Knocking-down Meloidogyne incognita proteases by plant-delivered dsRNA has negative pleiotropic effect on nematode vigor
The root-knot nematode Meloidogyne incognita causes serious damage and yield losses in numerous important crops worldwide. Analysis of the M. incognita genome revealed a vast number of proteases belonging to five different catalytic classes. Several reports indicate that M. incognita proteases could...
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creator | Antonino de Souza Júnior, José Dijair Ramos Coelho, Roberta Tristan Lourenço, Isabela da Rocha Fragoso, Rodrigo Barbosa Viana, Antonio Américo Lima Pepino de Macedo, Leonardo Mattar da Silva, Maria Cristina Gomes Carneiro, Regina Maria Engler, Gilbert de Almeida-Engler, Janice Grossi-de-Sa, Maria Fatima |
description | The root-knot nematode Meloidogyne incognita causes serious damage and yield losses in numerous important crops worldwide. Analysis of the M. incognita genome revealed a vast number of proteases belonging to five different catalytic classes. Several reports indicate that M. incognita proteases could play important roles in nematode parasitism, besides their function in ordinary digestion of giant cell contents for feeding. The precise roles of these proteins during parasitism however are still unknown, making them interesting targets for gene silencing to address protein function. In this study we have knocked-down an aspartic (Mi-asp-1), a serine (Mi-ser-1) and a cysteine protease (Mi-cpl-1) by RNAi interference to get an insight into the function of these enzymes during a host/nematode interaction. Tobacco lines expressing dsRNA for Mi-ser-1 (dsSER), Mi-cpl-1 (dsCPL) and for the three genes together (dsFusion) were generated. Histological analysis of galls did not show clear differences in giant cell morphology. Interestingly, nematodes that infected plants expressing dsRNA for proteases produced a reduced number of eggs. In addition, nematode progeny matured in dsSER plants had reduced success in egg hatching, while progeny resulting from dsCPL and dsFusion plants were less successful to infect wild-type host plants. Quantitative PCR analysis confirmed a reduction in transcripts for Mi-cpl-1 and Mi-ser-1 proteases. Our results indicate that these proteases are possibly involved in different processes throughout nematode development, like nutrition, reproduction and embryogenesis. A better understanding of nematode proteases and their possible role during a plant-nematode interaction might help to develop new tools for phytonematode control. |
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Analysis of the M. incognita genome revealed a vast number of proteases belonging to five different catalytic classes. Several reports indicate that M. incognita proteases could play important roles in nematode parasitism, besides their function in ordinary digestion of giant cell contents for feeding. The precise roles of these proteins during parasitism however are still unknown, making them interesting targets for gene silencing to address protein function. In this study we have knocked-down an aspartic (Mi-asp-1), a serine (Mi-ser-1) and a cysteine protease (Mi-cpl-1) by RNAi interference to get an insight into the function of these enzymes during a host/nematode interaction. Tobacco lines expressing dsRNA for Mi-ser-1 (dsSER), Mi-cpl-1 (dsCPL) and for the three genes together (dsFusion) were generated. Histological analysis of galls did not show clear differences in giant cell morphology. Interestingly, nematodes that infected plants expressing dsRNA for proteases produced a reduced number of eggs. In addition, nematode progeny matured in dsSER plants had reduced success in egg hatching, while progeny resulting from dsCPL and dsFusion plants were less successful to infect wild-type host plants. Quantitative PCR analysis confirmed a reduction in transcripts for Mi-cpl-1 and Mi-ser-1 proteases. Our results indicate that these proteases are possibly involved in different processes throughout nematode development, like nutrition, reproduction and embryogenesis. A better understanding of nematode proteases and their possible role during a plant-nematode interaction might help to develop new tools for phytonematode control.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0085364</identifier><identifier>PMID: 24392004</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animals ; Base Sequence ; Biology ; Catalysis ; Cell division ; Cell morphology ; Computer Simulation ; Cysteine proteinase ; Cytology ; Double-stranded RNA ; Eggs ; Embryogenesis ; Embryonic growth stage ; Environmental Sciences ; Enzymes ; Expressed Sequence Tags ; Female ; Galls ; Gene expression ; Gene Knockdown Techniques ; Gene silencing ; Genomes ; Hatching ; Host plants ; Life Sciences ; Meloidogyne incognita ; Nematodes ; Nicotiana - genetics ; Nutrition ; Offspring ; Ovum - growth & development ; Ovum - metabolism ; Parasites ; Parasitism ; Peptide Hydrolases - deficiency ; Peptide Hydrolases - genetics ; Plants, Genetically Modified ; Progeny ; Proteins ; RNA Interference ; RNA, Double-Stranded - genetics ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; RNA-mediated interference ; Serine ; Tobacco ; Tylenchoidea - enzymology ; Tylenchoidea - genetics ; Tylenchoidea - growth & development ; Tylenchoidea - physiology ; Vigor</subject><ispartof>PloS one, 2013-12, Vol.8 (12), p.e85364-e85364</ispartof><rights>2013 Antonino de Souza Júnior et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>2013 Antonino de Souza Júnior et al 2013 Antonino de Souza Júnior et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c560t-f8132ae2d21dda14bd6bec2ec819865503aa04451efbabb621ea1a88b11ba4ed3</citedby><cites>FETCH-LOGICAL-c560t-f8132ae2d21dda14bd6bec2ec819865503aa04451efbabb621ea1a88b11ba4ed3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3877404/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3877404/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79342,79343</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24392004$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.inrae.fr/hal-02647616$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Antonino de Souza Júnior, José Dijair</creatorcontrib><creatorcontrib>Ramos Coelho, Roberta</creatorcontrib><creatorcontrib>Tristan Lourenço, Isabela</creatorcontrib><creatorcontrib>da Rocha Fragoso, Rodrigo</creatorcontrib><creatorcontrib>Barbosa Viana, Antonio Américo</creatorcontrib><creatorcontrib>Lima Pepino de Macedo, Leonardo</creatorcontrib><creatorcontrib>Mattar da Silva, Maria Cristina</creatorcontrib><creatorcontrib>Gomes Carneiro, Regina Maria</creatorcontrib><creatorcontrib>Engler, Gilbert</creatorcontrib><creatorcontrib>de Almeida-Engler, Janice</creatorcontrib><creatorcontrib>Grossi-de-Sa, Maria Fatima</creatorcontrib><title>Knocking-down Meloidogyne incognita proteases by plant-delivered dsRNA has negative pleiotropic effect on nematode vigor</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>The root-knot nematode Meloidogyne incognita causes serious damage and yield losses in numerous important crops worldwide. Analysis of the M. incognita genome revealed a vast number of proteases belonging to five different catalytic classes. Several reports indicate that M. incognita proteases could play important roles in nematode parasitism, besides their function in ordinary digestion of giant cell contents for feeding. The precise roles of these proteins during parasitism however are still unknown, making them interesting targets for gene silencing to address protein function. In this study we have knocked-down an aspartic (Mi-asp-1), a serine (Mi-ser-1) and a cysteine protease (Mi-cpl-1) by RNAi interference to get an insight into the function of these enzymes during a host/nematode interaction. Tobacco lines expressing dsRNA for Mi-ser-1 (dsSER), Mi-cpl-1 (dsCPL) and for the three genes together (dsFusion) were generated. Histological analysis of galls did not show clear differences in giant cell morphology. Interestingly, nematodes that infected plants expressing dsRNA for proteases produced a reduced number of eggs. In addition, nematode progeny matured in dsSER plants had reduced success in egg hatching, while progeny resulting from dsCPL and dsFusion plants were less successful to infect wild-type host plants. Quantitative PCR analysis confirmed a reduction in transcripts for Mi-cpl-1 and Mi-ser-1 proteases. Our results indicate that these proteases are possibly involved in different processes throughout nematode development, like nutrition, reproduction and embryogenesis. A better understanding of nematode proteases and their possible role during a plant-nematode interaction might help to develop new tools for phytonematode control.</description><subject>Animals</subject><subject>Base Sequence</subject><subject>Biology</subject><subject>Catalysis</subject><subject>Cell division</subject><subject>Cell morphology</subject><subject>Computer Simulation</subject><subject>Cysteine proteinase</subject><subject>Cytology</subject><subject>Double-stranded RNA</subject><subject>Eggs</subject><subject>Embryogenesis</subject><subject>Embryonic growth stage</subject><subject>Environmental Sciences</subject><subject>Enzymes</subject><subject>Expressed Sequence Tags</subject><subject>Female</subject><subject>Galls</subject><subject>Gene expression</subject><subject>Gene Knockdown Techniques</subject><subject>Gene silencing</subject><subject>Genomes</subject><subject>Hatching</subject><subject>Host plants</subject><subject>Life Sciences</subject><subject>Meloidogyne incognita</subject><subject>Nematodes</subject><subject>Nicotiana - genetics</subject><subject>Nutrition</subject><subject>Offspring</subject><subject>Ovum - growth & development</subject><subject>Ovum - metabolism</subject><subject>Parasites</subject><subject>Parasitism</subject><subject>Peptide Hydrolases - deficiency</subject><subject>Peptide Hydrolases - genetics</subject><subject>Plants, Genetically Modified</subject><subject>Progeny</subject><subject>Proteins</subject><subject>RNA Interference</subject><subject>RNA, Double-Stranded - genetics</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>RNA-mediated interference</subject><subject>Serine</subject><subject>Tobacco</subject><subject>Tylenchoidea - enzymology</subject><subject>Tylenchoidea - genetics</subject><subject>Tylenchoidea - growth & development</subject><subject>Tylenchoidea - 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Isabela</au><au>da Rocha Fragoso, Rodrigo</au><au>Barbosa Viana, Antonio Américo</au><au>Lima Pepino de Macedo, Leonardo</au><au>Mattar da Silva, Maria Cristina</au><au>Gomes Carneiro, Regina Maria</au><au>Engler, Gilbert</au><au>de Almeida-Engler, Janice</au><au>Grossi-de-Sa, Maria Fatima</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Knocking-down Meloidogyne incognita proteases by plant-delivered dsRNA has negative pleiotropic effect on nematode vigor</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2013-12-31</date><risdate>2013</risdate><volume>8</volume><issue>12</issue><spage>e85364</spage><epage>e85364</epage><pages>e85364-e85364</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>The root-knot nematode Meloidogyne incognita causes serious damage and yield losses in numerous important crops worldwide. Analysis of the M. incognita genome revealed a vast number of proteases belonging to five different catalytic classes. Several reports indicate that M. incognita proteases could play important roles in nematode parasitism, besides their function in ordinary digestion of giant cell contents for feeding. The precise roles of these proteins during parasitism however are still unknown, making them interesting targets for gene silencing to address protein function. In this study we have knocked-down an aspartic (Mi-asp-1), a serine (Mi-ser-1) and a cysteine protease (Mi-cpl-1) by RNAi interference to get an insight into the function of these enzymes during a host/nematode interaction. Tobacco lines expressing dsRNA for Mi-ser-1 (dsSER), Mi-cpl-1 (dsCPL) and for the three genes together (dsFusion) were generated. Histological analysis of galls did not show clear differences in giant cell morphology. Interestingly, nematodes that infected plants expressing dsRNA for proteases produced a reduced number of eggs. In addition, nematode progeny matured in dsSER plants had reduced success in egg hatching, while progeny resulting from dsCPL and dsFusion plants were less successful to infect wild-type host plants. Quantitative PCR analysis confirmed a reduction in transcripts for Mi-cpl-1 and Mi-ser-1 proteases. Our results indicate that these proteases are possibly involved in different processes throughout nematode development, like nutrition, reproduction and embryogenesis. A better understanding of nematode proteases and their possible role during a plant-nematode interaction might help to develop new tools for phytonematode control.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>24392004</pmid><doi>10.1371/journal.pone.0085364</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2013-12, Vol.8 (12), p.e85364-e85364 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_1473341975 |
source | MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Free Full-Text Journals in Chemistry; Public Library of Science (PLoS) |
subjects | Animals Base Sequence Biology Catalysis Cell division Cell morphology Computer Simulation Cysteine proteinase Cytology Double-stranded RNA Eggs Embryogenesis Embryonic growth stage Environmental Sciences Enzymes Expressed Sequence Tags Female Galls Gene expression Gene Knockdown Techniques Gene silencing Genomes Hatching Host plants Life Sciences Meloidogyne incognita Nematodes Nicotiana - genetics Nutrition Offspring Ovum - growth & development Ovum - metabolism Parasites Parasitism Peptide Hydrolases - deficiency Peptide Hydrolases - genetics Plants, Genetically Modified Progeny Proteins RNA Interference RNA, Double-Stranded - genetics RNA, Messenger - genetics RNA, Messenger - metabolism RNA-mediated interference Serine Tobacco Tylenchoidea - enzymology Tylenchoidea - genetics Tylenchoidea - growth & development Tylenchoidea - physiology Vigor |
title | Knocking-down Meloidogyne incognita proteases by plant-delivered dsRNA has negative pleiotropic effect on nematode vigor |
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