Distribution and Inhibition of Liposomes on Staphylococcus aureus and Pseudomonas aeruginosa Biofilm

التفاصيل البيبلوغرافية
العنوان: Distribution and Inhibition of Liposomes on Staphylococcus aureus and Pseudomonas aeruginosa Biofilm
المؤلفون: Peter-John Wormald, Nicky Thomas, Dong Dong, Benjamin Thierry, Clive A. Prestidge, Sarah Vreugde
المساهمون: Dong, Dong, Thomas, Nicky, Thierry, Benjamin, Vreugde, Sarah, Prestidge, Clive A, Wormald, Peter-John
المصدر: PLoS ONE
PLoS ONE, Vol 10, Iss 6, p e0131806 (2015)
بيانات النشر: Public Library of Science, 2015.
سنة النشر: 2015
مصطلحات موضوعية: Staphylococcus aureus, Phospholipid, lcsh:Medicine, Biology, medicine.disease_cause, Staphylococcal infections, Microbiology, ionic lipsome, chemistry.chemical_compound, medicine, Humans, Cationic liposome, Pseudomonas Infections, lcsh:Science, Phospholipids, Liposome, Multidisciplinary, Microscopy, Confocal, biofilm growth, Pseudomonas aeruginosa, Vesicle, lcsh:R, Biofilm, drug, biochemical phenomena, metabolism, and nutrition, Staphylococcal Infections, medicine.disease, Anti-Bacterial Agents, chemistry, Biofilms, Liposomes, lcsh:Q, cationic, Research Article
الوصف: Background: Staphylococcus aureus and Pseudomonas aeruginosa are major pathogens in chronic rhinosinusitis (CRS) and their biofilms have been associated with poorer post surgical outcomes. This study investigated the distribution and anti-biofilm effect of cationic (+) and anionic (-) phospholipid liposomes with different sizes (unilamellar and multilamellar vesicle, ULV and MLV respectively) on S. aureus and P. aeruginosa biofilms. Method: Specific biofilm models for S. aureus ATCC 25923 and P. aeruginosa ATCC 15692 were established. Liposomal distribution was determined by observing SYTO9 stained biofilm exposed to DiI labeled liposomes using confocal scanning laser microscopy, followed by quantitative image analysis. The anti-biofilm efficacy study was carried out by using the alamarBlue assay to test the relative viability of biofilm treated with various liposomes for 24 hours and five minutes. Results: The smaller ULVs penetrated better than larger MLVs in both S. aureus and P. aeruginosa biofilm. Except that +ULV and –ULV displayed similar distribution in S. aureus biofilm, the cationic liposomes adhered better than their anionic counterparts. Biofilm growth was inhibited at 24-hour and five-minute exposure time, although the decrease of viability for P. aeruginosa biofilm after liposomal treatment did not reach statistical significance. Conclusion: The distribution and anti-biofilm effects of cationic and anionic liposomes of different sizes differed in S. aureus and P. aeruginosa biofilms. Reducing the liposome size and formulating liposomes as positively charged enhanced the penetration and inhibition of S. aureus and P. aeruginosa biofilms. Refereed/Peer-reviewed
اللغة: English
تدمد: 1932-6203
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d405518a951b540f07f0e76ae9171f8cTest
http://europepmc.org/articles/PMC4488362Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....d405518a951b540f07f0e76ae9171f8c
قاعدة البيانات: OpenAIRE