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P452 Estimation of the detection limit of extracted Candida DNA from spiked EDTA blood sample

POSTER SESSION 3, SEPTEMBER 23, 2022, 12:30 PM - 1:30 PM:   BACKGROUND: Candidemia caused by genus Candida, are opportunistic pathogens with life-threatening infection in immunocompromised individuals with a mortality rate being 40%–54% in patients. Blood culture is not a reliable and rapid method f...

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Autores principales: Subramanian, Anitha, Balakumar, Uthra, Kindo, Anupma Jyoti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9510004/
http://dx.doi.org/10.1093/mmy/myac072.P452
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author Subramanian, Anitha
Balakumar, Uthra
Kindo, Anupma Jyoti
author_facet Subramanian, Anitha
Balakumar, Uthra
Kindo, Anupma Jyoti
author_sort Subramanian, Anitha
collection PubMed
description POSTER SESSION 3, SEPTEMBER 23, 2022, 12:30 PM - 1:30 PM:   BACKGROUND: Candidemia caused by genus Candida, are opportunistic pathogens with life-threatening infection in immunocompromised individuals with a mortality rate being 40%–54% in patients. Blood culture is not a reliable and rapid method for the diagnosis of candidemia as its sensitivity is as low as 50%. Molecular diagnosis is an alternative to conventional culture for early detection of candidemia. An appropriate DNA isolation technique is needed to obtain high purity DNA from blood specimens and improves the sensitivity of the polymerase chain reaction (PCR). In this study, two different methods were used to extract Candida DNA from spiked EDTA blood specimens, the In-house phenol-chloroform and potassium acetate method. OBJECTIVES: DNA extraction from the spiked blood samples Quantification of the Candida DNA extracted from the spiked sample Comparison of the extracted DNA by phenol-chloroform and potassium acetate method METHODS: A total of 5 ml of EDTA blood samples from healthy volunteers were spiked with 104-108 Candida albicans cells (ATCC 90028) to determine the detection limit of our extraction method. DNA was extracted from whole blood using phenol-chloroform and the potassium acetate methods which involves pretreatment with erythrocytes, leukocytes and fungal lysis buffer. DNA from C. albicans were amplified using ITS1 and ITS4 based primers. PCR products were visualized by agarose gel electrophoresis. RESULTS: The spiked Candida cells taken were from 104-108 yeast cells. The total extracted DNA by phenol chloroform extraction method ranged from 18.29 to 51.64 ng/μl respectively. Whereas the total extracted DNA from potassium acetate extraction method ranged from 15.58 to 32.30 ng/μl respectively. The presence of a 535 base pair (bp) product was considered positive (Figs. 1 and 2). The lowest detection limit of PCR has been determined as 106-108 Candida cells for our spiked samples. CONCLUSION: In our study, till date, the extracted quantity of DNA was found to be higher by phenol-chloroform method as compared to the potassium acetate method. Greater numbers and processing are required to obtain conclusive data.
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spelling pubmed-95100042022-09-26 P452 Estimation of the detection limit of extracted Candida DNA from spiked EDTA blood sample Subramanian, Anitha Balakumar, Uthra Kindo, Anupma Jyoti Med Mycol Oral Presentations POSTER SESSION 3, SEPTEMBER 23, 2022, 12:30 PM - 1:30 PM:   BACKGROUND: Candidemia caused by genus Candida, are opportunistic pathogens with life-threatening infection in immunocompromised individuals with a mortality rate being 40%–54% in patients. Blood culture is not a reliable and rapid method for the diagnosis of candidemia as its sensitivity is as low as 50%. Molecular diagnosis is an alternative to conventional culture for early detection of candidemia. An appropriate DNA isolation technique is needed to obtain high purity DNA from blood specimens and improves the sensitivity of the polymerase chain reaction (PCR). In this study, two different methods were used to extract Candida DNA from spiked EDTA blood specimens, the In-house phenol-chloroform and potassium acetate method. OBJECTIVES: DNA extraction from the spiked blood samples Quantification of the Candida DNA extracted from the spiked sample Comparison of the extracted DNA by phenol-chloroform and potassium acetate method METHODS: A total of 5 ml of EDTA blood samples from healthy volunteers were spiked with 104-108 Candida albicans cells (ATCC 90028) to determine the detection limit of our extraction method. DNA was extracted from whole blood using phenol-chloroform and the potassium acetate methods which involves pretreatment with erythrocytes, leukocytes and fungal lysis buffer. DNA from C. albicans were amplified using ITS1 and ITS4 based primers. PCR products were visualized by agarose gel electrophoresis. RESULTS: The spiked Candida cells taken were from 104-108 yeast cells. The total extracted DNA by phenol chloroform extraction method ranged from 18.29 to 51.64 ng/μl respectively. Whereas the total extracted DNA from potassium acetate extraction method ranged from 15.58 to 32.30 ng/μl respectively. The presence of a 535 base pair (bp) product was considered positive (Figs. 1 and 2). The lowest detection limit of PCR has been determined as 106-108 Candida cells for our spiked samples. CONCLUSION: In our study, till date, the extracted quantity of DNA was found to be higher by phenol-chloroform method as compared to the potassium acetate method. Greater numbers and processing are required to obtain conclusive data. Oxford University Press 2022-09-20 /pmc/articles/PMC9510004/ http://dx.doi.org/10.1093/mmy/myac072.P452 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
Subramanian, Anitha
Balakumar, Uthra
Kindo, Anupma Jyoti
P452 Estimation of the detection limit of extracted Candida DNA from spiked EDTA blood sample
title P452 Estimation of the detection limit of extracted Candida DNA from spiked EDTA blood sample
title_full P452 Estimation of the detection limit of extracted Candida DNA from spiked EDTA blood sample
title_fullStr P452 Estimation of the detection limit of extracted Candida DNA from spiked EDTA blood sample
title_full_unstemmed P452 Estimation of the detection limit of extracted Candida DNA from spiked EDTA blood sample
title_short P452 Estimation of the detection limit of extracted Candida DNA from spiked EDTA blood sample
title_sort p452 estimation of the detection limit of extracted candida dna from spiked edta blood sample
topic Oral Presentations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9510004/
http://dx.doi.org/10.1093/mmy/myac072.P452
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