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Mixed cytomegalovirus genotypes in HIV-positive mothers show compartmentalization and distinct patterns of transmission to infants

Cytomegalovirus (CMV) is the commonest cause of congenital infection and particularly so among infants born to HIV-infected women. Studies of congenital CMV infection (cCMVi) pathogenesis are complicated by the presence of multiple infecting maternal CMV strains, especially in HIV-positive women, an...

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Autores principales: Pang, Juanita, Slyker, Jennifer A, Roy, Sunando, Bryant, Josephine, Atkinson, Claire, Cudini, Juliana, Farquhar, Carey, Griffiths, Paul, Kiarie, James, Morfopoulou, Sofia, Roxby, Alison C, Tutil, Helena, Williams, Rachel, Gantt, Soren, Goldstein, Richard A, Breuer, Judith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7806273/
https://www.ncbi.nlm.nih.gov/pubmed/33382036
http://dx.doi.org/10.7554/eLife.63199
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author Pang, Juanita
Slyker, Jennifer A
Roy, Sunando
Bryant, Josephine
Atkinson, Claire
Cudini, Juliana
Farquhar, Carey
Griffiths, Paul
Kiarie, James
Morfopoulou, Sofia
Roxby, Alison C
Tutil, Helena
Williams, Rachel
Gantt, Soren
Goldstein, Richard A
Breuer, Judith
author_facet Pang, Juanita
Slyker, Jennifer A
Roy, Sunando
Bryant, Josephine
Atkinson, Claire
Cudini, Juliana
Farquhar, Carey
Griffiths, Paul
Kiarie, James
Morfopoulou, Sofia
Roxby, Alison C
Tutil, Helena
Williams, Rachel
Gantt, Soren
Goldstein, Richard A
Breuer, Judith
author_sort Pang, Juanita
collection PubMed
description Cytomegalovirus (CMV) is the commonest cause of congenital infection and particularly so among infants born to HIV-infected women. Studies of congenital CMV infection (cCMVi) pathogenesis are complicated by the presence of multiple infecting maternal CMV strains, especially in HIV-positive women, and the large, recombinant CMV genome. Using newly developed tools to reconstruct CMV haplotypes, we demonstrate anatomic CMV compartmentalization in five HIV-infected mothers and identify the possibility of congenitally transmitted genotypes in three of their infants. A single CMV strain was transmitted in each congenitally infected case, and all were closely related to those that predominate in the cognate maternal cervix. Compared to non-transmitted strains, these congenitally transmitted CMV strains showed statistically significant similarities in 19 genes associated with tissue tropism and immunomodulation. In all infants, incident superinfections with distinct strains from breast milk were captured during follow-up. The results represent potentially important new insights into the virologic determinants of early CMV infection.
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spelling pubmed-78062732021-01-15 Mixed cytomegalovirus genotypes in HIV-positive mothers show compartmentalization and distinct patterns of transmission to infants Pang, Juanita Slyker, Jennifer A Roy, Sunando Bryant, Josephine Atkinson, Claire Cudini, Juliana Farquhar, Carey Griffiths, Paul Kiarie, James Morfopoulou, Sofia Roxby, Alison C Tutil, Helena Williams, Rachel Gantt, Soren Goldstein, Richard A Breuer, Judith eLife Genetics and Genomics Cytomegalovirus (CMV) is the commonest cause of congenital infection and particularly so among infants born to HIV-infected women. Studies of congenital CMV infection (cCMVi) pathogenesis are complicated by the presence of multiple infecting maternal CMV strains, especially in HIV-positive women, and the large, recombinant CMV genome. Using newly developed tools to reconstruct CMV haplotypes, we demonstrate anatomic CMV compartmentalization in five HIV-infected mothers and identify the possibility of congenitally transmitted genotypes in three of their infants. A single CMV strain was transmitted in each congenitally infected case, and all were closely related to those that predominate in the cognate maternal cervix. Compared to non-transmitted strains, these congenitally transmitted CMV strains showed statistically significant similarities in 19 genes associated with tissue tropism and immunomodulation. In all infants, incident superinfections with distinct strains from breast milk were captured during follow-up. The results represent potentially important new insights into the virologic determinants of early CMV infection. eLife Sciences Publications, Ltd 2020-12-31 /pmc/articles/PMC7806273/ /pubmed/33382036 http://dx.doi.org/10.7554/eLife.63199 Text en © 2020, Pang et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Genetics and Genomics
Pang, Juanita
Slyker, Jennifer A
Roy, Sunando
Bryant, Josephine
Atkinson, Claire
Cudini, Juliana
Farquhar, Carey
Griffiths, Paul
Kiarie, James
Morfopoulou, Sofia
Roxby, Alison C
Tutil, Helena
Williams, Rachel
Gantt, Soren
Goldstein, Richard A
Breuer, Judith
Mixed cytomegalovirus genotypes in HIV-positive mothers show compartmentalization and distinct patterns of transmission to infants
title Mixed cytomegalovirus genotypes in HIV-positive mothers show compartmentalization and distinct patterns of transmission to infants
title_full Mixed cytomegalovirus genotypes in HIV-positive mothers show compartmentalization and distinct patterns of transmission to infants
title_fullStr Mixed cytomegalovirus genotypes in HIV-positive mothers show compartmentalization and distinct patterns of transmission to infants
title_full_unstemmed Mixed cytomegalovirus genotypes in HIV-positive mothers show compartmentalization and distinct patterns of transmission to infants
title_short Mixed cytomegalovirus genotypes in HIV-positive mothers show compartmentalization and distinct patterns of transmission to infants
title_sort mixed cytomegalovirus genotypes in hiv-positive mothers show compartmentalization and distinct patterns of transmission to infants
topic Genetics and Genomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7806273/
https://www.ncbi.nlm.nih.gov/pubmed/33382036
http://dx.doi.org/10.7554/eLife.63199
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