Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (1/1 displayed)

  • 2009Internal Control for Nucleic Acid Testing Based on the Use of Purified <i>Bacillus atrophaeus</i> subsp. <i>globigii</i> Spores37citations

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Chart of shared publication
Peytavi, Regis
1 / 2 shared
Bernier, Marthe R.
1 / 1 shared
Bergeron, Michel G.
1 / 5 shared
Picard, Francois J.
1 / 3 shared
Gagnon, Martin
1 / 3 shared
Boissinot, Maurice
1 / 4 shared
Parham, Nicholas J.
1 / 2 shared
Chart of publication period
2009

Co-Authors (by relevance)

  • Peytavi, Regis
  • Bernier, Marthe R.
  • Bergeron, Michel G.
  • Picard, Francois J.
  • Gagnon, Martin
  • Boissinot, Maurice
  • Parham, Nicholas J.
OrganizationsLocationPeople

article

Internal Control for Nucleic Acid Testing Based on the Use of Purified <i>Bacillus atrophaeus</i> subsp. <i>globigii</i> Spores

  • Bastien, Martine
  • Peytavi, Regis
  • Bernier, Marthe R.
  • Bergeron, Michel G.
  • Picard, Francois J.
  • Gagnon, Martin
  • Boissinot, Maurice
  • Parham, Nicholas J.
Abstract

<jats:p>Commonly used internal controls (ICs) to monitor the efficiency of nucleic acid testing (NAT) assays do not allow verification of nucleic acid extraction efficiency. Since microbial cells are often difficult to lyse, it is important to ensure that nucleic acids are efficiently extracted from any target organism. For this purpose, we developed a cellular IC based on the use of nonpathogenic<jats:italic>Bacillus</jats:italic>spores. Purified<jats:italic>Bacillus atrophaeus</jats:italic>subsp.<jats:italic>globigii</jats:italic>(referred to hereafter as simply<jats:italic>B. atrophaeus</jats:italic>) spores were added to vaginal and anal samples, which were then subjected to rapid DNA extraction and subsequent PCR amplification. The proof of concept of this cellular IC was made through the use of both manual and automated DNA extraction methods, using vaginal or anal samples spiked with<jats:italic>B. atrophaeus</jats:italic>spores, combined with a multiplex real-time PCR assay for the specific detection of group B streptococci (GBS) and<jats:italic>B. atrophaeus</jats:italic>. The performance of the cellular IC was compared to that of a standard IC plasmid added to PCRs. Approximately 500<jats:italic>B. atrophaeus</jats:italic>spores per PCR was found to be optimal since this did not interfere significantly with GBS detection for either DNA extraction method and yielded reproducible amplification and/or detection of<jats:italic>B. atrophaeus</jats:italic>genomic DNA serving as an IC template. Performance of the cellular IC was comparable to that of the standard IC. This novel IC system using nonpathogenic and hard-to-lyse<jats:italic>B. atrophaeus</jats:italic>spores allowed validation of both the DNA extraction procedure and the amplification and detection process. Use of a spore-based control also provides a universal control for microbial cell lysis.</jats:p>

Topics
  • impedance spectroscopy
  • extraction
  • ion chromatography