Chia J S, Chang L Y, Shun C T, Chang Y Y, Tsay Y G, Chen J Y
Graduate Institute of Microbiology, College of Medicine National Taiwan University, National Taiwan University Hospital, Taipei, Taiwan, Republic of China.
Infect Immun. 2001 Nov;69(11):6987-98. doi: 10.1128/IAI.69.11.6987-6998.2001.
We have demonstrated previously by Western blotting that in naturally sensitized humans, the serum or salivary antibody response to Streptococcus mutans was directed predominantly to a protein antigen with a size of approximately 60-kDa. To identify this immunodominant antigen, specific serum antibodies were eluted from immunoblots and five positive clones with inserts ranging in length from 3 to 8 kb from identical chromosomal loci were obtained by screening a genomic expression library of Streptococcus mutans GS-5. Amino acid sequencing established the identity of this immunodominant antigen, a 60-kDa immunodominant glycoprotein (IDG-60), to be a cell wall-associated general stress protein GSP-781, which was originally predicted to have a molecular mass of approximately 45 kDa based on the derived nucleotide sequence. Discrepancy in the molecular mass was also observed in recombinant his-tagged IDG-60 (rIDG-60) expressed from Escherichia coli. Glycosylation, consisting of sialic acid, mannose galactose, and N-acetylgalactosamine, was detected by lectin binding to IDG-60 in cell wall extracts from S. mutans and rIDG-60 expressed in vivo or translated in vitro. Despite the presence of multiple Asn or Ser or Thr glycosylation sites, IDG-60 was resistant to the effect of N-glycosidase F and multiple O-glycosidase molecules but not to beta-galactosidase. Insertional inactivation of the gene encoding IDG-60, sagA, resulted in a retarded growth rate, destabilization of the cell wall, and pleiomorphic cell shape with multifold ingrowth of cell wall. In addition, distinct from the parental GS-5 strain, the isogenic mutant GS-51 was unable to survive the challenge of low pH and high osmotic pressure or high temperature. Expression of the wild-type gene in trans within GS-51 from plasmid pDL277 complemented the growth defect and restored normal cell shape. These results suggested that IDG-60 is essential for maintaining the integrity of the cell wall and the uniformity of cell shape, both of which are indispensable for bacteria survival under stress conditions.
我们之前通过蛋白质免疫印迹法证明,在自然致敏的人体中,血清或唾液对变形链球菌的抗体反应主要针对一种大小约为60 kDa的蛋白质抗原。为了鉴定这种免疫显性抗原,从免疫印迹中洗脱特异性血清抗体,并通过筛选变形链球菌GS-5的基因组表达文库,获得了五个阳性克隆,其插入片段长度在3至8 kb之间,来自相同的染色体位点。氨基酸测序确定了这种免疫显性抗原,即一种60 kDa的免疫显性糖蛋白(IDG-60),是一种细胞壁相关的一般应激蛋白GSP-781,根据推导的核苷酸序列,其最初预测的分子量约为45 kDa。在从大肠杆菌中表达的重组组氨酸标签IDG-60(rIDG-60)中也观察到分子量的差异。通过凝集素与变形链球菌细胞壁提取物中的IDG-60以及体内表达或体外翻译的rIDG-60结合,检测到由唾液酸、甘露糖、半乳糖和N-乙酰半乳糖胺组成的糖基化。尽管存在多个天冬酰胺或丝氨酸或苏氨酸糖基化位点,但IDG-60对N-糖苷酶F和多种O-糖苷酶分子的作用具有抗性,但对β-半乳糖苷酶不具有抗性。编码IDG-60的基因sagA的插入失活导致生长速率减慢、细胞壁不稳定以及细胞壁多倍向内生长的多形细胞形状。此外,与亲本GS-5菌株不同,同基因突变体GS-51无法在低pH、高渗透压或高温的挑战下存活。来自质粒pDL277的野生型基因在GS-51中反式表达弥补了生长缺陷并恢复了正常细胞形状。这些结果表明,IDG-60对于维持细胞壁的完整性和细胞形状的均匀性至关重要,而这两者对于细菌在应激条件下的存活都是不可或缺的。