Human Parechoviruses as an Important Viral Cause of Sepsislike Illness and Meningitis in Young Children (original) (raw)

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1

Department of Medical Microbiology, Laboratory of Clinical Virology

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Amsterdam, The Netherlands

Reprints or correspondence: Dr. Katja C. Wolthers, Dept. of Medical Microbiology, Laboratory of Clinical Virology K1-121, Academic Medical Center, Meibergdreef 15, 1105 AZ Amsterdam, The Netherlands (k.c.wolthers@amc.uva.nl).

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1

Department of Medical Microbiology, Laboratory of Clinical Virology

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Amsterdam, The Netherlands

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1

Department of Medical Microbiology, Laboratory of Clinical Virology

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Amsterdam, The Netherlands

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1

Department of Medical Microbiology, Laboratory of Clinical Virology

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Amsterdam, The Netherlands

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Department of Medical Microbiology, Laboratory of Clinical Virology

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Amsterdam, The Netherlands

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Departments of Medical Microbiology, Onze Lieve Vrouwe Gasthuis

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Amsterdam, The Netherlands

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Departments of Pediatrics, Onze Lieve Vrouwe Gasthuis

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Amsterdam, The Netherlands

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Department of Pediatric Infectious Diseases, Emma Children's Hospital, Academic Medical Center, University of Amsterdam

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Amsterdam, The Netherlands

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Received:

19 December 2007

Published:

01 August 2008

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Katja C. Wolthers, Kimberley S. M. Benschop, Janke Schinkel, Richard Molenkamp, Rosemarijn M. Bergevoet, Ingrid J. B. Spijkerman, H. Carlijn Kraakman, Dasja Pajkrt, Human Parechoviruses as an Important Viral Cause of Sepsislike Illness and Meningitis in Young Children, Clinical Infectious Diseases, Volume 47, Issue 3, 1 August 2008, Pages 358–363, https://doi.org/10.1086/589752
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Abstract

Background. Enteroviruses (EVs) belong to the family Picornaviridae and are a well-known cause of neonatal sepsis and viral meningitis. Human parechoviruses (HPeVs) type 1 and 2, previously named echovirus 22 and 23, have been associated with mild gastrointestinal or respiratory symptoms in young children. Six HPeV genotypes are currently known, of which HPeV3 is associated with neonatal sepsis and meningitis.

Methods. Cerebrospinal fluid samples from children aged <5 years previously tested by EV-specific polymerase chain reaction (PCR) during 2004–2006 were selected (n=761). Samples from 716 of those children were available for retrospective testing by HPeV-specific real-time PCR. The prevalence of EV and HPeV in these samples was compared. Data on clinical presentation of children infected with HPeV were retrospectively documented.

Results. HPeV was found in cerebrospinal fluid samples from 33 (4.6%) of the children. Yearly prevalence of HPeV in cerebrospinal fluid varied remarkably: 8.2% in 2004, 0.4% in 2005, and 5.7% in 2006. EV was detected in 14% (108 of 761 samples), with no variation in yearly prevalence. Children with HPeV in cerebrospinal fluid presented with clinical symptoms of sepsislike illness and meningitis, which led to hospitalization and antibiotic treatment.

Conclusion. EV-specific PCRs do not detect HPeVs. The addition of an HPeV-specific PCR has led to a 31% increase in detection of a viral cause of neonatal sepsis or central nervous system symptoms in children aged <5 years. HPeV can be considered to be the second cause of viral sepsis and meningitis in young children, and rapid identification of HPeV by PCR could contribute to shorter duration of both antibiotic use and hospital stay.

© 2008 by the Infectious Diseases Society of America

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