Related Experiment Video
Updated: Jan 30, 2026

A Method for Targeted 16S Sequencing of Human Milk Samples
Published on: March 23, 2018
Genetic diversity of human parechoviruses in stool samples, Germany
Corinna Pietsch1, Uwe G Liebert1
1Institute of Virology, Leipzig University, Leipzig, Germany.
Abstract:
Human parechoviruses (HPeV) are ubiquitous and mainly occur in early infancy. They are known to cause various clinical manifestations including acute gastroenteritis. To gain insight into the diversity of circulating HPeV genotypes, stool samples from patients (n = 539) with clinical signs of infectious gastroenteritis which showed negative results for other common viral and bacterial enteric pathogens were obtained during three years, 2008 to 2010. Real-time RT-PCR showed HPeV RNA in 34 (6.3%) of the samples. The HPeV detection rate was highest (8.8%) in samples derived from infants and young children under the age of two years. Genotyping was based on VP3/VP1 junction nucleic acid sequences and revealed predominant HPeV-1B (n = 16) and HPeV-3 (n = 12) strains. Those prevailed minor HPeV-6 (n = 3) as well as HPeV-2, -4 and -5 (n = 1, each) strains. To ascertain the assigned HPeV-2 genotype of uncommon strain LPZ04-2008, analysis of complete coding sequences was performed. In complete VP1 analysis strain LPZ04-2008 showed 81.2% nucleic acid identity with HPeV-2 reference strain Williamson. In phylogenetic analysis VP1 of strain LPZ04-2008 clustered with a recent HPeV-2 strain from the UK. Regarding clinical manifestations, severe disease occurred HPeV-1B, -3 and - 6 infections. In conclusion, this paper a high genetic diversity of HPeV in stool samples, including rare strains. The investigation adds data on the whole coding sequences of the rare HPeV-2 strain. Genotyping results confirm previously reported association of more severe illness with HPeV-3 and HPeV-1B strains.
Insights
Human parechoviruses (HPeV) cause gastroenteritis, especially in infants. This study found diverse HPeV genotypes in stool samples, with HPeV-1B and HPeV-3 being most common and associated with severe illness.
Area of Science:
- Virology
- Infectious Diseases
- Molecular Epidemiology
Background:
- Human parechoviruses (HPeV) are common viral pathogens.
- HPeV infections primarily affect infants and young children.
- Gastroenteritis is a known clinical manifestation of HPeV.
Purpose of the Study:
- To investigate the genetic diversity of circulating HPeV genotypes.
- To identify HPeV strains in patients with infectious gastroenteritis.
- To correlate HPeV genotypes with disease severity.
Main Methods:
- Real-time RT-PCR for HPeV RNA detection in stool samples.
- VP3/VP1 junction sequencing for HPeV genotyping.
- Complete coding sequence analysis for uncommon strains.
- Phylogenetic analysis of VP1 sequences.
Main Results:
- HPeV RNA detected in 6.3% of samples, with a higher rate (8.8%) in children under two.
- Predominant genotypes identified were HPeV-1B (47%) and HPeV-3 (35%).
- Rare strains including HPeV-2, -4, -5, and -6 were also detected.
- Severe disease was associated with HPeV-1B, -3, and -6 infections.
Conclusions:
- This study highlights significant genetic diversity among HPeV strains.
- HPeV-1B and HPeV-3 are key genotypes associated with severe gastroenteritis.
- The findings contribute to understanding HPeV epidemiology and clinical impact.
Related Concept Videos
Human Genetics
The complex relationship between genetics and psychology is observable through common biological components such...
Diversity of Archaea I
Cell Diversity
Multicellular...
Diversity of Archaea II
Diversity of Protists I
Diversity of Protists II

