Concentration and detection of hepatitis A virus and its indicator from artificial seawater using zeolite

•Zeolite was able to concentrate 99% of hepatitis A virus from artificial seawater.•SDS (5%, pH 11.2) was able to elute 5.5 out of 7.7 log units of HAV from zeolite.•The described concentration/elution process can be completed in 2h.•The concentration/elution efficiency was highest in 10ppt artifici...

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Published inJournal of virological methods Vol. 235; pp. 1 - 8
Main Authors Cormier, Jiemin, Janes, Marlene
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.09.2016
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Abstract •Zeolite was able to concentrate 99% of hepatitis A virus from artificial seawater.•SDS (5%, pH 11.2) was able to elute 5.5 out of 7.7 log units of HAV from zeolite.•The described concentration/elution process can be completed in 2h.•The concentration/elution efficiency was highest in 10ppt artificial seawater. Hepatitis A virus (HAV) infection is the leading worldwide cause of acute viral hepatitis, and outbreaks caused by this virus often occur in fecal polluted waters. Rapid concentration and detection of viral contamination in water environments can prevent economic loss and can identify the source of contamination within a short time. However, conventional methods for virus concentration are often laborious, time consuming, and subject to clogging. Furthermore, most methods require a secondary concentration step to reduce the final volume of samples. We developed a method to concentrate HAV from seawater using zeolite in aid of rapid detection. In this method,artificial seawater was inoculated with HAV (7–8 log TCID50) and filtered with zeolite. The viruses were then eluted from zeolite with sodium dodecyl sulfate and detected via real-time PCR (qPCR). Zeolite was able to concentrate HAV from artificial seawater with ∼99% efficiency in less than 5min and was more efficient in seawater than in fresh water. The entire concentration and detection can be done in approximately 2h. Compared to existing methods, this method eliminated the need for a secondary concentration step as well as the necessity to modify the pH or salinity of the seawater during concentration, and was simple and inexpensive.
AbstractList Hepatitis A virus (HAV) infection is the leading worldwide cause of acute viral hepatitis, and outbreaks caused by this virus often occur in fecal polluted waters. Rapid concentration and detection of viral contamination in water environments can prevent economic loss and can identify the source of contamination within a short time. However, conventional methods for virus concentration are often laborious, time consuming, and subject to clogging. Furthermore, most methods require a secondary concentration step to reduce the final volume of samples. We developed a method to concentrate HAV from seawater using zeolite in aid of rapid detection. In this method,artificial seawater was inoculated with HAV (7-8 log TCID50) and filtered with zeolite. The viruses were then eluted from zeolite with sodium dodecyl sulfate and detected via real-time PCR (qPCR). Zeolite was able to concentrate HAV from artificial seawater with ∼99% efficiency in less than 5min and was more efficient in seawater than in fresh water. The entire concentration and detection can be done in approximately 2h. Compared to existing methods, this method eliminated the need for a secondary concentration step as well as the necessity to modify the pH or salinity of the seawater during concentration, and was simple and inexpensive.
Hepatitis A virus (HAV) infection is the leading worldwide cause of acute viral hepatitis, and outbreaks caused by this virus often occur in fecal polluted waters. Rapid concentration and detection of viral contamination in water environments can prevent economic loss and can identify the source of contamination within a short time. However, conventional methods for virus concentration are often laborious, time consuming, and subject to clogging. Furthermore, most methods require a secondary concentration step to reduce the final volume of samples. We developed a method to concentrate HAV from seawater using zeolite in aid of rapid detection. In this method,artificial seawater was inoculated with HAV (7-8 log TCID50) and filtered with zeolite. The viruses were then eluted from zeolite with sodium dodecyl sulfate and detected via real-time PCR (qPCR). Zeolite was able to concentrate HAV from artificial seawater with 99% efficiency in less than 5min and was more efficient in seawater than in fresh water. The entire concentration and detection can be done in approximately 2h. Compared to existing methods, this method eliminated the need for a secondary concentration step as well as the necessity to modify the pH or salinity of the seawater during concentration, and was simple and inexpensive.
•Zeolite was able to concentrate 99% of hepatitis A virus from artificial seawater.•SDS (5%, pH 11.2) was able to elute 5.5 out of 7.7 log units of HAV from zeolite.•The described concentration/elution process can be completed in 2h.•The concentration/elution efficiency was highest in 10ppt artificial seawater. Hepatitis A virus (HAV) infection is the leading worldwide cause of acute viral hepatitis, and outbreaks caused by this virus often occur in fecal polluted waters. Rapid concentration and detection of viral contamination in water environments can prevent economic loss and can identify the source of contamination within a short time. However, conventional methods for virus concentration are often laborious, time consuming, and subject to clogging. Furthermore, most methods require a secondary concentration step to reduce the final volume of samples. We developed a method to concentrate HAV from seawater using zeolite in aid of rapid detection. In this method,artificial seawater was inoculated with HAV (7–8 log TCID50) and filtered with zeolite. The viruses were then eluted from zeolite with sodium dodecyl sulfate and detected via real-time PCR (qPCR). Zeolite was able to concentrate HAV from artificial seawater with ∼99% efficiency in less than 5min and was more efficient in seawater than in fresh water. The entire concentration and detection can be done in approximately 2h. Compared to existing methods, this method eliminated the need for a secondary concentration step as well as the necessity to modify the pH or salinity of the seawater during concentration, and was simple and inexpensive.
Author Cormier, Jiemin
Janes, Marlene
Author_xml – sequence: 1
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  fullname: Cormier, Jiemin
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  surname: Janes
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  email: mjanes@agcenter.lsu.edu
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Keywords Hepatitis A virus
Zeolite
Concentration
Seawater
Language English
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Snippet •Zeolite was able to concentrate 99% of hepatitis A virus from artificial seawater.•SDS (5%, pH 11.2) was able to elute 5.5 out of 7.7 log units of HAV from...
Hepatitis A virus (HAV) infection is the leading worldwide cause of acute viral hepatitis, and outbreaks caused by this virus often occur in fecal polluted...
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SubjectTerms Concentration
Filtration
financial economics
freshwater
Hepatitis A virus
Hepatitis A virus - isolation & purification
Hepatovirus A
quantitative polymerase chain reaction
rapid methods
Real-Time Polymerase Chain Reaction - economics
Real-Time Polymerase Chain Reaction - methods
RNA, Viral - analysis
Salinity
Seawater
Seawater - virology
Sensitivity and Specificity
Sodium Dodecyl Sulfate
viral hepatitis
viruses
Zeolite
Zeolites
Title Concentration and detection of hepatitis A virus and its indicator from artificial seawater using zeolite
URI https://dx.doi.org/10.1016/j.jviromet.2016.04.020
https://www.ncbi.nlm.nih.gov/pubmed/27150045
https://www.proquest.com/docview/1813621473
https://www.proquest.com/docview/1815711916
https://www.proquest.com/docview/2045823239
Volume 235
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