Flaviviruses are vector-borne RNA viruses that can emerge unexpectedly in human populations and cause a spectrum of potentially severe diseases including hepatitis, vascular shock syndrome, encephalitis, acute flaccid paralysis, congenital abnormalities and fetal death. This epidemiological pattern has occurred numerous times during the last 70 years, including epidemics of dengue virus and West Nile virus, and the most recent explosive epidemic of Zika virus in the Americas. Flaviviruses are now globally distributed and infect up to 400 million people annually. Of significant concern, outbreaks of other less well-characterized flaviviruses have been reported in humans and animals in different regions of the world. The potential for these viruses to sustain epidemic transmission among humans is poorly understood. In this Review, we discuss the basic biology of flaviviruses, their infectious cycles, the diseases they cause and underlying host immune responses to infection. We describe flaviviruses that represent an established ongoing threat to global health and those that have recently emerged in new populations to cause significant disease. We also provide examples of lesser-known flaviviruses that circulate in restricted areas of the world but have the potential to emerge more broadly in human populations. Finally, we discuss how an understanding of the epidemiology, biology, structure and immunity of flaviviruses can inform the rapid development of countermeasures to treat or prevent human infections as they emerge.
Flaviviruses are single-stranded RNA viruses vectored principally by arthropods that cause severe illnesses in humans. The extensive global spread and epidemic transmission of flaviviruses during the last seven decades has been remarkable. The mosquito-borne dengue viruses (DENV) infect an estimated 400 million humans each year; more than a quarter of the world’s population lives in areas where DENV is now endemic1. By comparison, only sporadic DENV epidemics were documented before the Second World War2. The introductions of West Nile (WNV) and Zika (ZIKV) viruses into the Western Hemisphere was followed by rapid geographical spread, large numbers of human infections and considerable morbidity3,4. Ongoing yellow fever virus (YFV) transmission and its encroachment on urban environments, despite the existence of an effective vaccine, poses a serious public health challenge5,6,7. Other flaviviruses present ongoing health risks or are beginning to emerge in different parts of the world, including Japanese encephalitis virus (JEV), tick-borne encephalitis virus (TBEV) and Usutu virus (USUV).
The epidemic potential of flaviviruses reflects many factors related to the unique characteristics of their insect vectors, the consequences of poorly planned urbanization that creates ideal arthropod breeding habitats, the geographical expansion of vectors, changing environmental conditions and extensive global travel8,9. Beyond arthropods and humans, flaviviruses are also known to infect a wide array of animal species and can be important veterinary pathogens that threaten economically important domesticated animals10,11,12,13,14. These vertebrate animal hosts may constitute important stable reservoirs and contribute to defining conditions that support the introduction of new viral species and transmission among humans15. The continued threat of flavivirus emergence and re-emergence highlights a need for a detailed fundamental understanding of the biology of these viruses, the immune responses that can contain them and the possible countermeasures that can blunt their impact on public health should new outbreaks occur.
Flavivirus structure and replication
Flaviviruses are small (~50 nm) spherical virus particles that incorporate a single genomic RNA of positive-sense polarity encoding three structural and seven non-structural proteins (Fig. 1a). Our knowledge of the biology of flaviviruses has advanced considerably with the availability of high-resolution structures of viral structural proteins and of virions at different stages of the replication cycle or in complex with antibodies or host factors16. Crystal structures of the enzymatic non-structural proteins also have been solved, accelerating advances in an understanding of virus replication and pathogenesis17,18,19 and enabling structure-guided drug discovery, as reviewed elsewhere20.
Virion structure and morphogenesis
Flaviviruses are assembled using three viral structural proteins (C, prM and E), a host lipid envelope and the viral genomic RNA. The structure of the envelope (E) protein, which mediates virus entry steps of the replication cycle, was solved first for TBEV21 and thereafter for multiple flaviviruses including DENV, WNV and ZIKV (reviewed in ref. 22). The E protein is a three-domain structure (referred to as domains E-DI, E-DII and E-DIII) tethered to the viral membrane by a helical stem and two antiparallel transmembrane domains (Fig. 1b). Most flavivirus E proteins are modified post-translationally by the addition of one or two asparagine-linked carbohydrates. The folding of the E protein in the endoplasmic reticulum (ER) is facilitated by interactions with the structural premembrane (prM) protein shortly after synthesis23. prM is incorporated into the viral envelope during virion morphogenesis as heterotrimeric prM–E spikes with icosahedral symmetry24 (Fig. 1c) and prevents conformational changes in the E protein that would allow adventitious fusion of virions with host membranes during egress. Cleavage of prM to M during transit of immature virions through the trans-Golgi network by a host furin-like serine protease is required for the formation of infectious mature forms of the virion25. On mature virions, E proteins are arranged as antiparallel dimers via extensive contacts between adjacent E-DIIs26,27,28,29. Ninety E dimers are incorporated into each mature virion and arranged in a herringbone pattern with icosahedral-like symmetry (Fig. 1c). The viral capsid (C) protein is a small helical protein with surfaces that bind either viral nucleic acids or host lipids and directs the incorporation of the viral genome into the virion30. Establishing the physical connection between membrane-anchored structural proteins and the C protein or RNA has been elusive. The application of asymmetric reconstruction techniques to the cryo-electron microscopy (cryo-EM) analysis of ZIKV provides evidence that the capsid interacts transiently with the other structural proteins during particle biogenesis31. C-protein incorporation into the virion is regulated further by the coordinated cleavage of the polyprotein by the viral non-structural protein 2B (NS2B)–NS3 serine protease32.
Flaviviruses bind to an array of mammalian cell types through interactions of asparagine-linked sugars on structural proteins with multiple C-type lectins including dendritic-cell-specific intercellular adhesion molecule-3-grabbing non-integrin (DC-SIGN)33,34, the binding of charged surfaces of the E protein to glycosaminoglycans on cell surfaces35 and interactions between the viral lipid envelope and proteins of the T-cell immunoglobulin domain and mucin domain (TIM) and Tyro3, Axl and Mertk (TAM) family of phosphatidylserine receptors36 (Fig. 2). The role of specific host proteins in the attachment and entry of viruses into cells varies. Host proteins classically defined as receptors are essential for the entry of viruses because they catalyse critical conformational events. For example, the CD4 molecule on T lymphocytes enables conformational transitions in the human immunodeficiency virus type 1 GP120 protein required for viral membrane fusion14. While host factors that increase the efficiency of flavivirus binding and infection of cells have been identified, they are not required to trigger the structural transitions that propel viral membrane fusion; instead, these are defined as attachment factors. Flaviviruses bound to synthetic lipid membranes devoid of host proteins are capable of stimulating E protein-mediated fusion once exposed to an acidic environment37,38. Identifying virus–host receptor interactions important for pathogenesis in humans and other vertebrate animals has been challenging, and even less is known about entry pathways in invertebrate host cells. Relationships between host attachment factor expression and viral tropism in vivo have not been established. Some flavivirus attachment factors (for example, TAM and integrin receptors) capable of binding virions also transduce signals into target cells, which has the potential to augment infection and further complicates the role and definition of host attachment molecules39,40,41,42.
Once attached to cells, flaviviruses are taken up by clathrin-dependent endocytic vesicles. While this same host machinery is involved in the internalization of multiple types of cellular cargo, recent studies identified host molecules required by flaviviruses to exploit the endocytic pathway for infectious entry including RNASEK, lymphocyte antigen locus 6 (LY6E) and microtubules43,44,45. Flavivirus membrane fusion occurs in the low pH compartments of the endosome and is catalysed by conformational changes in the E protein that involve the formation of E protein trimers, penetration of the highly conserved E-DII fusion loop into the adjacent host membranes and the folding of the E protein helical stem against the exterior surface of the newly formed E protein trimer46. A structural and kinetic understanding of flavivirus membrane fusion has informed the design of antiviral molecules that disrupt the entry process47 (Fig. 2).
The flavivirus genomic RNA encodes a single open reading frame flanked by highly structured untranslated regions (UTR) that coordinate viral translation, replication and regulation of the innate immune response48. The penetration of the viral genome into the cytoplasm allows for the cap-dependent translation of the viral polyprotein in association with membranes of the ER49. Viral translation products are believed to stimulate a shift in the use of the incoming viral genome from a substrate for translation to a template for genomic RNA replication. Flavivirus replication occurs on complex virus-induced membrane structures incorporating host and viral factors50. The ultrastructure of these flavivirus replication complexes (RCs) was solved using cryo-EM tomography, revealing invaginations of the ER that form spherical compartments in which viral components required for RNA replication can be located, including NS1, NS2A, NS3, NS4A and NS5 (refs. 50,51) (Fig. 2). Although the contents of these vesicle packets are protected from surveillance by cytoplasmic innate immune sensors, narrow connections exist to allow movement of viral RNA replication products to sites of translation and virion morphogenesis. Changes in host cell metabolism are important for the generation of RCs, including an increase in cholesterol, fatty acid and sphingomyelin synthesis; regulation of autophagy also has been suggested to contribute to virus-induced changes in lipid metabolism52,53. Host factors such as the reticulon protein 3.1A and DNAJC14 also are critical for RC formation54,55. As many of the enzymes involved in these metabolic changes are targets for therapeutics, a more detailed understanding of the host pathways and networks required to support flavivirus replication may identify new classes of antiviral agents56.
The clinical presentation of acute flavivirus infection in humans ranges from mild illness (asymptomatic infection or self-limiting febrile episodes) to severe and life-threatening disease (haemorrhagic fever, shock syndrome, encephalitis, paralysis, congenital defects, hepatitis and hepatic failure). Individual flavivirus infections fall into two broad categories, visceral and neurotropic, although some have features of both (for example, ZIKV) (Fig. 3). Variability in disease presentation among individual flaviviruses likely reflects the unique cellular and tissue tropism of each virus, differences in their capacity to evade or antagonize host immunity, and the interplay between the direct pathogenic effects of virus infection and injury caused by the requisite host response. Approximately 50–80% of flavivirus infections are asymptomatic and cause little to no illness57,58,59. Most symptomatic flavivirus infections result in self-limiting flu-like febrile illnesses with a headache, myalgia, arthralgia and a rash without long-term consequences. The factors that determine the penetrance of more severe disease phenotypes for different flaviviruses are not fully characterized, but likely reflect polymorphisms in key host genes (for example, CCR5 for WNV60, DC-SIGN for DENV61), age62, immune status and co-morbidities, and prior flavivirus immunity (for example, DENV63), in addition to differential pathogenicity of particular virus strains and perhaps other acquired factors including the microbiome64.
DENV, YFV and ZIKV are the principal flaviviruses that cause visceral disease in humans. DENV infection of myeloid cells in blood and tissues is believed to induce an immunopathogenesis cascade resulting in vascular leakage, thrombocytopenia, abnormal bleeding, haemoconcentration and hypotension65,66. The flavivirus NS1 protein may contribute to hypotension by virtue of its ability to bind endothelial cells, disrupt the integrity of underlying glycocalyx and alter vascular permeability67,68. YFV replicates to high levels in liver cells, and this results in severe hepatitis, renal failure, haemorrhage, shock and death69,70. ZIKV infects progenitor cells, epithelium and myeloid cells, and in peripheral tissues causes injury to the male and female reproductive tracts and the eye71. ZIKV persists in human semen for months72 and may cause oligospermia, lower levels of sex hormones and, possibly, compromised fertility73. The high viral load in seminal fluid also can lead to sexual transmission of ZIKV74.
WNV, JEV, TBEV, Powassan virus (POWV) and ZIKV are neurotropic viruses that can cause encephalitis, cognitive impairment, seizure disorders and paralysis75. The neurological and functional disability associated with these neurotropic flavivirus infections can cause considerable morbidity in patients long after their recovery from acute illness. These viruses cause injury to neurons (or neuroprogenitor cells in the case of ZIKV) through direct (virus infection-induced) and indirect (immune-mediated) mechanisms75,76. Microscopic examination of the brain reveals neuronal cell death, activation of microglia and infiltrating macrophages, and accumulation of CD4+ and CD8+ T cells. Depending on the flavivirus, these lesions can occur in the brainstem, cerebral cortex, hippocampus, thalamus, cerebellum or spinal cord77.
As well as being neurotropic, ZIKV is also teratogenic, in part because it infects and causes injury to the developing placenta78. The tropism of ZIKV for the placenta71 may not be unique among flaviviruses, as inoculation of human placental explants or pregnant mice with WNV or POWV also resulted in infection and injury to the placenta79.
Immune response to flavivirus infection
In this section, we highlight recent advances relating to cell-intrinsic host defence activation, and innate and adaptive immune response-dependent restriction of flavivirus infections. We discuss how these findings affect the development of candidate therapeutics.
The mammalian host detects and responds to flavivirus infection by recognizing viral RNA through several pathogen recognition receptors (PRRs), including the cell surface and endosomal RNA sensors Toll-like receptors 3 and 7, the cytoplasmic RNA sensors retinoic acid-inducible gene I (RIG-I) and melanoma-differentiation-associated gene 5 (ref. 80,81). Binding of single- and/or double-stranded viral RNA results in the downstream activation of adaptor molecules, such as mitochondrial antiviral signalling protein, MyD88, TIR domain-containing adaptor inducing IFN-β (TRIF), nuclear translocation of interferon (IFN) regulatory transcription factors 3 and 7 (IRF3 and IRF7) and NF-κB, which induce expression of type I and III IFNs. The cytoplasmic adaptor molecule stimulator of IFN genes (STING) also participates in immune responses generated against flaviviruses in the context of RIG-I recognition, by acting as a scaffold for the recruitment of signalling components required for IRF3 activation and IFN induction82,83,84.
Type I interferons (IFN-α and β) promote an antiviral state by inducing IFN-stimulated genes (ISGs) with direct and indirect antiviral functions (reviewed in refs. 85,86). Pre-treatment of cells with type I IFNs inhibits flavivirus replication in vitro, but treatment after infection is less effective. Although flaviviruses can antagonize IFN-induced responses after infection by preventing induction of IFNs and disrupting their signalling pathways87, IFN still restricts replication and spread in vivo. Mice lacking the type I IFN receptor (Ifnar1–/–) show expanded tropism and greater morbidity and mortality than wild-type mice after infection with multiple different flaviviruses88,89. Type III IFN-λ is an antiviral cytokine that binds a unique receptor and primarily functions at barrier surfaces90. In cell culture, IFN-λ has direct antiviral effects against flaviviruses through induction of ISGs91,92. IFN-λ also has inhibitory activity against ZIKV in the context of infection of the maternal-derived decidua and fetal-derived placenta during pregnancy in mice and humans93,94,95.
Some of the recently identified ISGs that display antiviral activity against flaviviruses85 in vitro include: C6orf150, DDX24, HPSE, MAFK, NAMPT, PAK3, PHF15, SAMD9L, SC4MOL, C19orf66, CH25H, IFI44L, IFIT1, IFIT2, IFI6, IFITM2, IFITM3, ISG20 and RSAD2 (viperin). ISGs with demonstrated antiviral activity against flaviviruses in vivo include: PKR, RNASEL, RSAD2, IFIT1, IFIT2, IFITM3, Ifi27l2a and CH25H96,97,98,99. The inhibitory mechanisms of some well-described ISGs have been reviewed98,100, with some targeting flavivirus entry and/or fusion (IFITM3 and CH25H), translation (IFIT1/2, PKR and C19orf66) or replication (RNASEL and RSAD2). However, the mechanisms by which many other ISGs restrict flavivirus infections remain to be determined. Further delineation of how specific ISGs restrict flaviviruses could create opportunities for pharmacological targeting and enhanced resistance to infection.
The importance of antiviral antibodies against flaviviruses is well-established101. Passive transfer of virus-reactive monoclonal or polyclonal antibodies confers significant protection in animal models102,103. Anti-flavivirus antibodies may also exert protective effects via effector functions mediated by the Fc portion of the antibody molecule, including complement fixation, antibody-mediated cellular cytotoxicity and antibody-mediated opsonization, all of which can facilitate viral clearance104,105. Protective antibodies against flaviviruses predominantly recognize epitopes on the E protein of the virion, but also can bind to regions of the cell surface and secreted forms of NS1 (refs. 106,107).
Neutralizing anti-flavivirus antibodies can inhibit infection at multiple steps in the virus lifecycle, including a blockade of virus attachment to host cells108, presumably by disrupting interactions with attachment factors or receptors. Flavivirus-reactive antibodies may also block infection after the attachment step. Many potently neutralizing and protective antibodies inhibit the pH-dependent structural changes required for endosomal fusion and nucleocapsid release109. In contrast, some flavivirus-reactive antibodies increase the efficiency of infection under certain conditions. Such antibody-dependent enhancement (ADE) of infection occurs when non-neutralizing amounts of antibody bind virions and promote more efficient infection of cells expressing activating Fc–γ receptors via enhancement of virion attachment and internalization110. While readily demonstrated in vitro with multiple flaviviruses using cell lines or primary Fc–γ-expressing cells, a role for ADE in vivo has only been demonstrated convincingly for DENV111,112.
Studies have established important roles for both CD4+ and CD8+ T cells in flavivirus pathogenesis and immunity (reviewed in refs. 107,113,114). The protective roles of CD4+ T cells may differ during primary and memory responses. In mice, CD4+ T cells control primary WNV, YFV, ZIKV and JEV infection and disease115. In comparison, CD4+ T cells were not required for controlling primary DENV infection, yet instead contributed to viral clearance after immunization and challenge116. CD4+ T cells can also protect against flavivirus infection by providing help for antibody responses, sustaining CD8+ T-cell responses that enable viral clearance, producing antiviral cytokines and lysing some infected cell targets. In humans, impaired JEV-specific CD4+ T-cell function was seen preferentially in patients with encephalitis and neurological sequelae117. As DENV-specific CD4+ T cells show cytolytic activity ex vivo and are associated with a protective class II major histocompatibility complex allele, they are believed to control DENV infection in humans118.
Memory CD4+ T cells can have protective or pathological consequences depending on the context. For DENV, immunization schemes that elicited antigen-specific CD4+ T cells prior to infection of mice resulted in diminished viral burden after challenge with homologous DENV116. Memory T-cell responses elicited by prior infection with DENV recognize ZIKV-derived peptides and influence the magnitude and quality of the ZIKV T-cell response119. Although cross-reactive CD4+ T cells against conserved peptides can be detected across flaviviruses, their effect on viral infection and disease remains uncertain. In some settings, the memory response may also have pathological consequences. For example, CD4+ T cells primed against one serotype of DENV can result in the over-exuberant production of inflammatory cytokines and an increased risk for severe disease in the context of infection with a second, heterologous DENV serotype120.
CD8+ T cells, by virtue of their ability to lyse infected target cells and produce pro-inflammatory cytokines, can also have protective or pathological effects against flaviviruses depending on the context. In mice, CD8+ T cells can be an essential component of protection against and for the resolution of primary infection by several different flaviviruses (such as WNV, ZIKV and DENV)121,122,123. Flavivirus-specific cytotoxic CD8+ T cells proliferate, release proinflammatory cytokines including IFN-γ and tumour necrosis factor (TNF), and lyse cells through the delivery of perforin and granzymes, or via Fas–Fas ligand or TNF-related apoptosis-inducing ligand (TRAIL) interactions113. Consequently, mice deficient in these molecules had increased viral burden124,125. Heterologous, memory T-cell responses also can have protective functions, as cross-reactive DENV-immune CD8+ T cells restrict ZIKV infection and disease, including in pregnancy126,127. Reciprocally, ZIKV-immune CD8+ T cells can protect against DENV infection in mice128.
In certain circumstances, flavivirus-specific CD8+ T cells can cause immunopathology. The antiviral activity of CD8+ T cells within the brain markedly limited ZIKV infection of neurons, but also triggered ZIKV-associated paralysis in mice129. CD8+ T cells induced immunopathology in the brain after infection with TBEV130, and for DENV, a pathogenic role of CD8+ T cells has been described during secondary infection. Serotype cross-reactive CD8+ T cells are preferentially activated during secondary infection in humans131 and exhibit altered cytokine production and reduced cytolytic activity132,133. Aberrant cytokine production by CD8+ T cells could contribute to severe DENV disease by promoting endothelial cell dysfunction or damage and plasma leakage134. Notwithstanding these data, other human studies suggest that CD8+ T cell responses, in the context of secondary DENV infection, may have beneficial consequences114,135.
Given this background on how flaviviruses replicate, are recognized by the host immune system and the clinical diseases they cause, in the next sections we will describe the flaviviruses that are considered established threats, those that have recently emerged as global health threats and, finally, those which may emerge to cause future epidemics.
After mosquito inoculation, the four serotypes of DENV can cause human clinical disease ranging from self-limited dengue fever to a life-threatening syndrome, termed ‘severe dengue’. DENV now causes an estimated 390 million total infections, 100 million clinically apparent cases and 500,000 presentations of severe dengue per year worldwide, with at least 2.5 billion people at risk1 (Table 1). Over the past 70 years, the number of people infected has risen steadily, making DENV the most prevalent arthropod-borne viral disease in the world. Severe dengue routinely occurs in more than 100 countries, including those in the Americas, Asia, Africa and Australia; in essence, wherever the primary mosquito vector Aedes aegypti is present (Fig. 4). In the continental United States, although some regions (the Gulf Coast and the south east) periodically experience dengue outbreaks136,137, sustained transmission has not occurred recently, possibly due to indoor lifestyles and rapid mosquito control efforts (such as spraying and larvicide strategies) implemented once DENV cases are detected.
The incidence of severe dengue varies between primary and secondary infections. A secondary DENV infection results when a person previously infected with one serotype is exposed to a different serotype, and is the single most important risk factor for severe dengue disease138,139. Severe dengue is characterized by rapid onset of capillary leakage accompanied by thrombocytopenia and mild to moderate liver damage140. Although haemorrhagic manifestations occur (for example, epistaxis, gastrointestinal tract bleeding and menorrhagia), fluid loss into tissue spaces and the resulting hypotension carries the greatest risk of mortality141. Whereas severe dengue occurs principally after secondary infection in children and adults142, in infants under the age of one born to dengue-immune mothers, a primary DENV infection can cause substantial morbidity and mortality143. Maternal anti-dengue antibody titers and the age of the infant correlated with disease. Severe dengue often occurs in infants (peaking at 7 months of age) when maternal serum antibodies wane and enhance rather than neutralize infection of monocytes via ADE112. Severe dengue is more prevalent in infants144 and has a higher mortality rate compared to other age groups145.
West Nile virus
WNV, which was first isolated in 1937 (ref. 146), cycles in nature between Culex mosquitoes and birds but also infects and causes disease in humans, horses and other mammals (Table 1). Although its enzootic cycle is between mosquitoes and birds, with mammals serving as ‘dead-end’ hosts because of low-level and transient viraemia, non-viraemic transmission of WNV between co-feeding mosquitoes suggests that some mammals could act as additional reservoirs147. Historically, WNV caused sporadic outbreaks of a febrile illness in regions of Africa, the Middle East, Asia and Australia that were not associated with severe human disease. However, in the 1990s, the epidemiology of infection changed. Cases in Eastern Europe were associated with neurological disease148. In 1999, WNV entered North America and caused seven human fatalities in the New York area as well a large number of avian and equine deaths. In the United States, some avian species were particularly vulnerable, with a large number of deaths in crows, jays and hawks recorded during the epidemic. Over the past two decades, WNV has spread to and circulated in continental United States as well in Canada, Mexico, the Caribbean and South America (Fig. 4). Because of the increased range, the number of human cases has continued to rise: in the United States, 51,747 cases were confirmed between 1999–2019. Forty-eight percent of these cases caused acute flaccid paralysis, meningitis and/or encephalitis and were associated with 2,381 deaths149. Based on blood supply screening, 2,000,000 to 4,000,000 total infections likely occurred in the United States between 1999 and 2010 (ref. 150). Moreover, WNV continues to emerge in parts of Eastern Europe151 with severe neurological disease and fatalities caused by a different genetic lineage, termed lineage 2 WNV152. In 2018, an unusually high number of infections in horses and people were reported in southern parts of Europe153. Although sequence determinants responsible for greater virulence in birds have been identified (for example, a T249P amino acid substitution in NS3 (ref. 154)), the basis for enhanced pathogenicity of contemporary American and European isolates in humans remains an unanswered question.
Japanese encephalitis virus
JEV causes severe neurological disease and is primarily prevalent in Asia, where it accounts for ~35,000 to 50,000 cases and 10,000 to 15,000 deaths annually155. JEV epidemics were originally described in Japan in the nineteenth century, and the virus was first recovered in 1935 from an infected human in Tokyo. While the majority of human infections are asymptomatic, many symptomatic cases result in meningitis, encephalitis and/or flaccid paralysis, and are fatal or cause devastating long-term neurological sequelae156 (Table 1). In one study of children with JEV encephalitis157, only 44% of patients recovered fully, with 8% dying during the acute phase and 31% having persistent neurological, developmental and psychiatric disease. The enzootic cycle of JEV is between water birds and Culex mosquitoes, with pigs also serving as an amplifying host. Humans are considered incidental dead-end hosts and generally do not produce viraemia sufficient to infect mosquitoes. Despite the introduction of inactivated and live-attenuated vaccines158, JEV remains an important global cause of viral encephalitis. JEV is classified into a single serotype with five genotypes, and infection and disease occur across a large range of Asian countries with outbreaks occurring in Japan, China, Taiwan, Korea, the Philippines, India and the eastern region of Russia (Fig. 4). Epidemic activity in India, Nepal and other parts of Southeast Asia appears to be escalating, and JEV more recently has been described in Pakistan, Papua New Guinea and Australia, suggesting that its geographic range may be expanding159. Indeed, autochthonous transmission of JEV was detected for the first time in Africa in a febrile patient from Angola160. Of concern, the more divergent genotype V strains (amino acid divergence from 8.4% to 10.0% compared to genotypes I–IV) have been detected in Malaysia161, Korea162 and China163, and may be covered poorly by existing genotype III-based vaccines. Currently, approximately 50 percent of the world’s population is living in regions that are endemic to JEV164. There is also concern that JEV could spread to the Americas, much like WNV did, since North American field-collected Culex mosquitoes are susceptible to JEV infection165, and several avian species in North America are susceptible to JEV and can potentially serve as amplification hosts.
Emerging and re-emerging threats
Yellow fever virus
YFV is the prototype and namesake of the flavivirus genus owing to the jaundice that characterizes severe infections. While most infections are asymptomatic, YFV causes an acute febrile illness that may result in hepatitis, renal failure, haemorrhage and shock70,166 (Table 1). Infection is fatal in 20– 60% of severe symptomatic cases167. Trade between Africa, where YFV is thought to have originated, and the New World or Europe drove devastating outbreaks in coastal cities during the eighteenth and nineteenth century that shaped the development and economies of the Americas168. These outbreaks ultimately were blunted by the deployment of a vaccine and measures to control mosquito populations.
Despite the existence of an effective vaccine, YFV remains endemic in many parts of the world (Fig. 4)169,170. YFV has an equatorial distribution across the African continent, bounded in the north by the Sahara Desert and Angola in the south. Periodic outbreaks of varying intensity occur, most frequently in West and East Africa70. It is estimated that 90% of YFV cases occur in Africa171. However, the burden of disease in Africa has proven difficult to measure due to the heterogeneity of clinical presentation of YFV. Modelling suggests ~130,000 severe cases of YFV occur each year, resulting in ~78,000 deaths170, mostly in West Africa. Only 12% of human YFV infections in Africa are estimated to cause severe illness166. Prior to the late 1990s, the distribution of YFV in South America occurred predominantly in the river basins of the Orinoco, Amazon and Araguaia rivers. Since then, multiple outbreaks in humans and non-human primates (NHPs) have occurred outside this endemic region in Brazil, Columbia, Argentina, Ecuador and Peru172. This expanding activity is characterized by human infections proximal to major urban centres and large numbers of unvaccinated individuals.
The epidemiology of YFV is determined by the distribution of its mosquito vector. In South America, YFV is maintained in an enzootic cycle between canopy mosquitoes of the Haemogogus and Sabethes genera and a variety of NHP species, whereas transmission among African primates is vectored by Aedes species mosquitoes169. These sylvatic cycles provide a reservoir for YFV and an opportunity for transmission when human activity encroaches on forest ecosystems. The presence of this reservoir virtually eliminates the possibility of YFV eradication through vaccination. Urban cycles of YFV transmission involving transmission cycles of A. aegypti and humans have not contributed significantly to YFV outbreaks in South America173. A study of the 2016–2017 YFV outbreak in Minas Gerais, Brazil, identified a temporal correlation between human infections and virus detection in NHPs, and established that YFV-infected individuals lived an average of 1.4 km from a YFV-positive NHP sampled by this study (as compared to 39 km for non-exposed human controls)5. The distribution of YFV cases in this outbreak also supported a model by which human infections originated from a sylvatic rather than urban cycle of enzootic transmission. While many factors contribute to the potential for YFV emergence in urban areas, the widespread distribution of A. aegypti populations capable of YFV transmission creates a significant risk for public health.
Prior to 2007, ZIKV was an obscure virus that caused a mild febrile illness in a small number of humans in Africa and parts of Asia. In late 2013 or early 2014, ZIKV was introduced into Brazil and other regions of the Americas174 with millions of infections occurring (Fig. 4). As part of this epidemic, some of the unique clinical features of ZIKV infection (for example, congenital malformations) were identified175,176 (Table 1). A key question is: how did ZIKV change to cause an epidemic of fetal microcephaly and other congenital anomalies?
Ecological factors have been proposed to explain the increased number of ZIKV infections in humans as a function of greater transmission by Aedes species mosquitoes. Potential factors that could have enhanced Aedes mosquito populations and transmission include changes in land use (for example, deforestation), climate change, population growth and human movement into urban areas177. Beyond this, changes in the ZIKV sequence during the pre- to post-epidemic transition may explain the expanded vector transmission. An alanine-to-valine (A188V) substitution in NS1 of epidemic ZIKV strains facilitated greater infectivity in A. aegypti laboratory mosquitoes and thus is postulated to enhance epidemic transmission178.
Genetic changes in ZIKV also may have affected its ability to replicate and cause injury to key neuroprogenitor cells in the brain. Initial phylogenetic analysis revealed eleven amino acid changes between ancestral strains and French Polynesian and American ZIKV isolates, and these differences were dispersed in prM, NS1, NS3 and NS5 proteins179. Subsequent experiments showed that a serine-to-asparagine substitution (S139N of the polyprotein) in prM resulted in increased ZIKV infectivity in neuroprogenitor cells and more severe microcephaly in neonatal mice180. The S139N substitution arose just prior to the 2013 outbreak in French Polynesia and has been maintained in virtually all American strains. The basis for how the S139N mutation in prM mediates increased pathogenicity is uncertain, although it is speculated to affect the maturation state and/or physical structure of the ZIKV particle181.
Sequence changes in the 3’-UTR also may contribute to pathogenic effects in neural cells. One group identified a putative Musashi protein binding element in the stem-loop 2 (SL2) of the 3’-UTR, with changes immediately upstream of this site in epidemic strains182. As Musashi proteins regulate progenitor cell growth and differentiation through posttranscriptional control of gene expression, they speculated that the binding elements in the 3’-UTR of ZIKV would affect the fate of neuronal progenitor cells in infected cells and pathogenesis. A second group showed that Musashi-1 interacts with ZIKV RNA and facilitates viral replication183. ZIKV infection disrupted the binding of Musashi-1 to its endogenous targets, which altered expression of factors implicated in neural stem cell function and differentiation. Thus, Musashi protein interactions with RNA elements from epidemic strains of ZIKV may contribute to the vulnerability of the fetal brain to infection and development.
The same amino acid change in NS1 (A188V) in epidemic strains that is speculated to affect vector transmission also may affect replication in human cells. A188V variants of NS1 show enhanced binding to human TANK-binding kinase 1 (TBK1), an enzyme that regulates the activity and nuclear translocation of IRF3. NS1 binding to TBK1 resulted in reduced levels of TBK1 phosphorylation and diminished IFN-β expression in human cells and mice184. Thus, this recent sequence change in NS1 can promote evasion of the innate immune response, enhance viraemia and possibly enhance ZIKV transmissibility from hosts to vectors, all of which facilitate epidemic transmission.
The immune status of the host may also influence ZIKV pathogenesis. While cross-reactive anti-DENV antibodies can readily enhance ZIKV infection in cell culture185,186, the significance of this finding to the epidemiology of ZIKV disease severity and transmission remains uncertain187. Indeed, passive transfer of cross-reactive, neutralizing E-dimer epitope antibodies raised against DENV prevented ZIKV pathogenesis in mice and NHPs188,189. However, in some settings, pre-existing anti-flavivirus antibodies have augmented ZIKV infection and disease; passive transfer of immune plasma raised against DENV or WNV enhanced ZIKV pathogenesis in Stat2–/– mice190,191. Yet in another study in Ifnar1–/– (A129) or Ifnar1–/– Ifngr–/– (AG129) mice, whilst inactivated ZIKV vaccination enhanced dengue disease severity, ADE was not observed after ZIKV infection in animals that were passively immunized or pre-infected with DENV181. Apart from the contrasting results, a major caveat to the passive transfer of antibody model is that these mice lack immune, cross-reactive CD8+ T cells, which can limit the pathological effects of ADE in the context of DENV immunity and subsequent ZIKV infection, including during pregnancy127,192.
In NHPs, the effects of pre-existing flavivirus immunity on ZIKV and DENV pathogenesis are also uncertain. In one study, no substantive differences in ZIKV infection viral titers, neutralizing antibody levels or immune cell kinetics were observed after inoculation of naïve and flavivirus-immune rhesus macaques193. Other groups also have found no evidence of enhancement of ZIKV pathogenesis in DENV-immune macaques194,195. However, in a study in rhesus macaques, prior exposure to ZIKV resulted in enhanced DENV peak viraemia196, and this was associated with delayed induction of memory cross-neutralizing antibody responses197. This observation may have implications for ZIKV vaccine development in areas endemic for DENV infections. More epidemiological studies in humans are necessary to establish whether clinically relevant ADE of ZIKV pathogenesis occurs. An analysis of Brazilian cohorts has not shown evidence of ADE, greater disease severity or effects on birth outcomes in DENV-experienced patients with acute ZIKV infection198,199.
The next possible emerging flaviviruses
The ZIKV epidemic showed that flaviviruses of relative obscurity can emerge as significant public health threats within a compressed time frame. Are there other esoteric flaviviruses that will appear soon and cause epidemics in vulnerable hosts? While it is difficult to predict the rise of a particular pathogen in the human population, six less well known flaviviruses could emerge to cause significant human disease in the near future (Fig. 4; Table 1).
Spondweni virus (SPOV) is the flavivirus most closely related to ZIKV. In the 1950s, SPOV was isolated from patients in Nigeria and South Africa200,201, and subsequently circulated in sub-Saharan Africa. Although most symptomatic SPOV infections result in mild illness, a subset reportedly progresses to more serious disease, including vascular leakage and shock or neurological involvement202. The enzootic cycle of SPOV likely is between mosquitoes and NHPs203. Historically, SPOV infection was not observed in A. aegypti, Aedes albopictus and Culex quinquefasciatus mosquitoes, and instead was isolated from other mosquitoes in the genera Aedes, Culex, Eretmapodites and Mansonia. Based on this vector biology, the potential for urban epidemic cycles of SPOV was considered low. However, the epidemiology may be changing, as SPOV was reportedly detected in field-caught C. quinquefasciatus mosquitoes in Haiti in 2016 (ref. 204). This finding suggests that SPOV may adapt to mosquito species that preferentially feed on humans. Given its relationship to ZIKV (~75% amino acid identity), there is concern that SPOV also might have the capacity to infect cells of the reproductive tract and be sexually transmitted in humans, as was reported in mice205.
USUV is a mosquito-transmitted flavivirus belonging to the JEV antigenic complex. USUV is classified into eight lineages with two major African and European groups206. USUV shares the same mosquito vectors (for example, Culex pipiens) with WNV and similar bird populations as amplifying hosts, and the two viruses can co-circulate207. Initially isolated in 1959 in South Africa, USUV appeared in 1996 in Italy (based on retrospective analysis of archived tissues) and in Central Europe in 2001, where it was associated with deaths in selected avian populations208. In 2015–2016, widespread USUV activity was reported in Germany, France, Austria, Belgium and the Netherlands, with mortality observed in blackbirds and grey owls209. USUV infection occurs in humans and seroprevalence studies suggest that it may be higher than WNV in areas of co-circulation210. Neuroinvasive disease in humans caused by USUV appears less common than WNV, although reports of meningoencephalitis, meningitis and paralysis exist211. As WNV and USUV are related (~76% amino acid identity), serological distinction may be challenging and thus, it is possible that USUV infection and disease are underestimated.
Ilheus virus (ILHV) is a mosquito-transmitted flavivirus closely related to viruses of the JEV serocomplex. It was first described in Brazil in 1944 and now circulates in South America where it sporadically causes a febrile syndrome in humans that can progress to encephalitis. ILHV infection in humans has been reported in Trinidad, Panama, Colombia, French Guyana, Brazil, Ecuador and Bolivia212. ILHV cycles in nature between birds and mosquitoes, and has been isolated from mosquitoes, sentinel monkeys, humans213 and birds. Moreover, high seroprevalence rates of ILHV have been detected in horses in parts of Brazil214. As this virus can propagate in some mosquitoes that feed on humans (such as the Aedes and Culex species)215, there is the potential for more extensive zoonotic emergence in the human population.
Rocio virus (ROCV) is a flavivirus in the JEV serocomplex and is closely related to ILHV. It was first isolated in 1975 from the brain of an affected individual during an epidemic of encephalitis in São Paulo, Brazil216. Its spread to more than 20 municipalities resulted in approximately 1,000 diagnosed cases217. During the epidemic, there was a case-fatality rate of 13%, with approximately 20% of survivors developing long-term neurological sequelae. Laboratory studies suggest that ROCV is mosquito-transmitted, as Culex tarsalis and C. pipiens were efficient experimental vectors218, and that birds may act as amplifying hosts219. Although no cases of ROCV infection and encephalitis have been reported after the initial outbreak, serological surveys suggest ROCV transmission among humans and animals in different regions of Brazil is still actively occurring220,221.
Wesselsbron virus (WSLV) is a mosquito-transmitted zoonotic agent that causes disease in sheep and other ruminants in Africa with spillover into human populations. WSLV infection was initially reported on a sheep farm in South Africa in 1955 and caused substantial mortality in newborn lambs and abortion in pregnant ewes213. In humans, WSLV infection can cause a sudden onset of influenza-like illness characterized by fever, rigors, headache, myalgia and arthralgia. Historical studies have suggested that WSLV circulation is widespread—at least in southern Africa213—and more recent analysis has demonstrated infection of rats, which could serve as a reservoir222. WSLV is likely present in many areas of Africa as viral isolations from mosquitoes have been reported in South Africa, Botswana, Zimbabwe, Uganda, Mozambique, Cameroon, Central African Republic, Mauritania, Senegal, Nigeria, Democratic Republic of Congo and Madagascar213. There is concern that WSLV could emerge beyond its traditional borders, spread more extensively and cause infection and disease in naïve human populations. Indeed, WSLV was isolated in Thailand from mosquitoes in 1966, although there is no recent evidence of circulation or transmission in Asia.
Transmission of tick-borne flaviviruses has been increasing worldwide. This group includes TBEV, which is principally located in regions of northern China and Japan, Russia, and Central and Eastern Europe, and can cause fatal neurological syndromes. TBEV causes several thousands of human cases per year, with recent increases attributed to changes in climate, population dynamics, the range of permissive ticks and shifts in land usage223,224. Other antigenically related tick-borne flaviviruses can cause severe human disease. This group includes Omsk haemorrhagic fever virus (OHFV), POWV, Kyasanur forest disease virus (KFDV), Alkhurma haemorrhagic fever virus (AHFV) and Karshi virus (KSIV), with some causing encephalitis (KSIV and POWV) and others resulting in haemorrhagic fever (OHFV, KFDV and AHFV).
POWV is the only known tick-borne flavivirus that circulates in North America. POWV was first isolated from a child who died of encephalitis in Powassan, Ontario in 1958. Human cases of POWV occur in the United States, Canada and also Russia225. Two genetic lineages of POWV circulate in North America, lineage I and lineage II (also called deer-tick virus (DTV)) that share at least 96% amino acid identity in their E proteins. POWV lineage I strains are predominantly maintained in Ixodes cookei ticks, whereas lineage II strains are found in Ixodes scapularis deer ticks226.
The natural cycle of POWV includes small mammals (such as rodents and lagomorphs), deer and ticks227, with peak transmission occurring during spring and summer. In humans, POWV infections can cause severe neuroinvasive disease, including meningitis and encephalitis, with an estimated case-fatality rate of 10–30% and with many survivors suffering long-term disabling sequelae. While POWV-induced disease can occur in all age groups, epidemiological studies suggest a greater risk in the elderly (> 60 years of age)224, which is similar to other encephalitic flaviviruses including WNV228. POWV is emerging, as increasing numbers of cases have been diagnosed over the past decade229 and up to 3–5% of I. scapularis ticks isolated in certain parts of the United States now test positive for POWV230,231. Moreover, seroprevalence rates of POWV infection in other mammals (for example, white-tailed deer) are rising and may be associated with the expanded range of I. scapularis in the United States232. Thus, an abundance of evidence suggests that POWV is an emerging flavivirus threat, which has triggered the development of countermeasures to minimize severe disease233.
Combating flavivirus emergence
Given the ongoing and likely future threats of flavivirus infections, the continued development and deployment of countermeasures that limit epidemic spread and disease in humans is urgent. This section focuses on the past successes and future challenges of flavivirus vaccines and the issues related to the development of direct-acting antiviral agents.
Licensed vaccines exist for five flaviviruses (YFV, DENV, JEV, KFDV and TBEV), and several others have been evaluated in preclinical and clinical studies. The live-attenuated YFV vaccine is among the most successful of all vaccines to prevent viral infections. Developed by Max Theiler in 1939 by iterative passage of the pathogenic Asibi strain in mouse and chicken embryos, more than 500 million doses of YFV 17D vaccine have been administered worldwide234. SA14-14-2, an extensively passaged vaccine for JEV, is also efficacious and is used extensively in Asia and India235. Molecular clone technology enabled the development of rationally-attenuated vaccines for DENV236,237,238,239,240 and JEV241 via the construction of chimeric viruses or those encoding deletions in the 3’-UTR of the genome. Additional modes of attenuation (for example, mutations in E, NS1 or NS5 genes) have been evaluated as flavivirus vaccine candidates in preclinical models242,243. Chemically-inactivated viruses of cell culture-derived viruses are currently used as vaccines for JEV244, TBEV245 and KFDV246. While they are protective, they require frequent iterative boosting to maintain protective immunity.
The severe clinical outcomes following DENV infections have made the development of a vaccine a global health imperative. However, vaccine design and development has been hampered by the risk that incomplete vaccine immunity against all four serotypes might paradoxically enhance pathogenesis in the setting of subsequent natural infection. As a result, the goal is to develop a vaccine that simultaneously elicits a balanced tetravalent neutralizing response against all four DENV serotypes. The live-attenuated, tetravalent Dengvaxia (from Sanofi Pasteur) was the first anti-DENV vaccine licensed in 2016, although it was restricted to individuals greater than 9 years of age247. In 2019, the United States Food and Drug Administration (FDA) approved Dengvaxia, but only for use in individuals between 9–16 years of age who have laboratory-confirmed prior dengue infection and are living in endemic areas. These relatively narrow indications are based in part on the finding that in the clinical trials, vaccinated children aged between 2–5 years were at greater risk of hospitalization as compared to controls248. Serological studies later demonstrated that individuals that were DENV-seropositive at the time of vaccine administration experienced benefit from Dengvaxia249, whereas DENV-naïve individuals were at increased risk for disease over this interval250. Further follow-up is required to evaluate the public health impact of the use of this vaccine candidate on children since its licensure. As two other live-attenuated tetravalent DENV vaccines (TV003 from the National Institute of Allergy and Infectious Diseases, and TAK-003 from Takeda Pharmaceutical Company) are in advanced stages of clinical trials251,252, the question remains as to whether they will provide superior protection to naïve individuals without the risk of sensitizing them to symptomatic or severe disease from subsequent natural DENV infection.
Despite the success of vaccines for some flaviviruses, challenges exist for the development of vaccine candidates to blunt epidemics caused by emerging flaviviruses. First, the extensive cross-reactivity of flavivirus-immune sera complicates the development and use of diagnostics to track and manage outbreaks. While neutralization assays provide some capacity to resolve antibody responses to homologous and heterologous viruses in convalescent sera, these approaches have limitations in sera from acutely infected individuals253,254. Since viraemia is typically transient, molecular assays to detect flavivirus infection are sensitive only for relatively small intervals after exposure, the timing of which is often unknown. While the discovery that RNA persists in the urine and semen of ZIKV-infected individuals extended the utility of these approaches during the 2015 epidemic72, serological assays remain an important tool for the management of the epidemics and evaluation of vaccine candidates255,256. Second, the presence of cross-reactive antibodies may shape the immune response to vaccination and influence the outcome of disease following infection, as reviewed elsewhere110. Third, while promising new platforms have been applied to create flavivirus vaccines, including synthetic nucleic expression systems, small differences in antigen design unpredictably modulate the potency of the immune response to vaccination, highlighting the need for additional study of the biology, structure and heterogeneity of vaccine antigens257. Fourth, even large epidemics of flavivirus infection and disease can be transient relative to the interval required to the development and evaluation of vaccine candidates. Despite the unprecedented speed of generating Zika virus vaccine candidates for early clinical evaluation, a requirement for advanced clinical trials in larger numbers of individuals to reveal efficacy and provide insights into correlates of protection may be jeopardized by the smaller number of new infections, which is characteristic of a waning epidemic258. Finally, limited availability or insufficient deployment may limit the utility of vaccines once developed. Notably, vaccine shortages have exacerbated ongoing YFV activity in South America and Africa, prompting vaccine sparing studies259. Moreover, considerable numbers of JEV and TBEV infections continue to occur in Asia and Europe despite the availability of safe and effective vaccine programs. Even when made available, effective vaccines have not always had the desired impact on global health.
The development of antiviral therapeutics will enable new approaches for the management of flavivirus outbreaks due to their potential for use as treatment and prophylaxis. Flaviviruses encode multiple potential targets for small molecule drugs. Extensive drug-discovery efforts have focused on the NS5 and NS3 proteins encoding enzymatic activity required for viral genome replication and polyprotein processing. Nucleoside260 and allosteric inhibitors261 of NS5-encoded RNA-dependent RNA polymerase activity have been described (reviewed in ref. 262). Compounds with broad activity against multiple classes of viruses, including flaviviruses, have also been characterized, including the adenosine analogue BCX4430 (refs. 263,264) and the nucleotide analogue prodrug Sofosbuvir265. The methyltransferase domain that comprises the amino terminus of NS5 responsible for the N-7 and 2’-O methylation of the viral RNA cap also is a potential target for small molecules266,267. Inhibition of viral protease activity has yielded important classes of drugs for multiple viruses, including hepatitis C, and has been aggressively pursued for other flaviviruses. While inhibitor design was guided by numerous structures of the NS3 protease in complex with NS2B, this complex has proven to be a challenging target due to the relatively flat structure of the substrate pocket, that ligands binding this motif are charged, and the conformational flexibility of the protease target268,269. Both small molecule and peptide protease inhibitors have been characterized; some of these function via an allosteric mechanism. Of interest, multiple repurposed compounds have been shown to inhibit flavivirus proteases, including several FDA-approved drugs capable of inhibiting ZIKV replication in cell culture and mice270,271. Flavivirus helicase inhibitors also have been characterized in preclinical studies272.
Structural proteins of the virion also may be targeted by antiviral compounds. Crystallographic studies of the E protein of DENV2 identified a lipid molecule in a hydrophobic pocket formed at the junction between ED-II and E-DI273. Compounds that target this pocket have been identified and are thought to block infection by interfering with the viral membrane fusion process274,275. Peptides derived from sequences present in the stem anchor domains of E also have antiviral activity276,277. The internal capsid protein has also been targeted for drug discovery efforts. High-throughput screening identified the small molecule ST-148 as capable of inhibiting cell death in a DENV propagation assay278. The proposed mechanism of this molecule is the stabilization of the capsid protein, which results in altered assembly and disassembly during virus entry279. A second chemically related compound has been described that also binds DENV capsid and inhibits infection280.
Targeting the vector
Progress has been made in reducing flavivirus transmission by limiting infection of the mosquito host281. For example, the infection of A. aegypti mosquitoes with selected strains of endosymbiotic Wolbachia resulted in bacterial invasion of mosquito populations and interference with DENV and ZIKV replication282,283. The wMel strain of Wolbachia-infected A. aegypti, when directly fed on viraemic dengue patients, has lower DENV transmission potential than their wild-type counterparts284. Mechanistic studies suggest that infection with Wolbachia reduces flavivirus replication, is associated with rapid viral RNA degradation in the cytoplasm and is mediated by the mosquito XRN1 enzyme285. The establishment of A. aegypti strains with Wolbachia infection in an endemic setting could abolish or reduce flavivirus transmission286. Wolbachia-infected A. aegypti mosquitoes have been released in Australia where outbreaks of dengue fever occur, and have been stable over several years287. The AWED trial (Applying Wolbachia to Eliminate Dengue) is underway to assess the efficacy of Wolbachia-infected mosquito deployments to reduce DENV incidence in Indonesia288.
Other groups have created genetically engineered A. aegypti mosquitoes that are resistant to DENV infection through the induction of an antiviral RNA interference response289. More recently, a polycistronic cluster of engineered, synthetic small RNAs targeting ZIKV was expressed in the midgut of mosquitoes, a site of early virus infection. Engineered A. aegypti mosquitoes harbouring the anti-ZIKV transgene had markedly reduced viral infection, dissemination and transmission rates of ZIKV in the laboratory290.
The recent outbreaks of less well-known flaviviruses highlight the transmission potential and dynamic state of emergence. While it is challenging to predict which flavivirus will transition next from relative obscurity to worldwide notoriety, their changing epidemiology raises concern for large-scale emergence and disease. Sustained research efforts on flaviviruses and likely other arboviruses (for example, alphaviruses, bunyaviruses and some orthomyxoviruses) are needed. Such a concerted program can prepare us to respond rapidly with countermeasures to new viral epidemics that cause known and unanticipated clinical syndromes.
A requirement to respond rapidly to an explosive ZIKV outbreak in the Americas identified aspects of flavivirus biology that may be particularly important for future preparedness efforts. While expensive to establish and maintain, surveillance programs to identify the changes in pathogen distribution that provide early signals to public health officials are critical, as has become clear with the global pandemic of severe acute respiratory syndrome coronavirus 2 infecton and COVID-19 disease. The emergence of WNV in North America in 1999 resulted in a considerable increase in arbovirus surveillance capacity to manage this outbreak, but this was not sustained291. The development of sensitive and specific flavivirus diagnostics is a challenge due to serological cross-reactivity and the relatively limited persistence of viral RNA in those infected. These technical obstacles hamper the management of an outbreak response, including the evaluation of vaccines. Enhanced and sustained investment in these areas are critical for an effective response to future flavivirus threats. Antibody discovery efforts for emerging flaviviruses will be a powerful component of preparedness efforts because they inform the development of diagnostics, allow for characterization of vaccine antigens and identify protective features of the immune response. Moreover, in vivo expression of potent flavivirus-reactive neutralizing antibodies using recently developed synthetic gene-expressing platforms, such as modified messenger RNA, provides a rapid pathway for the development of therapeutics292. While these gene-expression platforms also enable the rapid development of vaccine candidates, an understanding of structure–immunogen relationships and the correlates of protection may be insufficient to ensure rapid success for understudied flaviviruses in an outbreak setting. A continued emphasis on obtaining a fundamental understanding of the structure(s) of flavivirus vaccine antigens, the genetic and functional components of the antibody response to infection and vaccination, and viral pathogenesis in animal models strengthens our capacity to respond quickly to the next flavivirus threat. Because flaviviruses share an overall similar structure, antigen designs that lack features recognized by cross-reactive antibodies and that are compatible with increasingly powerful antigen expression or display platforms, may be particularly important first-generation vaccine candidates for use in an increasingly flavivirus-experienced world.
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This work is dedicated to the memory of Dr Michael Rossmann (1930–2019), who pioneered our structural understanding of flaviviruses and their interactions with the host. This work was supported by the intramural program of the National Institute of Allergy and Infectious Diseases and the National Institutes of Health (NIH; grant nos. R01 AI073755, R01 AI127828 and R01 HD091218 to M.S.D). We thank Ethan Tyler (NIH Office of the Director) for preparation of the figures. We also thank N. Vasilakis and S. Weaver for their editorial comments.
M.S.D. is a consultant for Inbios, is on the Scientific Advisory Board of Moderna and also receives funding from Emergent BioSolutions. The remaining author declares no competing interests.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
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Pierson, T.C., Diamond, M.S. The continued threat of emerging flaviviruses. Nat Microbiol 5, 796–812 (2020). https://doi.org/10.1038/s41564-020-0714-0
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