Evaluation of the real-time fluorescence loop-mediated isothermal amplification assay for the detection of Ureaplasma urealyticum

被引:2
作者
Shen, Jie-Ni [1 ,2 ]
Ye, Jing-Yi [2 ]
Lao, Meng-Xiao [3 ]
Wang, Chu-Qiao [2 ]
Wu, Dong-Hong [2 ]
Chen, Xiao-Ying [2 ]
Lin, Li-Hong [4 ]
Geng, Wen-Yan [1 ,5 ]
Guo, Xu-Guang [1 ,6 ,7 ]
机构
[1] Guangzhou Med Univ, Dept Clin Lab Med, Affiliated Hosp 3, Guangzhou, Peoples R China
[2] Guangzhou Med Univ, Dept Clin Med, Nanshan Sch, Guangzhou, Peoples R China
[3] Maternal & Child Hlth Care Hosp Guangming Dist, Dept Clin Lab Med, Shenzhen, Peoples R China
[4] Guangzhou Med Univ, Ctr Reprod Med, Key Lab Major Obstetr Dis Guangdong Prov, Clin Sch 3, Guangzhou, Peoples R China
[5] Guangzhou Med Univ, Dept Blood Transfus, Affiliated Hosp 3, Guangzhou, Peoples R China
[6] Guangzhou Med Univ, Key Lab Major Obstetr Dis Guangdong Prov, Affiliated Hosp 3, Guangzhou, Peoples R China
[7] Guangzhou Med Univ, Key Lab Reprod & Genet, Guangdong Higher Educ Inst, Affiliated Hosp 3, Guangzhou, Peoples R China
关键词
Ureaplasma urealyticum; Loop-mediated isothermal amplification; Real-time; POLYMERASE-CHAIN-REACTION; MYCOPLASMA-HOMINIS; RAPID DETECTION; PRETERM LABOR; DIAGNOSIS; PCR; COLONIZATION; LAMP;
D O I
10.1186/s13568-022-01357-2
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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/mu L (4.2 x 10(5) 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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页数:8
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