Human adenovirus species in children with acute respiratory illnesses

Varvara Probst1, Emily K Datyner1, Zaid Haddadin1

  • 1Departments of Pediatrics, Vanderbilt University Medical Center, 1161 21st Ave. South, Nashville, TN, 37232, USA.

Insights

Human adenovirus (HAdV) species C and B are common causes of pediatric acute respiratory illness (ARI). HAdV-C was linked to younger age, hospitalization, and seizures compared to HAdV-B, suggesting potential differences in severity.

Area of Science:

  • Pediatric Infectious Diseases
  • Virology
  • Respiratory Health

Background:

  • Human adenovirus (HAdV) species B, C, and E are frequent causes of acute respiratory illnesses (ARI).
  • Understanding the association between specific HAdV species and ARI severity in children is crucial for clinical management.

Purpose of the Study:

  • To investigate the relationship between HAdV species and the severity of acute respiratory illnesses in pediatric patients.
  • To compare clinical characteristics and outcomes among children infected with different HAdV species.

Main Methods:

  • Retrospective cohort study of pediatric HAdV cases identified via BioFire® FilmArray Respiratory Pathogen Panel 2.0.
  • Type-specific PCR assays were used to identify HAdV species (B, C, E).
  • Demographic, clinical, and outcome data were analyzed and compared between HAdV species.

Main Results:

  • HAdV species B and C were the most prevalent, detected in 44% and 48% of identified cases, respectively.
  • Patients with HAdV-C were more likely to be younger, hospitalized, and experience seizures compared to those with HAdV-B.
  • The majority of HAdV-positive specimens were from patients presenting to the Emergency Department (62%), with approximately one-third requiring hospitalization.

Conclusions:

  • HAdV-C and HAdV-B are the predominant species causing pediatric ARI, exhibiting distinct clinical presentations.
  • Further research with larger cohorts is needed to elucidate type-specific severity differences and inform HAdV vaccine development.
Abstract

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