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非O1群霍乱弧菌NRT36S的荚膜多糖结构与生物合成:相关基因嵌入脂多糖区域。

The capsule polysaccharide structure and biogenesis for non-O1 Vibrio cholerae NRT36S: genes are embedded in the LPS region.

作者信息

Chen Yuansha, Bystricky Peter, Adeyeye Jacob, Panigrahi Pinaki, Ali Afsar, Johnson Judith A, Bush C A, Morris J G, Stine O C

机构信息

Department of Epidemiology and Preventive Medicine, University of Maryland, Baltimore, Baltimore, MD 21201, USA.

出版信息

BMC Microbiol. 2007 Mar 15;7:20. doi: 10.1186/1471-2180-7-20.

Abstract

BACKGROUND

In V. cholerae, the biogenesis of capsule polysaccharide is poorly understood. The elucidation of capsule structure and biogenesis is critical to understanding the evolution of surface polysaccharide and the internal relationship between the capsule and LPS in this species. V. cholerae serogroup O31 NRT36S, a human pathogen that produces a heat-stable enterotoxin (NAG-ST), is encapsulated. Here, we report the covalent structure and studies of the biogenesis of the capsule in V. cholerae NRT36S.

RESULTS

The structure of the capsular (CPS) polysaccharide was determined by high resolution NMR spectroscopy and shown to be a complex structure with four residues in the repeating subunit. The gene cluster of capsule biogenesis was identified by transposon mutagenesis combined with whole genome sequencing data (GenBank accession DQ915177). The capsule gene cluster shared the same genetic locus as that of the O-antigen of lipopolysaccharide (LPS) biogenesis gene cluster. Other than V. cholerae O139, this is the first V. cholerae CPS for which a structure has been fully elucidated and the genetic locus responsible for biosynthesis identified.

CONCLUSION

The co-location of CPS and LPS biosynthesis genes was unexpected, and would provide a mechanism for simultaneous emergence of new O and K antigens in a single strain. This, in turn, may be a key element for V. cholerae to evolve new strains that can escape immunologic detection by host populations.

摘要

背景

在霍乱弧菌中,荚膜多糖的生物合成机制尚不清楚。阐明荚膜结构和生物合成对于理解该菌表面多糖的进化以及荚膜与脂多糖(LPS)之间的内在关系至关重要。霍乱弧菌O31 NRT36S血清型是一种能产生热稳定肠毒素(NAG-ST)的人类病原体,具有荚膜。在此,我们报告霍乱弧菌NRT36S荚膜的共价结构及其生物合成研究。

结果

通过高分辨率核磁共振光谱确定了荚膜多糖(CPS)的结构,显示其重复亚基中有四个残基,是一种复杂结构。通过转座子诱变结合全基因组测序数据(GenBank登录号DQ915177)鉴定了荚膜生物合成的基因簇。该荚膜基因簇与脂多糖(LPS)生物合成基因簇的O抗原位于相同的基因位点。除霍乱弧菌O139外,这是首个其结构已被完全阐明且负责生物合成的基因位点已被确定的霍乱弧菌CPS。

结论

CPS和LPS生物合成基因的共定位出乎意料,这可能为单个菌株中同时出现新的O抗原和K抗原提供一种机制。反过来,这可能是霍乱弧菌进化出能逃避宿主群体免疫检测的新菌株的关键因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7274/1847822/c5365b694823/1471-2180-7-20-1.jpg

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