Literature DB >> 35867576

Early Events in Reovirus Infection Influence Induction of Innate Immune Response.

Andrew T Abad1, Pranav Danthi1.   

Abstract

Mammalian orthoreovirus (reovirus) is a double-stranded RNA (dsRNA) virus which encapsidates its 10 genome segments within a double-layered viral particle. Reovirus infection triggers an antiviral response in host cells which serves to limit viral replication. This antiviral response is initiated by recognition of the incoming viral genome by host sensors present in the cytoplasm. However, how host sensors gain access to the reovirus genome is unclear, as this dsRNA is protected by the viral particle proteins throughout infection. To initiate infection, reovirus particles are endocytosed and the outer viral particle layer is disassembled through the action of host proteases. This disassembly event is required for viral escape into the cytoplasm to begin replication. We show that endosomal proteases are required even late in infection, when disassembly is complete, to induce an immune response to reovirus. Additionally, counter to dogma, our data demonstrate that at least some viral dsRNA genome is exposed and detectable during entry. We hypothesize that some proportion of reovirus particles remain trapped within endosomes, allowing for the breakdown of these particles and release of their genome. We show that rapidly uncoating mutants escape the endosome more rapidly and induce a diminished immune response. Further, we show that particles entering through dynamin-independent pathways evade detection by host sensors. Overall, our data provide new insight into how genomes from entering reovirus particles are detected by host cells. IMPORTANCE Viruses must infect host cells to replicate, often killing the host cell in the process. However, hosts can activate defenses to limit viral replication and protect the organism. To trigger these host defenses to viral infections, host cells must first recognize that they are infected. Mammalian orthoreovirus (reovirus) is a model system used to study host-virus interactions. This study identifies aspects of host and virus biology which determine the capacity of host cells to detect infection. Notably, entry of reovirus into host cells plays a critical role in determining the magnitude of immune response triggered during infection. Mutants of reovirus which can enter cells more rapidly are better at avoiding detection by the host. Additionally, reovirus can enter cells through multiple routes. Entry through some of these routes also helps reovirus evade detection.

Entities:  

Keywords:  innate immunity; reovirus

Mesh:

Substances:

Year:  2022        PMID: 35867576      PMCID: PMC9327682          DOI: 10.1128/jvi.00917-22

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   6.549


  67 in total

1.  The delta region of outer-capsid protein micro 1 undergoes conformational change and release from reovirus particles during cell entry.

Authors:  Kartik Chandran; John S L Parker; Marcelo Ehrlich; Tomas Kirchhausen; Max L Nibert
Journal:  J Virol       Date:  2003-12       Impact factor: 5.103

2.  Interferon production by double-stranded RNA: a comparison of induction by reovirus to that by a synthetic double-stranded polynucleotide.

Authors:  W F Long; D C Burke
Journal:  J Gen Virol       Date:  1971-07       Impact factor: 3.891

3.  Role of the mu 1 protein in reovirus stability and capacity to cause chromium release from host cells.

Authors:  J W Hooper; B N Fields
Journal:  J Virol       Date:  1996-01       Impact factor: 5.103

4.  Virion disassembly is required for apoptosis induced by reovirus.

Authors:  Jodi L Connolly; Terence S Dermody
Journal:  J Virol       Date:  2002-02       Impact factor: 5.103

5.  The epithelial cell response to rotavirus infection.

Authors:  E E Rollo; K P Kumar; N C Reich; J Cohen; J Angel; H B Greenberg; R Sheth; J Anderson; B Oh; S J Hempson; E R Mackow; R D Shaw
Journal:  J Immunol       Date:  1999-10-15       Impact factor: 5.422

6.  Amiloride inhibits macropinocytosis by lowering submembranous pH and preventing Rac1 and Cdc42 signaling.

Authors:  Mirkka Koivusalo; Christopher Welch; Hisayoshi Hayashi; Cameron C Scott; Moshe Kim; Todd Alexander; Nicolas Touret; Klaus M Hahn; Sergio Grinstein
Journal:  J Cell Biol       Date:  2010-02-15       Impact factor: 10.539

7.  Rotavirus structural proteins and dsRNA are required for the human primary plasmacytoid dendritic cell IFNalpha response.

Authors:  Emily M Deal; Maria C Jaimes; Sue E Crawford; Mary K Estes; Harry B Greenberg
Journal:  PLoS Pathog       Date:  2010-06-03       Impact factor: 6.823

8.  Activation of innate immune defense mechanisms by signaling through RIG-I/IPS-1 in intestinal epithelial cells.

Authors:  Yoshihiro Hirata; Alexis H Broquet; Luis Menchén; Martin F Kagnoff
Journal:  J Immunol       Date:  2007-10-15       Impact factor: 5.422

9.  Antiviral immunity via RIG-I-mediated recognition of RNA bearing 5'-diphosphates.

Authors:  Delphine Goubau; Martin Schlee; Safia Deddouche; Andrea J Pruijssers; Thomas Zillinger; Marion Goldeck; Christine Schuberth; Annemarthe G Van der Veen; Tsutomu Fujimura; Jan Rehwinkel; Jason A Iskarpatyoti; Winfried Barchet; Janos Ludwig; Terence S Dermody; Gunther Hartmann; Caetano Reis e Sousa
Journal:  Nature       Date:  2014-08-10       Impact factor: 49.962

Review 10.  Conventional and unconventional mechanisms for capping viral mRNA.

Authors:  Etienne Decroly; François Ferron; Julien Lescar; Bruno Canard
Journal:  Nat Rev Microbiol       Date:  2011-12-05       Impact factor: 60.633

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.