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Bat and pig IFN-induced transmembrane protein 3 restrict cell entry by influenza virus and lyssaviruses

IFN-induced transmembrane protein 3 (IFITM3) is a restriction factor that blocks cytosolic entry of numerous viruses that utilize acidic endosomal entry pathways. In humans and mice, IFITM3 limits influenza-induced morbidity and mortality. Although many IFITM3-sensitive viruses are zoonotic, whether...

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Autores principales: Benfield, Camilla T. O., Smith, Sarah E., Wright, Edward, Wash, Rachael S., Ferrara, Francesca, Temperton, Nigel J., Kellam, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for General Microbiology 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4631062/
https://www.ncbi.nlm.nih.gov/pubmed/25614588
http://dx.doi.org/10.1099/vir.0.000058
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author Benfield, Camilla T. O.
Smith, Sarah E.
Wright, Edward
Wash, Rachael S.
Ferrara, Francesca
Temperton, Nigel J.
Kellam, Paul
author_facet Benfield, Camilla T. O.
Smith, Sarah E.
Wright, Edward
Wash, Rachael S.
Ferrara, Francesca
Temperton, Nigel J.
Kellam, Paul
author_sort Benfield, Camilla T. O.
collection PubMed
description IFN-induced transmembrane protein 3 (IFITM3) is a restriction factor that blocks cytosolic entry of numerous viruses that utilize acidic endosomal entry pathways. In humans and mice, IFITM3 limits influenza-induced morbidity and mortality. Although many IFITM3-sensitive viruses are zoonotic, whether IFITMs function as antiviral restriction factors in mammalian species other than humans and mice is unknown. Here, IFITM3 orthologues in the microbat (Myotis myotis) and pig (Sus scrofa domesticus) were identified using rapid amplification of cDNA ends. Amino acid residues known to be important for IFITM3 function were conserved in the pig and microbat orthologues. Ectopically expressed pig and microbat IFITM3 co-localized with transferrin (early endosomes) and CD63 (late endosomes/multivesicular bodies). Pig and microbat IFITM3 restricted cell entry mediated by multiple influenza haemagglutinin subtypes and lyssavirus glycoproteins. Expression of pig or microbat IFITM3 in A549 cells reduced influenza virus yields and nucleoprotein expression. Conversely, small interfering RNA knockdown of IFITM3 in pig NPTr cells and primary microbat cells enhanced virus replication, demonstrating that these genes are functional in their species of origin at endogenous levels. In summary, we showed that IFITMs function as potent broad-spectrum antiviral effectors in two mammals – pigs and bats – identified as major reservoirs for emerging viruses.
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spelling pubmed-46310622015-11-16 Bat and pig IFN-induced transmembrane protein 3 restrict cell entry by influenza virus and lyssaviruses Benfield, Camilla T. O. Smith, Sarah E. Wright, Edward Wash, Rachael S. Ferrara, Francesca Temperton, Nigel J. Kellam, Paul J Gen Virol Animal IFN-induced transmembrane protein 3 (IFITM3) is a restriction factor that blocks cytosolic entry of numerous viruses that utilize acidic endosomal entry pathways. In humans and mice, IFITM3 limits influenza-induced morbidity and mortality. Although many IFITM3-sensitive viruses are zoonotic, whether IFITMs function as antiviral restriction factors in mammalian species other than humans and mice is unknown. Here, IFITM3 orthologues in the microbat (Myotis myotis) and pig (Sus scrofa domesticus) were identified using rapid amplification of cDNA ends. Amino acid residues known to be important for IFITM3 function were conserved in the pig and microbat orthologues. Ectopically expressed pig and microbat IFITM3 co-localized with transferrin (early endosomes) and CD63 (late endosomes/multivesicular bodies). Pig and microbat IFITM3 restricted cell entry mediated by multiple influenza haemagglutinin subtypes and lyssavirus glycoproteins. Expression of pig or microbat IFITM3 in A549 cells reduced influenza virus yields and nucleoprotein expression. Conversely, small interfering RNA knockdown of IFITM3 in pig NPTr cells and primary microbat cells enhanced virus replication, demonstrating that these genes are functional in their species of origin at endogenous levels. In summary, we showed that IFITMs function as potent broad-spectrum antiviral effectors in two mammals – pigs and bats – identified as major reservoirs for emerging viruses. Society for General Microbiology 2015-05 /pmc/articles/PMC4631062/ /pubmed/25614588 http://dx.doi.org/10.1099/vir.0.000058 Text en © 2015 The Authors http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Animal
Benfield, Camilla T. O.
Smith, Sarah E.
Wright, Edward
Wash, Rachael S.
Ferrara, Francesca
Temperton, Nigel J.
Kellam, Paul
Bat and pig IFN-induced transmembrane protein 3 restrict cell entry by influenza virus and lyssaviruses
title Bat and pig IFN-induced transmembrane protein 3 restrict cell entry by influenza virus and lyssaviruses
title_full Bat and pig IFN-induced transmembrane protein 3 restrict cell entry by influenza virus and lyssaviruses
title_fullStr Bat and pig IFN-induced transmembrane protein 3 restrict cell entry by influenza virus and lyssaviruses
title_full_unstemmed Bat and pig IFN-induced transmembrane protein 3 restrict cell entry by influenza virus and lyssaviruses
title_short Bat and pig IFN-induced transmembrane protein 3 restrict cell entry by influenza virus and lyssaviruses
title_sort bat and pig ifn-induced transmembrane protein 3 restrict cell entry by influenza virus and lyssaviruses
topic Animal
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4631062/
https://www.ncbi.nlm.nih.gov/pubmed/25614588
http://dx.doi.org/10.1099/vir.0.000058
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