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Cross-sectional study of cytomegalovirus shedding and immunological markers among seropositive children and their mothers
BACKGROUND: Congenital cytomegalovirus (CMV) is the leading infectious cause of birth defects in the United States. To better understand factors that may influence CMV transmission risk, we compared viral and immunological factors in healthy children and their mothers. METHODS: We screened for CMV I...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236433/ https://www.ncbi.nlm.nih.gov/pubmed/25388365 http://dx.doi.org/10.1186/s12879-014-0568-2 |
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author | Stowell, Jennifer D Mask, Karen Amin, Minal Clark, Rebekah Levis, Denise Hendley, Will Lanzieri, Tatiana M Dollard, Sheila C Cannon, Michael J |
author_facet | Stowell, Jennifer D Mask, Karen Amin, Minal Clark, Rebekah Levis, Denise Hendley, Will Lanzieri, Tatiana M Dollard, Sheila C Cannon, Michael J |
author_sort | Stowell, Jennifer D |
collection | PubMed |
description | BACKGROUND: Congenital cytomegalovirus (CMV) is the leading infectious cause of birth defects in the United States. To better understand factors that may influence CMV transmission risk, we compared viral and immunological factors in healthy children and their mothers. METHODS: We screened for CMV IgG antibodies in a convenience sample of 161 children aged 0-47 months from the Atlanta, Georgia metropolitan area, along with 32 mothers of children who screened CMV-seropositive. We assessed CMV shedding via PCR using saliva collected with oral swabs (children and mothers) and urine collected from diapers using filter paper inserts (children only). RESULTS: CMV IgG was present in 31% (50/161) of the children. Half (25/50) of seropositive children were shedding in at least one fluid. The proportion of seropositive children who shed in saliva was 100% (8/8) among the 4-12 month-olds, 64% (9/14) among 13-24 month-olds, and 40% (6/15) among 25-47 month-olds (P for trend = 0.003). Seropositive mothers had a lower proportion of saliva shedding (21% [6/29]) than children (P < 0.001). Among children who were shedding CMV, viral loads in saliva were significantly higher in younger children (P <0.001); on average, the saliva viral load of infants (i.e., <12 months) was approximately 300 times that of two year-olds (i.e., 24-35 months). Median CMV viral loads were similar in children's saliva and urine but were 10-50 times higher (P < 0.001) than the median viral load of the mothers' saliva. However, very high viral loads (> one million copies/mL) were only found in children's saliva (31% of those shedding); children's urine and mothers' saliva specimens all had fewer than 100,000 copies/mL. Low IgG avidity, a marker of primary infection, was associated with younger age (p = 0.03), higher viral loads in saliva (p = 0.02), and lower antibody titers (p = 0.005). CONCLUSIONS: Young CMV seropositive children, especially those less than one year-old may present high-risk CMV exposures to pregnant women, especially via saliva, though further research is needed to see if this finding can be generalized across racial or other demographic strata. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12879-014-0568-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4236433 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42364332014-11-19 Cross-sectional study of cytomegalovirus shedding and immunological markers among seropositive children and their mothers Stowell, Jennifer D Mask, Karen Amin, Minal Clark, Rebekah Levis, Denise Hendley, Will Lanzieri, Tatiana M Dollard, Sheila C Cannon, Michael J BMC Infect Dis Research Article BACKGROUND: Congenital cytomegalovirus (CMV) is the leading infectious cause of birth defects in the United States. To better understand factors that may influence CMV transmission risk, we compared viral and immunological factors in healthy children and their mothers. METHODS: We screened for CMV IgG antibodies in a convenience sample of 161 children aged 0-47 months from the Atlanta, Georgia metropolitan area, along with 32 mothers of children who screened CMV-seropositive. We assessed CMV shedding via PCR using saliva collected with oral swabs (children and mothers) and urine collected from diapers using filter paper inserts (children only). RESULTS: CMV IgG was present in 31% (50/161) of the children. Half (25/50) of seropositive children were shedding in at least one fluid. The proportion of seropositive children who shed in saliva was 100% (8/8) among the 4-12 month-olds, 64% (9/14) among 13-24 month-olds, and 40% (6/15) among 25-47 month-olds (P for trend = 0.003). Seropositive mothers had a lower proportion of saliva shedding (21% [6/29]) than children (P < 0.001). Among children who were shedding CMV, viral loads in saliva were significantly higher in younger children (P <0.001); on average, the saliva viral load of infants (i.e., <12 months) was approximately 300 times that of two year-olds (i.e., 24-35 months). Median CMV viral loads were similar in children's saliva and urine but were 10-50 times higher (P < 0.001) than the median viral load of the mothers' saliva. However, very high viral loads (> one million copies/mL) were only found in children's saliva (31% of those shedding); children's urine and mothers' saliva specimens all had fewer than 100,000 copies/mL. Low IgG avidity, a marker of primary infection, was associated with younger age (p = 0.03), higher viral loads in saliva (p = 0.02), and lower antibody titers (p = 0.005). CONCLUSIONS: Young CMV seropositive children, especially those less than one year-old may present high-risk CMV exposures to pregnant women, especially via saliva, though further research is needed to see if this finding can be generalized across racial or other demographic strata. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12879-014-0568-2) contains supplementary material, which is available to authorized users. BioMed Central 2014-11-12 /pmc/articles/PMC4236433/ /pubmed/25388365 http://dx.doi.org/10.1186/s12879-014-0568-2 Text en © Stowell et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Stowell, Jennifer D Mask, Karen Amin, Minal Clark, Rebekah Levis, Denise Hendley, Will Lanzieri, Tatiana M Dollard, Sheila C Cannon, Michael J Cross-sectional study of cytomegalovirus shedding and immunological markers among seropositive children and their mothers |
title | Cross-sectional study of cytomegalovirus shedding and immunological markers among seropositive children and their mothers |
title_full | Cross-sectional study of cytomegalovirus shedding and immunological markers among seropositive children and their mothers |
title_fullStr | Cross-sectional study of cytomegalovirus shedding and immunological markers among seropositive children and their mothers |
title_full_unstemmed | Cross-sectional study of cytomegalovirus shedding and immunological markers among seropositive children and their mothers |
title_short | Cross-sectional study of cytomegalovirus shedding and immunological markers among seropositive children and their mothers |
title_sort | cross-sectional study of cytomegalovirus shedding and immunological markers among seropositive children and their mothers |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236433/ https://www.ncbi.nlm.nih.gov/pubmed/25388365 http://dx.doi.org/10.1186/s12879-014-0568-2 |
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