聖塔非研究所

摘要 We used ultra deep sequencing to obtain tens of t

2010 · 已發表論文 · 更新 2026/08/30 下午12:48

摘要 We used ultra deep sequencing to obtain tens of thousands of HIV 1 sequences from regions targeted by CD8+ T lymphocytes from longitudinal samples from three acutely infected subjects, an…

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論文資訊

  • 類型:已發表論文
  • 日期:2010

摘要

We used ultra-deep sequencing to obtain tens of thousands of HIV-1 sequences from regions targeted by CD8+ T lymphocytes from longitudinal samples from three acutely infected subjects, and modeled viral 演化 during the critical first weeks of infection. Previous studies suggested that a single 病毒 established productive infection, but these conclusions were tempered because of limited sampling; now, we have greatly increased our confidence in this observation through modeling the observed earliest sample 多樣性 based on vastly more extensive sampling. Conventional sequencing of HIV-1 from acute/early infection has shown different patterns of escape at different epitopes; we investigated the earliest escapes in exquisite detail. Over 3-6 weeks, ultradeep sequencing revealed that the 病毒 explored a

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