TY - JOUR
T1 - Staphylococcus aureus strains exhibit heterogenous tolerance to direct cold atmospheric plasma therapy
AU - Baz, Abdullah
AU - Bakri, Ahmed
AU - Butcher, Mark
AU - Short, Bryn
AU - Ghimire, Bhagirath
AU - Gaur, Nishtha
AU - Jenkins, Toby
AU - Short, Robert D.
AU - Riggio, Marcello
AU - Williams, Craig
AU - Ramage, Gordon
AU - Brown, Jason L.
N1 - Funding Information:
The authors acknowledge funding from Engineering and Physical Sciences Research Council (EPSRC) for supporting this project ( EP/V005839/1 ). In addition, authors would like to thank GlaxoSmithKline Consumer Healthcare and the BBSRC Industrial GlaxoSmithKline CASE PhD studentship for Mark C. Butcher ( BB/V509541/1 ), the King AbdulAziz University, Saudi Arabia , and Ministry of Health of Malaysia, Malaysia for funding Abdullah Baz and Ahmed Bakri, respectively. The authors would also like to extend their gratitude to the Glasgow Imaging Facility, and especially Margaret Mullin for her continued help and support with the processing and imaging of the biofilm samples for scanning electron microscopy. Finally, a thank you to Dr Joey Shepherd, University of Sheffield, for generously providing the S. aureus SH1000 strain.
Data availability
Data will be made available on request.
PY - 2023/4/15
Y1 - 2023/4/15
N2 - The global clinical and socioeconomic impact of chronic wounds is substantial. The main difficulty that clinicians face during the treatment of chronic wounds is the risk of infection at the wound site. Infected wounds arise from an accumulation of microbial aggregates in the wound bed, leading to the formation of polymicrobial biofilms that can be largely resistant to antibiotic therapy. Therefore, it is essential for studies to identify novel therapeutics to alleviate biofilm infections. One innovative technique is the use of cold atmospheric plasma (CAP) which has been shown to possess promising antimicrobial and immunomodulatory properties. Here, different clinically relevant biofilm models will be treated with cold atmospheric plasma to assess its efficacy and killing effects. Biofilm viability was assessed using live dead qPCR, and morphological changes associated with CAP evaluated using scanning electron microscopy (SEM). Results indicated that CAP was effective against Candida albicans and Pseudomonas aeruginosa, both as mono-species biofilms and when grown in a triadic model system. CAP also significantly reduced viability in the nosocomial pathogen, Candida auris. Staphylococcus aureus Newman exhibited a level of tolerance to CAP therapy, both when grown alone or in the triadic model when grown alongside C. albicans and P. aeruginosa. However, this degree of tolerance exhibited by S. aureus was strain dependent. At a microscopic level, biofilm treatment led to subtle changes in morphology in the susceptible biofilms, with evidence of cellular deflation and shrinkage. Taken together, these results indicate a promising application of direct CAP therapy in combatting wound and skin-related biofilm infections, although biofilm composition may affect the treatment efficacy.
AB - The global clinical and socioeconomic impact of chronic wounds is substantial. The main difficulty that clinicians face during the treatment of chronic wounds is the risk of infection at the wound site. Infected wounds arise from an accumulation of microbial aggregates in the wound bed, leading to the formation of polymicrobial biofilms that can be largely resistant to antibiotic therapy. Therefore, it is essential for studies to identify novel therapeutics to alleviate biofilm infections. One innovative technique is the use of cold atmospheric plasma (CAP) which has been shown to possess promising antimicrobial and immunomodulatory properties. Here, different clinically relevant biofilm models will be treated with cold atmospheric plasma to assess its efficacy and killing effects. Biofilm viability was assessed using live dead qPCR, and morphological changes associated with CAP evaluated using scanning electron microscopy (SEM). Results indicated that CAP was effective against Candida albicans and Pseudomonas aeruginosa, both as mono-species biofilms and when grown in a triadic model system. CAP also significantly reduced viability in the nosocomial pathogen, Candida auris. Staphylococcus aureus Newman exhibited a level of tolerance to CAP therapy, both when grown alone or in the triadic model when grown alongside C. albicans and P. aeruginosa. However, this degree of tolerance exhibited by S. aureus was strain dependent. At a microscopic level, biofilm treatment led to subtle changes in morphology in the susceptible biofilms, with evidence of cellular deflation and shrinkage. Taken together, these results indicate a promising application of direct CAP therapy in combatting wound and skin-related biofilm infections, although biofilm composition may affect the treatment efficacy.
KW - Biofilm
KW - Candida albicans
KW - Candida auris
KW - Cold atmospheric plasma
KW - Heterogeneity
KW - Pseudomonas aeruginosa
KW - Staphylococcus aureus
KW - Tolerance
UR - http://www.scopus.com/inward/record.url?scp=85153104255&partnerID=8YFLogxK
U2 - 10.1016/j.bioflm.2023.100123
DO - 10.1016/j.bioflm.2023.100123
M3 - Article
AN - SCOPUS:85153104255
SN - 2590-2075
VL - 5
JO - Biofilm
JF - Biofilm
M1 - 100123
ER -