Persistent Reptarenavirus and Hartmanivirus Infection in Cultured Boid Cells

Microbiol Spectr. Article Link >
Annika Lintala, Leonora Szirovicza, Anja Kipar, Udo Hetzel, Jussi Hepojoki
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Gene Synthesis For producing a recombinant protein in Escherichia coli, we used a codon-optimized synthetic gene encoding the above-mentioned amino acid stretches separated by five glycine residues and followed by three glycine residues in the pET-20b(+) vector from Gene Universal. Get A Quote

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For producing a recombinant protein in Escherichia coli, we used a codon-optimized synthetic gene encoding the above-mentioned amino acid stretches separated by five glycine residues and followed by three glycine residues in the pET-20b(+) vector from Gene Universal.

Abstract

Mammarenaviruses establish a persistent infection in their rodent and bat hosts, and the evidence suggests that reptarenaviruses and hartmaniviruses found in captive snakes act similarly. In snakes, reptarenaviruses cause boid inclusion body disease (BIBD), which is often associated with secondary infections. Snakes with BIBD usually carry more than a single pair of reptarenavirus S and L segments and occasionally demonstrate hartmanivirus coinfection. Here, we reported the generation of cell lines persistently infected with a single or two reptarenavirus(es) and a cell line with persistent reptarenavirus-hartmanivirus coinfection. By RT-PCR we demonstrated that the amount of viral RNA within the persistently infected cells remains at levels similar to those observed following initial infection. Using antibodies against the glycoproteins (GPs) and nucleoprotein (NP) of reptarenaviruses, we studied the levels of viral protein in cells passaged 10 times after the original inoculation and observed that the expression of GPs declines dramatically during persistent infection, unlike the expression of NP. Immunofluorescence (IF) staining served to demonstrate differences in the distribution of NP within the persistently infected compared to freshly infected cells. IF staining of cells inoculated with the viruses secreted from the persistently infected cell lines produced similar NP staining compared to cells infected with a traditionally passaged virus, suggesting that the altered NP expression pattern of persistently infected cells does not relate to changes in the virus. The cell cultures described herein can serve as tools for studying the coinfection and superinfection interplay between reptarenaviruses and studying the BIBD pathogenesis mechanisms.

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