cris.boxmetadata.label.title
Direct analysis of bacterial viability in endotracheal tube biofilm from a pig model of methicillin-resistant Staphylococcus aureus pneumonia following antimicrobial therapy
cris.boxmetadata.label.dateissued
01 browse.startsWith.months.july 2012
cris.boxmetadata.label.accesslevel
metadata only access
cris.boxmetadata.label.resourcetype
journal article
cris.boxmetadata.label.authors
Fernández-Barat L.
Li Bassi G.
Ferrer M.
Bosch A.
Calvo M.
Vila J.
Gabarrús A.
Martínez-Olondris P.
Rigol M.
Esperatti M.
Torres A.
Instituto del Tórax
cris.boxmetadata.label.abstract
Confocal laser scanning microscopy (CLSM) helps to observe the biofilms formed in the endotracheal tube (ETT) of ventilated subjects and to determine its structure and bacterial viability using specific dyes. We compared the effect of three different treatments (placebo, linezolid, and vancomycin) on the bacterial biofilm viability captured by CLSM. Eight pigs with pneumonia induced by methicillin-resistant Staphylococcus aureus (MRSA) were ventilated up to 96 h and treated with linezolid, vancomycin, or placebo (controls). ETT images were microscopically examined after staining with the live/dead® BacLight™ Kit (Invitrogen, Barcelona, Spain) with a confocal laser scanning microscope. We analyzed 127 images obtained by CLSM. The median ratio of live/dead bacteria was 0.51, 0.74, and 1 for the linezolid, vancomycin, and control groups, respectively (P = 0.002 for the three groups); this ratio was significantly lower for the linezolid group, compared with the control group (P = 0.001). Images showed bacterial biofilm attached and non-attached to the ETT surface but growing within secretions accumulated inside ETT. Systemic treatment with linezolid is associated with a higher proportion of dead bacteria in the ETT biofilm of animals with MRSA pneumonia. Biofilm clusters not necessarily attach to the ETT surface. © 2012 Federation of European Microbiological Societies.
cris.boxmetadata.label.citationstartpage
309
cris.boxmetadata.label.citationendpage
317
cris.boxmetadata.label.volume
65
cris.boxmetadata.label.issue
2
cris.boxmetadata.label.language
English
cris.boxmetadata.label.ocdeknowledgeArea
Sistema respiratorio
cris.boxmetadata.label.doi
cris.boxmetadata.label.scopusidentifier
2-s2.0-84862688730
cris.boxmetadata.label.pubmedidentifier
cris.boxmetadata.label.source
FEMS Immunology and Medical Microbiology
cris.boxmetadata.label.containerissn
1574695X
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