Hood D W, Deadman M E, Allen T, Masoud H, Martin A, Brisson J R, Fleischmann R, Venter J C, Richards J C, Moxon E R
University of Oxford, Department of Paediatrics, John Radcliffe Hospital, Headington, UK.
Mol Microbiol. 1996 Dec;22(5):951-65. doi: 10.1046/j.1365-2958.1996.01545.x.
The availability of the complete 1.83-megabase-pair sequence of the Haemophilus influenzae strain Rd genome has facilitated significant progress in investigating the biology of H.influenzae lipopolysaccharide (LPS), a major virulence determinant of this human pathogen. By searching the H. influenzae genomic database, with sequences of known LPS biosynthetic genes from other organisms, we identified and then cloned 25 candidate LPS genes. Construction of mutant strains and characterization of the LPS by reactivity with monoclonal antibodies, PAGE fractionation patterns and electrospray mass spectrometry comparative analysis have confirmed a potential role in LPS biosynthesis for the majority of these candidate genes. Virulence studies in the infant rat have allowed us to estimate the minimal LPS structure required for intravascular dissemination. This study is one of the first to demonstrate the rapidity, economy and completeness with which novel biological information can be accessed once the complete genome sequence of an organism is available.
流感嗜血杆菌Rd菌株完整的183万个碱基对基因组序列的获得,推动了对流感嗜血杆菌脂多糖(LPS)生物学特性研究的重大进展,LPS是这种人类病原体的主要毒力决定因素。通过搜索流感嗜血杆菌基因组数据库,并结合来自其他生物体的已知LPS生物合成基因序列,我们鉴定并克隆了25个候选LPS基因。构建突变菌株,并通过与单克隆抗体反应、PAGE分级分离模式和电喷雾质谱比较分析对LPS进行表征,证实了这些候选基因中的大多数在LPS生物合成中具有潜在作用。在幼鼠身上进行的毒力研究使我们能够估计血管内传播所需的最小LPS结构。这项研究是首批证明一旦获得生物体的完整基因组序列,就能快速、经济且全面地获取新生物信息的研究之一。