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10.1080/22221751.2020.1717999

http://scihub22266oqcxt.onion/10.1080/22221751.2020.1717999
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31996093!7034077!31996093
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suck abstract from ncbi


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pmid31996093      Emerg+Microbes+Infect 2020 ; 9 (1): 246-255
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  • Discovery of a subgenotype of human coronavirus NL63 associated with severe lower respiratory tract infection in China, 2018 #MMPMID31996093
  • Wang Y; Li X; Liu W; Gan M; Zhang L; Wang J; Zhang Z; Zhu A; Li F; Sun J; Zhang G; Zhuang Z; Luo J; Chen D; Qiu S; Zhang L; Xu D; Mok CKP; Zhang F; Zhao J; Zhou R; Zhao J
  • Emerg Microbes Infect 2020[]; 9 (1): 246-255 PMID31996093show ga
  • Human coronavirus NL63 (HCoV-NL63) is primarily associated with common cold in children, elderly and immunocompromised individuals. Outbreaks caused by HCoV-NL63 are rare. Here we report a cluster of HCoV-NL63 cases with severe lower respiratory tract infection that arose in Guangzhou, China, in 2018. Twenty-three hospitalized children were confirmed to be HCoV-NL63 positive, and most of whom were hospitalized with severe pneumonia or acute bronchitis. Whole genomes of HCoV-NL63 were obtained using next-generation sequencing. Phylogenetic and single amino acid polymorphism analyses showed that this outbreak was associated with two subgenotypes (C3 and B) of HCoV-NL63. Half of patients were identified to be related to a new subgenotype C3. One unique amino acid mutation at I507 L in spike protein receptor binding domain (RBD) was detected, which segregated this subgenotype C3 from other known subgenotypes. Pseudotyped virus bearing the I507 L mutation in RBD showed enhanced entry into host cells as compared to the prototype virus. This study proved that HCoV-NL63 was undergoing continuous mutation and has the potential to cause severe lower respiratory disease in humans.
  • |*Coronavirus Infections[MESH]
  • |Child, Preschool[MESH]
  • |China[MESH]
  • |Coronavirus NL63, Human/*genetics/isolation & purification[MESH]
  • |Genotype[MESH]
  • |Humans[MESH]
  • |Infant[MESH]
  • |Phylogeny[MESH]


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