Evidence that pneumococcal serotype replacement in Massachusetts following conjugate vaccination is now complete

被引:114
作者
Hanage, William P. [1 ]
Finkelstein, Jonathan A. [2 ,3 ]
Huang, Susan S. [4 ]
Pelton, Stephen I. [5 ]
Stevenson, Abbie E. [5 ]
Kleinman, Ken [2 ,3 ]
Hinrichsen, Virginia L. [2 ,3 ]
Fraser, Christophe
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Infect Dis Epidemiol, London, England
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] Harvard Pilgrim Hlth Care, Boston, MA USA
[4] Univ Calif Irvine, Sch Med, Irvine, CA 92717 USA
[5] Boston Univ, Sch Med, Boston, MA 02118 USA
关键词
Streptococcus pneumoniae; Infectious disease epidemiology; Nasopharyngeal carriage; Population genetics;
D O I
10.1016/j.epidem.2010.03.005
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Invasive pneumococcal disease (IPD) has been reduced in the US following conjugate vaccination (PCV7) targeting seven pneumococcal serotypes in 2000. However, increases in IPD due to other serotypes have been observed, in particular 19A. How much this "serotype replacement" will erode the benefits of vaccination and over what timescale is unknown. We used a population genetic approach to test first whether the selective impact of vaccination could be detected in a longitudinal carriage sample, and secondly how long it persisted for following introduction of vaccine in 2000. To detect the selective impact of the vaccine we compared the serotype diversity of samples from pneumococcal carriage in Massachusetts children collected in 2001, 2004, and 2007 with others collected in the pre-vaccine era in Massachusetts, the UK, and Finland. The 2004 sample was significantly (p>0.0001) more diverse than pre-vaccine samples, indicating the selective pressure of vaccination. The 2007 sample showed no significant difference in diversity from the pre-vaccine period and exhibited similar population structure, but with different serotypes. In 2007 the carriage frequency of 19A was similar to that of the most common serotype in pre-vaccine samples. We suggest that serotype replacement involving 19A may be complete in Massachusetts due to similarities in population structure to pre-vaccine samples. These results suggest that the replacement phenomenon occurs rapidly with high vaccine coverage and may allay concerns about future increases in disease due to 19A. For other serotypes, the future course of replacement disease remains to be determined. (C) 2010 Elsevier B. V. All rights reserved.
引用
收藏
页码:80 / 84
页数:5
相关论文
共 23 条
[1]   Clonal relationships between invasive and carriage Streptococcus pneumoniae and serotype- and clone-specific differences in invasive disease potential [J].
Brueggemann, AB ;
Griffiths, DT ;
Meats, E ;
Peto, T ;
Crook, DW ;
Spratt, BG .
JOURNAL OF INFECTIOUS DISEASES, 2003, 187 (09) :1424-1432
[2]   Temporal trends of invasive disease due to Streptococcus pneumoniae among children in the Intermountain West:: Emergence of nonvaccine serogroups [J].
Byington, CL ;
Samore, MH ;
Stoddard, GJ ;
Barlow, S ;
Daly, J ;
Korgenski, K ;
Firth, S ;
Glover, D ;
Jensen, J ;
Mason, EO ;
Shutt, CK ;
Pavia, AT .
CLINICAL INFECTIOUS DISEASES, 2005, 41 (01) :21-29
[3]  
Centers for Disease Control Prevention, 2005, MMWR MORB MORTAL WKL, V54, P893
[4]   A multilocus sequence typing scheme for Streptococcus pneumoniae:: identification of clones associated with serious invasive disease [J].
Enright, MC ;
Spratt, BG .
MICROBIOLOGY-UK, 1998, 144 :3049-3060
[5]   Efficacy of a pneumococcal conjugate vaccine against acute otitis media [J].
Eskola, J ;
Kilpi, T ;
Palmu, A ;
Jokinen, J ;
Haapakoski, J ;
Herva, E ;
Takala, A ;
Käyhty, H ;
Karma, P ;
Kohberger, R ;
Siber, G ;
Mäkela, PH ;
Lockhart, S ;
Ecrola, M .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (06) :403-409
[6]   Neutral microepidemic evolution of bacterial pathogens [J].
Fraser, C ;
Hanage, WP ;
Spratt, BG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (06) :1968-1973
[7]   Effect of the 7-valent pneumococcal conjugate vaccine on nasopharyngeal colonization by Streptococcus pneumoniae in the first 2 years of life [J].
Ghaffar, F ;
Barton, T ;
Lozano, J ;
Muniz, LS ;
Hicks, P ;
Gan, V ;
Ahmad, N ;
McCracken, GH .
CLINICAL INFECTIOUS DISEASES, 2004, 39 (07) :930-938
[8]   Serotype-specific problems associated with pneumococcal conjugate vaccination [J].
Hanage, William P. .
FUTURE MICROBIOLOGY, 2008, 3 (01) :23-30
[9]   Diversity and antibiotic resistance among nonvaccine serotypes of Streptococcus pneumoniae carriage isolates in the post-heptavalent conjugate vaccine era [J].
Hanage, William P. ;
Huang, Susan S. ;
Lipsitch, Marc ;
Bishop, Cynthia J. ;
Godoy, Daniel ;
Pelton, Stephen I. ;
Goldstein, Richard ;
Huot, Heather ;
Finkelstein, Jonathan A. .
JOURNAL OF INFECTIOUS DISEASES, 2007, 195 (03) :347-352
[10]   Ability of pneumococcal serotypes and clones to cause acute otitis media:: Implications for the prevention of otitis media by conjugate vaccines [J].
Hanage, WP ;
Auranen, K ;
Syrjänen, R ;
Herva, E ;
Mäkelä, PH ;
Kilpi, T ;
Spratt, BG .
INFECTION AND IMMUNITY, 2004, 72 (01) :76-81