Cargando…
Rapid replacement by non-vaccine pneumococcal serotypes may mitigate the impact of the pneumococcal conjugate vaccine on nasopharyngeal bacterial ecology
There is growing concern that interventions that alter microbial ecology can adversely affect health. We characterised the impact of the seven-valent pneumococcal conjugate vaccine (PCV7) on pneumococcal carriage and the bacterial component of the nasopharyngeal microbiome during infancy. Newborns w...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557800/ https://www.ncbi.nlm.nih.gov/pubmed/28811633 http://dx.doi.org/10.1038/s41598-017-08717-0 |
_version_ | 1783257270157574144 |
---|---|
author | Kwambana-Adams, Brenda Hanson, Blake Worwui, Archibald Agbla, Schadrac Foster-Nyarko, Ebenezer Ceesay, Fatima Ebruke, Chinelo Egere, Uzochukwu Zhou, Yanjiao Ndukum, Maze Sodergren, Erica Barer, Michael Adegbola, Richard Weinstock, George Antonio, Martin |
author_facet | Kwambana-Adams, Brenda Hanson, Blake Worwui, Archibald Agbla, Schadrac Foster-Nyarko, Ebenezer Ceesay, Fatima Ebruke, Chinelo Egere, Uzochukwu Zhou, Yanjiao Ndukum, Maze Sodergren, Erica Barer, Michael Adegbola, Richard Weinstock, George Antonio, Martin |
author_sort | Kwambana-Adams, Brenda |
collection | PubMed |
description | There is growing concern that interventions that alter microbial ecology can adversely affect health. We characterised the impact of the seven-valent pneumococcal conjugate vaccine (PCV7) on pneumococcal carriage and the bacterial component of the nasopharyngeal microbiome during infancy. Newborns were recruited into three groups as follows: Group1 (n = 33) was the control group and comprised infants who received PCV7 after 6 months and came from unvaccinated communities. Group 2 (n = 30) came from unvaccinated communities and Group 3 (n = 39) came from vaccinated communities. Both group 2 and 3 received PCV7 at 2, 3 and 4 months. Culture and 16 S rRNA gene sequencing were performed on nasopharyngeal specimens collected at regular intervals from infants. Nasopharyngeal carriage of PCV7 serotypes in Group 1 was significantly higher than in Group 2 and 3 (p < 0.01). However, pneumococcal carriage remained comparable due to an expansion of non-vaccine serotypes in Groups 2 and 3. Determination of phylogenetic dis(similarities) showed that the bacterial community structures were comparable across groups. A mixed effects model showed no difference in community richness (p = 0.15) and Shannon α-diversity (p = 0.48) across the groups. Immediate replacement of pneumococcal vaccine serotypes with non-vaccine serotypes may mitigate the impact of PCV7 on nasopharyngeal bacterial community structure and ecology. |
format | Online Article Text |
id | pubmed-5557800 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55578002017-08-16 Rapid replacement by non-vaccine pneumococcal serotypes may mitigate the impact of the pneumococcal conjugate vaccine on nasopharyngeal bacterial ecology Kwambana-Adams, Brenda Hanson, Blake Worwui, Archibald Agbla, Schadrac Foster-Nyarko, Ebenezer Ceesay, Fatima Ebruke, Chinelo Egere, Uzochukwu Zhou, Yanjiao Ndukum, Maze Sodergren, Erica Barer, Michael Adegbola, Richard Weinstock, George Antonio, Martin Sci Rep Article There is growing concern that interventions that alter microbial ecology can adversely affect health. We characterised the impact of the seven-valent pneumococcal conjugate vaccine (PCV7) on pneumococcal carriage and the bacterial component of the nasopharyngeal microbiome during infancy. Newborns were recruited into three groups as follows: Group1 (n = 33) was the control group and comprised infants who received PCV7 after 6 months and came from unvaccinated communities. Group 2 (n = 30) came from unvaccinated communities and Group 3 (n = 39) came from vaccinated communities. Both group 2 and 3 received PCV7 at 2, 3 and 4 months. Culture and 16 S rRNA gene sequencing were performed on nasopharyngeal specimens collected at regular intervals from infants. Nasopharyngeal carriage of PCV7 serotypes in Group 1 was significantly higher than in Group 2 and 3 (p < 0.01). However, pneumococcal carriage remained comparable due to an expansion of non-vaccine serotypes in Groups 2 and 3. Determination of phylogenetic dis(similarities) showed that the bacterial community structures were comparable across groups. A mixed effects model showed no difference in community richness (p = 0.15) and Shannon α-diversity (p = 0.48) across the groups. Immediate replacement of pneumococcal vaccine serotypes with non-vaccine serotypes may mitigate the impact of PCV7 on nasopharyngeal bacterial community structure and ecology. Nature Publishing Group UK 2017-08-15 /pmc/articles/PMC5557800/ /pubmed/28811633 http://dx.doi.org/10.1038/s41598-017-08717-0 Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kwambana-Adams, Brenda Hanson, Blake Worwui, Archibald Agbla, Schadrac Foster-Nyarko, Ebenezer Ceesay, Fatima Ebruke, Chinelo Egere, Uzochukwu Zhou, Yanjiao Ndukum, Maze Sodergren, Erica Barer, Michael Adegbola, Richard Weinstock, George Antonio, Martin Rapid replacement by non-vaccine pneumococcal serotypes may mitigate the impact of the pneumococcal conjugate vaccine on nasopharyngeal bacterial ecology |
title | Rapid replacement by non-vaccine pneumococcal serotypes may mitigate the impact of the pneumococcal conjugate vaccine on nasopharyngeal bacterial ecology |
title_full | Rapid replacement by non-vaccine pneumococcal serotypes may mitigate the impact of the pneumococcal conjugate vaccine on nasopharyngeal bacterial ecology |
title_fullStr | Rapid replacement by non-vaccine pneumococcal serotypes may mitigate the impact of the pneumococcal conjugate vaccine on nasopharyngeal bacterial ecology |
title_full_unstemmed | Rapid replacement by non-vaccine pneumococcal serotypes may mitigate the impact of the pneumococcal conjugate vaccine on nasopharyngeal bacterial ecology |
title_short | Rapid replacement by non-vaccine pneumococcal serotypes may mitigate the impact of the pneumococcal conjugate vaccine on nasopharyngeal bacterial ecology |
title_sort | rapid replacement by non-vaccine pneumococcal serotypes may mitigate the impact of the pneumococcal conjugate vaccine on nasopharyngeal bacterial ecology |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557800/ https://www.ncbi.nlm.nih.gov/pubmed/28811633 http://dx.doi.org/10.1038/s41598-017-08717-0 |
work_keys_str_mv | AT kwambanaadamsbrenda rapidreplacementbynonvaccinepneumococcalserotypesmaymitigatetheimpactofthepneumococcalconjugatevaccineonnasopharyngealbacterialecology AT hansonblake rapidreplacementbynonvaccinepneumococcalserotypesmaymitigatetheimpactofthepneumococcalconjugatevaccineonnasopharyngealbacterialecology AT worwuiarchibald rapidreplacementbynonvaccinepneumococcalserotypesmaymitigatetheimpactofthepneumococcalconjugatevaccineonnasopharyngealbacterialecology AT agblaschadrac rapidreplacementbynonvaccinepneumococcalserotypesmaymitigatetheimpactofthepneumococcalconjugatevaccineonnasopharyngealbacterialecology AT fosternyarkoebenezer rapidreplacementbynonvaccinepneumococcalserotypesmaymitigatetheimpactofthepneumococcalconjugatevaccineonnasopharyngealbacterialecology AT ceesayfatima rapidreplacementbynonvaccinepneumococcalserotypesmaymitigatetheimpactofthepneumococcalconjugatevaccineonnasopharyngealbacterialecology AT ebrukechinelo rapidreplacementbynonvaccinepneumococcalserotypesmaymitigatetheimpactofthepneumococcalconjugatevaccineonnasopharyngealbacterialecology AT egereuzochukwu rapidreplacementbynonvaccinepneumococcalserotypesmaymitigatetheimpactofthepneumococcalconjugatevaccineonnasopharyngealbacterialecology AT zhouyanjiao rapidreplacementbynonvaccinepneumococcalserotypesmaymitigatetheimpactofthepneumococcalconjugatevaccineonnasopharyngealbacterialecology AT ndukummaze rapidreplacementbynonvaccinepneumococcalserotypesmaymitigatetheimpactofthepneumococcalconjugatevaccineonnasopharyngealbacterialecology AT sodergrenerica rapidreplacementbynonvaccinepneumococcalserotypesmaymitigatetheimpactofthepneumococcalconjugatevaccineonnasopharyngealbacterialecology AT barermichael rapidreplacementbynonvaccinepneumococcalserotypesmaymitigatetheimpactofthepneumococcalconjugatevaccineonnasopharyngealbacterialecology AT adegbolarichard rapidreplacementbynonvaccinepneumococcalserotypesmaymitigatetheimpactofthepneumococcalconjugatevaccineonnasopharyngealbacterialecology AT weinstockgeorge rapidreplacementbynonvaccinepneumococcalserotypesmaymitigatetheimpactofthepneumococcalconjugatevaccineonnasopharyngealbacterialecology AT antoniomartin rapidreplacementbynonvaccinepneumococcalserotypesmaymitigatetheimpactofthepneumococcalconjugatevaccineonnasopharyngealbacterialecology |