Volume 9, Number 1—January 2003
A Molecular Surveillance System for Global Patterns of Drug Resistance in Imported Malaria
Highlight and copy the desired format.
|EID||Labbé A, Patel SN, Crandall I, Kain KC. A Molecular Surveillance System for Global Patterns of Drug Resistance in Imported Malaria. Emerg Infect Dis. 2003;9(1):33-36. https://dx.doi.org/10.3201/eid0901.020121|
|AMA||Labbé A, Patel SN, Crandall I, et al. A Molecular Surveillance System for Global Patterns of Drug Resistance in Imported Malaria. Emerging Infectious Diseases. 2003;9(1):33-36. doi:10.3201/eid0901.020121.|
|APA||Labbé, A., Patel, S. N., Crandall, I., & Kain, K. C. (2003). A Molecular Surveillance System for Global Patterns of Drug Resistance in Imported Malaria. Emerging Infectious Diseases, 9(1), 33-36. https://dx.doi.org/10.3201/eid0901.020121.|
Analysis of imported malaria in travelers may represent a novel surveillance system for drug-resistant malaria. We analyzed consecutive falciparum malaria isolates from Canadian travelers from 1994 to 2000, for polymorphisms in pfcrt, dhfr, and dhps linked to chloroquine and pyrimethamine/sulfadoxine resistance. Forty percent of isolates possessed the K76 pfcrt allele, suggesting that many imported falciparum infections are still responsive to chloroquine. Travelers who had recently taken chloroquine had a significantly increased risk of harboring isolates with pfcrt resistance alleles (odds ratio = 4.47; p=0.03). The presence of two or more mutations in dhfr or dhps was found in 64.8% (95% confidence interval [CI] 54.6 to 73.9) and in 30.4% (95% CI 21.7 to 40.3) of isolates, respectively, and increased significantly over the course of the study. These molecular markers indicate that pyrimethamine/sulfadoxine resistance is increasing and is now too high to rely on this drug as a routine therapeutic agent to treat malaria in travelers.
Drug-resistant malaria is increasing, and novel strategies to monitor for resistance are needed. Over 50 million persons from the industrialized world visit malaria-endemic countries annually, and record numbers of imported malaria cases are being reported in North America and Europe (1). The first well-documented cases of chloroquine-resistant and sulfadoxine-pyrimethamine (SP)–resistant Plasmodium falciparum malaria were identified in tourists visiting East Africa in the late 1970s and early 1980s, which suggests that travelers may represent an important sentinel population to monitor for drug-resistant malaria (2,3). Although assessing travelers for malaria treatment and prophylaxis failures may be an effective strategy for detecting emerging drug resistance, traditional methods of detecting resistance, including in vivo treatment trials and in vitro drug susceptibility testing, are time- and labor-intensive and are not well suited to large-scale surveillance of travelers (4).
Molecular methods that detect genetic markers of drug resistance in parasites are potentially powerful tools to detect and track drug-resistant malaria. The molecular basis of resistance to antifolate drugs such as SP has been well characterized. High-level pyrimethamine resistance results from the accumulation of mutations in the dhfr gene, principally at codons 108, 59, and 51 (5,6). Similarly, point mutations in dhps have been associated with decreased susceptibility to sulfadoxine in vitro (7). Chloroquine resistance has been linked to mutations in two genes, pfmdr1 and pfcrt, that encode the digestive vacuole transmembrane proteins Pgh1 and PfCRT, respectively (8–13). Transfection studies with pfmdr1 suggest that mutations in Pgh1 may modulate the chloroquine resistance phenotype in vitro; however, in vivo studies have shown an inconsistent association between mutations in Pgh1 and chloroquine resistance (9–12). More recently, a series of point mutations in pfcrt have been associated with chloroquine resistance (13). One mutation at position 76 (K76T) was present in all in vitro resistant parasites and has been proposed as a molecular marker for surveillance of chloroquine-resistant falciparum malaria, particularly in nonimmune populations such as travelers (10,13).
The objectives of this study were to establish a molecular surveillance system for imported malaria, to determine and track the prevalence of putative molecular markers of drug resistance, and to examine risk factors for infection with isolates bearing resistance markers.
From January 1, 1994, to June 30, 2000, patients seen at the Toronto General Hospital or the Hospital for Sick Children in Toronto, Canada, with microscopically confirmed falciparum malaria were enrolled. Patient interviews were conducted or medical charts were reviewed for potential risk factors for infection and drug resistance by using a standardized data extraction form. This study was approved by the Institutional Review Boards of the Toronto General Hospital and the Hospital for Sick Children.
Falciparum isolates were characterized by polymerase chain reaction-restriction fragment length polymorphism analysis and sequencing for allelic variants of pfcrt and pfmdr1, dhfr, and dhps as described (5–17). Proportions were compared by using the chi-square test or Fisher exact test, as appropriate. The chi-square test for trend was used as required for variables that involved ordered categories. For the purpose of this analysis, we considered mixed isolates (e.g., isolates containing parasites with mutant and wild-type alleles) to be mutant ones and compared them against those possessing only wild-type alleles.
During the study period, 105 consecutive cases of imported falciparum malaria were recorded (69 males, 36 females; age range 1–70 years [mean 30.5]). The geographic regions in which these persons acquired their infections are shown in Table 1.
The prevalence of mutations in chloroquine-resistance markers (pfmdr1 and pfcrt) was significantly higher in isolates acquired in East Africa compared with West Africa (Table 1). Patients who acquired malaria infection in East Africa had a 4.5-fold higher risk of being infected by an isolate possessing the K76T mutation in pfcrt (odds ratio [OR] 4.53 [95% confidence interval (CI) 1.26 to 16.02]; p=0.03) than those visiting West Africa. The N86Y mutation in pfmdr1 was also found more often in isolates acquired in East Africa than in those acquired in West Africa (OR 3.56 [95% CI 1.16 to 10.80]; p=0.03). A linear trend for increasing prevalence of N86Y mutant isolates was evident during the study period (OR per year =1.21; p=0.07) (Table 2). We also examined the association between past chloroquine exposure and the prevalence of chloroquine-resistance markers. Nineteen (18.1%) patients had used chloroquine for prophylaxis (n=13) or treatment (n=6) while abroad. These persons had a significantly increased risk of being infected by an isolate harboring the K76T mutation when compared with other travelers (OR=4.47 [95% CI 1.13 to 25.45]; p=0.03).
We grouped the parasite dhfr and dhps genotypes into four categories on the basis of the cumulative number of mutations that have been linked to escalating SP resistance (Table 1). More mutations in dhps were found in isolates from travelers returning from West Africa versus East Africa (p=0.001, Fisher exact test). We found that the proportion of isolates with at least two mutations increased during the study period in both dhfr (OR for a 1-unit increase in year = 1.28; p=0.02, chi-square test for trend) and dhps (OR=1.29; p=0.03) (Table 2).
In this study, we demonstrate “proof-of-principle” that a molecular surveillance strategy based on imported malaria in travelers can be used to detect and track drug-resistant malaria. Monitoring travelers for imported drug-resistant malaria is a surveillance strategy that offers several potential advantages. Recommendations regarding treatment regimens and chemoprophylaxis for travelers should ideally be made on the basis of the efficacy of these drugs in nonimmune travelers rather than on partially immune persons residing in malaria-endemic areas. However, to date there has been little information on the rates of drug resistance in cases of imported malaria. Using travelers as a sentinel system provides a mechanism to study large numbers of persons returning from diverse malaria-endemic areas. In contrast, traditional studies have often been based on relatively small numbers of persons residing in geographically restricted areas. Travelers are generally nonimmune, facilitating the interpretation of treatment and prophylaxis studies since outcome measures are not confounded by reinfections and by the varying degrees of immunity present in residents of malaria-endemic areas. Similarly, correlating the molecular mechanisms of drug resistance to treatment outcome in travelers may be more straightforward since these confounding variables can largely be excluded. Knowledge of the resistance genotypes of malaria parasites obtained from returning travelers can provide credible and complementary data for evidence-based recommendations for both chemoprophylaxis and therapy of malaria in travelers.
The high correlation between mutations in DHFR and DHPS and in vitro resistance to pyrimethamine and sulfadoxine, further supported by site-directed mutagenesis and transfection experiments, suggests that the epidemiology of antifolate resistance in P. falciparum can be monitored by molecular techniques (5–7,14–17). Furthermore, evidence exists for an association between a stepwise increase in the number of mutations in DHFR and DHPS and a corresponding increase in the level of clinical resistance to SP. In recent in vivo studies in partially immune persons in Cameroon and Kenya, multiple mutations in DHFR (e.g., triple mutation at codons 108, 59, and 51) were associated with early treatment failure, suggesting that these could be useful markers for predicting the in vivo efficacy of SP (18–20).
Using molecular markers of antifolate resistance, our study provides important data on the appropriateness of drugs such as SP that are currently recommended in North America and Europe for treatment or self-treatment of malaria in travelers. We observed that 75%, 66%, and 28% of consecutive imported isolates had at least one, two, and three mutations in DHFR, respectively. In DHPS, corresponding figures were 80%, 30%, and 5%. Furthermore, we found a linear trend for increasing prevalence mutations in dhfr and dhps during this study. These results suggest that antifolate resistance in imported falciparum malaria is now common and escalating over time. These observations question the rationale of continued recommendation of SP as either standby therapy or combination therapy with quinine for the treatment of P. falciparum malaria in travelers. However, some caution is needed in extrapolating our data to predict the in vivo efficacy of SP. Additional prospective in vivo studies, especially in the nonimmune host, are required to definitively link antifolate molecular markers with in vivo resistance (18–20).
We have also collected data on the occurrence of mutations associated with chloroquine resistance in consecutive imported falciparum isolates. The overall prevalence of the N86Y mutation in pfmdr1 and K76T mutation in pfcrt was 47.0% and 60.2%, respectively. Recent in vivo studies have assessed the association between pfcrt mutations and chloroquine response and determined that the K76 allele correctly predicted successful outcome (9–11). A rapid assay to detect pfcrt K76T in travelers’ malaria may be useful, since the presence of the K76 allele would indicate the probable effectiveness of treatment with chloroquine alone. On the basis of these findings, we anticipate that at least 40% of our patients would have responded to chloroquine. However, in the absence of a rapid test, current recommendations from the World Health Organization and the Centers for Disease Control and Prevention must be applied, and P. falciparum infections acquired in areas of known chloroquine resistance should not be treated with chloroquine.
Chloroquine and SP resistance has been selected by drug pressure (5,6,10,21). In Mali, the K76T mutation in pfcrt was observed in persons with persistent or recurrent infection after chloroquine therapy, indicating selection for this mutation. Our study extends these observations to travelers; those who had taken chloroquine for prophylaxis or treatment had a 4.5-fold higher risk of being infected with an isolate carrying the K76T mutation. Although the number of isolates studied was relatively small, our results also indicate that the prevalence of genotypes associated with chloroquine resistance was significantly higher in isolates acquired in East Africa than in those acquired in West Africa. This observation is consistent with currently reported epidemiologic patterns (22). The distribution of chloroquine- and SP-resistant parasites and their degree of resistance are far from uniform, and regular assessment of the therapeutic efficacy of chloroquine and SP, such as obtained with World Health Organization in vivo studies, is required. Studies such as ours, using travelers as sentinels, can contribute in a novel and complementary way to the continuous monitoring and tracking of geographic drug-resistance patterns. A network of digitally linked sites in the developed world that are performing these analyses in cases of imported malaria could provide global and timely monitoring.
In summary, our study demonstrates that a molecular surveillance strategy based on imported malaria in travelers can be used to detect and track patterns of drug-resistant malaria. Given the high prevalence of observed mutations in dhfr and dhps, our data provide evidence that raises questions about the rationale of continued use of SP to treat falciparum malaria in returned travelers. Our data also indicate that a considerable proportion of imported falciparum infections are still responsive to chloroquine.
Dr. Labbé is microbiologist and infectious diseases consultant in the Department of Microbiology, Hôpital Maisonneuve-Rosemont, Assomption, Montréal, Canada.
This work was supported in part by the Physician Services Incorporated Foundation of Ontario and the Canadian Institutes of Health Research (MT-13721 to KCK). A.-C. Labbé is recipient of the Bayer Healthcare/University of Toronto fellowship in Medical Microbiology. K.C. Kain is supported by a Canada Research Chair and a Career Scientist Award from the Ontario Ministry of Health.
- Ryan ET, Kain KC. Health advice and immunizations for travelers. N Engl J Med. 2000;342:1716–25.
- Kean B. Chloroquine-resistant falciparum from Africa. JAMA. 1979;241:395.
- Onori E. The problem of Plasmodium falciparum drug resistance in Africa south of the Sahara. Bull World Health Organ. 1984;62:55–62.
- Lobel HO, Varma JK, Miani M, Green M, Todd GD, Grady K, Monitoring for mefloquine-resistant Plasmodium falciparum in Africa: implications for travelers' health. Am J Trop Med Hyg. 1998;59:129–32.
- Wang P, Lee CS, Bayoumi R, Djimde A, Doumbo O, Swedberg G, Resistance to antifolates in Plasmodium falciparum monitored by sequence analysis of dihydropteroate synthetase and dihydrofolate reductase alleles in a large number of field samples of diverse origins. Mol Biochem Parasitol. 1997;89:161–77.
- Plowe CV, Cortese JF, Djimde A, Nwanyanwu OC, Watkins WM, Winstanley PA, Mutations in Plasmodium falciparum dihydrofolate reductase and dihydropteroate synthase and epidemiologic patterns of pyrimethamine-sulfadoxine use and resistance. J Infect Dis. 1997;176:1590–6.
- Wang P, Brooks DR, Sims PF, Hyde JE. A mutation-specific PCR system to detect sequence variation in the dihydropteroate synthetase gene of Plasmodium falciparum. Mol Biochem Parasitol. 1995;71:115–25.
- Foote SJ, Kyle DE, Martin RK, Oduola AM, Forsyth K, Kemp DJ, Several alleles of the multidrug-resistance gene are closely linked to chloroquine resistance in Plasmodium falciparum. Nature. 1990;345:255–8.
- Dorsey G, Kamya MR, Singh B, Rosenthal PJ. Polymorphisms in the Plasmodium falciparum pfcrt and pfmdr-1 genes and clinical response to chloroquine in Kampala, Uganda. J Infect Dis. 2001;183:1417–20.
- Djimde A, Doumbo OK, Cortese JF, Kayentao K, Doumbo S, Diourte Y, A molecular marker for chloroquine-resistant falciparum malaria. N Engl J Med. 2001;344:257–63.
- Pillai DR, Labbe AC, Vanisaveth V, Hongvangthong B, Pomphida S, Inkathone S, Plasmodium falciparum malaria in Laos: chloroquine treatment outcome and predictive value of molecular markers. J Infect Dis. 2001;183:789–95.
- Reed MB, Saliba KJ, Caruana SR, Kirk K, Cowman AF. Pgh1 modulates sensitivity and resistance to multiple antimalarials in Plasmodium falciparum. Nature. 2000;403:906–9.
- Fidock AD, Nomura T, Talley KA, Cooper RA, Dzekunov SM, Ferdig MT, Mutations in the P. falciparum digestive vacuole transmembrane protein PfCRT and evidence for their role in chloroquine resistance. Mol Cell. 2000;6:861–71.
- Plowe CV, Djimde A, Bouare M, Doumbo O, Wellems TE. Pyrimethamine and proguanil resistance-conferring mutations in Plasmodium falciparum dihydrofolate reductase: polymerase chain reaction methods for surveillance in Africa. Am J Trop Med Hyg. 1995;52:565–8.
- Duraisingh MT, Curtis J, Warhurst DC. Plasmodium falciparum: detection of polymorphisms in the dihydrofolate reductase and dihydropteroate synthetase genes by PCR and restriction digestion. Exp Parasitol. 1998;89:1–8.
- Shaio MF, Wang P, Lee CS, Sims PF, Hyde JE. Development and comparison of quantitative assays for the dihydropteroate synthetase codon 540 mutation associated with sulfadoxine resistance in Plasmodium falciparum. Parasitology. 1998;116:203–10.
- Gyang FN, Peterson DS, Wellems TE. Plasmodium falciparum: rapid detection of dihydrofolate reductase mutations that confer resistance to cycloguanil and pyrimethamine. Exp Parasitol. 1992;74:470–2.
- Basco LK, Tahar R, Keundjian A, Ringwald P. Sequence variations in the genes encoding dihydropteroate synthase and dihydrofolate reductase and clinical response to sulfadoxine- pyrimethamine in patients with acute uncomplicated falciparum malaria. J Infect Dis. 2000;182:624–8.
- Nzila AM, Mberu EK, Sulo J, Dayo H, Winstanley PA, Sibley CH, Towards an understanding of the mechanism of pyrimethamine-sulfadoxine resistance in Plasmodium falciparum: genotyping of dihydrofolate reductase and dihydropteroate synthase of Kenyan parasites. Antimicrob Agents Chemother. 2000;44:991–6.
- Kublin JG, Dzinjalamala FK, Kamwendo DD, Malkin EM, Cortese JF, Martino LM, Molecular markers for failure of sulfadoxine-pyrimethamine and chlorproguanil-dapsone treatment of Plasmodium falciparum malaria. J Infect Dis. 2002;185:380–8.
- Curtis J, Duraisingh MT, Warhurst DC. In vivo selection for a specific genotype of dihydropteroate synthetase of Plasmodium falciparum by pyrimethamine-sulfadoxine but not chlorproguanil-dapsone treatment. J Infect Dis. 1998;177:1429–33.
- World Health Organization. The world health report 1999: making a difference. Geneva: The Organization; 1999.
- Table 1. Prevalence of molecular markers of drug resistance by region of malaria acquisition
- Table 2. Proportions of falciparum isolates with chloroquine- or sulfadoxine-pyrimethamine-associated resistance markers by year of acquisitiona
Please use the form below to submit correspondence to the authors or contact them at the following address:
Kevin C. Kain, Toronto General Hospital, EN G-224, 200 Elizabeth St., EN G-224, Toronto, ON, Canada, M5G 2C4; fax: 416-595-5826
Comment submitted successfully, thank you for your feedback.
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
- Page created: December 07, 2010
- Page last updated: December 07, 2010
- Page last reviewed: December 07, 2010
- Centers for Disease Control and Prevention,
National Center for Emerging and Zoonotic Infectious Diseases (NCEZID)
Office of the Director (OD)