Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/105238
DC FieldValueLanguage
dc.contributor.authorFerreira, Carolina-
dc.contributor.authorViana, Sofia D.-
dc.contributor.authorReis, Flávio-
dc.date.accessioned2023-02-10T10:19:44Z-
dc.date.available2023-02-10T10:19:44Z-
dc.date.issued2020-12-28-
dc.identifier.issn2076-2607pt
dc.identifier.urihttps://hdl.handle.net/10316/105238-
dc.description.abstractThe scientific knowledge already attained regarding the way severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infects human cells and the clinical manifestations and consequences for Coronavirus Disease 2019 (COVID-19) patients, especially the most severe cases, brought gut microbiota into the discussion. It has been suggested that intestinal microflora composition plays a role in this disease because of the following: (i) its relevance to an efficient immune system response; (ii) the fact that 5-10% of the patients present gastrointestinal symptoms; and (iii) because it is modulated by intestinal angiotensin-converting enzyme 2 (ACE2) (which is the virus receptor). In addition, it is known that the most severely affected patients (those who stay longer in hospital, who require intensive care, and who eventually die) are older people with pre-existing cardiovascular, metabolic, renal, and pulmonary diseases, the same people in which the prevalence of gut microflora dysbiosis is higher. The COVID-19 patients presenting poor outcomes are also those in which the immune system's hyperresponsiveness and a severe inflammatory condition (collectively referred as "cytokine storm") are particularly evident, and have been associated with impaired microbiota phenotype. In this article, we present the evidence existing thus far that may suggest an association between intestinal microbiota composition and the susceptibility of some patients to progress to severe stages of the disease.pt
dc.language.isoengpt
dc.publisherMDPI AGpt
dc.relationUIDP/04539/2020pt
dc.relationPTDC/SAU-NUT/31712/2017pt
dc.relationCENTRO-01-0145-FEDER-000012-HealthyAging2020pt
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UID/NEU/04539/2019/PTpt
dc.relationPTDC/SAU-NUT/31712/2017pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectCOVID-19pt
dc.subjectsusceptibility to progresspt
dc.subjectgutmicrobiota dysbiosispt
dc.subjectimmune responsept
dc.subjectinflammationpt
dc.titleIs Gut Microbiota Dysbiosis a Predictor of Increased Susceptibility to Poor Outcome of COVID-19 Patients? An Updatept
dc.typearticle-
degois.publication.firstPage53pt
degois.publication.issue1pt
degois.publication.titleMicroorganismspt
dc.peerreviewedyespt
dc.identifier.doi10.3390/microorganisms9010053pt
degois.publication.volume9pt
dc.date.embargo2020-12-28*
uc.date.periodoEmbargo0pt
item.fulltextCom Texto completo-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
item.openairetypearticle-
item.cerifentitytypePublications-
item.grantfulltextopen-
crisitem.project.grantnoCenter for Innovative Biomedicine and Biotechnology-
crisitem.project.grantnoCNC. IBILI-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.orcid0000-0002-1316-1319-
crisitem.author.orcid0000-0003-3401-9554-
Appears in Collections:FMUC Medicina - Artigos em Revistas Internacionais
I&D CIBB - Artigos em Revistas Internacionais
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