Proteomic analysis of murine norovirus-infected Raw 264.7 cells reveals the induction of Ras GTPases

Abstract The human norovirus (abbreviated as HuNV) is the most common agent responsible for acute viral gastroenteritis. Despite being recognized as a water-borne pathogenic virus for a long time, the cellular tropism of norovirus has not yet been clearly explained. The main reason is the lack of ap...

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Main Authors: Sung Ho Yun, Md Arif-Ur Rahman, Soo-Bin Nam, Soo Hyeon Kim, Gyuri Kim, Kun Cho, Jong-Soon Choi
Format: Article
Language:English
Published: SpringerOpen 2025-01-01
Series:Journal of Analytical Science and Technology
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Online Access:https://doi.org/10.1186/s40543-024-00470-0
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author Sung Ho Yun
Md Arif-Ur Rahman
Soo-Bin Nam
Soo Hyeon Kim
Gyuri Kim
Kun Cho
Jong-Soon Choi
author_facet Sung Ho Yun
Md Arif-Ur Rahman
Soo-Bin Nam
Soo Hyeon Kim
Gyuri Kim
Kun Cho
Jong-Soon Choi
author_sort Sung Ho Yun
collection DOAJ
description Abstract The human norovirus (abbreviated as HuNV) is the most common agent responsible for acute viral gastroenteritis. Despite being recognized as a water-borne pathogenic virus for a long time, the cellular tropism of norovirus has not yet been clearly explained. The main reason is the lack of appropriate cell culture and animal model systems for HuNV infection. Murine norovirus (abbreviated as MNV) is often used as a proxy for human norovirus when trying to understand the expression profiles left behind by norovirus infection in a host. In the current study, the host response to MNV was examined using the macrophage Raw 264.7 in terms of the altered host proteomes. After MNV infection, host Raw 264.7 cell lysates were collected for proteome profiling at the time points of 0.5 hpi (early phase, control), 16 hpi (mid-phase), and 24 hpi (late phase). LC–MS analysis was employed for label-free shotgun proteomics on the host cell proteomes. The progression of MNV infection status was monitored using an immunofluorescence-conjugated noroviral capsid protein VP1 and a confocal microscope. The up-regulation of Ras GTPases such Rab5A and Rab6A was found to be implicated in norovirus gastroenteritis, as revealed by proteomic profiling. Consequently, the recognition of Ras-related proteins can lead to a better understanding of how noroviral infection affects the immune system of the host cell.
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spelling doaj-art-009961b672c843b3a20e842371e355dd2025-01-19T12:26:37ZengSpringerOpenJournal of Analytical Science and Technology2093-33712025-01-0116111010.1186/s40543-024-00470-0Proteomic analysis of murine norovirus-infected Raw 264.7 cells reveals the induction of Ras GTPasesSung Ho Yun0Md Arif-Ur Rahman1Soo-Bin Nam2Soo Hyeon Kim3Gyuri Kim4Kun Cho5Jong-Soon Choi6Digital Omics Research Center, Korea Basic Science InstituteGraduate School of Analytical Science and Technology, Chungnam National UniversityGraduate School of Analytical Science and Technology, Chungnam National UniversityGraduate School of Analytical Science and Technology, Chungnam National UniversityDigital Omics Research Center, Korea Basic Science InstituteDigital Omics Research Center, Korea Basic Science InstituteDigital Omics Research Center, Korea Basic Science InstituteAbstract The human norovirus (abbreviated as HuNV) is the most common agent responsible for acute viral gastroenteritis. Despite being recognized as a water-borne pathogenic virus for a long time, the cellular tropism of norovirus has not yet been clearly explained. The main reason is the lack of appropriate cell culture and animal model systems for HuNV infection. Murine norovirus (abbreviated as MNV) is often used as a proxy for human norovirus when trying to understand the expression profiles left behind by norovirus infection in a host. In the current study, the host response to MNV was examined using the macrophage Raw 264.7 in terms of the altered host proteomes. After MNV infection, host Raw 264.7 cell lysates were collected for proteome profiling at the time points of 0.5 hpi (early phase, control), 16 hpi (mid-phase), and 24 hpi (late phase). LC–MS analysis was employed for label-free shotgun proteomics on the host cell proteomes. The progression of MNV infection status was monitored using an immunofluorescence-conjugated noroviral capsid protein VP1 and a confocal microscope. The up-regulation of Ras GTPases such Rab5A and Rab6A was found to be implicated in norovirus gastroenteritis, as revealed by proteomic profiling. Consequently, the recognition of Ras-related proteins can lead to a better understanding of how noroviral infection affects the immune system of the host cell.https://doi.org/10.1186/s40543-024-00470-0Murine norovirusViral infectionLabel-free shotgun proteomicsRas GTPase
spellingShingle Sung Ho Yun
Md Arif-Ur Rahman
Soo-Bin Nam
Soo Hyeon Kim
Gyuri Kim
Kun Cho
Jong-Soon Choi
Proteomic analysis of murine norovirus-infected Raw 264.7 cells reveals the induction of Ras GTPases
Journal of Analytical Science and Technology
Murine norovirus
Viral infection
Label-free shotgun proteomics
Ras GTPase
title Proteomic analysis of murine norovirus-infected Raw 264.7 cells reveals the induction of Ras GTPases
title_full Proteomic analysis of murine norovirus-infected Raw 264.7 cells reveals the induction of Ras GTPases
title_fullStr Proteomic analysis of murine norovirus-infected Raw 264.7 cells reveals the induction of Ras GTPases
title_full_unstemmed Proteomic analysis of murine norovirus-infected Raw 264.7 cells reveals the induction of Ras GTPases
title_short Proteomic analysis of murine norovirus-infected Raw 264.7 cells reveals the induction of Ras GTPases
title_sort proteomic analysis of murine norovirus infected raw 264 7 cells reveals the induction of ras gtpases
topic Murine norovirus
Viral infection
Label-free shotgun proteomics
Ras GTPase
url https://doi.org/10.1186/s40543-024-00470-0
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