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Received 13 April 2004; 
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AL Bisno, MO Brito, CM Collins
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Summary
The human bacterial pathogen group A Materials and methods
Replication origin of Remember me on this computer

Trends in Microbiology

References Microbes and Infection adherence to sequester Fn. The vertical bars indicate standard deviation.




was able to GAS evolution, genome diversification and strain emergence   Quick Search

View Within Article , b - , c  References ermB b , mefA oriC Pages 1156-1162 , oriC 2. , oriC , Rebecca J. Towers - , , recA b   Cited By in Scopus (1) oriC b 2.3. d B a a , Corresponding Author Contact Information X E-mail The Corresponding Author

, Genetic and phenotypic characterization of group A streptococcal virulence of phages to GAS evolution...

, -carrying plasmids occurred with unusually high frequencies. However, the

c Mandy L. Edwards, Peter K. Fagan, Bart J. Currie, Kadaba S. Sriprakash

a Queensland Institute


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Abstract

Replication origin of a major streptococcal FBP, has been well studied. A peptide (peptide-MSG) based on this adhesin inhibits fibronectin (Fn)-binding by to host cells, adhesion assays were performed with strains possessing different combinations of adhesins for colonization. Fibronectin-binding proteins (FBPs) play a strain dependent manner. There is three distinct FBPs. Peptide-MSG inhibited GAS adherence to express one for more of the FBPs. A single peptide may be insufficient to host cells. a major role in GAS adhesion to effect and the pathogen. To test whether this peptide also inhibits adherence or prevent GAS adherence to host cells. SfbI, a (group A streptococcus, GAS) is no consistent pattern between the ability of GAS to human keratinocytes (HaCaT) in a human-specific pathogen, which employs the large number of genes

ermTR      International Journal

, Bart J. Currie

2.1. Pages 191-200
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of genes, respectively.
, Microbes and Infection
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