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Published on: July 24, 2016
Human parechovirus central nervous system infections in southern California children
Susanna Felsenstein1, Shangxin Yang, Natalie Eubanks
1From the *Division of Pediatric Infectious Diseases; †Molecular Microbiology Laboratory Services; and ‡Department of Radiology, Children's Hospital Los Angeles, Los Angeles, CA.
Insights
Human parechoviruses (hPeV) are a significant cause of meningoencephalitis in infants. Testing for hPeV in cerebrospinal fluid (CSF) is crucial, even with normal CSF parameters, due to frequent neurological symptoms.
Area of Science:
- Virology
- Pediatric Neurology
- Infectious Diseases
Background:
- Human parechoviruses (hPeV) are increasingly identified as causes of meningoencephalitis in young children.
- Cerebrospinal fluid (CSF) testing for hPeV via PCR is not standard practice.
Purpose of the Study:
- To evaluate the prevalence and clinical presentation of hPeV in pediatric CSF samples.
- To compare hPeV infections with enterovirus (EV) infections in children with central nervous system symptoms.
Main Methods:
- Real-time reverse transcriptase PCR was used to detect hPeV serotypes 1-6 in 440 pediatric CSF samples.
- Prevalence and clinical features of hPeV-positive CSF were compared to EV-positive CSF.
Main Results:
- hPeV was detected in 2.7% of CSF samples, while EV was found in 10.7%.
- hPeV-positive infants were typically under 3 months old and often had normal CSF parameters.
- Neurological symptoms were more frequent in children with hPeV-positive CSF compared to those with EV-positive CSF.
Conclusions:
- hPeV central nervous system infections predominantly affect young infants and are associated with neurological symptoms, even with normal CSF findings.
- hPeV should be considered in the differential diagnosis for young children presenting with central nervous system symptoms or sepsis-like illness, irrespective of CSF results.
Background:
Human parechoviruses (hPeV) are increasingly recognized as significant etiological agents for meningoencephalitis especially in young children, but testing of cerebrospinal fluid (CSF) for hPeV by PCR is not routinely performed.
Methods:
We used real-time reverse transcriptase PCR for detection of serotypes 1-6 in CSF samples of 440 children who underwent a lumbar puncture to exclude an infectious etiology of their clinical presentation. We then compared the prevalence and clinical presentation of children with hPeV-positive CSF with that of children with enterovirus (EV)-positive CSF.
Results:
HPeV was detected in 2.7% and EV in 10.7% of CSF samples. Many hPeV-positive patients were <3 months of age and usually had CSF parameters within the age-adjusted normal range. However, children with hPeV-positive CSF presented with neurologic symptoms more frequently than those with EV-positive CSF.
Conclusions:
HPeV infections of the central nervous system occurred mainly in young infants and were more commonly associated with neurologic symptoms at presentation, despite the fact that CSF findings were within the normal range in the vast majority of these cases. HPeV should be included in the differential diagnosis of young children with central nervous system symptoms and sepsis-like illness, even in the presence of normal CSF parameters.
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