Cargando…
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...
Autores principales: | , , , , , , |
---|---|
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 |
_version_ | 1783661175152574464 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7936308 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT xiuleshan amolecularscreeningassaytoidentifychlamydiatrachomatisanddistinguishnewvariantsofctrachomatisfromwildtype AT liyamei amolecularscreeningassaytoidentifychlamydiatrachomatisanddistinguishnewvariantsofctrachomatisfromwildtype AT zhangchi amolecularscreeningassaytoidentifychlamydiatrachomatisanddistinguishnewvariantsofctrachomatisfromwildtype AT liyizhun amolecularscreeningassaytoidentifychlamydiatrachomatisanddistinguishnewvariantsofctrachomatisfromwildtype AT zengyaling amolecularscreeningassaytoidentifychlamydiatrachomatisanddistinguishnewvariantsofctrachomatisfromwildtype AT wangfeng amolecularscreeningassaytoidentifychlamydiatrachomatisanddistinguishnewvariantsofctrachomatisfromwildtype AT pengjunping amolecularscreeningassaytoidentifychlamydiatrachomatisanddistinguishnewvariantsofctrachomatisfromwildtype AT xiuleshan molecularscreeningassaytoidentifychlamydiatrachomatisanddistinguishnewvariantsofctrachomatisfromwildtype AT liyamei molecularscreeningassaytoidentifychlamydiatrachomatisanddistinguishnewvariantsofctrachomatisfromwildtype AT zhangchi molecularscreeningassaytoidentifychlamydiatrachomatisanddistinguishnewvariantsofctrachomatisfromwildtype AT liyizhun molecularscreeningassaytoidentifychlamydiatrachomatisanddistinguishnewvariantsofctrachomatisfromwildtype AT zengyaling molecularscreeningassaytoidentifychlamydiatrachomatisanddistinguishnewvariantsofctrachomatisfromwildtype AT wangfeng molecularscreeningassaytoidentifychlamydiatrachomatisanddistinguishnewvariantsofctrachomatisfromwildtype AT pengjunping molecularscreeningassaytoidentifychlamydiatrachomatisanddistinguishnewvariantsofctrachomatisfromwildtype |