Abstract
Extraintestinal strains of Escherichia coli possess a variety of virulence factors that enablethem to cause disease. These strains express a group 2 capsular polysaccharide which is important in the pathogenic process. Extraintestinal strains evaluated to date are also capable of producing the group 1 capsular polysaccharide colanic acid. The blood isolate CP9 (O4/K54/H5) constitutively produces the group 2, K54 capsule but can be induced to produce colanic acid. In this report we assess whether colanic acid contributes to the pathogenesis of this extraintestinal pathogen. CP9 and its derivatives that are deficient in their ability to produce colanic acid (TR94), the K54 group 2 capsule ± colanic acid (CP9.137, TR1374) and the 04 specific antigen ± colanic acid (CP921,CP925) were used to test whether the group 1 capsule colanic acid conferred protection against the bactericidal effects of serum and recombinant bactericidal/permeability-increasing protein (rBPI-23) in vitro. Additionally, CP9, CP9.137 and TR94 were evaluated in the rat granuloma pouch, an in vivo model for localized infection, and by intraperitoneal inoculation into mice, a systemic infection model. In summary, the inability of CP9 to produce colanic acid in the presence or absence of its K54 and O4 antigens had no effect on its ability to survive these host defenses in vitro and did not affect its virulence in these two in vivo models of infection.
| Original language | English |
|---|---|
| Pages (from-to) | 269-278 |
| Number of pages | 10 |
| Journal | Microbial Pathogenesis |
| Volume | 18 |
| Issue number | 4 |
| DOIs | |
| State | Published - Apr 1995 |
Keywords
- animal model
- bactericidal/permeability-increasing protein
- capsular polysaccharide
- colanic acid
- complement
- Escherichia coli, virulence
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