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A molecular screening assay to identify Chlamydia trachomatis and distinguish new variants of C. trachomatis from wild‐type

Chlamydia trachomatis is the most common sexually transmitted pathogen globally, causing serious health problems and representing a burden on public health. A new variant of C. trachomatis (nvCT) that carries mutations (C1514T, C1515T and G1523A) in the 23S rRNA gene has eluded detection in Aptima C...

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Autores principales: Xiu, Leshan, Li, Yamei, Zhang, Chi, Li, Yizhun, Zeng, Yaling, Wang, Feng, Peng, Junping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7936308/
https://www.ncbi.nlm.nih.gov/pubmed/33277967
http://dx.doi.org/10.1111/1751-7915.13724
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author Xiu, Leshan
Li, Yamei
Zhang, Chi
Li, Yizhun
Zeng, Yaling
Wang, Feng
Peng, Junping
author_facet Xiu, Leshan
Li, Yamei
Zhang, Chi
Li, Yizhun
Zeng, Yaling
Wang, Feng
Peng, Junping
author_sort Xiu, Leshan
collection PubMed
description Chlamydia trachomatis is the most common sexually transmitted pathogen globally, causing serious health problems and representing a burden on public health. A new variant of C. trachomatis (nvCT) that carries mutations (C1514T, C1515T and G1523A) in the 23S rRNA gene has eluded detection in Aptima Combo 2 assays. This has led to false negatives in diagnostics tests and poses a challenge for C. trachomatis diagnostics on a global level. In this study, we developed a simple and cost‐effective assay to identify C. trachomatis, with a potential application to screen for nvCT. We developed a screening assay based on high‐resolution melting (HRM), targeting the 23S rRNA gene and cryptic plasmid. To evaluate the performance of the assay, 404 archived C. trachomatis DNA specimens and 570 extracted clinical specimens were analysed. Our HRM assay not only identified C. trachomatis in clinical specimens, but also correctly differentiated nvCT carrying C1514T, C1515T and G1523A mutations from the wild‐type. We observed no cross‐reactions with other clinically related agents, and the limit of detection was 11.26 (95% CI; 7.61–31.82) copies per reaction. Implementation of this screening assay could reduce detection times and costs for C. trachomatis diagnoses, and facilitate increased research on the presence and monitoring of nvCT.
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spelling pubmed-79363082021-03-16 A molecular screening assay to identify Chlamydia trachomatis and distinguish new variants of C. trachomatis from wild‐type Xiu, Leshan Li, Yamei Zhang, Chi Li, Yizhun Zeng, Yaling Wang, Feng Peng, Junping Microb Biotechnol Research Articles Chlamydia trachomatis is the most common sexually transmitted pathogen globally, causing serious health problems and representing a burden on public health. A new variant of C. trachomatis (nvCT) that carries mutations (C1514T, C1515T and G1523A) in the 23S rRNA gene has eluded detection in Aptima Combo 2 assays. This has led to false negatives in diagnostics tests and poses a challenge for C. trachomatis diagnostics on a global level. In this study, we developed a simple and cost‐effective assay to identify C. trachomatis, with a potential application to screen for nvCT. We developed a screening assay based on high‐resolution melting (HRM), targeting the 23S rRNA gene and cryptic plasmid. To evaluate the performance of the assay, 404 archived C. trachomatis DNA specimens and 570 extracted clinical specimens were analysed. Our HRM assay not only identified C. trachomatis in clinical specimens, but also correctly differentiated nvCT carrying C1514T, C1515T and G1523A mutations from the wild‐type. We observed no cross‐reactions with other clinically related agents, and the limit of detection was 11.26 (95% CI; 7.61–31.82) copies per reaction. Implementation of this screening assay could reduce detection times and costs for C. trachomatis diagnoses, and facilitate increased research on the presence and monitoring of nvCT. John Wiley and Sons Inc. 2020-12-05 /pmc/articles/PMC7936308/ /pubmed/33277967 http://dx.doi.org/10.1111/1751-7915.13724 Text en © 2020 The Authors. Microbial Biotechnology published by Society for Applied Microbiology and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Xiu, Leshan
Li, Yamei
Zhang, Chi
Li, Yizhun
Zeng, Yaling
Wang, Feng
Peng, Junping
A molecular screening assay to identify Chlamydia trachomatis and distinguish new variants of C. trachomatis from wild‐type
title A molecular screening assay to identify Chlamydia trachomatis and distinguish new variants of C. trachomatis from wild‐type
title_full A molecular screening assay to identify Chlamydia trachomatis and distinguish new variants of C. trachomatis from wild‐type
title_fullStr A molecular screening assay to identify Chlamydia trachomatis and distinguish new variants of C. trachomatis from wild‐type
title_full_unstemmed A molecular screening assay to identify Chlamydia trachomatis and distinguish new variants of C. trachomatis from wild‐type
title_short A molecular screening assay to identify Chlamydia trachomatis and distinguish new variants of C. trachomatis from wild‐type
title_sort molecular screening assay to identify chlamydia trachomatis and distinguish new variants of c. trachomatis from wild‐type
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7936308/
https://www.ncbi.nlm.nih.gov/pubmed/33277967
http://dx.doi.org/10.1111/1751-7915.13724
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