Nelson Karen E, Fleischmann Robert D, DeBoy Robert T, Paulsen Ian T, Fouts Derrick E, Eisen Jonathan A, Daugherty Sean C, Dodson Robert J, Durkin A Scott, Gwinn Michelle, Haft Daniel H, Kolonay James F, Nelson William C, Mason Tanya, Tallon Luke, Gray Jessica, Granger David, Tettelin Hervé, Dong Hong, Galvin Jamie L, Duncan Margaret J, Dewhirst Floyd E, Fraser Claire M
The Institute for Genomic Research, Rockville, Maryland 20850, USA.
J Bacteriol. 2003 Sep;185(18):5591-601. doi: 10.1128/JB.185.18.5591-5601.2003.
The complete 2,343,479-bp genome sequence of the gram-negative, pathogenic oral bacterium Porphyromonas gingivalis strain W83, a major contributor to periodontal disease, was determined. Whole-genome comparative analysis with other available complete genome sequences confirms the close relationship between the Cytophaga-Flavobacteria-Bacteroides (CFB) phylum and the green-sulfur bacteria. Within the CFB phyla, the genomes most similar to that of P. gingivalis are those of Bacteroides thetaiotaomicron and B. fragilis. Outside of the CFB phyla the most similar genome to P. gingivalis is that of Chlorobium tepidum, supporting the previous phylogenetic studies that indicated that the Chlorobia and CFB phyla are related, albeit distantly. Genome analysis of strain W83 reveals a range of pathways and virulence determinants that relate to the novel biology of this oral pathogen. Among these determinants are at least six putative hemagglutinin-like genes and 36 previously unidentified peptidases. Genome analysis also reveals that P. gingivalis can metabolize a range of amino acids and generate a number of metabolic end products that are toxic to the human host or human gingival tissue and contribute to the development of periodontal disease.
已测定革兰氏阴性致病性口腔细菌牙龈卟啉单胞菌W83菌株完整的2343479碱基对基因组序列,该菌是牙周病的主要致病菌。与其他现有完整基因组序列进行的全基因组比较分析证实了噬纤维菌-黄杆菌-拟杆菌(CFB)门与绿硫细菌之间的密切关系。在CFB门内,与牙龈卟啉单胞菌基因组最相似的是嗜热栖热放线菌和脆弱拟杆菌的基因组。在CFB门之外,与牙龈卟啉单胞菌最相似的基因组是嗜热栖热放线菌的基因组,这支持了先前的系统发育研究,该研究表明绿菌门和CFB门是相关的,尽管关系较远。W83菌株的基因组分析揭示了一系列与这种口腔病原体新生物学相关的途径和毒力决定因素。在这些决定因素中,至少有六个假定的血凝素样基因和36种以前未鉴定的肽酶。基因组分析还表明,牙龈卟啉单胞菌能够代谢多种氨基酸,并产生一些对人类宿主或人类牙龈组织有毒的代谢终产物,这些产物会导致牙周病的发展。