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肺炎链球菌强毒株的全基因组序列

Complete genome sequence of a virulent isolate of Streptococcus pneumoniae.

作者信息

Tettelin H, Nelson K E, Paulsen I T, Eisen J A, Read T D, Peterson S, Heidelberg J, DeBoy R T, Haft D H, Dodson R J, Durkin A S, Gwinn M, Kolonay J F, Nelson W C, Peterson J D, Umayam L A, White O, Salzberg S L, Lewis M R, Radune D, Holtzapple E, Khouri H, Wolf A M, Utterback T R, Hansen C L, McDonald L A, Feldblyum T V, Angiuoli S, Dickinson T, Hickey E K, Holt I E, Loftus B J, Yang F, Smith H O, Venter J C, Dougherty B A, Morrison D A, Hollingshead S K, Fraser C M

机构信息

The Institute for Genomic Research (TIGR), 9712 Medical Center Drive, Rockville, MD 20850, USA.

出版信息

Science. 2001 Jul 20;293(5529):498-506. doi: 10.1126/science.1061217.

Abstract

The 2,160,837-base pair genome sequence of an isolate of Streptococcus pneumoniae, a Gram-positive pathogen that causes pneumonia, bacteremia, meningitis, and otitis media, contains 2236 predicted coding regions; of these, 1440 (64%) were assigned a biological role. Approximately 5% of the genome is composed of insertion sequences that may contribute to genome rearrangements through uptake of foreign DNA. Extracellular enzyme systems for the metabolism of polysaccharides and hexosamines provide a substantial source of carbon and nitrogen for S. pneumoniae and also damage host tissues and facilitate colonization. A motif identified within the signal peptide of proteins is potentially involved in targeting these proteins to the cell surface of low-guanine/cytosine (GC) Gram-positive species. Several surface-exposed proteins that may serve as potential vaccine candidates were identified. Comparative genome hybridization with DNA arrays revealed strain differences in S. pneumoniae that could contribute to differences in virulence and antigenicity.

摘要

肺炎链球菌是一种革兰氏阳性病原体,可导致肺炎、菌血症、脑膜炎和中耳炎。一株肺炎链球菌的基因组序列有2160837个碱基对,包含2236个预测的编码区;其中1440个(64%)被赋予了生物学功能。基因组约5%由插入序列组成,这些序列可能通过摄取外源DNA导致基因组重排。多糖和己糖胺代谢的细胞外酶系统为肺炎链球菌提供了大量的碳源和氮源,同时也会损害宿主组织并促进定植。在蛋白质信号肽中鉴定出的一个基序可能参与将这些蛋白质靶向低鸟嘌呤/胞嘧啶(GC)革兰氏阳性菌的细胞表面。鉴定出了几种可能作为潜在疫苗候选物的表面暴露蛋白。用DNA阵列进行的比较基因组杂交揭示了肺炎链球菌菌株之间的差异,这些差异可能导致毒力和抗原性的差异。

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