Structural characterization of lipo‐oligosaccharide (LOS) from Yersinia pestis: regulation of LOS structure by the PhoPQ system
Summary The two‐component regulatory system PhoPQ has been shown to regulate the expression of virulence factors in a number of bacterial species. For one such virulence factor, lipopolysaccharide (LPS), the PhoPQ system has been shown to regulate structural modifications in Salmonella enterica var...
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Veröffentlicht in: | Molecular microbiology 2002-06, Vol.44 (6), p.1637-1650 |
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Sprache: | eng |
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Zusammenfassung: | Summary
The two‐component regulatory system PhoPQ has been shown to regulate the expression of virulence factors in a number of bacterial species. For one such virulence factor, lipopolysaccharide (LPS), the PhoPQ system has been shown to regulate structural modifications in Salmonella enterica var Typhi‐murium. In Yersinia pestis,
which expresses lipo‐oligosaccharide (LOS), a PhoPQ regulatory system has been identified
and an isogenic mutant constructed. To investigate potential modifications to LOS
from Y. pestis, which to date has not been fully characterized, purified LOS
from wild‐type plague and the phoP defective mutant were analysed by mass
spectrometry. Here we report the structural characterization of LOS from Y. pestis
and the direct comparison of LOS from a phoP mutant. Structural modifications
to lipid A, the host signalling portion of LOS, were not detected but analysis of
the core revealed the expression of two distinct molecular species in wild‐type LOS,
differing in terminal galactose or heptose. The phoP mutant was restricted
to the expression of a single molecular species, containing terminal heptose. The
minimum inhibitory concentration of cationic antimicrobial peptides for the two strains
was determined and compared with the wild‐type: the phoP mutant was highly
sensitive to polymyxin. Thus, LOS modification is under the control of the PhoPQ
regulatory system and the ability to alter LOS structure may be required for survival
of Y. pestis within the mammalian and/or flea host. |
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ISSN: | 0950-382X 1365-2958 |
DOI: | 10.1046/j.1365-2958.2002.02990.x |