Molecular epidemiology of a post‐influenza pandemic outbreak of acute respiratory infections in Korea caused by human adenovirus type 3
Identifieur interne : 000C47 ( Main/Curation ); précédent : 000C46; suivant : 000C48Molecular epidemiology of a post‐influenza pandemic outbreak of acute respiratory infections in Korea caused by human adenovirus type 3
Auteurs : Wan-Ji Lee [Corée du Sud] ; Hee-Dong Jung [Corée du Sud] ; Hyang-Min Cheong [Corée du Sud] ; Kisoon Kim [Corée du Sud]Source :
- Journal of Medical Virology [ 0146-6615 ] ; 2015-01.
Descripteurs français
- KwdFr :
- ADN viral (), ADN viral (génétique), Adénovirus humains (), Adénovirus humains (génétique), Adénovirus humains (isolement et purification), Analyse de regroupements, Analyse de séquence d'ADN, Corée (épidémiologie), Données de séquences moléculaires, Enfant d'âge préscolaire, Grippe humaine (épidémiologie), Humains, Incidence, Infections de l'appareil respiratoire (virologie), Infections de l'appareil respiratoire (épidémiologie), Infections à Adenoviridae (virologie), Infections à Adenoviridae (épidémiologie), Mâle, Nourrisson, Pandémies, Phylogénie, Réaction de polymérisation en chaîne, Similitude de séquences, Sérotypage, Épidémiologie moléculaire.
- MESH :
- génétique : ADN viral, Adénovirus humains.
- isolement et purification : Adénovirus humains.
- virologie : Infections de l'appareil respiratoire, Infections à Adenoviridae.
- épidémiologie : Corée, Grippe humaine, Infections de l'appareil respiratoire, Infections à Adenoviridae.
- ADN viral, Adénovirus humains, Analyse de regroupements, Analyse de séquence d'ADN, Données de séquences moléculaires, Enfant d'âge préscolaire, Humains, Incidence, Mâle, Nourrisson, Pandémies, Phylogénie, Réaction de polymérisation en chaîne, Similitude de séquences, Sérotypage, Épidémiologie moléculaire.
English descriptors
- KwdEn :
- Adenoviridae Infections (epidemiology), Adenoviridae Infections (virology), Adenoviruses, Human (classification), Adenoviruses, Human (genetics), Adenoviruses, Human (isolation & purification), Child, Preschool, Cluster Analysis, DNA, Viral (chemistry), DNA, Viral (genetics), Humans, Incidence, Infant, Influenza, Human (epidemiology), Korea (epidemiology), Male, Molecular Epidemiology, Molecular Sequence Data, Pandemics, Phylogeny, Polymerase Chain Reaction, Respiratory Tract Infections (epidemiology), Respiratory Tract Infections (virology), Sequence Analysis, DNA, Sequence Homology, Serotyping.
- MESH :
- chemical , chemistry : DNA, Viral.
- geographic , epidemiology : Korea.
- classification : Adenoviruses, Human.
- epidemiology : Adenoviridae Infections, Influenza, Human, Respiratory Tract Infections.
- genetics : Adenoviruses, Human, DNA, Viral.
- isolation & purification : Adenoviruses, Human.
- virology : Adenoviridae Infections, Respiratory Tract Infections.
- Child, Preschool, Cluster Analysis, Humans, Incidence, Infant, Male, Molecular Epidemiology, Molecular Sequence Data, Pandemics, Phylogeny, Polymerase Chain Reaction, Sequence Analysis, DNA, Sequence Homology, Serotyping.
Abstract
An outbreak of upper respiratory tract infections associated with human adenovirus (HAdV) occurred on a national scale in Korea from September to December 2010, following a major H1N1 influenza pandemic. Data from the Korea Influenza and Respiratory Surveillance System (KINRESS) showed an unusually high positive rate accounting for up to 20% of all diagnosed cases. To determine the principal cause of the outbreak, direct polymerase chain reaction (PCR) amplification followed by sequence analysis targeting parts of the hexon gene of HAdV was performed. Serotypes of 1,007 PCR‐diagnosed HAdV‐positive samples from patients with an acute upper respiratory tract illness were determined and epidemiological characteristics including major aged group and clinical symptoms were analyzed. The principal symptom of HAdV infections was fever and the vulnerable aged group was 1–5 years old. Based on sequence analysis, HAdV‐3 was the predominant serotype in the outbreak, with an incidence of 74.3%. From the beginning of 2010 until May, the major serotypes were HAdV‐1, 2, and 5 (70–100%) in any given period. However, an outbreak dominated by HAdV‐3 started between July and August and peaked in September. Phylogenetic analysis revealed that there was no genetic variation in HAdV‐3. The results demonstrated that an outbreak of upper respiratory illness followed by H1N1 influenza pandemic in Korea was caused mainly by emerged HAdV‐3. J. Med. Virol. 87: 10–17, 2015. © 2014 Wiley Periodicals, Inc.
Url:
- https://api.istex.fr/ark:/67375/WNG-3PGHSPBT-3/fulltext.pdf
- http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7167096
DOI: 10.1002/jmv.23984
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Data from the Korea Influenza and Respiratory Surveillance System (KINRESS) showed an unusually high positive rate accounting for up to 20% of all diagnosed cases. To determine the principal cause of the outbreak, direct polymerase chain reaction (PCR) amplification followed by sequence analysis targeting parts of the hexon gene of HAdV was performed. Serotypes of 1,007 PCR‐diagnosed HAdV‐positive samples from patients with an acute upper respiratory tract illness were determined and epidemiological characteristics including major aged group and clinical symptoms were analyzed. The principal symptom of HAdV infections was fever and the vulnerable aged group was 1–5 years old. Based on sequence analysis, HAdV‐3 was the predominant serotype in the outbreak, with an incidence of 74.3%. From the beginning of 2010 until May, the major serotypes were HAdV‐1, 2, and 5 (70–100%) in any given period. However, an outbreak dominated by HAdV‐3 started between July and August and peaked in September. Phylogenetic analysis revealed that there was no genetic variation in HAdV‐3. The results demonstrated that an outbreak of upper respiratory illness followed by H1N1 influenza pandemic in Korea was caused mainly by emerged HAdV‐3. J. Med. Virol. 87: 10–17, 2015. © 2014 Wiley Periodicals, Inc.</div></front></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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