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    A genome-wide study of two-component signal transduction systems in eight newly sequenced mutans streptococci strains

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    Authors
    Song, Lifu
    Sudhakar, Padhmanand
    Wang, Wei
    Conrads, Georg
    Brock, Anke
    Sun, Jibin
    Wagner-Döbler, Irene
    Zeng, An-Ping
    Issue Date
    2012-04-04
    
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    Abstract
    Abstract Background Mutans streptococci are a group of gram-positive bacteria including the primary cariogenic dental pathogen Streptococcus mutans and closely related species. Two component systems (TCSs) composed of a signal sensing histidine kinase (HK) and a response regulator (RR) play key roles in pathogenicity, but have not been comparatively studied for these oral bacterial pathogens. Results HKs and RRs of 8 newly sequenced mutans streptococci strains, including S. sobrinus DSM20742, S. ratti DSM20564 and six S. mutans strains, were identified and compared to the TCSs of S. mutans UA159 and NN2025, two previously genome sequenced S. mutans strains. Ortholog analysis revealed 18 TCS clusters (HK-RR pairs), 2 orphan HKs and 2 orphan RRs, of which 8 TCS clusters were common to all 10 strains, 6 were absent in one or more strains, and the other 4 were exclusive to individual strains. Further classification of the predicted HKs and RRs revealed interesting aspects of their putative functions. While TCS complements were comparable within the six S. mutans strains, S. sobrinus DSM20742 lacked TCSs possibly involved in acid tolerance and fructan catabolism, and S. ratti DSM20564 possessed 3 unique TCSs but lacked the quorum-sensing related TCS (ComDE). Selected computational predictions were verified by PCR experiments. Conclusions Differences in the TCS repertoires of mutans streptococci strains, especially those of S. sobrinus and S. ratti in comparison to S. mutans, imply differences in their response mechanisms for survival in the dynamic oral environment. This genomic level study of TCSs should help in understanding the pathogenicity of these mutans streptococci strains.
    Citation
    BMC Genomics. 2012 Apr 04;13(1):128
    URI
    http://dx.doi.org/10.1186/1471-2164-13-128
    http://hdl.handle.net/10033/621030
    Type
    Journal Article
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    publications of the research group microbial communication (KOM)

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