Data on the structure and temperature-dependent variations of the lipopolysaccharide (LPS) of Yersinia pestis are summarized and compared with data of other enteric bacteria, including other Yersinia spp. A correlation between the LPS structure and properties of the LPS and bacterial cultures as well as the LPS biosynthesis control are briefly discussed.
Anisimov AP, Lindler LE, Pier GBIntraspecific diversity of Yersinia pestis. Clin Microbiol Rev2004; 17: 434—464.
2.
Perry RD, Fetherston JDYersinia pestis — etiologic agent of plague. Clin Microbiol Rev1997; 10: 35—66.
3.
Hinnebusch BJThe evolution of flea-borne transmission in Yersinia pestis. In: Carniel E, Hinnebusch BJ. (eds) Yersinia Molecular and Cellular Biology. Wymondham, Norfolk: Horizon Bioscience, 2004; 49—73.
4.
Zhou D., Han Y., Song Y., Huang P., Yang R.Comparative and evolutionary genomics of Yersinia pestis. Microbes Infect2004; 6: 1226—1234.
5.
Achtman M., Zurth K., Morelli G., Torrea G., Guiyoule A., Carniel E.Yersinia pestis, the cause of plague, is a recently emerged clone of Yersinia pseudotuberculosis. Proc Natl Acad Sci USA1999; 96: 14043—14048.
6.
Skurnik M., Peippo A., Ervelä E.Characterization of the O-antigen gene clusters of Yersinia pseudotuberculosis and the cryptic O-antigen gene cluster of Yersinia pestis shows that the plague bacillus is most closely related to and has evolved from Y. pseudotuberculosis serotype O: 1b. Mol Microbiol2000; 37: 316—330.
7.
Kukkonen M., Suomalainen M., Kyllonen P. et al. Lack of O-antigen is essential for plasminogen activation by Yersinia pestis and Salmonella enterica. Mol Microbiol2004; 51: 215—225.
8.
Vinogradov EV , Lindner B., Kocharova NA et al. The core structure of the lipopolysaccharide from the causative agent of plague, Yersinia pestis. Carbohydr Res2002; 337: 775—777.
9.
Hitchen PG, Prior JL, Oyston PC et al. Structural characterization of lipo-oligosaccharide (LOS) from Yersinia pestis: regulation of LOS structure by the PhoPQ system. Mol Microbiol2002; 44: 1637—1650.
10.
Gremyakova TA, Vinogradov EV, Lindner B. et al. The core structure of the lipopolysaccharide of Yersinia pestis strain KM218. Influence of growth temperature. Adv Exp Med Biol2003; 529: 229—232.
11.
Kawahara K. , Tsukano H., Watanabe H., Lindner B., Matsuura M.Modification of the structure and activity of lipid A in Yersinia pestis lipopolysaccharide by growth temperature. Infect Immun2002; 70: 4092—4098.
12.
Knirel YA, Lindner B., Vinogradov EV et al. Temperature-dependent variations and intraspecies diversity of the structure of the lipopolysaccharide of Yersinia pestis. Biochemistry2005; 44: 1731—1743.
13.
Knirel YA, Lindner B., Vinogradov EV et al. Cold temperature-induced modifications to the composition and structure of the lipopolysaccharide of Yersinia pestis. Carbohydr Res2005; 340: 1625—1630.
14.
Rebeil R., Ernst RK, Gowen BB, Miller SI, Hinnebusch BJVariation in lipid A structure in the pathogenic Yersiniae. Mol Microbiol2004; 52: 1363—1373.
15.
Aussel L., Thérisod H., Karibian D., Perry MB, Bruneteau M., Caroff M.Novel variation of lipid A structures in strains of different Yersinia species . FEBS Lett2000; 465: 87—92.
16.
Holst O.Chemical structure of the core region of lipopolysaccharides. In: Brade H, Opal SM, Vogel SN, Morrison DC. (eds) Endotoxin in Health and Disease. New York : Marcel Dekker, 1999; 115—154.
17.
Müller-Loennies S., Rund S., Ervelä E., Skurnik M., Holst O.The structure of the carbohydrate backbone of the core-lipid A region of the lipopolysaccharide from a clinical isolate of Yersinia enterocolitica 0:9. Eur J Biochem1999; 261: 19—24.
18.
Oertelt C., Lindner B., Skurnik M., Holst O.Isolation and structural characterization of an R-form lipopolysaccharide from Yersinia enterocolitica serotype O:8. Eur J Biochem2001; 268: 554—564.
19.
Raetz Crh, Whitfield C.Lipopolysaccharide endotoxins. Annu Rev Biochem2002; 71: 635—700.
20.
Feldman MF, Marolda CL, Monteiro MA, Perry MB, Parodi AJ, Valvano MAThe activity of a putative polyisoprenol-linked sugar translocase (Wzx) involved in Escherichia coli O antigen assembly is independent of the chemical structure of the O repeat. JBiol Chem1999; 274: 35129—35138.
21.
Ovodov YS, Gorshkova RP, Tomshich SV et al. Chemical and immunochemical studies on lipopolysaccharides of some Yersinia species. A review of some recent investigations. J Carbohydr Chem1992; 11: 21—35.
22.
Anisimov AP, Dentovskaya SV, Titareva GM, Bakhteeva IV, Shaikhutdinova RZ, Balakhonov SV et al. Intraspecies and temperature-dependent variations in susceptibility of Yersinia pestis to bactericidal action of serum and polymyxin B. Infect Immun2005; 73: 7324—7331.
23.
Kanipes MI, Lin S., Cotter RJ, Raetz Crh.Ca2+-induced phosphoethanolamine transfer to the outer 3-deoxy-D-mannooctulosonic acid moiety of Escherichia coli lipopolysaccharide. A novel membrane enzyme dependent upon phosphatidylethanolamine. J Biol Chem2001; 276: 1156—1163.
24.
Dentovskaya SV, Shaikhutdinova RZ, Knirel YA, Anisimov APConstruction of attenuated vaccine strains of Gram-negative bacteria. Mol Gen Mikrobiol Virusol2005; In press.
25.
Vorachek-Warren MK, Carty SM, Lin S., Cotter RJ, Raetz CRAn Escherichia coli mutant lacking the cold-shock induced palmitoleoyl transferase of lipid A biosynthesis. Absence of unsaturated acyl chains and antibiotic hypersensitivity at 12°C. J Biol Chem2002; 277: 14186—14193.
26.
Guo L., Lim KB, Gunn JS et al. Regulation of lipid A modifications by Salmonella typhimurium virulence genes phoP—phoQ. Science1997; 276: 250—253.
27.
Winfield MD , Latifi T., Groisman EATranscriptional regulation of the 4-amino-4-deoxy-L-arabinose biosynthetic genes in Yersinia pestis. J Biol Chem2005; 280: 14765—14772.
28.
Dimopoulos G.Insect immunity and its implication in mosquito—malaria interactions. Cell Microbiol2003; 5: 3—14.
