Literature DB >> 11497225

flaB-polymerase chain reaction (flaB-PCR) and its restriction fragment length polymorphism (RFLP) analysis are an efficient tool for detection and identification of Leptospira spp.

H Kawabata1, L A Dancel, S Y Villanueva, Y Yanagihara, N Koizumi, H Watanabe.   

Abstract

For establishment of a rapid-identification method of Leptospira species, a flaB gene of Leptospira was investigated and the following results were obtained. 1) HaeIII- or HindIII-restriction fragment length polymorphism (RFLP) of polymerase chain reaction (PCR) products (793 bp) of flaB gene was effectual for the classification of species of Leptospira. 2) Twenty cells of Leptospira in 1 ml of coagulated blood and 100 cells of Leptospira in 1 ml of anti-coagulated blood could be detected by flaB-PCR. These results suggested that PCR-RFLP based on the flaB gene was an efficient tool for rapid detection and identification of species of infected Leptospira from clinical specimens.

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Year:  2001        PMID: 11497225     DOI: 10.1111/j.1348-0421.2001.tb02649.x

Source DB:  PubMed          Journal:  Microbiol Immunol        ISSN: 0385-5600            Impact factor:   1.955


  15 in total

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9.  Molecular characterisation and disease severity of leptospirosis in Sri Lanka.

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10.  Development and validation of a real-time PCR for detection of pathogenic leptospira species in clinical materials.

Authors:  Ahmed Ahmed; Mirjam F M Engelberts; Kimberly R Boer; Niyaz Ahmed; Rudy A Hartskeerl
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