Rapid detection of non-enterobacteriaceae directly from positive blood culture using fluorescent in situ hybridization
Fluorescent in situ hybridization (FISH) was carried out using two different oligonucleotide probes specific for Pseudomonas spp. and Acinetobacter spp. These probes were tested against different organisms and were found to be highly specific. Sensitivity testing showed that the probes were able to...
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my.um.eprints.7232019-07-16T05:49:02Z http://eprints.um.edu.my/723/ Rapid detection of non-enterobacteriaceae directly from positive blood culture using fluorescent in situ hybridization Wong, E.H. Subramaniam, G. Navaratnam, P. Sekaran, S.D. RC Internal medicine Fluorescent in situ hybridization (FISH) was carried out using two different oligonucleotide probes specific for Pseudomonas spp. and Acinetobacter spp. These probes were tested against different organisms and were found to be highly specific. Sensitivity testing showed that the probes were able to detect as low as 10 3 CFU/mL. In addition, FISH was carried out directly on positive blood culture samples and the detection of microorganisms took less than 2 h. We believe that FISH is a rapid method that can be used as a routine laboratory diagnostic technique for the detection of Acinetobacter spp. and Pseudomonas spp. in clinical samples. Medknow Publications 2007-10 Article PeerReviewed Wong, E.H. and Subramaniam, G. and Navaratnam, P. and Sekaran, S.D. (2007) Rapid detection of non-enterobacteriaceae directly from positive blood culture using fluorescent in situ hybridization. Indian Journal of Medical Microbiology, 25 (4). pp. 391-4. ISSN 0255-0857 http://www.ncbi.nlm.nih.gov/pubmed/18087092 18087092 |
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RC Internal medicine Wong, E.H. Subramaniam, G. Navaratnam, P. Sekaran, S.D. Rapid detection of non-enterobacteriaceae directly from positive blood culture using fluorescent in situ hybridization |
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Fluorescent in situ hybridization (FISH) was carried out using two different oligonucleotide probes specific for Pseudomonas spp. and Acinetobacter spp. These probes were tested against different organisms and were found to be highly specific. Sensitivity testing showed that the probes were able to detect as low as 10 3 CFU/mL. In addition, FISH was carried out directly on positive blood culture samples and the detection of microorganisms took less than 2 h. We believe that FISH is a rapid method that can be used as a routine laboratory diagnostic technique for the detection of Acinetobacter spp. and Pseudomonas spp. in clinical samples. |
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Article |
author |
Wong, E.H. Subramaniam, G. Navaratnam, P. Sekaran, S.D. |
author_facet |
Wong, E.H. Subramaniam, G. Navaratnam, P. Sekaran, S.D. |
author_sort |
Wong, E.H. |
title |
Rapid detection of non-enterobacteriaceae directly from positive blood culture using fluorescent in situ hybridization |
title_short |
Rapid detection of non-enterobacteriaceae directly from positive blood culture using fluorescent in situ hybridization |
title_full |
Rapid detection of non-enterobacteriaceae directly from positive blood culture using fluorescent in situ hybridization |
title_fullStr |
Rapid detection of non-enterobacteriaceae directly from positive blood culture using fluorescent in situ hybridization |
title_full_unstemmed |
Rapid detection of non-enterobacteriaceae directly from positive blood culture using fluorescent in situ hybridization |
title_sort |
rapid detection of non-enterobacteriaceae directly from positive blood culture using fluorescent in situ hybridization |
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Medknow Publications |
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2007 |
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http://eprints.um.edu.my/723/ http://www.ncbi.nlm.nih.gov/pubmed/18087092 |
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