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dc.contributor.authorErcibengoa, María
dc.contributor.authorArostegi, Nerea
dc.contributor.authorMarimón Ortiz de Zarate, José María
dc.contributor.authorAlonso, Marta
dc.contributor.authorPérez Trallero, Emilio
dc.date.accessioned2012-08-31T07:45:20Z
dc.date.available2012-08-31T07:45:20Z
dc.date.issued2012-03-22
dc.identifier.citationBMC Infectious Diseases 12(69) : (2012)es
dc.identifier.issn1471-2334
dc.identifier.urihttp://hdl.handle.net/10810/8548
dc.description8 p.es
dc.description.abstractBackground: Pneumococcal nasopharyngeal carriage precedes invasive infection and is the source for dissemination of the disease. Differences in sampling methodology, isolation or identification techniques, as well as the period (pre -or post-vaccination) when the study was performed, can influence the reported rates of colonization and the distribution of serotypes carried.-- Objectives: To evaluate the prevalence and dynamics of pneumococcal nasopharyngeal colonization in healthy children aged 6-34 months attending a day care center with a high level of hygiene and no overcrowding. The study was performed 3-4 years after the 7-valent pneumococcal vaccine was introduced, using multiple methodologies to detect and characterize the isolates. -- Methods: Over 12 months, 25 children were sampled three times, 53 children twice and 27 children once. Three Streptococcus pneumoniae typing techniques were used: Quellung, Pneumotest-Latex-kit and multiplex-polymerase chain reaction (PCR). The similarity of isolates of the same serotype was established by pulsed field gel electrophoresis (PFGE) and occasionally the multilocus sequence type (ST) was also determined.-- Results: Overall pneumococcal carriage and multiple colonization rates were 89.5% (94/105) and 39%, respectively. Among 218 pneumococci detected, 21 different serotypes and 13 non-typeable isolates were found. The most prevalent serotypes were 19A, 16F and 15B. Serotypes 15B, 19A and 21 were mainly found as single carriage; in contrast serotypes 6B, 11A and 20, as well as infrequent serotypes, were isolated mainly as part of multiple carriage. Most 19A isolates were ST193 but most serotypes showed high genetic heterogeneity. Changes in the pneumococci colonizing each child were frequent and the same serotype detected on two occasions frequently showed a different genotype. By multiplex-PCR, 100% of pneumococci could be detected and 94% could be serotyped versus 80.3% by the Quellung reaction and Pneumotest-Latex in combination (p < 0.001). -- Conclusions: Rates of S. pneumoniae carriage and multiple colonization were very high. Prevalent serotypes differed from those found in similar studies in the pre-vaccination period. In the same child, clearance of a pneumococcal strain and acquisition of a new one was frequent in a short period of time. The most effective technique for detecting pneumococcal nasopharyngeal carriers was multiplex-PCR.es
dc.description.sponsorshipThis work was supported in part by GIU05/54 and GIU09-59 from the University of the Basque Country, UPV/EHU, Spain. The funder had no role in study design, data collection or analysis, decision to publish, or preparation of the manuscript.es
dc.language.isoenges
dc.publisherBioMed Centrales
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.subjectstreptococcus pneumoniaees
dc.subjectcocolonizationes
dc.subjectmultiple colonizationes
dc.subjectmultiplex PCRes
dc.subjectquellung reactiones
dc.titleDynamics of pneumococcal nasopharyngeal carriage in healthy children attending a day care center in northern Spain. Influence of detection techniques on the resultses
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© 2012 Ercibengoa et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.es
dc.relation.publisherversionhttp://www.biomedcentral.com/1471-2334/12/69es
dc.identifier.doi10.1186/1471-2334-12-69
dc.departamentoesMedicina preventiva y salud públicaes_ES
dc.departamentoeuPrebentzio medikuntza eta osasun publikoaes_ES
dc.subject.categoriaINFECTIOUS DISEASES


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