Davies Todd A, Yee Y Cheung, Bush Karen, Sahm Dan, Evangelista Alan, Goldschmidt Raul
Johnson & Johnson Pharmaceutical Research & Development, LLC, Raritan, New Jersey 08869, USA.
Microb Drug Resist. 2008 Sep;14(3):187-96. doi: 10.1089/mdr.2008.0805.
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.
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.
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.
PCV7 has led to extensive replacement of vaccine serotypes by nonvaccine serotypes among levofloxacin-resistant pneumococci.
七价肺炎球菌结合疫苗(PCV7)可预防侵袭性肺炎球菌疾病,这种保护作用可扩展至未接种疫苗的人群,如老年人或免疫功能低下的成年人。PCV7还可降低肺炎球菌对青霉素的耐药性。在本研究中,我们检测了PCV7对肺炎球菌氟喹诺酮耐药性的潜在影响。
对来自TRUST监测研究(1999 - 2004年)的美国左氧氟沙星耐药菌株(264株)进行血清分型,并对parC/E和gyrA/B的喹诺酮耐药决定区进行测序。通过回归分析和卡方趋势检验分析2000 - 2004年和1999 - 2004年期间疫苗/非疫苗血清型流行率的变化。
PCV7的引入(2000 - 2004年)并未影响氟喹诺酮耐药率,但疫苗血清型突变体以每年-6.6±0.8%的线性速率下降(p = 0.003),同时被非疫苗血清型所取代;与疫苗相关的血清型(6A、9N、19A和23N)有所增加(p = 0.04)。对于在ParC Ser79位点含有氨基酸替代或同时在ParC Ser79和GyrA Ser81位点含有氨基酸替代的突变体,疫苗和非疫苗血清型之间存在差异选择(分别为p = 0.01和p = 0.04)。在含有ParC Ser79替代的突变体中,疫苗血清型呈线性下降(p = 0.02),而非疫苗血清型则增加(p = 0.04)。此外,在1999 - 2004年期间,一种与疫苗无关的效应变得明显,因为氟喹诺酮耐药菌株中ParC Ser79和Asp83突变的发生率下降,这表明这些替代导致适应性降低。
在左氧氟沙星耐药的肺炎球菌中,PCV7已导致疫苗血清型被非疫苗血清型广泛取代。