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美国儿童中19A血清型肺炎链球菌的疫苗接种后基因结构

Postvaccine genetic structure of Streptococcus pneumoniae serotype 19A from children in the United States.

作者信息

Pai Rekha, Moore Matthew R, Pilishvili Tamara, Gertz Robert E, Whitney Cynthia G, Beall Bernard

机构信息

Division of Bacterial and Mycotic Diseases, Respiratory Diseases Branch, Centers for Disease Control and Prevention, Atlanta, GA 30333, USA.

出版信息

J Infect Dis. 2005 Dec 1;192(11):1988-95. doi: 10.1086/498043. Epub 2005 Nov 1.

Abstract

BACKGROUND

The introduction of the 7-valent conjugate pneumococcal vaccine (PCV7) in children may result in serotype replacement. We estimated the rate of increase of invasive pneumococcal disease (IPD) caused by serotype 19A in children <5 years old and determined the genetic composition of these isolates.

METHODS

Cases of IPD between July 1999 and June 2004 were identified through the Active Bacterial Core Surveillance. Serotype 19A isolates obtained from children <5 years old between January 2003 and June 2004 were characterized by serotyping, antibiotic susceptibility testing, and pulsed-field gel electrophoresis (PFGE). Select isolates representing homologous PFGE clusters were subjected to multilocus sequence typing, and eBURST was used to delineate clonal groups.

RESULTS

Between July 1999 and June 2004, the overall rate of IPD decreased from 23.3 to 13.1 cases/100,000 population (P<.00001). In children <5 years old, the rate decreased from 88.7 to 22.4 cases/100,000 population (P<.00001), whereas the rate in persons > or =5 years old decreased from 18.4 to 12.4 cases/100,000 population (P<.0001). The rate of serotype 19A IPD in children <5 years old increased significantly from 2.6 cases/100,000 population in 1999-2000 to 6.5 cases/100,000 population in 2003-2004; this was accompanied by significant increases in penicillin nonsusceptibility (P=.008) and multidrug resistance (P=.002) among serotype 19A isolates. As was observed during the pre-PCV7 era, clonal complex (CC) 199 predominated within serotype 19A, representing approximately 70% of invasive serotype 19A isolates from children <5 years old during 2003-2004. New serotype 19A genotypes were observed during 2003-2004, including 6 CCs that were not found among pneumococcal serotype 19A isolates during surveillance in 1999.

CONCLUSION

Serotype 19A is, at present, the most important cause of IPD by replacement serotypes, and it is increasingly drug resistant. CC199 is the predominant CC among type 19A serotypes in children <5 years old. Our data suggest that some of the increase in rates of infection with serotype 19A may be due to serotype switching within certain vaccine type strains.

摘要

背景

在儿童中引入7价肺炎球菌结合疫苗(PCV7)可能导致血清型替换。我们估计了5岁以下儿童中由19A血清型引起的侵袭性肺炎球菌疾病(IPD)的增加率,并确定了这些分离株的基因组成。

方法

通过主动细菌核心监测确定1999年7月至2004年6月期间的IPD病例。对2003年1月至2004年6月期间从5岁以下儿童中获得的19A血清型分离株进行血清分型、药敏试验和脉冲场凝胶电泳(PFGE)鉴定。选择代表同源PFGE簇的分离株进行多位点序列分型,并使用eBURST来划分克隆群。

结果

1999年7月至2004年6月期间,IPD的总体发病率从23.3例/10万人口降至13.1例/10万人口(P<0.00001)。在5岁以下儿童中,发病率从88.7例/10万人口降至22.4例/10万人口(P<0.00001),而5岁及以上人群的发病率从18.4例/10万人口降至12.4例/10万人口(P<0.0001)。5岁以下儿童中19A血清型IPD的发病率从1999 - 2000年的2.6例/10万人口显著增加到2003 - 2004年的6.5例/10万人口;这伴随着19A血清型分离株中青霉素不敏感性(P = 0.008)和多重耐药性(P = 0.002)的显著增加。如在PCV7时代之前所观察到的,克隆复合体(CC)199在19A血清型中占主导地位,在2003 - 2004年期间约占5岁以下儿童侵袭性19A血清型分离株的70%。在2003 - 2004年期间观察到了新的19A血清型基因型,包括1999年监测期间肺炎球菌19A血清型分离株中未发现的6个CC。

结论

目前,19A血清型是血清型替换导致IPD的最重要原因,并且其耐药性日益增加。CC199是5岁以下儿童19A血清型中的主要CC。我们的数据表明,19A血清型感染率的一些增加可能是由于某些疫苗型菌株内的血清型转换。

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