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Metabolomic profiling and its association with the bio-efficacy of Aspergillus niger strain against Fusarium wilt of guava
Bio-control agents are the best alternative to chemicals for the successful management of plant diseases. The fungus Aspergillus niger is known to produce diverse metabolites with antifungal activity, attracting researchers to exploit it as a bio-control agent for plant disease control. In the prese...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10165087/ https://www.ncbi.nlm.nih.gov/pubmed/37168123 http://dx.doi.org/10.3389/fmicb.2023.1142144 |
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author | Gangaraj, R. Kundu, Aditi Rana, Virendra Singh Das, Amrita Chawla, Gautham Prakash, G. Debbarma, Rubin Nagaraja, A. Bainsla, Naresh Kumar Gupta, Navin Chandra Kamil, Deeba |
author_facet | Gangaraj, R. Kundu, Aditi Rana, Virendra Singh Das, Amrita Chawla, Gautham Prakash, G. Debbarma, Rubin Nagaraja, A. Bainsla, Naresh Kumar Gupta, Navin Chandra Kamil, Deeba |
author_sort | Gangaraj, R. |
collection | PubMed |
description | Bio-control agents are the best alternative to chemicals for the successful management of plant diseases. The fungus Aspergillus niger is known to produce diverse metabolites with antifungal activity, attracting researchers to exploit it as a bio-control agent for plant disease control. In the present study, 11 A. niger strains were isolated and screened for their antagonism against the guava wilt pathogen under in vitro and in planta conditions. Strains were identified morphologically and molecularly by sequencing the internal transcribed spacer (ITS), β-tubulin, and calmodulin genes. The strains were evaluated through dual culture, volatile, and non-volatile methods under an in vitro study. AN-11, AN-6, and AN-2 inhibited the test pathogen Fusarium oxysporum f. sp. psidii (FOP) at 67.16%, 64.01%, and 60.48%, respectively. An in planta study was conducted under greenhouse conditions with 6 months old air-layered guava plants (var. Allahabad Safeda) by pre- and post-inoculation of FOP. The AN-11 strain was found to be effective under both pre- and post-inoculation trials. Furthermore, gas chromatography–mass spectrometry (GC–MS) analysis was carried out to characterize the volatile compounds of the most potential strain, A. niger. The hexane soluble fraction showed the appearance of characteristic peaks of hexadecenoic acid methyl ester (4.41%), 10-octadecanoic acid methyl ester (3.79%), dodecane (3.21%), undecane (3.19%), gibepyrone A (0.15%), 3-methylundecane (0.36%), and citroflex A (0.38%). The ethyl acetate fraction of the bio-control fungi revealed the occurrence of major antifungal compounds, such as acetic acid ethyl ester (17.32%), benzopyron-4-ol (12.17%), 1,2,6-hexanetriol (7.16%), 2-propenoic acid ethanediyl ester (2.95%), 1-(3-ethyloxiranyl)-ethenone (0.98%), 6-acetyl-8-methoxy dimethyl chromene (0.96%), 4-hexyl-2,5-dihydro dioxo furan acetic acid (0.19%), and octadecanoic acid (1.11%). Furthermore, bio-control abilities could be due to hyper-parasitism, the production of secondary metabolites, and competition for sites and nutrients. Indeed, the results will enrich the existing knowledge of metabolomic information and support perspectives on the bio-control mechanism of A. niger. |
format | Online Article Text |
id | pubmed-10165087 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101650872023-05-09 Metabolomic profiling and its association with the bio-efficacy of Aspergillus niger strain against Fusarium wilt of guava Gangaraj, R. Kundu, Aditi Rana, Virendra Singh Das, Amrita Chawla, Gautham Prakash, G. Debbarma, Rubin Nagaraja, A. Bainsla, Naresh Kumar Gupta, Navin Chandra Kamil, Deeba Front Microbiol Microbiology Bio-control agents are the best alternative to chemicals for the successful management of plant diseases. The fungus Aspergillus niger is known to produce diverse metabolites with antifungal activity, attracting researchers to exploit it as a bio-control agent for plant disease control. In the present study, 11 A. niger strains were isolated and screened for their antagonism against the guava wilt pathogen under in vitro and in planta conditions. Strains were identified morphologically and molecularly by sequencing the internal transcribed spacer (ITS), β-tubulin, and calmodulin genes. The strains were evaluated through dual culture, volatile, and non-volatile methods under an in vitro study. AN-11, AN-6, and AN-2 inhibited the test pathogen Fusarium oxysporum f. sp. psidii (FOP) at 67.16%, 64.01%, and 60.48%, respectively. An in planta study was conducted under greenhouse conditions with 6 months old air-layered guava plants (var. Allahabad Safeda) by pre- and post-inoculation of FOP. The AN-11 strain was found to be effective under both pre- and post-inoculation trials. Furthermore, gas chromatography–mass spectrometry (GC–MS) analysis was carried out to characterize the volatile compounds of the most potential strain, A. niger. The hexane soluble fraction showed the appearance of characteristic peaks of hexadecenoic acid methyl ester (4.41%), 10-octadecanoic acid methyl ester (3.79%), dodecane (3.21%), undecane (3.19%), gibepyrone A (0.15%), 3-methylundecane (0.36%), and citroflex A (0.38%). The ethyl acetate fraction of the bio-control fungi revealed the occurrence of major antifungal compounds, such as acetic acid ethyl ester (17.32%), benzopyron-4-ol (12.17%), 1,2,6-hexanetriol (7.16%), 2-propenoic acid ethanediyl ester (2.95%), 1-(3-ethyloxiranyl)-ethenone (0.98%), 6-acetyl-8-methoxy dimethyl chromene (0.96%), 4-hexyl-2,5-dihydro dioxo furan acetic acid (0.19%), and octadecanoic acid (1.11%). Furthermore, bio-control abilities could be due to hyper-parasitism, the production of secondary metabolites, and competition for sites and nutrients. Indeed, the results will enrich the existing knowledge of metabolomic information and support perspectives on the bio-control mechanism of A. niger. Frontiers Media S.A. 2023-04-24 /pmc/articles/PMC10165087/ /pubmed/37168123 http://dx.doi.org/10.3389/fmicb.2023.1142144 Text en Copyright © 2023 Gangaraj, Kundu, Rana, Das, Chawla, Prakash, Debbarma, Nagaraja, Bainsla, Gupta and Kamil. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Gangaraj, R. Kundu, Aditi Rana, Virendra Singh Das, Amrita Chawla, Gautham Prakash, G. Debbarma, Rubin Nagaraja, A. Bainsla, Naresh Kumar Gupta, Navin Chandra Kamil, Deeba Metabolomic profiling and its association with the bio-efficacy of Aspergillus niger strain against Fusarium wilt of guava |
title | Metabolomic profiling and its association with the bio-efficacy of Aspergillus niger strain against Fusarium wilt of guava |
title_full | Metabolomic profiling and its association with the bio-efficacy of Aspergillus niger strain against Fusarium wilt of guava |
title_fullStr | Metabolomic profiling and its association with the bio-efficacy of Aspergillus niger strain against Fusarium wilt of guava |
title_full_unstemmed | Metabolomic profiling and its association with the bio-efficacy of Aspergillus niger strain against Fusarium wilt of guava |
title_short | Metabolomic profiling and its association with the bio-efficacy of Aspergillus niger strain against Fusarium wilt of guava |
title_sort | metabolomic profiling and its association with the bio-efficacy of aspergillus niger strain against fusarium wilt of guava |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10165087/ https://www.ncbi.nlm.nih.gov/pubmed/37168123 http://dx.doi.org/10.3389/fmicb.2023.1142144 |
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