PCR Amplification with Primers Based on IS 2404 and GC-Rich Repeated Sequence Reveals Polymorphism in Mycobacterium ulcerans
Author:
Affiliation:
1. Mycobacteriology Unit, Institute of Tropical Medicine, Antwerp
2. Faculty of Chemistry, Gdansk University of Technology, Gdansk, Poland
3. Laboratorium voor Microbiologie, Universiteit Gent, Gent, Belgium
Abstract
Publisher
American Society for Microbiology
Subject
Microbiology (medical)
Link
https://journals.asm.org/doi/pdf/10.1128/JCM.43.1.448-451.2005
Reference11 articles.
1. Asiedu K. R. Scherpbier and M. Raviglione. 2000. Buruli ulcer infection: Mycobacterium ulcerans infection p. 1-4. (W.H.O./CDS/CPE/GBUI/2000.1) World Health Organization Geneva Switzerland.
2. Evaluation of PCR-Restriction Profile Analysis and IS 2404 Restriction Fragment Length Polymorphism and Amplified Fragment Length Polymorphism Fingerprinting for Identification and Typing of Mycobacterium ulcerans and M. marinum
3. Chemlal, K., K. de Ridder, P. A. Fonteyne, W. M. Meyers, J. Swings, and F. Portaels. 2001. The use of IS2404 restriction fragment length polymorphisms suggests the diversity of Mycobacterium ulcerans from different geographic areas. Am. J. Trop. Med. Hyg.64:270-273.
4. Characterization of an Unusual Mycobacterium: a Possible Missing Link between Mycobacterium marinum and Mycobacterium ulcerans
5. PCR-Based Genotyping of Mycobacterium tuberculosis with New GC-Rich Repeated Sequences and IS 6110 Inverted Repeats Used as Primers
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