Effects of the 7-valent pneumococcal conjugate vaccine on US levofloxacin-resistant streptococcus pneumoniae

被引:11
作者
Davies, Todd A. [1 ]
Yee, Y. Cheung [2 ]
Bush, Karen [1 ]
Sahm, Dan [3 ]
Evangelista, Alan [2 ]
Goldschmidt, Raul [1 ]
机构
[1] Johnson & Johnson Pharmaceut Res & Dev LLC, Raritan, NJ 08869 USA
[2] OrthoMcNeil Inc, Raritan, NJ USA
[3] Eurofins Inc, Herndon, VA USA
关键词
D O I
10.1089/mdr.2008.0805
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Seven-valent pneumococcal conjugate vaccine (PCV7) provides protection against invasive pneumococcal disease that extends to unvaccinated populations, such as elderly or immunocompromised adults. PCV7 also reduces incidence of pneumococcal penicillin resistance. In this study, the potential impact of PCV7 on pneumococcal fluoroquinolone resistance was examined. Methods: U.S. levofloxacin-resistant isolates (264) from TRUST surveillance studies (1999-2004) were serotyped and quinolone resistance-determining region of parC/E and gyrA/B sequenced. Changes in prevalence of vaccine/nonvaccine serotypes during 2000-2004 and 1999-2004 were analyzed by regression analyses and chi-square trend test. Results: The introduction of PCV7 (2000-2004) did not affect fluoroquinolone resistance prevalence, but mutants with vaccine serotypes declined linearly at -6.6 +/- 0.8% per year (p = 0.003), with concomitant replacement by nonvaccine serotypes; vaccine-related serotypes (6A, 9N, 19A, and 23N) increased (p = 0.04). Differential selection between vaccine and nonvaccine serotypes occurred for mutants containing amino acid substitutions at either ParC Ser79 (p = 0.01) or both ParC Ser79 and GyrA Ser81 (p = 0.04). Among mutants with ParC Ser79 substitutions, vaccine serotypes declined linearly (p = 0.02), whereas nonvaccine serotypes increased (p = 0.04). Additionally, a vaccine-independent effect became apparent during 1999-2004, as the incidence of ParC Ser79 and Asp83 mutations declined in fluoroquinolone-resistant strains, suggesting that these substitutions conferred decreased fitness. Conclusions: PCV7 has led to extensive replacement of vaccine serotypes by nonvaccine serotypes among levofloxacin-resistant pneumococci.
引用
收藏
页码:187 / 196
页数:10
相关论文
共 32 条
[1]  
[Anonymous], 2000, MMWR Recomm Rep, V49, P1
[2]  
[Anonymous], 1997, MMWR Recomm Rep, V46, P1
[3]  
Bartlett John G., 2000, Clinical Infectious Diseases, V31, P347, DOI 10.1086/313954
[4]   Streptococcus pneumoniae colonisation:: the key to pneumococcal disease [J].
Bogaert, D ;
de Groot, R ;
Hermans, PWM .
LANCET INFECTIOUS DISEASES, 2004, 4 (03) :144-154
[5]   Colonisation by Streptococcus pneumoniae and Staphylococcus aureus in healthy children [J].
Bogaert, D ;
van Belkum, A ;
Sluijter, M ;
Luijendijk, A ;
de Groot, R ;
Rümke, HC ;
Verbrugh, HA ;
Hermans, PWM .
LANCET, 2004, 363 (9424) :1871-1872
[6]  
Centers for Disease Control and Prevention, 2005, MMWR-MORBID MORTAL W, V54, P893, DOI DOI 10.2217/PME.13.57
[7]  
CLSI, 2007, M100S17 CLSI
[8]   Cross-resistance, relatedness and allele analysis of fluoroquinolone-resistant US clinical isolates of Streptococcus pneumoniae (1998-2000) [J].
Davies, TA ;
Goldschmidt, R ;
Pfleger, S ;
Loeloff, M ;
Bush, K ;
Sahm, DF ;
Evangelista, A .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2003, 52 (02) :168-175
[9]   Prevalence of single mutations in topoisomerase type II genes among levofloxacin-susceptible clinical strains of Streptococcus pneumoniae isolated in the United States in 1992 to 1996 and 1999 to 2000 [J].
Davies, TA ;
Evangelista, A ;
Pfleger, S ;
Bush, K ;
Sahm, DF ;
Goldschmidt, R .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (01) :119-124
[10]  
DRAGHI DC, 2005, 45 INT C ANT AG CHEM, P95