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Transcriptomic analyses in a benthic fish exposed to contaminated estuarine sediments through laboratory and in situ bioassays

datacite.subject.sdg14:Proteger a Vida Marinha
dc.contributor.authorCosta, Pedro M.
dc.contributor.authorMiguel, Célia
dc.contributor.authorCaeiro, Sandra
dc.contributor.authorLobo, Jorge
dc.contributor.authorMartins, Marta
dc.contributor.authorFerreira, Ana M.
dc.contributor.authorCaetano, Miguel
dc.date.accessioned2021-09-29T12:46:34Z
dc.date.available2021-09-29T12:46:34Z
dc.date.issued2011
dc.date.updated2021-09-20T09:46:56Z
dc.description.abstractThe transcription of contaminant responserelated genes was investigated in juvenile Senegalese soles exposed to sediments from three distinct sites (a reference plus two contaminated) of a Portuguese estuary (the Sado, W Portugal) through simultaneous 28-day laboratory and in situ bioassays. Transcription of cytochrome P450 1A (CYP1A), metallothionein 1 (MT1), glutathione peroxidase (GPx), catalase (CAT), caspase 3 (CASP3) and 90 kDa heat-shock protein alpha (HSP90AA) was surveyed in the liver by real-time PCR. CASP3 transcription analysis was complemented by surveying apoptosis through the TUNEL reaction. After 14 days of exposure, relative transcription was either reduced or decreased in fish exposed to the contaminated sediments, revealing a disturbance stress phase during which animals failed to respond to insult. After 28 days of exposure all genes’ transcription responded to contamination but laboratory and in situ assays depicted distinct patterns of regulation. Although sediments revealed a combination of organic and inorganic toxicants, transcription of the CYP1A gene was consistently correlated to organic contaminants. Metallothionein regulation was found correlated to metallic and organic xenobiotic contamination in the laboratory and in situ, respectively. The transcription of oxidative stress-related genes can be a good indicator of general stress but caution is mandatory when interpreting the results since regulation may be influenced by multiple factors. As for MT1, HSP90 up-regulation has potential to be a good indicator for total contamination, as well as the CASP3 gene, even though hepatocyte apoptosis depicted values inconsistent with sediment contamination, showing that programmed cell death did not directly depend on caspase transcription alone.pt_PT
dc.description.sponsorshipPOCTI/AMB 57281/104
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.doi10.1007/s10646-011-0708-zpt_PT
dc.identifier.eid2-s2.0-80054924869
dc.identifier.issn0963-9292
dc.identifier.slugcv-prod-74568
dc.identifier.urihttp://hdl.handle.net/10400.2/11147
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.subjectToxicogenomicspt_PT
dc.subjectTranscriptomicspt_PT
dc.subjectSolea senegalensispt_PT
dc.subjectQuantitative real-time RT-PCRpt_PT
dc.subjectApoptosispt_PT
dc.subjectEcological risk assessmentpt_PT
dc.titleTranscriptomic analyses in a benthic fish exposed to contaminated estuarine sediments through laboratory and in situ bioassayspt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/POSI/19815/PT
oaire.citation.endPage1764pt_PT
oaire.citation.issue8pt_PT
oaire.citation.startPage1749pt_PT
oaire.citation.titleEcotoxicologypt_PT
oaire.citation.volume20pt_PT
oaire.fundingStreamPOSI
person.familyNameCaeiro
person.familyNameCaetano
person.givenNameSandra
person.givenNameMiguel
person.identifier587808
person.identifier507243
person.identifier.ciencia-id8515-398A-D241
person.identifier.ciencia-id4F1D-56C9-BBFB
person.identifier.orcid 0000-0002-6079-3554
person.identifier.orcid0000-0001-5121-0719
person.identifier.ridK-3886-2014
person.identifier.scopus-author-id6603297853
person.identifier.scopus-author-id7003777195
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.cv.cienciaid8515-398A-D241 | SANDRA SOFIA FERREIRA DA SILVA CAEIRO
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
relation.isAuthorOfPublicatione2a8250a-8f09-4f11-a04e-1a3056644ff3
relation.isAuthorOfPublication8cf16fd9-7d07-4a51-abba-deca3df2aed2
relation.isAuthorOfPublication.latestForDiscoverye2a8250a-8f09-4f11-a04e-1a3056644ff3
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