Assessment of the vigour, vitality or viability of microorganisms must
be done on an individual basis and thus requires the non-invasive int
errogation of single organisms. For suspended organisms, flow cytometr
y provides a powerful means of measurement of a wide range of characte
ristics. Similar information for microbes in aggregates or growing on
surfaces may be obtained by use of confocal scanning laser microscopy.
For instance, membrane potential-sensitive fluorophores can distingui
sh between vigorous, frail and dead cells.