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Detection of nosocomial pneumonia pathogens using a fluorescence-based device

Authors
 Eun-Ha Jung  ;  Ji-Hye Yang  ;  So-Jung Mun  ;  Sun-Young Han 
Citation
 PHOTODIAGNOSIS AND PHOTODYNAMIC THERAPY, Vol.37 : 102621, 2022-03 
Journal Title
PHOTODIAGNOSIS AND PHOTODYNAMIC THERAPY
ISSN
 1572-1000 
Issue Date
2022-03
MeSH
Anti-Bacterial Agents ; Cross Infection* ; Healthcare-Associated Pneumonia* ; Humans ; Microbial Sensitivity Tests ; Photochemotherapy* / methods
Keywords
Autofluorescence ; Fluorescence property ; Fluorescence-based device ; Nosocomial pneumonia pathogens ; Porphyrin
Abstract
Background: Early detection of nosocomial pneumonia pathogens is a significant factor in hospital-acquired pneumonia care. This study aimed to determine the autofluorescence properties of five nosocomial pneumonia pathogens using a fluorescence-based device and to establish evidence for clinical guidelines.

Methods: The following bacterial strains were assessed: Acinetobacter baumannii (AB), Escherichia coli (EC), Enterococcus faecalis (EF), Klebsiella pneumoniae (KP), and Staphylococcus aureus (SA). The bacteria were cultured separately on tryptic soy agar at 37 °C under aerobic conditions for 168 h. Fluorescence photographs of each species were captured every 24 h using a fluorescence-based device with fixed camera settings. The images were analyzed by measuring the red and green values (R/G ratio) at a central point in each colony, and the R/G ratios were analyzed using the Kruskal-Wallis non-parametric test.

Results: KP and SA showed red fluorescence with their R/G values, which were significantly higher than those of the other strains (p < 0.001). In particular, the R/G ratio of KP increased steadily until 72 h of incubation, peaking at 3.65. In addition, AB and EC showed orange fluorescence with higher red ratios than green ratios. EF and SA showed green fluorescence all through 168 h of incubation, with R/G ratio less than 1.0.

Conclusions: Nosocomial pneumonia pathogens can be identified and classified via bacterial autofluorescence emission. It is possible to develop a rapid and easy-to-use identification technology based on bacterial autofluorescence for clinical applications.
Full Text
https://www.sciencedirect.com/science/article/pii/S1572100021004397
DOI
10.1016/j.pdpdt.2021.102621
Appears in Collections:
2. College of Dentistry (치과대학) > Dept. of Oral Pathology (구강병리학교실) > 1. Journal Papers
Yonsei Authors
Yang, Ji Hye(양지혜)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/194434
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