Investigating Klebsiella pneumoniae biofilm preservation for scanning electron microscopy.

Access Microbiology Pub Date : 2023-02-03 eCollection Date: 2023-01-01 DOI:10.1099/acmi.0.000470.v3
Renee M Fleeman, Michelle Mikesh, Bryan W Davies
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引用次数: 2

Abstract

Klebsiella pneumoniae biofilm formation is associated with chronic and relapsing infections. Scanning electron microscopy (SEM) is a powerful tool for characterizing biofilm structure and studying their formation. Reliable visualization of biofilm structure requires careful sample preservation, otherwise there may be loss of non-covalent interactions that are susceptible to damage during the dehydration and washing preparation steps. However, no standard procedure has been adopted in the literature to fix K. pneumoniae biofilm for scanning electron microscopy studies. This lack of standardization makes it challenging to compare results between studies and determine the degree to which native structures have been preserved. To advance this critical area of study, we investigated different scanning electron microscopy fixation methods for K. pneumoniae biofilm preservation. Our study reveals the impact preparation steps can have on retaining in biofilm architecture observed using scanning electron microscopy. Using fixation methods developed through our studies, we show that although species that overproduce capsular extracellular polysaccharides produced more robust biofilms, K. pneumoniae can form a developed biofilm in the absence of capsular polysaccharides.

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肺炎克雷伯菌生物膜保存的扫描电镜研究。
肺炎克雷伯菌生物膜的形成与慢性和复发性感染有关。扫描电子显微镜(SEM)是表征生物膜结构和研究生物膜形成的有力工具。生物膜结构的可靠可视化需要仔细的样品保存,否则可能会失去在脱水和洗涤制备步骤中容易受到破坏的非共价相互作用。然而,文献中没有采用标准的程序来固定肺炎克雷伯菌生物膜进行扫描电镜研究。这种标准化的缺乏使得比较研究结果和确定本地结构的保存程度具有挑战性。为了推进这一关键领域的研究,我们研究了不同的扫描电镜固定方法保存肺炎克雷伯菌生物膜。我们的研究揭示了利用扫描电子显微镜观察到的制备步骤对保留生物膜结构的影响。利用我们研究中开发的固定方法,我们发现虽然过量产生荚膜胞外多糖的物种产生更坚固的生物膜,但肺炎克雷伯菌可以在缺乏荚膜多糖的情况下形成发达的生物膜。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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