Seropositivity and epidemiology of human parechovirus types 1, 3, and 6 in Japan

K Watanabe1, C Hirokawa2, T Tazawa3

  • 1Division of Laboratory Science,Niigata University Graduate School of Health Sciences,Niigata,Japan.

Insights

Human parechoviruses (HPeVs) cause mild illness in children, but HPeV type 3 (HPeV3) is severe in infants. Adults lack HPeV3 antibodies, increasing susceptibility. Clinical symptoms depend on HPeV type and patient age.

Area of Science:

  • Virology
  • Epidemiology
  • Pediatrics

Background:

  • Human parechoviruses (HPeVs) are common viral pathogens, primarily affecting young children with gastrointestinal and respiratory symptoms.
  • Human parechovirus type 3 (HPeV3) is an exception, frequently causing severe systemic illness, including sepsis, in neonates and young infants.

Purpose of the Study:

  • To investigate the seropositivity and epidemiological characteristics of HPeV infections in different age groups in Niigata, Japan.
  • To correlate HPeV genotypes with clinical manifestations and patient demographics.

Main Methods:

  • Measurement of neutralizing antibody titers against various HPeV types in human serum samples across different age demographics.
  • Isolation and identification of HPeVs from diverse clinical specimens collected from patients.

Main Results:

  • Seropositivity for HPeV1, HPeV3, and HPeV6 was higher in older age groups, with HPeV1 and HPeV6 antibodies maintained in adults.
  • Significantly lower HPeV3 seropositivity was observed in individuals over 40 years old, suggesting increased adult susceptibility.
  • HPeV1 and HPeV6 were associated with gastroenteritis in infants and young children, while HPeV3 was exclusively isolated from neonates and young infants with severe sepsis-like illness, often with respiratory involvement.

Conclusions:

  • Clinical symptoms associated with HPeV infections are strongly dependent on the specific HPeV genotype and the age of the patient.
  • Adults over 40 may be more susceptible to severe HPeV3 infections due to a lack of pre-existing neutralizing antibodies.

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