In prospective studies, Staphylococcus aureus small-colony variants (SCVs)
have been linked to persistent and recurrent infections. SCVs are a natural
ly occurring subpopulation often defective in electron transport which may
be identified in the microbiological laboratory as nonpigmented, nonhemolyt
ic, slow-growing pinpoint colonies after incubation on rabbit blood agar. I
n addition, the often relatively unstable SCVs demonstrate a number of othe
r characteristics that are atypical for S. aureus including reduced alpha -
toxin production and delayed coagulase activity. A site-directed hemB mutan
t with a stable SCV phenotype provided strong evidence for the link between
these electron transport defective strains and persistent infections. The
hemB mutant was phagocytized by cultured endothelial cells, but did not lys
e these cells, because the mutant produced very little alpha -toxin. Thus,
SCVs can hide within the host cell, then revert to the highly virulent rapi
dly growing form and lyse the host cell, once the host immune response has
abated and antibiotic therapy is completed. The intracellular position shie
lds SCVs from host defenses and decreases exposure to antibiotics. This rev
iew discusses what is known of the biology of SCVs and describes the recove
ry and significance of Staphylococcus SCVs in clinical specimen.