Rift valley fever: diagnostic challenges and investment needs for vaccine development.

Rift valley fever virus (RVFV) is a causative agent of a viral zoonosis that constitutes a major clinical burden in wild and domestic ruminants. The virus causes major outbreaks in livestock (sheep, goats, cattle and camels) and can be transmitted to humans by contaminated animal products or via arthropod vectors. Human-to-human transmission has not been reported to date, but spill-over events from animals have led to outbreaks in humans in Africa and the Arabian Peninsula. Currently, there is no licensed human vaccine against RVFV and the virus is listed as a priority pathogen by the World Health Organisation (WHO) due to the high epidemic potential and the lack of effective countermeasures. Multiple large RVFV outbreaks have been reported since the virus was discovered. During the last two decades, over 4000 cases and ~1000 deaths have been reported. The lack of systematic surveillance to estimate the true burden and incidence of human RVF disease is a challenge for planning future vaccine efficacy evaluation. This creates a need for robust diagnostic methodologies that can be deployed in remote regions to aid case confirmation, assessment of seroprevalence as well as pathogen surveillance required for the different stages of vaccine evaluation. Here, we perform comprehensive landscaping of the available diagnostic solutions for detection of RVFV in humans. Based on the identified gaps in the currently available in-house and commercially available methods, we highlight the specific investment needs for diagnostics that are critical for accelerating the development of effective vaccines against RVFV. © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Rift valley fever virus (RVFV) causes major outbreaks in livestock and can be transmitted to humans by contaminated animal products or via arthropod vectors.

RVFV is listed as a priority pathogen by WHO due to its high epidemic potential and the lack of a licensed human vaccine or other effective countermeasures.

Despite the wide range of commercial and in-house developed diagnostic methods available, there is limited validation data for performance of different tests, particularly for human samples.

There is a need for validated tests that can be deployed in remote regions to aid case confirmation, assessment of seroprevalence as well as pathogen surveillance required for the different stages of vaccine evaluation.

There is a need for One Health approach to RVF disease management as well as local capacity strengthening to perform RVFV diagnostics in endemic regions to ensure early outbreak detection, case management and preparedness for future vaccine evaluation.

Introduction

Rift valley fever (RVF) is a disease caused by RVF virus (RVFV), an arbovirus member of the order Bunyavirales which can cause infections in a range of wild and domestic ruminants, as well as in humans. Humans are typically infected due to contact with infected animal products or via the bite of infected mosquito vectors.1 The first reported RVF outbreak was in 1931 in a sheep farm in Kenya2 and since then the virus has been a cause of multiple outbreaks in livestock leading to substantial number of deaths of domestic ruminants and consecutive negative health and economic impact on humans. Although human-to-human transmission has not been observed, the virus has caused several major outbreaks in humans in Africa (Republic of South Africa, Madagascar, Sudan) and Arabian Peninsula (Saudi Arabia, Yemen)3–5 (table 1).

Table 1

Ten largest outbreaks of RVF in humans since year 2000

Year	Location	No of cases	No of fatalities
2000	Yemen	1087	121
2007	Sudan	738	230
2006	Kenya	684	234
2000	Saudi Arabia	516	87
2006	Tanzania	264	109
2010	Republic of South Africa	237	26
2008	Madagascar	236	7
2003	Egypt	148	27
2006	Somalia	114	51
2016	Republic of Niger	105	28

Source: WHO reported data: https://www.who.int/news-room/fact-sheets/detail/rift-valley-fever

RVF, rift valley fever.

A large number of detected cases in humans is usually preceded by an outbreak in animals; detected or not. Despite the sporadic nature of outbreaks in humans and the limited antigenic diversity of the virus with the presence of a single serotype,6 RVFV is listed as one of the priority pathogens in WHO Blueprint list due to its epidemic potential and lack of effective countermeasures. RVFV is also considered a select agent by the Centers for Disease Control and Prevention (CDC) and US Department of Agriculture. The epidemic potential of the virus is largely driven by the global presence of competent arthropod vectors7 8 and the active international travel and trade of livestock which increase the potential of the virus to cause infections outside endemic regions.

In this analysis article, we present a comprehensive landscaping of the diagnostic solutions available for RVFV detection in humans, highlight key gaps and challenges for specific diagnostic use cases and outline the development areas that require stronger focus to facilitate RVFV vaccine development.

Clinical presentation and disease management of RVF

RVFV carries a tripartite negative ssRNA genome containing L, M and S genomic segments. The N and NS proteins are encoded by the S segment and the non-structural NS protein is the main virulence determinant driving virus escape from the innate immune response.9 10 The incubation period for human RVF disease is 3–6 days, and the disease in most cases presents in a flu-like febrile disease which is self-limiting. The early-disease symptoms are non-specific which likely leads to a large number of undetected cases. Less than 2% of cases develop severe disease with highly variable case fatality ratio11 (average 0.5%–2%, but up to 28% in specific endemic regions)12 and characterised with ocular disease, hepatitis and/or meningoencephalitis.13 Acute infection with RVFV during pregnancy has been linked to increased chance of miscarriage14 suggesting a possible additional disease burden in humans caused by vertical transmission. To better understand the impact of RVF, systematic longitudinal cohort studies on the interepidemic disease burden are warranted in the African region in particular.

Due to the lack of specific treatment available for RVF, the management of suspected cases is usually based on supportive therapy. According to CDC recommendations, the use of aspirin or non-steroid anti-inflammatory drugs in RVF cases should be avoided to reduce the risk of haemorrhagic complications.15 Severe cases are managed depending on the nature of the complications, with, for example, renal replacement therapy in patients with severe renal failure16 and artificial tear preparations and ophthalmic steroids in ocular disease cases.17 The use of ribavirin is recommended for prophylaxis and treatment of haemorrhagic fever caused by arenaviruses and other bunyaviruses,18 but its efficacy for treatment of RVF has not been demonstrated. Other antiviral drugs (benzavir-2, favipiravir T-705)19 20 as well as monoclonal antibodies against the virus21 are currently in development as RVF-specific treatment options, but they are yet to be evaluated and approved for clinical use.

Due to the lack of a licensed vaccine, prevention strategies for RVFV infection are limited to the use of personal protective equipment to prevent nosocomial infections22 as well as standard measures to prevent exposure to mosquito vectors (bed nets, long clothes).

Diagnostics for RVFV detection

Due to the high containment level (biosafety level 3 (BSL3)) required for handling of suspected RVF cases, diagnostic testing of RVFV is typically performed only in dedicated reference laboratories with trained biomedical staff. The limited laboratory capacity in endemic regions poses a major hurdle for timely diagnosis of RVF and leads to delays in outbreak detection. According to WHO recommendation,23 definitive diagnosis of RVFV infection requires: (1) detection of virus RNA in serum or plasma via real-time polymerase chain reaction (RT-PCR); (2) detection of anti-RVFV IgM and IgG antibodies; (3) detection of RVFV virus antigen and/or (4) RVFV isolation. The selection of an optimal assay depends on the timing of sampling relative to disease progression and the ability to detect antigenic (isolated virus, viral RNA) or immunological markers (IgM and IgG). A combination of molecular and serological assays is usually needed to confirm RVFV cases if the timing of infection is unknown.

Molecular tests

Molecular tests are most useful during viremia (2–4 days post infection)24 and up to 8 days after onset of symptoms.25 Since viral load is correlated with disease severity,26 27 qPCR methods are often preferable to ensure simultaneous diagnosis and prognostic prediction. A number of commercial kits for molecular testing are currently available (table 2). They are primarily based on RT-PCR and enable the detection of RVFV as a single test or in a panel of several RNA viruses (Techne/Cole Palmer). The kits produced by LifeRiver and Altona are the only two CE-certified tests, while alternative methods are for research use only. Comparative tests of the commercially available kits across laboratories and different specimen preparation protocols have not yet been published to our knowledge.

Table 2

In-house and commercially available molecular methods for RVFV detection in human samples

In-house nucleic acid test (NAT) methods for RVFV detection
Method	Publication	Target gene	Description
Real-time PCR (RT-PCR)	Bird et al30 (2007)	L	Two-step assay for high-throughput detection of 40 known strains.
RT-PCR	Busquets et al. (2010)54	L	One-step real-time TaqMan assay.
RT-PCR	Drolet et al. (2012)24	L	Can be performed in BSL-2 as it involves pathogen deactivation step.
qRT-PCR	Drosten et al. (2002)31	M	Part of a panel for differential diagnosis of six viral haemorrhagic fever pathogens.
RT-PCR	Garcia et al. (2001)55	NSs	Two-step real-time TaqМan.
RT-PCR	Liu et al. (2016)56	L	Developed as a TaqМan assay card for 26 pathogens. Suitable for outbreak investigation or surveillance.
RT-PCR	Mwaengo et al.(2012)57	L, S	Two-step real-time assay used for RVFV detection in mosquitos.
NestedRT-PCR	Sall et al.(2002)58	NSs	Qualitative. Used for 293 human and animal sera sampled during an RVF outbreak in Mauritania in 1998.
NestedRT-PCR	Sanchez-Seco et al.(2003)59	S, L	Nested PCR assay, qualitative. Uses degenerate primers in first round of PCR to capture all Phleboviruses.
RT-PCR	Weidmann et al.(2008)60	S	One-step assay, designed against 19 strains.
RT-PCR	Wilson et al.(2013)61	L, M, NSs	Multiplex RT-PCR which detects 3 segments: L and M segments as confirmatory targets, and NSs to differentiate between infection and vaccination (suitable for DIVA testing).

BSL3, biosafety level 3; CE, approved for clinical testing; DIVA, distinguish infected from vaccinated individuals; EBOV, Ebola virus; FTD, Fast-Track Diagnostics; qPCR, quantitative PCR; RUO, approved for research use only; RVFV, rift valley fever virus; YFV, yellow fever virus.

A range of in-house developed molecular methods are also available that use different protocols for detection of viral RNA. Unlike commercial methods, most of these in-house approaches have undergone some degree of external quality assessment (EQA).28 29 Two methods based on RT-PCR amplification (by Bird et al30 and by Drosten et al31) have been extensively tested across different laboratories and show high sensitivity, specificity and capacity for automation. The method of Bird et al30 uses primers for the L segment of the RVFV genome and is suitable for high-throughput analysis as it can detect 40 RVFV strains at once. The protocol developed by Drosten et al,31 targets the M segment and provides a better means for differential diagnosis as it offers a quantitative assay for detection of a panel of six viral haemorrhagic fever viruses including RVFV. In a comparative study of these two methods in 30 research laboratories across 16 countries, Escadafal et al,29 showed these to be comparable and to perform with high sensitivity and specificity.

Serological tests

Serological assays enable the assessment of ongoing disease by presence of circulating antigen, or prior exposure to RVFV as demonstrated by presence of specific IgM and/or IgG antibodies. Serological tests based on ELISA are typically based on recombinant nucleocapsid protein (NP) and offer high specificity and simple sample processing. Diagnosis can also be made by immunofluorescent antibody (IFA) assay. Serological assays are key to epidemiological studies for identification of active infection or previous exposure to the virus. Active infection is conferred by detection of viral antigens, and previous exposure—by measuring virus specific IgM or IgG antibodies. Due to the short viremia, virus antigens are no longer detectable after 4–5 days. Therefore, a reliable use of serological assays for RVF diagnosis should incorporate a combination of tests for detection of viral antigens and serum IgM. The majority of commercially available serological assays have been developed and approved for animal testing only. Two commercially available IFA assays for IgM and IgG (Euroimmun) are CE certified serological assays for humans, however, their performances have not been evaluated by external independent assessment (table 3). There are two commercial ELISA kits manufactured by Biological Diagnostic Supplies Limited (BDSL) and based on assays for detection of IgM and/or IgG antibodies in serological samples originally developed by Paweska et al,32 and Jansen van Vuren et al.33 An ELISA detecting anti-RVFV IgM is also currently in development by ID-Vet company but has not yet received CE certification for use in humans. The performance of BDSL and ID-Vet assays has been evaluated in animal serum samples as part of an European ring trail. This study shows high specificity and sensitivity of both assays and highlights their reliable use for serological testing.34 To our knowledge, similar assessment of commercial ELISA assays in human samples have not been performed to date.

In-house developed serological assays are typically based on recombinant RVFV NP or irradiated whole RVFV virions as a coating antigen for detection of IgG and IgM responses directed against the virus. Like molecular assays, ELISA-based methods have mainly been tested in ruminants and lack EQA in humans. The ability to distinguish infection from vaccination is essential for vaccine development. McElroy et al35 have developed a diagnostic assay that can distinguish infected from vaccinated individuals (DIVA) using an ELISA based on recombinant N and Ns proteins. The assay has been validated in humans but not yet tested by external independent assessment. In attempt to develop a serological assay that can be used in remote settings, Sobarzo et al36 have developed an immunosensor technique for detection of RVFV IgG antibodies using antigen-coated optical fiber. Although the technique shows high sensitivity in human samples and has the potential to be adapted in a portable format, it has not been evaluated as an alternative to standard ELISA techniques.

While ELISA methods can detect serological responses to one antigen at a time, detection of RVFV-specific antibodies can be performed in a multiplex fashion using bead-based assays. Such assays are typically based on recombinant virus proteins conjugated to microbeads and enable simultaneous screening for antibodies against a number of viral proteins.37 38

Rapid diagnostic tests

Rapid diagnostic tests (RDTs) can play a key role in early detection of potential RVFV outbreaks, in particular in areas distant from laboratories, and can play a key role in future potential vaccine efficacy trials if their sensitivity and specificity is comparable to the ‘gold-standard’ RT-PCR. Several methods for rapid molecular testing have been developed using protocols based on isothermal amplification (loop-mediated isothermal amplification and RPA-PCR) (by Le Roux et al39 and Euler et al,40 table 4). Both of these methods have under 45 min run time but there are no public data on how they perform compared with RT-PCR. As an alternative to amplification-based methods for detection of RVFV RNA, Zaher et al41 have developed a prototype of a colorimetric method for rapid identification of unamplified RNA with a detection limit of 10 RNA copies/reaction making rapid screening possible in settings with limited technical infrastructure. Further validation and development of this method beyond the prototype stage is still in progress. A report of a pen side veterinary test for diagnosis of RVF using chromatographic strips has also been published.42 This method uses gold-labelled monoclonal antibodies against RVFV N protein and has a detection limit of 103–105 pfu depending on the strain. This rapid test lacks quantitative results but could be used for first-line testing of livestock to detect early stages of suspected disease transmission, and serve as an early warning of potential subsequent human outbreaks.

Table 4

In-house RDTs in development for RVFV detection

Method	Publication	Description
LAMP	Peyrefitte et al. (2008)63	A 30 min qualitative assay. No independent EQA.
LAMP	Le Roux et al. (2009)39	A 30–45 min real-time assay. One EQA study with sensitivity limitations.
RPA-PCR	Eular et al. (2012)40	A qualitative assay with <30 min run time. Detection of a panel of 10 biothreat pathogens. Optimal performance on EQA study in 2012.
Rapid nanogold assay	Zaher et al. (2018)41	Colorimetric assay based on unmodified gold nanoparticles which detects unamplified RVFV RNA. Produces results in 30 min. Prototype stage. No independent EQA.
Pen-side test	Cêtre-Sossah et al. (2019)42	Chromatographic strip coated with antibodies against RVFV N protein. Non-quantitative. No independent EQA.

EQA, external quality assessment; LAMP, loop-mediated isothermal amplification; RDTs, rapid diagnostic tests; RVFV, rift valley fever virus.

Sequencing

Sequencing of the RVFV genome has been used to monitor virus epidemiological spread and geographic distribution of different strains.6 The ability to perform whole-genome sequencing on clinical specimens can aid the identification of new strains as well as the mapping of virus evolution and transmission. Despite the presence of a single serotype, there are 15 RVFV lineages identified43 and they show certain differences in virulence and pathogenicity in animal models,30 44 highlighting the importance of comprehensive genetic characterisation of RVFV for disease management as well. This genetic diversity of RVFV needs to be considered in the design of molecular diagnostic assays to ensure optimal assay sensitivity across all virus lineages. Recent advances in sequencing and comparative genomics for use in outbreak monitoring (eg, nextstrain.org) can further improve our understanding of transmission pathways.

Challenges in RVF diagnosis

Differential diagnosis of RVF is challenging due to the broad overlap of symptoms with other haemorrhagic fevers. Specimens from any suspected cases need to be handled under enhanced BSL-3 conditions and transferred under biological hazard regulations to a respective reference laboratory, requiring trained biomedical professionals. Despite the wide range of commercial and laboratory-developed methods, currently there is not a validated point-of-care diagnostic tool. The commercially available RT-PCR kits can be used for case confirmation, but the short period of viremia requires a combination of the molecular assay with a serological test to ensure reliable detection of cases. The lack of published independent studies evaluating any of the commercial molecular and ELISA assays for humans complicate the use of these tests for large-scale surveillance. Similarly, the quality of in-house methods requires further cross-validation between laboratories to evaluate their applicability for wider use. The necessity for BSL-3 facilities and trained biomedical staff for handling of suspected RVFV samples is particularly challenging in remote areas, close to farms or animal slaughtering facilities where outbreaks are mostly likely to occur. The high overlap of disease symptomology with other febrile illnesses, as well as the need for use of reference laboratories for testing likely lead to underreporting of cases and ongoing virus transmission which eventually increases the epidemic risk associated with RVFV. Epidemiological studies in cohorts or areas with evidence of prior outbreaks are recommended to enable estimation if the true disease burden and validation of existing molecular and serological tests, including RDTs when available.

Importance of diagnostics for RVFV vaccine development

The low antigenic diversity with the presence of a single serotype make RVFV a good target for vaccine development. A large variety of RVFV vaccines for livestock have been developed but primarily used in endemic regions due to the lack of licence for global veterinary use.45–47 Currently, there are no licensed RVFV vaccines for human use and the understanding of the correlates of protection is limited (see in-depth reviews by Faburay et al,48 Dungu et al49 and Ikegami50). As of 2017, there are 15 vaccine candidates at preclinical development stage and two vaccines that have reached clinical development.51 The Coalition for Epidemic Preparedness Innovations is supporting development of several RVF vaccines for use in humans in its portfolio and has currently signed funding agreements with two vaccine awardees to develop a human vaccine against RVFV. The first agreement, worth US$12.5 million is signed with Wageningen Bioveterinary Research in the Netherlands and will be used for vaccine manufacturing, preclinical research, and a phase I study to assess the safety, tolerability, and immunogenicity of a single-dose live attenuated vaccine candidate (RVFV-4s) against RVFV (https://www.larissa.online/about).

The second agreement, worth US$9.5 million is with Colorado State University52 and will be used for manufacturing and preclinical studies to assess a single-dose live attenuated vaccine candidate (DDVax) against RVF. DDVax is a second generation RVF vaccine, which was developed after knocking out the main disease-causing genes from the RVFV genome.

Diagnostics play several key roles in facilitating vaccine development, from mapping of disease burden to case confirmation in efficacy trials.51 A WHO report53 following a consultation on ‘RVF Vaccine and Treatment Evaluation’ highlights the case confirmation by RT-PCR and IgM ELISA as a primary endpoint for vaccine development as well as the DIVA testing as secondary endpoint to determine infection status as a surrogate of protection. The report further recommends the adoption of a One Health approach for diagnostic surveillance as well as vaccine development due to the tight relationship between outbreaks in livestock and in humans.

In addition to efficacy estimation, the reliable estimation of disease incidence in the study area is important for the planning of sample size and feasibility of clinical efficacy trials and their enrolment criteria (figure 1). Conducting clinical trials for development of an RVFV vaccine is complicated by the sporadic nature of RVF outbreaks and their relatively short period of activity (3–7 months), which has an impact on logistical planning of such trials. Therefore, sufficient resources need to be spent on surveillance strengthening both in humans and in livestock (who are the main source of outbreaks in humans) to ensure early detection of infections before an outbreak has occurred. Since outbreaks often occur in remote areas, coordination of efforts among affected areas might be required to determine if the incidence is enabling the setup of a clinical trial likely to be conclusive on vaccine evaluation. To ensure a rapid trial setup with emerging outbreaks, reliable diagnostics need to be validated ahead of time and supported to ensure they have the necessary regulatory approvals for use in the affected countries to be readily deployed.

Figure 1

Outline of diagnostic needs for vaccine development defined by the Coalition for Epidemic Preparedness Innovations (CEPI). RDT, rapid diagnostic tests; RT-PCR, real-time PCR; MERS, Middle-Eastern respiratory virus: NHPs, non-human primates; CMI, cell-mediated immunity;

The validation of molecular and serological assays for RVFV is a stepping stone for the design of epidemiological and ecological studies necessary to estimate the global seroprevalence to RVFV and the spectrum of disease severity in endemic regions and the pattern of disease progression in high-risk groups.

Investment needs in RVFV diagnostics for accelerating RVFV vaccine development

Based on the performed landscaping of diagnostic solutions for RVFV detection and the identified gaps in infrastructure and surveillance methods, we highlight several areas of research and investment needs that can be considered in future consultations to guide WHO recommendations for successful RVFV vaccine development:

Development of target product profile and validation protocols for evaluation of molecular and serological assays (including DIVA testing) for diagnosis of human RVFV.

Providing standards and sample panels to enable validation of diagnostic tests.

Development of RDTs to enable early detection of disease transmission in endemic regions and to facilitate future epidemiology studies.

Estimate incidence and seroprevalence of RVFV in areas and populations at particular risk, to prepare for potential future vaccine efficacy evaluation.

Undertake research to improve the understanding of underlying ecological factors for disease transmission.

Strengthening of surveillance systems in at risk areas and populationsthrough support of RVFV laboratory networks and sample transport systems, as well as through access to RDTs.

Improved RVF response protocols for differential diagnosis and early triaging of patients.

Estimate the societal and economic cost of the RVFV disease burden to evaluate the full public health value of access to a future human RVFV vaccine.

Conclusion

Despite its restricted prevalence in endemic regions in Africa and the Arabic Peninsula, RVFV is a pathogen with high epidemic potential due to the worldwide presence of competent arthropod vectors and the possibility of spill-over events from livestock subject to active international trade. In this context, the development of safe, effective and affordable vaccines for prevention of infection in animals and in humans is a priority. Robust and specific solutions for RVF diagnostics are required to determine seroprevalence, to perform case confirmation and to enable future vaccine efficacy evaluation. Diagnostics need to be easily deployable in areas with disease outbreaks and to provide a reliable measure to differentiate between previous exposure and vaccine-derived immunity. Despite the presence of established diagnostic tests developed to date, substantial efforts are recommended to validate these in field settings most affected by RVFV outbreaks. Due to the high containment level required for handling of suspected cases, local capacity strengthening and diagnostics is recommended to ensure early outbreak detection, case management, continuous pathogen surveillance, and readiness to enable future vaccine evaluation. Although this review focuses on mapping of diagnostic needs for RVFV sampling in humans, the management of RVFV disease should be performed in the context of the broader One Health paradigm. Therefore, any future strategies for RVFV vaccine development should incorporate combined efforts for human and animal prophylaxis to reduce disease prevalence in animals and mitigate the risk of recurrent human outbreaks.

Table 3

In-house and commercially available serological methods for RVFV detection in humans

In-house serological methods for RVFV detection
Method	Publication	Target antibodies	Description
ELISA (DIVA)	McElroy et al. (2009)35	IgM or IgG	Two parallel ELISAs which distinguish natural infections from vaccinations (recombinant N and NSs proteins). Validated in goat and human samples. Does not distinguish IgM versus IgG.
ELISA	Paweska et al. (2005)33	IgM and IgG	IgG sandwich and IgM capture assays for humans made using irradiated whole virus as antigen. Validated on human samples.
ELISA	Paweska et al. (2007)32	IgG	IgG assay for humans, made using recombinant N protein. Validated on human samples.
ELISA	van Vuren Jansen and Paweska (2009)33	IgM and IgG	Separate IgG, IgM indirect ELISAs for humans and ruminants, which uses recombinant N protein.
ELISA	van Vuren et al.(2009)33	IgM or IgG	Sandwich ELISA for ruminants and humans. Does not distinguish IgM versus IgG. Includes preincubation of samples at 56 C 1 hour to reduce biosafety requirements.
VNT	Winchger Schreur et al. (2017)62	Any neutralising antibodies	Uses avirulent RVFV which expresses eGFP. Takes 48 hours and is more sensitive than classic VNT. Not species-specific.
OFIS	Sobarzo et al.(2007)36	IgG	Based on sandwich ELISA. Irradiated RVFV and control antigen are immobilised on an optical fibre. More sensitive to low-levels of serum IgG than standard ELISA. Tested on human samples.
Luminex	Van der Wal et al.(2012)37	IgM and IgG	Bead-based assay for simultaneous detection of antibodies against RVFV Gn and N proteins. Demonstrated utility for DIVA testing.
Luminex	Wu et al.(2014)38	IgG	Designed as a multipathogen assay for virus haemorrhagic fevers including RVFV. No evaluation of diagnostic sensitivity for RVFV in clinical samples.

eGFP, enhanced green fluorescent protein; OFIS, optical fiber immunosensor; VNT, virus neutralisation test.

Commercially available serological methods for RVFV detection
Method	Manufacturer	Approval
IFA RVFV IIFT IgG	EUROIMMUN	CE
IFA RVFV IIFT IgM	EUROIMMUN	CE
ELISA RVFV IgM/IgG	Biological Diagnostic Supplies Limited	CE
ELISA RVFV IgM	ID-Vet	At development and validation stage.

CE, approved for clinical testing; DIVA, distinguish infected from vaccinated individuals; IFA, immunofluorescent antibody; IIFT, indirect immunofluorescence; RVFV, rift valley fever virus.