4.5 Article

A Vero-cell-adapted vaccine donor strain of influenza A virus generated by serial passages

期刊

VACCINE
卷 33, 期 2, 页码 374-381

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.vaccine.2014.11.007

关键词

Influenza A virus vaccine; Vero-cell adaptation; Serial passages

资金

  1. Chinese National Key Project of 973 [2013CB530504]
  2. Chinese National 863 Project [2012AA02A404, 2012AA020103]
  3. National Natural Science Foundation of China [81201280, 31030029, 31230024]
  4. Science and Technology Commission of Shanghai Municipality [12ZR1435000]
  5. Chinese National Science and Technology Major Project [2013ZX10004-101-005, 2013ZX10004-003-003, 2012ZX10002-007-003]
  6. CAS Key Project [KJZD-EW-L09-3]
  7. talent programs of the SA-SIBS Scholarship Program
  8. CAS Youth Innovation Association
  9. CAS-SIBS frontier research field foundation for young scientists
  10. private foundation of the Li Kha Shing Foundation

向作者/读者索取更多资源

A cell culture-based vaccine production system is preferred for the large-scale production of influenza vaccines and has advantages for generating vaccines against highly pathogenic influenza A viruses. Vero cells have been widely used in human vaccine manufacturing, and the safety of these cells has been well demonstrated. However, the most commonly used influenza-vaccine donor virus, A/Puerto Rico/8/1934 (PR8) virus, does not grow efficiently in Vero cells. Therefore, we adapted the PR8 virus to Vero cells by continuous passaging, and a high-growth strain was obtained after 20 passages. Sequence analysis and virological assays of the adapted strain revealed that mutations in four viral internal genes (NP, PB1, PA and NS1) were sufficient for adaptation. The recombinant virus harboring these mutations (PR8-4mut) displayed accelerated viral transport into the nucleus and increased RNP activity. Importantly, the PR8-4mut could serve as a backbone donor virus to support the growth of the H7N1, H9N2 and H5N1 avian viruses and the H1N1 and H3N2 human viruses in Vero cells without changing its pathogenicity in either chicken embryos or mice. Thus, our work describes the generation of a Vero-adapted, high-yield PR8-4mut virus that may serve as a promising candidate for an influenza-vaccine donor virus. (C) 2014 Elsevier Ltd. All rights reserved.

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