A simple PCR method for rapid genotype analysis of Mycobacterium ulcerans.

Abstract:

:Two high-copy-number insertion sequences, IS2404 and IS2606, were recently identified in Mycobacterium ulcerans and were shown by Southern hybridization to possess restriction fragment length polymorphism between strains from different geographic origins. We have designed a simple genotyping method that captures these differences by PCR amplification of the region between adjacent copies of IS2404 and IS2606. We have called this system 2426 PCR. The method is rapid, reproducible, sensitive, and specific for M. ulcerans, and it has confirmed previous studies suggesting a clonal population structure of M. ulcerans within a geographic region. M. ulcerans isolates from Australia, Papua New Guinea, Malaysia, Surinam, Mexico, Japan, China, and several countries in Africa were easily differentiated based on an array of 4 to 14 PCR products ranging in size from 200 to 900 bp. Numerical analysis of the banding patterns suggested a close evolutionary link between M. ulcerans isolates from Africa and southeast Asia. The application of 2426 PCR to total DNA, extracted directly from M. ulcerans-infected tissue specimens without culture, demonstrated the sensitivity and specificity of this method and confirmed for the first time that both animal and human isolates from areas of endemicity in southeast Australia have the same genotype.

journal_name

J Clin Microbiol

authors

Stinear T,Davies JK,Jenkin GA,Portaels F,Ross BC,Oppedisano F,Purcell M,Hayman JA,Johnson PD

doi

10.1128/JCM.38.4.1482-1487.2000

subject

Has Abstract

pub_date

2000-04-01 00:00:00

pages

1482-7

issue

4

eissn

0095-1137

issn

1098-660X

journal_volume

38

pub_type

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