Cargando…
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...
Autores principales: | , , , , , , , , , |
---|---|
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 |
_version_ | 1785053144210735104 |
---|---|
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. |
format | Online Article Text |
id | pubmed-10237378 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT liujiayin developmentandevaluationofadropletdigitalpcrassaytodetectbrucellainhumanwholeblood AT songzhichun developmentandevaluationofadropletdigitalpcrassaytodetectbrucellainhumanwholeblood AT tana developmentandevaluationofadropletdigitalpcrassaytodetectbrucellainhumanwholeblood AT tianguozhong developmentandevaluationofadropletdigitalpcrassaytodetectbrucellainhumanwholeblood AT yangxiaowen developmentandevaluationofadropletdigitalpcrassaytodetectbrucellainhumanwholeblood AT zhaohongyan developmentandevaluationofadropletdigitalpcrassaytodetectbrucellainhumanwholeblood AT piaodongri developmentandevaluationofadropletdigitalpcrassaytodetectbrucellainhumanwholeblood AT fanyu developmentandevaluationofadropletdigitalpcrassaytodetectbrucellainhumanwholeblood AT zhangyu developmentandevaluationofadropletdigitalpcrassaytodetectbrucellainhumanwholeblood AT jianghai developmentandevaluationofadropletdigitalpcrassaytodetectbrucellainhumanwholeblood |