A dual colour fluorescence in situ hybridization (FISH) assay for identifying the zoonotic malaria parasite Plasmodium knowlesi with a potential application for the specific diagnosis of knowlesi malaria in peripheral-level laboratories of Southeast Asia

Background Plasmodium knowlesi is primarily responsible for zoonotic malaria in several Southeast Asian countries. Precise identification of the parasite in the blood of patients presently relies on an expensive and elaborate PCR procedure because microscopic examination of blood and other available field identification techniques lack adequate specificity. Therefore, the use of a simple and inexpensive dual-colour fluorescence in situ hybridization (FISH) assay, analogous to FISH assays recently described for Plasmodium falciparum and Plasmodium vivax, was investigated as a potential tool for identifying P. knowlesi. Results A P. knowlesi 18S rDNA sequence-based DNA probe was used to test thin blood smears of P. knowlesi by FISH, and fluorescence viewed in a light microscope fitted with a light emitting diode light source and appropriate emission and barrier filters. The limit of detection in the P. knowlesi FISH assay was 84 parasites per μl in infected monkey blood and 61 parasites per μl for P. knowlesi cultured in human blood. The P. knowlesi-specific FISH probe detected only P. knowlesi and not P. falciparum, Plasmodium malariae, Plasmodium ovale, P. vivax or a panel of other human blood-borne pathogens. A previously described Plasmodium genus-specific probe used simultaneously in the P. knowlesi FISH assay reacted with all tested Plasmodium species. Conclusions To our knowledge, this is the first description of a FISH assay for P. knowlesi that is potentially useful for diagnosing infections in remote laboratories in endemic countries. Electronic supplementary material The online version of this article (doi:10.1186/s13071-017-2273-7) contains supplementary material, which is available to authorized users.


Background
The four common species of human malaria parasites, i.e. Plasmodium falciparum, Plasmodium vivax, Plasmodium malariae and Plasmodium ovale, transmitted between humans by anopheline mosquito vectors, have an ancient zoonotic origin [1]. Zoonotic malaria is currently a relatively neglected aspect of human malaria. Alterations in patterns of human settlements in the vicinity of forests, and deforestation, are increasing human proximity to primate malaria hosts in the tropics causing zoonotic malaria to become an emerging human health concern [1]. Primate malaria parasites that are naturally transmitted by anopheline mosquito vectors to humans at the present time include the catarrhine monkey parasites Plasmodium knowlesi and Plasmodium cynomolgi in Southeast Asia, the platyrrhine monkey parasites Plasmodium brasilianum and Plasmodium simium in South America, and Plasmodium vivax-like parasites from apes in West Africa [1]. The clinical significance of Plasmodium knowlesi malaria is increasingly recognized in Southeast Asia after the initial discovery of a focus of human infections in the Kapit division of the Sarawak state in Malaysian Borneo [2], subsequently in peninsular Malaysia [3][4][5] and then in other Southeast Asian countries [6]. Plasmodium knowlesi is normally a parasite of Macaca fascicularis (the long-tailed or crab-eating macaque), M. nemestrina (the pig-tailed macaque), Trachypithecus obscuras (the dusky leaf monkey or spectacled langur) and Presbytis melalophus (the banded leaf monkey or brown langur) ( [3,6] and references therein). Plasmodium knowlesi infections in humans are commonly misidentified as P. malariae and P. falciparum during routine microscopic examination of Giemsa-stained blood smears because of morphological similarities between the blood stages [2][3][4][5][6]. Therefore, the definitive identification of human infections caused by P. knowlesi presently relies on PCR-based techniques [2][3][4][5][6]. The diagnosis of P. knowlesi malaria is important in a clinical context because its pathogenicity and drug treatment options can differ from the human malaria caused by P. falciparum, P. malariae, P. ovale and P. vivax that are also prevalent in the Southeast Asian region. Rapid immunochromatographybased diagnostic tests (RDTs) are being increasingly used worldwide to detect malaria but a reliable RDT for specifically detecting P. knowlesi is not yet available [7]. PCRbased assays are sensitive enough to detect 1-5 parasites per μl of blood and able to discriminate between the different Plasmodium species that infect humans, including P. knowlesi [8]. However PCR-based assays are relatively expensive, time consuming, and require specialized equipment. PCR-based techniques are therefore not suitable for routine diagnosis in typical peripheral and district-level diagnostic laboratories in the P. knowlesi-endemic regions of Southeast Asia.
Fluorescence in situ hybridization (FISH) is a cytogenetic technique using short complementary probes labeled with fluorescent molecules to localize and detect specific target DNA or RNA sequences. Because there are many copies of ribosomal RNA (rRNA) in the cytoplasm able to react with specific probes, rRNA can be visualized without amplification of the target sequence. It is also possible to find short nucleotide stretches that are unique to a genus or species making rRNA suitable for differentiating closely related pathogens [9,10]. DNA probe-based FISH assays targeting 18S rRNA that detect P. falciparum and P. vivax in patient blood smears with appropriate diagnostic sensitivity and specificity, and suitable for use in peripheral laboratories in endemic areas, have recently been described [10]. The FISH assays can be performed with a light emitting diode (LED) light source with appropriate barrier and emission filters attached to a standard laboratory microscope [10]. To our knowledge, the development of an analogous FISH assay (termed the PK-FISH assay) capable of identifying P. knowlesi is described here for the first time.

Malaria parasites, other human pathogens and uninfected human blood
Thin smears of P. knowlesi on pre-cleaned microscope slides for FISH assays were prepared from two different sources of the parasite: (i) frozen blood from a West Malaysian strain of P. knowlesi first isolated in 1962 from M. fascicularis and subsequently maintained by serial passage in monkeys (ATCC 30192 obtained from American Type Culture Collection or ATCC, Atlanta, GA); and (ii) fresh in vitro cultures of the A1-H.1 clone, initially derived from the reference P. knowlesi H strain first isolated from a patient [11] and then recently adapted to grow in vitro in human red blood cells at the London School of Hygiene and Tropical Medicine, London, UK [12]. The P. knowlesi A1-H.1 strain parasites were grown in human blood obtained from the UK National Blood Transfusion Service using previously described culture conditions [12]. Plasmodium knowlesi cultures were synchronized by centrifugation through a cushion of Nycodenz (Axis-Shield, Oslo, Norway) as previously described [12].
Plasmodium falciparum, P. malariae and P. ovale blood smears from patients were provided by the Kenya Medical Research Institute/Walter Reed Project, Kisumu, Kenya, and P. vivax patient blood smears by the Kasturba Medical College Hospital, Mangalore, India, all being derived from anonymized left over patient samples as previously described [10]. In vitro cultures of P. falciparum strain 3D7 in human red blood cells were obtained from the London School of Hygiene and Tropical Medicine, London, UK.
Uninfected EDTA-treated human blood used as a control in the PK-FISH assay was obtained from ID-FISH Technology Inc., Palo Alto, CA. Bacterial and non-plasmodial protozoan blood-borne pathogens from different sources were used as additional specificity controls in the PK-FISH assay and these are detailed in Table 1.

FISH assay reagents
The Plasmodium knowlesi FISH assay kit (PK-FISH assay kit, catalogue number PkK04) used in the study was obtained from ID-FISH Technology Inc., Palo Alto, CA, USA. The kit contained Plasmodium genus-and P. knowlesi-specific DNA probes with hybridization buffer, smear preparation reagent (SPR), Plasmodium wash buffer, Plasmodium rinse buffer and Plasmodium mounting medium. The use of the Plasmodium genusspecific probe to detect the four common human Plasmodium species and also P. knowlesi by FISH has been previously described [10]. The P. knowlesi-specific probe in the PK-FISH assay kit (US patent application number 15/389,827) was based on a nucleotide sequence which has since been found to be conserved in all 18S rRNA sequences of different P. knowlesi isolates from humans and macaques deposited to date in GenBank. The PK-FISH assay was performed according to the manufacturer's instructions provided with the kit.
In the PK-FISH assay kit, the P. knowlesi-specific probe was labeled with Alexa 488 green fluorescent dye and the Plasmodium genus-specific probe with Atto 550 orange fluorescent dye. Therefore with LED illumination, only P. knowlesi parasites are expected to appear green under a green filter (excitation 492 nm; emission 530 nm band pass) in the assay. Under an orange filter (excitation 560; emission 630 nm long pass), all Plasmodium species, including P. knowlesi, are expected to appear orange.
Reactions of P. knowlesi and other blood-borne pathogens in the PK-FISH assay Thin blood smears of P. knowlesi from monkey blood and in vitro culture in human blood, together with control smears from uninfected human blood, other human malaria parasite species derived from patients and the reference set of non-plasmodial blood-borne pathogens were tested in the PK-FISH assay to estimate its potential specificity for detecting P. knowlesi.

Plasmodium knowlesi from infected monkey blood
This was done first at the ID-FISH laboratories, Palo Alto, CA, USA, in order to establish the P. knowlesi FISH assay procedure. EDTA-treated monkey blood containing parasites was mixed with SPR at 3 parts blood: 1 part SPR by volume. A set of four thin smears was prepared from each test sample. Each smear was prepared from 4 μl of the mixture, air-dried and fixed in methanol for subsequent testing in the PK-FISH assay. Briefly, after addition of the two probes in 12 μl of hybridization buffer to each methanol-fixed smear, the smear was covered with a plastic cover-slip and placed in a humid chamber at 37°C for 15 min for hybridization. After 15 min, each smear was washed twice for 2 min each with 1× Plasmodium wash buffer at ambient temperature, followed by a rinse with 1× Plasmodium rinse buffer. After drying the smears in complete darkness, a drop of Plasmodium mounting medium was added to each smear. The smear was then covered with a glass coverslip and viewed at ×1000 magnification, in an Olympus light microscope with an attached LED unit containing the filter set. A laboratory microscope with a LED light source and filter attachment is illustrated in Additional file 1: Figure S1.

Plasmodium knowlesi grown in vitro in human blood
A1-H.1 parasites from in vitro cultures in human red blood cells and synchronised as described to enrich for ring, trophozoite and schizont stages in different cultures [12] were used to prepare thin blood smears at the London School of Hygiene and Tropical Medicine and subsequently analyzed by the PK-FISH assay at the ID-FISH laboratories, Palo Alto, CA, USA, as described above for monkey blood. Limit of detection (LOD) of P. knowlesi in the PK-FISH assay In a manner previously described for P. falciparum and P. vivax [10], the lowest concentration of parasites that could be detected in every one of the replicated smears at different serial dilutions of P. knowlesi from monkey blood or human blood culture was determined as the LOD.

Plasmodium knowlesi in monkey blood
The parasitemia determined by Giemsa staining was 42,000 parasites per μl in the original monkey blood sample. This was serially diluted in EDTA-treated normal human venous blood (ID-FISH laboratories, Palo Alto, CA, USA) at 1:5, 1:10, 1:50, 1:100, 1:500 and 1:1000 dilutions. At each dilution multiple thin blood smears were made and three smears tested in the PK-FISH assay. The concentration of parasites at the greatest dilution at which parasites could be detected by the P. knowlesi-specific probe in all three replicate smears was considered to be the provisional LOD. Once a provisional LOD was determined, an additional 17 smears were tested at the same dilution for confirming the LOD.

Plasmodium knowlesi grown in vitro in human blood
A1-H.1 culture at 3.9% parasitemia was diluted 1:10, 1:100 and subsequently at serial two-fold dilutions in EDTA-treated normal human blood at the London School of Hygiene and Tropical Medicine, London, UK, to prepare smears for determining the LOD. Initially two smears at 1:200 and greater dilutions were tested to determine a provisional LOD where both duplicate smears were positive in the PK-FISH assay. Based on the provisional LOD, 20 replicate smears at the same dilution as well as two-fold higher and two-fold lower dilutions were made and transported for testing by the PK-FISH assay in the ID-FISH laboratories, Palo Alto, CA, USA. The concentration of parasites at the greatest dilution at which all 20 replicate smears were positive in the assay was considered to be the LOD.
Characteristics of the PK-FISH assay on blood smears containing both P. falciparum and P. knowlesi To determine whether the concomitant presence of P. falciparum affects the detection of P. knowlesi due to a possible cross-reaction of the P. knowlesi-specific FISH probe with P. falciparum, the PK-FISH assay was performed on serial dilutions of P. knowlesi containing a relatively high concentration of P. falciparum. In vitro cultures of P. falciparum 3D7 and P. knowlesi A1-H.1 at 4% parasitaemia were used as starting material for this purpose at the London School of Hygiene and Tropical Medicine, London, UK. Beginning at a 1:400 dilution in uninfected human red blood cells estimated to yield 500 P. knowlesi per μl, the P. knowlesi culture was serially diluted two-fold up to a dilution of 1:25,600 in a stock of 1:400 dilution of the original P. falciparum culture in fresh uninfected human red blood cells estimated to contain 500 P. falciparum per μl. A 1:1 v/v mixture of the 1:400 dilutions of the P. knowlesi and P. falciparum cultures at 4% parasitaemia was also prepared. Thin blood smears were then made from the mixed parasites at the London School of Hygiene and Tropical Medicine, London, UK, and triplicate blood smears at each dilution of P. knowlesi were tested by the PK-FISH assay at the ID-FISH laboratories, Palo Alto, CA, USA, using the procedures outlined above.

Results
Reactions of P. knowlesi and other human malaria parasites and pathogens in the PK-FISH assay Use of the dual fluorescence Plasmodium genus-specific and the P. knowlesi-specific probes in the PK-FISH assay showed that both probes reacted simultaneously with P. knowlesi present in the same microscopic field of monkey blood (Fig. 1). Similarly, both probes could also label P. knowlesi A1-H.1 strain parasites, grown in human red blood cells in vitro (Fig. 2). By using synchronized in vitro cultures of the A1-H.1 enriched for either ring, trophozoite or schizont-stage parasites, we were able to demonstrate reactivity of the P. knowlesi and Plasmodium genus-specific probes against each stage of asexual development in the blood, with distinct staining patterns discernable for each parasite stage (Fig. 2). Additional tests showed that the P. knowlesi-specific probe used in the PK-FISH assay did not react with patient-derived P. falciparum, P. vivax, P. malariae or P. ovale that were however detected by the Plasmodium genus-specific probe in the same microscope field (Fig. 3).
None of the other blood-borne bacterial and protozoan pathogens listed in Table 1 or uninfected human blood cells gave a positive reaction with either of the two probes in the PK-FISH assay. An example of nonreactive labelling is illustrated by the PK-FISH assay performed on B. duncani, another apicomplexan parasite closely related to the Plasmodium genus (Fig. 4). This shows that both the P. knowlesi-specific probe and the Plasmodium genus-specific probe fail to react with B. duncani. The B. duncani in the same hamster blood sample was however able to react with a Babesia genusspecific FISH probe (Fig. 4).

Limit of detection of P. knowlesi in the PK-FISH assay
The greatest dilution at which the monkey bloodderived P. knowlesi was detected in the PK-FISH assay in every one of the 20 replicate smears was 1:500. Based on the original parasitemia of 42,000 parasites per μl determined by Giemsa staining, this corresponded to a LOD of 84 P. knowlesi parasites per μl of blood.
The greatest dilution of the culture at which the in vitro grown P. knowlesi A1-H.1 could be detected in both duplicate smears in the PK-FISH assay was 1:6400. This corresponds to a provisional LOD of 61 parasites per μl of blood. The LOD was confirmed with the 20 additional smears tested at 1:6400 dilution as all smears were positive at this dilution. At a 1:3200 dilution corresponding to 123 parasites per μl, all 20 replicate smears were also positive in the PK-FISH assay and this was also the case with the duplicate smears initially tested at this and lower dilutions. At 1:12,800 dilution corresponding to 31 parasites per μl, 16 of the 20 replicate smears were positive giving a detection rate of 80%. At 1:25,600 and greater dilutions of the culture, parasites could not be Fig. 1 Fluorescence observed in the PK-FISH assay with the P. knowlesi-specific probe (green) and the Plasmodium genus-specific probe (orange) on monkey blood smears containing P. knowlesi. Dual colour fluorescence seen in a single microscope field at ×1000 magnification using the two different filters is shown in each set of paired photographs. The four sets of paired photographs are from four different fields (i) -(iv). Scale-bars: 5 μm Fig. 2 Fluorescence observed in the PK-FISH assay with the P. knowlesi-specific probe (green) and the Plasmodium genus-specific probe (orange) on different asexual stages of P. knowlesi A1-H.1 cultured in human blood. Dual colour fluorescence seen in the same microscope field at ×1000 magnification using the two different filters is shown in paired photographs R1 and R2, T1 and T2, and S1 and S2. Photographs of ring, trophozoite and schizont-stage parasites stained with Giemsa from smears prepared in parallel to the corresponding smears used in the PK-FISH assay are shown in R3, T3 and S3, respectively. Scale-bars: 5 μm. Abbreviations: R, rings; T, trophozoites; S, schizonts detected in either of the duplicate smears by the PK-FISH assay.
The LOD of P. knowlesi with the Plasmodium genusspecific probe observed under orange filter was the same as that observed with the P. knowlesi-specific probe under the green filter in both monkey blood and in vitro human red blood cell culture.
PK-FISH assay on mixed preparations of P. falciparum and P. knowlesi Mixed infections of multiple species of malaria parasite in a single patient are common and therefore we additionally tested the ability of the PK-FISH assay to detect P. knowlesi in the context of a mixed infection. For this, we artificially created mixed infections using in vitro cultured P. knowlesi and P. falciparum for the assay. The lowest concentration of P. knowlesi that could be detected in the presence of P. falciparum by the PK-FISH assay in all three replicate smears was 16 P. knowlesi parasites per μl. This was achieved in the concomitant presence of P. falciparum at approximately 500 parasites per μl. The absence of a reaction of the P. knowlesi-specific probe with P. falciparum in smears containing a mixture of P. knowlesi and P. falciparum at a final concentration of 250 parasite per μl each in the PK-FISH assay is illustrated in Fig. 5, where the Plasmodium genus-specific probe is concurrently shown to react with both P. falciparum and P. knowlesi.

Discussion
The FISH assays developed for P. falciparum and P. vivax were reported to be at least as sensitive and more specific than microscopic examination of Giemsa-stained slides, and directly applicable for diagnosis in malaria-endemic countries [10]. The desirable characteristics of these FISH assays were attributed to the selection of suitable probe sequences, appropriate smear preparation to facilitate penetration of DNA probes through the cell membrane and good hybridization properties. The present findings suggest that a similar FISH assay for P. knowlesi, described here for the first time can accurately identify the parasite, potentially overcoming the problem of misidentifying P. knowlesi as P. malariae or P. falciparum in Southeast Asia. The P. knowlesi-specific and the Plasmodium genusspecific probes in the PK-FISH assay were 100% accurate in detecting the two different P. knowlesi isolates tested and the 13 reference pathogens. The LOD of parasites in the PK-FISH assay was at least 84 P. knowlesi parasites per μl in thin blood smears which is comparable to routine microscopy with Giemsa-stained blood films [10]. The LOD of similar FISH assays for P. falciparum and P. vivax were reported to be 55 and 59 parasites per μl respectively [10]. The LOD may be improved if the FISH assay can be adapted to thick blood smears but our observations suggest that this is not yet possible. The PK-FISH assay is however likely to be equally effective on smears made directly from finger prick samples of patient blood as shown previously for the analogous P. falciparum-and Fig. 3 Fluorescence observed in the PK-FISH assay with the P. knowlesi-specific probe (green) and the Plasmodium genus-specific probe (orange) in blood smears containing Plasmodium spp. from monkey blood. Each set of paired photographs show the dual colour fluorescence in the same microscope field at ×1000 magnification using the two different filters. Scale-bars: 5 μm. Abbreviations: Pk, P. knowlesi; Pf, P. falciparum; Pm, P. malariae; Po, P. ovale; Pv, P. vivax Fig. 4 Fluorescence observed in the PK-FISH assay with the P. knowlesi-specific probe (green), the Plasmodium genus-specific probe (orange) and the Babesia genus-specific probe (green) in specificity control blood smears prepared from hamster blood infected with B. duncani. Two smears (Smear 1 and Smear 2) were made with the same B. duncani-infected hamster blood (ATCC PRA-302). Smear 1 was tested in the PK-FISH Assay and Smear 2 was tested in a Babesia genus-specific FISH assay. The results viewed at ×1000 magnification show a absence of a reaction in the PK-FISH assay with the P. knowlesi-specific probe on Smear 1, b absence of a reaction in the PK-FISH assay in the same microscope field with the Plasmodium genus-specific probe on Smear 1, and c reaction with the Babesia genus-specific FISH probe on Smear 2. Scale-bars: 5 μm P. vivax-specific FISH assays [10]. Because RNA is rapidly degraded in dying cells, the FISH assays preferentially detect live parasites in patient blood as previously reported [10]. Therefore the PK-FISH assay may also be useful for monitoring the in vivo response of P. knowlesi to drug treatment.
The PK-FISH assay described here has the added advantage of being potentially able to simultaneously detect mixed infections of P. knowlesi and other Plasmodium species seen in some patients [2,5]. This is because the other Plasmodium species will bind the Plasmodium genus-specific probe but not the P. knowlesi-specific probe and can subsequently be identified by other species-specific FISH assays [10]. There was no evidence for a cross-reaction of the P. knowlesispecific probe with P. falciparum when it was tested with a mixture of the two parasites derived from in vitro cultures because there was no indication that the LOD for P. knowlesi was reduced and no fluorescence reaction was observed with the probe on P. falciparum.
There is evidence for at least two genetically dimorphic P. knowlesi populations in Southeast Asia, likely to be associated with adaptation to the two main macaque hosts, M. fascicularis and M. nemestrina [13][14][15][16]. The rRNA sequences available in GenBank, which include reported sequences from the two populations [15], suggest that the specifically selected target rRNA sequence for the P. knowlesi-specific probe used here does not differ between the two populations. This can be further investigated with knowlesi malaria patients in Southeast Asia. Blood samples or smears from patients with P. knowlesi malaria in endemic areas of Southeast Asia were however not available for testing in the PK-FISH assay during the present investigation. Studies with a large number of such blood samples are necessary to determine the clinical diagnostic parameters and applicability of the PK-FISH assay in knowlesi malaria-endemic countries.
Another technique that rapidly detects P. knowlesi infections in human blood uses the loop-mediated isothermal amplification (LAMP) procedure, but this has not yet been adapted for routine use in endemic areas [17]. The advantages of FISH assays for malaria compared to the more sensitive nested PCR assays have been previously discussed in detail for the P. falciparum and P. vivax FISH assays [10], and the same considerations also apply to the PK-FISH assay. In essence, the FISH assays require no specialized equipment other than a light microscope with a LED source and filter attachments, and are less costly and simpler to perform than PCRbased tests. A single LED and filter attachment on a microscope may also be used for several different pathogen-specific FISH assays. The LED can be powered by low voltage batteries in areas where the mains electricity supply is not reliable and offers many other advantages over mercury arc lamps used in conventional fluorescence microscopes [10]. Another important consideration for delivery and use in tropical countries is that the PK-FISH assay kit is stable at 30°C for several months. The PK-FISH assay is therefore potentially useful for diagnosing P. knowlesi malaria in peripheral and district-level diagnostic laboratories in Southeast Asian countries. It also has similar advantages in this respect to the dual colour fluorescence FISH assays recently described for identifying Mycobacterium tuberculosis and Mycobacterium avium complexes [18].
The need for a simple and rapid assay for diagnosing P. knowlesi in peripheral and district-level endemic arealaboratories is illustrated by two recent case reports of knowlesi malaria in (i) a person working in a mining development in Indonesian Borneo [19] and (ii) a Sri Lankan soldier returning from training in peninsular Malaysia [20]. PCR-based diagnosis was the only available procedure for specific diagnosis in both cases and this involved recourse to a central molecular biology facility, in Jakarta in the Indonesian case and Singapore in the Sri Lankan case [19,20].  5 The reaction of a mixture of P. falciparum and P. knowlesi in the PK-FISH assay. In vitro cultures of P. falciparum and P. knowlesi were mixed 1:1 v/v to yield 250 parasites per μl of each parasite and then tested in the PK-FISH assay. The dual colour fluorescence observed in the same field viewed at ×1000 magnification with a the Plasmodium genus-specific probe (orange) and b the P. knowlesi-specific probe (green) are shown. Scale-bars: 5 μm Availability of data and materials All data generated and used to draw conclusions are provided in the manuscript. The PK-FISH assay kit with appropriate probes and reagents is available from ID-FISH Technology, Palo Alto, CA 94303 (www.idfishtechnology.com) with the catalogue number provided in the manuscript. The probe sequences employed in the PK-FISH assay are available on request subject to a confidentiality/ non-disclosure agreement while a patent is pending.
Authors' contributions JS and RR conceived the study, participated in experiments, analyzed data and wrote the manuscript. JS and OM designed the probes. AP and OM carried out experiments. UK coordinated the preparation of methanol-fixed smears from coded left over blood samples of vivax malaria patients. RWM and FM provided P. knowlesi A1-H.1 and P. falciparum 3D7 parasites and participated in relevant experimental work at the London School of Hygiene and Tropical Medicine. All authors read and approved the final manuscript.

Ethics approval
The study was reviewed and approved by the Institutional Review Boards of Kasturba Medical College, Mangalore, India and the Kenya Medical Research Institute/Walter Reed project, Kisumu, Kenya. Approval was granted to ID-FISH Technology Inc., for the use of archived de-identified samples submitted for routine testing that would otherwise have been discarded.

Consent for publication Not applicable.
Competing interests JS is the Founder and Chief Scientific Officer of ID-FISH and owns ID-FISH stock. OM is an employee and RR an affiliate of ID-FISH. Other authors have no affiliation with ID-FISH. JS and OM are inventors on the following relevant patents: Nucleic acid probes and methods for detecting Plasmodium parasites.

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