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Antimicrobial Agents and Chemotherapy, June 2001, p. 1746-1750, Vol. 45, No. 6
Unité de Parasitologie, Institut de
Médecine Tropicale du Service de Santé des
Armées, Le Pharo, 13998 Marseille, France
Received 12 January 2001/Returned for modification 20 February
2001/Accepted 19 March 2001
The in vitro activities of cyclines (tetracycline,
doxycycline, minocycline, oxytetracycline, and rolitetracycline),
macrolides (erythromycin, spiramycin, roxithromycin, and
lincomycin), quinolones (norfloxacin and ofloxacin), rifampin,
thiamphenicol, tobramycin, metronidazole, vancomycin, phosphomycin, and
cephalosporins (cephalexin, cefaclor, cefamandole, cefuroxime,
ceftriazone, cefotaxime, and cefoxitin) were evaluated on
Plasmodium falciparum clones, using an isotopic,
micro-drug susceptibility test. Only tetracyclines, macrolides,
quinolones, and rifampin demonstrated in vitro activity against
P. falciparum, which increased after a prolonged exposure (96 or 144 h). In the presence of iron (FeCl3), only
the activities of tetracyclines and norfloxacin were decreased. Their
in vitro activity against intraerythrocytic stages of
multidrug-resistant P. falciparum and their efficacy in
vivo favor the use of antibiotics as antimalarial drugs. However, due
to their slow antimalarial action and to the fact that they act better
after prolonged contact, they probably need to be administered in
conjunction with a rapidly acting antimalarial drug, such as a short
course of chloroquine or quinine.
0066-4804/01/$04.00+0 DOI: 10.1128/AAC.45.6.1746-1750.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
In Vitro Activities of Antibiotics against
Plasmodium falciparum Are Inhibited by Iron
*
Corresponding author. Mailing address: IMTSSA,
Unité de Parasitologie, Bd Charles Livon, Parc le Pharo, BP 46, 13998 Marseille Armées, France. Phone: 33 4 91 15 01 10. Fax: 33 4 91 15 01 64. E-mail: bruno.pradines{at}free.fr.
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