Automated Ribotyping and Pulsed-Field Gel Electrophoresis Reveal a Cluster of Group A Streptococci in Intravenous Drug Abusers

Infection ◽  
2000 ◽  
Vol 28 (5) ◽  
pp. 314-317 ◽  
Author(s):  
S. Brunner ◽  
F. Fleisch ◽  
C. Ruef ◽  
M. Altwegg
1996 ◽  
Vol 70 (3) ◽  
pp. 283-286 ◽  
Author(s):  
Daisuke TANAKA ◽  
Yotaku GYOBU ◽  
Hirohide KODAMA

2000 ◽  
Vol 125 (2) ◽  
pp. 299-301 ◽  
Author(s):  
S. POURNARAS ◽  
A. EFSTRATIOU ◽  
J. DOUBOYAS ◽  
R. C. GEORGE ◽  
A. TSAKRIS

Twenty-six isolates of the newly designated M90 serotype group A Streptococcus (GAS) from a large food-borne outbreak of pharyngitis in Greece and six M90 sporadic isolates from UK, were typed by pulsed-field gel electrophoresis (PFGE). Twenty-four outbreak isolates were identical and two closely related. The Greek isolates were possibly related with one UK isolate, while other sporadic isolates exhibited distinct PFGE profiles from the former isolates.


2003 ◽  
Vol 47 (7) ◽  
pp. 2370-2372 ◽  
Author(s):  
Kevin C. Katz ◽  
Allison J. McGeer ◽  
Carla L. Duncan ◽  
Aisha Ashi-Sulaiman ◽  
Barbara M. Willey ◽  
...  

ABSTRACT Of 500 group A streptococci isolated from pharyngeal swabs, 72 (14.4%) were macrolide resistant, compared to 2.1% in 1997. Of these, 66 (92%) were of the M phenotype and 6 (8.3%) were of the MLS phenotype. Pulsed-field gel electrophoresis found that two clones, with patterns identical to those of serotypes M1 and M4, accounted for 19.4 and 68.1% of the macrolide-resistant isolates, respectively.


2006 ◽  
Vol 3 (1) ◽  
pp. 138-141 ◽  
Author(s):  
Katharina Grif ◽  
Ingrid Heller ◽  
Martin Wagner ◽  
Manfred Dierich ◽  
Reinhard Würzner

1999 ◽  
Vol 37 (6) ◽  
pp. 1892-1898 ◽  
Author(s):  
Karine Rolland ◽  
Corinne Marois ◽  
Veronique Siquier ◽  
Blandine Cattier ◽  
Roland Quentin

A collection of 114 independent Streptococcus agalactiae strains, including 54 strains isolated from the cerebrospinal fluid (CSF) samples of neonates and 60 strains from asymptomatic patients, was characterized by pulsed-field gel electrophoresis (PFGE) of DNA restricted with SmaI and by PCR analysis of the hylB gene. All strains were previously studied by multilocus enzyme electrophoresis (MLEE) (R. Quentin, H. Huet, F.-S. Wang, P. Geslin, A. Goudeau, and R. K. Selander, J. Clin. Microbiol. 33:2576–2581, 1995). Among these 114 strains, there were 92 PFGE patterns. Eleven genetic groups (A to K) were identified with 38% divergence. A more homogeneous group (PFGE group A) was defined, consisting of 73% of the strains previously identified as belonging to a particular MLEE phylogenetic group. A 162-kb fragment was identified as a marker of strains that invaded the central nervous system of neonates. It was detected in 69% of the PFGE patterns obtained with CSF isolates and in only 1.8% of the PFGE patterns obtained with carrier strains. The hylB gene encoding hyaluronate lyase was amplified for all strains in our collection. Ten of 15 isolates belonging to an MLEE subgroup, previously described as being likely to cause invasive infection, had an insertion in the hylB gene (IS1548).


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