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PMID: 3509884 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Contribution of lipopolysaccharide to pathogenicity of Haemophilus influenzae: comparative virulence of genetically-related strains in rats.

Microbial pathogenesis ·Vol. 1 ·No. 5 ·1986-10-00 ·Pages 465-73

Zwahlen A, Rubin LG, Moxon ER

Abstract

The elaboration of type b capsule plays an important role in determining virulence of Haemophilus influenzae but the contribution of lipopolysaccharide to pathogenicity of this organism remains undefined. Using DNA from a virulent type b H. influenzae donor strain and a capsule-deficient recipient (Rd:01), we constructed capsular transformants having lipopolysaccharide characteristics either similar to (strain Rd/b+:01), or different from (strain Rd/b+:02), the recipient strain. These two type b transformants had similar type b capsule and outer membrane proteins. Comparative virulence studies in rats showed that strain Rd/b+:02 was more virulent than Rd/b+01 as assessed by magnitude of bacteraemia, incidence of meningitis and mortality. Similarly, strain Rd/b-:02 exhibited greater pathogenicity in C3-depleted rats than its genetically-related strain Rd:01. We conclude that lipopolysaccharide composition plays a significant role in mediating the potential of H. influenzae to cause invasive infections. In addition, the findings suggest that there is linkage of virulence genes involved in lipopolysaccharide and capsule expression.

MeSH Terms
Animals Haemophilus Infections/etiology Haemophilus influenzae/genetics,pathogenicity Lipopolysaccharides/genetics Rats Rats, Inbred Strains Species Specificity Transformation, Genetic Virulence
Chemicals
Lipopolysaccharides
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Zwahlen A
Department of Medicine, Hôpital de zone Saint-Loup-Orbe, Pompaples, Switzerland.
Rubin L G
Moxon E R
Article Info
Journal
Microbial pathogenesis
Abbr.
Microb Pathog
ISSN
0882-4010
Published
1986-10-00
Pages
465-73
Language
English
Region
England
NLM ID
8606191
Subset
IM
Grants
NINDS NIH HHS · NS-12554 · United States
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