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P497 Candida DNA extraction from positive blood culture bottles
POSTER SESSION 3, SEPTEMBER 23, 2022, 12:30 PM - 1:30 PM: BACKGROUND: Molecular technique of detecting candida from blood is a quick method to identify candidemia. A major limitation of the molecular method is the difficulty associated with breaking fungal cell wall, the DNA extraction step still...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9509939/ http://dx.doi.org/10.1093/mmy/myac072.P497 |
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author | Balakumar, Uthra Subramanian, Anitha Kindo, Anupma Jyoti |
author_facet | Balakumar, Uthra Subramanian, Anitha Kindo, Anupma Jyoti |
author_sort | Balakumar, Uthra |
collection | PubMed |
description | POSTER SESSION 3, SEPTEMBER 23, 2022, 12:30 PM - 1:30 PM: BACKGROUND: Molecular technique of detecting candida from blood is a quick method to identify candidemia. A major limitation of the molecular method is the difficulty associated with breaking fungal cell wall, the DNA extraction step still requires more than half of a working day. The successful extraction of DNA involves effective disruption of cells, denaturation of protein, and nucleoprotein complexes, and inactivation of nucleases such as DNase. The extracted DNA should have low contamination of proteins. OBJECTIVES: To perform DNA extraction using phenol-chloroform method. 2. To speciate candida using PCR-RFLP. METHODS: Candida DNA is isolated using phenol-chloroform method. The PCR products of different candida species obtained directly from blood samples were subjected to restriction enzyme (MspI). RESULTS: DNA was extracted from 50 samples, out of which 40 samples were from known positive blood culture bottles and the remaining 10 were known negative for candida. Of the 40 known positive blood culture bottles, 34 produced bands of various molecular weights and all 10 negative cultures did not show bands. Representative amplicon is shown in the gel picture (Figure 1). Out of 40 candida-positive blood culture samples, 7 species have been identified using PCR- RFLP method. CONCLUSION: The turn-around time can be highly reduced by extracting DNA from positive blood culture bottles and then performing PCR and RFLP for speciation compared with the conventional method. |
format | Online Article Text |
id | pubmed-9509939 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-95099392022-09-26 P497 Candida DNA extraction from positive blood culture bottles Balakumar, Uthra Subramanian, Anitha Kindo, Anupma Jyoti Med Mycol Oral Presentations POSTER SESSION 3, SEPTEMBER 23, 2022, 12:30 PM - 1:30 PM: BACKGROUND: Molecular technique of detecting candida from blood is a quick method to identify candidemia. A major limitation of the molecular method is the difficulty associated with breaking fungal cell wall, the DNA extraction step still requires more than half of a working day. The successful extraction of DNA involves effective disruption of cells, denaturation of protein, and nucleoprotein complexes, and inactivation of nucleases such as DNase. The extracted DNA should have low contamination of proteins. OBJECTIVES: To perform DNA extraction using phenol-chloroform method. 2. To speciate candida using PCR-RFLP. METHODS: Candida DNA is isolated using phenol-chloroform method. The PCR products of different candida species obtained directly from blood samples were subjected to restriction enzyme (MspI). RESULTS: DNA was extracted from 50 samples, out of which 40 samples were from known positive blood culture bottles and the remaining 10 were known negative for candida. Of the 40 known positive blood culture bottles, 34 produced bands of various molecular weights and all 10 negative cultures did not show bands. Representative amplicon is shown in the gel picture (Figure 1). Out of 40 candida-positive blood culture samples, 7 species have been identified using PCR- RFLP method. CONCLUSION: The turn-around time can be highly reduced by extracting DNA from positive blood culture bottles and then performing PCR and RFLP for speciation compared with the conventional method. Oxford University Press 2022-09-20 /pmc/articles/PMC9509939/ http://dx.doi.org/10.1093/mmy/myac072.P497 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of The International Society for Human and Animal Mycology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Oral Presentations Balakumar, Uthra Subramanian, Anitha Kindo, Anupma Jyoti P497 Candida DNA extraction from positive blood culture bottles |
title | P497 Candida DNA extraction from positive blood culture bottles |
title_full | P497 Candida DNA extraction from positive blood culture bottles |
title_fullStr | P497 Candida DNA extraction from positive blood culture bottles |
title_full_unstemmed | P497 Candida DNA extraction from positive blood culture bottles |
title_short | P497 Candida DNA extraction from positive blood culture bottles |
title_sort | p497 candida dna extraction from positive blood culture bottles |
topic | Oral Presentations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9509939/ http://dx.doi.org/10.1093/mmy/myac072.P497 |
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