How non-enveloped viruses hijack host machineries to cause infection
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作者:
Spriggs, Chelsey C.
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Univ Michigan, Sch Med, Dept Cell & Dev Biol, Ann Arbor, MI 48109 USAUniv Michigan, Sch Med, Dept Cell & Dev Biol, Ann Arbor, MI 48109 USA
Spriggs, Chelsey C.
[1
]
Harwood, Mara C.
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Univ Michigan, Sch Med, Dept Cell & Dev Biol, Ann Arbor, MI 48109 USA
Univ Michigan, Sch Med, Cellular & Mol Biol Program, Ann Arbor, MI 48109 USAUniv Michigan, Sch Med, Dept Cell & Dev Biol, Ann Arbor, MI 48109 USA
Harwood, Mara C.
[1
,2
]
Tsai, Billy
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Univ Michigan, Sch Med, Dept Cell & Dev Biol, Ann Arbor, MI 48109 USA
Univ Michigan, Sch Med, Cellular & Mol Biol Program, Ann Arbor, MI 48109 USAUniv Michigan, Sch Med, Dept Cell & Dev Biol, Ann Arbor, MI 48109 USA
Tsai, Billy
[1
,2
]
机构:
[1] Univ Michigan, Sch Med, Dept Cell & Dev Biol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Med, Cellular & Mol Biol Program, Ann Arbor, MI 48109 USA
Viruses must navigate the complex endomembranous network of the host cell to cause infection. In the case of a non-enveloped virus that lacks a surrounding lipid bilayer, endocytic uptake from the plasma membrane is not sufficient to cause infection. Instead, the virus must travel within organelle membranes to reach a specific cellular destination that supports exposure or arrival of the virus to the cytosol. This is achieved by viral penetration across a host endomembrane, ultimately enabling entry of the virus into the nucleus to initiate infection. In this review, we discuss the entry mechanisms of three distinct non-enveloped DNA viruses-adenovirus (AdV), human papillomavirus (HPV), and polyomavirus (PyV)-highlighting how each exploit different intracellular transport machineries and membrane penetration apparatus associated with the endosome, Golgi, and endoplasmic reticulum (ER) membrane systems to infect a host cell. These processes not only illuminate a highly-coordinated interplay between non-enveloped viruses and their host, but may provide new strategies to combat non-enveloped virus-induced diseases.
机构:
Univ Lille 2, Fac Med, CHRU Lille, Virol Lab,EA3610, F-59037 Lille, FranceUniv Lille 2, Fac Med, CHRU Lille, Virol Lab,EA3610, F-59037 Lille, France
Firquet, Swan
Beaujard, Sophie
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Univ Lille 2, Fac Med, CHRU Lille, Virol Lab,EA3610, F-59037 Lille, FranceUniv Lille 2, Fac Med, CHRU Lille, Virol Lab,EA3610, F-59037 Lille, France
Beaujard, Sophie
Lobert, Pierre-Emmanuel
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Univ Lille 2, Fac Med, CHRU Lille, Virol Lab,EA3610, F-59037 Lille, FranceUniv Lille 2, Fac Med, CHRU Lille, Virol Lab,EA3610, F-59037 Lille, France
Lobert, Pierre-Emmanuel
Sane, Famara
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Univ Lille 2, Fac Med, CHRU Lille, Virol Lab,EA3610, F-59037 Lille, FranceUniv Lille 2, Fac Med, CHRU Lille, Virol Lab,EA3610, F-59037 Lille, France
Sane, Famara
Caloone, Delphine
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Univ Lille 2, Fac Med, CHRU Lille, Virol Lab,EA3610, F-59037 Lille, FranceUniv Lille 2, Fac Med, CHRU Lille, Virol Lab,EA3610, F-59037 Lille, France
Caloone, Delphine
Izard, Daniel
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Univ Lille 2, Fac Med, CHRU Lille, Virol Lab,EA3610, F-59037 Lille, France
CHRU Lille, Bacteriol Lab, F-59037 Lille, FranceUniv Lille 2, Fac Med, CHRU Lille, Virol Lab,EA3610, F-59037 Lille, France
机构:
Univ Michigan, Dept Microbiol & Immunol, Med Sch, Ann Arbor, MI 48109 USA
Univ Ghana, Dept Biochem Cell & Mol Biol, West African Ctr Cell Biol Infect Pathogens, Legon, Accra, GhanaUniv Michigan, Dept Microbiol & Immunol, Med Sch, Ann Arbor, MI 48109 USA
Owusu, Irene A.
Quaye, Osbourne
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Univ Ghana, Dept Biochem Cell & Mol Biol, West African Ctr Cell Biol Infect Pathogens, Legon, Accra, GhanaUniv Michigan, Dept Microbiol & Immunol, Med Sch, Ann Arbor, MI 48109 USA
Quaye, Osbourne
Passalacqua, Karla D.
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Univ Michigan, Dept Microbiol & Immunol, Med Sch, Ann Arbor, MI 48109 USA
Henry Ford Hlth Syst, Detroit, MI 48202 USAUniv Michigan, Dept Microbiol & Immunol, Med Sch, Ann Arbor, MI 48109 USA
Passalacqua, Karla D.
Wobus, Christiane E.
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Univ Michigan, Dept Microbiol & Immunol, Med Sch, Ann Arbor, MI 48109 USAUniv Michigan, Dept Microbiol & Immunol, Med Sch, Ann Arbor, MI 48109 USA