Cargando…
Molecular surveillance of pneumococcal carriage following completion of immunization with the 13-valent pneumococcal conjugate vaccine administered in a 3 + 1 schedule
In a cross-sectional study, with the use of molecular methods, we aimed to gain insight into oropharyngeal pneumococcal colonization over time in 1212 Greek children recruited in general pediatric settings throughout the country; they were fully vaccinated with PCV13 (3 + 1 schedule). A single sampl...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718523/ https://www.ncbi.nlm.nih.gov/pubmed/34969968 http://dx.doi.org/10.1038/s41598-021-03720-y |
_version_ | 1784624746654072832 |
---|---|
author | Syrogiannopoulos, George A. Grivea, Ioanna N. Moriondo, Maria Nieddu, Francesco Michoula, Aspasia N. Calabrese, Maria Rita Anthracopoulos, Michael Azzari, Chiara |
author_facet | Syrogiannopoulos, George A. Grivea, Ioanna N. Moriondo, Maria Nieddu, Francesco Michoula, Aspasia N. Calabrese, Maria Rita Anthracopoulos, Michael Azzari, Chiara |
author_sort | Syrogiannopoulos, George A. |
collection | PubMed |
description | In a cross-sectional study, with the use of molecular methods, we aimed to gain insight into oropharyngeal pneumococcal colonization over time in 1212 Greek children recruited in general pediatric settings throughout the country; they were fully vaccinated with PCV13 (3 + 1 schedule). A single sample was obtained from each child at a time interval of 26 days to 70 months after administration of the 4th (booster) PCV13 dose; sampling time was divided into six time intervals. Carriage of Streptococcus pneumoniae was detected by real-time PCR targeting the lytA gene and isolates were serotyped by singleplex real-time PCR assays. Multiple control procedures to avoid false-positive results were applied. We showed an overall S. pneumoniae carriage rate of 48.6%. Serotyping identified typeable isolates in 82% of the total lytA-positive samples. Non-PCV13 serotypes represented 83.8% of total isolates when excluding serogroups with mixed PCV13 and non-PCV13 serotypes. In multivariate analysis daycare/school attendance emerged as the main contributing factor. Notably, serotypes 19A and 3 were the only two PCV13 serotypes the colonization rate of which increased over time (χ(2) for trend P < 0.001 and P = 0.012, respectively). The application of the SP2020 gene on lytA-positive serotyped samples showed pneumococcal colonization in 97% of cases, and the overall colonization profile over time closely resembled that of the lytA gene. With the provisions of the methodological approach and age group of our study, the use of the oropharynx emerges as a reliable alternative to the nasopharynx in estimating pneumococcal carriage in epidemiological studies. |
format | Online Article Text |
id | pubmed-8718523 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-87185232022-01-05 Molecular surveillance of pneumococcal carriage following completion of immunization with the 13-valent pneumococcal conjugate vaccine administered in a 3 + 1 schedule Syrogiannopoulos, George A. Grivea, Ioanna N. Moriondo, Maria Nieddu, Francesco Michoula, Aspasia N. Calabrese, Maria Rita Anthracopoulos, Michael Azzari, Chiara Sci Rep Article In a cross-sectional study, with the use of molecular methods, we aimed to gain insight into oropharyngeal pneumococcal colonization over time in 1212 Greek children recruited in general pediatric settings throughout the country; they were fully vaccinated with PCV13 (3 + 1 schedule). A single sample was obtained from each child at a time interval of 26 days to 70 months after administration of the 4th (booster) PCV13 dose; sampling time was divided into six time intervals. Carriage of Streptococcus pneumoniae was detected by real-time PCR targeting the lytA gene and isolates were serotyped by singleplex real-time PCR assays. Multiple control procedures to avoid false-positive results were applied. We showed an overall S. pneumoniae carriage rate of 48.6%. Serotyping identified typeable isolates in 82% of the total lytA-positive samples. Non-PCV13 serotypes represented 83.8% of total isolates when excluding serogroups with mixed PCV13 and non-PCV13 serotypes. In multivariate analysis daycare/school attendance emerged as the main contributing factor. Notably, serotypes 19A and 3 were the only two PCV13 serotypes the colonization rate of which increased over time (χ(2) for trend P < 0.001 and P = 0.012, respectively). The application of the SP2020 gene on lytA-positive serotyped samples showed pneumococcal colonization in 97% of cases, and the overall colonization profile over time closely resembled that of the lytA gene. With the provisions of the methodological approach and age group of our study, the use of the oropharynx emerges as a reliable alternative to the nasopharynx in estimating pneumococcal carriage in epidemiological studies. Nature Publishing Group UK 2021-12-30 /pmc/articles/PMC8718523/ /pubmed/34969968 http://dx.doi.org/10.1038/s41598-021-03720-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Syrogiannopoulos, George A. Grivea, Ioanna N. Moriondo, Maria Nieddu, Francesco Michoula, Aspasia N. Calabrese, Maria Rita Anthracopoulos, Michael Azzari, Chiara Molecular surveillance of pneumococcal carriage following completion of immunization with the 13-valent pneumococcal conjugate vaccine administered in a 3 + 1 schedule |
title | Molecular surveillance of pneumococcal carriage following completion of immunization with the 13-valent pneumococcal conjugate vaccine administered in a 3 + 1 schedule |
title_full | Molecular surveillance of pneumococcal carriage following completion of immunization with the 13-valent pneumococcal conjugate vaccine administered in a 3 + 1 schedule |
title_fullStr | Molecular surveillance of pneumococcal carriage following completion of immunization with the 13-valent pneumococcal conjugate vaccine administered in a 3 + 1 schedule |
title_full_unstemmed | Molecular surveillance of pneumococcal carriage following completion of immunization with the 13-valent pneumococcal conjugate vaccine administered in a 3 + 1 schedule |
title_short | Molecular surveillance of pneumococcal carriage following completion of immunization with the 13-valent pneumococcal conjugate vaccine administered in a 3 + 1 schedule |
title_sort | molecular surveillance of pneumococcal carriage following completion of immunization with the 13-valent pneumococcal conjugate vaccine administered in a 3 + 1 schedule |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718523/ https://www.ncbi.nlm.nih.gov/pubmed/34969968 http://dx.doi.org/10.1038/s41598-021-03720-y |
work_keys_str_mv | AT syrogiannopoulosgeorgea molecularsurveillanceofpneumococcalcarriagefollowingcompletionofimmunizationwiththe13valentpneumococcalconjugatevaccineadministeredina31schedule AT griveaioannan molecularsurveillanceofpneumococcalcarriagefollowingcompletionofimmunizationwiththe13valentpneumococcalconjugatevaccineadministeredina31schedule AT moriondomaria molecularsurveillanceofpneumococcalcarriagefollowingcompletionofimmunizationwiththe13valentpneumococcalconjugatevaccineadministeredina31schedule AT nieddufrancesco molecularsurveillanceofpneumococcalcarriagefollowingcompletionofimmunizationwiththe13valentpneumococcalconjugatevaccineadministeredina31schedule AT michoulaaspasian molecularsurveillanceofpneumococcalcarriagefollowingcompletionofimmunizationwiththe13valentpneumococcalconjugatevaccineadministeredina31schedule AT calabresemariarita molecularsurveillanceofpneumococcalcarriagefollowingcompletionofimmunizationwiththe13valentpneumococcalconjugatevaccineadministeredina31schedule AT anthracopoulosmichael molecularsurveillanceofpneumococcalcarriagefollowingcompletionofimmunizationwiththe13valentpneumococcalconjugatevaccineadministeredina31schedule AT azzarichiara molecularsurveillanceofpneumococcalcarriagefollowingcompletionofimmunizationwiththe13valentpneumococcalconjugatevaccineadministeredina31schedule |