Fuller R, Houghton S B, Brooker B E
Appl Environ Microbiol. 1981 Jun;41(6):1433-41. doi: 10.1128/aem.41.6.1433-1441.1981.
The counts of Streptococcus faecium SY1 in the duodenums of gnotobiotic chicks exceeded the counts in their crops, indicating that multiplication was occurring in the anterior small intestine. This growth was related to adhesion to the gut wall which could be demonstrated by viable counts of macerated washed duodenal tissue. Scanning electron microscopy demonstrated that adhesion occurred in restricted areas on the surface of the villus, and transmission studies showed the presence of a thick extracellular layer on the bacterium. Attachment of S. faecium SY1 was confirmed in vitro by using chicken duodenal brush borders. The washings, produced during the preparation of the brush borders, increased the number of S. faecium adhering to the brush borders. This enhancing effect was due to the presence of trypsin in the duodenal washings. However, the effect was not dependent on the enzymatic activity of the trypsin molecule. The initial adhesion was not prevented by pretreatment of the brush borders with soy bean trypsin inhibitor. There were, therefore, two adhesion systems operating, only one of which was dependent on trypsin. Pretreatment of brush borders with trypsin digested them, but they remained intact in the presence of S. faecium SY1, indicating that the enzymatic activity was being inhibited. This effect was specific for the adhering strain of S. faecium SY1; the nonadhering S. faecium strain CRS23 and an adhering strain of Lactobacillus sp. were inactive, as was strain SY1 when adhesion was prevented by including sodium periodate in the test system. The colonizations of the gut by strains of S. faecium of differing adhesive abilities were compared. The nonadhering strain CRS23 showed reduced ability to colonize the duodenum, but the penicillin-resistant mutant of S. faecium SY1, which had reduced adhesive ability but could still attach to a lesser degree, was able to colonize the duodenum as efficiently as the parent strain.
悉生雏鸡十二指肠中屎肠球菌SY1的数量超过了嗉囊中的数量,这表明在前小肠中发生了增殖。这种生长与对肠壁的黏附有关,这可以通过对研磨洗涤后的十二指肠组织进行活菌计数来证明。扫描电子显微镜显示黏附发生在绒毛表面的特定区域,透射研究表明该细菌表面存在一层厚厚的细胞外层。通过使用鸡十二指肠刷状缘在体外证实了屎肠球菌SY1的附着。在制备刷状缘的过程中产生的洗涤液增加了黏附在刷状缘上的屎肠球菌数量。这种增强作用是由于十二指肠洗涤液中存在胰蛋白酶。然而,这种作用并不依赖于胰蛋白酶分子的酶活性。用大豆胰蛋白酶抑制剂对刷状缘进行预处理并不能阻止初始黏附。因此,存在两种黏附系统,其中只有一种依赖于胰蛋白酶。用胰蛋白酶对刷状缘进行预处理会使其消化,但在屎肠球菌SY1存在的情况下它们仍保持完整,这表明酶活性受到了抑制。这种作用对黏附性屎肠球菌SY1菌株具有特异性;非黏附性屎肠球菌菌株CRS23和一种黏附性乳酸杆菌菌株没有活性,当在测试系统中加入高碘酸钠阻止黏附时,SY1菌株也没有活性。比较了不同黏附能力的屎肠球菌菌株在肠道中的定殖情况。非黏附性菌株CRS23在十二指肠中的定殖能力降低,但屎肠球菌SY1的青霉素抗性突变体黏附能力降低但仍能在较小程度上附着,它在十二指肠中的定殖效率与亲本菌株相同。