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Agrobacterium-mediated transformation of Guignardia citricarpa: An efficient tool to gene transfer and random mutagenesis

Authors :
Marcel Bellato Spósito
Anderson Ferreira
Léia Cecilia de Lima Fávaro
Maria Beatriz Calderan Rodrigues
Ana Paula de Souza Pallu
Fernanda Luiza de Souza Sebastianes
Welington Luiz Araújo
Aline Aparecida Pizzirani-Kleiner
Maria Juliana Calderan Rodrigues
Maria Beatriz Calderan Rodrigues, USP-ESALQ
LEIA CECILIA DE LIMA FAVARO, CNPAE
Ana Paula de Souza Pallu, USP-ESALQ
ANDERSON FERREIRA, CPAMT
Fernanda de Souza Sebastianes, USP-ESALQ
Maria Juliana Calderan Rodrigues, USP-ESALQ
Marcel Bellato Spósito, USP-ESALQ
Welington Luiz DE Araújo, UMC
Aline Aparecida Pizzirani-Kleiner, USP-ESALQ.
Source :
Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA-Alice), Empresa Brasileira de Pesquisa Agropecuária (Embrapa), instacron:EMBRAPA
Publication Year :
2013
Publisher :
Elsevier BV, 2013.

Abstract

Guignardia citricarpa is the causal agent of Citrus Black Spot (CBS), an important disease in Citriculture. Due to the expressive value of this activity worldwide, especially in Brazil, understanding more about the functioning of this fungus is of utmost relevance, making possible the elucidation of its infection mechanisms, and providing tools to control CBS. This work describes for the first time an efficient and successful methodology for genetic transformation of G. citricarpa mycelia, which generated transformants expressing the gene encoding for the gfp (green fluorescent protein) and also their interaction with citrus plant. Mycelia of G. citricarpa were transformed via Agrobacterium tumefaciens, which carried the plasmid pFAT-gfp, contains the genes for hygromycin resistance (hph) as well as gfp. The optimization of the agrotransformation protocol was performed testing different conditions (type of membrane; inductor agent concentration [acetosyringonee - AS] and cocultivation time). Results demonstrated that the best condition occurred with the utilization of cellulose?s ester membrane; 200µM of AS and 96 h as cocultivation time. High mitotic stability (82 %) was displayed by transformants using Polymerase Chain Reaction (PCR) technique to confirm the hph gene insertion. In addition, the presence of gfp was observed inside mycelia by epifluorescence optical microscopy. This technique easy visualization of the behaviour of the pathogen interacting with the plant for the first time, allowing future studies on the pathogenesis of this fungus. The establishment of a transformation method for G. citricarpa opens a range of possibilities and facilitates the study of insertional mutagenesis and genetic knockouts, in order to identify the most important genes involved in the pathogenesis mechanisms and plant-pathogen interaction. Made available in DSpace on 2017-08-10T23:53:57Z (GMT). No. of bitstreams: 1 cpamtFerreira187861462013.pdf: 2546936 bytes, checksum: 2e6c44d693e8209961e5bcc1042c2b08 (MD5) Previous issue date: 2014-02-03

Details

ISSN :
18786146
Volume :
117
Database :
OpenAIRE
Journal :
Fungal Biology
Accession number :
edsair.doi.dedup.....169de44e51886bb3391a88aa4cd807ec
Full Text :
https://doi.org/10.1016/j.funbio.2013.06.005