错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

Tracing household transmission of SARS-CoV-2 in New Zealand using genomics

  • Lauren Jelley,
  • Nayyereh Aminisani,
  • Meaghan O’Neill,
  • Tineke Jennings,
  • Jordan Douglas,
  • Srushti Utekar,
  • Helen Johnston,
  • David Welch,
  • James Hadfield,
  • Nikki Turner,
  • Tony Dowell,
  • Annette Nesdale,
  • Hazel C. Dobinson,
  • Priscilla Campbell-Stokes,
  • Michelle Balm,
  • Cameron C. Grant,
  • Karen Daniells,
  • Peter McIntyre,
  • Adrian Trenholme,
  • Cass Byrnes,
  • Ruth Seeds,
  • Tim Wood,
  • Megan Rensburg,
  • Jort Cueto,
  • Ernest Caballero,
  • Joshma John,
  • Emmanuel Penghulan,
  • Danielle Currin,
  • Mary Ryan,
  • Andrea Bowers,
  • Chor Ee Tan,
  • Judy Bocacao,
  • Wendy Gunn,
  • Bryden Bird,
  • Tegan Slater,
  • Farjana Ahmed,
  • Mai Anh Sam,
  • Elaisa Glampe,
  • Gabriella Davey,
  • Joep de Ligt,
  • David Winter,
  • Nigel French,
  • Paul G. Thomas,
  • Richard J. Webby,
  • Sue Huang,
  • Jemma L. Geoghegan

摘要

By early 2022, the highly transmissible Omicron variant of SARS-CoV-2 had spread across most of the world. For the first time since the pandemic began, New Zealand was experiencing high levels of community transmission of SARS-CoV-2. We enroled a cohort of households to better understand differences in transmission dynamics among subvariants of Omicron. We enroled 71 households, comprising 289 participants, and aimed to use viral genomes to gain a clearer understanding of variant-specific differences in epidemiological parameters affecting transmission dynamics. Approximately 80% of the households enroled experienced transmission of BA.2, while most of the remaining households had infections with BA.1 or BA.5. Using a logistic regression generalised linear mixed model, we found no difference in household secondary infection rate between Omicron subvariants BA.1, BA.2 and BA.5. Of the households recruited, the vast majority (92%) experienced a single chain of transmission with one inferred introduction. Further, we found that in 48% of the households studied, all household participants became infected following an index case. Most household participants tested positive within a week following an introduction, supporting the seven-day isolation requirement for household contacts that was in place in New Zealand at the time. By integrating genomic and epidemiological data, we show that viral transmission dynamics can be investigated with a higher level of granularity than with epidemiological data alone. Overall, households are a high risk setting for viral transmission in New Zealand.