Essential Site Maintenance: Authorea-powered sites will be updated circa 15:00-17:00 Eastern on Tuesday 5 November.
There should be no interruption to normal services, but please contact us at [email protected] in case you face any issues.

loading page

Early-life cytomegalovirus infection is associated with changes in the intestinal microbiota and increased risk of atopy
  • +8
  • Hind Sbihi,
  • Karen Simmons,
  • Malcolm Sears,
  • Theo Moraes,
  • Allen Becker,
  • Piush Mandhane,
  • Padmaja Subbarao,
  • Darlene Dai,
  • B. Brett Finlay,
  • Stuart Turvey,
  • Soren Gantt
Hind Sbihi
Univ of British Columbia
Author Profile
Karen Simmons
Univ of British Columbia
Author Profile
Malcolm Sears
McMaster University
Author Profile
Theo Moraes
University of Toronto
Author Profile
Allen Becker
University of Manitoba
Author Profile
Piush Mandhane
University of Alberta
Author Profile
Padmaja Subbarao
University of Toronto
Author Profile
Darlene Dai
British Columbia Children's Hospital
Author Profile
B. Brett Finlay
Univ British Columbia
Author Profile
Stuart Turvey
Univ of British Columbia
Author Profile
Soren Gantt
University of Montreal

Corresponding Author:[email protected]

Author Profile

Abstract

Background: The ‘old friends’ hypothesis posits that reduced exposure to previously ubiquitous microorganisms is one factor involved in the increased rates of allergic diseases. Cytomegalovirus (CMV) may be one of the “old friends” hypothesized to help prevent allergic diseases. We sought to elucidate whether early-life CMV infection is associated with childhood atopy via perturbations of the gut microbiota. Methods: Participants were recruited from a population-based birth cohort (CHILD study) and followed prospectively until age five years in four Canadian cities. A total of 928 participants provided stool microbiome data, urine for CMV testing, skin-prick tests, and questionnaires-based detailed environmental exposures. CMV infection was assessed in the first year of life while the main outcome was defined by persistent sensitization to any allergen at ages 1, 3, and 5 years. Results: Early CMV infection was associated with increased beta and decreased alpha diversity of the gut microbiota. Both changes in diversity measures and early CMV infection were associated with persistent allergic sensitization at age 5 years (aOR= 2.08; 95%CI: 1, 4.33). Mediation analysis demonstrated that perturbation of gut microbial composition explains 30% of the association. Conclusions: Early-life CMV infection is associated with an alteration in the intestinal microbiota, which mediates the effect of the infection on childhood atopy. This work indicates that preventing CMV infection would not put children at increased risk of developing atopy. Rather, a CMV vaccine, in addition to preventing CMV-associated morbidity and mortality, might reduce the risk of childhood allergic diseases.