Comparison of internal process control viruses for detection of food and waterborne viruses

Enteric viruses are pathogens associated with foodand waterborne outbreaks. The recovery of viruses from food or water samples is affected by the procedures applied to detect and concentrate them. The incorporation of an internal process control virus to the analyses allows monitoring the performanc...

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Autores principales: Blanco Fernández, María Dolores, Barrios, Melina Elizabeth, Cammarata, Robertina Viviana, Torres, Carolina, Taboga, Oscar Alberto, Mbayed, Viviana Andrea
Formato: Artículo
Lenguaje:Inglés
Publicado: 2017
Materias:
Acceso en línea:http://hdl.handle.net/20.500.12123/951
https://link.springer.com/article/10.1007%2Fs00253-017-8244-2
https://doi.org/10.1007/s00253-017-8244-2
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author Blanco Fernández, María Dolores
Barrios, Melina Elizabeth
Cammarata, Robertina Viviana
Torres, Carolina
Taboga, Oscar Alberto
Mbayed, Viviana Andrea
author_browse Barrios, Melina Elizabeth
Blanco Fernández, María Dolores
Cammarata, Robertina Viviana
Mbayed, Viviana Andrea
Taboga, Oscar Alberto
Torres, Carolina
author_facet Blanco Fernández, María Dolores
Barrios, Melina Elizabeth
Cammarata, Robertina Viviana
Torres, Carolina
Taboga, Oscar Alberto
Mbayed, Viviana Andrea
author_sort Blanco Fernández, María Dolores
collection INTA Digital
description Enteric viruses are pathogens associated with foodand waterborne outbreaks. The recovery of viruses from food or water samples is affected by the procedures applied to detect and concentrate them. The incorporation of an internal process control virus to the analyses allows monitoring the performance of the methodology. The aim of this study was to produce a recombinant adenovirus (rAdV) and apply it together with bacteriophage PP7 as process controls. The rAdV carries a DNA construction in its genome to differentiate it from wild-type adenovirus by qPCR. The stability of both control viruses was evaluated at different pH conditions. The rAdV was stable at pH 3, 7, and 10 for 18 h. PP7 infectious particles were stable at pH 7 and showed a 2.14 log reduction at pH 10 and total decay at pH 3 after 18 h. Three virus concentration methods were evaluated: hollow-fiber tap water ultrafiltration, wastewater ultracentrifugation, and elution-PEG precipitation from lettuce. Total and infectious viruses were quantified and their recoveries were calculated. Virus recovery for rAdV and PP7 by ultrafiltration showed a wide range (2.10–84.42 and 13.54–84.62%, respectively), whereas that by ultracentrifugation was 5.05–13.71 and 6.98–13.27%, respectively. The performance of ultracentrifugation to concentrate norovirus and enteroviruses present in sewage was not significantly different to the recovery of control viruses. For detection of viruses from lettuce, genomic copies of PP7 were significantly more highly recovered than adenovirus (14.74–18.82 and 0.00–3.44%, respectively). The recovery of infectious virus particles was significantly affected during sewage ultracentrifugation and concentration from lettuce. The simultaneous use of virus controls with dissimilar characteristics and behaviors might resemble different enteric viruses.
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spelling INTA9512019-03-22T12:47:15Z Comparison of internal process control viruses for detection of food and waterborne viruses Blanco Fernández, María Dolores Barrios, Melina Elizabeth Cammarata, Robertina Viviana Torres, Carolina Taboga, Oscar Alberto Mbayed, Viviana Andrea Food Technology Wterborne Diseases Disease Control Tecnología de Alimentos Enfermedades Transmitidas por Agua Control de Enfermedades Enteric viruses are pathogens associated with foodand waterborne outbreaks. The recovery of viruses from food or water samples is affected by the procedures applied to detect and concentrate them. The incorporation of an internal process control virus to the analyses allows monitoring the performance of the methodology. The aim of this study was to produce a recombinant adenovirus (rAdV) and apply it together with bacteriophage PP7 as process controls. The rAdV carries a DNA construction in its genome to differentiate it from wild-type adenovirus by qPCR. The stability of both control viruses was evaluated at different pH conditions. The rAdV was stable at pH 3, 7, and 10 for 18 h. PP7 infectious particles were stable at pH 7 and showed a 2.14 log reduction at pH 10 and total decay at pH 3 after 18 h. Three virus concentration methods were evaluated: hollow-fiber tap water ultrafiltration, wastewater ultracentrifugation, and elution-PEG precipitation from lettuce. Total and infectious viruses were quantified and their recoveries were calculated. Virus recovery for rAdV and PP7 by ultrafiltration showed a wide range (2.10–84.42 and 13.54–84.62%, respectively), whereas that by ultracentrifugation was 5.05–13.71 and 6.98–13.27%, respectively. The performance of ultracentrifugation to concentrate norovirus and enteroviruses present in sewage was not significantly different to the recovery of control viruses. For detection of viruses from lettuce, genomic copies of PP7 were significantly more highly recovered than adenovirus (14.74–18.82 and 0.00–3.44%, respectively). The recovery of infectious virus particles was significantly affected during sewage ultracentrifugation and concentration from lettuce. The simultaneous use of virus controls with dissimilar characteristics and behaviors might resemble different enteric viruses. Inst. de Biotecnología Fil: Blanco Fernández, María Dolores. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Cátedra de Virología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Barrios, Melina Elizabeth. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Cátedra de Virología; Argentina. Ministerio de Ciencia y Tecnología. Agencia Nacional de Promoción Científica y Tecnológica; Argentina Fil: Cammarata, Robertina Viviana. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Cátedra de Virología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Torres, Carolina. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Cátedra de Virología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Taboga, Oscar Alberto. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Biotecnología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Mbayed, Viviana Andrea. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Cátedra de Virología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina 2017-08-11T11:50:23Z 2017-08-11T11:50:23Z 2017-05 info:ar-repo/semantics/artículo info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://hdl.handle.net/20.500.12123/951 https://link.springer.com/article/10.1007%2Fs00253-017-8244-2 1432-0614 (Online) 0175-7598 (Print) https://doi.org/10.1007/s00253-017-8244-2 eng info:eu-repo/semantics/restrictedAccess application/pdf Applied microbiology and biotechnology 101 (10) : 4289–4298. (2017)
spellingShingle Food Technology
Wterborne Diseases
Disease Control
Tecnología de Alimentos
Enfermedades Transmitidas por Agua
Control de Enfermedades
Blanco Fernández, María Dolores
Barrios, Melina Elizabeth
Cammarata, Robertina Viviana
Torres, Carolina
Taboga, Oscar Alberto
Mbayed, Viviana Andrea
Comparison of internal process control viruses for detection of food and waterborne viruses
title Comparison of internal process control viruses for detection of food and waterborne viruses
title_full Comparison of internal process control viruses for detection of food and waterborne viruses
title_fullStr Comparison of internal process control viruses for detection of food and waterborne viruses
title_full_unstemmed Comparison of internal process control viruses for detection of food and waterborne viruses
title_short Comparison of internal process control viruses for detection of food and waterborne viruses
title_sort comparison of internal process control viruses for detection of food and waterborne viruses
topic Food Technology
Wterborne Diseases
Disease Control
Tecnología de Alimentos
Enfermedades Transmitidas por Agua
Control de Enfermedades
url http://hdl.handle.net/20.500.12123/951
https://link.springer.com/article/10.1007%2Fs00253-017-8244-2
https://doi.org/10.1007/s00253-017-8244-2
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