Publication:
Bacteriophages Improve Outcome in Experimental Staphylococcus Aureus Ventilator Associated Pneumonia.

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cris.virtualsource.author-orcide59e23e5-2f23-4a72-8f6f-29f09044000d
datacite.rightsopen.access
dc.contributor.authorPrazak, Josef
dc.contributor.authorIten, Manuela
dc.contributor.authorCameron, David Robert
dc.contributor.authorSave, Jonathan Florian
dc.contributor.authorGrandgirard, Denis
dc.contributor.authorResch, Gregory
dc.contributor.authorGöpfert, Christine
dc.contributor.authorLeib, Stephen
dc.contributor.authorTakala, Jukka
dc.contributor.authorJakob, Stephan
dc.contributor.authorQue, Yok-Ai
dc.contributor.authorHänggi, Matthias
dc.date.accessioned2024-10-28T17:09:27Z
dc.date.available2024-10-28T17:09:27Z
dc.date.issued2019-11-01
dc.description.abstractRATIONALE Infections caused by multidrug resistant bacteria are a major clinical challenge. Phage therapy is a promising alternative antibacterial strategy. OBJECTIVE To evaluate the efficacy of intravenous phage therapy for the treatment of ventilator associated pneumonia due to methicillin-resistant Staphylococcus aureus in rats. METHODS A randomized blinded controlled experimental study compared intravenous teicoplanin (3mg/kg, n=12), a cocktail of four phages (2-3 x 10^9 plaque forming units/ml of 2003, 2002, 3A and K, n=12) and combination of both (n=11), given two, 12 and 24 hours after induction of pneumonia, then once daily for four days. The primary outcome was survival at day four. Secondary outcomes were bacterial and phage densities in lungs and spleen, histopathological scoring of infection within the lungs and inflammatory biomarkers in blood. MEASUREMENTS AND MAIN RESULTS Treatment with either phages or teicoplanin increased survival from 0% to 58% and 50% respectively (p<0.005). Combination of phage with antibiotics did not further improve outcome (45% survival). Animal survival correlated with reduced bacterial burden in the lung (1.2 x 10^6 CFU/g of tissue for survivors versus 1.2 x 10^9 CFU/g for non-surviving animals, p<0.0001), as well as improved histopathological outcomes. Phage multiplication within the lung occurred during treatment. IL-1β increased for all treatment groups over the course of therapy. CONCLUSIONS Phage therapy was as effective as teicoplanin in improving survival and decreasing bacterial load within the lungs of rats infected with methicillin-resistant S. aureus. Combining antibiotics with phage therapy did not further improve outcomes. Key Words: bacteriophage; antibiotic resistance, microbial; pneumonia, ventilator associated.
dc.description.numberOfPages8
dc.description.sponsorshipUniversitätsklinik für Intensivmedizin
dc.description.sponsorshipInstitut für Infektionskrankheiten
dc.description.sponsorshipInstitut für Tierpathologie (ITPA)
dc.identifier.doi10.7892/boris.132564
dc.identifier.pmid31260638
dc.identifier.publisherDOI10.1164/rccm.201812-2372OC
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/181647
dc.language.isoen
dc.publisherAmerican Lung Association
dc.relation.ispartofAmerican journal of respiratory and critical care medicine
dc.relation.issn1073-449X
dc.relation.organizationDCD5A442C072E17DE0405C82790C4DE2
dc.relation.organizationDCD5A442BD12E17DE0405C82790C4DE2
dc.relation.organizationDCD5A442BADDE17DE0405C82790C4DE2
dc.subjectbacteriophage; antibiotic resistance
dc.subjectmicrobial; pneumonia
dc.subjectventilator associated
dc.subject.ddc600 - Technology::630 - Agriculture
dc.subject.ddc500 - Science::570 - Life sciences; biology
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleBacteriophages Improve Outcome in Experimental Staphylococcus Aureus Ventilator Associated Pneumonia.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.endPage1133
oaire.citation.issue9
oaire.citation.startPage1126
oaire.citation.volume200
oairecerif.author.affiliationUniversitätsklinik für Intensivmedizin
oairecerif.author.affiliationUniversitätsklinik für Intensivmedizin
oairecerif.author.affiliationUniversitätsklinik für Intensivmedizin
oairecerif.author.affiliationUniversitätsklinik für Intensivmedizin
oairecerif.author.affiliationInstitut für Infektionskrankheiten
oairecerif.author.affiliationInstitut für Tierpathologie (ITPA)
oairecerif.author.affiliationInstitut für Infektionskrankheiten
oairecerif.author.affiliationUniversitätsklinik für Intensivmedizin
oairecerif.author.affiliationUniversitätsklinik für Intensivmedizin
oairecerif.author.affiliationUniversitätsklinik für Intensivmedizin
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unibe.date.embargoChanged2020-07-02 00:30:06
unibe.date.licenseChanged2019-10-23 14:24:01
unibe.description.ispublishedpub
unibe.eprints.legacyId132564
unibe.journal.abbrevTitleAM J RESP CRIT CARE MED
unibe.refereedtrue
unibe.subtype.articlejournal

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