作者
Hervé Tettelin, Vega Masignani, Michael J Cieslewicz, Claudio Donati, Duccio Medini, Naomi L Ward, Samuel V Angiuoli, Jonathan Crabtree, Amanda L Jones, A Scott Durkin, Robert T DeBoy, Tanja M Davidsen, Marirosa Mora, Maria Scarselli, Immaculada Margarit y Ros, Jeremy D Peterson, Christopher R Hauser, Jaideep P Sundaram, William C Nelson, Ramana Madupu, Lauren M Brinkac, Robert J Dodson, Mary J Rosovitz, Steven A Sullivan, Sean C Daugherty, Daniel H Haft, Jeremy Selengut, Michelle L Gwinn, Liwei Zhou, Nikhat Zafar, Hoda Khouri, Diana Radune, George Dimitrov, Kisha Watkins, Kevin JB O'Connor, Shannon Smith, Teresa R Utterback, Owen White, Craig E Rubens, Guido Grandi, Lawrence C Madoff, Dennis L Kasper, John L Telford, Michael R Wessels, Rino Rappuoli, Claire M Fraser
发表日期
2005/9/27
期刊
Proceedings of the National Academy of Sciences
卷号
102
期号
39
页码范围
13950-13955
出版商
National Academy of Sciences
简介
The development of efficient and inexpensive genome sequencing methods has revolutionized the study of human bacterial pathogens and improved vaccine design. Unfortunately, the sequence of a single genome does not reflect how genetic variability drives pathogenesis within a bacterial species and also limits genome-wide screens for vaccine candidates or for antimicrobial targets. We have generated the genomic sequence of six strains representing the five major disease-causing serotypes of Streptococcus agalactiae, the main cause of neonatal infection in humans. Analysis of these genomes and those available in databases showed that the S. agalactiae species can be described by a pan-genome consisting of a core genome shared by all isolates, accounting for ≈80% of any single genome, plus a dispensable genome consisting of partially shared and strain-specific genes. Mathematical extrapolation …
引用总数
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