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小鼠实验性腹膜炎期间大肠杆菌1型菌毛程度的变化

Change in degree of type 1 piliation of Escherichia coli during experimental peritonitis in the mouse.

作者信息

Alkan M L, Wong L, Silverblatt F J

出版信息

Infect Immun. 1986 Nov;54(2):549-54. doi: 10.1128/iai.54.2.549-554.1986.

DOI:10.1128/iai.54.2.549-554.1986
PMID:2876964
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC260196/
Abstract

To determine whether expression of type 1 pili varies during the course of Escherichia coli infection in vivo, mice were injected intraperitoneally with 5 X 10(7) CFU of piliated or nonpiliated phase variants per ml, and the degree of piliation was measured in peritoneal exudate by an enzyme-linked immunosorbent assay inhibition method. In the animals challenged with the piliated bacteria, the numbers of organisms increased a log over 9 h and the amount of pilus antigen decreased from 3 to 0.075 micrograms/10 bacteria. After a 4-h delay, nonpiliated bacteria also increased by one log over 9 h; however, the amount of piliation remained virtually undetectable. Piliated E. coli were more virulent than nonpiliated variants in this model (50% lethal dose of 7.5 X 10(6) versus 3 X 10(7), respectively). The difference was significantly reduced by prior passive immunization with rabbit serum containing high titers of antipili antibody. Piliated bacteria adhered in significantly greater numbers to isolated mouse peritoneal membranes than did nonpiliated variants (15,400 +/- 2,700 versus 1,300 +/- 700 bacteria/mm2, respectively; P = 0.05). Adherence was inhibited by the presence of 0.1 M alpha methyl mannose (1,500 +/- 1,800 bacteria/mm2, P = 0.01). These results confirm the results of previous qualitative studies showing that phase variation of type 1 pili occurs in vivo and suggest that these pili may confer an initial advantage for growth of E. coli in the peritoneal cavity, presumably by fostering colonization of the peritoneal serosal surface.

摘要

为了确定1型菌毛的表达在体内大肠杆菌感染过程中是否会发生变化,给小鼠腹腔注射每毫升含5×10⁷CFU的菌毛化或非菌毛化相变变体,通过酶联免疫吸附测定抑制法测量腹腔渗出液中的菌毛化程度。在用菌毛化细菌攻击的动物中,细菌数量在9小时内增加了一个对数级,菌毛抗原量从3微克/10个细菌降至0.075微克/10个细菌。延迟4小时后,非菌毛化细菌在9小时内也增加了一个对数级;然而,菌毛化程度几乎仍无法检测到。在该模型中,菌毛化大肠杆菌比非菌毛化变体更具毒性(半数致死剂量分别为7.5×10⁶和3×10⁷)。用含有高滴度抗菌毛抗体的兔血清进行预先被动免疫可显著降低这种差异。与非菌毛化变体相比,菌毛化细菌黏附到分离的小鼠腹膜上的数量显著更多(分别为15400±2700和1300±700个细菌/mm²;P = 0.05)。0.1Mα-甲基甘露糖的存在可抑制黏附(1500±1800个细菌/mm²,P = 0.01)。这些结果证实了先前定性研究的结果,表明1型菌毛的相变发生在体内,并表明这些菌毛可能为大肠杆菌在腹腔内生长提供初始优势,大概是通过促进腹膜浆膜表面定植。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/490e/260196/193600892126/iai00098-0289-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/490e/260196/4d5df77e786e/iai00098-0288-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/490e/260196/193600892126/iai00098-0289-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/490e/260196/4d5df77e786e/iai00098-0288-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/490e/260196/193600892126/iai00098-0289-a.jpg

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