Loop-mediated isothermal amplification for rapid detection of Bacillus anthracis spores
被引:64
作者:
Yan-Mei Qiao
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机构:Chinese Acad Sci, Wuhan Inst Virol, State Key Lab Virol, Wuhan 430071, Peoples R China
Yan-Mei Qiao
Yong-Chao Guo
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机构:Chinese Acad Sci, Wuhan Inst Virol, State Key Lab Virol, Wuhan 430071, Peoples R China
Yong-Chao Guo
Xian-En Zhang
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Chinese Acad Sci, Wuhan Inst Virol, State Key Lab Virol, Wuhan 430071, Peoples R ChinaChinese Acad Sci, Wuhan Inst Virol, State Key Lab Virol, Wuhan 430071, Peoples R China
Xian-En Zhang
[1
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Ya-Feng Zhou
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机构:Chinese Acad Sci, Wuhan Inst Virol, State Key Lab Virol, Wuhan 430071, Peoples R China
Ya-Feng Zhou
Zhi-Ping Zhang
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机构:Chinese Acad Sci, Wuhan Inst Virol, State Key Lab Virol, Wuhan 430071, Peoples R China
Zhi-Ping Zhang
Hong-Ping Wei
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Hong-Ping Wei
Rui-Fu Yang
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Rui-Fu Yang
Dian-Bing Wang
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Dian-Bing Wang
机构:
[1] Chinese Acad Sci, Wuhan Inst Virol, State Key Lab Virol, Wuhan 430071, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R China
[3] Acad Mil Med Sci, Inst Microbiol & Epidemiol, Beijing 100071, Peoples R China
A loop-mediated isothermal amplification (LAMP) assay system was employed for detecting Bacillus anthracis spores in pure cultures as well as in various simulated powder samples. The specificity of the designed LAMP primer sets was validated by assaying 13 B. anthracis strains and 33 non-B. anthracis species. The detection limits of the LAMP assay were 10 spores/tube for pure cultures and 100 spores/2 mg powder for simulated powder samples. The results show that the LAMP protocol is a promising method for detecting B. anthracis.