Abstract
BackgroundFlaviviruses are representative arboviruses carried by arthropods and/or vertebrates; these viruses can pose a public health concern in many countries. By contrast, it is known that a novel virus group called insect-specific flaviviruses (ISFs) also infects arthropods, although no such virus has yet been isolated from vertebrates. The characteristics of ISFs, which affect replication of human-pathogenic flaviviruses within co-infected mosquito cells or mosquitoes without affecting the mosquitoes themselves, mean that we should pay attention to both ISFs and human-pathogenic flaviviruses, despite the fact that ISFs appear not to be directly hazardous to human health. To assess the risk of diseases caused by flaviviruses, and to better understand their ecology, it is necessary to know the extent to which flaviviruses are harbored by arthropods.MethodsWe developed a novel universal primer for use in a PCR-based system to detect a broad range of flaviviruses. We then evaluated its performance. The utility of the novel primer pair was evaluated in a PCR assay using artificially synthesized oligonucleotides derived from a template viral genome sequence. The utility of the primer pair was also examined by reverse transcription PCR (RT-PCR) using cDNA templates prepared from virus-infected cells or crude supernatants prepared from virus-containing mosquito homogenates.ResultsThe novel primer pair amplified the flavivirus NS5 sequence (artificially synthesized) in all samples tested (six species of flavivirus that can cause infectious diseases in humans, and flaviviruses harbored by insects). In addition, the novel primer pair detected viral genomes in cDNA templates prepared from mosquito cells infected with live flavivirus under different infectious conditions. Finally, the viral genome was detected with high sensitivity in crude supernatants prepared from pooled mosquito homogenates.ConclusionThis PCR system based on a novel primer pair makes it possible to detect arthropod-borne flaviviruses worldwide (the primer pair even detected viruses belonging to different genetic subgroups). As such, an assay based on this primer pair may help to improve public health and safety, as well as increase our understanding of flavivirus ecology.
Highlights
Flaviviruses are representative arboviruses carried by arthropods and/or vertebrates; these viruses can pose a public health concern in many countries
The intensity of the PCR products generated by FUDJ9166/ CFDJ9977 and pan-flavivirus FW/RV was high; the intensity of those generated by the other primer pairs (i.e., FU1/cFD2, MA/cFD2, and EMF1/VD8) were not as high as that generated by pan-flavivirus FW/ RV, indicating that these primer pairs are not the preferred choice for further analyses such as gene sequencing
The results showed that individual nucleotide sequences, excluding the PCR primers and unread regions at both ends of the PCR products, were 100% identical to the sequences of the templates (Type II Dengue virus (DENV), Zika virus (ZIKV), Japanese encephalitis virus (JEV), West Nile virus (WNV), Yellow fever virus (YFV), Tickborne encephalitis virus (TBEV), Aedes flavivirus, and Culex flavivirus)
Summary
Flaviviruses are representative arboviruses carried by arthropods and/or vertebrates; these viruses can pose a public health concern in many countries. It is known that a novel virus group called insect-specific flaviviruses (ISFs) infects arthropods, no such virus has yet been isolated from vertebrates. Because some ISFs enhance or suppress replication of humanpathogenic flaviviruses within co-infected mosquito cells or mosquito laboratory colonies [19, 33,34,35,36], attention should be paid to both ISFs and human-pathogenic flaviviruses, even though ISFs appear not to be directly hazardous to human health. To better assess the risk posed by flavivirus-induced diseases in humans, and to increase our understanding of the ecology of flaviviruses, we need to examine the distribution and diversity of flaviviruses using a broad detection system that can detect a wide range of these viruses in arthropods, which are known reservoirs
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