Affiliation:
1. Department of Microbiology and Immunology, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, Maryland 20814
2. Division of Bacterial, Parasitic, and Allergic Products, Centers for Biologics Evaluation and Research, 29 Lincoln Drive, Bethesda, Maryland 20892
Abstract
ABSTRACT
Bacillus collagen-like protein of anthracis (BclA) is the immunodominant glycoprotein on the exosporium of
Bacillus anthracis
spores. Here, we sought to assess the impact of BclA on spore germination in vitro and in vivo, surface charge, and interaction with host matrix proteins. For that purpose, we constructed a markerless
bclA
null mutant in
B. anthracis
Sterne strain 34F2. The growth and sporulation rates of the Δ
bclA
and parent strains were nearly indistinguishable, but germination of mutant spores occurred more rapidly than that of wild-type spores in vitro and was more complete by 60 min. Additionally, the mean time to death of A/J mice inoculated subcutaneously or intranasally with mutant spores was lower than that for the wild-type spores even though the 50% lethal doses of the two strains were similar. We speculated that these in vitro and in vivo differences between mutant and wild-type spores might reflect the ease of access of germinants to their receptors in the absence of BclA. We also compared the hydrophobic and adhesive properties of Δ
bclA
and wild-type spores. The Δ
bclA
spores were markedly less water repellent than wild-type spores, and, probably as a consequence, the extracellular matrix proteins laminin and fibronectin bound significantly better to mutant than to wild-type spores. These studies suggest that BclA acts as a shield to not only reduce the ease with which spores germinate but also change the surface properties of the spore, which, in turn, may impede the interaction of the spore with host matrix substances.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
89 articles.
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