Analysis of the bacterial biofilm formation in different models of the in vitro culture
DOI:
https://doi.org/10.15584/ejcem.2021.1.6Keywords:
in vitro biofilm, microtiter plate assay, RPMI 1640, tryptic soy brothAbstract
Introduction. Microtiter plate assay (MPA) remains one of workhorses of in vitro biofilm research but it requires optimization of experimental conditions to fulfill the biofilm formation requirements of different bacterial pathogens.
Aim. The aim was to determine the effect of TSB and RPMI1640 culture media and selected culture variables (O2 vs. 5% CO2, extended incubation time) on the biofilm production by bacteria commonly involved in biofilm-related infections: Enterococcus faecalis (EF), Escherichia coli (EC), Staphylococcus aureus (SA), Pseudomonas aeruginosa (PA), Klebsiella pneumoniae (KP).
Material and methods. The investigation was performed using the MPA with crystal violet. Results. Statistically significant (p<0.05) increase in biofilm production between 24h and 72h time points was observed for EF (TSBo2, RPMIo2 and RPMIco2 ), EC (TSBo2 ), SA (TSBo2, TSBco2), KP (TSBo2, TSBco2), PA (RPMIco2, TSBco2). The TSB caused a significantly greater stimulation of biofilm production compared to RPM1640. It outcompeted RPMI1640 irrespective of the atmospheric conditions for SA and KP and under aerobic conditions for EF.
Conclusion. Although the TSB provided the most optimal conditions for biofilm production, the process was influenced by the strain type, atmospheric conditions and period of cultivation which limits the ability to design a single universal model of the in vitro biofilm investigation.
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References
Fux CA, Costerton JW, Stewart PS, Stoodely P. Survival strategies of infectious biofilms. Trends Microbiol. 2005;13:34-40.
Hancock V, Witsø IL, Klemm P. Biofilm formation as a function of adhesin, growth medium, substratum and strain type. Int J Med Microbiol. 2011;301:570-576.
Høiby N, Bjarnsholt T, Moser C, et al. ESCMID guideline for the diagnosis and treatment of biofilm infections 2014. Clin Microbiol Infect. 2015;21:S1-S25.
Gupta P, Sarkar S, Das B, Bhattacharjee S, Tribedi P. Biofilm, pathogenesis and prevention - a journey to break the wall: a review. Arch Microbiol. 2016;198:1-15.
Stepanović S, Vuković D, Hola W, et al. Quantification of biofilm in microtiter plates: overview of testing conditions and practical recommendations for assessment of biofilm production by staphylococci. APMIS. 2007;115:891-899.
Roberts AE, Kragh KN, Bjarnsholt T, Diggle SP. The limitations of in vitro experimentation in understanding biofilms and chronic infection. J Mol Biol. 2015;427:3646-3661.
Senevirante CJ, Yip JWY, Chang JWW, Zhang CF, Samaranayake LP. Effect of culture media and nutrients on biofilm growth kinetics of laboratory and clinical strains of Enterococcus faecalis. Arch Oral Biol. 2013;58:1327-1334.
Singh AK, Prakash P, Achra A, Sing GP, Das A, Singh RK. Standarization and classification of in vitro biofilm formation by clinical isolates of Staphylococcus aureus. J Global Infect Dis. 2017;9:93-101.
Tan T, Leonhard M, Schneider-Stickler B. Evaluation of culture conditions for mixed biofilm formation with clinically isolated non-albicans Candida species and Staphylococcus epidermidis on silicone. Microb Pathog. 2017;112:215-220.
Wijensinghe G, Dilhari A, Gayani B, Kottegoda N, Samaranayake L, Weerasekera M. Influence of laboratory culture media on in vitro growth, adhesion, and biofilm formation of Pseudomonas aeruginosa and Staphylococcus aureus. Med Princ Pract. 2019;28(1):28-35.
Alves DR, Perez-Esteban P, Kot W, et al. A novel bacteriophage cocktail reduces and disperses Pseudomonas aeruginosa biofilms under static and flow conditions. Microb Biotechnol. 2016;9:61e74.
Bjarnsholt T, Alhede M, Eickhardt-Sørensen SR, et al. The in vivo biofilm. Trends Microbiol. 2013;21:466-474.
Knobloch JK-M, Horstkotte MA, Rohde H, Mack D. Evaluation of different detection methods of biofilm formation in Staphylococcus aureus. Med Microbiol Immunol. 2002;191:101-106.
Hood SK, Zottola EA. Adherence to stainless steel by foodvorne microorganisms during growth in model food systems. Int J Food Microbiol. 1997;37:145-153.
Van Loosdrecht MC, Lyklema J, Norde W, Schraa G, Zehnder, AJ. Electrophoretic mobility and hydrophobicity as a measured to predict the initial steps of bacterial adhesion. Appl Environ Microbiol. 1987;53:1898-1901.
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