Plasmodium vivax multidrug resistance-1 gene polymorphism in French Guiana

Abstract

Background

Plasmodium vivax malaria is a major public health problem in French Guiana. Some cases of resistance to chloroquine, the first-line treatment used against P. vivax malaria, have been described in the Brazilian Amazon region. The aim of this study is to investigate a possible dispersion of chloroquine-resistant P. vivax isolates in French Guiana. The genotype, polymorphism and copy number variation, of the P. vivax multidrug resistance gene-1 (pvmdr1) have been previously associated with modification of the susceptibility to chloroquine.

Methods

The pvmdr1 gene polymorphism was evaluated by sequencing and copy number variation was assessed by real-time PCR, in P. vivax isolates obtained from 591 symptomatic patients from 1997 to 2013.

Results

The results reveal that 1.0% [95% CI 0.4–2.2] of French Guiana isolates carry the mutations Y976F and F1076L, and that the proportion of isolates with multiple copies of pvmdr1 has significantly decreased over time, from 71.3% (OR = 6.2 [95% CI 62.9–78.7], p < 0.0001) in 1997–2004 to 12.8% (OR = 0.03 [95% CI 9.4–16.9], p < 0.0001) in 2009–2013. A statistically significant relationship was found between Guf-A (harboring the single mutation T958M) and Sal-1 (wild type) alleles and pvmdr1 copy number.

Conclusions

Few P. vivax isolates harboring chloroquine-resistant mutations in the pvmdr1 gene are circulating in French Guiana. However, the decrease in the prevalence of isolates carrying multiple copies of pvmdr1 might indicate that the P. vivax population in French Guiana is evolving towards a decreased susceptibility to chloroquine.

Background

Plasmodium vivax remains the most geographically widespread of the five Plasmodium species infecting humans. As the second most common cause of malaria worldwide, P. vivax is the main cause of malaria in South America, where 390,000 cases were reported by the World Health Organization in 2015 [1]. Approximately 95% of these P. vivax malaria cases occur in nine countries of the Amazon Basin, namely Brazil, Bolivia, Colombia, Ecuador, French Guiana, Guyana, Peru, Suriname and Venezuela [1]. A total of 311 P. vivax cases were reported in French Guiana in 2014, representing 70% of the total number of malaria cases [2]. Since 1995, the treatments of uncomplicated P. falciparum malaria, mefloquine or halofantrine were used in monotherapy until 2002 when they were replaced by the association atovaquone–proguanil and in 2009 by the combination of artemether–lumefantrine [2–4]. Like the other countries across the continent, chloroquine is still recommended as the first-line treatment for P. vivax in French Guiana.

In 1989, the first cases of chloroquine-resistant P. vivax infection were reported in Papua New Guinea [5]. First cases of P. vivax resistance to chloroquine in South America were described in clinical studies of unsupervised chloroquine treatment in 1989 and 1992, in Colombia and Brazil, respectively [6, 7]. It was only in 1996 that the first confirmed clinical case of resistance was described in Brazil [8]. Chloroquine resistance has spread around the world over the last decade [9], and is now found in Southeast Asia [10–14] but also in Africa [15, 16], South America [8, 17–22] and the Middle East [23, 24].

Polymorphisms in pvmdr1 gene (P. vivax multidrug resistance-1 gene, PVX_080100), orthologous to pfmdr1 gene in Plasmodium falciparum (PF3D7_0523000) [25], has been associated with chloroquine resistance in many studies. Pvmdr1 Y976F and F1076L mutations are found in all malaria-endemic regions where chloroquine is used as the first-line treatment [13, 14, 26, 27]. Isolates bearing only F1076L mutations were identified but were not associated with a chloroquine resistance [28, 29]. This observation supports the argument that P. vivax chloroquine resistance requires the presence of both mutations. It has been suggested that F1076L is the prerequisite for the secondary acquisition of Y976F, which is responsible for the decrease in chloroquine susceptibility [29]. However, no other studies have observed this correlation between Y976F mutation and resistance phenotype [15, 18]. Several studies have pinpointed an increase in pvmdr1 gene copy number, which seems to be related to an increased susceptibility to chloroquine [13, 14, 30, 31]. Furthermore, a recent study suggested that chloroquine resistance and clinical severity in vivax malaria were associated with increased expression levels of pvmdr1 and pvcrt-o genes [32].

This study aims to estimate the possible emergence of chloroquine-resistant P. vivax in French Guiana. The work is divided into two parts. Firstly, pvmdr1 gene polymorphism and copy number were assayed in P. vivax isolates obtained from blood samples of patients collected since 1997 and the temporal evolution of pvmdr1 gene polymorphism and copy number were studied.

Methods

Sample collection

Between 1997 and 2013, samples were collected from 591 symptomatic patients presenting with malaria symptoms at health centres in French Guiana. Plasmodium vivax mono-infections were diagnosed by rapid diagnostic tests and/or microscopic examination of the blood. Blood samples were collected in EDTA-coated tubes and sent to the National Reference Centre (NRC) for Malaria at the Institut Pasteur de la Guyane for further analysis and biobanking.

DNA extraction, amplification and sequencing

Parasite DNA was extracted from whole blood samples using the QIAamp DNA Blood Mini Kit (Qiagen, Courtaboeuf, France), following manufacturer’s instructions. The pvmdr1 gene was amplified and sequencing using protocol (primers and amplification condition) previously described by Lekweiry et al. [33] except the polymerase, 0.025 U/μl of Ampli Taq Gold™, 2.5 mM MgCl₂, 1× PCR Gold Buffer (Applied Biosystems). The amplification product was loaded on a 1.5% agarose gel and visualized after electrophoresis.

Sequencing of pvmdr1 PCR product was performed by using the nested primers [33] generating a product length of 547 bp (region between codon 931 and 1095). These sequence were compared with the reference sequence Sal-1 (Genbank accession number AY571984).

Pvmdr1 and pvaldolase cloning

As a reference sample with a known pvmdr1 copy number was not available, two reference plasmids containing one copy of the pvmdr1 and pvaldolase genes were generated, respectively, to use as positive controls for the real-time PCR (qPCR). They were created by PCR amplification of pvmdr1 and pvaldolase genes using A380 and A379 or A382 and A383 primers, respectively (Table 1). Each PCR product was cloned in pCR™4-TOPO^® plasmid using the TOPO^® TA Cloning^® kit (Invitrogen), following manufacturer’s protocol.

Table 1.

Primers and probes for quantification of the pvmdr1 copy number by qPCR

Primer and probe name	Sequence	Gene
A380	5′-GAG-AGG-ACG-TAA-ACG-TGC-TT-3′	pvmdr1
A379	5′-ACG-TTG-GTG-TCG-TAC-TGA-TTC-G-3′
A399	5′-FAM_TTT-GCC-GCA-ATT-GA_MGB/NFQ-3′
A382	5′-AGT-TTT-GTT-GGA-AGG-AGC-TTT-ATT-G-3′	pvaldolase
A383	5′-TGG-TTT-TCA-CAG-CAC-AGT-CGT-AT-3′
A397	5′-FAM_CCC-AAC-ATG-GTG-ACC-G_MGB/NFQ-3′

MGB/NFQ minor groove binder/non-fluorescent quencher, pvmdr1 Plasmodium vivax multi-drug resistance 1

Real-time PCR to quantify the pvmdr1 gene copy number

The pvmdr1 gene copy number was measured by performing a qPCR in comparison to the reference gene pvaldolase, using the method previously described by Lekweiry et al. [33]. The reproducibility problems encountered were solved by designing new probes using Primer Express^® software (Applied Biosystems). These primers and probes are listed in Table 1. The qPCR was carried out in a 25 μl reaction volume containing 1 μl of DNA, 300 nM of each primer, 200 nM of probe, 12.5 μl of TaqMan^® Universal Master Mix II (Applied Biosystems) and water. Real-time PCR was performed under the following conditions: 95 °C for 10 min, then 40 cycles at 95 °C for 15 s and 65 °C for 1 min. Samples were set up in triplicate and experiments were repeated independently twice.

Results analysis was executed by StepOne™ software (Applied Biosystems). The signal from the pvmdr1 gene was normalized to the single copy pvaldolase reference gene, then copy number was determined using the mathematical model described by Pfaffl [34].

Statistical analysis

All statistical analyses were performed with R software (version 3.0.2). Percentages were calculated for each parameter studied, namely single nucleotide polymorphisms and increased pvmdr1 copy number, in comparison to the total sample size. Corresponding 95% confidence intervals (CI) were calculated using the exact (Clopper-Pearson interval) method [35]. In this study, the pvmdr1 copy number was analysed as a qualitative variable and two groups were considered: samples with one copy and samples with at least two copies of the pvmdr1 gene.

A Chi square test for trend allowed comparison of the temporal evolution of pvmdr1 allele frequencies and gene copy number. A logistic regression was used to determine the association between polymorphisms and the pvmdr1 gene copy numbers. A p value below 0.05 was considered significant.

Nucleotide sequence accession numbers

The Guf-A, Guf-B and Guf-C allele sequences of the pvmdr1 gene reported in this study were deposited in GenBank under accession numbers KU196660, KU196661 and KU196662, respectively.

Results

Demographic information

A total of 547 patients for 591 sample, 362 men and 185 women with the sex ratio of 1.96, were included in this study. The average age was 29.2 years (1 month to 76 years, including 88 children under 15 years) with parasitaemia between 0.001 and 4% with an average of 0.32% (Table 2). Three time periods (1997–2004, 2005–2008 and 2009–2013) were considered according to the years 2005 when the P. vivax became the dominant species diagnosed in French Guiana, and 2009 when the combination of artemether and lumefantrine was adopted for the treatment of P. falciparum and mixed infections (P. falciparum/P. vivax) in French Guiana (Table 2). No significant association on all parameters (age, sex ratio and parasitaemia) and the time period.

Table 2.

Demographic information

Year	Number of patient	Age (mini–max)	Nb men	Nb women	Sex ratio	Parasitemia % (mini–max)
1997–2004	136	26.7 (0.46–56)	85	50	1.7	0.4 (0.01–2)
2005–2008	120	22.9 (0.08–63)	82	38	2.16	0.5 (0.01–4)
2009–2013	291	31.2 (0.67–76)	195	97	2.01	0.3 (0.001–2.3)
Total	547	29.2 (0.08–76)	362	185	1.96	0.32 (0.001–4)

Age were indicated in year; the parasitemia were indicated on percentage of red blood cell infected by P. vivax

Polymorphism of the pvmdr1 gene

Among the 591 genotyped samples, four non-synonymous mutations (T958 M, Y976F, F1070L and F1076L) and one synonymous mutation (L1022L) were identified. The French Guiana strains were then divided into four alleles (Fig. 1). The Sal-1 wild-type allele was present in 11.2% (n = 66/591, CI 95% [8.7–14.0]) of the samples while 86.5% (n = 511/591, CI 95% [83.4–89.1]) of isolates carried the T958 M mutation and this predominant allele was called Guf-A. Only 1.4% (n = 8/591, CI 95% [0.6–2.7]) of isolates carried the T958M/F1070L mutations and this double mutant allele was referenced as Guf-B. Finally, 1.0% (n = 6/591, CI 95% [0.4–2.2]) of isolates carried the T958M/Y976F/F1076L, this triple mutant was named Guf-C (Fig. 1).

Fig. 1.

Pvmdr1 sequence polymorphism (codon 931–1095) of 591 isolates collected in French Guiana between 1997 and 2013. Only polymorphic codons are indicated. Open symbols denote the wild-type (Sal-1-type) nucleotide sequence, and black symbols indicate the presence of the mutant sequence shown at the top. The number of isolates observed for each allele is indicated in brackets

The temporal evolution of these alleles was then determined (1997–2004, n = 136; 2005–2008, n = 120 and 2009–2013, n = 335; Fig. 2). No significant association was found between the frequency of Guf-B and Guf-C alleles and the time period (p = 0.44 and p = 0.35, respectively, Chi square test for trend). A statistically significant increase in the frequency of the Sal-1 allele through time (p < 0.0001) has detected, along with a statistically significant decrease for the Guf-A allele (p < 0.002) (Fig. 2). Furthermore, relationship between epidemiological data and genotype was not observed.

Fig. 2.

Temporal evolution of pvmdr1 allele frequencies. *p < 0.0002 and **p < 0.0001 denote significant differences in allele frequencies through time (Chi square test for trend)

Relationship between copy number and genotype of the pvmdr1 gene

The copy number of the pvmdr1 gene was determined for all samples and varied from 1 to 8 (mean 1.45, CI 95% [1.35–1.55]). The majority of the sample, 68.5% (n = 405/591, CI 95% [64.6–72.3]), had one copy while 31.5% (n = 186/591, CI 95% [27.7–35.4]) had two to eight copies. The frequency of isolates with multiple copies of the pvmdr1 gene was significantly higher in samples collected between 1997 and 2004 (97/136, 71.3%, CI 95% [62.9–78.7]) than in samples from 2005 to 2008 (45/120, 37.5%, CI 95% [28.8–46.8]) or even after 2008 (43/335, 12.8%, CI 95% [9.4–16.9]). This decrease over time was statistically significant (p < 0.0001, Chi square test for trend, see Fig. 3). Moreover, relationship between epidemiological data and copy number was not observed.

Fig. 3.

Temporal evolution of the proportion of isolates harbouring single or multiple pvmdr1 copy number. White represents the isolates with single copy number of pvmdr1 gene, and black indicates isolates with two or more pvmdr1 copy numbers. *p < 0.0001 for Chi square test for trend

The association between the copy number and genotype of the pvmdr1 gene was evaluated. The proportion of isolates harbouring multiple copies was not equally distributed among the different alleles. A statistically significant association was found between the Sal-1 allele and single copy pvmdr1 gene (p = 0.0006) as well as between the Guf-A allele and copy number greater than 1 (p = 0.0002). No statistically significant relationship was found between the Guf-B and Guf-C alleles and the pvmdr1 gene copy number (p = 0.93 and p = 0.58, respectively, Fig. 4).

Fig. 4.

Evaluation of the relationship between pvmdr1 copy number and genotype. *OR = 0.12 [95% CI 0.04–0.034], p = 0.00006. **OR = 5.57 [95% CI 2.51–12.36], p = 0.00002. ***OR = 0.73 [95% CI 0.15–3.64], p = 0.70. ****OR = 0.44 [95% CI 0.05–3.76], p = 0.45

Discussion

Vivax malaria is a major public health problem in South America. In French Guiana, it is currently responsible for two-thirds of malaria cases. Resistance to chloroquine, the main treatment used against vivax malaria [2], has been reported in the Brazilian Amazon Region [4, 17, 18, 20, 21, 32, 36, 37]. In French Guiana, the development of gold-mining activities and the consequent human migration between French Guiana and neighbouring countries, Brazil and Suriname [4, 38, 39], have raised fears that chloroquine-resistant P. vivax isolates may spread. It is therefore important to follow the circulation of resistant isolates. There are previous studies suggesting that Y976F and F1076L mutations in the pvmdr1 gene are associated with in vitro resistance to chloroquine [13, 14]. Pvmdr1 Y976F mutation alone is not sufficient to cause the failure of chloroquine treatment, as observed in Madagascar [15], Brazil [21] and Honduras [40]. It can only affect treatment outcome when associated with the F1076L mutation. In French Guiana, these two mutations were carried by 1.0% of the isolates (i.e., Guf-C allele). Therefore, these parasites could potentially be resistant to chloroquine; however, an association with clinical drug response or in vitro susceptibility have not been investigated. This value is similar to the 1.8% prevalence reported in Brazil [41].

Sal-1 and Guf-A alleles were present in 11.2 and 86.5% of the samples in French Guiana, respectively, showing significant and inverse trends in the temporal evolution of their frequency; while the frequency of the Sal-1 allele significantly increased over time, the frequency of the Guf-A allele decreased. These temporal variations of allele frequencies could be explained by different factors, such as the increased circulation of isolates between French Guiana and Brazil or changes in drug policy for the treatment of P. falciparum. This is supported by a recent study showing that the T958M mutation allele is the majority among Brazilian isolates collected between 2010 and 2014 [42]. Many studies in Southeast Asia have shown that isolates with pvmdr1 gene amplification were characterized by increased susceptibility to chloroquine but decreased susceptibility to mefloquine [13, 31]. A significant decrease of the proportion of isolates with multiple copies of pvmdr1 over this 16-year study period has been found, decreasing from 71.3% between 1997 and 2004 to only 12.8% between 2009 and 2013. A recent study comparing P. vivax isolates from French Guiana (collected between 2001 and 2003) and Southeast Asia (collected in 2010) showed the number of isolates with multiple copies of pvmdr1 gene to be higher in French Guiana than in Cambodia [43]. Moreover, pvmdr1 gene amplifications were rare (fewer than 2%) in countries where mefloquine has never been used for malaria treatment, such as Madagascar and Sudan [43]. In P. falciparum, multiple copies of pfmdr1 were associated with mefloquine-resistant isolates [44]. This has been confirmed in French Guiana where isolates with amplified copy number of pfmdr1 gene were significantly correlated with resistance to mefloquine and halofantrine, both used in monotherapy against uncomplicated P. falciparum malaria until 2002 [45]. P. vivax isolates were therefore subjected to indirect selection pressure by mefloquine during the treatment of P. falciparum or mixed infections (P. falciparum and P. vivax). When the use of mefloquine and halofantrine ceased in French Guiana, P. falciparum isolates with one copy of pfmdr1 increased [45]. This loss of selective pressure would also explain the increased frequency of P. vivax isolates with a single copy of the pvmdr1 gene, a genotype associated to chloroquine resistance [13].

Recently two studies analyzing the whole genome sequences of isolates collected in America, Africa and Asia, have shown great diversity of P. vivax isolates according to their geographical origin in particular for malaria drug antifolate resistance genes involved in resistance to (pvdhfr and pvdhps) [46, 47]. Nevertheless, the role of pvmdr1 in conferring resistance to chloroquine is still elusive and controversial and was recently further challenged by global population genomic studies of P. vivax. Indeed, Schousboe et al. studied the prevalence of polymorphisms and the diversity in microsatellite markers flanking the pvmdr1 gene in P. vivax isolates from seven endemic countries worldwide (Pakistan, Afghanistan, Nepal, Sri Lanka, Ecuador, Sao Tomé and Sudan). Although they showed that Y976F and F1076L mutations in pvmdr1 gene have developed on multiple haplotype backgrounds by convergent evolution in these countries, they highlighted high levels of diversity around mutant alleles, suggesting these alleles were not subject to a selective sweep [48].

Conclusions

The present study indicates that P. vivax isolates with mutations in pvmdr1 previously described as associated with chloroquine resistance are present at low frequency in French Guiana. In addition, the number of copies of the gene decreases over time. A continuous surveillance of these genetic markers in the P. vivax population circulating in this region should be maintained to ensure public health.