Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/2363
Title: Patterns of biofilm structure and formation kinetics among Acinetobacter baumannii clinical isolates with different antibiotic resistance profiles
Authors: Dahdouh, Elias
Orgaz, Belen
Gómez-Gil, Rosa
Mingorance, Jesús
Daoud, Ziad
Suarez, Monica
San Jose, Carmen
Affiliations: Faculty of Medicine 
Issue Date: 2016
Part of: Journal of medicinal chemistry communication
Volume: 7
Start page: 157
End page: 163
Abstract: 
Acinetobacter baumannii is a ubiquitous organism that has been involved in a wide range of nosocomial infections. Its ability to produce biofilms, among other characteristics, allows it to persist in hospitals for prolonged periods. In this study, in order to check the possible relationship between its resistance to different antibiotics and its ability to form biofilms on inert surfaces, the rate of biofilm formation as well as siderophore production and detection of OmpA and CsuE by PCR were investigated for 12 A. baumannii clinical isolates. The biofilms were cultured at 37 °C on steel coupons immersed in BHI broth and the attached viable cells were counted after 5, 24 and 48 h. Confocal Laser Scanning Microscopy (CLSM) images were obtained for some of the strains that were noted to produce a brown pigment. The biofilm volume and substratum coverage were estimated with an image analysis software program. Our data, though preliminary, show that the quicker biofilm formers were strains susceptible to aminoglycosides, whereas the biofilms providing thicker and more uniform surface coverage were produced by carbapenem-resistant strains, producing a brown pigment with a plausible siderophore role. Further investigation into a wider set of isolates could help better understand the relationship between biofilm formation and various clinical findings.
URI: https://scholarhub.balamand.edu.lb/handle/uob/2363
Open URL: Link to full text
Type: Journal Article
Appears in Collections:Faculty of Medicine

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