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2585. Changing Epidemiological Profile of Infantile Parechovirus-A3 Infection in Japan
BACKGROUND: Parechovirus-A3 (PeV-A3) causes severe disease, including sepsis and meningoencephalitis in young infants. The first case of PeV-A3 was reported in Japan in 1999 and, although epidemics have been reported every 2 to 3 years in more than 20 countries, no major epidemic has occurred in Jap...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6810139/ http://dx.doi.org/10.1093/ofid/ofz360.2263 |
Sumario: | BACKGROUND: Parechovirus-A3 (PeV-A3) causes severe disease, including sepsis and meningoencephalitis in young infants. The first case of PeV-A3 was reported in Japan in 1999 and, although epidemics have been reported every 2 to 3 years in more than 20 countries, no major epidemic has occurred in Japan since 2014. METHODS: This prospective study included febrile infants (<4 months of age) admitted at Niigata University and its affiliated hospitals, which serve about 2.5 million people, during the period from 2014 to 2018. Neonates and infants younger than 4 months presenting with fever and suspected of having viral sepsis underwent serum and/or cerebrospinal fluid (CSF) testing by real-time PCR for parechovirus-A (PeV-A) and enteroviruses (EVs), and for herpes simplex viruses, if suspected. Bacterial infection was excluded on the basis of the results of bacterial culture of blood, urine, and/or CSF. PeV-A genotype was identified by examining the viral protein 1 (VP1) sequence, and the phylogenetic tree of the VP1 sequence was constructed. RESULTS: Of the 277 patients evaluated, 135 (49%) were positive for PeV-A (n = 74, 27%) or EVs (n = 61, 22%). Among PeV-A patients, most had PeV-A3 (n = 69; 93%), followed by PeV-A4 (n = 4; 5%). There was a PeV-A3 epidemic in 2014 (n = 43); however, no cases were reported in 2015. In 2016–2018, small numbers of PeV-A3 cases were reported: 10 in 2016, 7 in 2017, and 9 in 2018. In contrast, EV cases were reported throughout this period: 8 in 2014, 22 in 2015, 10 in 2016, 5 in 2017, and 16 in 2018. When data were analyzed by season, the PeV-A3 detection rate in summer (June-August) was 93% (40/43) in 2014 and 65% (17/26) during 2016–2018, indicating an increase in the number of PeV-A3 cases in seasons other than summer. Phylogenetic analysis showed that PeV-A3 strains during 2016–2018 were part of a cluster of epidemics in 2011 and differed from those in 2014. CONCLUSION: After the major PeV-A3 epidemics in 2014, we observed changes in the PeV-A3 epidemic profile, namely, a small, but constant, number of cases every year in Niigata, Japan. A future study should investigate if this trend has continued in Japan and other countries and identify the causes of this change in epidemic profile. [Image: see text] DISCLOSURES: All authors: No reported disclosures. |
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