4.6 Article

A Live Attenuated H9N2 Avian Influenza Vaccine Prevents the Viral Reassortment by Exchanging the HA and NS1 Packaging Signals

Journal

FRONTIERS IN MICROBIOLOGY
Volume 11, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fmicb.2020.613437

Keywords

avian influenza virus; live-attenuated vaccine; HA; NS1; packaging signals

Categories

Funding

  1. National Key RD Project [2017YFD0500701]
  2. National Natural Science Foundation of China [31872477]
  3. Jiangsu Agriculture Science and Technology Innovation Fund [CX(19)3001]
  4. Six Talent Peaks Project in Jiangsu Province [NY-131]
  5. Jiangsu Provincial Natural Science Fund for Excellent Young Scholars [BK20200105]
  6. Priority Academic Program Development of Jiangsu Higher Education Institutions
  7. State Key Laboratory of Genetically Engineered Veterinary Vaccines [2015DQ741165]
  8. High-Level Talent Support Plan of Yangzhou University

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The H9N2 avian influenza virus is a significant zoonotic pathogen and can easily recombine with other subtypes to generate novel viruses. In this study, a new H9N2 live attenuated strain was developed to intercept reassortments and showed good genetic stability and immunogenicity in chickens.
The H9N2 avian influenza virus is not only an important zoonotic pathogen, it can also easily recombine with other subtypes to generate novel reassortments, such as the H7N9 virus. Although H9N2 live attenuated vaccines can provide good multiple immunities, including humoral, cellular, and mucosal immunity, the risk of reassortment between the vaccine strain and wild-type virus is still a concern. Here, we successfully rescued an H9N2 live attenuated strain [rTX-NS1-128 (mut)] that can interdict reassortment, which was developed by exchanging the mutual packaging signals of HA and truncated NS1 genes and confirmed by RT-PCR and sequencing. The dynamic growth results showed that rTX-NS1-128 (mut) replication ability in chick embryos was not significantly affected by our construction strategy compared to the parent virus rTX strain. Moreover, rTX-NS1-128 (mut) had good genetic stability after 15 generations and possessed low pathogenicity and no contact transmission characteristics in chickens. Furthermore, chickens were intranasally immunized by rTX-NS1-128 (mut) with a single dose, and the results showed that the hemagglutination inhibition (HI) titers peaked at 3 weeks after vaccination and lasted at least until 11 weeks. The cellular immunity (IL-6 and IL-12) and mucosal immunity (IgA and IgG) in the nasal and trachea samples were significantly increased compared to inactivated rTX. Recombinant virus provided a good cross-protection against homologous TX strain (100%) and heterologous F98 strain (80%) challenge. Collectively, these data indicated that rTX-NS1-128(mut) lost the ability for independent reassortment of HA and NS1-128 and will be expected to be used as a potential live attenuated vaccine against H9N2 subtype avian influenza.

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