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Nasopharynx Microbiome and Vaccination in Children
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2013-06-18 15:49:51 UTC
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Nasopharynx Microbiome and Vaccination in Children
Overview

The nasopharynx (NP) is home to many microorganisms that begin colonizing the body soon after birth. The collection of microbes, the microbiome, provides protection against pathogens, confers metabolic capabilities that humans lack, as well as other functions, and interacts extensively with the human host without provoking host defense responses. Microbes from the NP can cause diseases, such as pneumonia or meningitis, depending on which nearby tissues they invade. Normally these organisms do not cause disease, possibly because the complex ecosystem of the microbiome has evolved over millions of years to keep organisms mutually in check. Little is known about the detailed structure of the NP microbiome, especially in newborns and during early life as the microbiome is formed. Understanding how the microbiome is formed, what contributions come from parents, siblings, or caregivers, and how different geographical environments influence the NP microbiome is an important task of metagenomic research. Knowledge of these phenomena would allow abnormal situations to be recognized, offering the opportunity to prevent disease and ensure healthy development of the infant.
Vaccination is likely to have important consequences for the NP microbiome. Current pneumococcal vaccines are directed against multiple serotypes thus potentially eliminating these from the microbiome. Based on observations on this and other vaccines, new organisms are expected to move into the empty niches created by vaccine elimination of organisms. Thus the structure of the microbiome is altered by vaccines. The unintended consequences of this alteration remain to be seen. The aim of this exploratory study is to define the NP microbiome in newborns by sampling their NP monthly in the first year of life and analyzing these specimens with metagenomic DNA sequencing techniques. This analysis will reveal the organisms that comprise the microbiome, their abundances, and how their relative abundance changes over time. We will also collect a rich set of clinical data about the children and correlate the (changing) structure of the microbiome with the infants' health. These studies will be performed at four sites: Bangladesh, where the national vaccination program does not include pneumococcal conjugate vaccine (PCV); the Philippines where there is also no PCV in the national program but where half the children enrolled in the study will be given PCV; and two sites in Africa (The Gambia and South Africa) which both have already included PCV in their national programs and all children will be PCV-vaccinated. This range in geography and vaccine status will allow observations on the effects on the NP microbiome and the impact of this on infant health.
The results obtained from this study will lead to a better understanding of the consequences (side effects) of vaccination against pneumococci. Moreover, the metagenomic approach taken in this study naturally lends itself as a diagnostic. Future research could lead to the development of a tool to identify children at risk for disease because of an altered NP microbiome. Finally, the definition of the healthy NP microbiome and the at-risk microbiome that this study will yield also suggest that treatment of at-risk children with probiotics could reduce the possibility of disease.

Funding

Bill and Melinda Gates Foundation


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http://www.jcvi.org/cms/research/projects/nasopharynx-microbiome-and-vaccination-in-children/overview/#sthash.1uxMlzrJ.dpuf
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2013-06-18 15:54:14 UTC
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PLoS One. 2011; 6(6): e20229.
Published online 2011 June 10. doi: 10.1371/journal.pone.0020229
PMCID: PMC3112202
Effect of Seven-Valent Pneumococcal Conjugate Vaccine on Staphylococcus aureus Colonisation in a Randomised Controlled Trial
Elske J. M. van Gils,1,2,* Eelko Hak,3,4 Reinier H. Veenhoven,2 Gerwin D. Rodenburg,1,2 Debby Bogaert,1 Jacob P. Bruin,5 Loek van Alphen,6 and Elisabeth A. M. Sanders1
Eliane Namie Miyaji, Editor
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Abstract
Background
Heptavalent pneumococcal conjugate vaccine (PCV7) shifts nasopharyngeal colonisation with vaccine serotype pneumococci towards nonvaccine serotypes. Because of the reported negative association of vaccine serotype pneumococci and Staphylococcus aureus in the nasopharynx, we explored the effect of PCV7 on nasopharyngeal colonisation with S. aureus in children and parents.
Methodology/Principal Findings
This study was part of a randomised controlled trial on the effect of PCV7 on pneumococcal carriage, enrolling healthy newborns who were randomly assigned (111) to receive PCV7 (1) at 2 and 4 months of age (2) at 2, 4 and 11 months or (3) no PCV7 (controls). Nasopharyngeal colonisation of S. aureus was a planned secondary outcome. Nasopharyngeal swabs were obtained from all children over a 2-year period with 6-months interval and from one parent at the child's age of 12 and 24 months and cultured for Streptococcus pneumoniae and S. aureus. Between July 2005 and February 2006, 1005 children were enrolled and received either 2-doses of PCV7 (n=336), 2+1-doses (336) or no dose (n=333) before PCV7 implementation in the Dutch national immunization program. S. aureus colonisation had doubled in children in the 2+1-dose group at 12 months of age compared with unvaccinated controls (10.1% versus 5.0%; p=0.019). A negative association for co-colonisation of S. pneumoniae and S. aureus was observed for both vaccine serotype (adjusted odds ratio (aOR) 0.53, 95% confidence interval (CI) 0.38–0.74) and nonvaccine serotype pneumococci (aOR 0.67, 95% CI 0.52–0.88).
Conclusions/Significance
PCV7 induces a temporary increase in S. aureus colonisation in children around 12 months of age after a 2+1-dose PCV7 schedule. The potential clinical consequences are unknown and monitoring is warranted.
Trial Registration
ClinicalTrials.gov NCT00189020
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Introduction
Seven-valent CRM197-conjugated pneumococcal vaccine (PCV7) provides protection against vaccine serotype invasive pneumococcal disease (IPD) The following popper user interface control may not be accessible. Tab to the next button to revert the control to an accessible version.Destroy user interface control[1], pneumonia and acute otitis media in young children The following popper user interface control may not be accessible. Tab to the next button to revert the control to an accessible version.Destroy user interface control[2]. In the nasopharynx, PCV7 reduces colonisation with vaccine serotype pneumococci The following popper user interface control may not be accessible. Tab to the next button to revert the control to an accessible version.Destroy user interface control[3]–The following popper user interface control may not be accessible. Tab to the next button to revert the control to an accessible version.Destroy user interface control[5] and due to herd effects nasopharyngeal carriage of pneumococcal vaccine serotypes in children has virtually disappeared several years after widespread infant PCV7 vaccination The following popper user interface control may not be accessible. Tab to the next button to revert the control to an accessible version.Destroy user interface control[6]. The vacant ecological niche in the nasopharynx seems immediately occupied by nonvaccine serotype pneumococci resulting in a shift in serotype carriage with limited to no net reduction in overall pneumococcal carriage The following popper user interface control may not be accessible. Tab to the next button to revert the control to an accessible version.Destroy user interface control[3], The following popper user interface control may not be accessible. Tab to the next button to revert the control to an accessible version.Destroy user interface control[4], The following popper user interface control may not be accessible. Tab to the next button to revert the control to an accessible version.Destroy user interface control[5], The following popper user interface control may not be accessible. Tab to the next button to revert the control to an accessible version.Destroy user interface control[7].
S. pneumoniae is a frequent coloniser in the dynamic nasopharyngeal milieu interieure and pneumococcal serotype shifts following PCV7 vaccination may affect other bacteria present in the nasopharynx. For example, several studies found a negative association between the presence of S. aureus and PCV7 vaccine serotype pneumococci in the nasopharynx in unvaccinated children The following popper user interface control may not be accessible. Tab to the next button to revert the control to an accessible version.Destroy user interface control[8]–The following popper user interface control may not be accessible. Tab to the next button to revert the control to an accessible version.Destroy user interface control[10]. This may imply an upcoming presence of S. aureus after PCV7-vaccinations. A higher staphylococcal nasal load has been suggested to lead to higher dispersal to other extra-nasal sites harbouring S. aureus like the nasopharynx. Furthermore, S. aureus colonisation is associated with a higher risk of infection The following popper user interface control may not be accessible. Tab to the next button to revert the control to an accessible version.Destroy user interface control[11]. S. aureus is an important cause of respiratory tract infections such as chronic recurrent otitis media and pneumonia, skin infections and community-acquired bloodstream infections in particular in children under 5 years of age, with increasing prevalence of multi resistant strains The following popper user interface control may not be accessible. Tab to the next button to revert the control to an accessible version.Destroy user interface control[12].
Investigating the effect of PCV7 on nasopharyngeal presence of bacteria that may behave as disease pathogens is relevant. As part of a longitudinal randomised controlled trial on the effects of a 2-dose and 2+1-dose PCV7-schedule on nasopharyngeal pneumococcal colonisation during the first two years of life, we assessed the effects of PCV7 on S. aureus colonisation in children and parents as secondary outcomes.



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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3112202/?report=classic
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