Rapid and visual detection of Mycoplasma genitalium using recombinase polymerase amplification combined with lateral flow strips

被引:0
|
作者
Ren, Pufang [1 ]
Zeng, Yingmin [1 ]
Feng, Yao [1 ]
Hong, Honghai [1 ]
Xia, Yong [1 ]
机构
[1] Guangzhou Med Univ, Affiliated Hosp 3, Guangdong Prov Clin Res Ctr Obstet & Gynecol, Dept Clin Lab,Guangdong Prov Clin Res Ctr Obstet &, Guangzhou, Peoples R China
关键词
Recombinase polymerase amplification (RPA); Lateral flow (LF); Mycoplasma genitalium; Rapid detection; REAL-TIME PCR; EUROPEAN GUIDELINE; INFECTION; DNA; STRAINS; DISEASE; ASSAY;
D O I
10.1016/j.mimet.2024.107030
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Mycoplasma genitalium (MG) is an important sexually transmitted pathogen that can cause urethritis in males and pelvic inflammatory disease in females. Due to its complex growth requirements and lengthy incubation times, culturing MG in clinical laboratories is impractical. Here we describe a rapid and visual assay combining recombinase polymerase amplification (RPA) with lateral flow (LF) strips to detect MG (MG-RPA-LF). The limit of detection (LoD) of this method was 33.6 genome equivalents (GE) per reaction, using a dilution series of purified genomic DNA. Clinical performance was evaluated by testing 100 urogenital swabs. Compared to the Simultaneous Amplification and Testing assay, our MG-RPA-LF assay showed a sensitivity of 94 % (95 % CI, 82 %-98 %) and a specificity of 100 % (95 % CI, 91 %-100 %). The overall concordance between the two methods was 97 % (95 % CI, 91 %-99 %) with a kappa coefficient of 0.94 (P < 0.001). Without cumbersome and expensive instruments, this method is anticipated to be a promising alternative to diagnose MG infection, especially in resource-poor settings.
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页数:6
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