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Listerial meningitis: Atypical strain and misidentification by the automated identification system (Vitek2).
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DDG (Pension), Office of DGAFMS, Ministry of Defence, New Delhi, India.
Listeria in Adults - Truly Rare or Rarely Diagnosed in India?
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Senior Consultant.
Listeria monocytogenes is a facultative anaerobic intracellular Gram positive rod causing infection in pregnant women, extremes of age and immune-compromised hosts. In clinical specimens, the organisms may be gram-variable: laboratory misidentification of L. monocytogenes isolates as diphtheroids, streptococci, or enterococci is not uncommon and the isolation of a diphtheroid from blood or CSF should always alert the clinician to the possibility that the organism may be L.
View Article and Find Full Text PDFMisidentification of Listeria monocytogenes by the Vitek 2 system.
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National Salmonella, Shigella & Listeria Reference Laboratory, Medical Microbiology Department, University Hospital Galway, Galway, Ireland.
Evaluation of the VITEK 2 gram positive (GP) microbial identification test card: collaborative study.
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Q Laboratories, Inc., 1400 Harrison Ave, Cincinnati, OH 45214, USA.
A collaborative study was conducted to evaluate the performance of the VITEK 2 Gram Positive (GP) identification card for use with the VITEK 2 automated microbial identification system. The GP test card is used in the identification of selected Gram positive organisms, including Listeria and Staphylococcus species. The VITEK 2 GP card is based on 43 biochemical tests measuring carbon source utilization, inhibition and resistance, and enzymatic activities.
View Article and Find Full Text PDFGenotypic versus phenotypic methods in the detection of Listeria monocytogenes prosthetic joint infection.
J Med Microbiol
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Institute of Clinical Immunology and Allergology, Faculty of Medicine, Masaryk University, St Anne's University Hospital, Brno, Czech Republic.
A rare case of a severe prosthetic joint infection in a 71-year-old immunocompetent woman is presented. Listeria monocytogenes was identified in two consecutive samples using broad-range PCR and sequencing, whereas cultivation remained negative for the first sample and streptococci of a non-group A streptococci, non-group B streptococci type were detected for the second one. This report demonstrates that the phenotypic approach may lead to misidentification of L.
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