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Microscopic techniques to evaluate the biofilm formation ability of a marine bacterium Pseudomonas aeruginosa PFL‐P1 on different substrata

生物膜 细菌 扫描电子显微镜 聚苯乙烯 微生物学 陶瓷 天然橡胶 铜绿假单胞菌 原子力显微镜 材料科学 表面粗糙度 生物 化学 复合材料 纳米技术 聚合物 遗传学
作者
Kumari Uma Mahto,Surajit Das
出处
期刊:Microscopy Research and Technique [Wiley]
卷期号:84 (10): 2451-2461 被引量:24
标识
DOI:10.1002/jemt.23799
摘要

Abstract Biofilm formation in bacteria is strongly affected by the nature of substrata. Different substrata such as glass, polystyrene, steel, ceramic, and rubber were used to assess the biofilm forming ability of a marine bacterium Pseudomonas aeruginosa PFL‐P1 using a scanning electron microscope (SEM), atomic force microscope (AFM), and confocal laser scanning microscope (CLSM). The bacterium formed dense biofilms with varied aggregation on different substrata. SEM study revealed small rod‐shaped cells with diverse arrangements within the biofilms on all the substrata under study. The AFM study revealed the highest roughness of 545 nm on the ceramic substratum. The biofilms formed on ceramic substratum were characterized with maximum roughness (742 nm), maximum peak height (1,480 nm), and maximum arithmetic mean height (611 nm), significantly higher than all the other substrata ( p < .05). AFM studies confirmed that P. aeruginosa PFL‐P1 exhibited biofilm heterogeneity on all the substrata. The CLSM study indicated a higher fraction of nucleic acids to α‐polysaccharides ratio in the biofilms. COMSTAT analysis revealed the highest biofilm biomass of ~18 μm 3 /μm 2 on the ceramic substratum. The maximum biofilm thickness of ~50 μm in the native state on the ceramic substratum was significantly higher than glass ( p = .0015), polystyrene ( p = .0001), steel ( p = .0035), and rubber substrata ( p = .0001). The higher surface roughness of ceramic substratum is accountable for more area for colonization, as evident from higher biomass and thickness of the biofilm. This study provides insight into the substratum properties, which modulate the biofilm forming ability in bacteria.
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