Background

The protozoan parasite Plasmodium which causes malaria is a vector-borne infectious disease, estimated to infect approximately 350-500 million and kill more than a million people world wide every year [1]. There are five species of the Plasmodium parasite that can infect humans: the most virulent form of the disease is caused by Plasmodium falciparum and Plasmodium knowlesi. Malaria caused by Plasmodium vivax, Plasmodium ovale and Plasmodium malariae, are more chronic disease in humans. In the past three decades, with the globalization of economy and increasing immigration frequency, there has been a significant rise in the number of cases of imported malaria in non-endemic, developed countries, such as Canada [2]. Toronto is a large urban center in Canada with high rates of international travel and immigration and has recently been subjected to waves of imported outbreaks, such as SARS and swine H1N1 influenza [3].

Microscopic identification of malaria parasites relies on examination of Giemsa-stained peripheral blood smears. The sensitivity and specificity of this method are highly affected by the staining techniques used and the skill level of the microscopist [4–9]. Although light microscopy is capable of defining parasite density, parasite stage, and speciation, this method is labour-intensive and requires well-trained experts at reference centres, not to mention delays in specimen transport to such centres. In order to make the diagnosis of malaria faster and simpler to perform, rapid tests have been developed based on antigen-capture immuno-chromatographic tests (ICTs) as a valuable adjunct to microscopy for the diagnosis of malaria [2]. The ICTs are useful for identifying P. falciparum infection, but cannot be used to specifically identify non-P. falciparum species infections such as P. vivax, P. ovale, and P. malariae[7].

In the past few decades, with the advent of technology in molecular biology, new molecular methods have been introduced, such as polymerase chain reaction (PCR) and real-time quantitative polymerase chain reaction (QPCR). These molecular methods can detect malaria parasites to the species level by targeting the parasite DNA with good analytical sensitivity and specificity in laboratory studies [2, 10–13]. QPCR in particular has been a successful method for microbial detection from sterile sites with excellent sensitivity and has the ability to be quantitative. Many of the studies conducted to date seeking to validate malaria molecular diagnostics are limited to the research laboratory, but reports emphasizing the implementation of these techniques in clinical laboratory setup have not been adequately investigated in the past [14]. In the present study, validation of QPCR as compared to reference microscopy and two different ICTs was performed with particular attention to evaluating limits of detection, quality assurance, cost, staffing, and implementation in the clinical microbiology laboratory.

Materials and methods

Sample details

A total of 466 blood samples from individual patients (returning travelers) with fever or a history of fever and travel to a malaria-endemic area were tested by standard Giemsa stain microscopy for Plasmodium species detection. Summary statistics of patient clinical specimens are summarized in Table 1. Blood specimens were collected at community and hospital laboratories in Ontario, Canada and forwarded by courier the same day to the Public Health Reference Laboratory in Toronto (PHL Toronto) during the period May 2007 to January 2009. Infected blood aliquots were banked in a malaria bio-repository (-80°C monitored freezer) at PHL Toronto. Blood specimens positive by microscopy as well as a subset negative by microscopy were included in this study. Microscopy, ICTs (BINAXNOW® MALARIA [Binax, Seattle, WA] and CARESTART™ [Accessbio, Monmouth Junction, NJ]) detection and QPCR were performed in a blinded manner.

Table 1 Summary of clinical specimens used in this study.
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Conventional microscopy

Microscopy of thick and thin Giemsa-stained smears was performed according to standard methods by at least two experienced microscopists for each specimen reported here [15]. The parasitaemia is expressed as a percentage of erythroyctes. Microscopy performed here is considered reference microscopy and undergoes external quality assurance as a participant of the Insitut National de Santé Publique du Québec (INSPQ) blood parasitology programme.

Immuno-chromatographic tests (ICT)

Two rapid ICTs (BINAXNOW® MALARIA [Binax, Seattle, WA] and CARESTART ™, [Accessbio, Monmouth Junction, NJ]) were used in this study to detect the circulating Plasmodium antigen in the whole blood for the diagnosis of malaria. Both of the ICTs detect the Plasmodium falciparum-specific HRP2 antigen as well as a panmalarial antigen common to all Plasmodium species (aldolase in the case of BINAXNOW and pLDH in the case of CARESTART). The assays were performed according to the manufacturer's instructions. The test results were independently examined and interpreted by three blinded observers (one of whom was not a trained medical laboratory technologist). The final results of the test were recorded as either negative or positive based on the majority agreement. While ICT results reported here were on fresh frozen specimens,, all specimens were frozen only once, kept under monitored refrigerator conditions according to Clinical Laboratory Improvement Amendments (CLIA) guidelines. No difference was seen between single frozen and fresh frozen specimens when tested by ICT.

Multiplex real-time quantitative polymerase chain reaction (QPCR)

DNA was extracted from 100 μl of thawed EDTA-whole blood using the QIAamp DNA Mini Kit (Qiagen, Valencia, CA) according to the manufacturer's instructions. The extracted DNA was stored at -20°C in sterile capped containers until used. The qPCR was performed by using primers and reaction conditions described previously by Alberta Public Health Laboratory with the following modifications: fluorophores for probes of P. facliparum were changed to FAM-MGBNFQ and P. vivax to VIC-MGBNFQ [12]. Briefly, qPCR was performed under standard conditions (1 cycle of 50°C for 2 mins; 1 cycle of 95°C for 10 mins; 45 cycles of 95°C for 15 s and 60°C for 1 min) with the ABI TaqMan 7900 (Applied Biosystems Inc, Foster City, CA). The reaction was performed with a final volume of 25 μl containing 5 μl of template DNA, 12.5 μl of TaqMan universal master mix (ABI), and 7.5 μl of pooled primers and probes mix. Samples were confirmed Plasmodium positive with genus-specific primers Plasmo1 and Plasmo2 and the Plasprobe to detect a region of the Plasmodium 18S gene that is conserved across all five species. The Plasmodium species present in the sample were determined with species-specific forward primers, Plasmo2 and species-specific probes. The reaction was performed by multiplexing two plasmodium species in a single tube with distinct fluorophores for each probe, e.g. P. falciparum/P. vivax in a one tube and P. malariae/P. ovale in another tube. A cutoff of 40 cycles was used to define positive samples [12]. The test panel also included a number of controls: negative sample extraction as a negative control, β2-macroglobulin target amplification as a positive extraction control for the specimen, a positive reference control to detect any variation between runs, and no template negative controls for each of the master mixes.

Quality assurance

QPCR results were also compared with another reference provincial laboratory for public health, Edmonton, Alberta, Canada, using a blinded panel of 10 randomly selected blood specimens as part of quality assurance. The 10 blinded panel of blood specimens included P. vivax (n = 3), P. falciparum (n = 3), P. ovale (n = 3), mixed infection of P. falciparum and P. malariae (n = 1), and negative (n = 1). Microscopists used in this study are part of the INSPQ blood parasitology, quality assurance programme.

Limit of detection (LOD) for clinical isolates

To determine the minimum number of Plasmodium parasites detectable by two ICTs and QPCR, blood samples from twelve patients infected with P. falciparum (n = 3), P. vivax (n = 3), P. malariae (n = 3), and P. ovale (n = 3) were collected. The DNA purified from serial dilutions was performed in triplicate by QPCR. The ICTs were performed in parallel on all the blood sample serial dilutions, the results were interpreted by two different readers. The microscopy on serial dilutions was ruled out because the blood samples were already stored at -20°C in the malaria bio-repository. In addition, a LOD study was also done prospectively from three patients who from the Democratic Republic of Congo and were positive for P. falciparum by reference microscopy. To establish the ability of assays like ICT and QPCR to detect only the gametocyte stage of Plasmodium parasite, blood sample from one patient exclusively infected with P. falciparum gametocyte stage was used. All the blood samples were subjected to serial dilution with uninfected erythrocytes from healthy individuals with known baseline erythrocyte counts. The DNA purified from the dilutions was treated in triplicates for QPCR assay.

Limit of detection (LOD) for laboratory strains

The P. falciparum 3D7 strain was grown in two sets in human Rh+ erythrocytes at a haematocrit level of 5% in complete RPMI 1640 medium in tissue culture flasks (25 cm2 and 75 cm2) according to the method of Trager and Jensen [16]. The culture flask was replenished with a fresh batch of medium every 24 hours, and the culture was routinely monitored through Giemsa-staining of thin smears. The P. falciparum culture was synchronized to get only ring stages of P. falciparum as described earlier using 5% D-sorbitol [17]. The parasitaemia in the synchronized culture was determined from Giemsa-stained thin smears. In these malaria cultures to express the parasitaemia as number of parasites present in 1 μl of culture, the RBC/μl was counted using a standard Neubauer haemocytometer as per the manufacturer's instructions. The two sets of synchronized cultures were subjected to tenfold serial dilution with uninfected erythrocytes from healthy individuals. The DNA purified from the dilutions was performed in triplicates for QPCR assay. The microscopy and ICTs were performed in parallel on all the serial dilutions, the results were interpreted by two different readers.

Quantitating parasitaemia and ribosomal (r) DNA copy number from frozen specimens, fresh isolates, and laboratory strains

In frozen blood specimens to express the parasitaemia as number of parasites present in 1 μl of blood, it was assumed that 1 μl of blood contained 5 × 106 red blood cells, so 1% parasitaemia corresponds to 1 parasitized red blood cell/100 red blood cells or 50,000 parasites/μl of blood [18]. In the three fresh blood specimens to express the parasitaemia as number of parasites present in 1 μl of blood, the RBC/μl was calculated using a standard Neubauer haemocytometer as per the manufacturer's instructions. Infected blood samples were diluted with uninfected erythrocytes from healthy individuals with known baseline erythrocyte counts. Tenfold serial dilutions were made for each blood sample. The stage specific parasitaemia proportion was identified by a microscopist into different stages, such as single ring, double rings, triple rings, growing trophozoites, immature trophozoites, mature trophozoites, gametocytes, mature schizonts, and immature schizonts. The QPCR was performed on the ten-fold dilutions of these blood samples.

The rDNA copy number was calculated by using the following formula: rDNA copy number/reaction = (number. of parasitized RBC/μl)* ploidy * genecopy *5. The actual parasite ploidy number was determined as describes elsewhere [19]. Briefly, the ploidy for various stage of malarial parasites like, single ring and growing trophozoites was 1; double ring and gametocytes was 2; immature trophozoite, mature schizont and immature schizont was 8; and mature trophozoite was 16. The average rDNA gene copy number per parasite was considered as 6. A factor of 5 was multiplied, which accounts for the loading volume of DNA template per reaction.

Statistical data analysis

Sensitivity was calculated as follows: number of true positives divided by number of true positives plus false negatives × 100. Specificity was calculated as follows: number of true negatives divided by the number of true negatives plus false positives × 100. Separate analyses were conducted using reference microscopy and QPCR as gold standards. To determine the statistical significance of the results, the confidence interval (CI) and the margin of error for the sample size were determined [20]. The inter-reader variability was calculated by applying Kappa statistic [21].

Results

Comparison of microscopy, ICTs, and RTPCR

Evaluation of the sensitivity and specificity of microscopy, BINAXNOW, and CARESTART using QPCR and microscopy separately as the gold standard was carried out (Table 2). The microscopy was found to have higher sensitivity and specificity than the ICTs. The sensitivity of CARESTART (85.2%) was higher than BINAXNOW (83.67%), and both the ICTs had similar specificities (99.26%). The discordant results of microscopy, ICTs, and QPCR are summarized in Table 3. Among 466 patients in whom malaria was suspected, 170 (36.5%) were positive by microscopy. The remaining 296 samples were negative. Microscopy was used as the reference standard for comparison with the other methods. The CI for the sample size of 466 was 95% and the margin of error was 4.49%. The BINAXNOW detected malaria parasites in 166 of 170 microscopically positive samples with a sensitivity of 86.47% (95% confidence interval [CI] 81.98-90.96). The CARESTART detected malaria parasites in 169 of 170 microscopically positive samples with a sensitivity of 88.24% (95% CI 83.75-92.73). Among the 296 samples that were negative by microscopy, both ICTs detected malaria parasites in 19 samples with a specificity of 93.58% (95% CI 89.09-98.07). The QPCR detected malaria parasites in 169 of 170 microscopically positive samples with a sensitivity of 99.41% (95% CI 94.92-100). The QPCR detected malaria parasites in 27 of 296 microscopically negative samples with a specificity of 90.88% (95% CI 86.39-95.37). Out of these 27 QPCR positive but microscopy negative samples, 17 were also positive by ICTs. Ten samples were exclusively positive by QPCR and negative by microscopy and ICTs. The QPCR was negative in one out of 170 microscopically positive samples; this sample was also negative by ICTs. The QPCR has highest sensitivity (99.41%) in comparison to BINAXNOW (86.47%) and CARESTART (88.24%).

Table 2 Sensitivity and specificity expresessed as perecentarge of microscopy and ICTs (BINAXNOW and CARESTART) as alternately compared to QPCR and microscopy as gold standard method.
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Table 3 Discrepant analysis of different assays for the laboratory diagnosis of malaria based on results of QPCR.
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Conventional microscopy

A total of 170 out of 466 blood samples screened were positive for Plasmodium spp by microscopy. These 170 microscopy positive included 82 positive for P. falciparum, 63 positive for P. vivax, one positive for P. ovale, two positive for P. malariae, two positive for P. falciparum + P. ovale (mixed), one positive for P. falciparum + P. vivax (mixed), one positive for P. falciparum + P. malariae (mixed) and 18 positive for Plasmodium spp (species remained undetermined). 296 blood samples were negative for Plasmodium spp by microscopy. Microscopy was used as the reference standard for comparison with the other methods.

Immuno-chromatographic tests (ICT)

The BINAXNOW was positive for Plasmodium spp in 35.6% (166 out of 466) blood samples. These 166 BINAXNOW positive included 84 positive for P. falciparum/mixed Plasmodium species, 23 positive for P. falciparum, 59 positive for non P. falciparum species. The CARESTART was positive for Plasmodium spp in 36.3% (169 out of 466) blood samples. These 169 CARESTART positive included 84 positive for P. falciparum/mixed Plasmodium species, 22 positive for P. falciparum, 63 positive for non P. falciparum species. The Kappa value of inter-reader variability among three readers for BINAXNOW and CARESTART was calculated to be 0.872 and 0.898 respectively.

Multiplex-QPCR

The QPCR was positive for Plasmodium spp in 42.1% (196 out of 466) of blood samples. These 196 RTPCR positive included 111 positive for P. falciparum, 72 positive for P. vivax, five positive for P. ovale, three positive for P. malariae, one positive for P. malariae + P. ovale (mixed), and three positive for P. falciparum + P. vivax (mixed), one positive for P. falciparum + P. malariae (mixed). The result of multicentre validation of RTPCR on a blinded panel of 10 randomly selected blood specimens demonstrated 100% concordance. A different blinded panel was forwarded to the Alberta provincial reference laboratory, where 100% concordance was also achieved. This process was repeated six months later with a different blinded panel with 100% agreement as part of an ongoing quality control procedure. However, the comparative results of the multicentre validation showed that the Ct values were slightly lower than that performed by Alberta (see Additional File 1). All four Plasmodium species were successfully differentially detected in the species specific multiplex QPCR reaction.

Limit of detection analyses

The ability of QPCR to be quantitative was established by the comparison between the log of parasitaemia versus Ct value (threshold cycle) for all the four species of malaria. This was evaluated on representative clinical specimens for all four species of P. falciparum (n = 3), P. vivax (n = 3), P. malariae (n = 3), and P. ovale (n = 3). An increasing parasite concentration was reflected by lower Ct value with good linear correlation for both clinical isolates of all species (Figures 1, 2, 3, 4 and 5). To establish the minimum copy number of the target rDNA gene sequence detectable by QPCR, DNA from blood specimen exclusively positive for P. falciparum single ring stage was used. The standard curve for QPCR was constructed by using 10-fold serial dilutions of genomic DNA (115800 to 0.01158 rDNA copies/μl). A plot of rDNA copy number versus the Ct value is shown in Figure 6A. The detection limits was found to be 11 rDNA copies/μl for P. falciparum. A plot of the Ct versus the log of rDNA copy/μl showed a linear correlation (R2 = 0.9746). An amplification plot generated by QPCR for the 10-fold serial dilutions of P. falciparum rDNA is depicted in Figure 6B.

Figure 1
figure 1

A plot of log of parasitaemia versus threshold cycle for the 10-fold serial dilutions of P. falciparum (A) and a representative amplification plot for 10-fold serial dilutions (B) generated by QPCR are also shown. All clinical isolates were amplified in triplicate for each species with the linear correlation coefficient (R2) shown in the corresponding color.

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Figure 2
figure 2

A plot of log of parasitaemia versus threshold cycle for the 10-fold serial dilutions of P. vivax (A) and a representative amplification plot for 10-fold serial dilutions (B) generated by QPCR are also shown. All clinical isolates were amplified in triplicate for each species with the linear correlation coefficient (R2) shown in the corresponding color.

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Figure 3
figure 3

A plot of log of parasitaemia versus threshold cycle for the 10-fold serial dilutions of P. malariae (A) and a representative amplification plot for 10-fold serial dilutions (B) generated by QPCR are also shown. All clinical isolates were amplified in triplicate for each species with the linear correlation coefficient (R2) shown in the corresponding color.

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Figure 4
figure 4

A plot of log of parasitaemia versus threshold cycle for the 10-fold serial dilutions of P. ovale (A) and a representative amplification plot for 10-fold serial dilutions (B) generated by QPCR are also shown. All clinical isolates were amplified in triplicate for each species with the linear correlation coefficient (R2) shown in the corresponding color.

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Figure 5
figure 5

A plot of log of parasitaemia versus threshold cycle for the 10-fold serial dilutions of P. falciparum laboratory strain 3D7 (A) and a representative amplification plot for 10-fold serial dilutions (B) generated by QPCR are also shown. All clinical isolates were amplified in triplicate for each species with the linear correlation coefficient (R2) shown in the corresponding color.

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Figure 6
figure 6

A plot of rDNA copy number versus the threshold cycle for the 10-fold serial dilutions of P. falciparum specific QPCR (A) with the rDNA copy number in parentheses. The amplification plot generated by QPCR for 10-fold serial dilutions of P. falciparum rDNA is also shown (B).

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The comparative results of limit of detection showed that the QPCR had the highest sensitivity to detect parasite at lower levels (higher dilutions) as compared to microscopy and ICTs. For the three frozen biological replicates each of P. falciparum, P. vivax, P. malariae and P. ovale, there was an average log dilution difference of 2, 3, 4, and 4 respectively between QPCR and ICTs (Table 4). Similary, for the three fresh biological replicates of P. falciparum there was an average log dilution difference of 1 between QPCR and ICTs and an average log dilution difference of 2 between QPCR and Microscopy (Table 4). In order to understand the effect of different malarial parasite stage proportion on the QPCR detection system, a detailed evaluation of the various stages of malarial parasite and its contributing rDNA copy number for the LOD was also done (Table 5). For P. falciparum, detection of single ring infections required a higher rDNA copy number than double ring infections, and detection of gametocytes by QPCR required a higher rDNA copy number than for other Plasmodium spp. For non-P. falciparum species, detection of trophozoites required a higher rDNA copy number than ring stages.

Table 4 Comparative LOD results of Microscopy, ICTs and RTPCR performed on blood specimens from representative (n = 3 per species) patient specimens for each malaria species.
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Table 5 Average stage-specific detection limit of clinical specimens (n = 3 per species) by QPCR.
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Discussion

Performance characteristics, limit of detection, inter-reader variability and cost of QPCR, two ICTs (BINAXNOW and CARESTART) and reference microscopy was evaluated. QPCR quality assurance was sought by comparing the results of QPCR in two distinct reference lab settings. The results indicate that the QPCR is the most analytically sensitive method (sensitivity 99.41%), followed by CARESTART (sensitivity 88.24%), and BINAXNOW (sensitivity 86.47%) for the diagnosis of malaria in returning travelers when compared to microscopy. The results of the comparative LOD study between different assays suggest that the QPCR has the superior LOD. Microscopy was unable to specifically identify Plasmodia spp. in 18 out of 170 positive samples by QPCR. Moreover, the 17 samples that were negative by microscopy and positive by QPCR were also positive by ICTs.

Although microscopy can be sensitive to a threshold of 5-50 parasites/μl depending on the expertise of the microscopist, the average microscopist is likely to achieve a sensitivity closer to 100 parasites/μl or higher [22, 23]. The possible explanation for the discordance in these samples could be the inability of microscopy to appreciate the degraded parasite, merozoites stage, sequestered parasites in the splenic vasculature, or the occult exo-erythrocytic schizogony stage. More likely, the LOD studies suggest that reference microscopy is unable to detect parasites when below a certain threshold. Interestingly, this study revealed that the limit of detection was significantly affected by the stage of malarial parasite. For example, the two P. malariae positive specimens "Pm1" and "Pm3" (see Table 4) had the same parasitaemia of 0.06%, but there was a marked difference of ten fold in the limit of detection. This may be due to the difference between the parasite stage proportions between the specimens. The specimen "Pm1" had higher proportion of parasite stages like growing trophozoites and mature trophozoites in comparison to "Pm3". Our QPCR appeared to be more sensitive in the detection of the malarial parasite in blood specimens than performed by our comparator institution in Alberta (see Additional file 1). This is likely because of the difference in the number of targets amplified in one tube. The QPCR screens two targets in one tube as opposed to four targets in Alberta. This suggests that the PCR reaction kinetics favours the lesser number of targets per reaction due to competition among the targets for amplification. Of note, this marginal difference did not affect result interpretation.

It has been reported that the sensitivity of ICT to detect malarial parasites decreases as the parasitaemia decreases [24]. False-negative results, particularly for P. falciparum with its more virulent natural history of infection, are of concern. For BINAXNOW four false-negative results occurred for P. falciparum infections, 13 for P. vivax, four for P. ovale, and one for P. malariae. For CARESTART, three false-negative results occured for P. falciparum infections, 10 for P. vivax, four for P. ovale, one for P. malariae and one for a P. ovale and P. malariae mixed infection. In most cases the false negative results were due to low parasitaemia, but in a very few cases the false negative results was even at high parasitaemia. This may be attributed to the prozone phenomenon (antibody excess) making antigen unavailable to be detected by ICT or a possible mutant gene resulting in altered HRP-2 antigen [24]. The sensitivity of CARESTART (85.2%) was slightly higher than BINAXNOW (83.67%), and both ICTs had similar specificities (99.26%). CARESTART sensitivity was higher because it was able to pick up non-falciparum species on more occasions than BINAXNOW, this suggests that Plasmodium lactate dehydrogenase (pLDH) used in CARESTART is a more sensitive marker than aldolase used in BINAXNOW for detecting non-falciparum species. In the majority of samples, both the ICTs have identified P. falciparum monoinfections (detected by microscopy and QPCR) as P. falciparum/mixed because both bands (P. falciparum and pan-malarial) were positive, thereby not allowing the technologist to rule out mixed infection on the basis of the ICT alone. The sensitivity of both ICTs for the detection of only P. ovale and P. malariae infections was 0% and 50% respectively.

Previous reports suggest that the expression levels of the pan-Plasmodium antigen (LDH and aldolase) in P. ovale and P. malariae may be minimal and this in combination with low parasitaemia in these infections accounts for relatively lower sensitivity for the detection of these malaria species [25, 26]. It is important to note that both the ICTs have the limitation that does not distinguish between the non-P. falciparum species (P. vivax, P. ovale, and P. malariae), nor can it reliably distinguish pure P. falciparum infections from mixed falciparum infections. However, the test was found to be simple to conduct, rapid, and easy to interpret, with excellent inter-reader agreement for BINAXNOW and CARESTART as K value = 0.872 and K value = 0.898 respectively, indicating good agreement between trained and non-trained readers. Discrepancies between readers occurred mainly when the test result was weakly positive (faint band), especially in cases of low parasitaemia. Rapid diagnostic assays like ICTs may be a useful tool when expert microscopy is not available or onsite field survey is to be conducted on large population. Considering the inherent limitation and advantages of all the assays evaluated in the present study and the evidence from previous reports, ICTs are a useful diagnostic tool and can be used as an adjunct to conventional microscopy in front-line clinical laboratories in areas where malaria is not endemic. These laboratories frequently lack sufficient specimen volume to maintain expertise in diagnostic microscopy. A rapid diagnostic test like ICT could provide a fast although still preliminary diagnosis, while results are confirmed from a reference laboratory. There were three false-positive BINAXNOW results and two false-positive CARESTART results in this study. Occasional false-positive results due to the presence of rheumatoid factor have previously been reported with diagnostic methods based on the detection of HRP II [27]. It is important to note that, due to the incidental false-negative results with ICTs, malaria infection cannot be ruled out on the basis of a negative ICT result. Reference-level microscopy remains essential especially with the capability for species identification, parasite quantitation, and capacity to rule out gametocyte only infections. However, due to its excellent LOD, QPCR at the reference level serves the essential purpose of confirming or refuting microscopic speciation in certain cases (discussed below). A limitation of QPCR and ICT was that a positive result was obtained in one blood specimen with pure P. falciparum gametocytes. This shows that the QPCR can be positive in convalescence or clinically cured infections due to persistent sexual-stage forms (gametocytes) implying that the QPCR is unable to distinguish gametocyte only infections from true infections.

The cost and the processing time for all the four techniques employed for the laboratory diagnosis of malaria were evaluated (Table 6). At the time of writing, when purchased in bulk, the BINAXNOW kit was priced at US$5.20 per sample, whereas the CARESTART™ Malaria was priced at US$1.20 per sample. Of note, no significant difference was observed in this study between either ICT in spite of the cost differential. The BINAXNOW test has the approval from regulatory bodies in North America, such as the Food and Drug Administration and Health Canada. Reference microscopy of thick and thin smears costs US$2.50 for reagents in our reference laboratory setting. The ABI 7900HT Fast Real-Time PCR System used here for QPCR had a per sample cost of US$14.80 for reagents. Of note, QPCR requires a one time capital equipment purchase of the thermocycler. For example, the FC2500 SmartCycler System (Cepheid, Sunnyvale. CA) costs approximately US$36,000 and is capable of 14 reactions per run which seems appropriate given the frequency of malaria requests and the "stat" nature of the test in a non-endemic setting. The cost analysis clearly showed that the CARESTART was the cheapest method. While ICTs do not require trained staff, reference parasitology laboratories continue to place emphasis on microscopy training. A challenge to staffing of QPCR is the lack of equivalent training in molecular techniques. This is in contrast to virology and bacteriology sections where cross-training in molecular techniques is now common place in the reference laboratory.

Table 6 Comparison of the cost of different techniques employed for the diagnosis of malaria
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Conclusion

Taken together, QPCR should be implemented in all reference clinical laboratories and used in specific scenarios: (i) when a clinician does not agree with microscopic findings based on clinical pre-test probability of malaria; (ii) when two microscopists disagree on the findings particularly in cases of mixed infection, low parasitaemia, and sample degradation; (iii) when a microscopist does not visualize enough parasite stages to make a speciation call. Of note, the significance of a positive QPCR result following pharmacotherapy is still unclear as it could represent a fully treated infection with only DNA present and no live asexual stage organisms. As such, use of QPCR for test of cure is not encouraged until further studies are available. Due to the poor LOD with non-P. falciparum species and lack of advantage in diagnostic sensitivity when compared to reference microscopists for P. falciparum, the ICTs appear better suited to the community or hospital laboratory where experience with malaria smears may be limited and thus confer a diagnostic advantage.