Comparative genomics of the type VI secretion systems of Pantoea and Erwinia species reveals the presence of putative effector islands that may be translocated by the VgrG and Hcp proteins

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dc.contributor.author De Maayer, Pieter
dc.contributor.author Venter, S.N. (Stephanus Nicolaas)
dc.contributor.author Kamber, Tim
dc.contributor.author Duffy, Brion
dc.contributor.author Coutinho, Teresa A.
dc.contributor.author Smits, Theo H.M.
dc.date.accessioned 2012-01-12T12:02:37Z
dc.date.available 2012-01-12T12:02:37Z
dc.date.issued 2011
dc.description.abstract BACKGROUND: The Type VI secretion apparatus is assembled by a conserved set of proteins encoded within a distinct locus. The putative effector proteins Hcp and VgrG are also encoded within these loci. We have identified numerous distinct Type VI secretion system (T6SS) loci in the genomes of several ecologically diverse Pantoea and Erwinia species and detected the presence of putative effector islands associated with the hcp and vgrG genes. RESULTS: Between two and four T6SS loci occur among the Pantoea and Erwinia species. While two of the loci (T6SS-1 and T6SS-2) are well conserved among the various strains, the third (T6SS-3) locus is not universally distributed. Additional orthologous loci are present in Pantoea sp. aB-valens and Erwinia billingiae Eb661. Comparative analysis of the T6SS-1 and T6SS-3 loci showed non-conserved islands associated with the vgrG and hcp, and vgrG genes, respectively. These regions had a G+C content far lower than the conserved portions of the loci. Many of the proteins encoded within the hcp and vgrG islands carry conserved domains, which suggests they may serve as effector proteins for the T6SS. A number of the proteins also show homology to the C-terminal extensions of evolved VgrG proteins. CONCLUSIONS: Extensive diversity was observed in the number and content of the T6SS loci among the Pantoea and Erwinia species. Genomic islands could be observed within some of T6SS loci, which are associated with the hcp and vgrG proteins and carry putative effector domain proteins. We propose new hypotheses concerning a role for these islands in the acquisition of T6SS effectors and the development of novel evolved VgrG and Hcp proteins. en
dc.description.librarian nf2012 en
dc.description.sponsorship This study was partially supported by the National Research Foundation (NRF), the Tree Protection Co-operative Programme (TPCP), the NRF/Dept. of Science and Technology Centre of Excellence in Tree Health Biotechnology (CTHB), and the THRIP support program of the Department of Trade and Industry, South Africa, the Swiss Federal Office for Agriculture (BLW Fire Blight Research - Pathogen), and the Swiss Secretariat for Education and Research (SBF C07.0038). It was conducted within the European Science Foundation funded research network COST Action 864 and the Swiss ProfiCrops program. en_US
dc.description.uri http://www.biomedcentral.com/1471-2164/12/576 en_US
dc.identifier.citation De Maayer et al.: Comparative genomics of the type VI secretion systems of Pantoea and Erwinia species reveals the presence of putative effector islands that may be translocated by the VgrG and Hcp proteins. BMC Genomics 2011 12:576. en
dc.identifier.issn 1471-2172
dc.identifier.other 10.1186/1471-2164-12-576
dc.identifier.uri http://hdl.handle.net/2263/17767
dc.language.iso en en_US
dc.publisher BioMed Central en_US
dc.rights © 2011 De Maayer et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. en
dc.subject VgrG and Hcp proteins en
dc.subject Type VI secretion system (T6SS) en
dc.subject Pantoea en
dc.subject.lcsh Comparative genomics en
dc.subject.lcsh Erwinia en
dc.title Comparative genomics of the type VI secretion systems of Pantoea and Erwinia species reveals the presence of putative effector islands that may be translocated by the VgrG and Hcp proteins en
dc.type Article en


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