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Summary
The
BclA
protein is a major component of the outermost layer of spores of a number of bacterial species and
C
lostridium difficile
carries three
bclA
genes. Using insertional mutagenesis each gene was characterized and spores devoid of these proteins had surface aberrations, reduced hydrophobicity and germinated faster than wild‐type spores. Therefore the
BclA
proteins were likely major components of the spore surface and when absent impaired the protective shield effect of this outermost layer. Analysis of infection and colonization in mice and hamsters revealed that the 50% infectious dose (
ID
50
) of spores was significantly higher (2‐logs) in the
bclA1
−
mutant compared to the isogenic wild‐type control, but that levels of toxins (
A
and
B
) were indistinguishable from animals dosed with wild‐type spores.
bclA1
−
spores germinated faster than wild‐type spores yet mice were less susceptible to infection suggesting that
BclA
1 must play a key role in the initial (i.e. pre‐spore germination) stages of infection. We also show that the
ID
50
was higher in mice infected with
R
20291, a ‘hypervirulent’ 027 strain, that carries a truncated
BclA
1 protein.
Sprache
Englisch
Identifikatoren
ISSN: 0950-382X
eISSN: 1365-2958
DOI: 10.1111/mmi.12611
Titel-ID: cdi_crossref_primary_10_1111_mmi_12611
Format
–
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