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Evaluation of the real-time fluorescence loop-mediated isothermal amplification assay for the detection of Ureaplasma urealyticum.
Shen, Jie-Ni; Ye, Jing-Yi; Lao, Meng-Xiao; Wang, Chu-Qiao; Wu, Dong-Hong; Chen, Xiao-Ying; Lin, Li-Hong; Geng, Wen-Yan; Guo, Xu-Guang.
Afiliação
  • Shen JN; Department of Clinical Laboratory Medicine, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
  • Ye JY; Department of Clinical Medicine, The Nanshan School of Guangzhou Medical University, Guangzhou, China.
  • Lao MX; Department of Clinical Medicine, The Nanshan School of Guangzhou Medical University, Guangzhou, China.
  • Wang CQ; Department of Clinical Laboratory Medicine, Maternal and Child Health Care Hospital of Guangming District, Shenzhen, China.
  • Wu DH; Department of Clinical Medicine, The Nanshan School of Guangzhou Medical University, Guangzhou, China.
  • Chen XY; Department of Clinical Medicine, The Nanshan School of Guangzhou Medical University, Guangzhou, China.
  • Lin LH; Department of Clinical Medicine, The Nanshan School of Guangzhou Medical University, Guangzhou, China.
  • Geng WY; Center for Reproduction Medicine, Key Laboratory for Major Obstetric Diseases of Guangdong Province, The Third Clinical School of Guangzhou Medical University, Guangzhou, China. 81743150@qq.com.
  • Guo XG; Department of Clinical Laboratory Medicine, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China. gengwenyan0305@163.com.
AMB Express ; 12(1): 16, 2022 Feb 11.
Article em En | MEDLINE | ID: mdl-35147799
ABSTRACT
Ureaplasma urealyticum (UU) is commonly present in human reproductive tract, which frequently leads to genital tract infection. Hence, there is an urgent need to develop a rapid detection method for UU. In our study, a real-time fluorescence loop-mediated isothermal amplification (LAMP) assay was developed and evaluated for the detection of UU. Two primers were specifically designed based on the highly conserved regions of ureaseB genes. The reaction was carried out for 60 min in a constant temperature system using Bst DNA polymerase, and the process was monitored by real-time fluorescence signal, while polymerase chain reaction (PCR) was performed simultaneously. In real-time fluorescence LAMP reaction system, positive result was only obtained for UU among 9 bacterial strains, with detection sensitivity of 42 pg/µL (4.2 × 105 CFU/mL), and all 16 clinical samples of UU could be detected. In conclusion, real-time fluorescence LAMP is a simple, sensitive, specific and effective method compared with conventional PCR, which shows great promise in the rapid detection of UU.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article