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ESAT-6 a Major Virulence Factor of Mycobacterium tuberculosis

dc.contributor.authorAnes, Elsa
dc.contributor.authorPires, David
dc.contributor.authorMandal, Manoj
dc.contributor.authorAzevedo-Pereira, José Miguel
dc.date.accessioned2023-08-24T15:59:29Z
dc.date.available2023-08-24T15:59:29Z
dc.date.issued2023-06-09
dc.date.updated2023-06-15T13:29:51Z
dc.description.abstractMycobacterium tuberculosis (Mtb), the causative agent of human tuberculosis (TB), is one of the most successfully adapted human pathogens. Human-to-human transmission occurs at high rates through aerosols containing bacteria, but the pathogen evolved prior to the establishment of crowded populations. Mtb has developed a particular strategy to ensure persistence in the host until an opportunity for transmission arises. It has refined its lifestyle to obviate the need for virulence factors such as capsules, flagella, pili, or toxins to circumvent mucosal barriers. Instead, the pathogen uses host macrophages, where it establishes intracellular niches for its migration into the lung parenchyma and other tissues and for the induction of long-lived latency in granulomas. Finally, at the end of the infection cycle, Mtb induces necrotic cell death in macrophages to escape to the extracellular milieu and instructs a strong inflammatory response that is required for the progression from latency to disease and transmission. Common to all these events is ESAT-6, one of the major virulence factors secreted by the pathogen. This narrative review highlights the recent advances in understanding the role of ESAT-6 in hijacking macrophage function to establish successful infection and transmission and its use as a target for the development of diagnostic tools and vaccines.pt_PT
dc.description.sponsorshipThe research linked to this work was funded by Fundação para a Ciência e a Tecnologia (FCT) (grant numbers PTDC/SAU-INF/28182/2017 to E.A.; EXPL/SAU-INF/0742/2021 to D.P.; UIDB/04138/2020 to IMed-ULisboa; UIDB/04279/2020 to CIRH; and CEECINST/00070/2021 to Universidade Católica Portuguesa). M.M. is supported by a PhD fellowship from FCT with the reference 2021.07978.BD.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationAnes E, Pires D, Mandal M, Azevedo-Pereira JM. ESAT-6 a Major Virulence Factor of Mycobacterium tuberculosis. Biomolecules [Internet]. 2023 Jun 9;13(6):968. Available from: http://dx.doi.org/10.3390/biom13060968pt_PT
dc.identifier.doi10.3390/biom13060968pt_PT
dc.identifier.slugcv-prod-3286190
dc.identifier.urihttp://hdl.handle.net/10451/59007
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherMDPIpt_PT
dc.relationCEECINST/00070/2021pt_PT
dc.relationDevelopment and validation of a 3D cell culture model of the tuberculosis granuloma that can be applied for drug discovery and host cellular studies in the context of a latent infection and multicellular immunologic response.
dc.relationResearch Institute for Medicines
dc.relationCenter for Interdisciplinary Research in Health
dc.relationDeveloping host-directed-therapies for Mycobacterium tuberculosis infection and HIV co-infection based on Cystatins manipulation
dc.relation.publisherversionhttps://www.mdpi.com/2218-273X/13/6/968pt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjecttuberculosispt_PT
dc.subjectESAT-6pt_PT
dc.subjectESX-1pt_PT
dc.subjectvirulence factorspt_PT
dc.subjectPhoPR signal transductionpt_PT
dc.subjecthost-pathogen interactionspt_PT
dc.subjectTB vaccinespt_PT
dc.subjectTB diagnosispt_PT
dc.titleESAT-6 a Major Virulence Factor of Mycobacterium tuberculosispt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.awardTitleDevelopment and validation of a 3D cell culture model of the tuberculosis granuloma that can be applied for drug discovery and host cellular studies in the context of a latent infection and multicellular immunologic response.
oaire.awardTitleResearch Institute for Medicines
oaire.awardTitleCenter for Interdisciplinary Research in Health
oaire.awardTitleDeveloping host-directed-therapies for Mycobacterium tuberculosis infection and HIV co-infection based on Cystatins manipulation
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/3599-PPCDT/PTDC%2FSAU-INF%2F28182%2F2017/PT
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/3599-PPCDT/EXPL%2FSAU-INF%2F0742%2F2021/PT
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oaire.awardURIinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F04279%2F2020/PT
oaire.awardURIinfo:eu-repo/grantAgreement/FCT//2021.07978.BD/PT
oaire.citation.issue6pt_PT
oaire.citation.startPage968pt_PT
oaire.citation.titleBiomoleculespt_PT
oaire.citation.volume13pt_PT
oaire.fundingStream3599-PPCDT
oaire.fundingStream3599-PPCDT
oaire.fundingStream6817 - DCRRNI ID
oaire.fundingStream6817 - DCRRNI ID
person.familyNameRIBEIRO DOS SANTOS ANES
person.familyNameRODRIGUES PIRES
person.familyNameMandal
person.familyNameAzevedo Pereira
person.givenNameELSA MARIA
person.givenNameDAVID ALEXANDRE
person.givenNameManoj Kumar
person.givenNameJosé Miguel
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project.funder.identifierhttp://doi.org/10.13039/501100001871
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project.funder.nameFundação para a Ciência e a Tecnologia
project.funder.nameFundação para a Ciência e a Tecnologia
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project.funder.nameFundação para a Ciência e a Tecnologia
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.cv.cienciaid1A10-7DAD-D860 | ELSA MARIA RIBEIRO DOS SANTOS ANES
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
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