Author
Listed:
- Edvige Gambino
(Department of Biology, University of Naples “Federico II”, 80126 Naples, Italy
These authors contributed equally to this work.)
- Angela Maione
(Department of Biology, University of Naples “Federico II”, 80126 Naples, Italy
These authors contributed equally to this work.)
- Marco Guida
(Department of Biology, University of Naples “Federico II”, 80126 Naples, Italy)
- Luisa Albarano
(Department of Biology, University of Naples “Federico II”, 80126 Naples, Italy)
- Federica Carraturo
(Department of Biology, University of Naples “Federico II”, 80126 Naples, Italy)
- Emilia Galdiero
(Department of Biology, University of Naples “Federico II”, 80126 Naples, Italy)
- Valeria Di Onofrio
(Department of Sciences and Technologies, University of Naples “Parthenope”, 80143 Naples, Italy)
Abstract
Background: Biofilms have been found growing on implantable medical devices. This can lead to persistent clinical infections. The highly antibiotic-resistant property of biofilms necessitates the search for both potent antimicrobial agents and novel antibiofilm strategies. Natural product-based anti-biofilm agents were found to be as efficient as chemically synthesized counterparts with fewer side effects. In the present study, the effects of limonene as an antibiofilm agent were evaluated on Pseudomonas aeruginosa and Staphylococcus aureus biofilm formed on different surfaces using the CDC model system in continuous flow. The flgK gene and the pilA gene expression in P. aeruginosa, and the icaA gene and eno gene in S. aureus, which could be considered as efficient resistance markers, were studied. Methods: Mono- and dual-species biofilms were grown on polycarbonate, polypropylene, and stainless-steel coupons in a CDC biofilm reactor (Biosurface Technologies, Bozeman, MT, USA). To evaluate the ability of limonene to inhibit and eradicate biofilm, a sub-MIC concentration (10 mL/L) was tested. The gene expression of P. aeruginosa and S. aureus was detected by SYBR Green quantitative Real-Time PCR assay (Meridiana Bioline, Brisbane, Australia). Results: The limonene added during the formation of biofilms at sub-MIC concentrations works very well in inhibiting biofilms on all three materials, reducing their growth by about 2 logs. Of the same order of magnitude is the ability of limonene to eradicate both mono- and polymicrobial mature biofilms on all three materials. Greater efficacy was observed in the polymicrobial biofilm on steel coupons. The expression of some genes related to the virulence of the two microorganisms was differently detected in mono- and polymicrobial biofilm. Conclusions: These data showed that the limonene treatment expressed different levels of biofilm-forming genes, especially when both types of strains alone and together grew on different surfaces. Our findings showed that limonene treatment is also very efficient when biofilm has been grown under shear stress causing significant and irreversible damage to the biofilm structure. The effectiveness of the sanitation procedures can be optimized by applying antimicrobial combinations with natural compounds (e.g., limonene).
Suggested Citation
Edvige Gambino & Angela Maione & Marco Guida & Luisa Albarano & Federica Carraturo & Emilia Galdiero & Valeria Di Onofrio, 2022.
"Evaluation of the Pathogenic-Mixed Biofilm Formation of Pseudomonas aeruginosa / Staphylococcus aureus and Treatment with Limonene on Three Different Materials by a Dynamic Model,"
IJERPH, MDPI, vol. 19(6), pages 1-12, March.
Handle:
RePEc:gam:jijerp:v:19:y:2022:i:6:p:3741-:d:776162
Download full text from publisher
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:gam:jijerp:v:19:y:2022:i:6:p:3741-:d:776162. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: MDPI Indexing Manager (email available below). General contact details of provider: https://www.mdpi.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.