Literature DB >> 25929603

Enzymatic Pre-treatment of Wastewater to Minimize Recovery by Reverse Transcriptase PCR of RNA from Inactive Bacteriophages.

Veena V Unnithan1, Adrian Unc, Geoffrey B Smith.   

Abstract

Quantitative viral risk assessments for wastewaters are notoriously difficult. The often considered quantitative reverse transcriptase PCR reflects poorly on virus infectivity rates leading to inaccurate risk interpretations. Various techniques focused on the degradation of the nucleic acids of non-infective viruses were previously employed. We comparatively assessed the effectiveness of such enzymatic treatments for MS2 bacteriophage in treated wastewaters. The single use of RNase A at an appropriate concentration may be as effective as the combination of RNase followed by Proteinase K and more rapid. While all tested enzymatic treatments minimized recovery of RNA (>95 %) in the absence of infective MS2, none completely eliminated the signal recovery. Selection of any enzymatic protocol for minimizing recovery of RNA from degraded, non-infective viruses should balance the methods efficacy with its expediency.

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Year:  2015        PMID: 25929603     DOI: 10.1007/s00284-015-0830-x

Source DB:  PubMed          Journal:  Curr Microbiol        ISSN: 0343-8651            Impact factor:   2.188


  12 in total

1.  The detection of astrovirus in sludge biosolids using an integrated cell culture nested PCR technique.

Authors:  C D Chapron; N A Ballester; A B Margolin
Journal:  J Appl Microbiol       Date:  2000-07       Impact factor: 3.772

2.  Pretreatment to avoid positive RT-PCR results with inactivated viruses.

Authors:  Suphachai Nuanualsuwan; Dean O Cliver
Journal:  J Virol Methods       Date:  2002-07       Impact factor: 2.014

3.  A PCR-DGGE approach to evaluate the impact of wastewater source on the antibiotic resistance diversity in treated wastewater effluent.

Authors:  J Sigala; A Unc
Journal:  Water Sci Technol       Date:  2012       Impact factor: 1.915

4.  Quantitative PCR for determining the infectivity of bacteriophage MS2 upon inactivation by heat, UV-B radiation, and singlet oxygen: advantages and limitations of an enzymatic treatment to reduce false-positive results.

Authors:  Brian M Pecson; Luisa Valério Martin; Tamar Kohn
Journal:  Appl Environ Microbiol       Date:  2009-07-10       Impact factor: 4.792

5.  A unified view of polymer, dumbbell, and oligonucleotide DNA nearest-neighbor thermodynamics.

Authors:  J SantaLucia
Journal:  Proc Natl Acad Sci U S A       Date:  1998-02-17       Impact factor: 11.205

6.  Real-time fluorogenic reverse transcription-PCR assays for detection of bacteriophage MS2.

Authors:  Kevin P O'Connell; Jennifer R Bucher; Patricia E Anderson; Cheng J Cao; Akbar S Khan; Mark V Gostomski; James J Valdes
Journal:  Appl Environ Microbiol       Date:  2006-01       Impact factor: 4.792

7.  Effects of technological processes on the tenacity and inactivation of norovirus genogroup II in experimentally contaminated foods.

Authors:  Sascha Mormann; Mareike Dabisch; Barbara Becker
Journal:  Appl Environ Microbiol       Date:  2009-11-20       Impact factor: 4.792

8.  Evaluation of the persistence of infectious human noroviruses on food surfaces by using real-time nucleic acid sequence-based amplification.

Authors:  Safaa Lamhoujeb; Ismail Fliss; Solange E Ngazoa; Julie Jean
Journal:  Appl Environ Microbiol       Date:  2008-03-31       Impact factor: 4.792

9.  Primer-BLAST: a tool to design target-specific primers for polymerase chain reaction.

Authors:  Jian Ye; George Coulouris; Irena Zaretskaya; Ioana Cutcutache; Steve Rozen; Thomas L Madden
Journal:  BMC Bioinformatics       Date:  2012-06-18       Impact factor: 3.169

10.  RNase L mediated protection from virus induced demyelination.

Authors:  Derek D C Ireland; Stephen A Stohlman; David R Hinton; Parul Kapil; Robert H Silverman; Roscoe A Atkinson; Cornelia C Bergmann
Journal:  PLoS Pathog       Date:  2009-10-02       Impact factor: 6.823

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  1 in total

1.  Real-Time qPCR as a Method for Detection of Antibody-Neutralized Phage Particles.

Authors:  Anna Kłopot; Adriana Zakrzewska; Dorota Lecion; Joanna M Majewska; Marek A Harhala; Karolina Lahutta; Zuzanna Kaźmierczak; Łukasz Łaczmański; Marlena Kłak; Krystyna Dąbrowska
Journal:  Front Microbiol       Date:  2017-11-06       Impact factor: 5.640

  1 in total

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