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Transcriptional response of Meloidogyne incognita to non-fumigant nematicides
There is limited research about the impacts of new nematicides, including fluazaindolizine, fluopyram, and fluensulfone, on the plant-parasitic nematode Meloidogyne incognita, despite it being a pervasive agricultural pest. In this study, M. incognita second-stage juveniles were exposed for 24-h to...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9192767/ https://www.ncbi.nlm.nih.gov/pubmed/35697824 http://dx.doi.org/10.1038/s41598-022-13815-9 |
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author | Wram, Catherine L. Hesse, Cedar N. Zasada, Inga A. |
author_facet | Wram, Catherine L. Hesse, Cedar N. Zasada, Inga A. |
author_sort | Wram, Catherine L. |
collection | PubMed |
description | There is limited research about the impacts of new nematicides, including fluazaindolizine, fluopyram, and fluensulfone, on the plant-parasitic nematode Meloidogyne incognita, despite it being a pervasive agricultural pest. In this study, M. incognita second-stage juveniles were exposed for 24-h to fluensulfone, fluazaindolizine, fluopyram, and oxamyl and total RNA was extracted and sequenced using next-generation sequencing to determine gene expression. The effects of nematicide exposure on cellular detoxification pathways, common differentially expressed (DE) genes, and fatty acid and retinol-binding genes were examined. Fluopyram and oxamyl had the smallest impacts on the M. incognita transcriptome with 48 and 151 genes that were DE, respectively. These compounds also elicited a weak response in the cellular detoxification pathway and fatty acid and retinol-binding (FAR) genes. Fluensulfone and fluazaindolizine produced robust transcriptional responses with 1208 and 2611 DE genes, respectively. These compounds had strong impacts on cellular detoxification, causing differential regulation of transcription factors and genes in the detox pathway. These compounds strongly down-regulated FAR genes between 52–85%. Having a greater understanding of how these compounds function at a molecular level will help to promote proper stewardship, aid with nematicide discovery, and help to stay a step ahead of nematicide resistance. |
format | Online Article Text |
id | pubmed-9192767 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-91927672022-06-15 Transcriptional response of Meloidogyne incognita to non-fumigant nematicides Wram, Catherine L. Hesse, Cedar N. Zasada, Inga A. Sci Rep Article There is limited research about the impacts of new nematicides, including fluazaindolizine, fluopyram, and fluensulfone, on the plant-parasitic nematode Meloidogyne incognita, despite it being a pervasive agricultural pest. In this study, M. incognita second-stage juveniles were exposed for 24-h to fluensulfone, fluazaindolizine, fluopyram, and oxamyl and total RNA was extracted and sequenced using next-generation sequencing to determine gene expression. The effects of nematicide exposure on cellular detoxification pathways, common differentially expressed (DE) genes, and fatty acid and retinol-binding genes were examined. Fluopyram and oxamyl had the smallest impacts on the M. incognita transcriptome with 48 and 151 genes that were DE, respectively. These compounds also elicited a weak response in the cellular detoxification pathway and fatty acid and retinol-binding (FAR) genes. Fluensulfone and fluazaindolizine produced robust transcriptional responses with 1208 and 2611 DE genes, respectively. These compounds had strong impacts on cellular detoxification, causing differential regulation of transcription factors and genes in the detox pathway. These compounds strongly down-regulated FAR genes between 52–85%. Having a greater understanding of how these compounds function at a molecular level will help to promote proper stewardship, aid with nematicide discovery, and help to stay a step ahead of nematicide resistance. Nature Publishing Group UK 2022-06-13 /pmc/articles/PMC9192767/ /pubmed/35697824 http://dx.doi.org/10.1038/s41598-022-13815-9 Text en © This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Wram, Catherine L. Hesse, Cedar N. Zasada, Inga A. Transcriptional response of Meloidogyne incognita to non-fumigant nematicides |
title | Transcriptional response of Meloidogyne incognita to non-fumigant nematicides |
title_full | Transcriptional response of Meloidogyne incognita to non-fumigant nematicides |
title_fullStr | Transcriptional response of Meloidogyne incognita to non-fumigant nematicides |
title_full_unstemmed | Transcriptional response of Meloidogyne incognita to non-fumigant nematicides |
title_short | Transcriptional response of Meloidogyne incognita to non-fumigant nematicides |
title_sort | transcriptional response of meloidogyne incognita to non-fumigant nematicides |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9192767/ https://www.ncbi.nlm.nih.gov/pubmed/35697824 http://dx.doi.org/10.1038/s41598-022-13815-9 |
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