Table 1.
Test | Test Type | Virus Detected | Target Gene | Biological Matrix | Reference Assay | Sample Size | Sensitivity | Specificity | Author |
---|---|---|---|---|---|---|---|---|---|
RVFV RT-nested PCR | Homemade one-step RT-PCR nested method | RVFV different strains (Gabek forest, Gordil, saint Floris, Arumwot, Belterra, ArD38661, AnD100286, MP 12) | NS coding region of S segment | Virus produced in Vero E6 cells; serum from infected mice | Virus isolation method | ND | 0.5 pfu/reaction | Nd | Sall et al., 2001 [45] |
RVFV quantitative real-time PCR | qRT-PCR with fluorescent signal from probes for quality control | RVFV; MP12, ZH501, ZH548, ArD38661, 74 HB59 strains | NS coding region of S segment | Virus produced in Vero E6 cells; serum from infected mice | ND | ND | 50–100 copies/reaction | No amplification with Toscana, Icoraci, and Belterra closely related phlebovirus | Garcia et al., 2001 [46] |
RT-Real-time PCR | 5′ nuclease technology on a light cycler instrument | RVFV | G2 gene | Synthetic RNA | ND | ND | 2835 geq/mL | no cross-reactivity with other HCV, HBV, HSV1, CMV, Modoc virus, Mycobacterium tuberculosis, Mycobacterium leprae, Borrelia spp., Leptospira spp., Neisseria spp., Plasmodium spp., Leishmania spp. | Drosten et al., 2002 [48] |
RT-Real-time PCR homemade |
Fluorescent nested PCR TaqMan assay | RVFV | S segment | Synthetic RNA | ND | ND | 100 copies/reaction | SFNV cell culture | Weidmann et al., 2008 [47] |
Real-time qRT-PCR homemade |
qRT-PCR with fluorescent reporter dye detected at each PCR cycle | RVFV | G2 gene | Plasma of suspected patients with HVF | 272 RVFV confirmed cases | 2ND | 100 infectious particles/mL | IgM anti RVFV positive sera 100% |
Njenga et al., 2009 [49] |
RT-LAMP homemade |
Reverse transcription-loop-mediated isothermal amplification with a vertical | RVFV | L segment | Serum samples | TaqMan Real Time | 64 | Whole blood: LLOD: 10 copies RNA/reaction | No cross reactivity with phleboviruses; flaviviruses and chikungunja virus |
Peyrefitte et al., 2008 [50] |
RT-LAMP homemade |
Reverse transcription-loop-mediated isothermal amplification with a vertical | RVFV | L segment | Bleed samples from sheep (n = 20), human plasma from suspected cases (n = 65); 3 liver, kidney, serum from animals | Whole blood: LLOD: 10 copies/ reaction |
Six African phleboviruses and unrelated arbovirus did not give cross reactivity | Le Roux et al., 2009 [51] |
||
RT-LAMP homemade |
Reverse transcription-loop-mediated isothermal amplification | RVFV | S segment | Synthetic RNA | Real-time RT-PCR | ND | whole blood: LLOD: 1.94 copies/microliters within 60 min | No cross reactivity with JEV, H3N2 influenza virus, EBOV, MARV |
Han et al., 2020 [52] |
RT-LAMP homemade |
Reverse transcription-loop-mediated isothermal amplification | RVFV | M segment | Blood samples | Real-time RT-PCR | 130 | 98.36% sensitivity | 100%; no cross-reactivity with PPR and capripox viruses | Wekesa et al., 2023 [54] |
Isothermal recombinase polymerase amplification (RPA) | Isothermal exponential nucleic acid amplification and detection method | RVFV | S segment | Synthetic RNA | ND | ND | 19RNA molecules/reaction | No cross reactivity with Yersinia pestis, Francisella tularensis, Bacillus antracis, vaccinia virus, Ebola virus, Marburg virus, Crimean–Congo virus and phleboviruses |
Euler et al., 2012 [53] |
RT-qPCR genotyping assay | One step RT-qPCR for typing different strains of RVFV, melting curve to identify different strains of RVFV | RVFV | L, M, S segments | ND | Sanger sequencing | ND | Balaraman et al., 2023 [56] |
||
BioT DNA multiplex PCR-enzyme hybridization assay | Multiplex RT-PCR | RVFV | GP2 gene | 196 swabs, 45 skin swabs,15 serum, 7 sputum | ND | 260 clinical samples | 105–106 copies/mL with nucleic acid extraction | No cross reactivity with Influenza A, EBV, CMV, RSV A, ADV C, human metapneumovirus | He et al., 2009 [55] |
Oligonucleotide microarray | Microarray | RVFV | GP gene | Culture samples | Real-time PCR | 60 | 100% | Yao et al., 2021 [57] |
|
Real-time qRT-PCR commercial |
qRT-PCR with fluorescent reporter dye detected at each PCR cycle | RVFV | 0.89 copies/μL | cross-reactivity with flavivirus, Marburg virus, and Ebola virus | [61] |
ADV, adenovirus; CMV, cytomegalovirus; RSV, respiratory syncytial virus; JEV, Japanese encephalitis virus.