Development of a single-tube loop-mediated isothermal amplification assay for detection of four pathogens of bacterial meningitis

被引:38
作者
Nguyen Tien Huy [1 ]
Le Thi Thuy Hang [1 ]
Boamah, Daniel [1 ]
Nguyen Thi Phuong Lan [2 ]
Phan Van Thanh [2 ,3 ]
Watanabe, Kiwao [4 ]
Vu Thi Thu Huong [4 ]
Kikuchi, Mihoko [1 ]
Ariyoshi, Koya [4 ]
Morita, Kouichi [5 ,6 ]
Hirayama, Kenji [1 ,6 ]
机构
[1] Nagasaki Univ, Inst Trop Med NEKKEN, Dept Immunogenet, Nagasaki 8528523, Japan
[2] Inst Pasteur, Lab Arbovirus, Ho Chi Minh City, Vietnam
[3] Ho Chi Minh City Univ Sci, Fac Biol, Ho Chi Minh City, Vietnam
[4] Nagasaki Univ, Inst Trop Med, Dept Clin Med, Nagasaki 8528523, Japan
[5] Nagasaki Univ, Inst Trop Med, Dept Virol, Nagasaki 8528523, Japan
[6] Nagasaki Univ, Global COE Program, Nagasaki 8528523, Japan
关键词
assay; bacteria; diagnosis; LAMP; meningitis; simultaneous; REAL-TIME PCR; RIBOSOMAL-RNA; CEREBROSPINAL-FLUID; UNIVERSAL PRIMERS; RAPID DETECTION; DIAGNOSIS; SEQUENCES; CULTURE; GENE;
D O I
10.1111/1574-6968.12002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Several loop-mediated isothermal amplification (LAMP) assays have been developed to detect common causative pathogens of bacterial meningitis (BM). However, no LAMP assay is reported to detect Streptococcus agalactiae and Streptococcus suis, which are also among common pathogens of BM. Moreover, it is laborious and expensive by performing multiple reactions for each sample to detect bacterial pathogen. Thus, we aimed to design and develop a single-tube LAMP assay capable of detecting multiple bacterial species, based on the nucleotide sequences of the 16S rRNA genes of the bacteria. The nucleotide sequences of the 16S rRNA genes of main pathogens involved in BM were aligned to identify conserved regions, which were further used to design broad range specific LAMP assay primers. We successfully designed a set of broad range specific LAMP assay primers for simultaneous detection of four species including Staphylococcus aureus, Streptococcus pneumoniae, S. suis and S. agalactiae. The broad range LAMP assay was highly specific without cross-reactivity with other bacteria including Haemophilus influenzae, Neisseria meningitidis and Escherichia coli. The sensitivity of our LAMP assay was 1001000 times higher compared with the conventional PCR assay. The bacterial species could be identified after digestion of the LAMP products with restriction endonuclease DdeI and HaeIII.
引用
收藏
页码:25 / 30
页数:6
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