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Development and evaluation of a droplet digital PCR assay to detect Brucella in human whole blood

BACKGROUND: With the development of domestic animal husbandry, the spread of brucellosis has accelerated, and the scope of the epidemic has expanded. The timely and accurate diagnosis of human brucellosis continues to challenge clinicians in endemic areas. Droplet digital PCR (ddPCR) technology can...

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Autores principales: Liu, Jiayin, Song, Zhichun, Ta, Na, Tian, Guozhong, Yang, Xiaowen, Zhao, Hongyan, Piao, Dongri, Fan, Yu, Zhang, Yu, Jiang, Hai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10237378/
https://www.ncbi.nlm.nih.gov/pubmed/37267228
http://dx.doi.org/10.1371/journal.pntd.0011367
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author Liu, Jiayin
Song, Zhichun
Ta, Na
Tian, Guozhong
Yang, Xiaowen
Zhao, Hongyan
Piao, Dongri
Fan, Yu
Zhang, Yu
Jiang, Hai
author_facet Liu, Jiayin
Song, Zhichun
Ta, Na
Tian, Guozhong
Yang, Xiaowen
Zhao, Hongyan
Piao, Dongri
Fan, Yu
Zhang, Yu
Jiang, Hai
author_sort Liu, Jiayin
collection PubMed
description BACKGROUND: With the development of domestic animal husbandry, the spread of brucellosis has accelerated, and the scope of the epidemic has expanded. The timely and accurate diagnosis of human brucellosis continues to challenge clinicians in endemic areas. Droplet digital PCR (ddPCR) technology can quickly and accurately determine DNA load in samples, providing laboratory evidence for diagnosis, prognosis and management of brucellosis patients. In this study, a ddPCR method was established to accurately quantify Brucella DNA load in whole blood samples, and its diagnostic, prognostic, and therapeutic value for human brucellosis was evaluated. METHODS: Annealing temperature, primers, and probe targeting the Brucella bcsp31 gene were optimised, and the sensitivity, specificity and repeatability of the ddPCR assay were assessed using 94 whole blood samples from 61 confirmed and 33 suspected cases. Results were compared with those of quantitative PCR (qPCR). Nine follow-up brucellosis patients were also analysed by the two methods after 2 and 6 months of treatment. RESULTS: Optimal primer and probe concentrations were 800 nmol/L and 400 nmol/L, respectively, and the optimal annealing temperature was 55.3 °C. The ddPCR results showed that the limit of detection was 1.87 copies per reaction, with high repeatability. The positive rates for ddPCR and qPCR were 88.5% and 75.4% among 61 serum agglutination test (SAT) positive patients. In addition, 57.6% (19/33) of suspected sero-negative samples were positive by ddPCR, but only 36.3% (12/33) were positive by qPCR. Analysis of nine post-therapy follow-up brucellosis patients revealed that the Brucella DNA load in the whole blood samples decreased after 2 and 6 months of treatment, and was slightly increased following relapse and continuous exposure. CONCLUSION: The ddPCR assay showed good accuracy for whole blood samples, and could be a potential diagnostic and prognostic tool for detecting Brucella.
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spelling pubmed-102373782023-06-03 Development and evaluation of a droplet digital PCR assay to detect Brucella in human whole blood Liu, Jiayin Song, Zhichun Ta, Na Tian, Guozhong Yang, Xiaowen Zhao, Hongyan Piao, Dongri Fan, Yu Zhang, Yu Jiang, Hai PLoS Negl Trop Dis Research Article BACKGROUND: With the development of domestic animal husbandry, the spread of brucellosis has accelerated, and the scope of the epidemic has expanded. The timely and accurate diagnosis of human brucellosis continues to challenge clinicians in endemic areas. Droplet digital PCR (ddPCR) technology can quickly and accurately determine DNA load in samples, providing laboratory evidence for diagnosis, prognosis and management of brucellosis patients. In this study, a ddPCR method was established to accurately quantify Brucella DNA load in whole blood samples, and its diagnostic, prognostic, and therapeutic value for human brucellosis was evaluated. METHODS: Annealing temperature, primers, and probe targeting the Brucella bcsp31 gene were optimised, and the sensitivity, specificity and repeatability of the ddPCR assay were assessed using 94 whole blood samples from 61 confirmed and 33 suspected cases. Results were compared with those of quantitative PCR (qPCR). Nine follow-up brucellosis patients were also analysed by the two methods after 2 and 6 months of treatment. RESULTS: Optimal primer and probe concentrations were 800 nmol/L and 400 nmol/L, respectively, and the optimal annealing temperature was 55.3 °C. The ddPCR results showed that the limit of detection was 1.87 copies per reaction, with high repeatability. The positive rates for ddPCR and qPCR were 88.5% and 75.4% among 61 serum agglutination test (SAT) positive patients. In addition, 57.6% (19/33) of suspected sero-negative samples were positive by ddPCR, but only 36.3% (12/33) were positive by qPCR. Analysis of nine post-therapy follow-up brucellosis patients revealed that the Brucella DNA load in the whole blood samples decreased after 2 and 6 months of treatment, and was slightly increased following relapse and continuous exposure. CONCLUSION: The ddPCR assay showed good accuracy for whole blood samples, and could be a potential diagnostic and prognostic tool for detecting Brucella. Public Library of Science 2023-06-02 /pmc/articles/PMC10237378/ /pubmed/37267228 http://dx.doi.org/10.1371/journal.pntd.0011367 Text en © 2023 Liu et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Liu, Jiayin
Song, Zhichun
Ta, Na
Tian, Guozhong
Yang, Xiaowen
Zhao, Hongyan
Piao, Dongri
Fan, Yu
Zhang, Yu
Jiang, Hai
Development and evaluation of a droplet digital PCR assay to detect Brucella in human whole blood
title Development and evaluation of a droplet digital PCR assay to detect Brucella in human whole blood
title_full Development and evaluation of a droplet digital PCR assay to detect Brucella in human whole blood
title_fullStr Development and evaluation of a droplet digital PCR assay to detect Brucella in human whole blood
title_full_unstemmed Development and evaluation of a droplet digital PCR assay to detect Brucella in human whole blood
title_short Development and evaluation of a droplet digital PCR assay to detect Brucella in human whole blood
title_sort development and evaluation of a droplet digital pcr assay to detect brucella in human whole blood
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10237378/
https://www.ncbi.nlm.nih.gov/pubmed/37267228
http://dx.doi.org/10.1371/journal.pntd.0011367
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