Publication:
Global assessment of small RNAs reveals a non-coding transcript involved in biofilm formation and attachment in Acinetobacter baumannii ATCC 17978

dc.contributor.authorÁlvarez-Fraga, Laura
dc.contributor.authorRumbo-Feal, Soraya
dc.contributor.authorPerez, Astrid
dc.contributor.authorGomez, Manuel J
dc.contributor.authorGayoso, Carmen
dc.contributor.authorVallejo, Juan A.
dc.contributor.authorOhneck, Emily J.
dc.contributor.authorValle, Jaione
dc.contributor.authorActis, Luis A.
dc.contributor.authorBeceiro, Alejandro
dc.contributor.authorBou, Germán
dc.contributor.authorPoza, Margarita
dc.contributor.funderInstituto de Salud Carlos III
dc.contributor.funderMinisterio de Economía y Competitividad (España)
dc.contributor.funderSociedad Española de Enfermedades Infecciosas y Microbiología Clínica
dc.contributor.funderSocietat Catalana de Malalties Infeccioses i Microbiologia Clínica
dc.date.accessioned2017-10-20T10:23:10Z
dc.date.available2017-10-20T10:23:10Z
dc.date.issued2017
dc.description.abstractMany strains of Acinetobacter baumannii have been described as being able to form biofilm. Small non-coding RNAs (sRNAs) control gene expression in many regulatory circuits in bacteria. The aim of the present work was to provide a global description of the sRNAs produced both by planktonic and biofilm-associated (sessile) cells of A. baumannii ATCC 17978, and to compare the corresponding gene expression profiles to identify sRNAs molecules associated to biofilm formation and virulence. sRNA was extracted from both planktonic and sessile cells and reverse transcribed. cDNA was subjected to 454-pyrosequencing using the GS-FLX Titanium chemistry. The global analysis of the small RNA transcriptome revealed different sRNA expression patterns in planktonic and biofilm associated cells, with some of the transcripts only expressed or repressed in sessile bacteria. A total of 255 sRNAs were detected, with 185 of them differentially expressed in the different types of cells. A total of 9 sRNAs were expressed only in biofilm cells, while the expression of other 21 coding regions were repressed only in biofilm cells. Strikingly, the expression level of the sRNA 13573 was 120 times higher in biofilms than in planktonic cells, an observation that prompted us to further investigate the biological role of this non-coding transcript. Analyses of an isogenic mutant and over-expressing strains revealed that the sRNA 13573 gene is involved in biofilm formation and attachment to A549 human alveolar epithelial cells. The present work serves as a basis for future studies examining the complex regulatory network that regulate biofilm biogenesis and attachment to eukaryotic cells in A. baumannii ATCC 17978.
dc.description.peerreviewed
dc.description.sponsorshipThis work has been funded by Projects PI12/00552 and PI15/00860 to GB, PI11/01034 to MP, CP13/00226 to AB, and P14/000059 to MP and AB, all integrated in the National Plan for Scientific Research, Development and Technological Innovation 2013-2016 and funded by the ISCIII - General Subdirection of Assessment and Promotion of the Research European Regional Development Fund (FEDER) A way of making Europe. Miami University Research Funds from the department of Microbiology supported this work. We also want to thank the Spanish Network for Research in Infectious Diseases (REIPI RD12/0015/0014 to GB), co-financed by the European Development Regional Fund (EDRF) A Way to Achieve Europe, Instituto de Salud Carlos III, Subdireccion General de Redes y Centros de Investigacion Cooperativa, Ministerio de Economia y Competitividad as well as Sociedad Espanola de Enfermedades Infecciosas y Microbiologia Clinica (SEIMC). A.P. was financially supported by the Galician Plan for Research, Innovation and Growth (I2C Plan 2012-2016). J.A. Vallejo was financially supported by the Sara Borrell Programme (ISCIII, Spain CD13/00373). S. Rumbo-Feal was financially supported by the Agusti Pumarola Grant (Societat Catalana de Malalties Infeccioses i Microbiologia Clinica, SCMIMC) and Sociedad Espanola de Enfermedades Infecciosas y Microbiologia Clinica (SEIMC).; This work has been funded by Projects PI12/00552 and PI15/00860 to GB, PI11/01034 to MP, CP13/00226 to AB, and P14/000059 to MP and AB, all integrated in the National Plan for Scientific Research, Development and Technological Innovation 2013-2016 and funded by the ISCIII General Subdirection of Assessment and Promotion of the Research European Regional Development Fund (FEDER) ``A way of making Europe. Miami University Research Funds from the department of Microbiology supported this work. We also want to thank the Spanish Network for Research in Infectious Diseases (REIPI RD12/0015/0014 to GB), co financed by the European Development Regional Fund (EDRF) ``A Way to Achieve Europe, Instituto de Salud Carlos III, Subdireccion General de Redes y Centros de InvestigaciOn Cooperativa, Ministerio de Economia y Competitividad as well as Sociedad Espanola de Enfermedades Infecciosas y Microbiologia Clinica (SEIMC). A.P. was financially supported by the Galician Plan for Research, Innovation and Growth (12C Plan 2012-2016). J.A. Vallejo was financially supported by the Sara Borrell Programme (ISCIII, Spain CD13/00373). S. RumboFeal was financially supported by the Agusti Pumarola Grant (Societat Catalana de Malalties Infeccioses i Microbiologia Clinica, SCMIMC) and Sociedad Espanola de Enfermedades Infecciosas y Microbiologia Clinica (SEIMC). Finally, we thank Chua Kim Lee (University of Singapore) for providing pMo130-Te1<SUP>R</SUP>.
dc.format.volume12
dc.identifierISI:000406766500039
dc.identifier.citationPLoS One. 2017; 12(8):e0182084
dc.identifier.doi10.1371/journal.pone.0182084
dc.identifier.issn1932-6203
dc.identifier.journalPlos One
dc.identifier.pubmedID28763494
dc.identifier.urihttp://hdl.handle.net/20.500.12105/5103
dc.language.isoeng
dc.publisherPublic Library of Science (PLOS)
dc.relation.publisherversionhttps://doi.org/10.1371/journal.pone.0182084
dc.repisalud.institucionCNIC
dc.repisalud.orgCNICCNIC::Unidades técnicas::Bioinformática
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectSMALL REGULATORY RNAS
dc.subjectGENOME-WIDE IDENTIFICATION
dc.subjectSOLUBLE-RNAS
dc.subjectESCHERICHIA-COLI
dc.subjectPSEUDOMONAS-AERUGINOSA
dc.subjectBACTERIAL BIOFILMS
dc.subjectABIOTIC SURFACES
dc.subjectVIBRIO-CHOLERAE
dc.subjectLIFE-STYLE
dc.subjectVIRULENCE
dc.titleGlobal assessment of small RNAs reveals a non-coding transcript involved in biofilm formation and attachment in Acinetobacter baumannii ATCC 17978
dc.typeresearch article
dc.type.hasVersionVoR
dspace.entity.typePublication
relation.isAuthorOfPublicationa743c6ea-9abf-445b-9abd-b257dee0f6f9
relation.isAuthorOfPublication.latestForDiscoverya743c6ea-9abf-445b-9abd-b257dee0f6f9

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