Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/61313

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dc.contributor.authorOliveira, Hugo Alexandre Mendespor
dc.contributor.authorCosta, Ana Rita Martinspor
dc.contributor.authorFerreira, Alice Maria Fernandespor
dc.contributor.authorKonstantinides, Nicopor
dc.contributor.authorSantos, Sílvio Roberto Brancopor
dc.contributor.authorBoon, Maartenpor
dc.contributor.authorNoben, Jean-Paulpor
dc.contributor.authorLavigne, Robpor
dc.contributor.authorAzeredo, Joanapor
dc.date.accessioned2019-09-04T13:34:03Z-
dc.date.available2019-09-04T13:34:03Z-
dc.date.issued2019-
dc.identifier.citationOliveira, Hugo; Costa, Ana Rita; Ferreira, A.; Konstantinidis, Nico; Santos, Sílvio B.; Boon, Maarten; Noben, Jean-Paul; Lavigne, Rob; Azeredo, Joana, Functional analysis and antivirulence properties of a new depolymerase from a myovirus that infects Acinetobacter baumannii capsule K45. Journal of Virology, 93(4), e01163-18, 2019por
dc.identifier.issn0022-538Xpor
dc.identifier.urihttps://hdl.handle.net/1822/61313-
dc.description.abstractAcinetobacter baumannii is an important pathogen causative of healthcare-associated infections and is able to rapidly develop resistance to all known antibiotics including colistin. As an alternative therapeutic agent, we have isolated a novel myovirus (vB_AbM_B9) which specifically infects and makes lysis from without in strains of the K45 and K30 capsule type, respectively. Phage B9 has a genome of 93,641 bp and encodes 167 predicted proteins, of which 29 were identified by mass spectrometry. This phage holds a capsule depolymerase (B9gp69) able to digest extracted exopolysaccharides of both K30 and K45 strains and that remains active in a wide range of pH values (5 to 9), ionic strengths (0 to 500 mM), and temperatures (20 to 80\textdegreeC). B9gp69 demonstrated to be non-toxic in a cell line model of the human lung, and to make the K45 strain fully susceptible to serum killing in vitro. Contrary to the phage, no resistance development was observed by bacteria targeted with the B9gp69. Therefore, capsular depolymerases may represent attractive antimicrobial agents against A. baumannii infections.IMPORTANCE Currently, phage therapy has revived interest for controlling hard-to-treat bacterial infections. Acinetobacter baumannii is an emerging Gram-negative pathogen able to cause a variety of nosocomial infections. Additionally, this species is becoming more resistant to several classes of antibiotics. Herein, we describe the isolation of a novel lytic myophage B9 and its recombinant depolymerase. While the phage can be a promising alternative antibacterial agent, its success in the market will ultimately depend on new regulatory frameworks and general public acceptance. We therefore characterised the phage-encoded depolymerase which is a natural enzyme that can be more easily managed and used. To our knowledge, the therapeutic potential of phage depolymerase against A. baumannii is still unknown. We show for the first time that K45 capsule type is an important virulence factor of A. baumannii and that capsule removal via the recombinant depolymerase activity helps the host immune system to combat the bacterial infection.por
dc.description.sponsorshipThis study was supported by the Portuguese Foundation for Science and Technology (FCT) under the scope of the strategic funding of UID/BIO/04469/2013 unit, COMPETE 2020 (POCI-01-0145-FEDER-006684) and the Projects PTDC/BBB-BSS/ 6471/2014 (POCI-01-0145-FEDER-016678) and PTDC/CVT-CVT/29628/2017 (POCI-01- 0145-FEDER-029628). This work was also supported by the BioTecNorte operation (NORTE-01-0145-FEDER-000004) funded by the European Regional Development Fund under the scope of Norte2020—Programa Operacional Regional do Norte. H.O. and A.R.C. acknowledge FCT for grants SFRH/BPD/111653/2015 and SFRH/BPD/ 94648/2013, respectively. Support from Hercules Foundation project R-3986 for J.-P.N. is also acknowledged. The work of R.L. and M.B. was supported by a GOA grant from KU Leuven. J.-P.N. acknowledges the support of Hercules Foundation project R-3986.por
dc.language.isoengpor
dc.publisherAmerican Society for Microbiology (ASM)por
dc.relationinfo:eu-repo/grantAgreement/FCT/5876/147337/PTpor
dc.rightsopenAccesspor
dc.subjectAcinetobacter baumanniipor
dc.subjectAntivirulencepor
dc.subjectBacteriophagepor
dc.subjectDepolymerasepor
dc.titleFunctional analysis and antivirulence properties of a new depolymerase from a myovirus that infects Acinetobacter baumannii capsule K45por
dc.typearticle-
dc.peerreviewedyespor
dc.relation.publisherversionhttps://jvi.asm.org/por
dc.commentsCEB49262por
oaire.citationStartPagee01163-18 (1)por
oaire.citationEndPagee01163-18 (16)por
oaire.citationIssue4por
oaire.citationVolume93por
dc.date.updated2019-09-04T09:10:54Z-
dc.identifier.eissn1098-5514por
dc.identifier.doi10.1128/JVI.01163-18por
dc.identifier.pmid30463964por
dc.description.publicationversioninfo:eu-repo/semantics/publishedVersion-
dc.subject.wosScience & Technologypor
sdum.journalJournal of Virologypor
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