Experimental Infection of Rats with Influenza A Viruses: Implications for Murine Rodents in Influenza A Virus Ecology.

Long Li1 Rirong Chen1 Zhigang Yan1 Qinglong Cai1 Yi Guan1,2 Huachen Zhu1,2
Affiliations 2 institutions
  1. Guangdong-Hong Kong Joint Laboratory of Emerging Infectious Diseases, Joint Laboratory for International Collaboration in Virology and Emerging Infectious Diseases (Key Laboratory of Ministry of Education), Joint Institute of Virology (Shantou University-The University of Hong Kong), Shantou University Medical College, Shantou University, Shantou 515063, China.
  2. State Key Laboratory of Emerging Infectious Diseases (SKLEID), School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.

Abstract

Rattus norvegicus (brown rat), a widely distributed rodent and common biomedical model, is a known reservoir for many zoonotic pathogens but has not been traditionally recognized as a host for influenza A virus (IAV). To evaluate their susceptibility, we intranasally inoculated Sprague-Dawley rats with various IAV subtypes, including H5Nx, H7N9, H9N2, H10N8 and the 2009 pandemic H1N1. All strains productively infected the rats, inducing seroconversion without overt clinical signs. While replication efficiency varied, all viruses caused significant lung injury with a preferential tropism for the upper respiratory tract. Investigation of receptor distribution revealed a predominance of α2,3-linked sialic acid (SA) in the nasal turbinates and trachea, whereas α2,6-linked SA was more abundant in the lungs. Notably, both receptor types coexisted throughout the respiratory tract, aligning with the observed tissue-specific replication patterns and broad viral infectivity. These findings demonstrate that rats are permissive hosts for multiple IAV subtypes, challenging their exclusion from IAV ecology. The asymptomatic yet pathogenic nature of infection, combined with the global synanthropy of rats, underscores their potential role as cryptic reservoirs in viral maintenance and transmission. This study highlights the need for expanded surveillance of rodents in influenza ecology to mitigate zoonotic risks.

Supporting text Virus Host Location
host range 29 interspecies transmission 51 sialic acid receptor 16 surveillance 60 zoonotic influenza 2 Influenza A virus 186 Orthomyxoviridae Infections 228 Animals 1948 Disease Models, Animal 77 Humans 1440 Lung 65 Male 224 Mice 253 Rats 73 Rats, Sprague-Dawley 4 Viral Tropism 45 Virus Replication 191

Evidence records

3 total
Experimental Infection
2 records · 2 evidence types
Evidence type
1 records
OVE9089
Key finding

Intranasal inoculation of Sprague-Dawley rats with H5Nx, H7N9, H9N2, H10N8, and 2009 pandemic H1N1 influenza A viruses caused lung injury despite absence of overt clinical signs.

Virus
Host
Location
Not specified
Supporting text

We intranasally inoculated Sprague-Dawley rats with various IAV subtypes, including H5Nx, H7N9, H9N2, H10N8 and the 2009 pandemic H1N1. All strains productively infected the rats, inducing seroconversion without overt clinical signs. While replication efficiency varied, all viruses caused significant lung injury with a preferential tropism for the upper respiratory tract.

Method
intranasal inoculation | histopathological examination of lungs | virus replication assessment
Experimental system
intranasally inoculated Sprague-Dawley rat infection model
Evidence type
1 records
OVE9088
Key finding

Sprague-Dawley rats were intranasally inoculated with multiple influenza A virus subtypes (H5Nx, H7N9, H9N2, H10N8, and 2009 pandemic H1N1), and all strains productively infected the rats, demonstrating rat susceptibility to diverse IAVs.

Virus
Host
Location
Not specified
Supporting text

We intranasally inoculated Sprague-Dawley rats with various IAV subtypes, including H5Nx, H7N9, H9N2, H10N8 and the 2009 pandemic H1N1. All strains productively infected the rats, inducing seroconversion without overt clinical signs.

Method
intranasal inoculation | serological analysis (seroconversion) | virological assessment of infection and replication | histopathology of respiratory tissues
Sample type
lung tissue | nasal turbinates | trachea
Experimental system
animal challenge model (intranasal inoculation of live rats)
Functional Mechanism
1 records · 1 evidence types
Evidence type
1 records
OVE9090
Key finding

In rats, α2,3-linked sialic acid predominates in the nasal turbinates and trachea, while α2,6-linked sialic acid is more abundant in the lungs, indicating differing receptor distribution relevant to influenza A virus entry.

Virus
Host
Location
Not specified
Supporting text

Investigation of receptor distribution revealed a predominance of α2,3-linked sialic acid (SA) in the nasal turbinates and trachea, whereas α2,6-linked SA was more abundant in the lungs.

Method
receptor distribution analysis
Receptors
α2,3-linked sialic acid | α2,6-linked sialic acid