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dc.creatorRuiz de la Haba, Rafaeles
dc.creatorLópez Hermoso, Claraes
dc.creatorSánchez-Porro Álvarez, Cristinaes
dc.creatorVentosa Ucero, Antonioes
dc.creatorKonstantinidis, Konstantinos T.es
dc.date.accessioned2019-10-15T10:14:19Z
dc.date.available2019-10-15T10:14:19Z
dc.date.issued2019
dc.identifier.citationRuiz de la Haba, R., López Hermoso, C., Sánchez-Porro Álvarez, C., Ventosa Ucero, A. y Konstantinidis, K.T. (2019). Comparative Genomics and Phylogenomic Analysis of the Genus Salinivibrio. Frontiers in Microbiology, 10 (art. 2104), 1-15.
dc.identifier.issn1664-302Xes
dc.identifier.urihttps://hdl.handle.net/11441/89683
dc.description.abstractIn the genomic era phylogenetic relationship among prokaryotes can be inferred from the core orthologous genes (OGs) or proteins in order to elucidate their evolutionary history and current taxonomy should benefits of that. The genus Salinivibrio belongs to the family Vibrionaceae and currently includes only five halophilic species, in spite the fact that new strains are very frequently isolated from hypersaline environments. Species belonging to this genus have undergone several reclassifications and, moreover, there are many strains of Salinivibrio with available genomes which have not been affiliated to the existing species or have been wrongly designated. Therefore, a phylogenetic study using the available genomic information is necessary to clarify the relationships of existing strains within this genus and to review their taxonomic affiliation. For that purpose, we have also sequenced the first complete genome of a Salinivibrio species, Salinivibrio kushneri AL184T, which was employed as a reference to order the contigs of the draft genomes of the type strains of the current species of this genus, as well as to perform a comparative analysis with all the other available Salinivibrio sp. genomes. The genome of S. kushneri AL184T was assembled in two circular chromosomes (with sizes of 2.84 Mb and 0.60 Mb, respectively), as typically occurs in members of the family Vibrionaceae, with nine complete ribosomal operons, which might explain the fast growing rate of salinivibrios cultured under laboratory conditions. Synteny analysis among the type strains of the genus revealed a high level of genomic conservation in both chromosomes, which allow us to hypothesize a slow speciation process or homogenization events taking place in this group of microorganisms to be tested experimentally in the future. Phylogenomic and orthologous average nucleotide identity (OrthoANI)/average amino acid identity (AAI) analyses also evidenced the elevated level of genetic relatedness within members of this genus and allowed to group all the Salinivibrio strains with available genomes in seven separated species. Genome-scale attribute study of the salinivibrios identified traits related to polar flagellum, facultatively anaerobic growth and osmotic response, in accordance to the phenotypic features described for species of this genus.es
dc.description.sponsorshipSpanish Ministry of Economy and Competitiveness Project CGL2017- 83385-Pes
dc.description.sponsorshipEspaña Junta de Andalucía BIO-213es
dc.description.sponsorshipSpanish, University of Seville VIPPIT-US-2018es
dc.formatapplication/pdfes
dc.language.isoenges
dc.publisherFrontiers Mediaes
dc.relation.ispartofFrontiers in Microbiology, 10 (art. 2104), 1-15.
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectSalinivibrioes
dc.subjectSalinivibrio kushneries
dc.subjectcomplete genomees
dc.subjectphylogenomicses
dc.subjectgenomicses
dc.subjecthalophilic bacteriaes
dc.subjecthypersaline environmentses
dc.titleComparative Genomics and Phylogenomic Analysis of the Genus Salinivibrioes
dc.typeinfo:eu-repo/semantics/articlees
dcterms.identifierhttps://ror.org/03yxnpp24
dc.type.versioninfo:eu-repo/semantics/publishedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Microbiología y Parasitologíaes
dc.relation.projectIDVIPPIT-US-2018es
dc.relation.projectIDCGL2017- 83385-Pes
dc.relation.projectIDBIO-213es
dc.relation.publisherversionhttp://dx.doi.org/10.3389/fmicb.2019.02104es
dc.identifier.doi10.3389/fmicb.2019.02104es
idus.format.extent15 p.es
dc.journaltitleFrontiers in Microbiologyes
dc.publication.volumen10es
dc.publication.issueart. 2104es
dc.publication.initialPage1es
dc.publication.endPage15es

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