Distinct systemic and central nervous system disease patterns in enterovirus and parechovirus infected children

Heli Harvala1, Michael Griffiths2, Tom Solomon2

  • 1Specialist Virology Laboratory, Royal Infirmary of Edinburgh, Edinburgh EH16 4SA, UK; Infection and Immunity Division, Roslin Institute, University of Edinburgh, Easter Bush, Edinburgh EH25 9RG, UK.

Insights

Enterovirus (EV) and human parechovirus (HPeV) infections in children show distinct viral load patterns. Plasma viral loads are key for identifying sepsis cases, while CSF analysis is crucial for diagnosing central nervous system (CNS) disease.

Area of Science:

  • Virology
  • Pediatric Infectious Diseases
  • Neurovirology

Background:

  • Enteroviruses (EV) and human parechoviruses (HPeV) are significant causes of illness in neonates and young children.
  • These viruses are increasingly implicated in sepsis, meningitis, and encephalitis.

Purpose of the Study:

  • To investigate and compare viral loads of EV and HPeV in plasma and cerebrospinal fluid (CSF).
  • To understand the distinct infection profiles associated with sepsis versus central nervous system (CNS) disease.

Main Methods:

  • Compared detection frequencies and viral loads of EV and HPeV RNA in plasma and CSF.
  • Analyzed samples from children identified through sepsis or CNS screening.

Main Results:

  • Two distinct profiles emerged: CNS disease cases had higher/similar CSF than plasma viral loads (median ratio 0.5).
  • Sepsis cases showed low/undetectable CSF viral loads and high plasma viral loads (mean ratio 5700).
  • HPeV type 3 and coxsackievirus B2 were associated with sepsis.

Conclusions:

  • EV/HPeV RNA detection in CSF alone does not predict CNS disease, especially without pleocytosis.
  • Plasma screening identifies a substantial proportion of EV/HPeV sepsis cases missed by CSF screening alone.
Abstract

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