Literature DB >> 28507461

Washed Away; How Not to Lose Your RNA during Isolation.

Birgitte K Hønsvall1,2, Lucy J Robertson3.   

Abstract

Cryptosporidium oocysts have extremely robust walls that protect the parasite against environmental pressures. Analyses must be sensitive to detect the few organisms (if any) present in environmental samples. After a series of negative nucleic acid amplification results on spiked samples, following a standard RNA isolation protocol, it seemed probable that oocyst RNA had been lost in the washing steps of the isolation protocol. By reducing both the volume of wash buffer and the number of washing steps, positive results could be re-established. Insufficient washing, however, seemed to prevent downstream analysis, probably because of inhibitory substances remaining in the RNA isolate. Nucleic acid isolation protocols for low numbers of "difficult" organisms should be adapted, according to the material to optimize the balance between removal of inhibitors and retention of target, thereby improving the performance of the technique.

Entities:  

Keywords:  Boom extraction method; Cryptosporidium; Escherichia coli

Mesh:

Substances:

Year:  2017        PMID: 28507461      PMCID: PMC5408326          DOI: 10.7171/jbt.17-2802-004

Source DB:  PubMed          Journal:  J Biomol Tech        ISSN: 1524-0215


  9 in total

1.  Real-time nucleic acid sequence-based amplification using molecular beacons for detection of enterovirus RNA in clinical specimens.

Authors:  Marie L Landry; Robin Garner; David Ferguson
Journal:  J Clin Microbiol       Date:  2005-07       Impact factor: 5.948

2.  Real-time detection of noroviruses in surface water by use of a broadly reactive nucleic acid sequence-based amplification assay.

Authors:  Saskia A Rutjes; Harold H J L van den Berg; Willemijn J Lodder; Ana Maria de Roda Husman
Journal:  Appl Environ Microbiol       Date:  2006-08       Impact factor: 4.792

3.  Rapid and simple method for purification of nucleic acids.

Authors:  R Boom; C J Sol; M M Salimans; C L Jansen; P M Wertheim-van Dillen; J van der Noordaa
Journal:  J Clin Microbiol       Date:  1990-03       Impact factor: 5.948

4.  Nucleic acid sequence-based amplification.

Authors:  J Compton
Journal:  Nature       Date:  1991-03-07       Impact factor: 49.962

5.  Detection of viable oocysts of Cryptosporidium parvum following nucleic acid sequence based amplification.

Authors:  A J Baeumner; M C Humiston; R A Montagna; R A Durst
Journal:  Anal Chem       Date:  2001-03-15       Impact factor: 6.986

6.  Real-time nucleic acid sequence-based amplification (NASBA) assay targeting MIC1 for detection of Cryptosporidium parvum and Cryptosporidium hominis oocysts.

Authors:  Birgitte K Hønsvall; Lucy J Robertson
Journal:  Exp Parasitol       Date:  2016-12-18       Impact factor: 2.011

7.  Optimization of influencing factors of nucleic acid adsorption onto silica-coated magnetic particles: application to viral nucleic acid extraction from serum.

Authors:  Ning Sun; Congliang Deng; Yi Liu; Xiaoli Zhao; Yan Tang; Renxiao Liu; Qiang Xia; Wenlong Yan; Guanglu Ge
Journal:  J Chromatogr A       Date:  2013-12-11       Impact factor: 4.759

8.  Quantitation of human immunodeficiency virus type 1 RNA in cell free seminal plasma: comparison of NASBA with Amplicor reverse transcription-PCR amplification and correlation with quantitative culture.

Authors:  J R Dyer; B L Gilliam; J J Eron; L Grosso; M S Cohen; S A Fiscus
Journal:  J Virol Methods       Date:  1996-07       Impact factor: 2.014

9.  Rapid real-time nucleic Acid sequence-based amplification-molecular beacon platform to detect fungal and bacterial bloodstream infections.

Authors:  Yanan Zhao; Steven Park; Barry N Kreiswirth; Christine C Ginocchio; Raphaël Veyret; Ali Laayoun; Alain Troesch; David S Perlin
Journal:  J Clin Microbiol       Date:  2009-04-29       Impact factor: 5.948

  9 in total

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