Literature DB >> 21183638

Development and application of a tool to assess laboratory hygiene in contained-use facilities.

S A Rutjes1, F Lodder-Verschoor, J P Tijssen, A M de Roda Husman.   

Abstract

To gain information on laboratory hygiene in contained-use laboratories, a method was developed to study the presence of microorganisms on laboratory equipment. Focusing detection on genetically modified organisms (GMOs) containing the universal M13 primer binding sites enabled the detection of a broad range of GMOs using a single PCR. Swabbing surfaces in three different contained-use laboratories led to detection of M13-containing PCR products in 26 out of 34 swabs. Most sequences (up to five per sample) were detected in swabs from the centrifuge and sink, followed by swabs taken from the bin and incubator (up to four sequences per sample). The obtained sequences varied in length from 171 nucleotides (nt) to 878 nt. In most cases, sequences were only partially similar to sequences published in GenBank. The lengths of the regions with high similarity varied from 94 nt to 795 nt, and these similarities ranged from 81% to 100%. Similarities with more than one sequence were commonly found, complicating the identification of detected sequences. Nonetheless, 84% of the detected sequences were actually handled in the laboratory at the time of sampling. This demonstrates that the method may be used as a quality control tool to assess the efficacy of decontamination and cleaning of commonly used surfaces, such as laboratory benches, freezer doors, and centrifuge rotors, without prior knowledge of the identity or characteristics of the GMOs.

Mesh:

Year:  2010        PMID: 21183638      PMCID: PMC3067214          DOI: 10.1128/AEM.01781-10

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  13 in total

1.  Inactivation of caliciviruses.

Authors:  Erwin Duizer; Paul Bijkerk; Barry Rockx; Astrid De Groot; Fleur Twisk; Marion Koopmans
Journal:  Appl Environ Microbiol       Date:  2004-08       Impact factor: 4.792

Review 2.  Promises and pitfalls of recent advances in chemical means of preventing the spread of nosocomial infections by environmental surfaces.

Authors:  Syed A Sattar
Journal:  Am J Infect Control       Date:  2010-06       Impact factor: 2.918

3.  Laboratory efforts to eliminate contamination problems in the real-time RT-PCR detection of noroviruses.

Authors:  Ambroos Stals; Hadewig Werbrouck; Leen Baert; Nadine Botteldoorn; Lieve Herman; Mieke Uyttendaele; Els Van Coillie
Journal:  J Microbiol Methods       Date:  2009-01-30       Impact factor: 2.363

4.  Studies on lysogenesis. I. The mode of phage liberation by lysogenic Escherichia coli.

Authors:  G BERTANI
Journal:  J Bacteriol       Date:  1951-09       Impact factor: 3.490

5.  Use of bleach to eliminate contaminating DNA from the surface of bones and teeth.

Authors:  Brian M Kemp; David Glenn Smith
Journal:  Forensic Sci Int       Date:  2005-11-10       Impact factor: 2.395

6.  Avoiding false positives with PCR.

Authors:  S Kwok; R Higuchi
Journal:  Nature       Date:  1989-05-18       Impact factor: 49.962

7.  Is it safe to use Escherichia coli K12 in recombinant DNA experiments?

Authors:  H W Smith
Journal:  J Infect Dis       Date:  1978-05       Impact factor: 5.226

8.  Attachment of noroviruses to stainless steel and their inactivation, using household disinfectants.

Authors:  Maryline Girard; Solange Ngazoa; Kirsten Mattison; Julie Jean
Journal:  J Food Prot       Date:  2010-02       Impact factor: 2.077

9.  Fast, broad-range disinfection of bacteria, fungi, viruses and prions.

Authors:  Michael Beekes; Karin Lemmer; Achim Thomzig; Marion Joncic; Kathrin Tintelnot; Martin Mielke
Journal:  J Gen Virol       Date:  2009-10-28       Impact factor: 3.891

10.  Disinfection efficacy against parvoviruses compared with reference viruses.

Authors:  M Eterpi; G McDonnell; V Thomas
Journal:  J Hosp Infect       Date:  2009-07-30       Impact factor: 3.926

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