasitism and the signal transduction pathway leading to secondary metabolite production under CSR-T-3 treatment. The plants in the field study showed a reduced disease severity index (1.14) with high phenological growth and yield indices when treated with T. reesei isolate CSR-T-3 formulation. We report here an effective biocontrol-based management technological transformation from lab to thefield for successful control of Fusarium wilt disease caused by Foc TR4 in bananas.
Description: Not Available
Type(s) of content: Article
Sponsors: Not Available
Language: English
Name of Journal: Frontiers in Microbology
NAAS Rating: 10.23
Volume No.: 11
Page Number: Not Available
Name of the Division/Regional Station: ICAR-Central Soil Salinity Research Institute , Regional Research Station, Lucknow
Source, DOI or any other URL: 10.3389/fmicb.2020.595845
URI: http://krishi.icar.gov.in/jspui/handle/123456789/50210
Appears in Collections:NRM-CSSRI-Publication

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