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The type III effectors HsvG and HsvB of gall‐forming Pantoea agglomerans determine host specificity and function as transcriptional activators
Author(s) -
Nissan Gal,
ManulisSasson Shulamit,
Weinthal Dan,
Mor Henia,
Sessa Guido,
Barash Isaac
Publication year - 2006
Publication title -
molecular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 247
eISSN - 1365-2958
pISSN - 0950-382X
DOI - 10.1111/j.1365-2958.2006.05301.x
Subject(s) - biology , pantoea agglomerans , effector , microbiology and biotechnology , plasmid , type three secretion system , genetics , bacteria , virulence , gene
Summary Pantoea agglomerans pv. gypsophilae ( Pag ) elicits galls on gypsophila and a hypersensitive response on beet, whereas P. agglomerans pv. betae ( Pab ) induces galls on both beet and gypsophila. The pathogenicity of both pathovars is dependent on the presence of a plasmid harbouring type III secretion system (TTSS) components and effectors. The HsvG TTSS effectors of Pag (HsvG‐ Pag ) and Pab (HsvG‐ Pab ) determine the host specificity of both pathovars on gypsophila. Here we describe a novel HsvG homologue, HsvB, which determines the host specificity of Pag and Pab on beet. HsvG requires two direct amino acid repeats for pathogenicity on gypsophila, whereas one repeat in HsvB is sufficient for pathogenicity on beet. Exchanging repeats between HsvG‐ Pag and HsvB‐ Pab resulted in a switch of host specificities. Transient expression of GFP–HsvG or GFP–HsvB fusions in gypsophila, beet or melon leaves showed that HsvG and HsvB were localized to the nuclei of host and non‐host plants. A yeast one‐hybrid assay revealed that a single repeat of HsvG or HsvB was sufficient to activate transcription. By employing random binding‐site selection and gel‐shift assay HsvG was demonstrated to be a double‐stranded DNA‐binding protein with an ACACC/aAA consensus binding site. These results suggest that HsvG and HsvB are host‐specificity determinants and bear the potential to affect the host transcriptional machinery.