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Rapid Microbial Sample Preparation from Blood Using a Novel Concentration Device

Appropriate care for bacteremic patients is dictated by the amount of time needed for an accurate diagnosis. However, the concentration of microbes in the blood is extremely low in these patients (1–100 CFU/mL), traditionally requiring growth (blood culture) or amplification (e.g., PCR) for detectio...

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Autores principales: Boardman, Anna K., Campbell, Jennifer, Wirz, Holger, Sharon, Andre, Sauer-Budge, Alexis F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4326418/
https://www.ncbi.nlm.nih.gov/pubmed/25675242
http://dx.doi.org/10.1371/journal.pone.0116837
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author Boardman, Anna K.
Campbell, Jennifer
Wirz, Holger
Sharon, Andre
Sauer-Budge, Alexis F.
author_facet Boardman, Anna K.
Campbell, Jennifer
Wirz, Holger
Sharon, Andre
Sauer-Budge, Alexis F.
author_sort Boardman, Anna K.
collection PubMed
description Appropriate care for bacteremic patients is dictated by the amount of time needed for an accurate diagnosis. However, the concentration of microbes in the blood is extremely low in these patients (1–100 CFU/mL), traditionally requiring growth (blood culture) or amplification (e.g., PCR) for detection. Current culture-based methods can take a minimum of two days, while faster methods like PCR require a sample free of inhibitors (i.e., blood components). Though commercial kits exist for the removal of blood from these samples, they typically capture only DNA, thereby necessitating the use of blood culture for antimicrobial testing. Here, we report a novel, scaled-up sample preparation protocol carried out in a new microbial concentration device. The process can efficiently lyse 10 mL of bacteremic blood while maintaining the microorganisms’ viability, giving a 30‑μL final output volume. A suite of six microorganisms (Staphylococcus aureus, Streptococcus pneumoniae, Escherichia coli, Haemophilus influenzae, Pseudomonas aeruginosa, and Candida albicans) at a range of clinically relevant concentrations was tested. All of the microorganisms had recoveries greater than 55% at the highest tested concentration of 100 CFU/mL, with three of them having over 70% recovery. At the lowest tested concentration of 3 CFU/mL, two microorganisms had recoveries of ca. 40–50% while the other four gave recoveries greater than 70%. Using a Taqman assay for methicillin-sensitive S. aureus (MSSA)to prove the feasibility of downstream analysis, we show that our microbial pellets are clean enough for PCR amplification. PCR testing of 56 spiked-positive and negative samples gave a specificity of 0.97 and a sensitivity of 0.96, showing that our sample preparation protocol holds great promise for the rapid diagnosis of bacteremia directly from a primary sample.
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spelling pubmed-43264182015-02-24 Rapid Microbial Sample Preparation from Blood Using a Novel Concentration Device Boardman, Anna K. Campbell, Jennifer Wirz, Holger Sharon, Andre Sauer-Budge, Alexis F. PLoS One Research Article Appropriate care for bacteremic patients is dictated by the amount of time needed for an accurate diagnosis. However, the concentration of microbes in the blood is extremely low in these patients (1–100 CFU/mL), traditionally requiring growth (blood culture) or amplification (e.g., PCR) for detection. Current culture-based methods can take a minimum of two days, while faster methods like PCR require a sample free of inhibitors (i.e., blood components). Though commercial kits exist for the removal of blood from these samples, they typically capture only DNA, thereby necessitating the use of blood culture for antimicrobial testing. Here, we report a novel, scaled-up sample preparation protocol carried out in a new microbial concentration device. The process can efficiently lyse 10 mL of bacteremic blood while maintaining the microorganisms’ viability, giving a 30‑μL final output volume. A suite of six microorganisms (Staphylococcus aureus, Streptococcus pneumoniae, Escherichia coli, Haemophilus influenzae, Pseudomonas aeruginosa, and Candida albicans) at a range of clinically relevant concentrations was tested. All of the microorganisms had recoveries greater than 55% at the highest tested concentration of 100 CFU/mL, with three of them having over 70% recovery. At the lowest tested concentration of 3 CFU/mL, two microorganisms had recoveries of ca. 40–50% while the other four gave recoveries greater than 70%. Using a Taqman assay for methicillin-sensitive S. aureus (MSSA)to prove the feasibility of downstream analysis, we show that our microbial pellets are clean enough for PCR amplification. PCR testing of 56 spiked-positive and negative samples gave a specificity of 0.97 and a sensitivity of 0.96, showing that our sample preparation protocol holds great promise for the rapid diagnosis of bacteremia directly from a primary sample. Public Library of Science 2015-02-12 /pmc/articles/PMC4326418/ /pubmed/25675242 http://dx.doi.org/10.1371/journal.pone.0116837 Text en © 2015 Boardman et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Boardman, Anna K.
Campbell, Jennifer
Wirz, Holger
Sharon, Andre
Sauer-Budge, Alexis F.
Rapid Microbial Sample Preparation from Blood Using a Novel Concentration Device
title Rapid Microbial Sample Preparation from Blood Using a Novel Concentration Device
title_full Rapid Microbial Sample Preparation from Blood Using a Novel Concentration Device
title_fullStr Rapid Microbial Sample Preparation from Blood Using a Novel Concentration Device
title_full_unstemmed Rapid Microbial Sample Preparation from Blood Using a Novel Concentration Device
title_short Rapid Microbial Sample Preparation from Blood Using a Novel Concentration Device
title_sort rapid microbial sample preparation from blood using a novel concentration device
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4326418/
https://www.ncbi.nlm.nih.gov/pubmed/25675242
http://dx.doi.org/10.1371/journal.pone.0116837
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