Assessment of biofilm formation by pseudomonas aeruginosa and hydrodynamic evaluation of microtiter plate assay.

Objective: To assess the biofilm formation in clinical and environmental isolates of Pseudomonas aeruginosa and to evaluate the hydrodynamics in microtiter plate assay and compare it with conventional assays for biofilm formation. Methods: The cross-sectional study was conducted at the Department of Microbiology, Quaid-i-Azam University, Islamabad, Pakistan, in 2013-14, while the computational work was done at the National University of Science and Technology, Islamabad. The study comprised environmental and clinical isolates of pseudomonas aeruginosa. Pseudomonas citramide agar was used as a selective media, and further confirmation was done by biochemical tests. Biofilm formation was assessed by Congo red assay, air liquid interfaceassay and microtiter plate assay. Computational Fluid Dynamics (CFD) simulations were also used to improve the microtiter plate assay for biofilm formation assessment. Polymerase chain reaction was used for screening of pelA and pelG genes. Results: Of the 50 isolates, 25(50%) each were environmental and clinical. The number of biofilm producers observed in Congo red assay, air liquid interface assay and microtiter plate assay were 7(14%), 15(30%) and 30(60%) respectively. Biofilm former gene pelA was observed in 22(44%) isolates while 36(72%) isolates showed the presence of pelG gene. Conclusions: Microtiter plate assay was found to be a reliable method to detect biofilm forming pseudomonas aeruginosa isolates which further provides a base for development of methods to detect biofilms readily and accurately.