Amanda H. Seekings , Elizabeth Billington , Sahar Mahmood , Saumya S. Thomas , Anita Puranik , Simon Johnson , Alejandro Nunez , Samantha Watson , Jill Banks , Sharon M. Brookes , Ian H. Brown , Marek J. Slomka
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引用次数: 0
Abstract
H7N7 low-pathogenicity avian influenza virus (H7N7-LPAIV) incursions preceded emergence of H7N7 high-pathogenicity (HP)AIV at several European layer hen outbreaks. Evidence from a UK layer H7N7-HPAIV (2008) outbreak informed in vivo modelling of sequential events, beginning with H7N7-LPAIV precursor incursion. Three groups of 17-week-old (point-of-lay) hens were inoculated with H7N7-LPAIVs, which possessed different haemagglutinin cleavage sites (CS). Groups 1 and 2 were inoculated with H7N7-LPAIVs which possessed single and di-basic cleavage sites (SBCS and DBCS, the latter having occurred at the 2008 outbreak), along with the H7N7-HPAIV's internal genes. Group 3 was inoculated with a contemporary H7N7-LPAIV which possessed the DBCS, but different internal genes. In Groups 1–3, initial H7N7-LPAIV exposure caused limited viral shedding, restricted H7-antibody responses and no deaths by 14-days post-inoculation (dpi). H7N7-HPAIV challenge of all groups (n = 8 per challenge group, including AIV-naïve hens in Group 4) followed at 14 dpi, with 3/8 (37.5 %) survival in Group 4, by 14-days post-challenge (dpc). Prior H7N7-LPAIV inoculation protected against H7N7-HPAIV challenge mortality to varying degrees (6/8-8/8 [75 %–100 %] survival range) by 14 dpc, when all 21 Group1-3 survivors had strongly seroconverted. Among these survivors, 20/21 (95 %) shed H7N7-HP, indicating that immunity acquired during initial H7N7-LPAIV exposure did not arrest H7N7-HPAIV replication. Prior H7N7-LPAIV exposure elicited clinical protection against H7N7-HPAIV challenge, but did not prevent H7N7-HPAIV shedding, which in the field would represent a potential source for spread and further HPAIV outbreaks.
期刊介绍:
Launched in 1955, Virology is a broad and inclusive journal that welcomes submissions on all aspects of virology including plant, animal, microbial and human viruses. The journal publishes basic research as well as pre-clinical and clinical studies of vaccines, anti-viral drugs and their development, anti-viral therapies, and computational studies of virus infections. Any submission that is of broad interest to the community of virologists/vaccinologists and reporting scientifically accurate and valuable research will be considered for publication, including negative findings and multidisciplinary work.Virology is open to reviews, research manuscripts, short communication, registered reports as well as follow-up manuscripts.