St. Zhang et Sa. Crow, Toxic effects of Ag(I) and Hg(II) on Candida albicans and C-maltosa: a flow cytometric evaluation, APPL ENVIR, 67(9), 2001, pp. 4030-4035
The effects of Ag(I) and Hg(II) on membrane potential and integrity of cell
s of Candida albicans and C. maltosa were determined with a flow cytometric
procedure that employed an anionic membrane potential-sensitive dye, bis-(
1,3-dibutylbarbituric acid) trimethine oxonol, and a membrane integrity ind
icator, propidium iodide. The membrane potentials of cells of both species
were reduced rapidly within 15 min of exposure to Ag(I). No threshold dose
for Hg(II) existed, and cells of both species lost membrane potential gradu
ally in Hg(II) solutions. Cells of both species lost membrane integrity mor
e rapidly in Ag(I) solutions than in Hg(II) solutions. In Ag(I) solutions,
the decrease in the numbers of cells recoverable in culture occurred at a r
ate similar to the rate of cell depolarization and membrane permeabilizatio
n. In Hg(II) solutions, loss of cell recoverability preceded the loss of me
mbrane potential and membrane integrity. C. albicans, in contrast to C. mal
tosa, showed no loss of membrane integrity after exposure to Hg(II) solutio
ns for I h. Different rates of binding of Ag(I) and Hg(II) between the two
species suggest that the two ions target different primary sites.