In Vitro and In Vivo Models for the Study of Human Polyomavirus Infection

被引:18
|
作者
Barth, Heidi [1 ,2 ]
Solis, Morgane [1 ,2 ]
Kack-Kack, Wallys [1 ,2 ]
Soulier, Eric [2 ]
Velay, Aurelie [1 ,2 ]
Fafi-Kremer, Samira [1 ,2 ]
机构
[1] Hop Univ Strasbourg, Lab Virol, 3 Rue Koeberle, F-67000 Strasbourg, France
[2] Univ Strasbourg, INSERM, IRM UMR S 1109, 4 Rue Kirschleger, F-67000 Strasbourg, France
来源
VIRUSES-BASEL | 2016年 / 8卷 / 10期
关键词
polyomavirus; in vitro models; animal models; tropism; entry; pathogenesis; MERKEL CELL POLYOMAVIRUS; PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY; MAJOR CAPSID PROTEINS; SMALL-MOLECULE INHIBITORS; JC VIRUS; BK VIRUS; T-ANTIGENS; TRICHODYSPLASIA-SPINULOSA; CEREBROSPINAL-FLUID; FREQUENT INFECTION;
D O I
10.3390/v8100292
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Developments of genome amplification techniques have rapidly expanded the family of human polyomaviruses (PyV). Following infection early in life, PyV persist in their hosts and are generally of no clinical consequence. High-level replication of PyV can occur in patients under immunosuppressive or immunomodulatory therapy and causes severe clinical entities, such as progressive multifocal leukoencephalopathy, polyomavirus-associated nephropathy or Merkel cell carcinoma. The characterization of known and newly-discovered human PyV, their relationship to human health, and the mechanisms underlying pathogenesis remain to be elucidated. Here, we summarize the most widely-used in vitro and in vivo models to study the PyV-host interaction, pathogenesis and anti-viral drug screening. We discuss the strengths and limitations of the different models and the lessons learned.
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页数:17
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