Proteomic analysis of the food spoiler Pseudomonas fluorescens ITEM 17298 reveals the antibiofilm activity of the pepsin-digested bovine lactoferrin

2019 ◽  
Vol 82 ◽  
pp. 177-193 ◽  
Author(s):  
Laura Quintieri ◽  
Daniela Zühlke ◽  
Francesca Fanelli ◽  
Leonardo Caputo ◽  
Vania Cosma Liuzzi ◽  
...  
2020 ◽  
Vol 21 (22) ◽  
pp. 8526
Author(s):  
Angela Di Somma ◽  
Federica Recupido ◽  
Arianna Cirillo ◽  
Alessia Romano ◽  
Alessandra Romanelli ◽  
...  

Biofilms consist of a complex microbial community adhering to biotic or abiotic surfaces and enclosed within a protein/polysaccharide self-produced matrix. The formation of this structure represents the most important adaptive mechanism that leads to antibacterial resistance, and therefore, closely connected to pathogenicity. Antimicrobial peptides (AMPs) could represent attractive candidates for the design of new antibiotics because of their specific characteristics. AMPs show a broad activity spectrum, a relative selectivity towards their targets (microbial membranes), the ability to act on both proliferative and quiescent cells, a rapid mechanism of action, and above all, a low propensity for developing resistance. This article investigates the effect at subMIC concentrations of Temporin-L (TL) on biofilm formation in Pseudomonas fluorescens (P. fluorescens) both in static and dynamic conditions, showing that TL displays antibiofilm properties. Biofilm formation in static conditions was analyzed by the Crystal Violet assay. Investigation of biofilms in dynamic conditions was performed in a commercial microfluidic device consisting of a microflow chamber to simulate real flow conditions in the human body. Biofilm morphology was examined using Confocal Laser Scanning Microscopy and quantified via image analysis. The investigation of TL effects on P. fluorescens showed that when subMIC concentrations of this peptide were added during bacterial growth, TL exerted antibiofilm activity, impairing biofilm formation both in static and dynamic conditions. Moreover, TL also affects mature biofilm as confocal microscopy analyses showed that a large portion of preformed biofilm architecture was clearly perturbed by the peptide addition with a significative decrease of all the biofilm surface properties and the overall biomass. Finally, in these conditions, TL did not affect bacterial cells as the live/dead cell ratio remained unchanged without any increase in damaged cells, confirming an actual antibiofilm activity of the peptide.


2020 ◽  
Author(s):  
Arianna Cirillo ◽  
Angela Di Somma ◽  
Alessia Romano ◽  
Federica Recupido ◽  
Sergio Caserta ◽  
...  

<p>Introduction</p> <p>Biofilm consists of a complex self-produced matrix of polysaccharides, DNA and proteins that </p> <p>protects bacteria from the environment including the host immune system and constitutes the main</p> <p>cause of bacterial resistance against antibiotics. Research is then focused on finding alternative </p> <p>antimicrobial substances able to either hamper biofilm formation or to prevent bacterial growth. </p> <p>Recently, we showed that the antimicrobial peptide Temporin-L impairs E.coli growth by inhibiting </p> <p>cell division (Di Somma et al.; 2020; BBA). Here we investigate the effect of Temporin-L (TL) on </p> <p>biofilm formation in Pseudomonas fluorescens (P. fluorescens) both in static and dynamic conditions, </p> <p>showing that TL displays antibiofilm properties. </p> <p>Materials and methods</p> <p>Biofilm formation in static conditions was performed on coverslips and analyzed by the Crystal Violet </p> <p>assay. Biofilm morphology was assessed using imaging techniques. Investigation of biofilms in </p> <p>dynamic conditions was performed in a flow chamber using a microfluidic system and images were </p> <p>recorded by confocal microscopy.</p> <p>Results</p> <p>The P. fluorescens cells were either grown in the presence of TL or incubated with the antimicrobial </p> <p>peptide after biofilm formation both in static and dynamic conditions using different concentrations </p> <p>of the peptide. When TL was added during cell growth, the peptide affected biofilm formation at 25 </p> <p>µM. Confocal microscopy demonstrated that at this concentration P. fluorescens cells were still alive</p> <p>but a clear disruption of the biofilm architecture was observed. These results had to be ascribed to a </p> <p>specific antibiofilm effect of TL. At 100 µM TL antibiofilm activity biofilm thickness was nearly </p> <p>negligible. </p> <p>When P. fluorescens cells were treated with TL following biofilm formation, confocal images </p> <p>demonstrated that the peptide exerted a strong antibiofilm effect leading to cell detachment and </p> <p>disruption the biofilm architecture. </p> <p>Discussion and Conclusions </p> <p>Investigation of TL effect on P. fluorescens showed that when added during bacterial growth this </p> <p>peptide exerted antibiofilm activity at low concentration impairing biofilm formation both in static </p> <p>and dynamic conditions, leaving most of bacterial cells still alive. However, confocal microscopy </p> <p>measurements could not detect the long necklace-like structures observed in E.coli indicating a </p> <p>different mechanism of action of TL on P. fluorescens. Furthermore, when TL was added to a </p> <p>preformed P. fluorescens biofilm, the peptide showed a strong antibiofilm activity both in static and </p> <p>dynamic conditions, suggesting that TL might penetrate biofilm architecture with a still unknown </p> <p>mechanism leading to disruption of P. fluorescens biofilm.</p>


Food Control ◽  
2021 ◽  
Vol 123 ◽  
pp. 107834
Author(s):  
Shimo Kang ◽  
Chunlei Shi ◽  
Jiang Chang ◽  
Fanhua Kong ◽  
Mohan Li ◽  
...  

2015 ◽  
Vol 46 ◽  
pp. 15-24 ◽  
Author(s):  
Leonardo Caputo ◽  
Laura Quintieri ◽  
Daniela Manila Bianchi ◽  
Lucia Decastelli ◽  
Linda Monaci ◽  
...  

2007 ◽  
Vol 177 (4S) ◽  
pp. 297-297
Author(s):  
Kristina Schwamborn ◽  
Rene Krieg ◽  
Ruth Knüchel-Clarke ◽  
Joachim Grosse ◽  
Gerhard Jakse

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