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Environmental modulation of lipopolysaccharide chain length alters the sensitivity of Escherichia coli to the neutrophil bactericidal/permeability-increasing protein.

作者信息

Weiss J, Hutzler M, Kao L

出版信息

Infect Immun. 1986 Feb;51(2):594-9. doi: 10.1128/iai.51.2.594-599.1986.

DOI:10.1128/iai.51.2.594-599.1986
PMID:3510983
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC262384/
Abstract

We have shown previously that the sensitivity of Escherichia coli to the neutrophil bactericidal/permeability-increasing protein (BPI) depends mainly on the polysaccharide chain length of outer membrane lipopolysaccharides (LPS) (J. Weiss, S. Beckerdite-Quagliata, and P. Elsbach, J. Clin. Invest. 65:619-628, 1980). Thus, rough strains of E. coli producing only short-chain LPS are more sensitive to BPI than smooth strains that produce LPS with varied chain lengths. We now show that changes in the bacterial growth environment can modify BPI sensitivity of smooth E. coli as much as 30-fold depending on the bacterial strain and the growth conditions examined. Changes in BPI sensitivity paralleled differences in binding affinity of E. coli for BPI and closely correlated with changes in the chain length of LPS produced under different growth conditions, as assessed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. No concomitent changes in either the number of LPS molecules per cell or the bacterial protein profile were detected. Rough strains showed little or no growth-dependent variation in BPI sensitivity, further indicating that subtle alterations in bacterial constituents other than LPS do not significantly affect bacterial sensitivity to BPI. Thus, the BPI sensitivity of E. coli can be modulated not only by the genotypic conversion of the LPS phenotype, but also by environmental effects on LPS-polysaccharide formation in wild-type strains.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66c3/262384/16a0eda69c5e/iai00107-0233-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66c3/262384/b25f82e0f39f/iai00107-0233-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66c3/262384/16a0eda69c5e/iai00107-0233-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66c3/262384/b25f82e0f39f/iai00107-0233-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66c3/262384/16a0eda69c5e/iai00107-0233-b.jpg

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Metabolic labeling to characterize the overall composition of Francisella lipid A and LPS grown in broth and in human phagocytes.
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Recombinant bactericidal/permeability-increasing protein rBPI21 protects against pneumococcal disease.重组杀菌/通透性增加蛋白rBPI21可预防肺炎球菌疾病。
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Hemin-induced modifications of the antigenicity and hemin-binding capacity of Porphyromonas gingivalis lipopolysaccharide.血红素诱导牙龈卟啉单胞菌脂多糖抗原性及血红素结合能力的改变
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Reactivity of the human antiendotoxin immunoglobulin M monoclonal antibody HA-1A with lipopolysaccharides from rough and smooth gram-negative organisms.人抗内毒素免疫球蛋白M单克隆抗体HA-1A与革兰氏阴性粗糙型及光滑型菌属脂多糖的反应活性。
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Effect of lipopolysaccharide (LPS) chain length on interactions of bactericidal/permeability-increasing protein and its bioactive 23-kilodalton NH2-terminal fragment with isolated LPS and intact Proteus mirabilis and Escherichia coli.脂多糖(LPS)链长度对杀菌/通透性增加蛋白及其具有生物活性的23千道尔顿氨基末端片段与分离的LPS以及完整的奇异变形杆菌和大肠杆菌相互作用的影响。
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The region around residue 115 of human bactericidal/permeability-increasing protein is not involved in lipopolysaccharide binding or bactericidal activity. Chemical synthesis and expression of a gene coding for the active domain and characterization of recombinant proteins.人杀菌/通透性增加蛋白115位残基周围区域不参与脂多糖结合或杀菌活性。活性结构域编码基因的化学合成与表达及重组蛋白的特性分析。
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The microbicidal mechanisms of human neutrophils and eosinophils.人类中性粒细胞和嗜酸性粒细胞的杀菌机制。
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Size heterogeneity of Salmonella typhimurium lipopolysaccharides in outer membranes and culture supernatant membrane fragments.鼠伤寒沙门氏菌外膜及培养上清膜片段中脂多糖的大小异质性
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Lipopolysaccharide heterogeneity in Salmonella typhimurium analyzed by sodium dodecyl sulfate polyacrylamide gel electrophoresis.通过十二烷基硫酸钠聚丙烯酰胺凝胶电泳分析鼠伤寒沙门氏菌中的脂多糖异质性。
Eur J Biochem. 1980;107(1):137-43. doi: 10.1111/j.1432-1033.1980.tb04634.x.
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Mechanism of assembly of the outer membrane of Salmonella typhimurium. Translocation and integration of an incomplete mutant lipid A into the outer membrane.鼠伤寒沙门氏菌外膜组装机制。不完全突变脂质A在外膜中的转运与整合。
J Biol Chem. 1980 May 10;255(9):4246-51.
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Resistance of gram-negative bacteria to purified bactericidal leukocyte proteins: relation to binding and bacterial lipopolysaccharide structure.革兰氏阴性菌对纯化杀菌白细胞蛋白的抗性:与结合及细菌脂多糖结构的关系。
J Clin Invest. 1980 Mar;65(3):619-28. doi: 10.1172/JCI109707.
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Sensitivity of K1-encapsulated Escherichia coli to killing by the bactericidal/permeability-increasing protein of rabbit and human neutrophils.K1 包膜大肠杆菌对兔和人中性粒细胞杀菌/通透性增加蛋白杀伤作用的敏感性。
Infect Immun. 1982 Dec;38(3):1149-53. doi: 10.1128/iai.38.3.1149-1153.1982.