Literature DB >> 1564440

Variable cross-reactivity of Pseudomonas aeruginosa lipopolysaccharide-code-specific monoclonal antibodies and its possible relationship with serotype.

S Yokota1, M Terashima, J Chiba, H Noguchi.   

Abstract

The core region of Pseudomonas aeruginosa lipopolysaccharide (LPS) was analysed by four LPS-core-specific human monoclonal antibodies (mAbs; FK-2E7, MH-4H7, OM-1D6 and NM-3G8). Reactivity of these mAbs to about 180 P. aeruginosa strains was tested. FK-2E7 bound to strains of Homma serotype E and I at a frequency of about 90%, to strains of serotype M at about 50%, and to strains of serotype A and G at about 30%. MH-4H7 bound to P. aeruginosa strains of serotype A, F, G, H, K and M at a high frequency (45-87%), but did not bind to any strains of serotype B, C, E and I. OM-1D6 and NM-3G8 bound to P. aeruginosa strains in a nearly serotype-specific manner. OM-1D6 reacted with all strains of serotype G so far tested, and a few strains of serotype M. Furthermore, L-rhamnose in the LPS core of serotype G was an immunodominant sugar recognized by OM-1D6 as an epitope. NM-3G8 bound to only a few strains of serotype B and M. The variable reactivity of these mAbs suggests that antigenic heterogeneity of the LPS core is somewhat related with (O-polysaccharide-based) serotype. Among these mAbs, MH-4H7 and OM-1D6 showed a high level of protective activity against P. aeruginosa in an experimental infection model using normal mice. In vivo protective activity was shown to be closely related to in vitro binding activity to whole cells as determined by agglutination and flow cytometry, but not ELISA.

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Year:  1992        PMID: 1564440     DOI: 10.1099/00221287-138-2-289

Source DB:  PubMed          Journal:  J Gen Microbiol        ISSN: 0022-1287


  9 in total

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3.  Defining function of lipopolysaccharide O-antigen ligase WaaL using chemoenzymatically synthesized substrates.

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Journal:  J Biol Chem       Date:  2011-12-12       Impact factor: 5.157

4.  Membrane-anchored CD14 is important for induction of interleukin-8 by lipopolysaccharide and peptidoglycan in uroepithelial cells.

Authors:  Toshiaki Shimizu; Shin-ichi Yokota; Satoshi Takahashi; Yasuharu Kunishima; Koh Takeyama; Naoya Masumori; Atsushi Takahashi; Masanori Matsukawa; Naoki Itoh; Taiji Tsukamoto; Nobuhiro Fujii
Journal:  Clin Diagn Lab Immunol       Date:  2004-09

5.  Antibody responses to lipid A, core, and O sugars of the Pseudomonas aeruginosa lipopolysaccharide in chronically infected cystic fibrosis patients.

Authors:  G Kronborg; A Fomsgaard; C Galanos; M A Freudenberg; N Høiby
Journal:  J Clin Microbiol       Date:  1992-07       Impact factor: 5.948

6.  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

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

Authors:  S Yokota; T Hayashi; H Matsumoto
Journal:  J Bacteriol       Date:  1994-09       Impact factor: 3.490

8.  Biologic activities of antibodies to the neutral-polysaccharide component of the Pseudomonas aeruginosa lipopolysaccharide are blocked by O side chains and mucoid exopolysaccharide (alginate).

Authors:  K Hatano; J B Goldberg; G B Pier
Journal:  Infect Immun       Date:  1995-01       Impact factor: 3.441

9.  Monoclonal antibodies that distinguish inner core, outer core, and lipid A regions of Pseudomonas aeruginosa lipopolysaccharide.

Authors:  T R de Kievit; J S Lam
Journal:  J Bacteriol       Date:  1994-12       Impact factor: 3.490

  9 in total

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