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Vitek2 ms system

Manufactured by bioMérieux
Sourced in France, United States

The VITEK2 MS system is a compact and automated mass spectrometry-based platform designed for the rapid identification of microorganisms. It utilizes matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) technology to generate unique protein profiles for the accurate identification of a wide range of clinically relevant microorganisms.

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2 protocols using vitek2 ms system

1

Rapid Identification of Enterococcal Isolates

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Further testing of isolates was carried out at the Institute of Medical Microbiology and Infections Epidemiology, Leipzig University, Leipzig, Germany. Isolates were identified by matrix-assisted laser desorption/ionization time - off light (MALDI-TOF) Mass spectrometry using VITEK2 MS system (Biomerieux, France) and verified by specie specific enterococcal ddl PCR6 (link). MALDI TOF Mass spectrometry is a mass spectrometry based technology that offers accurate, rapid, and inexpensive identification of microorganisms. Briefly, bacterial colonies are removed from agar culture plates, mixed with an excess of UV-absorbing matrix, and dried on steel target plates. The dried preparations are exposed to laser pulses, resulting in energy transfer from the matrix to the nonvolatile analyte molecules, with desorption of analyte into the gas phase. The ionized molecules are accelerated by electric potentials through a flight tube to the mass spectrometer, with separation of the biomarkers determined by their mass/charge ratio. The profile of biomarkers is then compared with profiles of a collection of well characterized organisms7 . vanC genotype was determined by identification of organisms as E. gallinarum and E. casseliflavus since these species express the vanC genotype constitutively.
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2

MALDI-TOF MS Identification of Clinical Isolates

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Samples were collected from 15 July 2013 to 30 September 2013 (three-month period). Bacteria and yeast isolates retrieved from clinical samples from an academic diagnostic microbiology laboratory (National Health Laboratory Service [NHLS], Universitas Hospital, Bloemfontein, Free State, South Africa) and three other laboratories, one at Kimberly Hospital (Northern Cape, South Africa) and two private pathology laboratories (Bloemfontein, Free State, South Africa), were analysed. The laboratories identified isolates to the species level with standard biochemical methods using either the MicroScan Walkaway system (Siemens Healthcare Diagnostics, Sacramento, California, United States) or the VITEK 2 MS system (bioMérieux, Marcy l’Etoile, France). Isolates were tested in parallel with the MALDI-TOF MS assay (Bruker Daltonics, Bremen, Germany). The technician who carried out the MALDI-TOF MS assay was blinded to the identity of the isolates. The analysis of the isolates from the academic diagnostic microbiology laboratory was done in real time, whereas the samples from regional and private laboratories were assayed in batches.
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