ArticleScientific reports2015
Superinfection exclusion is absent during acute Junin virus infection of Vero and A549 cells.
Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed.
- Lassa Virus Genetics.Current topics in microbiology and immunology · 2023Article
- Virological and Immunological Outcomes of Coinfections.Clinical microbiology reviews · 2018Review
- It's in the mix: Reassortment of segmented viral genomes.PLoS pathogens · 2018Review
- Crossing the Iron Gate: Why and How Transferrin Receptors Mediate Viral Entry.Annual review of nutrition · 2018Review
- Xapuri virus, a novel mammarenavirus: natural reassortment and increased diversity between New World viruses.Emerging microbes & infections · 2018Article
- New World Arenavirus Biology.Annual review of virology · 2017Review
- Identification and Characterization of a Novel Broad-Spectrum Virus Entry Inhibitor.Journal of virology · 2016Article
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Authors and funding
2 authors.
Funding
Abstract
Many viruses have evolved strategies of so-called "superinfection exclusion" to prevent re-infection of a cell that the same virus has already infected. Although Old World arenavirus infection results in down-regulation of its viral receptor and thus superinfection exclusion, whether New World arenaviruses have evolved such a mechanism remains unclear. Here we show that acute infection by the New World Junin virus (JUNV) failed to down-regulate the transferrin receptor and did not induce superinfection exclusion. We observed that Vero cells infected by a first round of JUNV (Candid1 strain) preserve an ability to internalize new incoming JUNV particles that is comparable to that of non-infected cells. Moreover, we developed a dual infection assay with the wild-type Candid1 JUNV and a recombinant JUNV-GFP virus to discriminate between first and second infections at the transcriptional and translational levels. We found that Vero and A549 cells already infected by JUNV were fully competent to transcribe viral RNA from a second round of infection. Furthermore, flow cytometry analysis of viral protein expression indicated that viral translation was normal, regardless of whether cells were previously infected or not. We conclude that in acutely infected cells, Junin virus lacks a superinfection exclusion mechanism.
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