Analysis of Bacteriophage-Host Interaction by Raman Tweezers

Investor logo

Warning

This publication doesn't include Faculty of Sports Studies. It includes Faculty of Medicine. Official publication website can be found on muni.cz.
Authors

PILAT Zdenek JONAS Alexandr PILATOVA Jana KLEMENTOVA Tereza BERNATOVA Silvie SILER Martin MANKA Tadeas KIZOVSKY Martin RŮŽIČKA Filip PANTŮČEK Roman NEUGEBAUER Ute SAMEK Ota ZEMANEK Pavel

Year of publication 2020
Type Article in Periodical
Magazine / Source Analytical chemistry
MU Faculty or unit

Faculty of Medicine

Citation
web https://doi.org/10.1021/acs.analchem.0c01963
Doi http://dx.doi.org/10.1021/acs.analchem.0c01963
Keywords Infectious diseases; Viruses; Bioinorganic chemistry; Genetics; Raman spectroscopy
Description Bacteriophages, or "phages" for short, are viruses that replicate in bacteria. The therapeutic and biotechnological potential of phages and their lytic enzymes is of interest for their ability to selectively destroy pathogenic bacteria, including antibiotic-resistant strains. Introduction of phage preparations into medicine, biotechnology, and food industry requires a thorough characterization of phage-host interaction on a molecular level. We employed Raman tweezers to analyze the phage-host interaction of Staphylococcus aureus strain FS159 with a virulent phage JK2 (=812K1/420) of the Myoviridae family and a temperate phage 80 alpha of the Siphoviridae family. We analyzed the timeline of phage-induced molecular changes in infected host cells. We reliably detected the presence of replicating phages in bacterial cells within 5 min after infection. Our results lay the foundations for building a Raman-based diagnostic instrument capable of real-time, in vivo, in situ, nondestructive characterization of the phage-host relationship on the level of individual cells, which has the potential of importantly contributing to the development of phage therapy and enzybiotics.
Related projects:

You are running an old browser version. We recommend updating your browser to its latest version.

More info