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1. (Article ID: 3975)
Marr N, Novikov A, Hajjar AM, Caroff M, Fernandez RC
Variability in the lipooligosaccharide structure and endotoxicity among Bordetella pertussis strains
Journal of Infectious Diseases 202(12) (2010)
1897-1906
Bordetella endotoxins show remarkable structural variability both among each other and in comparison to other gram-negative bacteria. Here we demonstrate that, in contrast to the common Bordetella pertussis laboratory strain and Tohama I derivative BP338, lipooligosaccharide from mouse challenge strain 18-323 is a poor inducer of inflammatory cytokines in human and murine macrophages, is greatly impaired in Toll-like receptor 4-mediated activation of nuclear factor-kappaB in transfected HEK-293 cells, and functions as a Toll-like receptor 4 antagonist. Comparison of lipid A and lipooligosaccharide structures of B. pertussis strains BP338 and 18-323 revealed that 18-323 (1) lacks the ability to modify its lipid A phosphate groups with glucosamine, (2) is distinct in its acylation at the C3' position of the lipid A diglucosamine backbone, and (3) expresses molecular lipooligosaccharide species that lack a terminal heptose. Our findings have important implications for interpreting previous studies of host defenses to B. pertussis infection in mice and in vitro.
lipopolysaccharides, Lipooligosaccharide, lipid A, Bordetella pertussis, gram negative bacteria, cytokines, macrophage, NF-kappa B, endotoxicity
NCBI PubMed ID: 21050116Publication DOI: 10.1086/657409Journal NLM ID: 0413675Publisher: Oxford: Oxford University Press
Correspondence: rachelf

interchange.ubc.ca
Institutions: Department of Microbiology & Immunology, University of British Columbia, Vancouver, British Columbia, Canada, Equipe Structure et Activités des Endotoxines, UMR 8621 du Centre National de la Recherche Scientifique, IGM, Université de Paris-Sud, Orsay, France, Department of Comparative Medicine, University of Washington, Seattle, Washington
Methods: GC, MALDI-MS, statistical analysis
The publication contains the following compound(s):
- Compound ID: 9323
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3HODco-(1-3)-+
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?%a-D-GlcpN-(1--P--1)--+ |
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?%a-D-GlcpN-(1--P--4)--+ | |
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Myr-(1-3)-3HOMyr-(1-2)-b-D-GlcpN-(1-6)-a-D-GlcpN
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3HOMyr-(1-3)-+ 3HOMyr-(1-2)-+ |
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Structure type: oligomer
; 1559 [M-H]-, 1720 [M-H]-, 1881 [M-H]-
Compound class: lipid A
- Compound ID: 9324
|
/Variants 0/-+ 3HOMyr-(1-2)-+
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Myr-(1-3)-3HOMyr-(1-2)-b-D-GlcpN-(1-6)-a-D-GlcpN-(1-P
| |
P-4)-+ 3HODco-(1-3)-+
/Variants 0/ is:
3HOLau-(1-3)-
OR (exclusively)
3HODco-(1-3)- |
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Structure type: oligomer
; 1503 [M-H]-, 1531 [M-H]-
Compound class: lipid A
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