Publication:
The mangotoxin biosynthetic operon (mbo) is specifically distributed within Pseudomonas syringae genomospecies 1 and was acquired only once during evolution

Consultable a partir de

Date

2013

Authors

Carrión, Víctor J.
Gutiérrez Barranquero, José Antonio
Arrebola, Eva
Codina, Juan Carlos
Vicente, Antonio de
Cazorla, Francisco M.

Director

Publisher

American Society for Microbiology
Acceso abierto / Sarbide irekia
Artículo / Artikulua
Versión publicada / Argitaratu den bertsioa

Project identifier

ES/6PN/AGL2008-55311

Abstract

Mangotoxin production was first described in Pseudomonas syringae pv. syringae strains. A phenotypic characterization of 94 P. syringae strains was carried out to determine the genetic evolution of the mangotoxin biosynthetic operon (mbo). We designed a PCR primer pair specific for the mbo operon to examine its distribution within the P. syringae complex. These primers amplified a 692-bp DNA fragment from 52 mangotoxin-producing strains and from 7 non-mangotoxin-producing strains that harbor the mbo operon, whereas 35 non-mangotoxin-producing strains did not yield any amplification. This, together with the analysis of draft genomes, allowed the identification of the mbo operon in five pathovars (pathovars aptata, avellanae, japonica, pisi, and syringae), all of which belong to genomospecies 1, suggesting a limited distribution of the mbo genes in the P. syringae complex. Phylogenetic analyses using partial sequences from housekeeping genes differentiated three groups within genomospecies 1. All of the strains containing the mbo operon clustered in groups I and II, whereas those lacking the operon clustered in group III; however, the relative branching order of these three groups is dependent on the genes used to construct the phylogeny. The mbo operon maintains synteny and is inserted in the same genomic location, with high sequence conservation around the insertion point, for all the strains in groups I and II. These data support the idea that the mbo operon was acquired horizontally and only once by the ancestor of groups I and II from genomospecies 1 within the P. syringae complex.

Keywords

Mangotoxin, Phylogeny, Diagnostic PCR, Antimetabolite toxins, Virulence, Mango apical necrosis, Lateral gene transfer

Department

Producción Agraria / Nekazaritza Ekoizpena

Faculty/School

Degree

Doctorate program

Editor version

Funding entities

This work was supported by grants from the regional government of Andalucía (Spain), grants from CICE-Junta de Andalucía, Ayudas Grupo PAIDI AGR-169, and Proyecto de Excelencia (P07-AGR-02471) and Plan Nacional IDI grant AGL2008-55311-CO2-01 (Ministerio de Ciencia e Innovación), cofinanced by FEDER (European Union). Plan Propio of the University of Málaga funded a stay by V.J.C. at the Universidad Pública de Navarra, Spain.

© 2013 American Society for Microbiology. All Rights Reserved

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