Why the study?
A novel human parechovirus 3 Australian recombinant strain emerged in 2013 and coincided with biennial sepsis-like outbreaks in infants, prompting evaluation of its molecular evolution and association with severe disease.
Is the HPeV3-AR strain associated with increased clinical severity among hospitalized infants compared to other strains?
Observational (n=54)
Yes
Is the HPeV3-AR strain associated with increased clinical severity among hospitalized infants compared to other strains?
Answers are grounded in this paper and cite their sources.
The HPeV3-AR strain was the dominant cause of outbreaks in Australian infants between 2013 and 2020 but was not associated with increased clinical severity compared to other strains.
BACKGROUND: A novel human parechovirus 3 Australian recombinant (HPeV3-AR) strain emerged in 2013 and coincided with biennial outbreaks of sepsis-like illnesses in infants. We evaluated the molecular evolution of the HPeV3-AR strain and its association with severe HPeV infections. METHODS: HPeV3-positive samples collected from hospitalized infants aged 5-252 days in 2 Australian states (2013-2020) and from a community-based birth cohort (2010-2014) were sequenced. Coding regions were used to conduct phylogenetic and evolutionary analyses. A recombinant-specific polymerase chain reaction was designed and utilized to screen all clinical and community HPeV3-positive samples. RESULTS: Complete coding regions of 54 cases were obtained, which showed the HPeV3-AR strain progressively evolving, particularly in the 3' end of the nonstructural genes. The HPeV3-AR strain was not detected in the community birth cohort until the initial outbreak in late 2013. High-throughput screening showed that most (>75%) hospitalized HPeV3 cases involved the AR strain in the first 3 clinical outbreaks, with declining prevalence in the 2019-2020 season. The AR strain was not statistically associated with increased clinical severity among hospitalized infants. CONCLUSIONS: HPeV3-AR was the dominant strain during the study period. Increased hospital admissions may have been from a temporary fitness advantage and/or increased virulence.
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Bialasiewicz et al. (2022) conducted an observational in Human parechovirus 3 (HPeV3) infection (n=54). HPeV3-AR strain vs. Non-AR HPeV3 strains was evaluated on Clinical severity.
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