Literature DB >> 2825323

Molecular analysis of bacterial cytolysins.

T Chakraborty1, S Kathariou, J Hacker, H Hof, B Huhle, W Wagner, M Kuhn, W Goebel.   

Abstract

Results of molecular and pathogenic studies of three different bacterial hemolysins (cytolysins) are presented. These exoproteins derive from the two gram-negative bacteria Escherichia coli and Aeromonas hydrophila and from the gram-positive pathogen Listeria monocytogenes. The hemolysin of E. coli is determined by an 8-kilobase (kb) region that includes four clustered genes (hlyC, hlyA, hlyB, and hlyD). This hemolysin determinant is part either of large transmissible plasmids or of the chromosome. The genes located chromosomally are found predominantly in E. coli strains that can cause pyelonephritis and/or other extraintestinal infections. A detailed analysis of the chromosomal hyl determinants of one nephropathogenic E. coli strain revealed the existence of specific, large chromosomal insertions 75 kb and 100 kb in size that carry the hly genes but that also influence the expression of other virulence properties, i.e., adhesion and serum resistance. The direct involvement of E. coli hemolysin in virulence could be demonstrated in several model systems. The genetic determinants for hemolysin (cytolysin) formation in A. hydrophila (aerolysin) and L. monocytogenes (listeriolysin) are less complex. Both cytolysins seem to be encoded by single genes, although two loci (aerB and aerC) that affect the expression and activity of aerolysin have been identified distal and proximal to the structural gene for aerolysin (aerA). Cytolysin-negative mutants of both bacteria were obtained by site-specific deletion and/or transposon mutagenesis. These mutants show a drastic reduction in the virulence of the respective bacteria.

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Year:  1987        PMID: 2825323     DOI: 10.1093/clinids/9.supplement_5.s456

Source DB:  PubMed          Journal:  Rev Infect Dis        ISSN: 0162-0886


  7 in total

1.  Enterohemolysin production is associated with a temperate bacteriophage in Escherichia coli serogroup O26 strains.

Authors:  L Beutin; L Bode; M Ozel; R Stephan
Journal:  J Bacteriol       Date:  1990-11       Impact factor: 3.490

2.  Actinobacillus pleuropneumoniae hlyX gene homology with the fnr gene of Escherichia coli.

Authors:  J I MacInnes; J E Kim; C J Lian; G A Soltes
Journal:  J Bacteriol       Date:  1990-08       Impact factor: 3.490

3.  Haemolytic activity of Campylobacter pylori.

Authors:  B L Wetherall; A M Johnson
Journal:  Eur J Clin Microbiol Infect Dis       Date:  1989-08       Impact factor: 3.267

4.  Molecular cloning and characterization of a hemolysin gene from Actinobacillus (Haemophilus) pleuropneumoniae.

Authors:  C J Lian; S Rosendal; J I MacInnes
Journal:  Infect Immun       Date:  1989-11       Impact factor: 3.441

5.  The extracellular cytolysin of Vibrio vulnificus: inactivation and relationship to virulence in mice.

Authors:  A C Wright; J G Morris
Journal:  Infect Immun       Date:  1991-01       Impact factor: 3.441

6.  Cloning and expression of the damselysin gene from Vibrio damsela.

Authors:  D L Cutter; A S Kreger
Journal:  Infect Immun       Date:  1990-01       Impact factor: 3.441

7.  Characterization of Burkholderia pseudomallei protein BPSL1375 validates the Putative hemolytic activity of the COG3176 N-Acyltransferase family.

Authors:  Laziana Ahmad; Teng Loong Hung; Nor Azurah Mat Akhir; Rahmah Mohamed; Sheila Nathan; Mohd Firdaus-Raih
Journal:  BMC Microbiol       Date:  2015-11-23       Impact factor: 3.605

  7 in total

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