Rifabutin is a spiro-piperidyl-rifamycin derived from rifamycin-S. It
is structurally related to rifampin and shares many of its properties.
Rifabutin has a broad spectrum of antimicrobial activity. It is consi
derably more active than rifampin in vitro against the Mycobacterium a
vium complex (MAC), Mycobacterium tuberculosis, and Mycobacterium lepr
ae. It also is active against most atypical mycobacteria, including My
cobacterium kansasii, but Mycobacterium chelonae is relatively resista
nt. Rifabutin also is active against staphylococci, group A streptococ
ci, Neisseria gonorrhoeae, Neisseria meningitidis, Haemophilus influen
zae, Haemophilus ducreyi, Campylobacter jejuni, Helicobacter pylori, C
hlamydia trachomatis, and Toxoplasma gondii. It has poor activity agai
nst Enterobacteriaceae and Pseudomonas species. This review focuses on
the antimicrobial profile of rifabutin in relation to its pharmacolog
ical properties. Special emphasis is placed on its in vitro activity a
gainst MAC and other mycobacteria, its efficacy in cell culture and an
imal models, and its potential as a component of multidrug therapy for
mycobacterial and other infectious diseases.