|
Sign In to gain access to subscriptions and/or personal tools.
|
CRITICAL REVIEWS IN ORAL BIOLOGY & MEDICINE |
Lipopolysaccharide Heterogeneity: Innate Host Responses to Bacterial Modification of Lipid A Structure
D.R. Dixon1,2 and
R.P. Darveau1,*
1 Department of Periodontics, University of Washington, Health Sciences Center, Box 357444, Seattle, WA 98195, USA; and
2 The United States Army Dental Corps;
Correspondence: * corresponding author,rdarveau{at}u.washington.edu
The innate host response system is composed of various mechanisms designed to detect and facilitate host responses to microbial components, such as lipopolysaccharides (LPS). To enable this to occur, innate systems contain multiple pattern recognition receptors (i.e., LBP, CD14, and TLRs), which identify certain features within bacterial LPS that are foreign to the host, as well as essential and uniquely specific for bacteria. Innate host identification of unique bacterial components or patterns, therefore, relies on the inability of bacteria to alter these essential or critical components dramatically. Historically, LPS have been viewed as essential outer-membrane molecules containing both a highly variable outer region (O-segment) as well as a relatively conserved inner region (lipid A). However, over the last decade, new evidence has emerged, revealing that increased natural diversity or heterogeneity within specific components of LPS, such as lipid A—resulting in minor to moderate changes in lipid A structure—can produce dramatic host responses. Therefore, examples of natural lipid A heterogeneity, and the mechanisms that control it, represent a novel approach in which bacteria modulate host responses and may thereby confer specific advantages to certain bacterial species under changing environmental host conditions.
Key Words: lipopolysaccharide (LPS) lipid A CD14 TLR innate immunity
Journal of Dental Research, Vol. 84, No. 7,
584-595 (2005)
DOI: 10.1177/154405910508400702

CiteULike Complore Connotea Del.icio.us Digg Reddit Technorati Twitter What's this?
This article has been cited by other articles:

|
 |

|
 |
 
C. Cekic, C. R. Casella, C. A. Eaves, A. Matsuzawa, H. Ichijo, and T. C. Mitchell
Selective Activation of the p38 MAPK Pathway by Synthetic Monophosphoryl Lipid A
J. Biol. Chem.,
November 13, 2009;
284(46):
31982 - 31991.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A. El Hamidi, A. Novikov, D. Karibian, M. B. Perry, and M. Caroff
Structural characterization of Bordetella parapertussis lipid A
J. Lipid Res.,
May 1, 2009;
50(5):
854 - 859.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. Haiko, M. Suomalainen, T. Ojala, K. Lahteenmaki, and T. K. Korhonen
Invited review: Breaking barriers -- attack on innate immune defences by omptin surface proteases of enterobacterial pathogens
Innate Immunity,
April 1, 2009;
15(2):
67 - 80.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
B. W. Bainbridge, L. Karimi-Naser, R. Reife, F. Blethen, R. K. Ernst, and R. P. Darveau
Acyl Chain Specificity of the Acyltransferases LpxA and LpxD and Substrate Availability Contribute to Lipid A Fatty Acid Heterogeneity in Porphyromonas gingivalis
J. Bacteriol.,
July 1, 2008;
190(13):
4549 - 4558.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
N. Marr, A. Tirsoaga, D. Blanot, R. Fernandez, and M. Caroff
Glucosamine Found as a Substituent of Both Phosphate Groups in Bordetella Lipid A Backbones: Role of a BvgAS-Activated ArnT Ortholog
J. Bacteriol.,
June 15, 2008;
190(12):
4281 - 4290.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S. Hadina, J. P. Weiss, P. B. McCray Jr., K. Kulhankova, and P. S. Thorne
MD-2-Dependent Pulmonary Immune Responses to Inhaled Lipooligosaccharides: Effect of Acylation State
Am. J. Respir. Cell Mol. Biol.,
June 1, 2008;
38(6):
647 - 654.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. Rangarajan, J. Aduse-Opoku, N. Paramonov, A. Hashim, N. Bostanci, O. P. Fraser, E. Tarelli, and M. A. Curtis
Identification of a Second Lipopolysaccharide in Porphyromonas gingivalis W50
J. Bacteriol.,
April 15, 2008;
190(8):
2920 - 2932.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
R. S. Munford
Sensing Gram-Negative Bacterial Lipopolysaccharides: a Human Disease Determinant?
Infect. Immun.,
February 1, 2008;
76(2):
454 - 465.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
Y. Asai, Y. Makimura, A. Kawabata, and T. Ogawa
Soluble CD14 Discriminates Slight Structural Differences between Lipid As That Lead to Distinct Host Cell Activation
J. Immunol.,
December 1, 2007;
179(11):
7674 - 7683.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
Q. Zhou and S. Amar
Identification of Signaling Pathways in Macrophage Exposed to Porphyromonas gingivalis or to Its Purified Cell Wall Components
J. Immunol.,
December 1, 2007;
179(11):
7777 - 7790.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
G. Tang, T. Ruiz, R. Barrantes-Reynolds, and K. P. Mintz
Molecular heterogeneity of EmaA, an oligomeric autotransporter adhesin of Aggregatibacter (Actinobacillus) actinomycetemcomitans
Microbiology,
August 1, 2007;
153(8):
2447 - 2457.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|
|