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一种60千道尔顿的免疫显性糖蛋白对于变形链球菌的细胞壁完整性和细胞形态维持至关重要。

A 60-kilodalton immunodominant glycoprotein is essential for cell wall integrity and the maintenance of cell shape in Streptococcus mutans.

作者信息

Chia J S, Chang L Y, Shun C T, Chang Y Y, Tsay Y G, Chen J Y

机构信息

Graduate Institute of Microbiology, College of Medicine National Taiwan University, National Taiwan University Hospital, Taipei, Taiwan, Republic of China.

出版信息

Infect Immun. 2001 Nov;69(11):6987-98. doi: 10.1128/IAI.69.11.6987-6998.2001.

Abstract

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.

摘要

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。

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