Salyers A A, Pajeau M, McCarthy R E
Department of Microbiology, University of Illinois, Urbana 61801.
Appl Environ Microbiol. 1988 Aug;54(8):1970-6. doi: 10.1128/aem.54.8.1970-1976.1988.
We used two approaches to determine whether the mucopolysaccharide chondroitin sulfate is an important source of carbon and energy for Bacteroides thetaiotaomicron in the intestinal tracts of germfree mice. First, we tested the ability of three mutants that grew poorly or not at all on chondroitin sulfate to colonize the intestinal tract of a germfree mouse and to compete with wild-type B. thetaiotaomicron in this model system. One mutant (CG10) was rapidly outcompeted by the wild type. However, since this mutant was unable to grow on chondroitin sulfate because it could not grow on N-acetyl-galactosamine, one of its monosaccharide components, this mutant might also be unable to utilize glycoprotein mucins. Two mutants (46-1 and 46-4) were isolated that grew poorly on chondroitin sulfate but normally on both component sugars. One of them was outcompeted by the wild type, but the percent wild type increased more slowly than with CG10. In one experiment, the percent wild type never reached 100%. The other (46-4) was not outcompeted by the wild type. These results indicate that, although chondroitin sulfate may be a carbon source in the animal, it is not of major importance. Our second approach was to determine by immunoblot analysis whether a 28-kilodalton outer membrane protein that is produced by B. thetaiotaomicron only when it is grown on chondroitin sulfate or hyaluronic acid was being produced at induced level by B. thetaiotaomicron growing in the ceca of exgermfree mice. There was no evidence for induction of this protein in vivo. Thus, the immunoblot results are consistent with results of the mutant competition experiments.
我们采用了两种方法来确定黏多糖硫酸软骨素是否是无菌小鼠肠道中多形拟杆菌的重要碳源和能量来源。首先,我们测试了三种在硫酸软骨素上生长不良或完全不生长的突变体在无菌小鼠肠道中定殖的能力,以及在该模型系统中与野生型多形拟杆菌竞争的能力。一个突变体(CG10)很快就被野生型淘汰了。然而,由于这个突变体不能在硫酸软骨素上生长,因为它不能在其单糖成分之一的N - 乙酰半乳糖胺上生长,所以这个突变体可能也无法利用糖蛋白黏蛋白。分离出了两个突变体(46 - 1和46 - 4),它们在硫酸软骨素上生长不良,但在两种组成糖上生长正常。其中一个被野生型淘汰,但野生型的百分比增长比CG10慢。在一个实验中,野生型的百分比从未达到100%。另一个(46 - 4)没有被野生型淘汰。这些结果表明,尽管硫酸软骨素可能是动物体内的一种碳源,但它并不重要。我们的第二种方法是通过免疫印迹分析来确定多形拟杆菌仅在以硫酸软骨素或透明质酸为培养基生长时产生的一种28千道尔顿的外膜蛋白,在无菌小鼠盲肠中生长的多形拟杆菌是否在诱导水平产生该蛋白。没有证据表明该蛋白在体内被诱导产生。因此,免疫印迹结果与突变体竞争实验的结果一致。