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Tracking Human Adenovirus Inactivation by Gamma Radiation under Different Environmental Conditions.
Pimenta, Andreia I; Guerreiro, Duarte; Madureira, Joana; Margaça, Fernanda M A; Cabo Verde, Sandra.
Afiliação
  • Pimenta AI; Centro de Ciências e Tecnologias Nucleares (C2TN), Instituto Superior Técnico, Universidade de Lisboa, Bobadela, Loures, Portugal.
  • Guerreiro D; Centro de Ciências e Tecnologias Nucleares (C2TN), Instituto Superior Técnico, Universidade de Lisboa, Bobadela, Loures, Portugal.
  • Madureira J; Centro de Ciências e Tecnologias Nucleares (C2TN), Instituto Superior Técnico, Universidade de Lisboa, Bobadela, Loures, Portugal.
  • Margaça FM; Centro de Ciências e Tecnologias Nucleares (C2TN), Instituto Superior Técnico, Universidade de Lisboa, Bobadela, Loures, Portugal.
  • Cabo Verde S; Centro de Ciências e Tecnologias Nucleares (C2TN), Instituto Superior Técnico, Universidade de Lisboa, Bobadela, Loures, Portugal sandracv@ctn.tecnico.ulisboa.pt.
Appl Environ Microbiol ; 82(17): 5166-73, 2016 09 01.
Article em En | MEDLINE | ID: mdl-27316961
ABSTRACT
UNLABELLED Adenovirus is the most prevalent enteric virus in waters worldwide due to its environmental stability, which leads to public health concerns. Mitigation strategies are therefore required. The aim of this study was to assess the inactivation of human adenovirus type 5 (HAdV-5) by gamma radiation in aqueous environments. Various substrates with different organic loads, including domestic wastewater, were inoculated with HAdV-5 either individually or in a viral pool (with murine norovirus type 1 [MNV-1]) and were irradiated in a Cobalt-60 irradiator at several gamma radiation doses (0.9 to 10.8 kGy). The infectivity of viral particles, before and after irradiation, was tested by plaque assay using A549 cells. D10 values (dose required to inactivate 90% of a population or the dose of irradiation needed to produce a 1 log10 reduction in the population) were estimated for each substrate based on virus infectivity inactivation exponential kinetics. The capability of two detection methods, nested PCR and enzyme-linked immunosorbent assay (ELISA), to track inactivated viral particles was also assessed. After irradiation at 3.5 kGy, a reduction of the HAdV-5 titer of 4 log PFU/ml on substrates with lower organic loads was obtained, but in highly organic matrixes, the virus titer reduction was only 1 log PFU/ml. The D10 values of HAdV-5 in high organic substrates were significantly higher than in water suspensions. The obtained results point out some discrepancies between nested PCR, ELISA, and plaque assay on the assessments of HAdV-5 inactivation. These results suggest that the inactivation of HAdV-5 by gamma radiation, in aqueous environments, is significantly affected by substrate composition. This study highlights the virucidal potential of gamma radiation that may be used as a disinfection treatment for sustainable water supplies. IMPORTANCE Human adenovirus (HAdV) is the most prevalent of the enteric viruses in environmental waters worldwide. The purposes of this study are to provide new insights on the inactivation of enteric virus by gamma irradiation and to introduce new concepts and reinforce the benefits and utility of radiation technologies as disinfection processes. This may be an effective tool to guarantee the reduction of viral pathogens and to contribute to public health and sustainable water supplies.
Assuntos

Texto completo: 1 Coleções: 01-internacional Temas: Geral / Agentes_cancerigenos Base de dados: MEDLINE Assunto principal: Adenovírus Humanos / Desinfecção / Inativação de Vírus / Água Doce Tipo de estudo: Evaluation_studies Limite: Humans Idioma: En Revista: Appl Environ Microbiol Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Portugal

Texto completo: 1 Coleções: 01-internacional Temas: Geral / Agentes_cancerigenos Base de dados: MEDLINE Assunto principal: Adenovírus Humanos / Desinfecção / Inativação de Vírus / Água Doce Tipo de estudo: Evaluation_studies Limite: Humans Idioma: En Revista: Appl Environ Microbiol Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Portugal