Evaluation of different RNA-extraction kits for sensitive detection of Hepatitis A virus in strawberry samples

The efficiency of different commercial RNA extraction kits for the detection of hepatitis A virus (HAV) from seeded strawberry samples was assessed by standard RT-PCR and real time RT-PCR (RT-qPCR). The best results with standard RT-PCR were achieved with Aurum™ Total RNA extraction kit (BioRad), ob...

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Published inFood microbiology Vol. 28; no. 1; pp. 38 - 42
Main Authors Bianchi, Silvia, Vecchio, Anna Dal, Vilariño, María Luz, Romalde, Jesús L.
Format Journal Article
LanguageEnglish
Published Kidlington Elsevier Ltd 01.02.2011
Elsevier
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Abstract The efficiency of different commercial RNA extraction kits for the detection of hepatitis A virus (HAV) from seeded strawberry samples was assessed by standard RT-PCR and real time RT-PCR (RT-qPCR). The best results with standard RT-PCR were achieved with Aurum™ Total RNA extraction kit (BioRad), obtaining a detection limit of 5–6.25 pfu/mg of tissue. A slightly lower sensitivity was rendered by the RNeasy ® Plant mini kit (Qiagen) (10–12.5 pfu/mg tissue), while the Total Quick RNA Cells and Tissues kit version mini (Talent) rendered a detection limit of 50–100 pfu/mg of tissue. The other tested commercial kits showed worse detection limits (>500 pfu/mg). With RT-qPCR and ten fold diluted RNA all the kits showed an increase of sensitivity, detecting the kits from Qiagen, Talent and BioRad down to 0.05 pfu/mg of strawberry homogenate. These findings indicate that the use of Aurum™ Total RNA extraction kit, with standard RT-PCR technique or RT-qPCR, can not only be labor and time saving but also helpful to improve the sensitivity for the HAV detection from fruits and to facilitate the standardization of detection methods among laboratories.
AbstractList The efficiency of different commercial RNA extraction kits for the detection of hepatitis A virus (HAV) from seeded strawberry samples was assessed by standard RT-PCR and real time RT-PCR (RT-qPCR). The best results with standard RT-PCR were achieved with Aurum™ Total RNA extraction kit (BioRad), obtaining a detection limit of 5-6.25 pfu/mg of tissue. A slightly lower sensitivity was rendered by the RNeasy® Plant mini kit (Qiagen) (10-12.5 pfu/mg tissue), while the Total Quick RNA Cells and Tissues kit version mini (Talent) rendered a detection limit of 50-100 pfu/mg of tissue. The other tested commercial kits showed worse detection limits (>500 pfu/mg). With RT-qPCR and ten fold diluted RNA all the kits showed an increase of sensitivity, detecting the kits from Qiagen, Talent and BioRad down to 0.05 pfu/mg of strawberry homogenate. These findings indicate that the use of Aurum™ Total RNA extraction kit, with standard RT-PCR technique or RT-qPCR, can not only be labor and time saving but also helpful to improve the sensitivity for the HAV detection from fruits and to facilitate the standardization of detection methods among laboratories.
The efficiency of different commercial RNA extraction kits for the detection of hepatitis A virus (HAV) from seeded strawberry samples was assessed by standard RT-PCR and real time RT-PCR (RT-qPCR). The best results with standard RT-PCR were achieved with Aurum™ Total RNA extraction kit (BioRad), obtaining a detection limit of 5–6.25 pfu/mg of tissue. A slightly lower sensitivity was rendered by the RNeasy ® Plant mini kit (Qiagen) (10–12.5 pfu/mg tissue), while the Total Quick RNA Cells and Tissues kit version mini (Talent) rendered a detection limit of 50–100 pfu/mg of tissue. The other tested commercial kits showed worse detection limits (>500 pfu/mg). With RT-qPCR and ten fold diluted RNA all the kits showed an increase of sensitivity, detecting the kits from Qiagen, Talent and BioRad down to 0.05 pfu/mg of strawberry homogenate. These findings indicate that the use of Aurum™ Total RNA extraction kit, with standard RT-PCR technique or RT-qPCR, can not only be labor and time saving but also helpful to improve the sensitivity for the HAV detection from fruits and to facilitate the standardization of detection methods among laboratories.
The efficiency of different commercial RNA extraction kits for the detection of hepatitis A virus (HAV) from seeded strawberry samples was assessed by standard RT-PCR and real time RT-PCR (RT-qPCR). The best results with standard RT-PCR were achieved with Aurum(TM) Total RNA extraction kit (BioRad), obtaining a detection limit of 5-6.25pfu/mg of tissue. A slightly lower sensitivity was rendered by the RNeasyA registered Plant mini kit (Qiagen) (10-12.5pfu/mg tissue), while the Total Quick RNA Cells and Tissues kit version mini (Talent) rendered a detection limit of 50-100pfu/mg of tissue. The other tested commercial kits showed worse detection limits (>500pfu/mg). With RT-qPCR and ten fold diluted RNA all the kits showed an increase of sensitivity, detecting the kits from Qiagen, Talent and BioRad down to 0.05pfu/mg of strawberry homogenate. These findings indicate that the use of Aurum(TM) Total RNA extraction kit, with standard RT-PCR technique or RT-qPCR, can not only be labor and time saving but also helpful to improve the sensitivity for the HAV detection from fruits and to facilitate the standardization of detection methods among laboratories.
The efficiency of different commercial RNA extraction kits for the detection of hepatitis A virus (HAV) from seeded strawberry samples was assessed by standard RT-PCR and real time RT-PCR (RT-qPCR). The best results with standard RT-PCR were achieved with Aurum™ Total RNA extraction kit (BioRad), obtaining a detection limit of 5-6.25 pfu/mg of tissue. A slightly lower sensitivity was rendered by the RNeasy® Plant mini kit (Qiagen) (10-12.5 pfu/mg tissue), while the Total Quick RNA Cells and Tissues kit version mini (Talent) rendered a detection limit of 50-100 pfu/mg of tissue. The other tested commercial kits showed worse detection limits (>500 pfu/mg). With RT-qPCR and ten fold diluted RNA all the kits showed an increase of sensitivity, detecting the kits from Qiagen, Talent and BioRad down to 0.05 pfu/mg of strawberry homogenate. These findings indicate that the use of Aurum™ Total RNA extraction kit, with standard RT-PCR technique or RT-qPCR, can not only be labor and time saving but also helpful to improve the sensitivity for the HAV detection from fruits and to facilitate the standardization of detection methods among laboratories.
Author Bianchi, Silvia
Vilariño, María Luz
Romalde, Jesús L.
Vecchio, Anna Dal
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Issue 1
Keywords Hepatitis A virus
Detection
Commercial RNA extraction kits
Fruits
Evaluation
Fruit
RNA
Picornaviridae
Hepatovirus
Virus
Analysis method
Strawberry
Kit
Extraction
Control method
Language English
License CC BY 4.0
Copyright © 2010 Elsevier Ltd. All rights reserved.
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Elsevier
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Snippet The efficiency of different commercial RNA extraction kits for the detection of hepatitis A virus (HAV) from seeded strawberry samples was assessed by standard...
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SubjectTerms Biological and medical sciences
Commercial RNA extraction kits
Detection
Extraction
Food Analysis
Food engineering
Food industries
Food Microbiology
Foods
Fragaria
Fragaria - virology
Fruits
Fundamental and applied biological sciences. Psychology
General aspects
Hepatitis A virus
Hepatitis A virus - genetics
Hepatitis A virus - isolation & purification
Microbiology
Mini
Reagent Kits, Diagnostic
Reverse Transcriptase Polymerase Chain Reaction - methods
Ribonucleic acids
RNA - metabolism
RNA, Viral - analysis
RNA, Viral - genetics
Sensitivity and Specificity
Strawberries
Title Evaluation of different RNA-extraction kits for sensitive detection of Hepatitis A virus in strawberry samples
URI https://dx.doi.org/10.1016/j.fm.2010.08.002
https://www.ncbi.nlm.nih.gov/pubmed/21056773
https://search.proquest.com/docview/1671423116
https://search.proquest.com/docview/763165756
https://search.proquest.com/docview/855683353
Volume 28
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