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Streptococcus pyogenes in human plasma: adaptive mechanisms analyzed by mass spectrometry based proteomics.

Type Information
Nr 27 (Research article)
Authors Malmström, Johan; Karlsson, Christofer; Nordenfelt, Pontus; Ossola, Reto; Weisser, Hendrik; Quandt, Andreas; Hansson, Karin; Aebersold, Ruedi; Malmström, Lars; Bjorck, Lars
Title Streptococcus pyogenes in human plasma: adaptive mechanisms analyzed by mass spectrometry based proteomics.
Journal J Biol Chem (2011) 287 1415-25
DOI 10.1074/jbc.M111.267674
Citations 36 citations (journal impact: 4.77)
Abstract Streptococcus pyogenes is a major bacterial pathogen and a potent inducer of inflammation causing plasma leakage at the site of infection. A combination of label free quantitative mass spectrometry-based proteomics strategies were used to measure how the intracellular proteome homeostasis of S. pyogenes is influenced by the presence of human plasma identifying and quantifying 842 proteins. In plasma the bacterium modifies its production of 213 proteins and the most pronounced change was the complete down-regulation of proteins required for fatty acid biosynthesis FAB. Fatty acids are transported by albumin HSA in plasma. S. pyogenes expresses HSA-binding surface proteins and HSA carrying fatty acids reduced the amount of FAB proteins to the same extent as plasma. The results clarify the function of HSA-binding proteins in S. pyogenes and underline the power of the quantitative mass spectrometry strategy used here to investigate bacterial adaptation to a given environment.
Synopsis This paper describes how the human pathogen S. pyogenes re-organizes its proteome in response to increasing amount of human blood plasma in the growth medium.