Recently, three novel human polyomaviruses KIPyV, WUPyV and MCPyV were uncovered in biological specimens of patients with different underlying clinical conditions. Although it is too early to draw firm conclusions on their role in human pathology, this finding has revitalized the scientific debate on the Polyomaviridae family and their relation to human disease. Seroepidemiological studies showed that, similarly to BKPyV and JCPyV, benign primary exposure to these new viruses occurs early in childhood. The viruses then remain latent in the body, and reactivate in immunosuppressed patients with possible pathological consequences. Furthermore, the discovery of MCPyV in a rare and aggressive skin cancer named Merckel cell carcinoma and its clonal integration within the tumor genome suggests that MCPyV infection may represent an early event in the pathogenesis of this disease. This review describes the general aspects of human polyomavirus infection and pathogenesis. Current topics of investigation and future directions in the field are also discussed.

Babakir Mina, M., Ciccozzi, M., Perno, C.f., Ciotti, M. (2011). The novel KI, WU, MC polyomaviruses: possible human pathogens?. NEW MICROBIOLOGICA, 34(1), 1-8.

The novel KI, WU, MC polyomaviruses: possible human pathogens?

PERNO, CARLO FEDERICO;
2011-01-01

Abstract

Recently, three novel human polyomaviruses KIPyV, WUPyV and MCPyV were uncovered in biological specimens of patients with different underlying clinical conditions. Although it is too early to draw firm conclusions on their role in human pathology, this finding has revitalized the scientific debate on the Polyomaviridae family and their relation to human disease. Seroepidemiological studies showed that, similarly to BKPyV and JCPyV, benign primary exposure to these new viruses occurs early in childhood. The viruses then remain latent in the body, and reactivate in immunosuppressed patients with possible pathological consequences. Furthermore, the discovery of MCPyV in a rare and aggressive skin cancer named Merckel cell carcinoma and its clonal integration within the tumor genome suggests that MCPyV infection may represent an early event in the pathogenesis of this disease. This review describes the general aspects of human polyomavirus infection and pathogenesis. Current topics of investigation and future directions in the field are also discussed.
gen-2011
Pubblicato
Rilevanza internazionale
Articolo
Sì, ma tipo non specificato
Settore MED/07 - MICROBIOLOGIA E MICROBIOLOGIA CLINICA
English
Con Impact Factor ISI
Viremia; Polyomavirus Infections; Gastrointestinal Tract; Central Nervous System; Humans; Virus Latency; Skin Neoplasms; Respiratory System; Tumor Virus Infections; Carcinoma, Merkel Cell; Immunocompromised Host; Polyomavirus; Virus Activation
Babakir Mina, M., Ciccozzi, M., Perno, C.f., Ciotti, M. (2011). The novel KI, WU, MC polyomaviruses: possible human pathogens?. NEW MICROBIOLOGICA, 34(1), 1-8.
Babakir Mina, M; Ciccozzi, M; Perno, Cf; Ciotti, M
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/18802
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