Journalartikel

The Change P82L in the Rift Valley Fever Virus NSs Protein Confers Attenuation in Mice


AutorenlisteBorrego, B; Moreno, S; de la Losa, N; Weber, F; Brun, A

Jahr der Veröffentlichung2021

ZeitschriftViruses

Bandnummer13

Heftnummer4

eISSN1999-4915

Open Access StatusGold

DOI Linkhttps://doi.org/10.3390/v13040542

VerlagMDPI


Abstract

Rift Valley fever virus (RVFV) is a mosquito-borne bunyavirus that causes an important disease in ruminants, with great economic losses. The infection can be also transmitted to humans; therefore, it is considered a major threat to both human and animal health. In a previous work, we described a novel RVFV variant selected in cell culture in the presence of the antiviral agent favipiravir that was highly attenuated in vivo. This variant displayed 24 amino acid substitutions in different viral proteins when compared to its parental viral strain, two of them located in the NSs protein that is known to be the major virulence factor of RVFV. By means of a reverse genetics system, in this work we have analyzed the effect that one of these substitutions, P82L, has in viral attenuation in vivo. Rescued viruses carrying this single amino acid change were clearly attenuated in BALB/c mice while their growth in an interferon (IFN)-competent cell line as well as the production of interferon beta (IFN-beta) did not seem to be affected. However, the pattern of nuclear NSs accumulation was modified in cells infected with the mutant viruses. These results highlight the key role of the NSs protein in the modulation of viral infectivity.




Zitierstile

Harvard-ZitierstilBorrego, B., Moreno, S., de la Losa, N., Weber, F. and Brun, A. (2021) The Change P82L in the Rift Valley Fever Virus NSs Protein Confers Attenuation in Mice, Viruses, 13(4), Article 542. https://doi.org/10.3390/v13040542

APA-ZitierstilBorrego, B., Moreno, S., de la Losa, N., Weber, F., & Brun, A. (2021). The Change P82L in the Rift Valley Fever Virus NSs Protein Confers Attenuation in Mice. Viruses. 13(4), Article 542. https://doi.org/10.3390/v13040542



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