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从兔结肠分离出的粘蛋白可抑制大肠杆菌RDEC-1的体外结合。

Mucin isolated from rabbit colon inhibits in vitro binding of Escherichia coli RDEC-1.

作者信息

Mack D R, Sherman P M

机构信息

Department of Pediatrics, Hospital for Sick Children, University of Toronto, Canada.

出版信息

Infect Immun. 1991 Mar;59(3):1015-23. doi: 10.1128/iai.59.3.1015-1023.1991.

Abstract

The rabbit enteric pathogen Escherichia coli RDEC-1 (serotype O15:H-) mediates attaching and effacing binding to colonic epithelium in a manner morphologically identical to that observed in both human enteropathogenic E. coli and enterohemorrhagic E. coli infections. The aim of this study was to determine if colonic mucus and its constituents, including mucin derived from goblet cells, inhibited RDEC-1 adherence in vitro. Crude mucus was prepared from mucosal scrapings of rabbit colon and separated by buoyant density into eight fractions. Purified mucin was characterized by gel electrophoresis, dot immunoblotting, indirect immunofluorescence, and amino acid composition. RDEC-1 bacteria were grown to promote and suppress the expression of mannose-resistant, hydrophobic pili. A nonpiliated mutant, strain M34, was also used as a negative control. Binding of radiolabeled RDEC-1 expressing pili was quantitated in the presence of crude mucus, purified mucin, and nonmucin fractions. Binding of piliated RDEC-1 to hydrophobic polystyrene wells was greater than for both nonpiliated RDEC-1 and strain M34 (P less than 0.05). Both crude mucus and purified mucin mediated a concentration-dependent inhibition of piliated-RDEC-1 binding. Fractions of mucus without immunoreactive mucin did not inhibit the binding of RDEC-1 expressing hydrophobic pili. We conclude that colonic goblet cell-derived mucin mediates inhibition of piliated RDEC-1 attachment in vitro. Inhibition of bacterial adherence could prevent access of attaching and effacing E. coli enteric pathogens to the colonic mucosa in vivo.

摘要

兔肠道病原体大肠杆菌RDEC-1(血清型O15:H-)介导与结肠上皮的紧密黏附并造成局部侵蚀,其形态学方式与人类肠致病性大肠杆菌和肠出血性大肠杆菌感染中观察到的相同。本研究的目的是确定结肠黏液及其成分,包括杯状细胞衍生的黏蛋白,是否在体外抑制RDEC-1的黏附。从兔结肠黏膜刮片中制备粗黏液,并通过浮力密度分离成八个部分。通过凝胶电泳、斑点免疫印迹、间接免疫荧光和氨基酸组成对纯化的黏蛋白进行表征。培养RDEC-1细菌以促进和抑制甘露糖抗性疏水菌毛的表达。非菌毛突变体M34菌株也用作阴性对照。在存在粗黏液、纯化黏蛋白和非黏蛋白部分的情况下,对表达菌毛的放射性标记RDEC-1的结合进行定量。有菌毛的RDEC-1与疏水聚苯乙烯孔的结合大于无菌毛的RDEC-1和M34菌株(P小于0.05)。粗黏液和纯化黏蛋白均介导了对有菌毛RDEC-1结合的浓度依赖性抑制。没有免疫反应性黏蛋白的黏液部分不抑制表达疏水菌毛的RDEC-1的结合。我们得出结论,结肠杯状细胞衍生的黏蛋白在体外介导了对有菌毛RDEC-1黏附的抑制。抑制细菌黏附可以防止紧密黏附并造成局部侵蚀的大肠杆菌肠道病原体在体内进入结肠黏膜。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc8/258361/9ba32ad09d3b/iai00039-0283-a.jpg

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