Degradation and inactivation of adenovirus in water by photo-electro-oxidation
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Brazilian Journal of Biology |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1519-69842015000900037 |
Resumo: | The present study analyzed the efficiency of the photo-electro-oxidation process as a method for degradation and inactivation of adenovirus in water. The experimental design employed a solution prepared from sterile water containing 5.107 genomic copies/L (gc/L) of a standard strain of human adenovirus type 5 (HAdV-5) divided into two equal parts, one to serve as control and one treated by photo-electro-oxidation (PEO) for 3 hours and with a 5A current. Samples collected throughout the exposure process were analyzed by real-time polymerase chain reaction (qPCR) for viral genome identification and quantitation. Prior to gene extraction, a parallel DNAse treatment step was carried out to assess the integrity of viral particles. Integrated cell culture (ICC) analyses assessed the viability of infection in a cell culture. The tested process proved effective for viral degradation, with a 7 log10 reduction in viral load after 60 minutes of treatment. The DNAse-treated samples exhibited complete reduction of viral load after a 75 minute exposure to the process, and ICC analyses showed completely non-viable viral particles at 30 minutes of treatment. |
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Brazilian Journal of Biology |
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Degradation and inactivation of adenovirus in water by photo-electro-oxidationadenovirusadvanced oxidation processphoto-electro-oxidationwaterThe present study analyzed the efficiency of the photo-electro-oxidation process as a method for degradation and inactivation of adenovirus in water. The experimental design employed a solution prepared from sterile water containing 5.107 genomic copies/L (gc/L) of a standard strain of human adenovirus type 5 (HAdV-5) divided into two equal parts, one to serve as control and one treated by photo-electro-oxidation (PEO) for 3 hours and with a 5A current. Samples collected throughout the exposure process were analyzed by real-time polymerase chain reaction (qPCR) for viral genome identification and quantitation. Prior to gene extraction, a parallel DNAse treatment step was carried out to assess the integrity of viral particles. Integrated cell culture (ICC) analyses assessed the viability of infection in a cell culture. The tested process proved effective for viral degradation, with a 7 log10 reduction in viral load after 60 minutes of treatment. The DNAse-treated samples exhibited complete reduction of viral load after a 75 minute exposure to the process, and ICC analyses showed completely non-viable viral particles at 30 minutes of treatment.Instituto Internacional de Ecologia2015-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1519-69842015000900037Brazilian Journal of Biology v.75 n.4 suppl.2 2015reponame:Brazilian Journal of Biologyinstname:Instituto Internacional de Ecologia (IIE)instacron:IIE10.1590/1519-6984.00813supplinfo:eu-repo/semantics/openAccessMonteiro,G. S.Staggemeier,R.Klauck,C. R.Bernardes,A. M.Rodrigues,M. A. S.Spilki,F. R.eng2016-01-18T00:00:00Zoai:scielo:S1519-69842015000900037Revistahttps://www.scielo.br/j/bjb/https://old.scielo.br/oai/scielo-oai.phpbjb@bjb.com.br||bjb@bjb.com.br1678-43751519-6984opendoar:2016-01-18T00:00Brazilian Journal of Biology - Instituto Internacional de Ecologia (IIE)false |
dc.title.none.fl_str_mv |
Degradation and inactivation of adenovirus in water by photo-electro-oxidation |
title |
Degradation and inactivation of adenovirus in water by photo-electro-oxidation |
spellingShingle |
Degradation and inactivation of adenovirus in water by photo-electro-oxidation Monteiro,G. S. adenovirus advanced oxidation process photo-electro-oxidation water |
title_short |
Degradation and inactivation of adenovirus in water by photo-electro-oxidation |
title_full |
Degradation and inactivation of adenovirus in water by photo-electro-oxidation |
title_fullStr |
Degradation and inactivation of adenovirus in water by photo-electro-oxidation |
title_full_unstemmed |
Degradation and inactivation of adenovirus in water by photo-electro-oxidation |
title_sort |
Degradation and inactivation of adenovirus in water by photo-electro-oxidation |
author |
Monteiro,G. S. |
author_facet |
Monteiro,G. S. Staggemeier,R. Klauck,C. R. Bernardes,A. M. Rodrigues,M. A. S. Spilki,F. R. |
author_role |
author |
author2 |
Staggemeier,R. Klauck,C. R. Bernardes,A. M. Rodrigues,M. A. S. Spilki,F. R. |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Monteiro,G. S. Staggemeier,R. Klauck,C. R. Bernardes,A. M. Rodrigues,M. A. S. Spilki,F. R. |
dc.subject.por.fl_str_mv |
adenovirus advanced oxidation process photo-electro-oxidation water |
topic |
adenovirus advanced oxidation process photo-electro-oxidation water |
description |
The present study analyzed the efficiency of the photo-electro-oxidation process as a method for degradation and inactivation of adenovirus in water. The experimental design employed a solution prepared from sterile water containing 5.107 genomic copies/L (gc/L) of a standard strain of human adenovirus type 5 (HAdV-5) divided into two equal parts, one to serve as control and one treated by photo-electro-oxidation (PEO) for 3 hours and with a 5A current. Samples collected throughout the exposure process were analyzed by real-time polymerase chain reaction (qPCR) for viral genome identification and quantitation. Prior to gene extraction, a parallel DNAse treatment step was carried out to assess the integrity of viral particles. Integrated cell culture (ICC) analyses assessed the viability of infection in a cell culture. The tested process proved effective for viral degradation, with a 7 log10 reduction in viral load after 60 minutes of treatment. The DNAse-treated samples exhibited complete reduction of viral load after a 75 minute exposure to the process, and ICC analyses showed completely non-viable viral particles at 30 minutes of treatment. |
publishDate |
2015 |
dc.date.none.fl_str_mv |
2015-12-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1519-69842015000900037 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1519-69842015000900037 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/1519-6984.00813suppl |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Instituto Internacional de Ecologia |
publisher.none.fl_str_mv |
Instituto Internacional de Ecologia |
dc.source.none.fl_str_mv |
Brazilian Journal of Biology v.75 n.4 suppl.2 2015 reponame:Brazilian Journal of Biology instname:Instituto Internacional de Ecologia (IIE) instacron:IIE |
instname_str |
Instituto Internacional de Ecologia (IIE) |
instacron_str |
IIE |
institution |
IIE |
reponame_str |
Brazilian Journal of Biology |
collection |
Brazilian Journal of Biology |
repository.name.fl_str_mv |
Brazilian Journal of Biology - Instituto Internacional de Ecologia (IIE) |
repository.mail.fl_str_mv |
bjb@bjb.com.br||bjb@bjb.com.br |
_version_ |
1752129882068877312 |