دورية أكاديمية
Use of real-time PCR as an alternative to conventional genotyping methods for the laboratory detection of lymphogranuloma venereum (LGV).
العنوان: | Use of real-time PCR as an alternative to conventional genotyping methods for the laboratory detection of lymphogranuloma venereum (LGV). |
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المؤلفون: | Woodson EN; Laboratory Leadership Service, Centers for Disease Control and Prevention, Atlanta, GA, USA; Division of STD Prevention, National Center for HIV, Hepatitis, STD, TB Prevention, Centers for Disease Control and Prevention, Atlanta, GA, USA. Electronic address: phy2@cdc.gov., Katz SS; Division of STD Prevention, National Center for HIV, Hepatitis, STD, TB Prevention, Centers for Disease Control and Prevention, Atlanta, GA, USA., Mosley SS; Division of STD Prevention, National Center for HIV, Hepatitis, STD, TB Prevention, Centers for Disease Control and Prevention, Atlanta, GA, USA., Danavall DC; Division of STD Prevention, National Center for HIV, Hepatitis, STD, TB Prevention, Centers for Disease Control and Prevention, Atlanta, GA, USA., Bowden KE; Division of STD Prevention, National Center for HIV, Hepatitis, STD, TB Prevention, Centers for Disease Control and Prevention, Atlanta, GA, USA., Chi KH; Division of STD Prevention, National Center for HIV, Hepatitis, STD, TB Prevention, Centers for Disease Control and Prevention, Atlanta, GA, USA., Raphael BH; Division of STD Prevention, National Center for HIV, Hepatitis, STD, TB Prevention, Centers for Disease Control and Prevention, Atlanta, GA, USA. |
المصدر: | Diagnostic microbiology and infectious disease [Diagn Microbiol Infect Dis] 2021 Dec; Vol. 101 (4), pp. 115532. Date of Electronic Publication: 2021 Aug 27. |
نوع المنشور: | Journal Article |
اللغة: | English |
بيانات الدورية: | Publisher: Elsevier Biomedical Country of Publication: United States NLM ID: 8305899 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-0070 (Electronic) Linking ISSN: 07328893 NLM ISO Abbreviation: Diagn Microbiol Infect Dis Subsets: MEDLINE |
أسماء مطبوعة: | Original Publication: [New York, NY] : Elsevier Biomedical, [c1983- |
مواضيع طبية MeSH: | Chlamydia trachomatis/*isolation & purification , Lymphogranuloma Venereum/*diagnosis , Molecular Diagnostic Techniques/*methods , Real-Time Polymerase Chain Reaction/*methods, Bacterial Outer Membrane Proteins/genetics ; Chlamydia trachomatis/classification ; Chlamydia trachomatis/genetics ; DNA, Bacterial/genetics ; Genome, Bacterial/genetics ; Genotype ; Humans ; Lymphogranuloma Venereum/microbiology ; Molecular Diagnostic Techniques/standards ; Real-Time Polymerase Chain Reaction/standards ; Rectum/microbiology ; Reproducibility of Results ; Sensitivity and Specificity ; Sequence Analysis, DNA ; Serogroup |
مستخلص: | Lymphogranuloma venereum (LGV) can be differentiated from non-LGV chlamydial infection using Sanger sequencing or molecular assays, including those that are commercially-available internationally. Here, we describe the performance of a rapid real-time PCR (RT-PCR)-based strategy in differentiating Chlamydia trachomatis infections associated with LGV or non-LGV serovars. One hundred three rectal swabs, previously genotyped using Sanger sequencing of the ompA gene as a reference method, were tested in the RT-PCR assays. All non-LGV specimens were correctly identified, but the RT-PCR failed to detect 1 LGV specimen, resulting in a sensitivity of 87.5% for the non-LGV/LGV RT-PCR assay. Additional performance characteristics (e.g., specificity, accuracy, and reproducibility) were all between 93% and 100% with a limit of detection ≤100 copies/reaction. Thus, this rapid RT-PCR method for LGV detection in clinical specimens is comparable to the reference method. Competing Interests: Declaration of competing interest The authors report no conflicts of interest relevant to this article. (Published by Elsevier Inc.) |
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معلومات مُعتمدة: | CC999999 United States ImCDC Intramural CDC HHS |
فهرسة مساهمة: | Keywords: Chlamydia trachomatis; Lymphogranuloma venereum; Outer membrane protein A (ompA); Real-time PCR |
المشرفين على المادة: | 0 (Bacterial Outer Membrane Proteins) 0 (DNA, Bacterial) 149024-69-1 (OMPA outer membrane proteins) |
تواريخ الأحداث: | Date Created: 20210927 Date Completed: 20220131 Latest Revision: 20221202 |
رمز التحديث: | 20240628 |
مُعرف محوري في PubMed: | PMC8650105 |
DOI: | 10.1016/j.diagmicrobio.2021.115532 |
PMID: | 34571353 |
قاعدة البيانات: | MEDLINE |
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