Figures
Abstract
Background
We compared the performance of two new commercial tests for the detection of dengue NS1 protein during the clinical phase of dengue virus (DENV) infection—an immunochromatographic test allowing rapid detection of the NS1 antigen, Dengue NS1 Ag STRIP (Bio-Rad Laboratories - Marnes La Coquette, France), and a two-step sandwich-format microplate enzyme-linked immunosorbent assay (ELISA), pan-E Dengue Early ELISA (Panbio - Brisbane, Australia)—with a one-step sandwich-format microplate ELISA, the Platelia Dengue NS1 Ag test (Bio-Rad).
Methods
We tested 272 serum samples from patients with dengue disease. Of these, 222 were from patients with acute infection of one of the four dengue serotypes, detected by RT-PCR and/or virus isolation. Forty-eight acute-phase serum samples from patients not infected with dengue virus were also included.
Results
The sensitivity of the Platelia Dengue NS1 Ag test on acute serum samples (n = 222) was 87.4% (95% confidence interval: 82.3% to 91.5%); that of Dengue NS1 Ag STRIP was 81.5% (95% CI: 75.8% to 86.4%) after 15 minutes and 82.4% (95% CI: 76.8% to 87.2%) after 30 minutes. Both tests had a specificity of 100% (97.5% CI, one-sided test: 92.6% to 100.0%). The pan-E Dengue Early ELISA had a sensitivity of 60.4% (95% CI: 53.4% to 66.8%) and a specificity of 97.9% (95% CI: 88.9% to 99.9%).
Conclusion
Our findings support the use of diagnostic tools based on the NS1 antigen detection for the diagnosis of acute DENV infection. The immunochromatographic test, Dengue NS1 Ag STRIP—the first rapid diagnostic test for DENV infection—was highly sensitive and specific, and would therefore be a suitable first-line test in the field. The pan-E Dengue Early ELISA was less sensitive than the Platelia test; this two-step ELISA should be combined with DENV IgM antibody detection for the diagnosis of DENV infection.
Author Summary
Dengue is a viral disease transmitted by mosquitoes that is endemic in more than 100 countries in tropical areas, threatening over 2.5 billion people. It causes a wide range of symptoms and has severe forms. In reference laboratories, dengue disease is confirmed by virus isolation or genome detection during the acute phase, and by serological methods during the early convalescent phase. The viral NS1 protein circulates in the sera of infected patients throughout the clinical phase of the disease. Novel diagnostic tests based on NS1 detection have been recently developed and marketed. We compared the performance of two tests for detecting dengue NS1 protein during the clinical phase of dengue infection (an immunochromatographic test (ICT) from Bio-Rad allowing rapid detection of the NS1 antigen and a two-step sandwich-format ELISA from Panbio) with the one-step sandwich-format microplate ELISA (Bio-Rad). The ICT test performed better than the ELISA test from Panbio. This study confirms that diagnostic tests based on NS1 could be used in routine clinical practice in poorly equipped laboratories and that dengue diagnosis could therefore be confirmed without the need for testing in reference laboratories. This represents a crucial step towards the control of dengue disease in the human population.
Citation: Dussart P, Petit L, Labeau B, Bremand L, Leduc A, Moua D, et al. (2008) Evaluation of Two New Commercial Tests for the Diagnosis of Acute Dengue Virus Infection Using NS1 Antigen Detection in Human Serum. PLoS Negl Trop Dis 2(8): e280. https://doi.org/10.1371/journal.pntd.0000280
Editor: Eva Harris, University of California Berkeley, United States of America
Received: February 14, 2008; Accepted: July 18, 2008; Published: August 20, 2008
Copyright: © 2008 Dussart et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by the Centre National de Reference des Arbovirus et virus influenza, Région Antilles-Guyane, at the Institut Pasteur de la Guyane. Laure Petit was supported by a grant from the European Commission (FP6-2005-INCO-DEV2-517711). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Dengue virus (DENV) is a mosquito-borne virus (family Flaviviridae, genus Flavivirus). Four viral serotypes of DENV (DENV-1 to DENV-4) cause disease in humans. Symptoms range from mild fever, the most common form, to potentially fatal dengue hemorrhagic fever (DHF) and dengue shock syndrome (DSS) or encephalitis and hepatitis. The disease is now endemic in more than 100 countries in tropical areas, threatening over 2.5 billion people. It currently affects around 100 million people every year [1]. Among affected individuals, 500,000 have DHF and around 25,000, mostly children, die. According to World Health Organization estimates, the incidence of dengue disease has increased by a factor of 30 over the past 50 years [2]. Many of these epidemiological changes can be attributed to the increase and spread of the vector Stegomyia aegypti (formerly Aedes aegypti), an urban mosquito, together with population growth, urbanization and increases in human travel [3].
Flaviviruses are enveloped, single-stranded, positive-sense RNA viruses. The genomic RNA is about 11 kb long and contains 10 genes encoding three structural proteins (capsid [C], envelope [E], and membrane [M]), and seven nonstructural proteins (NS1, NS2a, NS2b, NS3, NS4a, NS4b, and NS5) [4]. The polycistronic coding region is flanked by non-coding regions at its 5′ and 3′ ends. The nonstructural protein, NS1, is a highly conserved glycoprotein, but its biological activity has not been established. During in vitro infection, the flavivirus NS1 protein is expressed as an intracellular membrane-associated form essential for viral replication [5],[6] or as a cell surface-associated form that may be involved in signal transduction [7]. In solution, secreted NS1 protein behaves as a hexamer; it circulates and accumulates in the sera of dengue virus-infected patients throughout the clinical phase of the disease [8]–[10]. A recent study demonstrated that soluble NS1 protein binds to endothelial cells and, following recognition by anti-NS1 antibodies, could contribute to plasma leakage during severe dengue virus infection [11].
The detection of secreted NS1 protein represents a new approach to the diagnosis of acute dengue infection. A recently developed commercially available diagnostic test based on dengue NS1 antigen-capture ELISA (Platelia Dengue NS1 Ag test, Bio-Rad Laboratories, Marnes la Coquette, France), was investigated in two studies (one in South America and the other in Southeast Asia); the test had an overall sensitivity of 88.7% and 93.4% in the two studies, with 100% specificity [12],[13].
We evaluated and compared the performance of the Platelia Dengue NS1 Ag test from Bio-Rad Laboratories with two new commercial tests for the detection of dengue virus NS1 antigen (Ag) in patients with clinically diagnosed DENV infection: Dengue NS1 Ag STRIP, an immunochromatographic assay developed by Bio-Rad Laboratories, and pan-E Dengue Early ELISA, an enzyme-linked immunosorbent assay developed by Panbio (Brisbane, Australia).
Materials and Methods
Clinical samples
We used a panel of human serum samples from the collection of the Centre National de Référence des Arbovirus et virus Influenza (the French National Reference Center (NRC) for Arboviruses and Influenza viruses), Région Antilles-Guyane, based at the Institut Pasteur de la Guyane. Sera were collected from patients previously diagnosed with Dengue infection. No clinical investigation was conducted and no personal identifiers were included; therefore, no IRB approval was sought for this study. The laboratory as NRC conducted the collection of serum samples with approval from the French Ministry of Health. The database used by the NRC is registered with the Commission Nationale de l'Informatique et des Libertés (CNIL). This database provided clinical information about the age and sex of each patient, the date of serum collection and the day on which symptoms occurred (onset of fever taken as day 0, i.e. first 24 hours). Clinical data and serum samples were collected from patients presenting a dengue-like illness in the context of the dengue surveillance activity of the NRC.
Dengue infection diagnosis
DENV was isolated by cell culture and the DENV genome was detected by RT-PCR, as previously described, in acute-phase serum samples [14],[15]. Briefly, for virus isolation, acute-phase serum samples from febrile patients were diluted 10-fold in Leibowitz medium containing 3% fetal calf serum, and dilutions were injected into subconfluent AP 61 cell cultures, as previously described. After 7 days of culture, cells were harvested, and dengue viruses were identified according to serotype by an indirect immunofluorescence assay (IFA) with monoclonal antibodies specific for DENV-1, -2, -3, and -4 viruses (provided by CDC, Fort Collins, CO, USA). DENV was isolated from 104 samples, and DENV RNA was detected in an additional 82 samples by RT-PCR. A third set of 36 samples was positive for both virus isolation and RT-PCR. Based on the epidemiological situation for dengue in French Guiana, we considered patients with positive detection of the genome associated with dengue-like syndrome to be confirmed cases of dengue infection.
Acute- and early convalescence-phase serum samples were tested for IgM antibodies against DENV, using the MAC-ELISA test, as previously described [16]. All sera were tested for the presence of DENV IgG antibody using a test adapted from a previously described indirect ELISA [17]. Briefly, the wells of flat-bottomed microplates (Polysorp, Nunc) were coated with 100 µl of dengue antigen diluted 1∶2,000 in phosphate-buffered saline (PBS). Normal mouse brain antigen was diluted in an identical manner and used to coat other adjacent wells. After overnight incubation at 4°C, the microplates were washed three times with PBS containing 0.1% Tween 20 (PBS-T; both reagents from Sigma Laboratories, l'Isle d'Abeau Chesnes, France). The sera were diluted (1∶100) in PBS containing 0.1% Tween 20 and 5% nonfat dried milk (PBS-T-NDM) and added to each well (100 µl/well). Six negative and two positive reference sera were included in each plate as controls. The negative controls consisted of sera from patients with other febrile illnesses but negative for dengue infection. The plates were then incubated for 2 h at 37°C and washed three times with PBS-T. Bound IgG was detected by adding 100 µl of horseradish peroxidase-conjugated goat anti-human IgG (Jackson Immunoresearch Laboratories, West Grove, PA, USA) diluted 1∶2,000 in PBS-T-NDM to each well. The plates were incubated for 1 h at 37°C and washed with PBS-T. Bound antibodies were visualized by adding 100 µl of tetramethylbenzidine (Sigma Laboratories) to each well. After incubation for 15 min at room temperature, absorbance at 650 nm (A650) was read with a microplate reader, and the ΔA650 was calculated (ΔA650 = ΔA650 Den Ag−ΔA650 control Ag). For validation of the test, the ΔA650 of the positive control serum had to be ≥0.5 and the ΔA650 of the negative control serum had to be ≤0.2. The mean (±the standard deviation) ΔA650 values for the negative controls were then determined. A result was considered negative if ΔA650 was less than the mean value for the negative control plus two standard deviations, indeterminate when ΔA650 was between two and three standard deviations, and positive when ΔA650 values was more than three standard deviations greater than the mean of the negative control.
We studied a panel of 320 sera previously tested for NS1 antigen with the Platelia Dengue NS1 Ag kit [12]. Two hundred seventy-two DENV-infected sera were characterized as follows: (i) DENV-1 (n = 33), DENV-2 (n = 42), DENV-3 (n = 101) and DENV-4 (n = 46) acute sera (n = 222 in total), (ii) 50 non serotyped serum samples containing DENV IgM antibody detected during different dengue outbreaks from French Guiana (Table 1). We also included 48 additional acute-phase serum samples (days one to four) from patients presenting dengue-like syndrome (temperature of ≥38.5°C, arthralgia, headache and/or myalgia), for whom recent dengue infection was ruled out based on acute and convalescent sera. Of the 222 acute serum samples with dengue virus detected by RT-PCR and/or virus isolation, 194 (87.4%; 95% CI: 82.3% to 91.5%) were positive for the Platelia Dengue NS1 Ag test; four sera (1.8%) with equivocal results were considered negative based on further statistical analysis. We used these well-characterized sera to compare the performance of Dengue NS1 Ag STRIP and pan-E Dengue Early ELISA with the Platelia Dengue NS1 Ag test.
Based on the WHO criteria for case definitions of dengue fever, DHF and DSS, all serum samples tested were collected from patients with clinical symptoms of classical dengue fever (fever, headache, myalgia, and arthralgia) with or without a rash or minor hemorrhagic manifestations. No patient presented severe clinical symptoms of DHF or DSS [18].
New commercial tests based on dengue NS1 antigen detection
Dengue NS1 Ag STRIP (Bio-Rad Laboratories) is an immunochromatographic test (ICT) for the rapid detection of NS1 antigen. Briefly, one drop of migration buffer was added to 50 µL serum in a specimen tube and a strip was placed in the tube. The strip has two lines: a control line (C) (“biotin – gold colloidal particles coated with streptavidin” complex) and a test line (T) (“monoclonal anti-NS1 antibodies (mAb) – NS1 Ag – gold colloidal particles coated with anti-NS1 mAb” complex). The appearance of the T and C lines after a migration time of 15 minutes (min) indicates a positive result. The appearance of the C line alone indicates a negative result. If the C line is not present, the test is considered invalid and is repeated. It is recommended that strips giving ambiguous (faint color at the T line) or negative results are put back in the tube after the initial reading and left for a further 15 min for re-evaluation. We evaluated all samples at 15 min (ICT 15 min) and then at 30 min (ICT 30 min).
The pan-E Dengue Early ELISA (Panbio) is a two-step sandwich-format microplate enzyme-linked immunosorbent assay for the detection of NS1 antigen. The test uses polyclonal and monoclonal antibodies for capture and detection, respectively. Panel serum samples and control serum samples provided in the kit were diluted 1∶10 (135 µL of serum diluents and 15 µL of each serum sample and control sample). Diluted serum and control samples (100 µL) were placed in microplate wells coated with anti-NS1 polyclonal antibodies. The microplate was incubated for one hour at 37°C, and then washed six times. Horseradish peroxidase-conjugated anti-NS1 Mab (100 µL) was added to each well and the microplate was incubated for one hour at 37°C, then washed six times. Immune complexes were detected using a color development reaction (100 µL of tetramethylbenzidine added to each well). The plate was incubated for 10 minutes room temperature, and the enzymatic reaction was then stopped with phosphoric acid. Absorbance at 450/620 nm was determined within 30 minutes.
We used the average absorbance of triplicate readings from the calibrator, multiplied by the calibration factor (provided in the kit), to calculate the cut-off value (CO). An index value was calculated by dividing the sample absorbance by the CO. Panbio Units were calculated by multiplying the index value by ten. According to the manufacturer's recommendations, samples with index values less than 0.9 were considered negative (no detectable dengue NS1 Ag); those with index values between 0.9 and 1.1 were equivocal for the presence of dengue NS1 Ag, and samples with index values greater than 1.1 were considered positive (presence of detectable dengue NS1 Ag).
The technicians carrying out Dengue NS1 Ag STRIP and pan-E Dengue Early ELISA were blind to the DENV-infection status of the panel of serum samples. For each strip, two people read the results independently. When discordance was observed between Platelia and ICT and/or pan-E results, the discordant serum was retested with all three tests to avoid discrepancies due to the effects of serum sample storage.
Statistical analysis was performed with STATA version 9.0 (STATA Corporation, College Station, TX, USA).
Results
The sensitivity of each of the three NS1 antigen detection tests with the 272 DENV-infected sera is detailed in Table 2. All sera testing positive for the presence of NS1 with the pan-E Dengue Early ELISA also tested positive with the Dengue NS1 Ag STRIP and Platelia Dengue NS1 Ag tests. Similarly, all sera testing positive for NS1 with the Dengue NS1 Ag STRIP also tested positive with the Platelia Dengue NS1 Ag test (Table 2). Using the Dengue NS1 Ag STRIP, 207 (76.1%; 95% CI: 70.6% to 81.0%) samples gave positive results at 15 minutes and 211 (77.6%; 95% CI: 72.1% to 82.4%) samples gave positive results at 30 minutes. One serum sample, collected on day four, gave ambiguous results at 15 minutes (faint Dengue NS1 Ag STRIP T line), and a positive result after 30 minutes (positive with the Platelia test, with a ratio greater than 5.0). A second serum sample, collected on day 0, was considered negative after 15 minutes and positive after 30 minutes (positive with the Platelia test, with a ratio of 3.9). With the pan-E Dengue Early ELISA, 150 serum samples (55.1%; 95% CI: 49.0% to 61.2%) tested positive. Nine other serum samples collected on day 1 (n = 1), day 2 (n = 2), day 3 (n = 2), day 4 (n = 2) and day 6 (n = 2) were considered equivocal with the pan-E Dengue Early ELISA, whereas these samples had ratios of 2.8 (n = 1) or greater than 5.0 (n = 8) with the Platelia test.
Table 3 details the sensitivities of the three NS1 tests and of the MAC-ELISA according to the number of days after onset of fever. The sensitivity of ICT at 30 minutes was 94.2%, using the Platelia Dengue NS1 Ag test as a reference (100%), whereas that of the pan-E Dengue Early ELISA was 66.9%. The sensitivity of pan-E Dengue Early ELISA for DENV diagnosis between days 0 and 4 (60.0%) increased significantly, to 64.0%, when combined with IgM detection (McNemar's test: 9.0 p = 0.003) (Data not shown).
Table 4 compares the sensitivity of the Dengue NS1 Ag STRIP and pan-E Dengue Early ELISA tests with that of the Platelia Dengue NS1 Ag test, as a function of DENV serotype. No significant difference was observed between the four DENV serotypes for sensitivity of the Platelia test (χ2 = 0.49, P = 0.92), the ICT at 15 min (χ2 = 0.05, P = 0.99) or the ICT at 30 min (χ2 = 0.25, P = 0.97). However, a significantly lower sensitivity (21.7%; 95% CI: 10.9% to 36.4%) for DENV-4 serum samples was observed with the Panbio test (χ2 = 40.1, P<0.0001).
The sensitivity of Platelia Dengue NS1 Ag, ICT at 15 min and 30 min, and pan-E Dengue Early ELISA tests for acute sera with positive RT-PCR or viral culture results is presented in Table 5. No significant difference was observed between the sensitivity (Se) of ICT 15 min (Se = 81.8%; 180/220), ICT 30 min (Se = 82.7%; 182/220) and Platelia Dengue NS1 Ag (Se = 87.7%; 193/220) (χ2 = 3.3, P = 0.19) for acute serum samples collected between days 0 and 4 after fever onset. However, a significant difference in sensitivity was observed between pan-E Dengue Early ELISA (Se = 60.0%; 132/220) and Platelia Dengue NS1 Ag (χ2 = 43.8, P<0.0001), ICT 15 min (χ2 = 25.4, P<0.0001) and ICT 30 min (χ2 = 27.8, P<0.0001).
There was a significant difference in the sensitivity of NS1 detection tests between serum samples with positive and negative results for DENV IgG detection (Platelia: χ2 = 24.5, P<0.0001; ICT 15 min. χ2 = 37.2, P<0.0001; ICT 30 min. χ2 = 33.3, P<0.0001; Pan-E: χ2 = 27.0, P<0.0001) (Table 6). This difference was observed regardless of the timing of serum sample collection (Figures 1A & 1B). Furthermore, we observed an increase in the sensitivity of the three NS1 detection tests between sera collected at day 0 and those collected on day 3, with the largest increase observed with the pan-E Dengue Early ELISA (Figure 1B).
A: Serum samples with no IgG: Platelia Dengue NS1 Ag test (—⋄—), Dengue NS1 Ag STRIP 15 min (- - -□- - -) and 30 min (– –▵– –), and pan-E Dengue Early ELISA (– –+– –). B: Serum samples positive for IgG: Platelia Dengue NS1 Ag test (—⧫—), Dengue NS1 Ag STRIP 15 min (- - -▪- - -) and 30 min, (– –▴– –) and pan-E Dengue Early ELISA (- - + - -).
The specificity testing was conducted with the 48 acute-phase serum samples from dengue-negative patients. The Platelia Dengue NS1 Ag test, ICT 15 min and 30 min had a specificity of 100% (48/48; 97.5% CI: 92.6% to 100%, one-sided test), whereas the specificity of the pan-E Dengue Early ELISA was 97.9% (47/48; 95% CI: 88.9% to 99.9%). For one patient, we considered the positive Panbio test for the acute-phase serum sample to be a false positive result because virus isolation, genome and IgM detection tests were all negative. Moreover, for the 48 non-DENV-infected patients, all acute-phase and early convalescent sera were tested for IgM directed against two other flaviviruses (Saint-Louis encephalitis and yellow fever antigen, data not shown), and for the false-positive Panbio result, the paired sera were retested to confirm the absence of cross-reactivity with these two flaviviruses.
Discussion
We compared three diagnostic tests for early detection of the NS1 antigen secreted in the plasma of patients with dengue infection during the acute phase of the disease. The Platelia Dengue NS1 Ag test has been already demonstrated to be effective for NS1 detection [12]–[13]. We show here a high rate of detection in samples from patients with the rapid immunochromatographic test, Dengue NS1 Ag STRIP — the first ICT test developed for NS1 detection — for all four DENV serotypes. This rapid diagnostic test (RDT) is convenient, easy to use, and the results are obtained in 15 minutes, or 30 minutes for ambiguous results. The RDT does not involve any specific laboratory equipment, except a microcentrifuge for serum separation. This test can detect NS1 Ag from serum samples, but not from whole blood. The development of an ICT for the NS1 detection in whole blood would allow rapid diagnosis of dengue in the field or during medical consultations in health care centers with minimal equipment. Moreover, an early ICT for NS1 could be performed in parallel with an RDT for malaria in tropical areas in which these two diseases are endemic.
The sensitivity of the pan-E Dengue Early ELISA was significantly lower than that of the Platelia Dengue NS1 Ag test or the Dengue NS1 Ag STRIP. This observation is consistent with a previous study performed in Southeast Asia with fewer serum samples (n = 92), in which the pan-E Dengue Early ELISA had a sensitivity of 63.2% (95% CI: 53.4% to 73.0%) for sera collected between days four and seven after fever onset [19]. We also show that this test differed significantly from the Platelia Dengue NS1 Ag and Dengue NS1 Ag STRIP tests for patients with the DENV-4 serotype and with acute serum samples collected between days 0 and four. Thus, the pan-E Dengue Early ELISA should not be used alone for acute diagnosis of DENV infection and should instead be combined with MAC-ELISA, as suggested by Blacksell et al. Furthermore, in practical terms, the Platelia Dengue NS1 Ag test, which has a one-step sandwich-format (one incubation period), is more convenient for technicians than the pan-E Dengue Early ELISA test, which has two steps (two incubation periods).
During the acute phase of the disease, the presence of DENV IgM antibody alone suggests primary infection, and the concomitant detection of DENV IgM and IgG antibodies is suggestive of secondary infection [18],[20]. The absence of DENV IgG antibody in serum samples collected between days 0 and eight makes it possible to classify the case as primary DENV infection. It has also been shown that, during the IgG antibody response, NS1-specific IgG antibodies start to appear on day 8 of primary infection and are still present during the first few days of DENV secondary infection [21]. As suggested by Table 6, the sensitivity of NS1 Ag detection with the three commercial tests would be expected to be higher during primary infection than during secondary infection, and we clearly showed greater sensitivity with the Platelia Dengue NS1 Ag test or the Dengue NS1 Ag STRIP than with the pan-E Dengue Early ELISA. This observation is consistent with recent findings with the Platelia Dengue NS1 Ag assay [13]. During these first few days of secondary infection, a substantial amount of NS1 protein may be bound to NS1-specific IgG antibodies from previous acute-phase infection and trapped within immune complexes [9],[22]. This difference in the kinetics of NS1-specific IgG antibodies between primary and secondary DENV infection is certainly similar to the kinetics observed for total DENV IgG antibodies. In addition, as observed in Table 3, the sensitivity of NS1 detection rapidly decreases on day five of secondary DENV infection, requiring NS1 detection between days 0 and four for an accurate diagnosis.
The accurate laboratory diagnosis of DENV infection is now possible with Dengue NS1 Ag detection tests, taking into account the timing of serum collection after the onset of fever. Previous studies have demonstrated a diagnostic strategy combining NS1 Ag detection in acute-phase sera and DENV IgM detection in early-convalescent-phase sera, providing a sensitivity of about 90% for dengue diagnosis [12],[23]. The development of a single immunochromatographic assay combining NS1 antigen and DENV IgM antibody detection would provide clinicians with a rapid test for dengue diagnosis sensitive during both the acute and early convalescence phases, between days 0 and 8 after the onset of fever.
NS1 detection has been shown to be suitable for early dengue diagnosis, whatever the DENV serotype responsible for dengue disease in Latin America and Southeast Asia, but only in two retrospective studies [12],[13]. Although these new diagnostic tools have been designed using two monoclonal antibodies (Platelia and ICT from Bio-Rad) or one monoclonal and one polyclonal antibody (pan-E from Panbio) for NS1 capture, and given the existence of different DENV genotypes within each serotype [24], it would be interesting to evaluate these two new diagnostic tools based on NS1 detection in prospective clinical studies in Asia and Latin America. It would also be useful to evaluate the performances of these kits taking into account different patient profiles such as ethnicity or disease severity. However, the severe fatal forms of the disease, such as DHF/DSS, are known to occur between four and six days after fever onset, whereas NS1 detection is optimized for all sera collected during the first five days of the disease.
We show that the sensitivity of NS1 detection with the Dengue NS1 Ag STRIP and Pan-E Dengue Early ELISA tests increased from day 0 to day 3 after fever onset, with the largest effect observed for serum samples without DENV IgG antibody. This phenomenon may be correlated with an increase in NS1 secretion over the first three days after fever onset [9]. This increase was not detectable with the Platelia Dengue NS1 Ag test, possibly due to the greater analytical sensitivity of the Platelia than of the Dengue NS1 Ag STRIP and pan-E Dengue Early ELISA tests.
We observed an increase in the sensitivity of the Platelia Dengue NS1 Ag and Dengue NS1 Ag STRIP tests on day 6 for serum samples positive for DENV IgG antibody, probably correlated with an increase in the amount of secreted NS1, but the number of serum samples was small (n = 15). Soluble NS1 protein binds to the human endothelium in situ [11] and accumulates in hepatocytes [25], possibly contributing to viral propagation. The release of soluble NS1 protein from the endothelium or from hepatocytes during DENV secondary infection may therefore play a role in the pathophysiology of the disease. Alternatively, the persistence of viral particles in capillary blood longer than in peripheral blood promotes the late release of soluble NS1 protein [26]. Further studies quantifying NS1 protein as a function of viral load in acute-phase and early convalescence-phase sera will provide further insight into these aspects.
In conclusion, this evaluation of two new commercial tests for dengue diagnosis, Dengue NS1 Ag STRIP and pan-E Dengue Early ELISA, and their comparison with the Platelia Dengue NS1 Ag test confirm that NS1 will be beneficial as a new marker in the diagnosis of acute DENV infection. The first rapid immunochromatographic test, Dengue NS1 Ag STRIP, which performs well, is suitable as a first-line test in the field, whereas pan-E Dengue Early ELISA should be used with DENV IgM antibody detection for the diagnosis of DENV infection.
Supporting Information
Alternative Language Abstract S1.
Translation of the Abstract into Portuguese by Pedro Fernando Vasconcelos, Instituto Evandro Chagas, Belém, Brazil
https://doi.org/10.1371/journal.pntd.0000280.s001
(0.05 MB PDF)
Alternative Language Abstract S2.
Translation of the Abstract into Spanish by Samantha Brandler, Institut Pasteur, Paris, France
https://doi.org/10.1371/journal.pntd.0000280.s002
(0.05 MB PDF)
Alternative Language Abstract S3.
Translation of the Abstract into French by Philippe Dussart
https://doi.org/10.1371/journal.pntd.0000280.s003
(0.05 MB PDF)
Acknowledgments
Dengue NS1 Ag STRIP tests were provided by Bio-Rad Laboratories, Marnes La Coquette, France.
Author Contributions
Conceived and designed the experiments: PD LB. Performed the experiments: BL LB DM SM. Analyzed the data: PD LP LB. Contributed reagents/materials/analysis tools: LP BL LB AL SM. Wrote the paper: PD LB.
References
- 1. Guzman MG, Kouri G (2002) Dengue: an update. Lancet Infect Dis 2: 33–42.
- 2.
World Health Organization Available: [Online.] http://www.who.int/csr/disease/dengue/impact/en/index.html.
- 3. Gubler DJ (1998) Dengue and dengue hemorrhagic fever. Clin Microbiol Rev 11: 480–496.
- 4. Chambers TJ, Hahn CS, Galler R, Rice CM (1990) Flavivirus genome organization, expression and replication. Annu Rev Microbiol 44: 649–688.
- 5. Lindenbach BD, Rice CM (1997) Trans-complementation of yellow fever virus NS1 reveals a role in early RNA replication. J Virol 71: 9608–9617.
- 6. Mackenzie JM, Jones MK, Young PR (1996) Immunolocalization of the dengue virus nonstructural glycoprotein NS1 suggests a role in viral RNA replication. Virology 220: 232–240.
- 7. Winkler G, Maxwell SE, Ruemmler C, Stollar V (1989) Newly synthesized dengue-2 virus nonstructural protein NS1 is a soluble protein but becomes partially hydrophobic and membrane-associated after dimerization. Virology 171: 302–305.
- 8. Young PR, Hilditch PA, Bletchly C, Halloran W (2000) An antigen capture enzyme-linked immunosorbent assay reveals high levels of dengue virus protein NS1 in the sera of infected patients. J Clin Microbiol 38: 1053–1057.
- 9. Libraty DH, Young PR, Pickering D, Endy TP, Kalayanarooj S, et al. (2002) High circulating levels of the dengue virus nonstructural protein NS1 early in dengue illness correlate with the development of dengue hemorrhagic fever. J Infect Dis 186: 1165–1168.
- 10. Alcon S, Talarmin A, Debruyne M, Falconar A, Deubel V, et al. (2002) Enzyme-linked immunosorbent assay specific to Dengue virus type 1 nonstructural protein NS1 reveals circulation of the antigen in the blood during the acute phase of disease in patients experiencing primary or secondary infections. J Clin Microbiol 40: 376–381.
- 11. Avirutnan P, Zhang L, Punyadee N, Manuyakorn A, Puttikhunt C, et al. (2007) Secreted NS1 of dengue virus attaches to the surface of cells via interactions with heparan sulfate and chondroitin sulfate E. PLoS Pathog 3: e183. doi:10.1371/journal.ppat.0030183.
- 12. Dussart P, Labeau B, Lagathu G, Louis P, Nunes MR, et al. (2006) Evaluation of an enzyme immunoassay for detection of dengue virus NS1 antigen in human serum. Clin Vaccine Immunol 13: 1185–1189.
- 13. Kumarasamy V, Wahab AH, Chua SK, Hassan Z, Chem YK, et al. (2007) Evaluation of a commercial dengue NS1 antigen-capture ELISA for laboratory diagnosis of acute dengue virus infection. J Virol Methods 140: 75–79.
- 14. Gubler DJ, Kuno G, Sather GE, Velez M, Oliver A (1984) Mosquito cell cultures and specific monoclonal antibodies in surveillance for dengue viruses. Am J Trop Med Hyg 33: 158–65.
- 15. Lanciotti RS, Calisher CH, Gubler DJ, Chang GJ, Vorndam AV (1992) Rapid detection and typing of dengue viruses from clinical samples by using reverse transcriptase-polymerase chain reaction. J Clin Microbiol 30: 545–551.
- 16. Talarmin A, Labeau B, Lelarge J, Sarthou JL (1998) Immunoglobulin A-specific capture enzyme-linked immunosorbent assay for diagnosis of Dengue fever. J Clin Microbiol 36: 1189–1192.
- 17. Matheus S, Deparis X, Labeau B, Lelarge J, Morvan J, et al. (2005) Discrimination between primary and secondary dengue virus infection by an immunoglobulin G avidity test using a single acute-phase serum sample. J Clin Microbiol 43: 2793–2797.
- 18.
World Health Organization (1997) Dengue haemorrhagic fever: diagnosis, treatment and control. World Health Organization, Geneva. Switzerland. [Online.] http://who.int/csr/resources/publications/dengue/Denguepublication/en/index.html.
- 19. Blacksell SD, Mammen MP Jr, Thongpaseuth S, Gibbons RV, Jarman RG, et al. (2008) Evaluation of the Panbio dengue virus nonstructural 1 antigen detection and immunoglobulin M antibody enzyme-linked immunosorbent assays for the diagnosis of acute dengue infections in Laos. Diagn Microbiol Infect Dis 60: 43–49.
- 20. Shu PY, Huang JH (2004) Current advances in dengue diagnosis. Clin Diagn Lab Immunol 11: 642–650.
- 21. Shu PY, Chen LK, Chang SF, Yueh YY, Chow L, et al. (2003) Comparison of capture immunoglobulin M (IgM) and IgG enzyme-linked immunosorbent assay (ELISA) and nonstructural protein NS1 serotype-specific IgG ELISA for differentiation of primary and secondary dengue virus infections. Clin Diagn Lab Immunol 10: 622–630.
- 22. Lapphra K, Sangcharaswichai A, Chokephaibulkit K, Tiengrim S, Piriyakarnsakul W, et al. (2008) Evaluation of an NS1 antigen detection for diagnosis of acute dengue infection in patients with acute febrile illness. Diagn Microbiol Infect Dis 4: 387–391.
- 23. Chuansumrit A, Chaiyaratana W, Pongthanapisith V, Tangnararatchakit K, Lertwongrath S, et al. (2008) The use of Dengue nonstructural protein 1 antigen for the early diagnosis during the febrile stage in patients with dengue infection. Pediatr Infect Dis J 27: 43–48.
- 24. Rico-Hesse R (2003) Microevolution and virulence of dengue viruses. Adv Virus Res 59: 315–41.
- 25. Alcon-LePoder S, Drouet MT, Roux P, Frenkiel MP, Arborio M, et al. (2005) The secreted form of dengue virus nonstructural protein NS1 is endocytosed by hepatocytes and accumulates in late endosomes: implications for viral infectivity. J Virol 79: 11403–11411.
- 26. Matheus S, Meynard JB, Lacoste V, Morvan J, Deparis X (2007) Use of capillary blood samples as a new approach for diagnosis of Dengue virus infection. J Clin Microbiol 45: 887–890.