Tropical Parasitology

: 2016  |  Volume : 6  |  Issue : 1  |  Page : 30--41

Antimalarial drug resistance: An overview

Hiasindh Ashmi Antony, Subhash Chandra Parija 
 Department of Microbiology, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India

Correspondence Address:
Subhash Chandra Parija
Department of Microbiology, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry - 605 006


Malaria is a major public health burden throughout the world. Resistance to the antimalarial drugs has increased the mortality and morbidity rate that is achieved so far through the malaria control program. Monitoring the drug resistance to the available antimalarial drugs helps to implement effective drug policy, through the in vivo efficacy studies, in vitro drug susceptibility tests and detection of molecular markers. It is important to understand the mechanism of the antimalarial drugs, as it is one of the key factors in the emergence and spread of drug resistance. This review summarizes the commonly used antimalarial drugs, their mechanism of action and the genetic markers validated so far for the detection of drug-resistant parasites.

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Antony HA, Parija SC. Antimalarial drug resistance: An overview.Trop Parasitol 2016;6:30-41

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Antony HA, Parija SC. Antimalarial drug resistance: An overview. Trop Parasitol [serial online] 2016 [cited 2019 Jul 16 ];6:30-41
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Malaria is one of the deadliest diseases which claim millions of life throughout the world. Five known species of Plasmodium genus that causes malaria in human are Plasmodium falciparum, Plasmodium vivax, Plasmodium malariae, Plasmodium ovale, and Plasmodium knowlesi. Of these, P. falciparum is the most virulent parasite, with high mortality and morbidity rate. The discovery of synthetic drug chloroquine (CQ) in the 1940s helped to treat, prevent and eradicate malaria through National Malaria Control and Eradication Programme throughout the world in 1950s. [1],[2] However, the therapeutic efficacy of CQ and efforts to eradicate malaria worldwide were diminished due to the occurrence of CQ resistance. The failure of these eradication programs led to re-emergence of malaria and spread of CQ-resistant parasite in Southeast Asia and South America. [1],[2],[3],[4],[5] Due to the lack of potent and affordable drug for malaria treatment, the spread of CQ-resistant parasite to Africa around 1980s claimed 2-3-fold increase in malaria-related death. [5],[6] Hence, CQ was replaced with sulfadoxine/pyrimethamine (SP) as the first-line of treatment for malaria; however, parasite became resistant to SP and spread widely. [7],[8],[9] Use of antimalarial drugs as combination therapy instead of monotherapy has been in practice to increase the efficacy of drug and to delay the emergence of drug resistance parasite. Since then, artemisinin-based combination therapies (ACTs) has been most widely and effectively used for malaria treatment. Recently, resistance to artemisinin has been reported in Southeast Asia increasing the global alarm for malaria treatment and control. [10],[11]

The emergence of antimalarial drug-resistant parasite will not only demise the malaria control efforts achieved but to look for new treatment regimes to treat and control the disease. Thus, an in-depth knowledge to understand the mechanism of action of antimalarial drug used and the molecular marker involved for the surveillance of drug-resistant parasite will aid in designing an effective drug policy in all malaria endemic regions and affected countries.


WHO estimated malaria burden worldwide with approximately 1.2 billion people at risk of infection and its distribution as shown in [Figure 1]. [12] Globally, 198 million malaria cases have been reported in 2013 with 584,000 deaths indicating a decrease in malaria infection and mortality rate since 2000. [12] WHO African Region contributed 90% of all malaria deaths worldwide, and 78% of deaths reported belong to children <5 years age. [12]{Figure 1}

In the 10 malaria-endemic countries from South East Asia region, about 352 million people are at high risk for malaria, and there was a decrease in malaria reported cases from 2.9 to 1.5 million during 2000-2013. [12] India, Indonesia, and Myanmar were found to carry a heavy load with 55%, 21%, and 21% of malaria cases, respectively, contributing to 97% cases totally in 2013. [12]

Antimalarial drug resistance has been observed for P. falciparum, P. vivax, and P. malariae globally. [13] Resistance to various antimalarial drugs (quinolones and antifolate family) has been reported in P. falciparum and artemisinin derivate resistance has also been documented recently in western Cambodia. [13],[14] [Figure 2]a-c illustrate the worldwide surveillance of antimalarial drug resistance obtained from WWARN Molecular Surveyor. [15] The WWARN Molecular Surveyor website ( exhibits a range of tools and filters to access the spread of molecular markers associated with various antimalarials. In P. vivax, resistance to CQ, primaquine, mefloquine (MQ), and SP has been reported from various regions of the world and is emerging rapidly. CQ-resistant P. malariae has been reported recently in South Sumatra, Indonesia. [16]{Figure 2}

Based on the National Vector Borne Disease Control Programme surveillance in India, the malaria cases has reduced from 2 million annually in the 1990s to 1 million in 2012, with a declining trend since 2002. [17] However, the P. falciparum cases reported has increased to 50.01% in 2012 from 39% in 1995. [17] In India, CQ resistance was first reported from Karbi-Anglong district, Assam, in 1973. [18] Since then, resistance to commonly used antimalarial drugs (CQ, MQ, and SP) has been reported for P. falciparum across the country and National Drug Policy recommends the use of ACT as first-line of treatment for P. falciparum since 2010. [19],[20] Resistance to CQ has also been reported for P. vivax in few cases. [21],[22]

 Antimalarials Used Against Malaria

Based on the mode of action, the antimalarial drugs were mainly classified into three groups: quinolone, antifolate, and artemisinin derivatives. [Table 1] summarizes the widely used antimalarials adapted from "Drug resistance in malaria" [23] and modified indicating their mechanism of action and validated molecular markers for drug resistance. Most of the antimalarial drugs target the asexual erythrocytic stages of the parasite, hence called as blood schizonticidal drugs. [24] Tissue schizonticidal drugs target the hypnozoites (dormant stage of the parasite) in the liver whereas gametocytocidal drugs kill the sexual stages of the parasite in the bloodstream. [24] These antimalarial drugs have a different mode of action and mechanism within the parasite that was explained in [Table 1] and illustrated in [Figure 3]. Due to the emergence and spread of CQ and SP resistant parasite, antimalarials are being administrated as combination therapies. [Table 2] depicts the currently available ACT drugs. In ACT, each antimalarial drug targets different mechanism of action within the parasite, thereby decreasing the emergence of the multidrug-resistant parasite. Understanding the mechanism of action of drugs will depict in the identification of the specific molecular marker for drug resistance and thereby monitoring the level and spread of resistance can be carried out through the drug-resistant markers. Thus, continuous assessment of markers and therapeutic efficacy studies in malaria endemic regions will help to detect the resistant parasite, and also to understand the degree and extent of resistance associated with a particular population. These studies will aid in timely changes for an effective drug policy when the treatment failure rate exceeds 10% at the end of follow-up based on the WHO guidelines. [25]{Figure 3}{Table 1}{Table 2}

 Drug Resistance Genetic Markers

Identification of potent drug-resistant molecular marker is an important tool to determine the emergence and spread of antimalarial drug resistance worldwide. Genetic crosslink and mapping studies of parasites assisted in identifying the genetic markers for drug resistance. Crosslink studies between the CQ-sensitive and resistant strains localized a 36 kb segment on chromosome 7 of P. falciparum.[26] Further molecular analyses revealed mutation in the P. falciparum chloroquine resistance transporter (Pfcrt) gene associated strongly with CQ-susceptible and resistant strains in both laboratory and field studies. [27],[28],[29],[30] Antifolate drugs, SP, inhibits P. falciparum dihydropteroate synthetase (PfDHPS) and P. falciparum bifunctional dihydrofolate reductase-thymidylate synthase (PfDHFR) enzyme involved in folate biosynthesis pathway. In P. falciparum, biochemical and genetic cross-linkage studies allowed the identification of mutation in Pfdhps and Pfdhfr gene involved in the reduced drug susceptibility of SP respectively. [31],[32],[33],[34],[35] Whole genome sequencing of the artemisinin-resistant parasite revealed mutation in the Kelch 13 (K13) propeller protein associated with the artemisinin resistance in both clinical and field isolates. [11],[36],[37] Molecular marker detection by polymerase chain reaction for drug resistance: Overcome the in vivo and in vitro tests used, many isolates and markers screened in a short time, samples collected and stored for prolonged duration can also be studied. [38] The various drug-resistant markers identified for P. falciparum and P. vivax antimalarial drugs are discussed below; thus emergence and spread of resistance can determine easily, and necessary drug policy decisions for malaria treatment be made at the right time.

 Plasmodium falciparum Chloroquine Resistance Transporter

Pfcrt gene has 13 exons, localized to chromosome 7 encoding 424 amino acid transmembrane protein with a molecular mass of 48.6 kDa. [27] PfCRT protein belongs to the drug/metabolite transporter superfamily and chloroquine resistance transporter-like transporter family with 10 putative transmembrane domain spanning the digestive vacuole membrane of the parasite. [39] Several studies comparing the wild and mutant PfCRT allele expression showed less CQ accumulation in mutant PfCRT when compared to wild PfCRT [40],[41] and this difference in CQ accumulation is due to the active transport mechanism of mutant PfCRT in the resistant parasite. [42],[43] Recently, recombinant CQ-sensitive protein (PfCRT3D7) and CQ-resistant protein (PfCRTDd2, PfCRT7G8, PfCRTK76T [with K76T mutation in the 3D7 gene background]) were purified and found that both the CQ-sensitive and resistant protein transport CQ molecule. In addition, higher CQ transport activity was observed in CQ-resistant protein whereas higher accumulation of CQ measured in CQ-sensitive protein by proteoliposome study. Thus, the CQ-resistant variants showed decreased affinity toward CQ with increased transport activity, which lead to less accumulation of CQ in the digestive vacuole, conferring CQ resistance. [44]

Mutation in Pfcrt gene plays a significant role in determining the CQ resistance and its phenotype. The K76T mutation is the primary determinant of CQ resistance and susceptibility. [27] K76T mutation located in the first transmembrane domain of PfCRT protein, where the positively charged lysine residue is replaced by neutrally charged threonine residue at 76 th position, could allow the efflux of diprotonated CQ out of the digestive vacuole by active transport. [39] Most common mutation in other regions (C72S, M74I, N75E, A220S, Q271E, N326S, I356T, and R371I) also confer resistance, but only in association with K76T mutation.

Variation in the PfCRT protein influences antimalarial drug susceptibility and resistance to quinine, amodiaquine (AQ), piperaquine, and lumefantrine. [45],[46],[47],[48] CQ shows cross-resistance with AQ and quinine mainly mediated by 76T, whereas lumefantrine exhibits an inverse cross-resistance having reduced susceptibility in association with wild-type K76. [5] The PfCRT mutations at 72-76 codons confer higher resistance to CQ and medium level AQ resistance in Southeast Asia and Africa, whereas linked with greater AQ resistance in South America. [38] Thus, K76T mutation in PfCRT protein is a potent molecular marker for the antimalarial drug, depending on their previous use in the region.

 Plasmodium falciparum Multidrug Resistance Protein 1

The P. falciparum multidrug resistance protein 1 (Pfmdr1) gene located on chromosome 5 has one exon, encoding for P-glycoprotein homolog 1 protein with 1419 amino acid and 162.25 kDa molecular mass. [49],[50] PfMDR1 protein is a transmembrane protein, with two domains each consisting of 6 helical transmembrane domains and a nucleotide binding fold region that act as a site for ATP binding, present in the digestive vacuole of the parasite similar to PfCRT protein and belongs to the ATP-binding cassette (ABC) superfamily. [49],[50] Polymorphism, amplification, and variation in mRNA expression level of the Pfmdr1 gene have involved in resistance to various antimalarials and emergence of multi-drug resistance parasites. [50]

Mutation in Pfmdr1 gene at the following position (N86Y, Y184F, S1034C, N1042D, and D1246Y) have been reported to involve in determining the drug susceptibility to CQ, quinine, MQ, halofantrine, lumefantrine, and artemisinin. [38],[51],[52],[53] PfMDR1 mutations at N86Y and N1042D position have associated with AQ resistance. [54] K76T and A220S mutation in the Pfcrt gene and N86Y mutation in the Pfmdr1 gene associated with high resistance to CQ in field isolates. In addition, copy number variation of Pfmdr1 gene has been linked to higher level of resistance to quinine, MQ, halofantrine, lumefantrine, and artemisinin. [55]

 Plasmodium falciparum Multidrug Resistance-Associated Protein

P. falciparum multidrug resistance-associated protein (Pfmrp) gene has one exon located on chromosome 1 belonging to ABC transporter family, similar to PfMDR1. [56] PfMRP is a transmembrane protein localized to the plasma membrane of the parasite encoding 1822 amino acid with a molecular mass of 214.44 kDa and is predicted to have two nucleotide binding domains and two membrane-spanning domains with each consisting of 6 helical transmembrane domains. [56],[57] MRP helps in the transport of organic anionic substrates such as oxidized glutathione, glucuronate, sulfate conjugates, and also in drug transport. [56] Two mutations at position Y191H and A437S in PfMRP were found associated with CQ and quinine resistance. [58] Genetic knockout of Pfmrp gene in the resistant parasite, showed high sensitivity to various antimalarial drugs such as CQ, quinine, primaquine, piperaquine, and artemisinin, whereas more accumulation of CQ and quinine observed in the sensitive parasite. [57] Thus, PfMRP is involved in varying the antimalarial response to resistance but not in determining the drug resistance mainly, and also hypothesized that PfMRP protein effluxes various metabolites and drugs out of the parasite in association with other transporters. [57]

 Plasmodium falciparum Sodium Hydrogen Exchanger

P. falciparum contains a candidate gene Pfnhe1 in chromosome 13 with two exons, coding for sodium hydrogen exchanger (Na + /H + exchanger or PfNHE) protein associated with quinine resistance. [59] PfNHE1 is a transmembrane protein localized in the plasma membrane of the parasite with 1920 amino acid of 226 kDa molecular mass and predicted to have 12 transmembrane domains. [60] The role of PfNHE was not understood fully but hypothesized that it is involved in active efflux of protons to maintain pH 7.4 within the parasite, in response to acidification by anaerobic glycolysis, the primary energy source for the parasite. [61]

In field and in vitro culture studies, polymorphism in the microsatellite ms470 region exhibited a decrease in quinine susceptibility with an increase in DNNND repeat motif whereas increase in quinine susceptibility observed with a rise in NHNDNHNNDDD motif. [62] Three mutations at 790, 894, and 950 codons and polymorphism in the microsatellite region (msR1 and ms3580) showed no association with quinine resistance. [62] Thus, repeat polymorphism in Pfnhe1 gene may be used as a valid genetic marker to determine the quinine resistance in some regions [5] and resistance to quinine also mediated by other genetic markers such as Pfcrt, Pfmrd1, and Pfmrp. [63]

 Plasmodium falciparum Bifunctional Dihydrofolate Reductase-Thymidylate Synthase

The Pfdhfr-ts gene has one exon located on chromosome 4 encoding for PfDHFR protein with an appropriate molecular mass of 71.73 kDa and 608 amino acids in length. It is a bifunctional enzyme involved in two main folate metabolic activity: the biosynthesis of dTMP by thymidylate synthase activity and the reduction of dihydrofolate into tetrahydrofolate by dihydrofolate reductase activity. [64] The folate mechanism of PfDHFR enzyme inhibited by the action of antifolate drugs such as pyrimethamine and cycloguanil, thus reducing the production of pyrimidine for DNA replication. [65]

Pyrimethamine resistance has mainly associated with point mutation in the PfDHFR protein at S108D codon, further mutation at N51I, C59N, and I164L positions strengthen their resistance besides amplification of gene. [38],[66],[67],[68],[68] Double mutation at A16V and S108T positions in PfDHFR linked with the resistance of P. falciparum to cycloguanil. [69]

 Plasmodium falciparum Dihydropteroate Synthetase

The Pfdhps gene located on chromosome 8 with three exons that encode for PfDHPS protein consisting of 706 amino acid and 83.37 kDa molecular weight. PfDHPS enzyme catalyzes the reaction of the p-aminobenzoic acid (PABA) with a pterin derivative in synthesizing dihydrofolate, a folate precursor that is essential for the synthesis of pyrimidine in the parasite. [64] This catalytic enzyme action to synthesize dihydrofolate inhibited by sulfa drugs (sulfadoxine and dapsone), which act as an analog to PABA. [5],[64]

Five mutations in the PfDHPS protein (S436A/F, A437G, L540E, A581G, and A613T/S) have linked with resistance to sulfadoxine in P. falciparum. [38],[68] Mutation at 436, 581, and 613 codons are associated with higher level of resistance, whereas mutation at 437 and 540 contribute a low level of resistance with modulation effects in association with other mutation in PfDHPS. [69] Since the antimalarial drug resistance as monotherapy has emerged, sulfadoxine is always provided in combination with pyrimethamine, known as SP or Fansidar, and resistance to SP have associated with point mutation in both Pfdhfr and Pfdhps gene. [5],[31],[38],[67]

 Cytochrome B

Cytochrome b (cytb) gene is a subunit of cytochrome bc1 complex, which catalyses the transfer of electrons across the inner mitochondrial membrane to maintain the electrochemical potential of the membrane. [70] It is a mitochondrial membrane protein belonging to cytb family with 376 amino acid and 43.37 KDa molecular mass. It is predicted to have 10 putative helical transmembrane domains spanning the mitochondrial inner membrane of the parasite.

The antimalarial drug atovaquone binds to the ubiquinol binding site of cytb, thus disrupting the electrochemical potential of the mitochondrial membrane, which is fatal for the parasite survival. [70] Ubiquinol binding site is a highly conserved region of the protein and mutation in this region confers atovaquone resistance. [71],[72] Single mutation at Y268N/S/C codon in the cytb gene associated with resistance to atovaquone in P. falciparum field isolates. [38]

Kelch 13

K13 protein has one exon located on the chromosome 13 with 726 amino acid and 83.66 kDa molecular mass. The C-terminal region of K13 protein has six kelch motifs consisting of beta sheets that folded into a propeller domain and mutation in this region is predicted to disrupt the domain scaffold and alter its function. [36],[73] The kelch family proteins have diverse cellular functions, such as in organizing and interacting with other proteins. [36],[73] Furthermore, several studies are required to understand the function of K13 protein, various mutation effects on the protein and the mechanism of drug action concerning protein fully.

Recently, the point mutation in the propeller region of K13 protein has been identified as a key determinant for artemisinin resistance in P. falciparum. Nonsynonymous polymorphism at Y493H, R539T, I543T, and C580Y position observed in the kelch repeat region of K13 propeller domain have associated with higher resistance to artemisinin. [36] M476I mutation in the kelch repeat no. 2 and D56V mutation in PF3D7_0110400 gene increased the artemisinin resistance in Tanzania. [36] In cultured and field isolates, mutation at these codons F446I, Y493H, P574L, R539T, and C580Y have contributed to a higher degree of resistance to artemisinin, and the frequency of C580Y allele mutation is higher and takes longer time for parasite clearance when compared to variation in other sites. [11],[36] Thus, polymorphism in K13 propeller protein is a potent molecular marker in determining the emergence and spread of artemisinin-resistant P. falciparum. [36]

 Drug Resistance In Vivax Malaria

Malaria infection due to P. vivax is prevalent in many areas of the world except Africa, where P. falciparum infection remains higher. [12] The primary treatment for P. vivax consists of two drugs mainly: CQ (blood schizonticide) to eliminate the asexual blood stages of the parasite and primaquine (tissue schizonticide) to remove the dormant live stage (hypnozoites) of the parasite, which causes relapse in malaria infection. [12] Resistance to CQ in P. vivax emerged first in Papua New Guinea and Indonesia in the late 1980s, since then it has been reported in many parts of the world. [74] WHO recommends the use of ACT for P. vivax infection in areas where CQ resistance has been documented. [12]

The quest to find the molecular drug-resistant markers in P. vivax was based on the known molecular determinant markers in P. falciparum. [5] Increased susceptibility to CQ in P. vivax has strongly associated with the Y976F mutation in Pvmdr1 gene, which is a homolog of Pfmdr1. [75],[76],[77] Pvcrt gene in P. vivax, a homolog of Pfcrt, have not been associated with CQ resistance unlike in P. falciparum where the mutation in this gene exhibit a higher degree of resistance. [78] MQ resistance in P. vivax has associated with amplification of Pvmdr1 gene. [77],[79] In addition, mutation at Y976F position of PvMRD1 in vitro has been observed with resistance to MQ and artesunate, which requires further clinical studies. [77],[79]

The point mutation at F57L/I, S58R, T61M, and S117T/N codons of Pvdhfr gene have linked with pyrimethamine resistance and treatment failure in P. vivax. [80],[81],[82] The wild type residue V585 in Pvdhps gene showed innate resistance to sulfadoxine and is enhanced by the mutation in A383G and A553G codons in PvDHPS, which is similar to PfDHPS mutation at codons A347G and A581G. [83] In summary, drug resistance genetic markers contribute in determining the emergence and spread of resistance in P. vivax.


Emergence and spread of antimalarial drug resistance constitute a major threat toward the treatment of malaria and if not handled properly, could reverse the malaria control program and containment achieved so far worldwide. Till date, drug resistance has been reported mainly for P. falciparum and P. vivax. Antimalarial combination therapy targeting different mechanism of action could prolong the emergence and spread of drug-resistant parasites. Understanding the site of action and mechanism of the antimalarials is an important tool to identify drug-resistant marker, to prevent the development of drug resistance further and in the development of new antimalarial drugs/vaccines. The molecular markers of drug resistance play a vital role in the detection of resistance in clinical and field isolates when compared to the in vivo efficacy studies and in vitro tests. Thus, earlier detection of drug-resistant parasites in clinical isolates will aid in employing immediate and appropriate treatment that in turn reduces treatment failure and thereby mortality, and also prevents the spread of resistance. Hence, continuous monitoring and surveillance of drug-resistant molecular markers in malaria endemic regions is important in determining and assisting an effective national drug policy for malaria treatment. Therefore, more research is necessary to find new antimalarial drugs/vaccines for multidrug resistance parasites and in identification and validation of genetic markers for multidrug resistance, thereby containment and treatment of malaria can be achieved hand in hand.

Financial support and sponsorship

This work was supported by the Institute Research Grant from Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER), Pondicherry, India. The first author acknowledges the Indian Council of Medical Research (ICMR), New Delhi, for providing senior research fellowship. We thank Manochitra Kumar and Shashiraja Padukone for revising the manuscript critically.

Conflicts of interest

There are no conflicts of interest.


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