Twist Bioscience
2021 年 1 月 18 日
8 分で読む

SARS-CoV-2 パンデミックを終息させるために不可欠な変異株サーベイランス

最近出現したSARS-CoV-2の変異株は、パンデミックに効果的に対応するためには、新たな株を検出するための世界規模の NGS シーケンシングが必要であることを示しています。
SARS-CoV-2 パンデミックを終息させるために不可欠な変異株サーベイランス

 (以下 英文ブログを元にした和訳例)この2ヶ月間で、英国、南アフリカ、ブラジルにおいて、集団内の感染拡大に関連する新たな SARS-CoV-2 変異株が確認されました。迅速かつ定期的な NGS シーケンシングによる陽性サンプルの株サーベイランスにより、私たちの健康にさらなる脅威をもたらす変異株の特定が可能になります。このような脅威を早期に把握することは、効果的なパンデミック対応に不可欠であり、世界中で医療の逼迫を避けることにつながります。 

 

しかし、世界的な変異株のサーベイランスのインフラはまだ初期段階にあり、 SARS-CoV-2 の変異が疫学的にどのような影響を与えているかについては、まだほとんど知られていない現状です。本稿では、この2か月間に焦点を当てて、サーベイランスの成功事例をご紹介します。また、私たちは今後数ヶ月の間に必要とされる世界的な株サーベイランスの取り組みの強化を支持します。 

 

サーベイランスによって、懸念される新たな株を確認

 

Toward the end of 2020, the UK government locked down the country to stem the increase in SARS-CoV-2 (COVID-19) infections. Scientists tracking the spread of the virus noticed that the southeast county of Kent was not following a typical trend in this lockdown period. While cases in the rest of the country were going down, cases in the southeast were rising.

 

On December 10th, Public Health England (PHE) first published the identification of a new Coronavirus strain, VoC-202012/01 (B.1.1.7), concentrated in Kent and parts of London. Retrospective studies showed cases originated in September. Current scientific understanding states that VoC-202012/01, which contains 23 mutations, has greatly increased transmissibility (it spreads faster). This strain can likely be attributed to the unusual increase in cases in the UK.

 

Epidemiological evidence shows that VoC-202012/01 doesn’t lead to a more severe SARS-CoV-2 infection. However, the increased transmissibility dramatically increases the risk of overwhelming health services and ultimately increases mortality rate. As of the 18th January, over 45 countries have reported at least one case of this variant. 

 

SARS-CoV-2 の英国変異株の感染拡大を示す地図
2020年1月18日時点でVoC-202012/01の症例が確認されている国々

 

English scientists identified VoC-202012/01 by studying the routinely available SARS-CoV-2 sequencing data available due to the ongoing sequencing efforts in place in the UK through the COVID-19 Genomics UK consortium (COG-UK).

 

COG-UK formed in March 2020, consisting of hundreds of scientists across 16 sequencing hubs throughout the UK. To date, COG-UK has sequenced over 200,000 SARS-CoV-2 genomes, approximately 7% of the country’s positive tests. Before this, the largest dataset for epidemiological studies during an epidemic was 1,500 Ebola genomes. COG-UK surpassed this during their first month. COG-UK is currently aiming to sequence 20,000 genomes per week.

 

COG-UK has developed software that automatically analyzes the large volume of sequencing data produced, including the identification of mutations. Data is then distributed to the four public health institutions in the UK, which merge this with broader epidemiological data from PCR-based screening efforts. Mutations that have implications on public health are then identified, and advice is subsequently passed on to governing bodies. Positive strains are also submitted to the Global Initiative on Sharing Avian Influenza Data (GISAID), which has curated the global database of coronavirus genomes.

 

On 2020 年 12 月 21 日, the Africa Centers for Disease Control and Prevention announced that their surveillance work led to the identification of a unique coronavirus strain (501Y.V2). Three mutations were identified in the strain’s spike protein, one of which (N501Y) was also observed in the UK strain VoC-202012/01 and implicated in increased transmissibility. In light of 501Y.V2, The African CDC states that they are increasing surveillance efforts across Africa.

 

On January 6th, 2021, Japan’s National Institute of Infectious Diseases announced it had identified a new strain in four passengers traveling from Brazil, showing mutations implicated in increased transmissibility also present in VoC-202012/01 and 501Y.V2. A publication from the Instituto Leônidas e Maria Deane, Brazil, analyzed 148 genome sequences from positive cases in the Amazonas region. Results suggest this variant arose from the Amazonas region around December. With the recency of the strain, the authors state they are in the process of sequencing samples from new patients in the Amazonas region to understand the epidemiological impact. 

 

SARS-CoV-2 の南アフリカ変異株の感染拡大を示す地図
2020年1月18日時点で501Y.V2の症例が確認されている国々

 

変異株ばかりになる

 

During a pandemic, especially one of the scale and impact of SARS-CoV-2, the NGS sequencing of cases is essential to monitor changes in a viral genome for an effective pandemic response. Such surveillance is essential to “keeping ahead” of any new strains that pose an increased threat to human health. Understanding the scale and spread of these new strains allows governing bodies to allocate resources appropriately. As new strains are detected, one of the first and most salient questions to be asked is, “are current vaccines still effective?”For the UK and South Africa strains, early data suggests the answer is yes. Unfortunately, it is naive to assume this is the case for all strains in circulation when we have such a limited picture of sequence variation across the global population.

 

Logically, Japan, South Africa, and the UK have been among the first to identify coronavirus variants to date – all three nations have well-established sequencing infrastructure for strain surveillance. This begs two questions: what strains of concern may exist in countries that do not currently have adequate surveillance, and how far have these strains spread? A significant improvement to global strain surveillance infrastructure is required to provide answers.

 

Current WHO advice states that where feasible, countries with sequencing capacity should increase routine systematic sequencing of SARS-CoV-2 viruses from known cases to understand SARS-CoV-2 transmission patterns, and to monitor the emergence of new variants. Countries that do not have NGS capacity are encouraged to collaborate with public and private sequencing laboratories from the COVID-19 reference laboratory network. On January 8th, 2021, the WHO published comprehensive guidelines for the genomic sequencing of SARS-CoV-2 and the implementation of sequencing programs.

 

Recognizing the need for increased surveillance, the European Centre for Disease Prevention and Control has stated, “Member States need to perform timely genome sequencing of a significant and representative selection of isolates. Ideally, Member States should aim for similar timeliness, and fraction of samples sequenced [to the UK].”In a similar model to the UK response, positive cases will be reported to Europe’s Early Warning and Detection System and The European Surveillance System for epidemiological study. 

 

The United States of America bears one of the most significant coronavirus surveillance challenges. In the first nine days of 2021, over two million cases were confirmed. Since the pandemic began, the US has submitted only 56,000 genome sequences of the 23 million US positive samples to GISAID. The country needs to screen three times this amount every week if it is to achieve surveillance numbers matching the UK and European goals. Currently, the CDC’s surveillance capacity is less than 3,000 genomes per week. The good news is efforts are underway to increase this capacity, and a surveillance network has recently been established.

 

Twist Bioscienceのサーベイランス活動への貢献

 

Twist Bioscience recognizes the need for tools that enable the scientific community to perform rapid, efficient, and accurate sequencing of SARS-CoV-2 samples to identify variants. In November 2020, Twist launched its SARS-CoV-2 NGS Assay - RUO, a Research Use Only targeted sequencing assay designed to comprehensively hybridize with and capture the entire 30kb coronavirus genome from a patient sample. 

 

In the WHO’s newly released advice on the sequencing of SARS-CoV-2 genomes, they say the following about target capture-based assays: “One advantage of using a capture-based approach... is that capture-based approaches can tolerate viral sequence differences from the probe sequences of 10–20%. This is higher than the mismatch tolerated by PCR, where such a divergence from the primer sequences would result in a high risk of amplicon failure. Capture-based approaches can therefore be used to enrich successfully for relatively divergent SARS-CoV-2 sequences.” 

 

Twist offers a broad range of synthetic SARS-CoV-2 controls, allowing for verification of screens and sequencing assays and providing measures to determine the limit of detection and monitor test-to-test variance. Two controls for UK variant VoC-202012/01 are now available in response to the rapidly changing screening landscape.

 

Click the link for more information on tools for addressing the SARS-CoV-2 pandemic from Twist Bioscience.

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