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Published on: July 24, 2016
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.
Objectives:
Enteroviruses (EV) and human parechoviruses (HPeV) infections are increasingly identified in neonates and young children with sepsis, meningitis and encephalitis. We investigated EV and HPeV viral loads in plasma and cerebrospinal fluid (CSF) among those presenting with sepsis or central nervous system (CNS) disease to gain understanding of the nature of these infections.
Methods:
Detections frequencies and viral loads of EV and HPeV RNA were compared in plasma and CSF obtained from infected children originally identified on sepsis or CNS screening.
Results:
Two distinct infection profiles were identified; 11 subjects with CNS disease, showed higher or similar viral loads in CSF than in plasma (median plasma:CSF ratio 0.5), whereas 14 children with sepsis showed low or undetectable viral loads in CSF and high viral loads in plasma (mean ratio 5700). HPeV type 3 and one EV serotype (coxsackievirus B2) were primarily associated with the latter presentation.
Conclusions:
Simple detection of EV or HPeV RNA in CSF is not predictive of CNS disease, especially in the absence of clinical markers (i.e. pleocytosis). Screening of plasma can identify EV and HPeV RNA in a substantial proportion of sepsis cases, some of which will be missed if CSF samples alone are screened.
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