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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Veröffentlicht in:PloS one 2013-12, Vol.8 (12), p.e85364-e85364
Hauptverfasser: 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
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container_issue 12
container_start_page e85364
container_title PloS one
container_volume 8
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.
doi_str_mv 10.1371/journal.pone.0085364
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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. 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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. 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Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Meteorological &amp; Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Advanced Technologies &amp; Aerospace Database</collection><collection>ProQuest Advanced Technologies &amp; Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Antonino de Souza Júnior, José Dijair</au><au>Ramos Coelho, Roberta</au><au>Tristan Lourenço, 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>
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1932-6203
language eng
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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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