Utilize este identificador para referenciar este registo: http://hdl.handle.net/10362/36468
Título: Implications of hepatitis C virus subtype 1a migration patterns for virus genetic sequencing policies in Italy
Autor: Cuypers, Lize
Vrancken, Bram
Fabeni, Lavinia
Marascio, Nadia
Cento, Valeria
Di Maio, Velia Chiara
Aragri, Marianna
Pineda-Peña, Andrea Clemencia
Schrooten, Yoeri
Van Laethem, Kristel
Balog, Daniel
Focà, Alfredo
Torti, Carlo
Nevens, Frederik
Perno, Carlo Federico
Vandamme, Anne Mieke
Ceccherini-Silberstein, Francesca
Palavras-chave: Europe
HCV
HCV1a
Italy
Phylogeography
Public health policy
Q80K
US
Ecology, Evolution, Behavior and Systematics
SDG 3 - Good Health and Well-being
SDG 10 - Reduced Inequalities
Data: 7-Mar-2017
Resumo: Background: In-depth phylogeographic analysis can reveal migration patterns relevant for public health planning. Here, as a model, we focused on the provenance, in the current Italian HCV subtype 1a epidemic, of the NS3 resistance-associated variant (RAV) Q80K, known to interfere with the action of NS3/4A protease inhibitor simeprevir. HCV1a migration patterns were analysed using Bayesian phylodynamic tools, capitalising on newly generated and publicly available time and geo-referenced NS3 encoding virus genetic sequence data. Results: Our results showed that both immigration and local circulation fuel the current Italian HCV1a epidemic. The United States and European continental lineages dominate import into Italy, with the latter taking the lead from the 1970s onwards. Since similar migration patterns were found for Q80K and other lineages, no clear differentiation of the risk for failing simeprevir can be made between patients based on their migration and travel history. Importantly, since HCV only occasionally recombines, these results are readily transferable to the genetic sequencing policy concerning NS5A RAVs. Conclusions: The patient migration and travel history cannot be used to target only part of the HCV1a infected population for drug resistance testing before start of antiviral therapy. Consequently, it may be cost-effective to expand genotyping efforts to all HCV1a infected patients eligible for simeprevir-based therapies.
Peer review: yes
URI: http://www.scopus.com/inward/record.url?scp=85014646353&partnerID=8YFLogxK
DOI: https://doi.org/10.1186/s12862-017-0913-3
ISSN: 1471-2148
Aparece nas colecções:IHMT: MM - Artigos em revista internacional com arbitragem científica

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