J Bacteriol 1994, 176:2398–2406.PubMed Authors’ contributions MH conceived the study, participated in the design, performed laboratory work, and drafted parts of the manuscript. DMV performed statistical analysis and drafted parts of the manuscript. BZ conceived the study, participated in its design and coordination, edited the manuscript, and is the holder of the research grand used to fund the study. All authors have read and approved the final manuscript.”
“Background Horizontal gene transfer and recombination, although recognized as important mechanisms in the evolution of certain phenotypes

such as penicillin resistance in both Neisseria meningitidis and Streptococcus selleck chemical pneumoniae, were considered to be rare [1, 2]. Full genome sequences and extensive surveys of bacterial populations using multilocus sequence typing (MLST) have challenged this view and established the essential role of horizontal gene transfer and recombination in bacterial evolution, revealing the high frequency of these events [3, 4]. Streptococcus pneumoniae (pneumococcus) is an important human pathogen, taxonomically recognized as a group within the pneumoniae-mitis-pseudopneumoniae

cluster of the Streptococcus genus [5]. The capacity of pneumococci to undergo genetic transformation was recognized early in the study of this bacterium [6] and it was later found that competence presented the intriguing

property GDC-0973 price of being tightly controlled at the population level [7]. Competence was thus one of the first examples of a multicellular bacterial response coordinated by a diffusible signal. These processes were later termed quorum-sensing and found to be used by both Gram positive and Gram negative bacteria to synchronize the switch of genetic programs simultaneously at the population level in order to achieve goals that are unattainable by single cells Phospholipase D1 [8]. Several molecules are used by bacteria to regulate their quorum-sensing mechanisms, with modified or unmodified oligopeptides being used by Gram positive and Gram-negative bacteria [8]. In S. pneumoniae, a secreted unmodified 17-aminoacid peptide pheromone, termed the competence-stimulating peptide (CSP), is responsible for quorum-sensing [9]. The product of the comC gene is secreted and processed by an ABC transporter (ComAB) resulting in the accumulation of CSP in the medium. A two-component regulatory system consisting of a histidine kinase receptor (ComD) and its cognate response regulator (ComE) are then responsible for sensing the CSP concentration and triggering the competence response. In pneumococci several distinct mature CSPs have been identified, although the vast majority of strains produce one of two variants: CSP-1 or CSP-2 (also designated CSP-α and CSP-β, respectively) [5, 10–12].