Literature DB >> 21421371

Ectopic expression of a Meloidogyne incognita dorsal gland protein in tobacco accelerates the formation of the nematode feeding site.

Djair Dos Santos de Lima e Souza1, José Dijair Antonino de Souza, Maíra Grossi-de-Sá, Thales Lima Rocha, Rodrigo da Rocha Fragoso, Aulus Estevão Anjos de Deus Barbosa, Gustavo Ramos de Oliveira, Erich Yukio Tempel Nakasu, Bruna Araújo de Sousa, Natália Faustino Pires, Diva Maria de Alencar Dusi, Regina Maria Dechechi Gomes Carneiro, Eduardo Romano, Janice de Almeida-Engler, Gilbert Engler, Cezar Martins-de-Sá, Maria Fátima Grossi-de-Sá.   

Abstract

Meloidogyne spp., plant-parasitic nematodes present worldwide, are intensively studied because of the damage caused to a large variety of agronomically important crops. Several reports indicate that proteins from the Meloidogyne spp. dorsal gland might play an important role to allow proper establishment of a functional nematode feeding site. The precise role of these proteins in the process of feeding cell development is unknown. To gain insights into the function of these secreted M. incognita proteins, we constitutively (ectopically) expressed the nematodes dorsal gland protein 7E12 in tobacco plants. It was found that the number of galls at 8 and 16 days after nematode infection was significantly higher in transgenic plants compared to control plants. Eggs from nematodes in transgenic plants hatched faster than those in control plants. Histological analysis of nematode induced galls in transgenic plants clearly shows a different morphology. Giant feeding cells harbor more vacuoles and an increased amount of cell wall invaginations, while neighboring cells surrounding feeding cells are more numerous. These results suggest that the presence of the 7E12 protein in tobacco accelerates gall formation. This assumption is supported by our data illustrating faster gall formation and egg eclosion in transgenic plants.
Copyright © 2010 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 21421371     DOI: 10.1016/j.plantsci.2010.09.003

Source DB:  PubMed          Journal:  Plant Sci        ISSN: 0168-9452            Impact factor:   4.729


  5 in total

1.  Knocking-down Meloidogyne incognita proteases by plant-delivered dsRNA has negative pleiotropic effect on nematode vigor.

Authors:  José Dijair Antonino de Souza Júnior; Roberta Ramos Coelho; Isabela Tristan Lourenço; Rodrigo da Rocha Fragoso; Antonio Américo Barbosa Viana; Leonardo Lima Pepino de Macedo; Maria Cristina Mattar da Silva; Regina Maria Gomes Carneiro; Gilbert Engler; Janice de Almeida-Engler; Maria Fatima Grossi-de-Sa
Journal:  PLoS One       Date:  2013-12-31       Impact factor: 3.240

2.  Life-stage specific transcriptomes of a migratory endoparasitic plant nematode, Radopholus similis elucidate a different parasitic and life strategy of plant parasitic nematodes.

Authors:  Xin Huang; Chun-Ling Xu; Si-Hua Yang; Jun-Yi Li; Hong-Le Wang; Zi-Xu Zhang; Chun Chen; Hui Xie
Journal:  Sci Rep       Date:  2019-04-18       Impact factor: 4.379

Review 3.  Effectors of Root-Knot Nematodes: An Arsenal for Successful Parasitism.

Authors:  Shounak Jagdale; Uma Rao; Ashok P Giri
Journal:  Front Plant Sci       Date:  2021-12-22       Impact factor: 5.753

Review 4.  Identification and functional analysis of secreted effectors from phytoparasitic nematodes.

Authors:  Sajid Rehman; Vijai K Gupta; Aakash K Goyal
Journal:  BMC Microbiol       Date:  2016-03-21       Impact factor: 3.605

5.  The root-knot nematode effector MiPFN3 disrupts plant actin filaments and promotes parasitism.

Authors:  Natthanon Leelarasamee; Lei Zhang; Cynthia Gleason
Journal:  PLoS Pathog       Date:  2018-03-15       Impact factor: 6.823

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.