Your browser doesn't support javascript.
loading
A regional genomic surveillance program is implemented to monitor the occurrence and emergence of SARS-CoV-2 variants in Yubei District, China.
Liu, Fangyuan; Deng, Peng; He, Jiuhong; Chen, Xiaofeng; Jiang, Xinyu; Yan, Qi; Xu, Jing; Hu, Sihan; Yan, Jin.
Afiliação
  • Liu F; Chongqing Yubei Center for Disease Control and Prevention, Chongqing, China.
  • Deng P; Chongqing Yubei Center for Disease Control and Prevention, Chongqing, China.
  • He J; Chongqing Yubei Center for Disease Control and Prevention, Chongqing, China.
  • Chen X; Chongqing Yubei Center for Disease Control and Prevention, Chongqing, China.
  • Jiang X; Chongqing Yubei Center for Disease Control and Prevention, Chongqing, China.
  • Yan Q; Chongqing Yubei Center for Disease Control and Prevention, Chongqing, China.
  • Xu J; Chongqing Yubei Center for Disease Control and Prevention, Chongqing, China.
  • Hu S; Chongqing Yubei Center for Disease Control and Prevention, Chongqing, China.
  • Yan J; Chongqing Yubei Center for Disease Control and Prevention, Chongqing, China. yanjinkin@163.com.
Virol J ; 21(1): 13, 2024 01 08.
Article em En | MEDLINE | ID: mdl-38191416
ABSTRACT

BACKGROUND:

In December 2022, Chongqing experienced a significant surge in coronavirus disease 2019 (COVID-19) epidemic after adjusting control measures in China. Given the widespread immunization of the population with the BA.5 variant, it is crucial to actively monitor severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variant evolution in Chongqing's Yubei district.

METHODS:

In this retrospective study based on whole genome sequencing, we collected oropharyngeal and nasal swab of native COVID-19 cases from Yubei district between January to May 2023, along with imported cases from January 2022 to January 2023. Through second-generation sequencing, we generated a total of 578 genomes.

RESULTS:

Phylogenetic analyses revealed these genomes belong to 47 SARS-CoV-2 Pango lineages. BA.5.2.48 was dominant from January to April 2023, rapidly replaced by XBB* variants from April to May 2023. Bayesian Skyline Plot reconstructions indicated a higher evolutionary rate (6.973 × 10-4 subs/site/year) for the XBB.1.5* lineage compared to others. The mean time to the most recent common ancestor (tMRCA) of BA.5.2.48* closely matched BA.2.75* (May 27, 2022). Using multinomial logistic regression, we estimated growth advantages, with XBB.1.9.1 showing the highest growth advantage (1.2, 95% HPI1.1-1.2), followed by lineage FR.1 (1.1, 95% HPI1.1-1.2).

CONCLUSIONS:

Our monitoring reveals the rapid replacement of the previously prevalent BA.5.2.48 variant by XBB and its sub-variants, underscoring the ineffectiveness of herd immunity and breakthrough BA.5 infections against XBB variants. Given the ongoing evolutionary pressure, sustaining a SARS-CoV-2 genomic surveillance program is imperative.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: SARS-CoV-2 / COVID-19 Tipo de estudo: Observational_studies / Risk_factors_studies / Screening_studies Limite: Humans País/Região como assunto: Asia Idioma: En Revista: Virol J Assunto da revista: VIROLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Assunto principal: SARS-CoV-2 / COVID-19 Tipo de estudo: Observational_studies / Risk_factors_studies / Screening_studies Limite: Humans País/Região como assunto: Asia Idioma: En Revista: Virol J Assunto da revista: VIROLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China