Literature DB >> 11796592

Relationships between Staphylococcus aureus genetic background, virulence factors, agr groups (alleles), and human disease.

Sophie Jarraud1, Christophe Mougel, Jean Thioulouse, Gerard Lina, Hélène Meugnier, Françoise Forey, Xavier Nesme, Jerome Etienne, François Vandenesch.   

Abstract

The expression of most Staphylococcus aureus virulence factors is controlled by the agr locus, which encodes a two-component signaling pathway whose activating ligand is an agr-encoded autoinducing peptide (AIP). A polymorphism in the amino acid sequence of the AIP and of its corresponding receptor divides S. aureus strains into four major groups. Within a given group, each strain produces a peptide that can activate the agr response in the other member strains, whereas the AIPs belonging to different groups are usually mutually inhibitory. We investigated a possible relationship between agr groups and human S. aureus disease by studying 198 S. aureus strains isolated from 14 asymptomatic carriers, 66 patients with suppurative infection, and 114 patients with acute toxemia. The agr group and the distribution of 24 toxin genes were analyzed by PCR, and the genetic background was determined by means of amplified fragment length polymorphism (AFLP) analysis. The isolates were relatively evenly distributed among the four agrgroups, with 61 strains belonging to agr group I, 49 belonging to group II, 43 belonging to group III, and 45 belonging to group IV. Principal coordinate analysis performed on the AFLP distance matrix divided the 198 strains into three main phylogenetic groups, AF1 corresponding to strains of agr group IV, AF2 corresponding to strains of agr groups I and II, and AF3 corresponding to strains of agr group III. This indicated that the agr type was linked to the genetic background. A relationship between genetic background, agr group, and disease type was observed for several toxin-mediated diseases: for instance, agr group IV strains were associated with generalized exfoliative syndromes, and phylogenetic group AF1 strains with bullous impetigo. Among the suppurative infections, endocarditis strains mainly belonged to phylogenetic group AF2 and agr groups I and II. While these results do not show a direct role of the agr type in the type of human disease caused by S. aureus, the agr group may reflect an ancient evolutionary division of S. aureus in terms of this species' fundamental biology.

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Year:  2002        PMID: 11796592      PMCID: PMC127674          DOI: 10.1128/IAI.70.2.631-641.2002

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  21 in total

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  374 in total

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2.  Surveillance of methicillin-resistant Staphylococcus aureus in a pediatric hospital in Mexico City during a 7-year period (1997 to 2003): clonal evolution and impact of infection control.

Authors:  M E Velazquez-Meza; M Aires de Sousa; G Echaniz-Aviles; F Solórzano-Santos; G Miranda-Novales; J Silva-Sanchez; H de Lencastre
Journal:  J Clin Microbiol       Date:  2004-08       Impact factor: 5.948

3.  Restriction modification (RM) tests associated to additional molecular markers for screening prevalent MRSA clones in Brazil.

Authors:  C O Beltrame; A M N Botelho; M C Silva-Carvalho; R R Souza; R R Bonelli; M S Ramundo; M A Guimarães; L R Coelho; A M S Figueiredo
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2012-01-13       Impact factor: 3.267

4.  Species identification of staphylococci by amplification and sequencing of the tuf gene compared to the gap gene and by matrix-assisted laser desorption ionization time-of-flight mass spectrometry.

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Journal:  Eur J Clin Microbiol Infect Dis       Date:  2010-10-22       Impact factor: 3.267

5.  Molecular epidemiology of Panton-Valentine leukocidin-positive Staphylococcus aureus in Spain: emergence of the USA300 clone in an autochthonous population.

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7.  Nasal carriage of Staphylococcus aureus in healthy humans with different levels of contact with animals in Tunisia: genetic lineages, methicillin resistance, and virulence factors.

Authors:  K Ben Slama; H Gharsa; N Klibi; A Jouini; C Lozano; E Gómez-Sanz; M Zarazaga; A Boudabous; C Torres
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2010-11-11       Impact factor: 3.267

8.  Low-molecular weight chitosan enhances antibacterial effect of antibiotics and permeabilizes cytoplasmic membrane of Staphylococcus epidermidis biofilm cells.

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9.  Structural characterization of native autoinducing peptides and abiotic analogues reveals key features essential for activation and inhibition of an AgrC quorum sensing receptor in Staphylococcus aureus.

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Journal:  J Am Chem Soc       Date:  2013-11-25       Impact factor: 15.419

10.  The agr function and polymorphism: impact on Staphylococcus aureus susceptibility to photoinactivation.

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Journal:  J Photochem Photobiol B       Date:  2013-10-23       Impact factor: 6.252

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