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Unprecedented outbreaks caused by the H5N1 highly pathogenic avian influenza virus (HPAIV) among dairy cows in the United States have raised significant concerns. Whether other subtypes of influenza A viruses (IAVs) can infect and transmit in cattle remains largely unknown. Herein, we infected cattle respiratory and mammary gland cells with different IAVs and two groups of Holstein calves intranasally or orally with a swine H3N2 virus to determine their susceptibility. Naive calves were co-housed with infected animals to investigate virus transmission. Results showed that tested swine and avian IAVs could infect cattle primary nasal turbinate and tracheal epithelial cells, as well as immortalized mammary gland epithelial cells and fibroblasts. No obvious clinical signs, including fever, were observed in infected and contact calves, but macroscopic lung lesions were found in necropsied animals in both groups on day 5 post-infection. Viral shedding was detected in three out of four nasally infected calves but not in orally infected or the two groups of contact animals. Interestingly, viral RNA and antigen could not be detected in all tissues from individual necropsied animals from either infection group, but viral RNA and sequences were detected in serum samples of two nasally infected calves on day 7 post-infection, not on other days and in other animals. Additionally, only the nasally infected animals seroconverted. Our results indicate that in addition to H5N1 HPAIV, swine H3N2 virus can infect cattle but does not transmit efficiently among them, suggesting that other subtypes of IAVs could infect and replicate in cattle.IMPORTANCEHighly pathogenic avian influenza H5N1 virus outbreaks in U.S. dairy herds have raised questions about whether other subtypes of influenza A viruses (IAVs) can infect and transmit in cattle. In this study, we investigated the susceptibility and infection of different IAVs in bovine primary and immortalized cells and Holstein calves. Results showed that avian H5N1 and H9N2, and swine H3N2 IAVs could infect beef cattle primary nasal turbinate and tracheal epithelial cells, as well as immortalized mammary gland epithelial cells and fibroblasts. Moreover, the swine H3N2 could infect the calves through intranasal infection, but not through oral infection, despite no obvious clinical signs and efficient transmission being observed. Our results demonstrate that other subtypes of IAVs can infect cattle and might pose threats to public and animal health.
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http://dx.doi.org/10.1128/mbio.03957-24 | DOI Listing |
PLoS Pathog
September 2025
State Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China.
Influenza B viruses (IBVs), though often overshadowed by influenza A viruses (IAVs), remain a significant global public health concern, particularly during seasons when they predominate. However, the molecular mechanisms underlying IBV pathogenicity remain largely unknown. In this study, we identified two amino acid substitutions, PB2-N460S and NP-I163T, from IBV clinical isolates with distinct replication and pathogenicity profiles.
View Article and Find Full Text PDFmSphere
September 2025
Influenza Division, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
The ferret model is widely used to study influenza A viruses (IAVs) isolated from multiple avian and mammalian species, as IAVs typically replicate in the respiratory tract of ferrets without the need for prior host adaptation. During standard IAV risk assessments, tissues are routinely collected from ferrets at a fixed time point post-inoculation to assess the capacity for systemic spread. Here, we describe a data set of virus titers in tissues collected from both respiratory tract and extrapulmonary sites 3 days post-inoculation from over 300 ferrets inoculated with more than 100 unique IAVs (inclusive of H1, H2, H3, H5, H7, and H9 IAV subtypes, both mammalian and zoonotic origin).
View Article and Find Full Text PDFJ Virol
September 2025
Laboratory of Ultrastructural Virology, Institute for Life and Medical Sciences, Kyoto University, Kyoto, Japan.
Double-stranded RNA (dsRNA), which induces an innate immune response against viral infections, is rarely detected in influenza A virus (IAV)-infected cells. Nevertheless, we previously reported that the influenza A viral ribonucleoprotein (vRNP) complex generates looped dsRNAs during RNA synthesis . This finding suggests that IAV possesses a specific mechanism for sequestering dsRNA within infected cells, thereby enabling viral evasion of the innate immune response.
View Article and Find Full Text PDFThe evolutionary dynamics of seasonal influenza A viruses (IAVs) have been well characterized at the population level, with antigenic drift known to be a major force in driving strain turnover. The evolution of IAV populations at the within-host level, however, is still less well characterized. Improving our understanding of within-host IAV evolution has the potential to shed light on the source of new strains, including new antigenic variants, at the population level.
View Article and Find Full Text PDFCurr Microbiol
August 2025
Department of Biotechnology, Quaid-I-Azam University, Islamabad, 45320, Pakistan.
The emergence of zoonotic infections in humans is intensifying the need for awareness of the viruses circulating in animals that can cross the species barrier. Among these are the group of influenza viruses causing seasonal outbreaks and epidemics in humans and animals. As compared to the familiar human and avian influenza viruses, bat influenza viruses are relatively unknown.
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