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Design and Evaluation of a Novel Multiplex Real-Time PCR Melting Curve Assay for the Simultaneous Detection of Nine Sexually Transmitted Disease Pathogens in Genitourinary Secretions

Background: Sexually transmitted diseases (STD) are a major cause of infertility, long-term disability, ectopic pregnancy, and premature birth. Therefore, the development of fast and low-cost laboratory STD diagnostic screening methods will contribute to reducing STD-induced reproductive tract damag...

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Autores principales: Hu, Xiao-Mei, Xu, Jiang-Xia, Jiang, Li-Xia, Deng, Lian-Rui, Gu, Zhen-Mei, Xie, Xiao-Ying, Ji, Hui-Cai, Wang, Wei-Hua, Li, Li-Ming, Tian, Cheng-Nan, Song, Fang-Li, Huang, Shao, Zheng, Lei, Zhong, Tian-Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6861374/
https://www.ncbi.nlm.nih.gov/pubmed/31781517
http://dx.doi.org/10.3389/fcimb.2019.00382
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author Hu, Xiao-Mei
Xu, Jiang-Xia
Jiang, Li-Xia
Deng, Lian-Rui
Gu, Zhen-Mei
Xie, Xiao-Ying
Ji, Hui-Cai
Wang, Wei-Hua
Li, Li-Ming
Tian, Cheng-Nan
Song, Fang-Li
Huang, Shao
Zheng, Lei
Zhong, Tian-Yu
author_facet Hu, Xiao-Mei
Xu, Jiang-Xia
Jiang, Li-Xia
Deng, Lian-Rui
Gu, Zhen-Mei
Xie, Xiao-Ying
Ji, Hui-Cai
Wang, Wei-Hua
Li, Li-Ming
Tian, Cheng-Nan
Song, Fang-Li
Huang, Shao
Zheng, Lei
Zhong, Tian-Yu
author_sort Hu, Xiao-Mei
collection PubMed
description Background: Sexually transmitted diseases (STD) are a major cause of infertility, long-term disability, ectopic pregnancy, and premature birth. Therefore, the development of fast and low-cost laboratory STD diagnostic screening methods will contribute to reducing STD-induced reproductive tract damage and improve women's health worldwide. In this study, we evaluated a novel multiplex real-time PCR melting curve assay method for the simultaneous detection of 9 STD pathogens, including Chlamydia trachomatis, Neisseria gonorrhoeae, Mycoplasma genitalium, Trichomonas vaginalis, Mycoplasma hominis, Ureaplasma urealyticum, Ureaplasma parvum, and herpes simplex virus. Methods: The analytical performance of the method, including its limit of detection (LOD), specificity, repeatability, and effect on different DNA extraction kits were evaluated. Additionally, we obtained 1,328 clinical specimens from 3 hospitals to detect the 9 STD pathogens using multiplex real-time PCR melting curve and Sanger sequencing, to evaluate the sensitivity, specificity, and consistency of the assay method. Results: The results showed that the analytical sensitivity of the novel multiplex real-time PCR melting curve assay is very excellent, with LOD of DNA corresponding to <200 copies/μL for the DNA of the 9 STDs and 1.00 × 10(4) color change unit /ml for those of UU and UP. Additionally, this assay demonstrated excellent analytical specificity, excellent repeatability, and its results had no effect of different DNA extraction kits. The performance, in terms of sensitivity (91.06–100%) and specificity (99.14–100%), was remarkable, since the consistency between it and Sanger sequencing was more than 0.85 in the clinic. Conclusion: The novel multiplex real-time PCR melting curve assay method has high sensitivity and specificity, relatively low cost, and simple to use for the simultaneous detection of 9 STD pathogens in genitourinary secretions.
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spelling pubmed-68613742019-11-28 Design and Evaluation of a Novel Multiplex Real-Time PCR Melting Curve Assay for the Simultaneous Detection of Nine Sexually Transmitted Disease Pathogens in Genitourinary Secretions Hu, Xiao-Mei Xu, Jiang-Xia Jiang, Li-Xia Deng, Lian-Rui Gu, Zhen-Mei Xie, Xiao-Ying Ji, Hui-Cai Wang, Wei-Hua Li, Li-Ming Tian, Cheng-Nan Song, Fang-Li Huang, Shao Zheng, Lei Zhong, Tian-Yu Front Cell Infect Microbiol Cellular and Infection Microbiology Background: Sexually transmitted diseases (STD) are a major cause of infertility, long-term disability, ectopic pregnancy, and premature birth. Therefore, the development of fast and low-cost laboratory STD diagnostic screening methods will contribute to reducing STD-induced reproductive tract damage and improve women's health worldwide. In this study, we evaluated a novel multiplex real-time PCR melting curve assay method for the simultaneous detection of 9 STD pathogens, including Chlamydia trachomatis, Neisseria gonorrhoeae, Mycoplasma genitalium, Trichomonas vaginalis, Mycoplasma hominis, Ureaplasma urealyticum, Ureaplasma parvum, and herpes simplex virus. Methods: The analytical performance of the method, including its limit of detection (LOD), specificity, repeatability, and effect on different DNA extraction kits were evaluated. Additionally, we obtained 1,328 clinical specimens from 3 hospitals to detect the 9 STD pathogens using multiplex real-time PCR melting curve and Sanger sequencing, to evaluate the sensitivity, specificity, and consistency of the assay method. Results: The results showed that the analytical sensitivity of the novel multiplex real-time PCR melting curve assay is very excellent, with LOD of DNA corresponding to <200 copies/μL for the DNA of the 9 STDs and 1.00 × 10(4) color change unit /ml for those of UU and UP. Additionally, this assay demonstrated excellent analytical specificity, excellent repeatability, and its results had no effect of different DNA extraction kits. The performance, in terms of sensitivity (91.06–100%) and specificity (99.14–100%), was remarkable, since the consistency between it and Sanger sequencing was more than 0.85 in the clinic. Conclusion: The novel multiplex real-time PCR melting curve assay method has high sensitivity and specificity, relatively low cost, and simple to use for the simultaneous detection of 9 STD pathogens in genitourinary secretions. Frontiers Media S.A. 2019-11-12 /pmc/articles/PMC6861374/ /pubmed/31781517 http://dx.doi.org/10.3389/fcimb.2019.00382 Text en Copyright © 2019 Hu, Xu, Jiang, Deng, Gu, Xie, Ji, Wang, Li, Tian, Song, Huang, Zheng and Zhong. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular and Infection Microbiology
Hu, Xiao-Mei
Xu, Jiang-Xia
Jiang, Li-Xia
Deng, Lian-Rui
Gu, Zhen-Mei
Xie, Xiao-Ying
Ji, Hui-Cai
Wang, Wei-Hua
Li, Li-Ming
Tian, Cheng-Nan
Song, Fang-Li
Huang, Shao
Zheng, Lei
Zhong, Tian-Yu
Design and Evaluation of a Novel Multiplex Real-Time PCR Melting Curve Assay for the Simultaneous Detection of Nine Sexually Transmitted Disease Pathogens in Genitourinary Secretions
title Design and Evaluation of a Novel Multiplex Real-Time PCR Melting Curve Assay for the Simultaneous Detection of Nine Sexually Transmitted Disease Pathogens in Genitourinary Secretions
title_full Design and Evaluation of a Novel Multiplex Real-Time PCR Melting Curve Assay for the Simultaneous Detection of Nine Sexually Transmitted Disease Pathogens in Genitourinary Secretions
title_fullStr Design and Evaluation of a Novel Multiplex Real-Time PCR Melting Curve Assay for the Simultaneous Detection of Nine Sexually Transmitted Disease Pathogens in Genitourinary Secretions
title_full_unstemmed Design and Evaluation of a Novel Multiplex Real-Time PCR Melting Curve Assay for the Simultaneous Detection of Nine Sexually Transmitted Disease Pathogens in Genitourinary Secretions
title_short Design and Evaluation of a Novel Multiplex Real-Time PCR Melting Curve Assay for the Simultaneous Detection of Nine Sexually Transmitted Disease Pathogens in Genitourinary Secretions
title_sort design and evaluation of a novel multiplex real-time pcr melting curve assay for the simultaneous detection of nine sexually transmitted disease pathogens in genitourinary secretions
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6861374/
https://www.ncbi.nlm.nih.gov/pubmed/31781517
http://dx.doi.org/10.3389/fcimb.2019.00382
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