1. The Flavivirus NS1
NS1 is a highly conserved nonstructural glycoprotein (46 kDa) encoded by most flaviviruses [1]. These viruses, transmitted mainly by arthropods, are the causative agent of many severe diseases, including dengue fever, West Nile, yellow fever, Zika, and more [2]. Flaviviruses are small, enveloped viruses containing a positive-sense single-strand RNA genome. This genome encodes a large polyprotein precursor that is further processed, co-translationally and post-translationally, by viral and cellular proteases into three structural proteins (capsid protein, membrane protein and envelop protein) and seven nonstructural proteins (NS1, NS2A, NS2B, NS3, NS4A, NS4B, NS5). The structural proteins build the virion, whereas the nonstructural proteins are involved in viral replication [1,2,3]. NS1 can be found both as a membrane-associated, highly stable dimer and a secreted soluble, lipid-associated hexamer [4,5]. In the infected cell, NS1 is synthesized as a soluble monomer and dimerizes after it is post-translationally modified in the lumen of the endoplasmic reticulum [4]. The membrane-associated NS1 can be found both in cellular compartments and on the cell surface [4]. Secreted NS1 is transported to the cell surface and accumulates extracellularly as a hexamer [6], which also binds the plasma membrane of cells through interactions with specific sulfated glycosaminoglycans [7,8]. Soluble NS1 is present in serum and other body fluids [9,10,11,12]. Although it does not have a known catalytic function, it is clear that NS1 is essential for efficient viral RNA replication [5,13]. NS1 proteins also modulate endothelial permeability in a tissue-specific manner, correlating with disease pathology [14]. It has been shown that the immune response against NS1 might damage endothelial cells due to a cross-reaction of the antibodies and immune complex formation, which can elicit autoantibodies that react with platelets and extracellular matrix proteins [15].
Specific antibodies to membrane-associated NS1 and antibodies against soluble NS1 further enhance the activation of the complement system [8]. The connection between those antibodies and the complement system can result in hemorrhage and capillary-leakage, which is part of the characteristics of a severe disease [8,14,15,16].
2. The Role of NS1 in Dengue Fever Diagnosis
Dengue fever (DF) is an arthropod-borne viral disease that is responsible for the greatest human disease burden [17,18]. The estimation of annual deaths is 10,000 and the estimation of apparent infection cases is between 100–400 million [17,19,20]. About 50% of the world’s population lives in dengue virus (DENV) endemic areas [20,21]. DENV infection is caused by four distinct serotypes (DENV 1-4), which are antigenically distinct [19]. All four serotypes may cause different forms of the disease, ranging from an asymptomatic infection and febrile illness to the more severe dengue hemorrhagic fever (DHF), dengue shock syndrome (DSS), and their related complications [22]. Infection with one of the DENV serotypes provides lifelong immunity to that specific serotype. However, immunity against other serotypes is limited and usually does not last for more than a few months [23]. Clinical diagnosis of DF as primary or secondary infection is important, as the greatest risk for DHF/DSS is considered to be with a second DENV serotype exposure (while the risk for DHF with a third or fourth dengue infection is very low) [23,24,25,26].
2.1. NS1 in Serum Samples
DF is diagnosed using several assays, which are all based on DENV markers in the host. These markers are antibodies against the envelope protein of DENV (IgM\IgG) and the RNA of the virus [27,28].
The serological assays, based on the detection of IgM and IgG antibodies against the envelope protein, have several advantages. They are available at a low cost and do not require high-end equipment [29]. However, a significant disadvantage of this method is its inability to diagnose the disease in the acute phase of infection since IgM levels in the serum become detectable only after 3–5 days from symptoms onset, and peak approximately two weeks after the onset of fever [25,29,30,31]. Another critical issue regarding serology-based diagnosis is the cross-reactivity among flaviviruses [32]. Flaviviruses share common antigenic epitopes; therefore, antibodies against these common epitopes may cause false positive results when using an IgM- or IgG-based assay [30,32,33,34]. This issue makes the diagnosis of specific flavivirus infection more complex and less accurate, especially in regions that are endemic for several flaviviruses. Thus, for early detection of acute DF, the current immunological assays are not sensitive or specific enough [35,36,37]. Of note, dengue antibodies might be falsely detected due to past infection, infection with other flaviviruses, or past flavivirus vaccination [38], thus, making the diagnosis of secondary DENV infection challenging. Secondary DENV infection is considered a risk factor for severe dengue, emphasizing the clinical significance of diagnosis [39].
Molecular methods are based on DENV RNA detection by real-time RT-PCR. This method allows the detection of the virus at an early stage of the infection [40]. The main disadvantages of the molecular methods are their costs and availability, a serious consideration in low-income countries where DENV is endemic. Additionally, the window for virus detection using PCR is relatively narrow, and its highest sensitivity is achieved within the beginning of the illness. RT-PCR sensitivity varies greatly between various studies [41,42].
NS1-based assays may overcome several of the previously mentioned problems. NS1 levels in serum are highly correlated with DENV viremia [43] and become detectable at the beginning of the febrile illness, peaking 3 to 5 days following symptom onset. Furthermore, NS1 can still be detected in some cases until day 12 post-symptom onset, when RT-PCR can no longer detect viral RNA in most cases [38,44].
The commercial kits for detecting NS1 proteins are primarily based on ELISA. However, rapid one-step assays based on in-vitro immunochromatography are also available. Thus, NS1-based assays are readily available, simple to use as a rapid test, and cost-effective.
The assay’s sensitivity depends on the sampling time, the serotype of DENV, and the detection kit. Studies have evaluated the sensitivity of these assays and found it to be highest during the first days from fever onset (Table 1). A study conducted on returning travelers showed a sensitivity of 87% during the first three days of symptoms, that decreased to 69.4% when sampled during days 0–12 [38]. Other studies using a different commercial kit showed sensitivities of up to 95% during the first days [41,45,46]. The sensitivity of the NS1 antigen-capture assay was significantly higher for DENV-1 than for the three other serotypes [46,47].
The specificity of these assays was found to vary between 86% to 100% [9,38,41,53,54].
Sensitivity is significantly enhanced by combining the NS1 antigen kit with an IgM-based detection assay by approximately 28% [47,55]. The sensitivity of this combination is somewhat lower than the combination of RT-PCR together with an IgM-detection-based assay, and higher than the sensitivity of RT-PCR alone [47].
Several studies have found that during a secondary DENV infection, when IgG antibodies against NS1 are already present in serum, there is a lower sensitivity of the NS1-based assay [38,47,48]. Other studies have shown no significant difference in the sensitivity for the NS1-based assay between the first and second infection [56,57,58]. One study has shown a substantial decrease in the sensitivity (91.6% to 48.3%) of the NS1-based assay due to the presence of IgM antibodies against NS1 in the serum [58]
Another method that can contribute to detecting DENV is the Dried Blood Spot (DBS), a technique used when venous blood cannot be taken or where a laboratory does not exist. It requires a small amount of blood that can be collected from finger prick samples. This method involves minor discomfort, can be performed without medical assistance and does not require low temperature storage as is the case with serum samples. Several studies have shown the advantages of the DBS method [59,60,61] and its high sensitivity for NS1 detection, 98.7% during days 2–4 after the onset of the disease and 92.3% during days 5–7 [62].
The half-life of NS1 in plasma is about one hour [16]. The amount of free NS1 in the serum correlates with the viremia and, thus, it is a potential marker of the clinical outcome of DHF and DSS [47,63,64], suggesting that early quantitative detection of NS1 may provide a significant benefit. It can enable adequate follow-up for patients at high risk of developing DSS and DHF, whereas it can save unnecessary medications and hospitalization for patients with low risk. However, other studies found no correlation between NS1 levels in serum and disease severity [55,63].
In conclusion, NS1 is an important marker for detecting acute DENV infection. It offers an excellent serologic alternative to dengue viral RNA detection by RT-PCR, which is very sensitive and specific but expensive and not readily available in endemic regions (Figure 1). NS1 detection is useful for early DF diagnosis and whether quantifying the level of NS1 may identify patients at higher risk for severe dengue infection needs further studies.
2.2. Dengue NS1 Detection in Other Body Fluids
DENV-RNA and NS1 were also detected in urine and saliva samples [10,51,65,66,67] (Table 2). A study in Helsinki tested 14 Finnish travelers with DF, examining the presence of DENV-RNA and NS1 in saliva, urine and serum concurrently, and found that DENV-RNA in urine samples can be detectable at a later stage than serum samples [10] (Schemes Ι). This phenomenon, corroborated in other studies, is fundamental because it extends the time that DENV can be detectable using a molecular technique to the convalescent phase of infection. DENV-RNA levels in saliva were found to be similar to those in serum [10]. However, other studies found DENV-RNA levels in saliva were less sensitive, but taking longer to be detected in comparison to the levels in serum [65]. These results highlight the different kinetics of viral RNA in the urine and saliva.
NS1 levels in urine were found to correlate with reduced platelet counts and urine total protein concentration. Both urine NS1 levels and total protein concentration were found to correlate with serum DENV-RNA levels, suggesting that NS1 is the main DENV component in urine during the peak of the viremia [10].
A study performed in Japan [52] on 96 Japanese travelers with DF examined the utility of NS1 antigen detection in urine and serum samples. This study and others showed that, in some cases, NS1 could be detected in urine samples even after it reaches undetectable levels in serum. The NS1 detection rate in the serum showed a decrease after day 10, while the NS1 detection rate in the urine was relatively low (approximately 30%) but consistent until day 14. Similarly, detection based on the presence of urine DENV-RNA compared to the serum showed similar detection rates as those of NS1, with better results in detecting DENV-RNA in the urine than in the serum after day 11 [52,65].
A different study compared serum and urine samples obtained from 55 patients, of whom 19 had DF and 36 developed DHF with evidence of plasma leakage [9]. While NS1 levels in serum did not correlate with disease severity, the detection rates of NS1 in urine samples were higher in DHF patients, suggesting that the presence of NS1 in urine could be due to plasma leakage or the production of viral antigens by infected kidney cells [51]. In addition, the assays used in all the studies are designed and calibrated for serum; therefore, their sensitivities for urine and saliva must be evaluated. As for NS1 detection by ELISA in urine, most studies show high specificity but much lower sensitivity, around 100% and 20–68%, respectively [9,10,50,51,52]. Thus, more studies are needed to assess the performance and application of DENV diagnosis in urine and saliva.
2.3. CSF NS1 for Diagnosis of Dengue-Associated Encephalitis
Unlike other arboviral infections, DENV does not usually cause neurological manifestations [68]. The prevalence of CNS involvement in patients with dengue infection varies with the severity of dengue disease. However, the presence of CNS involvement does not affect the prognosis of dengue infection.
Although some studies suggest that DENV actively enters the CNS, this has not been demonstrated. Thus, it is still possible that the virus passively crosses the blood–brain barrier [69].
The presence of NS1 in CSF has not been well studied. One study examined the performance of IgM- and NS1-based assays (Pan-E Dengue Early ELISA) on CSF samples from dengue-infected patients vs. non-dengue patients obtained during autopsies [12]. The results showed that when used during viremia, the NS1-based assay can also detect NS1 in CSF with a sensitivity of 50%, while the sensitivity of the same kit in serum ranges from 60.4% to 91.6% [70]. As in serum, the combination of NS1 and IgM-based assays in CSF increases dengue diagnosis. However, similar to the observation in the serum, once IgM is detected, the sensitivity of NS1 Ag detection decreases significantly [70].
Another study from Brazil examined CSF samples from 209 patients with suspected viral meningitis or meningoencephalitis (26 of them died from suspected meningitis). All the samples were analyzed using RT-PCR, ELISA for NS1 (Pan-E Dengue Early ELISA), IgM, and a rapid immunochromatography test for IgG. Results demonstrate that out of 209 samples, 8 (3.8%) had shown positive results for DENV in at least one of the assays. Those findings are similar to other studies from Jamaica [71] and Vietnam [72].
Although more research is needed, these studies [12,73] show that NS1 kits for detecting NS1 antigen in serum can be used for CSF samples in dengue patients with neurological manifestations. As mentioned, it is recommended to use the combination of IgM- and NS1-based assays to increase the sensitivity of the diagnosis.
2.4. Detection of Dengue NS1 Is Tissue Specimens
To detect DENV in tissues, most studies have used RT-PCR, in situ hybridization, or immunostaining [74,75,76,77]. Another understudied alternative method for DENV tissue detection is the identification of NS1. The main application of this method is to reveal information about the cause of death that may lead to a better understanding of viral tropism in the human body in fatal cases.
Evidence for the presence of DENV antigens has been previously demonstrated in liver cells, brain inflammatory cells, spleen, lung, and pulmonary endothelium cells [59,60,62,74,77,78,79,80,81].
A study analyzed tissues from 13 children who died of DHF/DSS using immunohistochemistry and found NS1 in at least one tissue in all 13 cases using frozen and paraffin-embedded tissues [82]. The analyzed tissues were from organs, including the liver, spleen, lymph nodes, heart, lungs, kidney, bone marrow, and brain. In the liver, NS1 was identified in the cytoplasm of hepatocytes and Kupffer cells. Still, there was no evidence for NS1 in the sinusoidal endothelial cells. In the spleen, NS1 was identified in several mononuclear cells scattered within white and red pulps. In the lymph nodes, NS1 was found in the germinal centers. No evidence for NS1, or other DENV proteins, was found in other tissue specimens from the heart, lungs, kidneys, and bone marrow. However, other morphological changes related to DENV infection have been observed in some of these tissues.
Another study that assessed the usefulness of NS1-based assays on tissue specimens took 74 tissue samples from various organs from 23 fatal dengue cases [74]. For DENV detection, three different kits were used—Early ELISA (Panbio), Platelia NS1 (Biorad), and NS1 Ag Strip (Biorad). Per specimen, NS1 Ag Strip had the highest sensitivity of 78.3%; the Platelia NS1 sensitivity was 45.9%, and the Early ELISA sensitivity was 22.9%. Per case, the detection rates were 91.3%, 60.8%, and 34.7%, respectively. However, the overall sensitivity of this new approach in confirming the fatal cases was 87.0%. The specificity was 100% for all kits, and no cross-reactivity was observed with control tissues from fatal cases of yellow fever. It is important to note that each of the tissues had been detected in at least one case with one kit. For example, the NS1 Ag Strip, which had the best sensitivity, detected NS1 in the following tissue specimens: liver (91.3%), lung (71.4%), kidney (100%), brain (80%), spleen (66.6%) and thymus (100%). Similar results in liver and spleen tissue had been shown in another recent study [75].
The identity of the cells and tissues which DENV infects and replicates in humans are still incompletely understood. One possible explanation for the detection of NS1 in some of the tissue specimens is its presence in the blood supporting these tissues and, indeed, some of those organs that were well-diagnosed have high blood circulation. Yet, the liver seems to be an adequate tissue for NS1 detection.
These results encourage further studies and evaluation of the use of DENV NS1 in detection in tissues. Different postmortem preservation techniques and time of detection after death should also be examined. These methods are rapid, require less laboratory expertise and equipment, and cost less than the molecular and immunohistochemical methods that are currently in use.
This method, which can be performed following a needle biopsy, can dramatically improve the diagnosis and confirmation of postmortem fatal dengue cases in some parts of the world.
3. NS1 in Zika Infection
The Zika virus outbreak spread in the last years to a total of 89 countries and territories [83,84]. The Americas, and South Asia have significantly complicated flavivirus diagnosis. Cross-reactivity between DENV and ZIKV antibodies resulted in low specificity of ELISAs-based serology detecting flaviviral envelope-epitopes. More importantly, this cross-reactivity also occurs in viral neutralization assays, considered the gold standard for flavivirus diagnosis [85,86]. However, due to the substantial amino acid differences in NS1 between ZIKV and DENV, several ELISA kits have been developed to detect ZIKV NS1 antibodies [87,88,89,90] rather than envelope antibodies. In contrast to envelope-based assays, ZIKV NS1-based ELISA is highly specific and showed almost no cross-reactivity was detected in patients with previous DENV, WNV, YF, and Japanese encephalitis viral infections [89]. Interestingly, while IgG sensitivity was high, IgM sensitivity of the assay was demonstrated to be dependent on flavivirus background, and samples obtained from people living in areas with endemic ZIKV exhibited lower IgM sensitivity [89]. A study examining the sensitivity and kinetics of ZIKV NS1-based ELISA among travelers with ZIKV infection demonstrated higher IgM sensitivity of 79% in the first month and 68% up to two months post-symptoms onset [88] suggesting that levels of IgM against the NS1 may be declining much faster than IgM antibodies against the envelope protein. Indeed, while envelope IgM persisted for years after infection [91], NS1 IgM levels were shown to have a 75% decline by 44 days after symptom onset [92]. This suggests that measuring IgM against NS1 may be better suited for detecting the acute phase of the disease as it allows distinguishing between recent and past infections. Moreover, the limited cross-reactivity of NS1-based ELISA and its ability to serve as a first-line screening tool for travelers [93] allows the exclusion of ZIKV infection in travelers returning from ZIKV-endemic countries and, together with RT-PCR, minimizes the risk of false-negative results which is especially important for those who are pregnant or wish for preconception screening.
As a result of the excellent performance of the ZIKV NS1-based ELISA, DENV NS1-based ELISAs are currently being developed. They may provide better diagnostic capabilities for DENV, especially in areas with co-circulation of both DENV and ZIKV.
It is important to note that while NS1-based ELISA are a standard diagnostic tool in Europe and the Middle East, the Center for Disease Control and Prevention (CDC) uses an FDA-approved envelope-based ELISA and does not recommend serology testing for asymptomatic pregnant women or preconception screening [94].
4. The Role of NS1 for Other Flaviviruses Diagnosis
The development of assays for detecting DENV NS1 antigens in serum allowed easy and affordable diagnosis of dengue patients at the acute phase, as discussed above [38]. However, NS1 antigen detection tests against other flaviviruses are not commercially available. Two studies generated antibodies against WNV NS1 protein and investigated the secretion of WNV NS1 during WNV infection in vivo and in vitro using an ELISA assay [95,96]. NS1 was detectable up to day five in infected hamsters [95] and up to day three post-infection in mice [96] suggesting that NS1 secretion during infection is low. Still, the detection of WNV NS1 is comparable to the detection of WNV RNA by qRT-PCR.
5. The Role of Dengue NS1 Testing to Differentiate Dengue vs. COVID-19 Infection
The pandemic of SARS-CoV-2 rapidly spread around the globe, including areas endemic to dengue. DF and COVID-19 are difficult to distinguish as they share similar clinical and laboratory features [97]. Interestingly, recent reports from several countries in Asia showed cross-reactivity of either IgM and/or IgG antibodies between these two, despite being unrelated viruses [98,99,100,101]. This effect might have an impact on the clinical outcome if diagnosis is delayed. On the other hand, other evidence downsized the concern of cross-reactivity [102]. Hence, further studies are warranted to explore the pathophysiology of this cross-reactivity and to better elucidate the accuracy of the different commercial kits. Given that a possible cross-reactivity between DENV and SARS-CoV-2 could lead to false-positive results for both diseases and the consideration that DENV has been extensively spread in recent decades, a serological test alone might be misleading. However, using dengue NS1 antigen for diagnosis can prevent cross-reactive results and leads to a more accurate diagnosis.
6. In Summary
NS1 is an essential flavivirus protein that has a central role in efficient viral RNA replication. This protein accumulates intracellularly and is secreted from infected cells. Soluble NS1 is present in blood serum and other body fluids and, therefore, can be used as an antigen-detection diagnosis. Since antibodies are produced against this protein they can be used for serology diagnosis. There are advantages of using NS1-based diagnosis (antigen and/or antibodies) in several aspects:
Epidemiologically, its highly specific properties differ in each flavivirus, and therefore minimize cross-reactive results among the flaviviruses group. The amounts of NS1 antigen are high during dengue infection, while during Zika infection, the amount of NS1 antibodies are high. Better methods of detecting low concentration of NS1 may also allow its use in the diagnosis of other flaviviruses as well. Currently a reliable serological diagnosis to differentiate each virus within the family of flaviviruses is less than optimal and introducing NS1-based serology can give more precise diagnosis and better epidemiological understating of the global distribution of each flavivirus.
From the clinical point of view, a correct identification of the virus might have great significance. For example, Zika virus infection is highly important in a pregnant woman as there is a need for further evaluation of in-utero infection.
Regarding DF, the amount of NS1 antigen is important as it correlates with the level of viremia, which makes it a potential marker of severe disease.
Regarding a virology aspect, detection of the specific NS1 antibodies against each DENV serotype can give an assessment of previous infection with DF and which serotype it was.
Regardless, NS1-based diagnosis does not replace other serology, especially when the diagnosis is made long after the infection, nor the very sensitive but expensive PCR.
The authors declare no conflict of interest.
Footnotes
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.
Enlarge this image.Figure 1. Schematic time line (D = days) of the different DENV detection methods and their sensitivities. The sensitivity range reflects the variety of results in different studies.
Comparison of sensitivity and specificity of NS1 DENV detection in serum samples, accordance to timeline from symptoms-onset.
| Source | Method | % Sensitivity According to Days Post Symptoms Onset | Specificity % | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | 13 | |||
| Blessmann et al., 2020 [ |
RDT (SD Bioline Dengue Duo) | 78.3 | 60 | 42.9 | 28.6 | ND | ND | ND | ND | ND | >96 | ||||
| ELISA (Platelia, Bio-Rad) | 65.2 | 50 | 42.9 | 28.6 | ND | ND | ND | ND | ND | >96 | |||||
| Liu et al., 2020 |
RDT (Bio-Rad) | 89.9 | 80.6 | ND | ND | ND | ND | ND | ND | ND | 94.6 | ||||
| RDT (SD Dengue Duo) | 95.7 | 83.6 | ND | ND | ND | ND | ND | ND | ND | 91.9 | |||||
| RDT (CTK) | 95.7 | 82.1 | ND | ND | ND | ND | ND | ND | ND | 73 | |||||
| Hunsperger et al., 2016 |
ELISA (InBios) | 93 | 93 | 85 | 83 | 84 | 60 | 57 | 47 | 86 | 67 | ND | ND | ND | ND |
| ELISA (Panbio) | 86 | 93 | 78 | 71 | 71 | 52 | 50 | 33 | 57 | 33 | ND | ND | ND | ND | |
| Andries et al., 2016 [ |
ELISA (NS1) | 94.4 | 66.7 | 21.3 | ND | ND | |||||||||
| Andries et al., 2015 [ |
ELISA (NS1) | 83.3 | 91.6 | 79 | 55.9 | 29.1 | ND | ||||||||
| Fuchs et al., 2014 |
ELISA (Panbio) | 87.5 | ND | ND | ND | ND | ND | ND | ND | ND | ND | ND | 88.8–100 | ||
| 73.9 | ND | ND | ND | ND | ND | ND | ND | ND | |||||||
| 72.5 | ND | ND | ND | ND | |||||||||||
| 69.4 | ND | ||||||||||||||
| Saito et al., 2015 [ |
ELISA (Platelia, Bio-Rad) | >90 | 33 | ND | |||||||||||
| Huhtamo et al., 2010 [ |
ELISA (Platelia, Bio-Rad) | 78.6 | 74.1 | 84.2 | 70.6 | ND | ND | ND | 100 | ||||||
| Ramirez et al., 2009 [ |
ELISA (Panbio) | 60.9 | ND | ND | ND | ND | ND | ND | 94.4 | ||||||
| ELISA (Platelia, Bio-Rad) | 71.3 | ND | ND | ND | ND | ND | ND | 86.1 | |||||||
| RDT (AG Strip (BIO-RAD) | 67.8 | ND | ND | ND | ND | ND | ND | 94.4 | |||||||
| Chuansumrit et al., 2011 |
ELISA (Platelia, Bio-Rad) | ND | ND | 94.7 | ND | ND | ND | 100 | |||||||
| RDT (Bio-Rad) | ND | ND |
|
ND | ND | ND | 100 | ||||||||
Abbreviation: ND—Not done; RDT—Rapid diagnostic test; ELISA—Enzyme-linked immunosorbent assay.
Comparison of sensitivity and specificity of NS1 detection in urine and saliva samples, accordance to timeline from symptoms-onset.
| Source | Method | % Sensitivity According to Days Post Symptoms Onset | Specificity % | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | 13 | |||
| Urine | |||||||||||||||
| Andries et al., 2016 [ |
ELISA | 9.9 | 19.2 | 3.4 | ND | 100 | |||||||||
| RDT | 11.1 | 21 | 2.3 | ND | ND | ||||||||||
| Andries et al., 2015 [ |
ELISA | 0 | 10.8 | 28.6 | 18.6 | 0 | ND | ||||||||
| Saito et al., 2015 [ |
ELISA | 36 | 43 | 12 | ND | ||||||||||
| real-time RT-PCR (for reference) | 32 | 30 | 33 | ND | |||||||||||
| Korhonen et al., 2014 [ |
ELISA | ND | 59.1 | 50 | 100 | ||||||||||
| Chuansumrit et al., 2011 [ |
ELISA | ND | ND | 68.4 | ND | ND | ND | 100 | |||||||
| RDT | ND | ND | 52.6 | ND | ND | ND | 100 | ||||||||
| Saliva | |||||||||||||||
| Andries et al., 2016 [ |
ELISA (NS1-Saliva) | 25.5 | 29.9 | 8.3 | ND | ND | |||||||||
| RDT (NS1-Saliva) | 14.9 | 25.7 | 10.2 | ND | ND | ||||||||||
| Andries et al., 2015 [ |
ELISA (NS1-Saliva) | 16.7 | 33.7 | 41 | 28.8 | 10.9 | ND | ||||||||
| Korhonen et al., 2014 [ |
Antigen EIA (NS1-Saliva) | ND | 59.1 | 52.2 | 95 | ||||||||||
Abbreviation: ND—Not done; RDT—Rapid diagnostic test; ELISA—Enzyme-linked immunosorbent assay.
References
1. Lindenbach, B.D.; Rice, C.M. Molecular Biology of Flavivirus. Adv. Virus Res.; 2003; 59, pp. 1317-1542. [DOI: https://dx.doi.org/10.1152/physrev.00004.2012]
2. Blitvich, B.J.; Firth, A.E. A Review of Flaviviruses that Have No Known Arthropod Vector. Viruses; 2017; 9, 154. [DOI: https://dx.doi.org/10.3390/v9060154] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/28635667]
3. Akey, D.L.; Brown, W.C.; Dutta, S.; Konwerski, J.; Jose, J.; Jurkiw, T.J.; DelProposto, J.; Ogata, C.M.; Skiniotis, G.; Kuhn, R.J. et al. Flavivirus NS1 structures reveal surfaces for associations with membranes and the immune system. Science (80-.); 2014; 343, pp. 881-885. [DOI: https://dx.doi.org/10.1126/science.1247749] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/24505133]
4. Winkler, G.; Maxwell, S.E.; Ruemmler, C.; Stollar, V. Newly synthesized dengue-2 virus nonstructural protein NS1 is a soluble protein but becomes partially hydrophobic and membrane-associated after dimerization. Virology; 1989; 171, pp. 302-305. [DOI: https://dx.doi.org/10.1016/0042-6822(89)90544-8]
5. Akey, D.L.; Brown, W.C.; Jose, J.; Kuhn, R.J.; Smith, J.L. Structure-guided insights on the role of NS1 in flavivirus infection. BioEssays; 2015; 37, pp. 489-494. [DOI: https://dx.doi.org/10.1002/bies.201400182]
6. Megret, O.; Mathieu, M.; Lepault, J.; Rey, L.I.X.A.; Deubel, V. Dengue Virus Type 1 Nonstructural Glycoprotein NS1 Is Secreted from Mammalian Cells as a Soluble Hexamer in a Glycosylation-Dependent Fashion. J. Virol.; 1999; 73, pp. 6104-6110.
7. Avirutnan, P.; Zhang, L.; Punyadee, N.; Manuyakorn, A.; Puttikhunt, C.; Kasinrerk, W.; Malasit, P.; Atkinson, J.P.; Diamond, M.S. Secreted NS1 of dengue virus attaches to the surface of cells via interactions with heparan sulfate and chondroitin sulfate E. PLoS Pathog.; 2007; 3, e183. [DOI: https://dx.doi.org/10.1371/journal.ppat.0030183]
8. Avirutnan, P.; Hauhart, R.E.; Somnuke, P.; Blom, A.M.; Diamond, M.S.; Atkinson, J.P. Binding of Flavivirus Nonstructural Protein NS1 to C4b Binding Protein Modulates Complement Activation. J. Immunol.; 2011; 187, pp. 424-433. [DOI: https://dx.doi.org/10.4049/jimmunol.1100750]
9. Chuansumrit, A.; Chaiyaratana, W.; Tangnararatchakit, K.; Yoksan, S.; Flamand, M.; Sakuntabhai, A. Dengue nonstructural protein 1 antigen in the urine as a rapid and convenient diagnostic test during the febrile stage in patients with dengue infection. Diagn. Microbiol. Infect. Dis.; 2011; 71, pp. 467-469. [DOI: https://dx.doi.org/10.1016/j.diagmicrobio.2011.08.020]
10. Korhonen, E.M.; Huhtamo, E.; Virtala, A.M.; Kantele, A.; Vapalahti, O. Approach to non-invasive sampling in dengue diagnostics: Exploring virus and NS1 antigen detection in saliva and urine of travelers with dengue. J. Clin. Virol.; 2014; 61, pp. 353-358. [DOI: https://dx.doi.org/10.1016/j.jcv.2014.08.021]
11. Poloni, T.R.; Oliveira, A.S.; Alfonso, H.L.; Galvo, L.R.; Amarilla, A.A.; Poloni, D.F.; Figueiredo, L.T.; Aquino, V.H. Detection of dengue virus in saliva and urine by real time RT-PCR. Virol. J.; 2010; 7, pp. 2-5. [DOI: https://dx.doi.org/10.1186/1743-422X-7-22]
12. Araujo, F.M.; Brilhante, R.S.; Cavalcanti, L.P.; Rocha, M.F.; Cordeiro, R.A.; Perdigao, A.C.; Miralles, I.S.; Araujo, L.C.; Araujo, R.M.; Lima, E.G. et al. Detection of the dengue non-structural 1 antigen in cerebral spinal fluid samples using a commercially available enzyme-linked immunosorbent assay. J. Virol. Methods; 2011; 177, pp. 128-131. [DOI: https://dx.doi.org/10.1016/j.jviromet.2011.07.003]
13. Lindenbach, B.D.; Rice, C.M. trans-Complementation of Yellow Fever Virus NS1 Reveals a Role in Early RNA Replication. J. Virol.; 1997; 71, pp. 9608-9617. [DOI: https://dx.doi.org/10.1128/jvi.71.12.9608-9617.1997]
14. Puerta-guardo, H.; Glasner, D.R.; Espinosa, D.A.; Wang, C.; Beatty, P.R.; Harris, E.; Puerta-guardo, H.; Glasner, D.R.; Espinosa, D.A.; Biering, S.B. et al. Flavivirus NS1 Triggers Tissue-Specific Vascular Endothelial Dysfunction Reflecting Disease Tropism Article Flavivirus NS1 Triggers Tissue-Specific Vascular Endothelial Dysfunction Reflecting Disease Tropism. Cell Rep.; 2019; 26, pp. 1598-1613. [DOI: https://dx.doi.org/10.1016/j.celrep.2019.01.036]
15. Falconar, A.K.I. The dengue virus nonstructural-1 protein (NS1) generates antibodies to common epitopes on human blood clotting, integrin/adhesin proteins and binds to human endothelial cells: Potential implications in haemorrhagic fever pathogenesis. Arch. Virol.; 1997; 142, pp. 897-916. [DOI: https://dx.doi.org/10.1007/s007050050127]
16. Avirutnan, P.; Punyadee, N.; Noisakran, S.; Komoltri, C.; Thiemmeca, S.; Auethavornanan, K.; Jairungsri, A.; Kanlaya, R.; Tangthawornchaikul, N.; Puttikhunt, C. et al. Vascular leakage in severe dengue virus infections: A potential role for the nonstructural viral protein NS1 and complement. J. Infect. Dis.; 2006; 193, pp. 1078-1088. [DOI: https://dx.doi.org/10.1086/500949]
17. Messina, J.P.; Brady, O.J.; Golding, N.; Kraemer, M.U.G.; Wint, G.R.W.; Ray, S.E.; Pigott, D.M.; Shearer, F.M.; Johnson, K.; Earl, L. et al. The current and future global distribution and population at risk of dengue. Nat. Microbiol.; 2019; 4, pp. 1508-1515. [DOI: https://dx.doi.org/10.1038/s41564-019-0476-8]
18. Stanaway, J.D.; Shepard, D.S.; Undurraga, E.A.; Halasa, Y.A.; Coffeng, L.E.; Brady, O.J.; Hay, S.I.; Bedi, N.; Bensenor, I.M.; Castañeda-Orjuela, C.A. et al. The global burden of dengue: An analysis from the Global Burden of Disease Study 2013. Lancet Infect. Dis.; 2016; 16, pp. 712-723. [DOI: https://dx.doi.org/10.1016/S1473-3099(16)00026-8]
19. Bhatt, S.; Gething, P.W.; Brady, O.J.; Messina, J.P.; Farlow, A.W.; Moyes, C.L.; Drake, J.M.; Brownstein, J.S.; Hoen, A.G.; Sankoh, O. et al. The global distribution and burden of dengue. Nature; 2013; 496, pp. 504-507. [DOI: https://dx.doi.org/10.1038/nature12060]
20. World Health Organization (WHO). Dengue and Severe Dengue. Available online: https://www.who.int/news-room/fact-sheets/detail/dengue-and-severe-dengue#:~:text=Global%20burden&text=One%20modelling%20estimate%20indicates%20390,with%20any%20severity%20of%20disease (accessed on 10 January 2022).
21. Brady, O.J.; Gething, P.W.; Bhatt, S.; Messina, J.P.; Brownstein, J.S.; Hoen, A.G.; Moyes, C.L.; Farlow, A.W.; Scott, T.W.; Hay, S.I. Refining the Global Spatial Limits of Dengue Virus Transmission by Evidence-Based Consensus. PLoS Negl. Trop. Dis.; 2012; 6, e1760. [DOI: https://dx.doi.org/10.1371/journal.pntd.0001760]
22. Mathew, A.; Rothman, A.L. Understanding the contribution of cellular immunity to dengue disease pathogenesis. Immunol. Rev.; 2008; 225, pp. 300-313. [DOI: https://dx.doi.org/10.1111/j.1600-065X.2008.00678.x] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/18837790]
23. Anantapreecha, S.; Chanama, S.; A-Nuegoonpipat, A.; Naemkhunthot, S.; Sa-Ngasang, A.; Sawanpanyalert, P.; Kurane, I. Serological and virological features of dengue fever and dengue haemorrhagic fever in Thailand from 1999 to 2002. Epidemiol. Infect.; 2005; 133, pp. 503-507. [DOI: https://dx.doi.org/10.1017/S0950268804003541] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/15962557]
24. Gibbons, R.V.; Kalanarooj, S.; Jarman, R.G.; Nisalak, A.; Vaughn, D.W.; Endy, T.P.; Mammen, M.P., Jr.; Srikiatkhachorn, A. Analysis of repeat hospital admissions for dengue to estimate the frequency of third or fourth dengue infections resulting in admissions and dengue hemorrhagic fever, and serotype sequences. Am. J. Trop. Med. Hyg.; 2007; 77, pp. 910-913. [DOI: https://dx.doi.org/10.4269/ajtmh.2007.77.910] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/17984352]
25. Meltzer, E.; Schwartz, E. A travel medicine view of dengue and dengue hemorrhagic fever. Travel Med. Infect. Dis.; 2009; 7, pp. 278-283. [DOI: https://dx.doi.org/10.1016/j.tmaid.2009.05.002]
26. Thein, S.O.E.; Aung, M.Y.O.M.I.N.; Shwe, T.N.U.; Aye, M.Y.O.; Zaw, A.; Aye, K.; Aye, K.M.A.R.; Aaskov, A. Risk factors in dengue shock syndrome. Am. J. Trop. Med. Hyg.; 1997; 56, pp. 566-572. [DOI: https://dx.doi.org/10.4269/ajtmh.1997.56.566]
27. World Health Organization Dengue: Guidelines for diagnosis, treatment, prevention, and control. Spec. Program. Res. Train. Trop. Dis.; 2009; 1, pp. 91-104. [DOI: https://dx.doi.org/10.13140/RG.2.2.19008.76807]
28. Simmons, C.P.; Farrar, J.J.; van Nguyen, V.C.; Wills, B. Dengue. N. Engl. J. Med.; 2012; 366, pp. 1423-1432. [DOI: https://dx.doi.org/10.1056/NEJMra1110265]
29. Kao, C.L.; King, C.C.; Chao, D.Y.; Wu, H.L.; Chang, G.J. Laboratory diagnosis of dengue virus infection: Current and future perspectives in clinical diagnosis and public health. J. Microbiol. Immunol. Infect.; 2005; 38, pp. 5-16.
30. Schwartz, E.; Mileguir, F.; Grossman, Z.; Mendelson, E. Evaluation of ELISA-based sero-diagnosis of dengue fever in travelers. J. Clin. Virol.; 2000; 19, pp. 169-173. [DOI: https://dx.doi.org/10.1016/S1386-6532(00)00114-1]
31. Guzman, M.G.; Halstead, S.B.; Artsob, H.; Buchy, P.; Farrar, J.; Gubler, D.J.; Hunsperger, E.; Kroeger, A.; Margolis, H.S.; Martinez, E. et al. Dengue: A continuing global threat. Nat. Rev. Microbiol.; 2010; 8, pp. S7-S16. [DOI: https://dx.doi.org/10.1038/nrmicro2460]
32. Kuno, G. Serodiagnosis of flaviviral infections and vaccinations in humans. Adv. Virus. Res.; 2003; 61, pp. 3-65.
33. Cardosa, M.J.; Wang, S.M.; Sum, M.S.; Tio, P.H. Antibodies against prM protein distinguish between previous infection with dengue and Japanese encephalitis viruses. BMC Microbiol.; 2002; 2, 9. [DOI: https://dx.doi.org/10.1186/1471-2180-2-9]
34. Oceguera, L.F., 3rd; Patiris, P.J.; Chiles, R.E.; Busch, M.P.; Tobler, L.H.; Hanson, C.V. Flavivirus serology by Western blot analysis. Am. J. Trop. Med. Hyg.; 2007; 77, pp. 159-163. [DOI: https://dx.doi.org/10.4269/ajtmh.2007.77.159]
35. Tezcan, S.; Kizildamar, S.; Ulger, M.; Aslan, G.; Tiftik, N.; Ozkul, A.; Emekdas, G.; Niedrig, M.; Ergunay, K. Flavivirus seroepidemiology in blood donors in Mersin province, Turkey. Mikrobiyoloji Bul.; 2014; 48, pp. 606-617. [DOI: https://dx.doi.org/10.5578/mb.8301]
36. Kim, J.H.; Chong, C.K.; Sinniah, M.; Sinnadurai, J.; Song, H.O.; Park, H. Clinical diagnosis of early dengue infection by novel one-step multiplex real-time RT-PCR targeting NS1 gene. J. Clin. Virol.; 2015; 65, pp. 11-19. [DOI: https://dx.doi.org/10.1016/j.jcv.2015.01.018]
37. Rathore, A.P.S.; John, A.L.S. Cross-Reactive Immunity Among Flaviviruses. Front. Immunol.; 2020; 11, pp. 1-9. [DOI: https://dx.doi.org/10.3389/fimmu.2020.00334]
38. Fuchs, I.; Bin, H.; Schlezinger, S.; Schwartz, E. NS1 antigen testing for the diagnosis of dengue in returned Israeli travelers. J. Med. Virol.; 2014; 86, pp. 2005-2010. [DOI: https://dx.doi.org/10.1002/jmv.23879]
39. Tesh, R.B.; Travassos da Rosa, A.P.; Guzman, H.; Araujo, T.P.; Xiao, S.Y. Immunization with heterologous flaviviruses protective against fatal West Nile encephalitis. Emerg. Infect. Dis.; 2002; 8, pp. 245-251. [DOI: https://dx.doi.org/10.3201/eid0803.010238]
40. Lemmer, K.; Donoso, O.; Bae, H.; Groen, J.; Drosten, C.; Niedrig, M. External quality control assessment in PCR diagnostics of dengue virus infections. J. Clin. Virol.; 2004; 30, pp. 291-296. [DOI: https://dx.doi.org/10.1016/j.jcv.2003.11.002]
41. Huhtamo, E.; Hasu, E.; Uzcategui, N.Y.; Erra, E.; Nikkari, S.; Kantele, A.; Vapalahti, O.; Piiparinen, H. Early diagnosis of dengue in travelers: Comparison of a novel real-time RT-PCR, NS1 antigen detection and serology. J. Clin. Virol.; 2010; 47, pp. 49-53. [DOI: https://dx.doi.org/10.1016/j.jcv.2009.11.001]
42. Ahamed, S.F.; Vivek, R.; Kotabagi, S.; Nayak, K.; Chandele, A.; Kaja, M.K.; Shet, A. Enhancing the sensitivity of Dengue virus serotype detection by RT-PCR among infected children in India. J. Virol. Methods; 2017; 244, pp. 46-54. [DOI: https://dx.doi.org/10.1016/j.jviromet.2017.02.014] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/28254680]
43. Libraty, D.H.; Young, P.R.; Pickering, D.; Endy, T.P.; Kalayanarooj, S.; Green, S.; Vaughn, D.W.; Nisalak, A.; Ennis, F.A.; Rothman, A.L. 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.; 2002; 186, pp. 1165-1168. [DOI: https://dx.doi.org/10.1086/343813] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/12355369]
44. Allonso, D.; Meneses, M.D.; Fernandes, C.A.; Ferreira, D.F.; Mohana-Borges, R. Assessing positivity and circulating levels of NS1 in samples from a 2012 dengue outbreak in Rio de Janeiro, Brazil. PLoS ONE; 2014; 9, e113634. [DOI: https://dx.doi.org/10.1371/journal.pone.0113634] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/25412084]
45. McBride, W.J.H. Evaluation of dengue NS1 test kits for the diagnosis of dengue fever. Diagn. Microbiol. Infect. Dis.; 2009; 64, pp. 31-36. [DOI: https://dx.doi.org/10.1016/j.diagmicrobio.2009.01.002]
46. Liu, L.T.; Chen, C.H.; Tsai, C.Y.; Lin, P.C.; Hsu, M.C.; Huang, B.Y.; Wang, Y.H.; Tsai, J.J. Evaluation of rapid diagnostic tests to detect dengue virus infections in Taiwan. PLoS ONE; 2020; 15, e0239710. [DOI: https://dx.doi.org/10.1371/journal.pone.0239710]
47. Duong, V.; Ly, S.; Lorn Try, P.; Tuiskunen, A.; Ong, S.; Chroeung, N.; Lundkvist, A.; Leparc-Goffart, I.; Deubel, V.; Vong, S. et al. Clinical and virological factors influencing the performance of a NS1 antigen-capture assay and potential use as a marker of dengue disease severity. PLoS Negl. Trop. Dis.; 2011; 5, e1244. [DOI: https://dx.doi.org/10.1371/journal.pntd.0001244]
48. Blessmann, J.; Winkelmann, Y.; Keoviengkhone, L.; Sopraseuth, V.; Kann, S.; Hansen, J.; Halas, H.E.; Emmerich, P.; Schmidt-Chanasit, J.; Schmitz, H. et al. Assessment of diagnostic and analytic performance of the SD Bioline Dengue Duo test for dengue virus (DENV) infections in an endemic area (Savannakhet province, Lao People’s Democratic Republic). PLoS ONE; 2020; 15, e0230337. [DOI: https://dx.doi.org/10.1371/journal.pone.0230337]
49. Hunsperger, E.A.; Muñoz-Jordán, J.; Beltran, M.; Colón, C.; Carrión, J.; Vazquez, J.; Acosta, L.N.; Medina-Izquierdo, J.F.; Horiuchi, K.; Biggerstaff, B.J. et al. Performance of Dengue Diagnostic Tests in a Single-Specimen Diagnostic Algorithm. J. Infect. Dis.; 2016; 214, pp. 836-844. [DOI: https://dx.doi.org/10.1093/infdis/jiw103]
50. Andries, A.C.; Duong, V.; Ong, S.; Ros, S.; Sakuntabhai, A.; Horwood, P.; Dussart, P.; Buchy, P. Evaluation of the performances of six commercial kits designed for dengue NS1 and anti-dengue IgM, IgG and IgA detection in urine and saliva clinical specimens. BMC Infect. Dis.; 2016; 16, 201. [DOI: https://dx.doi.org/10.1186/s12879-016-1551-x]
51. Andries, A.C.; Duong, V.; Ly, S.; Cappelle, J.; Kim, K.S.; Lorn Try, P.; Ros, S.; Ong, S.; Huy, R.; Horwood, P. et al. Value of Routine Dengue Diagnostic Tests in Urine and Saliva Specimens. PLoS Negl. Trop. Dis.; 2015; 9, e0004100. [DOI: https://dx.doi.org/10.1371/journal.pntd.0004100]
52. Saito, Y.; Moi, M.L.; Kotaki, A.; Ikeda, M.; Tajima, S.; Shiba, H.; Hosono, K.; Saijo, M.; Kurane, I.; Takasaki, T. Detection of Dengue Virus Nonstructural Protein 1 (NS1) in Urine Samples using ELISA as a Laboratory Diagnostic Method for Dengue Virus Infection. Jpn. J. Infect. Dis.; 2015; 68, pp. 455-460. [DOI: https://dx.doi.org/10.7883/yoken.JJID.2014.441]
53. Ramirez, A.H.; Moros, Z.; Comach, G.; Zambrano, J.; Bravo, L.; Pinto, B.; Vielma, S.; Cardier, J.; Liprandi, F. Evaluation of dengue NS1 antigen detection tests with acute sera from patients infected with dengue virus in Venezuela. Diagn. Microbiol. Infect. Dis.; 2009; 65, pp. 247-253. [DOI: https://dx.doi.org/10.1016/j.diagmicrobio.2009.07.022]
54. Blacksell, S.D.; Jarman, R.G.; Bailey, M.S.; Tanganuchitcharnchai, A.; Jenjaroen, K.; Gibbons, R.V.; Paris, D.H.; Premaratna, R.; De Silva, H.J.; Lalloo, D.G. et al. Evaluation of six commercial point-of-care tests for diagnosis of acute dengue infections: The need for combining NS1 antigen and IgM/IgG antibody detection to achieve acceptable levels of accuracy. Clin. Vaccine Immunol.; 2011; 18, pp. 2095-2101. [DOI: https://dx.doi.org/10.1128/CVI.05285-11]
55. Guzman, M.G.; Jaenisch, T.; Gaczkowski, R.; Ty Hang, V.T.; Sekaran, S.D.; Kroeger, A.; Vazquez, S.; Ruiz, D.; Martinez, E.; Mercado, J.C. et al. Multi-country evaluation of the sensitivity and specificity of two commercially-available NS1 ELISA assays for dengue diagnosis. PLoS Negl. Trop. Dis.; 2010; 4, e811. [DOI: https://dx.doi.org/10.1371/journal.pntd.0000811]
56. Alcon, S.; Talarmin, A.; Debruyne, M.; Falconar, A.; Deubel, V.; Flamand, M. 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.; 2002; 40, pp. 376-381. [DOI: https://dx.doi.org/10.1128/JCM.40.02.376-381.2002]
57. Moi, M.L.; Omatsu, T.; Tajima, S.; Lim, C.K.; Kotaki, A.; Ikeda, M.; Harada, F.; Ito, M.; Saijo, M.; Kurane, I. et al. Detection of dengue virus nonstructural protein 1 (NS1) by using ELISA as a useful laboratory diagnostic method for dengue virus infection of international travelers. J. Travel Med.; 2013; 20, pp. 185-193. [DOI: https://dx.doi.org/10.1111/jtm.12018]
58. Sekaran, S.D.; Lan, E.C.; Mahesawarappa, K.B.; Appanna, R.; Subramaniam, G. Evaluation of a Dengue NS1 capture ELISA assay for the rapid detection of Dengue. J. Infect. Dev. Ctries.; 2007; 1, pp. 182-188.
59. Matheus, S.; Meynard, J.B.; Lavergne, A.; Girod, R.; Moua, D.; Labeau, B.; Dussart, P.; Lacoste, V.; Deparis, X. Dengue-3 outbreak in Paraguay: Investigations using capillary blood samples on filter paper. Am. J. Trop. Med. Hyg.; 2008; 79, pp. 685-687. [DOI: https://dx.doi.org/10.4269/ajtmh.2008.79.685]
60. Aubry, M.; Roche, C.; Dupont-Rouzeyrol, M.; Aaskov, J.; Viallon, J.; Marfel, M.; Lalita, P.; Elbourne-Duituturaga, S.; Chanteau, S.; Musso, D. et al. Use of serum and blood samples on filter paper to improve the surveillance of Dengue in Pacific Island Countries. J. Clin. Virol.; 2012; 55, pp. 23-29. [DOI: https://dx.doi.org/10.1016/j.jcv.2012.05.010]
61. Chakravarti, A.; Siddiqui, O.; Malik, S.; Uppal, B. Use of dried blood blotted on filter paper to detect dengue IgM antibody and dengue NS1 antigen. Southeast Asian J. Trop. Med. Public Health; 2013; 44, pp. 226-231.
62. Matheus, S.; Pham, T.B.; Labeau, B.; Huong, V.T.; Lacoste, V.; Deparis, X.; Marechal, V. Kinetics of dengue non-structural protein 1 antigen and IgM and IgA antibodies in capillary blood samples from confirmed dengue patients. Am. J. Trop. Med. Hyg.; 2014; 90, pp. 438-443. [DOI: https://dx.doi.org/10.4269/ajtmh.13-0458] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/24470561]
63. Chau, T.N.; Anders, K.L.; Lien, L.B.; Hung, N.T.; Hieu, L.T.; Tuan, N.M.; Thuy, T.T.; Phuong, L.T.; Tham, N.T.; Lanh, M.N. et al. Clinical and virological features of Dengue in Vietnamese infants. PLoS Negl. Trop. Dis.; 2010; 4, e657. [DOI: https://dx.doi.org/10.1371/journal.pntd.0000657]
64. Ghetia, C.; Bhatt, P.; Mukhopadhyay, C. Association of dengue virus non-structural-1 protein with disease severity: A brief review. Trans. R. Soc. Trop. Med. Hyg.; 2022; 116, pp. 986-995. [DOI: https://dx.doi.org/10.1093/trstmh/trac087] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/36125197]
65. Humaidi, M.; Tien, W.P.; Yap, G.; Chua, C.R.; Ng, L.C. Non-invasive dengue diagnostics—The use of saliva and urine for different stages of the illness. Diagnostics; 2021; 11, 1345. [DOI: https://dx.doi.org/10.3390/diagnostics11081345]
66. Mendonça, P.D.; Santos, L.K.B.; Foguel, M.V.; Rodrigues, M.A.B.; Cordeiro, M.T.; Gonçalves, L.M.; Marques, E.T.A.; Dutra, R.F. NS1 glycoprotein detection in serum and urine as an electrochemical screening immunosensor for dengue and Zika virus. Anal. Bioanal. Chem.; 2021; 413, pp. 4873-4885. [DOI: https://dx.doi.org/10.1007/s00216-021-03449-7] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/34152457]
67. Munasinghe, E.; Athapaththu, M.; Abeyewickreme, W. Immuno-dominant dengue NS1 peptides as antigens for production of monoclonal antibodies. Front. Mol. Biosci.; 2022; 9, pp. 1-11. [DOI: https://dx.doi.org/10.3389/fmolb.2022.935456]
68. Khanna, A.; Atam, V.; Gupta, A. A case of dengue encephalitis with intracerebral hemorrhage. J. Glob. Infect. Dis.; 2011; 3, pp. 206-207. [DOI: https://dx.doi.org/10.4103/0974-777X.81707]
69. Domingues, R.B.; Kuster, G.W.; Onuki-Castro, F.L.; Souza, V.A.; Levi, J.E.; Pannuti, C.S. Involvement of the central nervous system in patients with dengue virus infection. J. Neurol. Sci.; 2008; 267, pp. 36-40. [DOI: https://dx.doi.org/10.1016/j.jns.2007.09.040]
70. Dussart, P.; Petit, L.; Labeau, B.; Bremand, L.; Leduc, A.; Moua, D.; Matheus, S.; Baril, L. 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.; 2008; 2, e280. [DOI: https://dx.doi.org/10.1371/journal.pntd.0000280]
71. Jackson, S.T.; Mullings, A.; Bennett, F.; Khan, C.; Gordon-Strachan, G.; Rhoden, T. Dengue infection in patients presenting with neurological manifestations in a dengue endemic population. West Indian Med. J.; 2008; 57, pp. 373-376.
72. Solomon, T.; Dung, N.M.; Vaughn, D.W.; Kneen, R.; Thao, L.T.; Raengsakulrach, B.; Loan, H.T.; Day, N.P.; Farrar, J.; Myint, K.S. et al. Neurological manifestations of dengue infection. Lancet; 2000; 355, pp. 1053-1059. [DOI: https://dx.doi.org/10.1016/S0140-6736(00)02036-5]
73. Araujo, F.; Nogueira, R.; Araujo Mde, S.; Perdigao, A.; Cavalcanti, L.; Brilhante, R.; Rocha, M.; Vilar, D.F.; Holanda, S.S.; Braga Dde, M. et al. Dengue in patients with central nervous system manifestations, Brazil. Emerg. Infect. Dis.; 2012; 18, pp. 677-679. [DOI: https://dx.doi.org/10.3201/eid1804.111522]
74. Lima Mda, R.; Nogueira, R.M.; Schatzmayr, H.G.; de Filippis, A.M.; Limonta, D.; dos Santos, F.B. A new approach to dengue fatal cases diagnosis: NS1 antigen capture in tissues. PLoS Negl. Trop. Dis.; 2011; 5, e1147. [DOI: https://dx.doi.org/10.1371/journal.pntd.0001147]
75. Takami, C.; Roxane, K.; Fontes, M.; Silvia, P.; Iglézias, D.A.; Cirqueira, C.; Sansone, M.; Moutinho, J.; Dayane, P.; Teixeira, L. et al. Anti-DENV-NS1 monoclonal antibody for the differential histopathological diagnosis of hemorrhagic fever caused by dengue. Braz. J. Microbiol.; 2022; 53, pp. 777-783. [DOI: https://dx.doi.org/10.1007/s42770-022-00697-2]
76. Póvoa, T.F.; Alves, A.M.B.; Oliveira, C.A.B.; Nuovo, G.J.; Chagas, V.L.A.; Paes, M.V. The Pathology of Severe Dengue in Multiple Organs of Human Fatal Cases: Histopathology, Ultrastructure and Virus Replication. PLoS ONE; 2014; 9, e83386. [DOI: https://dx.doi.org/10.1371/journal.pone.0083386]
77. Jessie, K.; Fong, M.Y.; Devi, S.; Lam, S.K.; Wong, K.T. Localization of dengue virus in naturally infected human tissues, by immunohistochemistry and in situ hybridization. J. Infect. Dis.; 2004; 189, pp. 1411-1418. [DOI: https://dx.doi.org/10.1086/383043]
78. Miagostovich, M.P.; Ramos, R.G.; Nicol, A.F.; Nogueira, R.M.; Cuzzi-Maya, T.; Oliveira, A.V.; Marchevsky, R.S.; Mesquita, R.P.; Schatzmayr, H.G. Retrospective study on dengue fatal cases. Clin. Neuropathol.; 1997; 16, pp. 204-208.
79. Couvelard, A.; Marianneau, P.; Bedel, C.; Drouet, M.T.; Vachon, F.; Henin, D.; Deubel, V. Report of a fatal case of dengue infection with hepatitis: Demonstration of dengue antigens in hepatocytes and liver apoptosis. Hum. Pathol.; 1999; 30, pp. 1106-1110. [DOI: https://dx.doi.org/10.1016/S0046-8177(99)90230-7]
80. Huerre, M.R.; Lan, N.T.; Marianneau, P.; Hue, N.B.; Khun, H.; Hung, N.T.; Khen, N.T.; Drouet, M.T.; Huong, V.T.; Ha, D.Q. et al. Liver histopathology and biological correlates in five cases of fatal dengue fever in Vietnamese children. Virchows Arch.; 2001; 438, pp. 107-115. [DOI: https://dx.doi.org/10.1007/s004280000329]
81. Limonta, D.; Capo, V.; Torres, G.; Perez, A.B.; Guzman, M.G. Apoptosis in tissues from fatal dengue shock syndrome. J. Clin. Virol.; 2007; 40, pp. 50-54. [DOI: https://dx.doi.org/10.1016/j.jcv.2007.04.024]
82. Aye, K.S.; Charngkaew, K.; Win, N.; Wai, K.Z.; Moe, K.; Punyadee, N.; Thiemmeca, S.; Suttitheptumrong, A.; Sukpanichnant, S.; Prida, M. et al. Pathologic highlights of dengue hemorrhagic fever in 13 autopsy cases from Myanmar. Hum. Pathol.; 2014; 45, pp. 1221-1233. [DOI: https://dx.doi.org/10.1016/j.humpath.2014.01.022] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/24767772]
83. World Health Organization (WHO). Zika Epidemiology Update-February 2022. Available online: https://www.who.int/publications/m/item/zika-epidemiology-update---february-2022 (accessed on 8 February 2022).
84. World Health Organization (WHO). Countries and Territories with Current or Previous Zika Virus Transmission. Updated February 2023. Available online: https://www.who.int/publications/m/item/countries-and-territories-with-current-or-previous-zika-virus-transmission (accessed on 10 January 2023).
85. Wilson, H.L.; Tran, T.; Druce, J.; Dupont-Rouzeyrol, M.; Catton, M. Neutralization Assay for Zika and Dengue Viruses by Use of Real-Time-PCR-Based Endpoint Assessment. J. Clin. Microbiol.; 2017; 55, 3104. [DOI: https://dx.doi.org/10.1128/JCM.00673-17] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/28794181]
86. Lanciotti, R.S.; Kosoy, O.L.; Laven, J.J.; Velez, J.O.; Lambert, A.J.; Johnson, A.J.; Stanfield, S.M.; Duffy, M.R. Genetic and serologic properties of Zika virus associated with an epidemic, Yap State, Micronesia, 2007. Emerg. Infect. Dis.; 2008; 14, pp. 1232-1239. [DOI: https://dx.doi.org/10.3201/eid1408.080287] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/18680646]
87. Kadkhoda, K.; Gretchen, A.; Racano, A. Evaluation of a commercially available Zika virus IgM ELISA: Specificity in focus. Diagn. Microbiol. Infect. Dis.; 2017; 88, pp. 233-235. [DOI: https://dx.doi.org/10.1016/j.diagmicrobio.2017.04.002] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/28478111]
88. Lustig, Y.; Zelena, H.; Venturi, G.; Van Esbroeck, M.; Rothe, C.; Perret, C.; Koren, R.; Katz-Likvornik, S.; Mendelson, E.; Schwartz, E. Sensitivity and kinetics of an NS1-based Zika virus enzyme-linked immunosorbent assay in Zika virus-infected travelers from Israel, the Czech Republic, Italy, Belgium, Germany, and Chile. J. Clin. Microbiol.; 2017; 55, pp. 1894-1901. [DOI: https://dx.doi.org/10.1128/JCM.00346-17]
89. Steinhagen, K.; Probst, C.; Radzimski, C.; Schmidt-Chanasit, J.; Emmerich, P.; Van Esbroeck, M.; Schinkel, J.; Grobusch, M.P.; Goorhuis, A.; Warnecke, J.M. et al. Serodiagnosis of Zika virus (ZIKV) infections by a novel NS1-based ELISA devoid of cross-reactivity with dengue virus antibodies: A multicohort study of assay performance, 2015 to 2016. Eurosurveillance; 2016; 21, 30426. [DOI: https://dx.doi.org/10.2807/1560-7917.ES.2016.21.50.30426]
90. Pasquier, C.; Joguet, G.; Mengelle, C.; Chapuy-Regaud, S.; Pavili, L.; Prisant, N.; Izopet, J.; Bujan, L.; Mansuy, J.M. Kinetics of anti-ZIKV antibodies after Zika infection using two commercial enzyme-linked immunoassays. Diagn. Microbiol. Infect. Dis.; 2018; 90, pp. 26-30. [DOI: https://dx.doi.org/10.1016/j.diagmicrobio.2017.09.001]
91. Griffin, I.; Martin, S.W.; Fischer, M.; Chambers, T.V.; Kosoy, O.L.; Goldberg, C.; Falise, A.; Villamil, V.; Ponomareva, O.; Gillis, L.D. et al. Zika Virus IgM 25 Months after Symptom Onset. Emerg. Infect. Dis.; 2019; 25, pp. 2264-2265. [DOI: https://dx.doi.org/10.3201/eid2512.191022]
92. Lustig, Y.; Zuckerman, N.; Koren, R.; Katz-Likvornik, S.; Yizchaki, M.; Mendelson, E.; Freedman, L.; Schwartz, E. Rapid Decline of Zika Virus IgM Antibodies against the NS1 Protein in Imported Israeli Cases. Am. J. Trop. Med. Hyg.; 2022; 106, pp. 1121-1125. [DOI: https://dx.doi.org/10.4269/ajtmh.21-0099]
93. Lustig, Y.; Koren, R.; Biber, A.; Zuckerman, N.; Mendelson, E.; Schwartz, E. Screening and exclusion of Zika virus infection in travellers by an NS1-based ELISA and qRT-PCR. Clin. Microbiol. Infect.; 2020; 26, 1687.e7–1687.e11. [DOI: https://dx.doi.org/10.1016/j.cmi.2020.02.037]
94. Centers for Disease Control and Prevention (CDC); National Center for Emerging and Zoonotic Infectious Diseases (NCEZID). Division of Vector-Borne Diseases (DVBD) Testing Guidance-Zika and Dengue Testing Guidance (Updated November 2019). Available online: https://www.cdc.gov/zika/hc-providers/testing-guidance.html (accessed on 29 September 2022).
95. Macdonald, J.; Tonry, J.; Hall, R.A.; Williams, B.; Palacios, G.; Ashok, M.S.; Jabado, O.; Clark, D.; Tesh, R.B.; Briese, T. et al. NS1 Protein Secretion during the Acute Phase of West Nile Virus Infection. J. Virol.; 2005; 79, pp. 13924-13933. [DOI: https://dx.doi.org/10.1128/JVI.79.22.13924-13933.2005]
96. Kyung, M.C.; Diamond, M.S. Defining the levels of secreted non-structural protein NS1 after West Nile virus infection in cell culture and mice. J. Med. Virol.; 2008; 80, pp. 547-556. [DOI: https://dx.doi.org/10.1002/jmv.21091]
97. Patil, S.V.; Bhadake, M.; Acharya, A. ‘Dengue-COVID-19 overlap’: Is it an ‘antigenic mimicry’ or coexistent two different viral genotypic diseases? Prospective, observational study in tertiary care setting in India. Electron. J. Gen. Med.; 2022; 19, em400. [DOI: https://dx.doi.org/10.29333/ejgm/12279]
98. Lustig, Y.; Keler, S.; Kolodny, R.; Ben-Tal, N.; Atias-Varon, D.; Shlush, E.; Gerlic, M.; Munitz, A.; Doolman, R.; Asraf, K. et al. Potential Antigenic Cross-reactivity Between Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) and Dengue Viruses. Clin. Infect. Dis.; 2021; 73, pp. e2444-e2449. [DOI: https://dx.doi.org/10.1093/cid/ciaa1207]
99. Yan, G.; Lee, C.K.; Lam, L.T.M.; Yan, B.; Chua, Y.X.; Lim, A.Y.N.; Phang, K.F.; Kew, G.S.; Teng, H.; Ngai, C.H. et al. Covert COVID-19 and false-positive dengue serology in Singapore. Lancet Infect. Dis.; 2020; 20, 536. [DOI: https://dx.doi.org/10.1016/S1473-3099(20)30158-4]
100. Luvira, V.; Leaungwutiwong, P.; Thippornchai, N.; Thawornkuno, C.; Chatchen, S.; Chancharoenthana, W.; Tandhavanant, S.; Muangnoicharoen, S.; Piyaphanee, W.; Chantratita, N. False Positivity of Anti-SARS-CoV-2 Antibodies in Patients with Acute Tropical Diseases in Thailand. Trop. Med. Infect. Dis.; 2022; 7, 132. [DOI: https://dx.doi.org/10.3390/tropicalmed7070132]
101. Santoso, M.S.; Masyeni, S.; Haryanto, S.; Yohan, B.; Hibberd, M.L.; Sasmono, R.T. Assessment of dengue and COVID-19 antibody rapid diagnostic tests cross-reactivity in Indonesia. Virol. J.; 2021; 18, pp. 1-5. [DOI: https://dx.doi.org/10.1186/s12985-021-01522-2]
102. Spinicci, M.; Bartoloni, A.; Mantella, A.; Zammarchi, L.; Rossolini, G.M.; Antonelli, A. Low risk of serological cross-reactivity between dengue and COVID-19. Mem. Inst. Oswaldo Cruz; 2020; 115, e200225. [DOI: https://dx.doi.org/10.1590/0074-02760200225]
© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Details
; Lustig, Yaniv 2 ; Sklan, Ella H 3
; Schwartz, Eli 4 1 Department of Otolaryngology/Head & Neck Surgery, Hadassah Hebrew; University Medical Center, Jerusalem 91120, Israel
2 Central Virology Laboratory, Ministry of Health, Sheba Medical Center, Ramat-Gan 52621, Israel; Sackler Faculty of Medicine, Tel-Aviv University, Tel Aviv 69978, Israel
3 Sackler Faculty of Medicine, Tel-Aviv University, Tel Aviv 69978, Israel
4 Sackler Faculty of Medicine, Tel-Aviv University, Tel Aviv 69978, Israel; The Center of Geographic Medicine and Tropical Diseases, Sheba Medical Center, Ramat-Gan 52621, Israel