Center for Biofilm Engineering
Abstract:
"Selective detection of live bacteria combining propidium monoazide
sample treatment with microarray technology"
09-007
The use of DNA-based molecular detection tools for bacterial diagnostics is
hampered by the inability to distinguish signals originating from live and dead
cells. The detection of live cells is typically most relevant in molecular
diagnostics. DNA-intercalating dyes like ethidium monoazide and propidium
monoazide (PMA) offer a possibility to selectively remove cells with compromised
cell membranes from the analysis. Once these dyes enter a cell, they bind to DNA
and can be covalently crosslinked to it by light exposure. PCR amplification of
such modified DNA is strongly inhibited. In this study we evaluated the
suitability of propidium monoazide treatment to exclude isopropanol-killed cells
from detection in defined mixtures using diagnostic microarray technology. The
organisms comprised Pseudomonas aeruginosa, Listeria monocytogenes,
Salmonella typhimurium, Serratia marcescens, and Escherichia
coli O157:H7. PCR products obtained from amplification of chaperonin 60
genes (cpn60; coding for GroEL) were hybridized to a custom-designed microarray
containing strain-specific cpn60-based 35-mer oligonucleotide probes. Results
were compared with data from quantitative PCR, which confirmed that PMA could
successfully inhibit amplification of DNA from killed cells in the mixtures.
Although microarray data based on analysis of end-point PCR amplicons is not
quantitative, results showed a significant signal reduction when targeting
killed cells and consistently agreed with qPCR results. Treatment of samples
with PMA in combination with diagnostic microarray detection can therefore be
considered beneficial when analyzing mixtures of intact and membrane-compromised
cells. Minimization of detection signals deriving from dead cells will render
data more relevant in studies including pathogen risk assessment.
Nocker A, Mazza A, Masson L, Camper AK, Brousseau R, "Selective detection of
live bacteria combining propidium monoazide sample treatment with microarray
technology," J. Microbiol. Methods 2009; 76(3):253-261
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