Affiliation:
1. Molecular Biology Unit, Virus Reference Division,1 and
2. Streptococcus and Diphtheria Reference Unit, WHO Collaborating Centre for Diphtheria and Streptococcal Infections,2 Central Public Health Laboratory, London NW9 5HT, United Kingdom
Abstract
ABSTRACT
We have used fluorescent amplified-fragment length polymorphism (FAFLP) analysis to subtype clinical isolates of
Streptococcus pyogenes
serotype M1. Established typing methods define most M1 isolates as members of a clone that has a worldwide distribution and that is strongly associated with invasive diseases. FAFLP analysis simultaneously sampled 90 to 120 loci throughout the M1 genome. Its discriminatory power, precision, and reproducibility were compared with those of other molecular typing methods. Irrespective of disease symptomatology or geographic origin, the majority of the clinical M1 isolates shared a single ribotype, pulsed-field gel electrophoresis macrorestriction profile, and
emm
1 gene sequence. Nonetheless, among these isolates, FAFLP analysis could differentiate 17 distinct profiles, including seven multi-isolate groups. The FAFLP profiles of M1 isolates reproducibly exhibited between 1 and more than 20 amplified fragment differences. The high discriminatory power of genotyping by FAFLP analysis revealed genetic microheterogeneity and differentiated otherwise “identical” M1 isolates as members of a clone complex.
Publisher
American Society for Microbiology
Cited by
20 articles.
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