Literature DB >> 23294413

A rapid, high-throughput screening method for carriage of methicillin-resistant Staphylococcus aureus.

Hege S Tunsjø1, Benoit Follin-Arbelet, Nina M Clausen, Yngve Ness, Truls M Leegaard, Vahid Bemanian.   

Abstract

Rapid screening of methicillin-resistant Staphylococcus aureus (MRSA) colonization prior to hospital admittance is important to reduce nosocomial infections and health care costs. Molecular detection of mecA and S. aureus specific target genes has become widely established for this purpose. However, there are still limitations in potential for high-throughput screening in the methods described. We have compared the time aspects and workload of four different DNA preparation platforms, resulting in an automated and simple MRSA screening method which combines two liquid handling systems and a simple lysis buffer. We have further transferred our in-house dual real-time PCR to a fast-PCR protocol, reducing the time and labour spent on these samples to a minimum.
© 2013 APMIS. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  DNA preparation; Methicillin-resistant Staphylococcus aureus; high-throughput; real-time PCR; screening

Mesh:

Substances:

Year:  2013        PMID: 23294413     DOI: 10.1111/apm.12049

Source DB:  PubMed          Journal:  APMIS        ISSN: 0903-4641            Impact factor:   3.205


  2 in total

1.  High frequency of occupied attB regions in Norwegian Staphylococcus aureus isolates supports a two-step MRSA screening algorithm.

Authors:  H S Tunsjø; S Kalyanasundaram; M M Worren; T M Leegaard; A E F Moen
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2016-09-09       Impact factor: 3.267

2.  DNA extraction of microbial DNA directly from infected tissue: an optimized protocol for use in nanopore sequencing.

Authors:  Karin Helmersen; Hege Vangstein Aamot
Journal:  Sci Rep       Date:  2020-02-19       Impact factor: 4.379

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.