Genetic analysis of the capsular biosynthetic locus from all 90 pneumococcal serotypes

被引:556
作者
Bentley, Stephen D.
Aanensen, David M.
Mavroidi, Angeliki
Saunders, David
Rabbinowitsch, Ester
Collins, Matthew
Donohoe, Kathy
Harris, David
Murphy, Lee
Quail, Michael A.
Samuel, Gabby
Skovsted, Ian C.
Kaltoft, Margit Staum
Barrell, Bart
Reeves, Peter R.
Parkhill, Julian
Spratt, Brian G.
机构
[1] Sanger Inst, Cambridge, England
[2] Imperial Coll, Dept Infect Dis Epidemiol, London, England
[3] Univ Sydney, Sch Mol & Microbial Biosci, Sydney, NSW 2006, Australia
[4] State Serum Inst, Copenhagen, Denmark
来源
PLOS GENETICS | 2006年 / 2卷 / 03期
关键词
D O I
10.1371/journal.pgen.0020031
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Several major invasive bacterial pathogens are encapsulated. Expression of a polysaccharide capsule is essential for survival in the blood, and thus for virulence, but also is a target for host antibodies and the basis for effective vaccines. Encapsulated species typically exhibit antigenic variation and express one of a number of immunochemically distinct capsular polysaccharides that define serotypes. We provide the sequences of the capsular biosynthetic genes of all 90 serotypes of Streptococcus pneumoniae and relate these to the known polysaccharide structures and patterns of immunological reactivity of typing sera, thereby providing the most complete understanding of the genetics and origins of bacterial polysaccharide diversity, laying the foundations for molecular serotyping. This is the first time, to our knowledge, that a complete repertoire of capsular biosynthetic genes has been available, enabling a holistic analysis of a bacterial polysaccharide biosynthesis system. Remarkably, the total size of alternative coding DNA at this one locus exceeds 1.8 Mbp, almost equivalent to the entire S. pneumoniae chromosomal complement.
引用
收藏
页码:262 / 269
页数:8
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