Affiliation:
1. Laboratory of Pharmaceutical Microbiology, Ghent University, Ghent, Belgium
2. Laboratory of Pharmaceutical Microbiology, Istanbul University, Istanbul, Turkey
Abstract
ABSTRACT
In young cystic fibrosis (CF) patients,
Staphylococcus aureus
is typically the most prevalent organism, while in adults,
Pseudomonas aeruginosa
is the major pathogen. More recently, it was observed that also
Streptococcus anginosus
plays an important role in exacerbations of respiratory symptoms. These species are often coisolated from CF lungs, yet little is known about whether antibiotic killing of one species is influenced by the presence of others. In the present study, we compared the activities of various antibiotics against
S. anginosus
,
S. aureus
, and
P. aeruginosa
when grown in monospecies biofilms with the activity observed in a multispecies biofilm. Our results show that differences in antibiotic activity against species grown in mono- and multispecies biofilms are species and antibiotic dependent. Fewer
S. anginosus
cells are killed by antibiotics that interfere with cell wall synthesis (amoxicillin plus sulbactam, cefepime, imipenem, meropenem, and vancomycin) in the presence of
S. aureus
and
P. aeruginosa
, while for ciprofloxacin, levofloxacin, and tobramycin, no difference was observed. In addition, we observed that the cell-free supernatant of
S. aureus
, but not that of
P. aeruginosa
biofilms, also caused this decrease in killing. Overall,
S. aureus
was more affected by antibiotic treatment in a multispecies biofilm, while for
P. aeruginosa
, no differences were observed between growth in mono- or multispecies biofilms. The results of the present study suggest that it is important to take the community composition into account when evaluating the effect of antimicrobial treatments against certain species in mixed biofilms.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
43 articles.
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