Hérias M V, Midtvedt T, Hanson L A, Wold A E
Department of Clinical Immunology, University of Göteborg, Sweden.
Infect Immun. 1997 Feb;65(2):531-6. doi: 10.1128/iai.65.2.531-536.1997.
The role of capsule expression in the capacity of Escherichia coli to colonize in the large intestinal environment was studied in a gnotobiotic rat model. The rats were given perorally a mixture of two mutant strains differing in K5 expression. After 2 weeks, the rats were sacrificed, and subsequently intestinal contents, intestinal mucosae, and mesenteric lymph nodes were homogenized and bacterial numbers were quantified. Two E. coli mutant pairs were used, the first pair (972-998) lacking the O-specific side chain and the second pair (973-997) carrying the O75 lipopolysaccharide. The K5+ mutants established themselves at a higher level than the K5- mutants (10(9) versus 10(6) CFU/g [P < 0.001] for the first pair and 10(9) versus 10(8) CFU/g [P < 0.01] for the second pair, respectively). The results were confirmed by serology showing a K5+ phenotype for practically all isolates. The bacterial population associated with the mucosa was similar to that in the luminal contents with respect to the proportions of the respective mutants, and translocation occurred in numbers proportional to the intestinal population densities of the respective mutants. All mutants were able to express type 1 as well as P fimbriae. After colonization, the expression of P fimbriae remained high whereas only a minority of the isolates expressed type 1 fimbriae. The results suggest that capsule expression and P fimbriae enhance intestinal colonization by E. coli and that these virulence factors, by increasing bacterial densities in the intestine, secondarily increase translocation.
在无菌大鼠模型中研究了荚膜表达在大肠杆菌在大肠环境中定殖能力方面的作用。给大鼠经口投喂两种K5表达不同的突变菌株的混合物。2周后,处死大鼠,随后将肠内容物、肠黏膜和肠系膜淋巴结匀浆并对细菌数量进行定量。使用了两对大肠杆菌突变体,第一对(972 - 998)缺乏O特异性侧链,第二对(973 - 997)携带O75脂多糖。K5 +突变体比K5 -突变体定殖水平更高(第一对分别为10⁹对10⁶CFU/g [P < 0.001],第二对分别为10⁹对10⁸CFU/g [P < 0.01])。血清学结果证实了几乎所有分离株的K5 +表型。就各自突变体的比例而言,与黏膜相关的细菌群体与管腔内容物中的相似,并且转位发生的数量与各自突变体的肠道群体密度成比例。所有突变体都能够表达1型菌毛以及P菌毛。定殖后,P菌毛的表达仍然很高,而只有少数分离株表达1型菌毛。结果表明荚膜表达和P菌毛增强了大肠杆菌在肠道中的定殖,并且这些毒力因子通过增加肠道中的细菌密度,继而增加转位。