Abstract

BackgroundStaphylococcus aureus or MRSA (Methicillin Resistant S. aureus), is an acquired pathogen and the primary cause of nosocomial infections worldwide. In S. aureus, teichoic acid is an essential component of the cell wall, and its biosynthesis is not yet well characterized. Studies in Bacillus subtilis have discovered two different pathways of teichoic acid biosynthesis, in two strains W23 and 168 respectively, namely teichoic acid ribitol (tar) and teichoic acid glycerol (tag). The genes involved in these two pathways are also characterized, tarA, tarB, tarD, tarI, tarJ, tarK, tarL for the tar pathway, and tagA, tagB, tagD, tagE, tagF for the tag pathway. With the genome sequences of several MRSA strains: Mu50, MW2, N315, MRSA252, COL as well as methicillin susceptible strain MSSA476 available, a comparative genomic analysis was performed to characterize teichoic acid biosynthesis in these S. aureus strains.ResultsWe identified all S. aureus tar and tag gene orthologs in the selected S. aureus strains which would contribute to teichoic acids sythesis.Based on our identification of genes orthologous to tarI, tarJ, tarL, which are specific to tar pathway in B. subtilis W23, we also concluded that tar is the major teichoic acid biogenesis pathway in S. aureus. Further analyses indicated that the S. aureus tar genes, different from the divergon organization in B. subtilis, are organized into several clusters in cis. Most interesting, compared with genes in B. subtilis tar pathway, the S. aureus tar specific genes (tarI,J,L) are duplicated in all six S. aureus genomes.ConclusionIn the S. aureus strains we analyzed, tar (teichoic acid ribitol) is the main teichoic acid biogenesis pathway. The tar genes are organized into several genomic groups in cis and the genes specific to tar (relative to tag): tarI, tarJ, tarL are duplicated. The genomic organization of the S. aureus tar pathway suggests their regulations are different when compared to B. subtilis tar or tag pathway, which are grouped in two operons in a divergon structure.

Highlights

  • Staphylococcus aureus or Methicillin Resistant Staphylococcus Aureus (MRSA) (Methicillin Resistant S. aureus), is an acquired pathogen and the primary cause of nosocomial infections worldwide

  • The phylogenetic tree shows the orthologs of B. subtilis Tar/Tag ORFs in S. aureus strains Mu50, MW2, N315, MRSA252, MSSA476 and COL

  • We report the genomic organization of the teichoic acid biogenesis genes, which is different from the divergon organization in B. subtilis W23 and 168

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Summary

Introduction

Staphylococcus aureus or MRSA (Methicillin Resistant S. aureus), is an acquired pathogen and the primary cause of nosocomial infections worldwide. The genes involved in these two pathways are characterized, tarA, tarB, tarD, tarI, tarJ, tarK, tarL for the tar pathway, and tagA, tagB, tagD, tagE, tagF for the tag pathway. In strain 168, the biosynthesis of teichoic acid poly(GroP) involves genes tagA, tagB, tagD, tagE, and tagF. These tag genes are organized in a divergon of two divergently transcribed operons, tagAB and tagDEF[4,5]. Based on high sequence similarity, tarA, tarB, tarD, and tarF are believed to perform similar enzymatic reactions as tagA, tagB, tagD, and tagF do respectively [2], while tarI, tarJ, tarK and tarL carry functions specific to poly(RboP) teichoic acid biosynthesis [2]

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