AAC
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Other Versions of this Article:
AAC.00527-07v1
51/10/3485    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Dahl, E. L.
Right arrow Articles by Rosenthal, P. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Dahl, E. L.
Right arrow Articles by Rosenthal, P. J.

 Previous Article  |  Next Article 

Antimicrobial Agents and Chemotherapy, October 2007, p. 3485-3490, Vol. 51, No. 10
0066-4804/07/$08.00+0     doi:10.1128/AAC.00527-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Multiple Antibiotics Exert Delayed Effects against the Plasmodium falciparum Apicoplast{triangledown}

Erica L. Dahl and Philip J. Rosenthal*

Department of Medicine, Box 0811, University of California San Francisco, San Francisco, California 94143

Received 20 April 2007/ Returned for modification 20 June 2007/ Accepted 1 August 2007

Several classes of antibiotics exert antimalarial activity. The mechanisms of action of antibiotics against malaria parasites have been unclear, and prior studies have led to conflicting results, in part because they studied antibiotics at suprapharmacological concentrations. We examined the antimalarial effects of azithromycin, ciprofloxacin, clindamycin, doxycycline, and rifampin against chloroquine-resistant (W2) and chloroquine-sensitive (3D7) Plasmodium falciparum strains. At clinically relevant concentrations, rifampin killed parasites quickly, preventing them from initiating cell division. In contrast, pharmacological concentrations of azithromycin, ciprofloxacin, clindamycin, and doxycycline were relatively inactive against parasites initially but exerted a delayed death effect, in which the progeny of treated parasites failed to complete erythrocytic development. The drugs that caused delayed death did not alter the distribution of apicoplasts into developing progeny. However, the apicoplasts inherited by the progeny of treated parasites were abnormal. The loss of apicoplast function became apparent as the progeny of antibiotic-treated parasites initiated cell division, with the failure of schizonts to fully mature or for erythrocyte rupture to take place. These findings explain the slow antimalarial action of multiple antibiotics.


* Corresponding author. Mailing address: Box 0811, University of California San Francisco, San Francisco, CA 94143-0811. Phone: (415) 206-8845. Fax: (415) 648-8425. E-mail: philip.rosenthal{at}ucsf.edu

{triangledown} Published ahead of print on 13 August 2007.


Antimicrobial Agents and Chemotherapy, October 2007, p. 3485-3490, Vol. 51, No. 10
0066-4804/07/$08.00+0     doi:10.1128/AAC.00527-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
Clin. Vaccine Immunol. Clin. Microbiol. Rev.
J. Clin. Microbiol. ALL ASM JOURNALS

Copyright © 2007 by the American Society for Microbiology. All rights reserved.