Rapid identification of medically important Candida to species level by polymerase chain reaction and single-strand conformational polymorphism
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作者:
Hui, M
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Chinese Univ Hong Kong, Dept Microbiol, Hong Kong, Hong Kong, Peoples R ChinaChinese Univ Hong Kong, Dept Microbiol, Hong Kong, Hong Kong, Peoples R China
Hui, M
[1
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Ip, M
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Chinese Univ Hong Kong, Dept Microbiol, Hong Kong, Hong Kong, Peoples R ChinaChinese Univ Hong Kong, Dept Microbiol, Hong Kong, Hong Kong, Peoples R China
Ip, M
[1
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Chan, PKS
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Chinese Univ Hong Kong, Dept Microbiol, Hong Kong, Hong Kong, Peoples R ChinaChinese Univ Hong Kong, Dept Microbiol, Hong Kong, Hong Kong, Peoples R China
Chan, PKS
[1
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Chin, ML
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Chinese Univ Hong Kong, Dept Microbiol, Hong Kong, Hong Kong, Peoples R ChinaChinese Univ Hong Kong, Dept Microbiol, Hong Kong, Hong Kong, Peoples R China
Chin, ML
[1
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Cheng, AFB
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Chinese Univ Hong Kong, Dept Microbiol, Hong Kong, Hong Kong, Peoples R ChinaChinese Univ Hong Kong, Dept Microbiol, Hong Kong, Hong Kong, Peoples R China
Cheng, AFB
[1
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机构:
[1] Chinese Univ Hong Kong, Dept Microbiol, Hong Kong, Hong Kong, Peoples R China
Invasive fungal disease has taken a great toll on immunocompromised patients. With the emergence of fluconazole and amphotericin B resistance, the rapid identification of fungi to species level is of clinical relevance in guiding appropriate antifungal therapy. Among these opportunistic fungi, Candida species are the most commonly encountered. We had developed a molecular method utilizing single-strand conformational polymorphism (SSCP) to delineate different patterns on a 260-bp amplicon from the 28S rRNA gene from six medically important Candida species. The SSCP banding patterns obtained from a total of 52 isolates were sufficiently unique to allow distinction between the species, thus indicated a high level of specificity. This method of PCR-SSCP can provide a simple and specific method for the rapid identification of medically important Candida to species level. (C) 2000 Elsevier Science Inc. All rights reserved.
机构:
Chinese Acad Sci, Inst Microbiol, Systemat Mycol & Lichenol Lab, Beijing 100101, Peoples R China
Chinese Acad Sci, Grad Sch, Beijing 100101, Peoples R ChinaChinese Acad Sci, Inst Microbiol, Systemat Mycol & Lichenol Lab, Beijing 100101, Peoples R China
Li, Juan
Bai, Feng-Yan
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Chinese Acad Sci, Inst Microbiol, Systemat Mycol & Lichenol Lab, Beijing 100101, Peoples R ChinaChinese Acad Sci, Inst Microbiol, Systemat Mycol & Lichenol Lab, Beijing 100101, Peoples R China
机构:
Lincoln Univ, Agr & Life Sci Div, Gene Marker Lab, Cell Biol Grp, Lincoln 7647, New ZealandLincoln Univ, Agr & Life Sci Div, Gene Marker Lab, Cell Biol Grp, Lincoln 7647, New Zealand
Zhou, H.
Hickford, J. G. H.
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Lincoln Univ, Agr & Life Sci Div, Gene Marker Lab, Cell Biol Grp, Lincoln 7647, New ZealandLincoln Univ, Agr & Life Sci Div, Gene Marker Lab, Cell Biol Grp, Lincoln 7647, New Zealand
Hickford, J. G. H.
Fang, Q.
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Lincoln Univ, Agr & Life Sci Div, Gene Marker Lab, Cell Biol Grp, Lincoln 7647, New ZealandLincoln Univ, Agr & Life Sci Div, Gene Marker Lab, Cell Biol Grp, Lincoln 7647, New Zealand
Fang, Q.
Byun, S. O.
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Lincoln Univ, Agr & Life Sci Div, Gene Marker Lab, Cell Biol Grp, Lincoln 7647, New ZealandLincoln Univ, Agr & Life Sci Div, Gene Marker Lab, Cell Biol Grp, Lincoln 7647, New Zealand