4.4 Review

New insights into the spread of resistance to artemisinin and its analogues

Journal

JOURNAL OF GLOBAL ANTIMICROBIAL RESISTANCE
Volume 27, Issue -, Pages 142-149

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.jgar.2021.09.001

Keywords

Artemisinin; Plasmodium falciparum; Malaria; Resistance; Kelch 13 mutation

Funding

  1. King Khalid University, Saudi Arabia [R.G.P.2/26/42]

Ask authors/readers for more resources

Plasmodium falciparum, the causative agent of malaria, has developed resistance to multiple drugs, including the latest drug artemisinin. This resistance undermines the effectiveness of current treatment strategies, posing a threat to global efforts in malaria elimination. Research has identified genetic factors and molecular pathways associated with artemisinin resistance, highlighting the need for novel strategies to combat the spread of resistant parasites.
Plasmodium falciparum, the causative agent of malaria, has been developing resistance to several drugs worldwide for more than five decades. Initially, resistance was against drugs such as chloroquine, pyrimethamine, sulfadoxine, mefloquine and quinine. Research studies are now reporting parasites with resistance to the most effective and novel drug used against malaria infection worldwide, namely artemisinin. For this reason, the first-line treatment strategy of artemisinin-based combination therapy is becoming unsuccessful in areas where drug resistance is highly prevalent. The increase in artemisinin-resistant P. falciparum strains has threatened international effort s to eliminate malarial infections and to reduce the disease burden. Detection of several phenotypes that display artemisinin resistance, specifica-tion of basic genetic factors, the discovery of molecular pathways, and evaluation of its clinical outcome are possible by the current series of research on genomics and transcriptomic levels in Asia and Africa. In artemisinin resistance, slow parasite clearance among malaria-infected patients and enhanced in vitro survival of parasites occurs at the early ring stage. This resistance is due to single nucleotide polymor-phisms within the Kelch 13 gene of the parasite and is related to significantly upregulated resistance signalling pathways; thus, the pro-oxidant action of artemisinins can be antagonised. New strategies are required to halt the spread of artemisinin-resistant malarial parasites. (c) 2021 The Author(s). Published by Elsevier Ltd on behalf of International Society for Antimicrobial Chemotherapy. This is an open access article under the CC BY license ( http://creativecommons.org/licenses/by/4.0/ )

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available