The post-vaccine microevolution of invasive Streptococcus pneumoniae

被引:28
|
作者
Cremers, Amelieke J. H. [1 ]
Mobegi, Fredrick M. [1 ,2 ,3 ]
de Jonge, Marien I. [1 ]
van Hijum, Sacha A. F. T. [2 ,3 ]
Meis, Jacques F. [4 ,5 ]
Hermans, Peter W. M. [1 ]
Ferwerda, Gerben [1 ]
Bentley, Stephen D. [6 ]
Zomer, Aldert L. [1 ,2 ,3 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Lab Pediat Infect Dis, NL-6525 ED Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Bacterial Genom Grp, NL-6525 ED Nijmegen, Netherlands
[3] Radboud Univ Nijmegen, Ctr Mol & Biomol Informat, NL-6525 ED Nijmegen, Netherlands
[4] Canisius Wilhelmina Hosp, Dept Med Microbiol & Infect Dis, Nijmegen, Netherlands
[5] Radboud Univ Nijmegen, Med Ctr, Dept Med Microbiol, NL-6525 ED Nijmegen, Netherlands
[6] Wellcome Trust Sanger Inst, Pathogen Genom Grp, Hinxton Cambridge, England
来源
SCIENTIFIC REPORTS | 2015年 / 5卷
关键词
PNEUMOCOCCAL CONJUGATE VACCINE; SEROTYPE REPLACEMENT; MULTIPLE ALIGNMENT; DISEASE; CARRIAGE; POPULATION; CHILDREN; EPIDEMIOLOGY; LIKELIHOOD; SEQUENCE;
D O I
10.1038/srep14952
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The 7-valent pneumococcal conjugated vaccine (PCV7) has affected the genetic population of Streptococcus pneumoniae in pediatric carriage. Little is known however about pneumococcal population genomics in adult invasive pneumococcal disease (IPD) under vaccine pressure. We sequenced and serotyped 349 strains of S. pneumoniae isolated from IPD patients in Nijmegen between 2001 and 2011. Introduction of PCV7 in the Dutch National Immunization Program in 2006 preluded substantial alterations in the IPD population structure caused by serotype replacement. No evidence could be found for vaccine induced capsular switches. We observed that after a temporary bottleneck in gene diversity after the introduction of PCV7, the accessory gene pool re-expanded mainly by genes already circulating pre-PCV7. In the post-vaccine genomic population a number of genes changed frequency, certain genes became overrepresented in vaccine serotypes, while others shifted towards non-vaccine serotypes. Whether these dynamics in the invasive pneumococcal population have truly contributed to invasiveness and manifestations of disease remains to be further elucidated. We suggest the use of whole genome sequencing for surveillance of pneumococcal population dynamics that could give a prospect on the course of disease, facilitating effective prevention and management of IPD.
引用
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页数:8
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