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The validation of the role of several genes related to Bombyx mori nucleopolyhedrovirus infection in vivo.

Authors :
Wang XY
Zhao CX
Wang X
Zhao ZQ
Su ZH
Xu PZ
Li MW
Wu YC
Source :
Archives of insect biochemistry and physiology [Arch Insect Biochem Physiol] 2021 Feb; Vol. 106 (2), pp. e21762. Date of Electronic Publication: 2021 Jan 08.
Publication Year :
2021

Abstract

Bombyx mori nucleopolyhedrovirus (BmNPV) is one of primary silkworm pathogens and causes a serious damage of cocoon losses every year. Recent years, many works have been done to clarify the silkworm anti-BmNPV mechanism, and a significant progress has been made in screening and studying of genes and proteins related to BmNPV infection, but several of them lacked the proofs in vivo. In this study, to further validate the function of seven newly reported genes in vivo, including BmAtlatin-n, Bmferritin-heavy chain (BmFerHCH), Bmthymosin (BmTHY), Bmseroin1, Bmseroin2, Bmnuclear hormone receptors 96 (BmNHR96), and BmE3 ubiquitin-protein ligase SINA-like 10 (BmSINAL10), the response of them in the midgut, fat body, and hemolymph of differentially resistant strains (resistant strain YeA and susceptible strain YeB) at 48 h following BmNPV infection were analyzed. The results showed that the relative stable or upregulated expression level of BmAtlatin-n, BmTHY, Bmseroin1, and Bmseroin2 in YeA resistant strain following BmNPV infection further indicated their antiviral role in vivo, compared with susceptible YeB strain. Moreover, the significant downregulation of BmFerHCH, BmNHR96, and BmSINAL10 in both strains following BmNPV infection revealed their role in benefiting virus infection, as well as the upregulation of BmFerHCH in YeB midgut and BmSINAL10 in YeB hemolymph. These data could be used to complementary the proofs of the function of these genes in response to BmNPV infection.<br /> (© 2020 Wiley Periodicals LLC.)

Details

Language :
English
ISSN :
1520-6327
Volume :
106
Issue :
2
Database :
MEDLINE
Journal :
Archives of insect biochemistry and physiology
Publication Type :
Academic Journal
Accession number :
33415772
Full Text :
https://doi.org/10.1002/arch.21762