Literature detail

Replication Fitness of Human Influenza B Viruses in Swine Primary Respiratory Epithelial Cells.

Sunayana S Jandhyala1 Chithra C Sreenivasan2 Shalini Soni2 Kripa Giri2 Radhey S Kaushik1 Feng Li2 Dan Wang2
Affiliations 2 institutions
  1. Department of Biology and Microbiology, South Dakota State University, Brookings, South Dakota, USA.
  2. Maxwell H. Gluck Equine Research Center, Department of Veterinary Science, University of Kentucky, Lexington, Kentucky, USA.
PMID 41891518 2026 J Med Virol eng ppublish
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Article

Publication summary

Influenza B virus (IBV) is a significant pathogen and contributes to seasonal influenza epidemics worldwide yearly. Humans are thought to be a reservoir and amplification host for IBV. However, natural infections of IBVs in other species such as pigs probably from a spillover event from humans can sporadically occur. Here, we examined and compared the replication fitness of two human IBV lineages in swine primary respiratory epithelial cells (nasal turbinate, trachea, and lung). IBV strains used in this study included two Victoria lineage viruses (B/Brisbane/60/2008 (BR08) and B/HongKong/286/2017 (HK17)) and two Yamagata lineage viruses (B/Florida/04/06 (FL06) and B/Utah/09/2014 (UT14)). Results of our experiments showed that IBVs replicated efficiently in swine primary respiratory epithelial cells regardless of the virus lineage with higher titers observed at 33°C than at 37°C. HK17 (Victoria lineage) grew to the highest titers in nasal turbinate and lung cells, while the other Victoria lineage strain BR08 showed a modest replication fitness. In sum, the swine primary respiratory epithelial cells representing the upper, middle, and lower respiratory tract of swine support IBV replication, which can be further explored as the in vitro model system to study IBV adaptation to swine, the mixing vessel in generating zoonotic influenza viruses.

influenza B virus replication fitness swine swine primary respiratory epithelial cells Epithelial Cells Influenza B virus Respiratory Mucosa Virus Replication Animals Cells, Cultured Humans Influenza, Human Lung Orthomyxoviridae Infections Swine Trachea Turbinates

Structured evidence records

Evidence records

2 total
1 records
Extraction confidence 0.95
Key finding

Human Influenza B viruses replicated efficiently in swine primary respiratory epithelial cells from nasal turbinate, trachea, and lung, demonstrating swine cell susceptibility to these human IBV lineages.

Virus
Location
Not specified
Supporting text

Here, we examined and compared the replication fitness of two human IBV lineages in swine primary respiratory epithelial cells (nasal turbinate, trachea, and lung). Results of our experiments showed that IBVs replicated efficiently in swine primary respiratory epithelial cells regardless of the virus lineage with higher titers observed at 33°C than at 37°C.

Method
replication assay; in vitro infection
Sample type
nasal turbinate; trachea; lung
Experimental system
in vitro cell culture
1 records
Extraction confidence 0.90
Key finding

Pigs can occasionally be naturally infected with human influenza B viruses, indicating a human-to-swine spillback event.

Virus
Location
Not specified
Supporting text

Natural infections of IBVs in other species such as pigs probably from a spillover event from humans can sporadically occur.

Transmission direction
human-to-animal