Influence of interspecies interactions on biomass and extracellular polymeric substances of bacterial biofilms

IF 0.2 Q4 MEDICINE, GENERAL & INTERNAL Universa Medicina Pub Date : 2023-04-10 DOI:10.18051/univmed.2023.v42.84-93
Mercedes Baltazara Schettini Alava, N. R. Maddela
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Abstract

BackgroundStudies with emphasis on pure and mixed-species biofilms are of significant importance in understanding biofilm formation mechanisms during microbial infections. This research aims to evaluate pure- and dual-species biofilms of Escherichia coli (code A), Staphylococcus aureus (code B), Klebsiella pneumoniae (code C) and Pseudomonas aeruginosa (code D) pathogenic bacterial species and their production of biofilm exopolysaccharides at laboratory scale. MethodsBiofilm biomass (A595) of pure- and dual-species cultures was determined by means of a microtiter plate assay in triplicate using a microplate photometer (Fisher Scientific, type-357). Extracellular polymeric substances (EPS) and soluble microbial products (SMP) were extracted from the biofilm cells (pure- and dual-species cultures) using the alkaline-heat extraction method. Dry weights (g/L) of EPS and SMP were determined by drying the samples at 105 °C for 8 hours. ResultsKlebsiella pneumoniae biofilm biomass accounted for a 28-72% greater biofilm biomass than the other bacteria. Experimental values of dual-species biofilm biomasses were in the range of 6% to 30% over theoretical values. The experimental value of one dual-species (bacteria B + D) biofilm biomass was 30% higher than its expected value. Decrease or increase in the dual-species biofilm biomass of either bacteria A+C or bacteria B+C combinations was totally dependent on the cell density of bacteria C. Conclusions Biofilm biomass of pure-species cultures was totally species-dependent, and the biofilm biomass of four species was in the following order: bacteria C > D > A > B. Relation between biofilm biomasses and SMP or EPS was inconsistent.
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种间相互作用对细菌生物膜生物量和细胞外聚合物的影响
背景以纯生物膜和混合生物膜为重点的研究对于理解微生物感染过程中生物膜的形成机制具有重要意义。本研究旨在在实验室规模上评估大肠杆菌(代码A)、金黄色葡萄球菌(代码B)、肺炎克雷伯菌(代码C)和铜绿假单胞菌(代码D)的纯生物膜和双物种生物膜及其生物膜胞外多糖的产生。方法采用微量板光度计(Fisher Scientific,357型),通过一式三份的微量滴定板测定纯物种和双物种培养物的生物膜生物量(A595)。采用碱性热提取法从生物膜细胞(纯和双菌种培养物)中提取胞外聚合物(EPS)和可溶性微生物产物(SMP)。通过在105°C下干燥样品8小时来测定EPS和SMP的干重(g/L)。结果肺炎克雷伯菌生物膜生物量比其他细菌高28~72%。双物种生物膜生物质的实验值在理论值的6%至30%的范围内。一种双菌种(细菌B+D)生物膜生物量的实验值比预期值高出30%。细菌A+C或细菌B+C组合的双物种生物膜生物量的减少或增加完全取决于细菌C的细胞密度。生物膜生物量和SMP或EPS之间的关系不一致。
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来源期刊
Universa Medicina
Universa Medicina MEDICINE, GENERAL & INTERNAL-
自引率
0.00%
发文量
27
审稿时长
20 weeks
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