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Development of a Broad-Range 23S rDNA Real-Time PCR Assay for the Detection and Quantification of Pathogenic Bacteria in Human Whole Blood and Plasma Specimens

Molecular methods are important tools in the diagnosis of bloodstream bacterial infections, in particular in patients treated with antimicrobial therapy, due to their quick turn-around time. Here we describe a new broad-range real-time PCR targeting the 23S rDNA gene and capable to detect as low as...

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Autores principales: Gaibani, Paolo, Mariconti, Mara, Bua, Gloria, Bonora, Sonia, Sassera, Davide, Landini, Maria Paola, Mulatto, Patrizia, Novati, Stefano, Bandi, Claudio, Sambri, Vittorio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3613074/
https://www.ncbi.nlm.nih.gov/pubmed/23586027
http://dx.doi.org/10.1155/2013/264651
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author Gaibani, Paolo
Mariconti, Mara
Bua, Gloria
Bonora, Sonia
Sassera, Davide
Landini, Maria Paola
Mulatto, Patrizia
Novati, Stefano
Bandi, Claudio
Sambri, Vittorio
author_facet Gaibani, Paolo
Mariconti, Mara
Bua, Gloria
Bonora, Sonia
Sassera, Davide
Landini, Maria Paola
Mulatto, Patrizia
Novati, Stefano
Bandi, Claudio
Sambri, Vittorio
author_sort Gaibani, Paolo
collection PubMed
description Molecular methods are important tools in the diagnosis of bloodstream bacterial infections, in particular in patients treated with antimicrobial therapy, due to their quick turn-around time. Here we describe a new broad-range real-time PCR targeting the 23S rDNA gene and capable to detect as low as 10 plasmid copies per reaction of targeted bacterial 23S rDNA gene. Two commercially available DNA extraction kits were evaluated to assess their efficiency for the extraction of plasma and whole blood samples spiked with different amount of either Staphylococcus aureus or Escherichia coli, in order to find the optimal extraction method to be used. Manual QIAmp extraction method with enzyme pre-treatment resulted the most sensitive for detection of bacterial load. Sensitivity of this novel assay ranged between 10 and 10(3) CFU per PCR reaction for E. coli and S. aureus in human whole blood samples depending on the extraction methods used. Analysis of plasma samples showed a 10- to 100-fold reduction of bacterial 23S rDNA in comparison to the corresponding whole blood specimens, thus indicating that whole blood is the preferential sample type to be used in this real-time PCR protocol. Our results thus show that the 23S rDNA gene represents an optimal target for bacteria quantification in human whole blood.
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spelling pubmed-36130742013-04-12 Development of a Broad-Range 23S rDNA Real-Time PCR Assay for the Detection and Quantification of Pathogenic Bacteria in Human Whole Blood and Plasma Specimens Gaibani, Paolo Mariconti, Mara Bua, Gloria Bonora, Sonia Sassera, Davide Landini, Maria Paola Mulatto, Patrizia Novati, Stefano Bandi, Claudio Sambri, Vittorio Biomed Res Int Research Article Molecular methods are important tools in the diagnosis of bloodstream bacterial infections, in particular in patients treated with antimicrobial therapy, due to their quick turn-around time. Here we describe a new broad-range real-time PCR targeting the 23S rDNA gene and capable to detect as low as 10 plasmid copies per reaction of targeted bacterial 23S rDNA gene. Two commercially available DNA extraction kits were evaluated to assess their efficiency for the extraction of plasma and whole blood samples spiked with different amount of either Staphylococcus aureus or Escherichia coli, in order to find the optimal extraction method to be used. Manual QIAmp extraction method with enzyme pre-treatment resulted the most sensitive for detection of bacterial load. Sensitivity of this novel assay ranged between 10 and 10(3) CFU per PCR reaction for E. coli and S. aureus in human whole blood samples depending on the extraction methods used. Analysis of plasma samples showed a 10- to 100-fold reduction of bacterial 23S rDNA in comparison to the corresponding whole blood specimens, thus indicating that whole blood is the preferential sample type to be used in this real-time PCR protocol. Our results thus show that the 23S rDNA gene represents an optimal target for bacteria quantification in human whole blood. Hindawi Publishing Corporation 2013 2013-03-17 /pmc/articles/PMC3613074/ /pubmed/23586027 http://dx.doi.org/10.1155/2013/264651 Text en Copyright © 2013 Paolo Gaibani et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Gaibani, Paolo
Mariconti, Mara
Bua, Gloria
Bonora, Sonia
Sassera, Davide
Landini, Maria Paola
Mulatto, Patrizia
Novati, Stefano
Bandi, Claudio
Sambri, Vittorio
Development of a Broad-Range 23S rDNA Real-Time PCR Assay for the Detection and Quantification of Pathogenic Bacteria in Human Whole Blood and Plasma Specimens
title Development of a Broad-Range 23S rDNA Real-Time PCR Assay for the Detection and Quantification of Pathogenic Bacteria in Human Whole Blood and Plasma Specimens
title_full Development of a Broad-Range 23S rDNA Real-Time PCR Assay for the Detection and Quantification of Pathogenic Bacteria in Human Whole Blood and Plasma Specimens
title_fullStr Development of a Broad-Range 23S rDNA Real-Time PCR Assay for the Detection and Quantification of Pathogenic Bacteria in Human Whole Blood and Plasma Specimens
title_full_unstemmed Development of a Broad-Range 23S rDNA Real-Time PCR Assay for the Detection and Quantification of Pathogenic Bacteria in Human Whole Blood and Plasma Specimens
title_short Development of a Broad-Range 23S rDNA Real-Time PCR Assay for the Detection and Quantification of Pathogenic Bacteria in Human Whole Blood and Plasma Specimens
title_sort development of a broad-range 23s rdna real-time pcr assay for the detection and quantification of pathogenic bacteria in human whole blood and plasma specimens
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3613074/
https://www.ncbi.nlm.nih.gov/pubmed/23586027
http://dx.doi.org/10.1155/2013/264651
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