Affiliation:
1. Department of Biomedical Engineering, The Cleveland Clinic Foundation, 9500 Euclid Avenue, Cleveland, Ohio 44195-5254
2. Department of Microbiology, The Cleveland Clinic Foundation, 9500 Euclid Avenue, Cleveland, Ohio 44195-5254
Abstract
Magnetic deposition, quantitation, and identification of bacteria reacting with the paramagnetic trivalent lanthanide ion, Er
3+
, was evaluated. The magnetic deposition method was dubbed thin-film magnetopheresis. The optimization of the magnetic deposition protocol was accomplished with
Escherichia coli
as a model organism in 150 mM NaCl and 5 mM ErCl
3
solution. Three gram-positive bacteria,
Staphylococcus epidermidis, Staphylococcus saprophyticus,
and
Enterococcus faecalis,
and four gram-negative bacteria,
E. coli, Pseudomonas aeruginosa, Proteus mirabilis,
and
Klebsiella pneumoniae,
were subsequently investigated. Quantitative analysis consisted of the microscopic cell count and a scattered-light scanning of the magnetically deposited material aided by the computer data acquisition system. Qualitative analysis consisted of Gram stain differentiation and fluorescein isothiocyanate staining in combination with selected antisera against specific types of bacteria on the solid substrate. The magnetic deposition protocol allowed quantitative detection of
E. coli
down to the concentration of 10
5
CFU ml
-1
, significant in clinical diagnosis applications such as urinary tract infections. Er
3+
did not interfere with the typical appearance of the Gram-stained bacteria nor with the antigen recognition by the antibody in the immunohistological evaluations. Indirect antiserum-fluorescein isothiocyanate labelling correctly revealed the presence of
E. faecalis
and
P. aeruginosa
in the magnetically deposited material obtained from the mixture of these two bacterial species. On average, the reaction of gram-positive organisms was significantly stronger to the magnetic field in the presence of Er
3+
than the reaction of gram-negative organisms. The thin-film magnetophoresis offers promise as a rapid method for quantitative and qualitative analysis of bacteria in solutions such as urine or environmental water.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
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