Genome Sequence of a Nephritogenic and Highly Transformable M49 Strain of<i>Streptococcus pyogenes</i>

  • W. Michael McShan
    Department of Pharmaceutical Sciences
  • Joseph J. Ferretti
    Department of Microbiology and Immunology, The University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma
  • Tadahiro Karasawa
    Department of Bacteriology, Graduate School of Medical Science, Kanazawa University, Kanazawa, Japan
  • Alexander N. Suvorov
    Department of Molecular Microbiology, Institute of Experimental Medicine, St. Petersburg, Russia
  • Shaoping Lin
    Department of Chemistry, The University of Oklahoma, Norman, Oklahoma
  • Biafang Qin
    Department of Chemistry, The University of Oklahoma, Norman, Oklahoma
  • Honggui Jia
    Department of Chemistry, The University of Oklahoma, Norman, Oklahoma
  • Steve Kenton
    Department of Chemistry, The University of Oklahoma, Norman, Oklahoma
  • Fares Najar
    Department of Chemistry, The University of Oklahoma, Norman, Oklahoma
  • Hongmin Wu
    Department of Chemistry, The University of Oklahoma, Norman, Oklahoma
  • Julie Scott
    Department of Pharmaceutical Sciences
  • Bruce A. Roe
    Department of Chemistry, The University of Oklahoma, Norman, Oklahoma
  • Dragutin J. Savic
    Department of Pharmaceutical Sciences

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<jats:title>ABSTRACT</jats:title><jats:p>The 1,815,783-bp genome of a serotype M49 strain of<jats:italic>Streptococcus pyogenes</jats:italic>(group A streptococcus [GAS]), strain NZ131, has been determined. This GAS strain (FCT type 3;<jats:italic>emm</jats:italic>pattern E), originally isolated from a case of acute post-streptococcal glomerulonephritis, is unusually competent for electrotransformation and has been used extensively as a model organism for both basic genetic and pathogenesis investigations. As with the previously sequenced<jats:italic>S. pyogenes</jats:italic>genomes, three unique prophages are a major source of genetic diversity. Two clustered regularly interspaced short palindromic repeat (CRISPR) regions were present in the genome, providing genetic information on previous prophage encounters. A unique cluster of genes was found in the pathogenicity island-like<jats:italic>emm</jats:italic>region that included a novel Nudix hydrolase, and, further, this cluster appears to be specific for serotype M49 and M82 strains. Nudix hydrolases eliminate potentially hazardous materials or prevent the unbalanced accumulation of normal metabolites; in bacteria, these enzymes may play a role in host cell invasion. Since M49<jats:italic>S. pyogenes</jats:italic>strains have been known to be associated with skin infections, the Nudix hydrolase and its associated genes may have a role in facilitating survival in an environment that is more variable and unpredictable than the uniform warmth and moisture of the throat. The genome of NZ131 continues to shed light upon the evolutionary history of this human pathogen. Apparent horizontal transfer of genetic material has led to the existence of highly variable virulence-associated regions that are marked by multiple rearrangements and genetic diversification while other regions, even those associated with virulence, vary little between genomes. The genome regions that encode surface gene products that will interact with host targets or aid in immune avoidance are the ones that display the most sequence diversity. Thus, while natural selection favors stability in much of the genome, it favors diversity in these regions.</jats:p>

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