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IFITM-Family Proteins: The Cell's First Line of Antiviral Defense

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TLDR
The discovery and characterization of the IFITM proteins are reviewed, the spectrum of their antiviral activities are described, and potential mechanisms underlying these effects are discussed.
Abstract
Animal cells use a wide variety of mechanisms to slow or prevent replication of viruses. These mechanisms are usually mediated by antiviral proteins whose expression and activities can be constitutive but are frequently amplified by interferon induction. Among these interferon-stimulated proteins, members of the IFITM (interferon-induced transmembrane) family are unique because they prevent infection before a virus can traverse the lipid bilayer of the cell. At least three human IFITM proteins—IFITM1, IFITM2, and IFITM3—have antiviral activities. These activities limit infection in cultured cells by many viruses, including dengue virus, Ebola virus, influenza A virus, severe acute respiratory syndrome coronavirus, and West Nile virus. Murine Ifitm3 controls influenza A virus infection in vivo, and polymorphisms in human IFITM3 correlate with the severity of both seasonal and highly pathogenic avian influenza virus. Here we review the discovery and characterization of the IFITM proteins, describe the spectrum of their antiviral activities, and discuss potential mechanisms underlying these effects.

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Journal ArticleDOI

SARS-CoV-2 Receptor ACE2 Is an Interferon-Stimulated Gene in Human Airway Epithelial Cells and Is Detected in Specific Cell Subsets across Tissues.

Carly G. K. Ziegler, +135 more
- 28 May 2020 - 
TL;DR: The data suggest that SARS-CoV-2 could exploit species-specific interferon-driven upregulation of ACE2, a tissue-protective mediator during lung injury, to enhance infection.
Journal ArticleDOI

The Multifaceted Functions of Neutrophils

TL;DR: Primordial neutrophil functions are discussed, and more recent evidence that interactions between neutrophils and adaptive immune cells establish a feed-forward mechanism that amplifies pathologic inflammation is presented.
Journal ArticleDOI

Human Coronavirus: Host-Pathogen Interaction.

TL;DR: The current knowledge of host factors co-opted and signaling pathways activated during HCoV infection is summarized, with an emphasis on H CoV-infection-induced stress response, autophagy, apoptosis, and innate immunity.
Journal ArticleDOI

Interplay between SARS-CoV-2 and the type I interferon response.

TL;DR: The potential benefits of a well-timed IFN-I treatment and strategies to boost pDC-mediated IFN responses during the early stages of viral infection are discussed.
Journal ArticleDOI

Fusion of Enveloped Viruses in Endosomes

TL;DR: A key take‐home message is that enveloped viruses that enter cells by fusing in endosomes traverse the endocytic pathway until they reach an endosome that has all of the environmental conditions to trigger the fusion protein and to support membrane fusion.
References
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Journal ArticleDOI

Angiotensin-converting enzyme 2 is a functional receptor for the SARS coronavirus.

TL;DR: It is found that a soluble form of ACE2, but not of the related enzyme ACE1, blocked association of the S1 domain with Vero E6 cells, indicating that ACE2 is a functional receptor for SARS-CoV.
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A diverse range of gene products are effectors of the type I interferon antiviral response

TL;DR: It is shown that different viruses are targeted by unique sets of ISGs, and that each viral species is susceptible to multiple antiviral genes, which together encompass a range of inhibitory activities.
Journal ArticleDOI

A molecular programme for the specification of germ cell fate in mice

TL;DR: It is shown that fragilis, an interferon-inducible transmembrane protein, marks the onset of germ cell competence, and it is proposed that through homotypic association, it demarcates germ cells from somatic neighbours.
Journal ArticleDOI

Endosomal Proteolysis of the Ebola Virus Glycoprotein Is Necessary for Infection

TL;DR: Biochemical studies demonstrate that CatB and CatL mediate entry by carrying out proteolysis of the EboV GP subunit GP1 and support a multistep mechanism that explains the relative contributions of these enzymes to infection.
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