Surveillance for Chlamydia trachomatis variants escaping detection with the Aptima Combo 2 assay in Canada from 2019 to 2021.

IF 3.8 2区 生物学 Q2 MICROBIOLOGY Microbiology spectrum Pub Date : 2025-03-04 Epub Date: 2025-01-23 DOI:10.1128/spectrum.02062-24
Felicia Roy, Jennifer Beirnes, Jason J LeBlanc, Suzanne Gibbons, Aida Sivro, Alberto Severini
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Abstract

Nucleic acid amplification tests (NAATs) are the method of choice for Chlamydia trachomatis diagnosis, but these strategies are susceptible to target site mutations. C. trachomatis variants escaping detection with the Aptima Combo 2 (AC2) assay on the Hologic Panther instrument from 23S rRNA mutations have been reported in Nordic countries, England, Japan, and the United States. Given the potential for false negative results, this study investigated whether strains of C. trachomatis with AC2 target site mutations were present in Canada. Surveillance was conducted in Canadian laboratories from 2019 to 2021. Specimens suspected of AC2 target site mutations included those with low-value detections on the AC2 assay, with subsequent high-value detections on the Aptima Chlamydia Trachomatis (ACT) assay used for confirmatory testing. Specimens with AC2/ACT discrepant results were subjected to sequencing of the AC2 target (i.e., 23S rRNA). Sequencing revealed 15 (4.8%) diagnostic escape variants which were carrying either C1514T, G1523A, or G1526A mutations. All specimens with a diagnostic escape mutation were detected with a reformulated version of the AC2 assay. Overall, while the prevalence of C. trachomatis variants was rare, their presence in the Canadian population supports the use of the new AC2 kit formulation and the need for ongoing genetic surveillance for NAAT-based assays.

Importance: Molecular tests are commonly used for the detection of sexually transmitted infections (STIs) like Chlamydia trachomatis. Mutations impacting C. trachomatis molecular target detection on the Hologic Panther AC2 assay have been reported in several countries, raising concerns about potential false negative results. This study showed C. trachomatis target detection failures in specimens submitted for C. trachomatis testing in Canadian laboratories from 2019 to 2021. A reformulated version of the AC2 molecular test is now available that can identify C. trachomatis strains harboring target site mutations that were impacted by the previous test formulation. While target site mutations were rare in Canada, revealing their presence is important to ensure accurate molecular detection of C. trachomatis with existing testing methods. This study supports ongoing genetic monitoring of C. trachomatis molecular test target sites, as well as the use of the reformulated test to avoid false negative results and subsequent transmissions.

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2019 - 2021年加拿大Aptima Combo 2检测漏检沙眼衣原体变异的监测
核酸扩增试验(NAATs)是沙眼衣原体诊断的首选方法,但这些方法容易受到靶位点突变的影响。在Hologic Panther仪器上,从23S rRNA突变中逃脱Aptima Combo 2 (AC2)检测的沙眼衣原体变异在北欧国家、英国、日本和美国都有报道。考虑到假阴性结果的可能性,本研究调查了在加拿大是否存在AC2靶位点突变的沙眼衣原体菌株。2019年至2021年在加拿大实验室进行了监测。疑似AC2靶位突变的标本包括AC2检测值较低的标本,随后用于确认检测的Aptima沙眼衣原体(ACT)检测值较高的标本。对AC2/ACT结果不一致的标本进行AC2靶点(即23S rRNA)测序。测序显示15个(4.8%)诊断性逃逸变异携带C1514T、G1523A或G1526A突变。所有具有诊断性逃逸突变的标本均采用重新配制的AC2测定法检测。总的来说,虽然沙眼衣原体变异的流行率很少见,但它们在加拿大人群中的存在支持了新的AC2试剂盒配方的使用,并且需要对基于naat的检测进行持续的遗传监测。重要性:分子检测通常用于检测性传播感染,如沙眼衣原体。一些国家报道了影响Hologic Panther AC2检测沙眼衣原体分子靶标检测的突变,引起了对潜在假阴性结果的担忧。该研究显示,2019年至2021年,加拿大实验室提交沙眼原体检测的标本中沙眼原体靶检测失败。AC2分子检测的重新制定版本现在可用,可以识别沙眼衣原体菌株,这些菌株含有受先前测试配方影响的靶位点突变。虽然靶位点突变在加拿大很少见,但揭示它们的存在对于确保现有检测方法准确检测沙眼衣原体分子非常重要。本研究支持沙眼衣原体分子检测靶点的持续遗传监测,以及使用重新制定的检测方法以避免假阴性结果和随后的传播。
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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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