克雷伯氏菌内生液滴自组装及拓扑结构变化的时间研究

Bhavani Balasundaraekar, R Akash Pande, P. Karthikeyan, P. Dhasarathan
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引用次数: 0

摘要

来自患者的传染性液滴根据细菌与底物和液体的相互作用自行组装成一种新的模式。细菌在液滴内的空间位置随非共价力而波动。在蒸发的传染性液滴中,变形和脱水引起的应力改变了细菌的生存能力和传染性。采用自然蒸发的方法研究了克雷伯菌(Klebsiella oxytoca, KO)在传染性无根液滴中的自组装。随着液滴的排出,KO形成了新的模式,从而揭示了控制生存和感染策略的未探索的拓扑变化。将细菌悬浮液和体积为0.95±0.1 μl的SRF滴滴放置在玻璃材料上,以评估自组装。细菌悬浮液在干燥前被染色。利用明暗场光学方法记录了蒸发结束时细菌的趋化性和沉积。随机的时间间隔也被测量来跟踪细菌的运动。研究表明,由于边缘紧密堆积,大多数细菌种群向液滴边缘移动,从而提高了众所周知的“咖啡环”的生存能力和发病机制,并且很少有细菌存在于液滴中心,这代表了细菌的趋化性。通过我们的研究获得的机制见解可以对通过飞沫(例如通过开放伤口)进行细菌感染具有深远的意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Investigation of self-assembly and topological changes in the sessile droplets of Klebsiella oxytoca by Chronological study
The infectious droplet from the patient self-assembles into a novel pattern depending on bacterial interaction with substrate and liquid. The spatial location of bacteria inside the droplet fluctuates depending on the non-covalent forces. The deformation and dehydration induced stress on bacteria in evaporating contagious-fluid droplets alters the viability and infectivity. The self-assembly of Klebsiella oxytoca (KO) in contagious sessile droplets was studied by natural evaporation. KO forms novel patterns as the droplets exsiccate, thus revealing the unexplored topological changes that govern its survival and infection strategies. The droplets of both bacterial suspension in Milli-Q and SRF of volume 0.95 ± 0.1 μl were placed on the glass material for assessment of the self-assembly. The bacterial suspension was stained before allowing them to desicate. The bacterial chemotaxis and deposition near the end of evaporation are recorded using the bright and dark field optical method. The random time interval is also measured to track the bacterial movement. The investigation shows that the majority of the bacterial population moves toward the rim of the droplet because of edge closely packing, leading to enhanced viability and pathogenesis on the famously known “coffee ring” and few bacteria are present at the centre of the droplet which represents chemotaxis of bacteria. The mechanistic insight gained via our study can have far-reaching implications for bacterial infection through droplets e.g., through open wounds.
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