Prevalence and clonal distribution of pcpA, psrP and Pilus-1 among pediatric isolates of Streptococcus pneumoniae.

Prevalence and clonal distribution of pcpA, psrP and Pilus-1 among pediatric isolates of Streptococcus pneumoniae.
复制标题

DOI:
10.1371/journal.pone.0041587
复制
发表时间:
2012
期刊:
影响因子:
3.7
通讯作者:
Muñoz-Almagro C
Muñoz-Almagro C
中科院分区:
综合性期刊3区
文献类型:
--
作者:
Selva L;Ciruela P;Blanchette K;del Amo E;Pallares R;Orihuela CJ;Muñoz-Almagro C

文献摘要

参考文献

被引文献

相似文献

Streptococcus pneumoniae is the leading cause of vaccine-preventable deaths globally. The objective of this study was to determine the distribution and clonal type variability of three potential vaccine antigens: Pneumococcal serine-rich repeat protein (PsrP), Pilus-1, and Pneumococcal choline binding protein A (PcpA) among pneumococcal isolates from children with invasive pneumococcal disease and healthy nasopharyngeal carriers. We studied by Real-Time PCR a total of 458 invasive pneumococcal isolates and 89 nasopharyngeal pneumococcal isolates among children (total = 547 strains) collected in Barcelona, Spain, from January 2004 to July 2010. pcpA, psrP and pilus-1 were detected in 92.8%, 51.7% and 14.4% of invasive isolates and in 92.1%, 48.3% and 18% of carrier isolates, respectively. Within individual serotypes the prevalence of psrP and pilus-1 was highly dependent on the clonal type. pcpA was highly prevalent in all strains with the exception of those belonging to serotype 3 (33.3% in serotype 3 isolates vs. 95.1% in other serotypes; P<.001). psrP was significantly more frequent in those serotypes that are less apt to be detected in carriage than in disease; 58.7% vs. 39.1% P<.001. Antibiotic resistance was associated with the presence of pilus-1 and showed a negative correlation with psrP. These results indicate that PcpA, and subsequently Psrp and Pilus-1 together might be good candidates to be used in a next-generation of multivalent pneumococcal protein vaccine.
DOI: 10.1371/journal.pone.0019650
发表时间: 2011-05-05
期刊: PloS one
影响因子: 3.7
作者:
Harvey RM;Stroeher UH;Ogunniyi AD;Smith-Vaughan HC;Leach AJ;Paton JC
通讯作者: Paton JC
DOI: 10.1128/iai.01126-07
发表时间: 2008-06-01
影响因子: 3.1
作者:
Glover, David T.;Hollingshead, Susan K.;Briles, David E.
通讯作者: Briles, David E.
DOI: 10.1128/jb.00673-06
发表时间: 2006-11-01
影响因子: 3.2
作者:
Moscoso, Miriam;Garcia, Ernesto;Lopez, Rubens
通讯作者: Lopez, Rubens
DOI: 10.1371/journal.ppat.1000026
发表时间: 2008-03-21
期刊: PLoS pathogens
影响因子: 6.7
作者:
Hilleringmann M;Giusti F;Baudner BC;Masignani V;Covacci A;Rappuoli R;Barocchi MA;Ferlenghi I
通讯作者: Ferlenghi I
DOI: 10.1073/pnas.0511017103
发表时间: 2006-02-21
影响因子: 11.1
作者:
Barocchi, MA;Rie, J;Henriques-Normark, B
通讯作者: Henriques-Normark, B