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A magneto-DNA nanoparticle system for the rapid and sensitive diagnosis of enteric fever
There is currently no widely available optimal assay for diagnosing patients with enteric fever. Here we present a novel assay designed to detect amplified Salmonella nucleic acid (mRNA) using magneto-DNA probes and a miniaturized nuclear magnetic resonance device. We designed primers for genes spec...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5015101/ https://www.ncbi.nlm.nih.gov/pubmed/27605393 http://dx.doi.org/10.1038/srep32878 |
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author | Park, Ki Soo Chung, Hyun Jung Khanam, Farhana Lee, Hakho Rashu, Rasheduzzaman Bhuiyan, Md. Taufiqur Berger, Amanda Harris, Jason B. Calderwood, Stephen B. Ryan, Edward T. Qadri, Firdausi Weissleder, Ralph Charles, Richelle C. |
author_facet | Park, Ki Soo Chung, Hyun Jung Khanam, Farhana Lee, Hakho Rashu, Rasheduzzaman Bhuiyan, Md. Taufiqur Berger, Amanda Harris, Jason B. Calderwood, Stephen B. Ryan, Edward T. Qadri, Firdausi Weissleder, Ralph Charles, Richelle C. |
author_sort | Park, Ki Soo |
collection | PubMed |
description | There is currently no widely available optimal assay for diagnosing patients with enteric fever. Here we present a novel assay designed to detect amplified Salmonella nucleic acid (mRNA) using magneto-DNA probes and a miniaturized nuclear magnetic resonance device. We designed primers for genes specific to S. Typhi, S. Paratyphi A, and genes conserved among Salmonella enterica spp. and utilized strongly magnetized nanoparticles to enhance the detection signal. Blood samples spiked with in vitro grown S. Typhi, S. Paratyphi A, S. Typhimurium, and E. coli were used to confirm the specificity of each probe-set, and serial 10-fold dilutions were used to determine the limit of the detection of the assay, 0.01–1.0 CFU/ml. For proof of principle, we applied our assay to 0.5 mL blood samples from 5 patients with culture-confirmed enteric fever from Bangladesh in comparison to 3 healthy controls. We were able to detect amplified target cDNA in all 5 cases of enteric fever; no detectable signal was seen in the healthy controls. Our results suggest that a magneto-DNA nanoparticle system, with an assay time from blood collection of 3.5 hours, may be a promising platform for the rapid and culture-free diagnosis of enteric fever and non-typhoidal Salmonella bacteremia. |
format | Online Article Text |
id | pubmed-5015101 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50151012016-09-12 A magneto-DNA nanoparticle system for the rapid and sensitive diagnosis of enteric fever Park, Ki Soo Chung, Hyun Jung Khanam, Farhana Lee, Hakho Rashu, Rasheduzzaman Bhuiyan, Md. Taufiqur Berger, Amanda Harris, Jason B. Calderwood, Stephen B. Ryan, Edward T. Qadri, Firdausi Weissleder, Ralph Charles, Richelle C. Sci Rep Article There is currently no widely available optimal assay for diagnosing patients with enteric fever. Here we present a novel assay designed to detect amplified Salmonella nucleic acid (mRNA) using magneto-DNA probes and a miniaturized nuclear magnetic resonance device. We designed primers for genes specific to S. Typhi, S. Paratyphi A, and genes conserved among Salmonella enterica spp. and utilized strongly magnetized nanoparticles to enhance the detection signal. Blood samples spiked with in vitro grown S. Typhi, S. Paratyphi A, S. Typhimurium, and E. coli were used to confirm the specificity of each probe-set, and serial 10-fold dilutions were used to determine the limit of the detection of the assay, 0.01–1.0 CFU/ml. For proof of principle, we applied our assay to 0.5 mL blood samples from 5 patients with culture-confirmed enteric fever from Bangladesh in comparison to 3 healthy controls. We were able to detect amplified target cDNA in all 5 cases of enteric fever; no detectable signal was seen in the healthy controls. Our results suggest that a magneto-DNA nanoparticle system, with an assay time from blood collection of 3.5 hours, may be a promising platform for the rapid and culture-free diagnosis of enteric fever and non-typhoidal Salmonella bacteremia. Nature Publishing Group 2016-09-08 /pmc/articles/PMC5015101/ /pubmed/27605393 http://dx.doi.org/10.1038/srep32878 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Park, Ki Soo Chung, Hyun Jung Khanam, Farhana Lee, Hakho Rashu, Rasheduzzaman Bhuiyan, Md. Taufiqur Berger, Amanda Harris, Jason B. Calderwood, Stephen B. Ryan, Edward T. Qadri, Firdausi Weissleder, Ralph Charles, Richelle C. A magneto-DNA nanoparticle system for the rapid and sensitive diagnosis of enteric fever |
title | A magneto-DNA nanoparticle system for the rapid and sensitive diagnosis of enteric fever |
title_full | A magneto-DNA nanoparticle system for the rapid and sensitive diagnosis of enteric fever |
title_fullStr | A magneto-DNA nanoparticle system for the rapid and sensitive diagnosis of enteric fever |
title_full_unstemmed | A magneto-DNA nanoparticle system for the rapid and sensitive diagnosis of enteric fever |
title_short | A magneto-DNA nanoparticle system for the rapid and sensitive diagnosis of enteric fever |
title_sort | magneto-dna nanoparticle system for the rapid and sensitive diagnosis of enteric fever |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5015101/ https://www.ncbi.nlm.nih.gov/pubmed/27605393 http://dx.doi.org/10.1038/srep32878 |
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