ArticlePLoS neglected tropical diseases2012
Role of Bunyamwera Orthobunyavirus NSs protein in infection of mosquito cells.
Article in PLoS neglected tropical diseases, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
31 citing papers in PubMed, 42 citations in OpenAlex.
- Jamestown Canyon Virus Rapidly Adapts to Mosquito Cells Through Multiple M Segment Mutations.Viruses · 2026Article
- Schmallenberg virus non-structural proteins NSs and NSm are not essential for experimental infection ofJournal of virology · 2025Article
- Dicer-2 mutations inThe Journal of general virology · 2024Article
- Bunyamwera Virus Infection ofViruses · 2024Article
- Comparison of Immunogenicity Between a Candidate Live Attenuated Vaccine and an Inactivated Vaccine for Cache Valley Virus.Viral immunology · 2023Article
- Article
- Replication Kinetics of a Candidate Live-Attenuated Vaccine for Cache Valley Virus inVector borne and zoonotic diseases (Larchmont, N.Y.) · 2022Article
- Comparative characterization of the reassortant Orthobunyavirus Ngari with putative parental viruses, Bunyamwera and Batai:The Journal of general virology · 2021Article
- Article
- Characterization of Ebinur Lake Virus and Its Human Seroprevalence at the China-Kazakhstan Border.Frontiers in microbiology · 2019Article
- Arboviruses and the Challenge to Establish Systemic and Persistent Infections in Competent Mosquito Vectors: The Interaction With the RNAi Mechanism.Frontiers in physiology · 2019Review
- Comparison of Schmallenberg virus sequences isolated from mammal host and arthropod vector.Virus genes · 2018Article
- Development of reverse genetics systems and investigation of host response antagonism and reassortment potential for Cache Valley and Kairi viruses, two emerging orthobunyaviruses of the Americas.PLoS neglected tropical diseases · 2018Article
- Antiviral Immunity and Virus-Mediated Antagonism in Disease Vector Mosquitoes.Trends in microbiology · 2018Review
- A Review of Bunyamwera, Batai, and Ngari Viruses: UnderstudiedFrontiers in veterinary science · 2018Review
- Isolation of a novel orthobunyavirus from bat flies (Eucampsipoda africana).The Journal of general virology · 2017Article
- Yellow fever virus capsid protein is a potent suppressor of RNA silencing that binds double-stranded RNA.Proceedings of the National Academy of Sciences of the United States of America · 2016Article
- Review
- Evolutionary and phenotypic analysis of live virus isolates suggests arthropod origin of a pathogenic RNA virus family.Proceedings of the National Academy of Sciences of the United States of America · 2015Article
- Flexibility of bunyavirus genomes: creation of an orthobunyavirus with an ambisense S segment.Journal of virology · 2015Article
Corrections and comments
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Authors and funding
3 authors at 2 institutions in 2 countries.
Funding
Abstract
backgroundBunyamwera orthobunyavirus is both the prototype and study model of the Bunyaviridae family. The viral NSs protein seems to contribute to the different outcomes of infection in mammalian and mosquito cell lines. However, only limited information is available on the growth of Bunyamwera virus in cultured mosquito cells other than the Aedes albopictus C6/36 line. METHODOLOGY AND PRINCIPAL
findingsTo determine potential functions of the NSs protein in mosquito cells, replication of wild-type virus and a recombinant NSs deletion mutant was compared in Ae. albopictus C6/36, C7-10 and U4.4 cells, and in Ae. aegypti Ae cells by monitoring N protein production and virus yields at various times post infection. Both viruses established persistent infections, with the exception of NSs deletion mutant in U4.4 cells. The NSs protein was nonessential for growth in C6/36 and C7-10 cells, but was important for productive replication in U4.4 and Ae cells. Fluorescence microscopy studies using recombinant viruses expressing green fluorescent protein allowed observation of three stages of infection, early, acute and late, during which infected cells underwent morphological changes. In the absence of NSs, these changes were less pronounced. An RNAi response efficiently reduced virus replication in U4.4 cells transfected with virus specific dsRNA, but not in C6/36 or C7/10 cells. Lastly, Ae. aegypti mosquitoes were exposed to blood-meal containing either wild-type or NSs deletion virus, and at various times post-feeding, infection and disseminated infection rates were measured. Compared to wild-type virus, infection rates by the mutant virus were lower and more variable. If the NSs deletion virus was able to establish infection, it was detected in salivary glands at 6 days post-infection, 3 days later than wild-type virus. CONCLUSIONS/SIGNIFICANCE: Bunyamwera virus NSs is required for efficient replication in certain mosquito cell lines and in Ae. aegypti mosquitoes.
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