Detection of parechovirus‐A in hospitalized children with acute lower respiratory infection in Myanmar, 2017–2018

Author:

Tachikawa Jun1ORCID,Aizawa Yuta1ORCID,Kobayashi Tetsuya1,Ikuse Tatsuki1ORCID,Kamata Kazuhiro12,Win Su Mon Kyaw2,Di Ja Lasham2,Thein Khin Nyo3,Win Nay Chi2,Thida Aye4,Tun Aye5,Suzuki Yuko1,Ito Ai1,Osada Hidekazu26,Chon Irina6,Phyu Wint Wint6,Ota Tomomi2,Kyaw Yadanar4,Tin Htay Htay7,Watanabe Kanako8,Shobugawa Yugo9,Watanabe Hisami2,Saito Reiko6,Saitoh Akihiko1ORCID

Affiliation:

1. Department of Pediatrics Niigata University Graduate School of Medical and Dental Sciences Niigata Japan

2. Infectious Diseases Research Center of Niigata University in Myanmar Yangon Myanmar

3. Yankin Children Hospital Yangon Myanmar

4. University of Medicine 2 Yangon Myanmar

5. Ministry of Health Myanmar

6. Division of International Health, Graduate School of Medical and Dental Science Niigata University Niigata Japan

7. University of Medical Technology Yangon Myanmar

8. Department of Medical Technology Niigata University Graduate School of Health Sciences Niigata Japan

9. Department of Active Ageing Niigata University Graduate School of Medical and Dental Sciences Niigata Japan

Abstract

AbstractParechovirus‐A (PeV‐A) causes emerging infection in children, and clinical presentation depends on genotype. The virus has been investigated mainly in developed countries; however, data from developing countries, especially in Asia, are sparse. This study investigated whether PeV‐A circulated in children in Myanmar. This retrospective study evaluated PeV‐A in nasopharyngeal samples from children aged 1 month to 12 years who were hospitalized with acute lower respiratory infection at Yankin Children Hospital, Yangon, Myanmar, during the period from May 2017 to April 2019. Real‐time polymerase chain reaction (PCR) was used to detect PeV‐A, and PCR‐positive samples were used for genotyping and phylogenetic analysis. In total, 11/570 (1.9%) of samples were positive for PeV‐A; 7 were successfully genotyped by sequencing the VP3/VP1 region, as follows: PeV‐A1 (n = 4), PeV‐A5 (n = 1), PeV‐A6 (n = 1), and PeV‐A14 (n = 1). Median age was 10.0 months (interquartile range 4.0–12.0 months), and other respiratory viruses were detected in all cases. Phylogenetic analysis showed that all detected PeV‐A1 strains were in clade 1 A, which was a minor clade worldwide. Four PeV‐A genotypes were detected in Myanmar. The clinical impact of PeV‐A in children should be evaluated in future studies.

Publisher

Wiley

Subject

Infectious Diseases,Virology

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