Skip to main content

Apicoplast Translation, Transcription, and Genome Replication

  • Living reference work entry
  • First Online:
Encyclopedia of Malaria
  • 380 Accesses

Synonyms

Organelle; Plastid

Definition

The apicoplast is an organelle of malaria parasites related to the plastid of plant cells. The apicoplast has limited biochemical functions in erythrocytic parasites, but it is essential, as antibiotics that target the apicoplast block parasite development, although in most cases their antimalarial activity is slow.

Introduction

A number of antibiotics possess antimalarial activity, although the mechanisms by which most of these drugs kill malaria parasites were until recently poorly understood. Recent data suggest that the target for multiple antimalarial antibiotics is the apicoplast, a plastid-like organelle. Treatment with prokaryotic protein synthesis inhibitors including tetracyclines, clindamycin, and macrolides causes modest antimalarial effects initially and then much more potent effects in the progeny of treated parasites. Inhibiting apicoplast functions with these antibiotics causes the next generation to inherit nonfunctional...

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Institutional subscriptions

References

  • Botté CY, Dubar F, McFadden GI, Maréchal E, Biot C. Plasmodium falciparum apicoplast drugs: targets or off-targets? Chem Rev. 2012;112:1269–83.

    Article  PubMed  Google Scholar 

  • Dahl EL, Rosenthal PJ. Apicoplast translation, transcription and genome replication: targets for antimalarial antibiotics. Trends Parasitol. 2008;24:279–84.

    Article  CAS  PubMed  Google Scholar 

  • Dahl EL, Shock JL, Shenai BR, Gut J, DeRisi JL, Rosenthal PJ. Tetracyclines specifically target the apicoplast of the malaria parasite Plasmodium falciparum. Antimicrob Agents Chemother. 2006;50:3124–31.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Fichera ME, Roos DS. A plastid organelle as a drug target in apicomplexan parasites. Nature. 1997;390:407–9.

    Article  CAS  PubMed  Google Scholar 

  • Foth BJ, Ralph SA, Tonkin CJ, Struck NS, Fraunholz M, Roos DS, Cowman AF, McFadden GI. Dissecting apicoplast targeting in the malaria parasite. Science. 2003;299:705–8.

    Article  CAS  PubMed  Google Scholar 

  • Goodman CD, McFadden GI. Targeting apicoplasts in malaria parasites. Expert Opin Ther Targets. 2013;17:167–77.

    Article  CAS  PubMed  Google Scholar 

  • Goodman CD, Su V, McFadden GI. The effects of anti-bacterials on the malaria parasite Plasmodium falciparum. Mol Biochem Parasitol. 2007;152:181–91.

    Article  CAS  PubMed  Google Scholar 

  • Howe CJ, Purton S. The little genome of apicomplexan plastids: its raison d’etre and a possible explanation for the ‘delayed death’ phenomenon. Protist. 2007;158:121–33.

    Article  CAS  PubMed  Google Scholar 

  • Jomaa H, Wiesner J, Sanderbrand S, Altincicek B, Weidemeyer C, Hintz M, Türbachova I, Eberl M, Zeidler J, Lichtenthaler HK, Soldati D, Beck E. Inhibitors of the nonmevalonate pathway of isoprenoid biosynthesis as antimalarial drugs. Science. 1999;285:1573–6.

    Article  CAS  PubMed  Google Scholar 

  • McFadden GI. The apicoplast. Protoplasma. 2011;248:641–50.

    Article  PubMed  Google Scholar 

  • Ralph SA, van Dooren GG, Waller RF, Crawford MJ, Fraunholz MJ, Foth BJ, Tonkin CJ, Roos DS, McFadden GI. Tropical infectious diseases: metabolic maps and functions of the Plasmodium falciparum apicoplast. Nat Rev Microbiol. 2004;2:203–16.

    Article  CAS  PubMed  Google Scholar 

  • Vaughan AM, O’Neill MT, Tarun AS, Camargo N, Phuong TM, Aly AS, Cowman AF, Kappe SH. Type II fatty acid synthesis is essential only for malaria parasite late liver stage development. Cell Microbiol. 2009;11:506–20.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Yeh E, DeRisi JL. Chemical rescue of malaria parasites lacking an apicoplast defines organelle function in blood-stage Plasmodium falciparum. PLoS Biol. 2011;9:e1001138.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Yu M, Kumar TR, Nkrumah LJ, Coppi A, Retzlaff S, Li CD, Kelly BJ, Moura PA, Lakshmanan V, Freundlich JS, Valderramos JC, Vilcheze C, Siedner M, Tsai JH, Falkard B, Sidhu AB, Purcell LA, Gratraud P, Kremer L, Waters AP, Schiehser G, Jacobus DP, Janse CJ, Ager A, Jacobs Jr WR, Sacchettini JC, Heussler V, Sinnis P, Fidock DA. The fatty acid biosynthesis enzyme FabI plays a key role in the development of liver-stage malarial parasites. Cell Host Microbe. 2008;4:567–78.

    Article  PubMed Central  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Philip J. Rosenthal .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2013 Springer Science+Business Media New York

About this entry

Cite this entry

Rosenthal, P.J. (2013). Apicoplast Translation, Transcription, and Genome Replication. In: Hommel, M., Kremsner, P. (eds) Encyclopedia of Malaria. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-8757-9_28-1

Download citation

  • DOI: https://doi.org/10.1007/978-1-4614-8757-9_28-1

  • Received:

  • Accepted:

  • Published:

  • Publisher Name: Springer, New York, NY

  • Online ISBN: 978-1-4614-8757-9

  • eBook Packages: Springer Reference MedicineReference Module Medicine

Publish with us

Policies and ethics