Complete genome sequence of an M1 strain of <i>Streptococcus pyogenes</i>

Joseph J. Ferretti(University of Oklahoma Health Sciences Center), W. Michael McShan(University of Oklahoma Health Sciences Center), Dragana Ajdić(University of Oklahoma Health Sciences Center), Dragutin J. Savić(University of Oklahoma Health Sciences Center), Gorana Savić(University of Oklahoma Health Sciences Center), Kevin Lyon(University of Oklahoma Health Sciences Center), Charles Primeaux(University of Oklahoma Health Sciences Center), S. Sezate(University of Oklahoma Health Sciences Center), А. Н. Суворов(Academy of Medical Sciences), Steve Kenton(University of Oklahoma Health Sciences Center), Hong Shing Lai(University of Oklahoma Health Sciences Center), Shao Ping Lin(University of Oklahoma Health Sciences Center), Yudong Qian(University of Oklahoma Health Sciences Center), Hong Jia(University of Oklahoma Health Sciences Center), Fares Z. Najar(University of Oklahoma Health Sciences Center), Qun Ren(University of Oklahoma Health Sciences Center), Hua Zhu(University of Oklahoma Health Sciences Center), Lin Song(University of Oklahoma Health Sciences Center), Jim White(University of Oklahoma Health Sciences Center), Xiling Yuan(University of Oklahoma Health Sciences Center), Sandra W. Clifton(Washington University in St. Louis), Bruce A. Roe(University of Oklahoma Health Sciences Center), Robert E. McLaughlin(University of Oklahoma Health Sciences Center)
Proceedings of the National Academy of Sciences
April 10, 2001
Cited by 940Open Access
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Abstract

The 1,852,442-bp sequence of an M1 strain of Streptococcus pyogenes, a Gram-positive pathogen, has been determined and contains 1,752 predicted protein-encoding genes. Approximately one-third of these genes have no identifiable function, with the remainder falling into previously characterized categories of known microbial function. Consistent with the observation that S. pyogenes is responsible for a wider variety of human disease than any other bacterial species, more than 40 putative virulence-associated genes have been identified. Additional genes have been identified that encode proteins likely associated with microbial "molecular mimicry" of host characteristics and involved in rheumatic fever or acute glomerulonephritis. The complete or partial sequence of four different bacteriophage genomes is also present, with each containing genes for one or more previously undiscovered superantigen-like proteins. These prophage-associated genes encode at least six potential virulence factors, emphasizing the importance of bacteriophages in horizontal gene transfer and a possible mechanism for generating new strains with increased pathogenic potential.


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