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基于桑格的测序技术用于黄热病疫苗遗传质量控制。

Sanger-based sequencing technology for yellow fever vaccine genetic quality control.

机构信息

Fiocruz, Bio-Manguinhos, Brazilian Ministry of Health, Avenida Brasil 4365, Manguinhos, Rio de Janeiro, RJ 21040-900, Brazil.

Fiocruz, Bio-Manguinhos, Brazilian Ministry of Health, Avenida Brasil 4365, Manguinhos, Rio de Janeiro, RJ 21040-900, Brazil.

出版信息

J Virol Methods. 2018 Oct;260:82-87. doi: 10.1016/j.jviromet.2018.07.006. Epub 2018 Jul 26.

Abstract

Yellow Fever (YF) is an acute viral hemorrhagic disease prevalent mainly in Africa and Americas, with 20-60% fatality rate in severe forms. Currently, antiviral drugs for the infection are not available, reinforcing the importance of vaccination in resident populations and travelers. Manufactured in 7 different countries, the YF vaccine was first created in 1937 and two substrains are used for production, 17DD and 17D-204. The vaccine produced in Bio-Manguinhos/Brazil uses 17DD substrain and more than 160 million doses have been exported to over 74 countries. The World Health Organization (WHO) recommends that new seed- and working-lots should have the viral genome sequenced in order to check vaccine genetic stability. The aim of this study was to develop and standardize a Sanger-based sequencing protocol for the genetic monitoring of the Brazilian 17DD vaccine. We designed 54 oligos to access the complete YF vaccine genome by RT-PCR and sequencing approach. After protocol standardization, we tested 45 vaccine lots and the corresponding secondary and working seed lots. All 45 lots presented 100% nucleotide identity to each other and to the seed lots. We also detected 2 heterogeneous positions at nucleotides 4523 (C/T) and 6673 (C/T) that may indicate a quasispecies diversity of YF 17DD strain. When compared to the Brazilian GenBank sequence YFU17066, the Brazilian 17DD vaccine presented 6 silent mutations. By applying the sequencing methodology to two YF 17D-204 strains, we showed that our method can also be used to sequence different YF vaccine virus. In summary, we have developed a robust method for the genetic monitoring of YF vaccines, which has been successfully applied in Bio-Manguinhos since 2009 and could also be used by other manufacturers for YF17D-based vaccines. There were no genetic variation in the Brazilian tested lots, highlighting the safety, production consistency and, more importantly, the genetic stability of Bio-Manguinhos' YF vaccine in the last 3 decades.

摘要

黄热病(YF)是一种主要在非洲和美洲流行的急性病毒性出血性疾病,重症患者的死亡率为 20-60%。目前,针对这种感染尚无抗病毒药物,因此疫苗在当地居民和旅行者中的接种就显得尤为重要。黄热病疫苗由 7 个不同国家生产,于 1937 年首次问世,目前使用 17DD 和 17D-204 两种亚株进行生产。巴西布坦坦研究所(Bio-Manguinhos)生产的疫苗使用 17DD 亚株,已向 74 多个国家出口了超过 1.6 亿剂疫苗。世界卫生组织(WHO)建议对新的种子和工作种子批进行病毒基因组测序,以检查疫苗遗传稳定性。本研究旨在开发和标准化基于 Sanger 的测序方案,用于监测巴西 17DD 疫苗的遗传变异。我们设计了 54 条 oligo,通过 RT-PCR 和测序方法对完整的黄热病疫苗基因组进行了测序。在方案标准化后,我们对 45 批疫苗和相应的二级和工作种子批进行了检测。所有 45 批疫苗之间的核苷酸序列完全一致,与种子批也完全一致。我们还在核苷酸 4523(C/T)和 6673(C/T)处检测到 2 个异质性位置,这可能表明黄热 17DD 株存在准种多样性。与巴西 GenBank 序列 YFU17066 相比,巴西 17DD 疫苗有 6 个沉默突变。通过将测序方法应用于两种 17D-204 黄热病毒株,我们表明我们的方法也可用于测序不同的黄热病疫苗病毒。总之,我们已经开发出一种用于监测黄热病疫苗的稳健方法,该方法自 2009 年以来一直在布坦坦研究所成功应用,其他制造商也可以将其用于基于 17D 的黄热病疫苗。在过去 30 年中,巴西测试的疫苗批次未发生遗传变异,这突显了布坦坦研究所黄热病疫苗的安全性、生产一致性,更重要的是遗传稳定性。

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