Lancefield acid extracts of Streptococcus pyogenes, type 22 (T12, M22, OF positive) gave good yields of M protein and little opacity factor (OF), but sodium dodecyl sulphate (SDS) extracts contained high titres of OF (greater than 20000) and little M protein. Acid-extracted OF could be separated from M protein by Sepharose 4B chromatography, but some of the OF-positive fractions that did not precipitate with the absorbed homologous anti-M rabbit serum, were able to neutralise opsonic antibodies present in human serum. The isoelectric-focusing profiles of the two antigens showed partial similarity. Some strains of the OF-positive serotypes, e.g., M-types 22 and 49, lost both M antigen and OF activity on serial transfer in Todd-Hewitt broth, but this was not seen in a representative of M-type 60, and no M-negative OF-negative variants could be detected after six subcultures. Among the OF-negative serotypes some, e.g., M-types 5 and 6, were completely stable, whereas others, e.g., M-types 12, 55 and 57, lost their M antigens after serial subculture. One explanation is that the genes that code for M antigen are plasmid borne in some serotypes and, moreover, are carried on the same plasmid as the gene for OF in some OF-positive serotypes. However, analysis of cell lysates by agarose-gel electrophoresis failed to demonstrate the presence of plasmid DNA in any of the strains tested.
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http://dx.doi.org/10.1099/00222615-16-1-13 | DOI Listing |
Sci Rep
December 2023
Centers for Disease Control and Prevention, National Center for Immunization and Respiratory Diseases, Division of Bacterial Diseases, Respiratory Diseases Branch, Atlanta, GA, USA.
Group A streptococcal strains potentially acquire new M protein gene types through genetic recombination (emm switching). To detect such variants, we screened 12,596 invasive GAS genomes for strains of differing emm types that shared the same multilocus sequence type (ST). Through this screening we detected a variant consisting of 16 serum opacity factor (SOF)-positive, emm pattern E, emm82 isolates that were ST36, previously only associated with SOF-negative, emm pattern A, emm12.
View Article and Find Full Text PDFJ Lipid Res
November 2023
Center for Bioenergetics, Houston Methodist, Houston, TX, USA; Department of Medicine, Weill Cornell Medicine, New York, NY, USA. Electronic address:
J Lipid Res
February 2023
Center for Bioenergetics and the Department of Medicine, Houston Methodist Research Institute, Houston, TX, USA; Weill Cornell Medicine, Department of Medicine, New York, NY, USA.
Porcine Health Manag
February 2021
Department of Veterinary and Biomedical Sciences, College of Veterinary Medicine, University of Minnesota, Saint Paul, MN, USA.
Background: There is limited information on the distribution of virulence-associated genes (VAGs) in U.S. Streptococcus suis isolates, resulting in little understanding of the pathogenic potential of these isolates.
View Article and Find Full Text PDFIndian Pediatr
April 2019
Department of Pediatrics, Maulana Azad Medical College, New Delhi, India.
Objective: To determine the diagnostic accuracy of polymerase chain reaction-based detection of sof gene compared to throat swab culture for S. pyogenes infection in patients with acute rheumatic fever and those with recurrence of rheumatic activity.
Methods: 40 patients between 3 to 18 years of age, with clinical diagnosis of acute rheumatic fever or new activity in established rheumatic heart disease were included.
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