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

Author:

Pang Juanita1ORCID,Slyker Jennifer A2,Roy Sunando1,Bryant Josephine1,Atkinson Claire3,Cudini Juliana1,Farquhar Carey4,Griffiths Paul3,Kiarie James5,Morfopoulou Sofia1,Roxby Alison C4,Tutil Helena1,Williams Rachel1,Gantt Soren6ORCID,Goldstein Richard A1ORCID,Breuer Judith7ORCID

Affiliation:

1. Division of Infection and Immunity, University College London, Cruciform Building, London, United Kingdom

2. Departments of Global Health and Epidemiology, University of Washington, Seattle, United States

3. Institute of Immunology and Transplantation, Division of Infection and Immunity, University College London, London, United Kingdom

4. Departments of Global Health, Epidemiology, Medicine (Div. Allergy and Infectious Diseases), University of Washington, Seattle, United States

5. University of Nairobi, Department of Obstetrics and Gynaecology, World Health Organization, Nairobi, Kenya

6. Research Centre of the Sainte-Justine University Hospital, Department of Microbiology, Infectious Diseases and Immunology, University of Montréal QC, Montréal, Canada

7. Department of Infection, Immunity and Inflammation, UCL Great Ormond Street Institute of Child Health, University College London, London, United Kingdom

Abstract

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.

Funder

EUFP7

Wellcome Trust

National Institute of Allergy and Infectious Diseases

National Institute of Child Health and Human Development

Rosetreees Trust PhD Studentship

UCL/UCLH NIHR Biomedical Research Centre

Sir Henry Wellcome Fellowship

Sir Henry Wellcome Fellowships

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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