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非发酵革兰氏阴性菌的生物膜形成活性

BIOFILM FORMING ACTIVITY OF NON-FERMENTING GRAM-NEGATIVE BACTERIA.

作者信息

Kovalchuk Valentyn P, Nazarchuk Oleksandr A, Burkot Vita M, Fomina Nadiia S, Prokopchuk Zoіa M, Dobrovanov Oleksandr

机构信息

NATIONAL PIROGOV MEMORIAL MEDICAL UNIVERSITY, VINNYTSIA, UKRAINE.

3RD CHILDREN'S CLINIC OF SLOVAK MEDICAL UNIVERSITY, BRATISLAVA, SLOVAK REPUBLIC.

出版信息

Wiad Lek. 2021;74(2):252-256.

Abstract

OBJECTIVE

The aim: To study the influence of chemical, physical factors on the biofilm forming activity of P. aeruginosa, A. baumannii.

PATIENTS AND METHODS

Materials and methods: Biofilm forming activity of P. aeruginosa (10 isolates) and A. baumannii (10 isolates) was studied in nutrient media of different composition. There was used the method in 96-well crystalline violet staining plates with spectrophotometry (STAT FAX®4300, wavelength of 620 nm).

RESULTS

Results: Results showed that in standard medium (trypto-soy broth), strains of P. aeruginosa (90%) and A. baumannii (60%) obtained high biofilm forming activity. A. baumannii formed biofilms even in sterile water. Biofilm forming activity of urease positive P. aeruginosa increased in the medium with 1.0% urea. Both Acinetbacteria and Pseudomonas intensively produced their biofilms in the presence of 5% serum or sub-bacteriostatic concentrations of levofloxacin in the media. High concentrations of sodium chloride inhibited their biofilm activity.

CONCLUSION

Conclusions: Isolates of Acinetobacter and Pseudomonas obtain the protective biofilm-forming ability under such adverse environmental conditions as insufficient nutrients, high osmotic pressure, the presence of antibiotics but at high concentrations sodium chloride biofilm-formation is stimulated only in the first bacteria and suppressed in the second one.

摘要

目的

研究化学、物理因素对铜绿假单胞菌和鲍曼不动杆菌生物膜形成活性的影响。

患者与方法

材料和方法:在不同成分的营养培养基中研究了铜绿假单胞菌(10株分离株)和鲍曼不动杆菌(10株分离株)的生物膜形成活性。采用96孔结晶紫染色板结合分光光度法(STAT FAX®4300,波长620nm)。

结果

结果表明,在标准培养基(胰蛋白胨大豆肉汤)中,铜绿假单胞菌菌株(90%)和鲍曼不动杆菌菌株(60%)具有较高的生物膜形成活性。鲍曼不动杆菌甚至能在无菌水中形成生物膜。在含有1.0%尿素的培养基中,脲酶阳性的铜绿假单胞菌的生物膜形成活性增加。在培养基中存在5%血清或亚抑菌浓度的左氧氟沙星时,不动杆菌属和假单胞菌属均大量产生生物膜。高浓度的氯化钠会抑制它们的生物膜活性。

结论

结论:不动杆菌属和假单胞菌属的分离株在营养不足、高渗透压、存在抗生素等不利环境条件下获得保护性生物膜形成能力,但高浓度氯化钠仅刺激第一种细菌形成生物膜,而抑制第二种细菌形成生物膜。

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