Cargando…

Water Stress Differentially Modulates the Expression of Tomato Cell Wall Metabolism-Related Genes in Meloidogyne incognita Feeding Sites

Microscopic observations and transcriptomic RNA-Seq analyses were applied to investigate the effect of water stress during the formation of tomato galls formation 1 and 2 weeks after inoculation with the root-knot nematode Meloidogyne incognita. Water stress affected root growth and the nematode abi...

Descripción completa

Detalles Bibliográficos
Autores principales: Veronico, Pasqua, Rosso, Laura Cristina, Melillo, Maria Teresa, Fanelli, Elena, De Luca, Francesca, Ciancio, Aurelio, Colagiero, Mariantonietta, Pentimone, Isabella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9051518/
https://www.ncbi.nlm.nih.gov/pubmed/35498686
http://dx.doi.org/10.3389/fpls.2022.817185
_version_ 1784696576014286848
author Veronico, Pasqua
Rosso, Laura Cristina
Melillo, Maria Teresa
Fanelli, Elena
De Luca, Francesca
Ciancio, Aurelio
Colagiero, Mariantonietta
Pentimone, Isabella
author_facet Veronico, Pasqua
Rosso, Laura Cristina
Melillo, Maria Teresa
Fanelli, Elena
De Luca, Francesca
Ciancio, Aurelio
Colagiero, Mariantonietta
Pentimone, Isabella
author_sort Veronico, Pasqua
collection PubMed
description Microscopic observations and transcriptomic RNA-Seq analyses were applied to investigate the effect of water stress during the formation of tomato galls formation 1 and 2 weeks after inoculation with the root-knot nematode Meloidogyne incognita. Water stress affected root growth and the nematode ability to mount an efficient parasitism. The effects of water stress on the feeding site development were already observed at 1 week after nematode inoculation, with smaller giant cells, delayed development, and thinner cell walls. These features suggested changes in the expression levels of genes involved in the feeding site formation and maintenance. Gene Ontology (GO) enrichment and expression patterns were used to characterize differentially expressed genes. Water stress modified the expression profile of genes involved in the synthesis, degradation, and remodeling of the cell wall during the development of nematode feeding site. A comparison of gene expression with unstressed galls revealed that water stress intensified the up or downregulation of most genes. However, it particularly influenced the expression pattern of expansin A11 (Solyc04g081870.4.1), expansin-like B1(Solyc08g077910.3.1), a pectin acetylesterase (Solyc08g005800.4.1), and the pectin methylesterase pmeu1 (Solyc03g123630.4.1) which were upregulated in unstressed galls and repressed by water stress, at both sampling times. The expression of most members of the genes involved in cell wall metabolism, i.e., those coding for Csl, fasciclin, and COBRA proteins, were negatively influenced. Interestingly, alteration in the expression profiles of most dirigent protein genes (DIRs) and upregulation of five gene coding for Casparian strip domain protein (CASP)-like proteins were found. Gene expression analysis of galls from water stressed plants allowed us to better understand the molecular basis of M. incognita parasitism in tomato. Specific genes, including those involved in regulation of cellulose synthesis and lignification process, require further study to develop defense strategies against root-knot nematodes.
format Online
Article
Text
id pubmed-9051518
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-90515182022-04-30 Water Stress Differentially Modulates the Expression of Tomato Cell Wall Metabolism-Related Genes in Meloidogyne incognita Feeding Sites Veronico, Pasqua Rosso, Laura Cristina Melillo, Maria Teresa Fanelli, Elena De Luca, Francesca Ciancio, Aurelio Colagiero, Mariantonietta Pentimone, Isabella Front Plant Sci Plant Science Microscopic observations and transcriptomic RNA-Seq analyses were applied to investigate the effect of water stress during the formation of tomato galls formation 1 and 2 weeks after inoculation with the root-knot nematode Meloidogyne incognita. Water stress affected root growth and the nematode ability to mount an efficient parasitism. The effects of water stress on the feeding site development were already observed at 1 week after nematode inoculation, with smaller giant cells, delayed development, and thinner cell walls. These features suggested changes in the expression levels of genes involved in the feeding site formation and maintenance. Gene Ontology (GO) enrichment and expression patterns were used to characterize differentially expressed genes. Water stress modified the expression profile of genes involved in the synthesis, degradation, and remodeling of the cell wall during the development of nematode feeding site. A comparison of gene expression with unstressed galls revealed that water stress intensified the up or downregulation of most genes. However, it particularly influenced the expression pattern of expansin A11 (Solyc04g081870.4.1), expansin-like B1(Solyc08g077910.3.1), a pectin acetylesterase (Solyc08g005800.4.1), and the pectin methylesterase pmeu1 (Solyc03g123630.4.1) which were upregulated in unstressed galls and repressed by water stress, at both sampling times. The expression of most members of the genes involved in cell wall metabolism, i.e., those coding for Csl, fasciclin, and COBRA proteins, were negatively influenced. Interestingly, alteration in the expression profiles of most dirigent protein genes (DIRs) and upregulation of five gene coding for Casparian strip domain protein (CASP)-like proteins were found. Gene expression analysis of galls from water stressed plants allowed us to better understand the molecular basis of M. incognita parasitism in tomato. Specific genes, including those involved in regulation of cellulose synthesis and lignification process, require further study to develop defense strategies against root-knot nematodes. Frontiers Media S.A. 2022-04-15 /pmc/articles/PMC9051518/ /pubmed/35498686 http://dx.doi.org/10.3389/fpls.2022.817185 Text en Copyright © 2022 Veronico, Rosso, Melillo, Fanelli, De Luca, Ciancio, Colagiero and Pentimone. 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 Plant Science
Veronico, Pasqua
Rosso, Laura Cristina
Melillo, Maria Teresa
Fanelli, Elena
De Luca, Francesca
Ciancio, Aurelio
Colagiero, Mariantonietta
Pentimone, Isabella
Water Stress Differentially Modulates the Expression of Tomato Cell Wall Metabolism-Related Genes in Meloidogyne incognita Feeding Sites
title Water Stress Differentially Modulates the Expression of Tomato Cell Wall Metabolism-Related Genes in Meloidogyne incognita Feeding Sites
title_full Water Stress Differentially Modulates the Expression of Tomato Cell Wall Metabolism-Related Genes in Meloidogyne incognita Feeding Sites
title_fullStr Water Stress Differentially Modulates the Expression of Tomato Cell Wall Metabolism-Related Genes in Meloidogyne incognita Feeding Sites
title_full_unstemmed Water Stress Differentially Modulates the Expression of Tomato Cell Wall Metabolism-Related Genes in Meloidogyne incognita Feeding Sites
title_short Water Stress Differentially Modulates the Expression of Tomato Cell Wall Metabolism-Related Genes in Meloidogyne incognita Feeding Sites
title_sort water stress differentially modulates the expression of tomato cell wall metabolism-related genes in meloidogyne incognita feeding sites
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9051518/
https://www.ncbi.nlm.nih.gov/pubmed/35498686
http://dx.doi.org/10.3389/fpls.2022.817185
work_keys_str_mv AT veronicopasqua waterstressdifferentiallymodulatestheexpressionoftomatocellwallmetabolismrelatedgenesinmeloidogyneincognitafeedingsites
AT rossolauracristina waterstressdifferentiallymodulatestheexpressionoftomatocellwallmetabolismrelatedgenesinmeloidogyneincognitafeedingsites
AT melillomariateresa waterstressdifferentiallymodulatestheexpressionoftomatocellwallmetabolismrelatedgenesinmeloidogyneincognitafeedingsites
AT fanellielena waterstressdifferentiallymodulatestheexpressionoftomatocellwallmetabolismrelatedgenesinmeloidogyneincognitafeedingsites
AT delucafrancesca waterstressdifferentiallymodulatestheexpressionoftomatocellwallmetabolismrelatedgenesinmeloidogyneincognitafeedingsites
AT ciancioaurelio waterstressdifferentiallymodulatestheexpressionoftomatocellwallmetabolismrelatedgenesinmeloidogyneincognitafeedingsites
AT colagieromariantonietta waterstressdifferentiallymodulatestheexpressionoftomatocellwallmetabolismrelatedgenesinmeloidogyneincognitafeedingsites
AT pentimoneisabella waterstressdifferentiallymodulatestheexpressionoftomatocellwallmetabolismrelatedgenesinmeloidogyneincognitafeedingsites