Literature DB >> 8071200

Identification of the lipopolysaccharide core region as the receptor site for a cytotoxin-converting phage, phi CTX, of Pseudomonas aeruginosa.

S Yokota1, T Hayashi, H Matsumoto.   

Abstract

A temperate phage, phi CTX, is a cytotoxin-converting phage of Pseudomonas aeruginosa. In this study, we characterized the lipopolysaccharide (LPS) structures of phi CTX-resistant mutants derived from phi CTX-sensitive strains. phi CTX infectivity was neutralized by LPS preparations derived from sensitive strains but not by those from resistant strains. phi CTX-resistant mutants had lower-molecular-weight rough (R)-type LPS than the parental strains and lacked the reactivity of some anti-LPS core monoclonal antibodies. Some LPS core components were lacking or significantly decreased in the resistant mutants. These results suggested that a receptor site of the cytotoxin-converting phage phi CTX was the LPS core region and that especially L-rhamnose and D-glucose residues in the outer core were involved in phage binding. The host range of phi CTX was nearly O-serotype dependent, probably because of the diversity of the LPS core structure among P. aeruginosa strains. phi CTX bound to most strains of Homma serotypes A, G, and I but not to strains of serotypes B and E. Furthermore, we found that a genetic locus specifying phi CTX sensitivity (and consequently participating in the biosynthesis of part of the LPS core) existed in or near the locus participating in the determination of O-serotype specificity (somA), which has been mapped between leu-10 and eda-9001. phi CTX, as well as anti-LPS core monoclonal antibodies, will be a good tool for structural characterization of the P. aeruginosa LPS core region.

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Year:  1994        PMID: 8071200      PMCID: PMC196709          DOI: 10.1128/jb.176.17.5262-5269.1994

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  30 in total

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Authors:  T Shinomiya; S Shiga
Journal:  J Virol       Date:  1979-12       Impact factor: 5.103

2.  A sensitive silver stain for detecting lipopolysaccharides in polyacrylamide gels.

Authors:  C M Tsai; C E Frasch
Journal:  Anal Biochem       Date:  1982-01-01       Impact factor: 3.365

3.  Structure of the Core oligosaccharide from the lipopolysaccharide of Pseudomonas aeruginosa PAC1R and its defective mutants.

Authors:  P S Rowe; P M Meadow
Journal:  Eur J Biochem       Date:  1983-05-02

4.  Genetic circularity of the Pseudomonas aeruginosa PAO chromosome.

Authors:  P L Royle; H Matsumoto; B W Holloway
Journal:  J Bacteriol       Date:  1981-01       Impact factor: 3.490

5.  The extraction and analysis of lipopolysaccharides from Pseudomonas aeruginosa strain PAO, and three rough mutants.

Authors:  A M Kropinski; L C Chan; F H Milazzo
Journal:  Can J Microbiol       Date:  1979-03       Impact factor: 2.419

6.  Construction of recombination-deficient strains of Pseudomonas aeruginosa.

Authors:  R Früh; J M Watson; D Haas
Journal:  Mol Gen Genet       Date:  1983

7.  Clustering of mutations affecting central pathway enzymes of carbohydrate catabolism in Pseudomonas aeruginosa.

Authors:  R A Roehl; T W Feary; P V Phibbs
Journal:  J Bacteriol       Date:  1983-12       Impact factor: 3.490

8.  A new common polysaccharide antigen of strains of Pseudomonas aeruginosa detected with a monoclonal antibody.

Authors:  S Sawada; T Kawamura; Y Masuho; K Tomibe
Journal:  J Infect Dis       Date:  1985-12       Impact factor: 5.226

9.  The isolation and characterization of lipopolysaccharide-defective mutants of Pseudomonas aeruginosa PAC1.

Authors:  S F Koval; P M Meadow
Journal:  J Gen Microbiol       Date:  1977-02

10.  Genetic determinant of pyocin R2 in Pseudomonas aeruginosa PAO. II. Physical characterization of pyocin R2 genes using R-prime plasmids constructed from R68.45.

Authors:  T Shinomiya; S Shiga; A Kikuchi; M Kageyama
Journal:  Mol Gen Genet       Date:  1983
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  9 in total

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2.  Characterization of Pseudomonas aeruginosa Bacteriophage L5 Which Requires Type IV Pili for Infection.

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3.  Identification of outer membrane proteins as target antigens of Pseudomonas aeruginosa Homma serotype M.

Authors:  S Yokota
Journal:  Clin Diagn Lab Immunol       Date:  1995-11

4.  The core oligosaccharide and thioredoxin of Vibrio cholerae are necessary for binding and propagation of its typing phage VP3.

Authors:  Jingyun Zhang; Wei Li; Qian Zhang; Hongxia Wang; Xiao Xu; Baowei Diao; Lijuan Zhang; Biao Kan
Journal:  J Bacteriol       Date:  2009-02-06       Impact factor: 3.490

5.  Antibacterial efficacy of phages against Pseudomonas aeruginosa infections in mice and Drosophila melanogaster.

Authors:  Yun-Jeong Heo; Yu-Rim Lee; Hyun-Hee Jung; JungEun Lee; GwangPyo Ko; You-Hee Cho
Journal:  Antimicrob Agents Chemother       Date:  2009-04-13       Impact factor: 5.191

6.  Heterogenous Susceptibility to R-Pyocins in Populations of Pseudomonas aeruginosa Sourced from Cystic Fibrosis Lungs.

Authors:  Madeline Mei; Jacob Thomas; Stephen P Diggle
Journal:  mBio       Date:  2021-05-04       Impact factor: 7.867

7.  Genetic and Functional Diversity of Pseudomonas aeruginosa Lipopolysaccharide.

Authors:  Joseph S Lam; Véronique L Taylor; Salim T Islam; Youai Hao; Dana Kocíncová
Journal:  Front Microbiol       Date:  2011-06-01       Impact factor: 5.640

8.  Genetic Evidence for O-Specific Antigen as Receptor of Pseudomonas aeruginosa Phage K8 and Its Genomic Analysis.

Authors:  Xuewei Pan; Xiaoli Cui; Fenjiao Zhang; Yang He; Lingyan Li; Hongjiang Yang
Journal:  Front Microbiol       Date:  2016-03-02       Impact factor: 5.640

Review 9.  The Role of Pseudomonas aeruginosa Lipopolysaccharide in Bacterial Pathogenesis and Physiology.

Authors:  Steven M Huszczynski; Joseph S Lam; Cezar M Khursigara
Journal:  Pathogens       Date:  2019-12-19
  9 in total

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