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A simple and efficient fluorescent labeling method in Staphylococcus aureus for real-time tracking of invasive bacteria.


ABSTRACT: Bacterial fluorescent labeling is a powerful tool for the diagnosis and treatment of bacterial infections. Here, we present a simple and efficient labeling strategy for Staphylococcus aureus. Intracellular labeling of bacteria was achieved by heat shock using Cyanine 5.5 (Cy5.5) near-infrared-I dyes in S. aureus (Cy5.5@S. aureus). Several key factors, such as Cy5.5 concentration and labeling time, were systematically evaluated. Further, the cytotoxicity of Cy5.5 and the stability of Cy5.5@S. aureus was evaluated by flow cytometry, inverted fluorescence microscopy, and transmission electron microscopy. In addition, Cy5.5@S. aureus were used to explore the phagocytic behavior of RAW264.7 macrophages. These results proved that Cy5.5@S. aureus had a uniform fluorescence intensity and high luminance; additionally, our method had no significant adverse effects on S. aureus compared to unlabeled S. aureus infections. Our method provides researchers with a useful option for analyzing the behavior of S. aureus as an infectious agent. This technique can be broadly applied to study host cell-bacteria interactions at the molecular level, and to in vivo tracing of bacterial infections.

SUBMITTER: Liu F 

PROVIDER: S-EPMC9950555 | biostudies-literature | 2023

REPOSITORIES: biostudies-literature

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A simple and efficient fluorescent labeling method in <i>Staphylococcus aureus</i> for real-time tracking of invasive bacteria.

Liu Fei F   Chen Sijie S   Zou Yingxin Y   Jiao Yong Y   Tang Ying Y  

Frontiers in microbiology 20230210


Bacterial fluorescent labeling is a powerful tool for the diagnosis and treatment of bacterial infections. Here, we present a simple and efficient labeling strategy for <i>Staphylococcus aureus</i>. Intracellular labeling of bacteria was achieved by heat shock using Cyanine 5.5 (Cy5.5) near-infrared-I dyes in <i>S. aureus</i> (<i>Cy5.5@S. aureus</i>). Several key factors, such as Cy5.5 concentration and labeling time, were systematically evaluated. Further, the cytotoxicity of Cy5.5 and the stab  ...[more]

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