Rahman M M, Guard-Petter J, Carlson R W
Complex Carbohydrate Research Center, The University of Georgia, Athens 30602, USA.
J Bacteriol. 1997 Apr;179(7):2126-31. doi: 10.1128/jb.179.7.2126-2131.1997.
The lipopolysaccharide (LPS) of Salmonella enteritidis has been implicated as a virulence factor of this organism. Therefore, the LPS from a stable virulent isolate, SE6-E21, was compared with that from an avirulent isolate, SE6-E5. The LPSs were extracted, and the high-molecular-weight (HMW) LPS was separated from the low-molecular-weight (LMW) LPS for both isolates. Both the HMW and LMW LPSs were characterized by glycosyl composition and linkage analyses. Immunochemical characterization was performed by Western blotting using factor 9 antiserum and using S. typhimurium antiserum which contains factors 1, 4, 5, and 12(2). In addition, the polysaccharides released by mild acid hydrolysis were isolated and subjected to hydrolysis by bacteriophage P22, which contains endorhamnosidase activity. The resulting oligosaccharides were purified by using Bio-Gel P4 gel permeation chromatography and characterized by nuclear magnetic resonance spectroscopy, fast atom bombardment mass spectrometry (FAB-MS), tandem MS-MS, and matrix-assisted laser desorption time of flight MS. The results show that the HMW LPS O-antigen polysaccharides from both isolates are comprised of two different repeating units, -[-->2)-[alpha-Tyvp-(1-->3)]beta-D-Manp-(1-->4)-alpha-L-R hap-(1-->3)-alpha-D-Galp-(1-->]- (structure I) and [-->2)-[alpha-Tyvp-(1-->3)]beta-D-Manp-(1-->4)-alpha--L-R hap-(1-->3)-[alpha-D-Glcp-(1-->4)]alpha-D-Galp-(1-->]- (structure II). The LMW LPSs from both isolates contains truncated O-antigen polysaccharide which is comprised of only structure I. In the virulent SE6-E21 isolate, the HMW LPS has a structure I/II ratio of 1:1, while in the avirulent SE6-E5 isolate, this ratio is 7:1. While the 7:1 ratio represents the published level of glucosylation for S. enteritidis LPS as well as for S. enteritidis LPS purchased from Sigma Chemical Co., the 1:1 ratio found for the virulent SE6-E21 is identical to the high level of glucosylation reported for S. typhi LPS. Thus, the LPS from the virulent SE6-E21 isolate produces an S. typhi-like LPS. Furthermore, the amount of O-antigen polysaccharide in SE6-E21 was twice that in SE6-E5.
肠炎沙门氏菌的脂多糖(LPS)被认为是该菌的一种毒力因子。因此,对来自稳定强毒株SE6-E21的LPS与无毒株SE6-E5的LPS进行了比较。提取了两种菌株的LPS,并将高分子量(HMW)LPS与低分子量(LMW)LPS分离。通过糖基组成和连接分析对HMW和LMW LPS进行了表征。使用因子9抗血清以及含有因子1、4、5和12(2)的鼠伤寒沙门氏菌抗血清通过蛋白质印迹法进行免疫化学表征。此外,分离出温和酸水解释放的多糖,并使其受到含有内鼠李糖苷酶活性的噬菌体P22的水解作用。使用Bio-Gel P4凝胶渗透色谱法纯化得到的寡糖,并通过核磁共振光谱、快原子轰击质谱(FAB-MS)、串联MS-MS和基质辅助激光解吸飞行时间质谱对其进行表征。结果表明,两种菌株的HMW LPS O抗原多糖均由两个不同的重复单元组成,即-[→2)-[α-Tyvp-(1→3)]β-D-Manp-(1→4)-α-L-Rhap-(1→3)-α-D-Galp-(1→]-(结构I)和[→2)-[α-Tyvp-(1→3)]β-D-Manp-(1→4)-α-L-Rhap-(1→3)-[α-D-Glcp-(1→4)]α-D-Galp-(1→]-(结构II)。两种菌株的LMW LPS均含有仅由结构I组成的截短O抗原多糖。在强毒株SE6-E21中,HMW LPS的结构I/II比例为1:1,而在无毒株SE6-E5中,该比例为7:1。虽然7:1的比例代表了肠炎沙门氏菌LPS以及从Sigma Chemical Co.购买的肠炎沙门氏菌LPS的已公布糖基化水平,但在强毒株SE6-E21中发现的1:1比例与伤寒沙门氏菌LPS报道的高糖基化水平相同。因此,来自强毒株SE6-E21的LPS产生了类似伤寒沙门氏菌的LPS。此外,SE6-E21中O抗原多糖的量是SE6-E5中的两倍。