ISSN: 0973-7510

E-ISSN: 2581-690X

Research Article | Open Access
Deepak Kumar Pankaj1, Manoj Kumar1 , Shanmugasundaram Nagarajan1, Chakradhar Tosh1, Harshad V. Murugkar1, K. Rajukumar1, Megha Sharma2, Shefali Udayakumar Tiwari1, Kumar Gaurav1,
Pushpendra Kumar Namdeo1 and Aniket Sanyal1
1ICAR-National Institute of High Security Animal Diseases (NIHSAD), WOAH Reference Laboratory for Avian Influenza, Bhopal, Madhya Pradesh, India.
2ICAR-Indian Veterinary Research Institute, Izatnagar, Bareilly, Uttar Pradesh, India.
Article Number: 11559 | © The Author(s). 2026
J Pure Appl Microbiol. 2026;20(2):1706-1714. https://doi.org/10.22207/JPAM.20.2.58
Received: 13 March 2026 | Accepted: 20 April 2026 | Published online: 05 June 2026
Issue online: June 2026
Abstract

Avian influenza (AI), especially H5Nx viruses of clade 2.3.4.4b gained global attention due to their rapid evolution and widespread circulation. The infection by this clade have been documented in mammals held in captivity and the wild, together with confirmed human cases, which suggest its expansion of host range. Using the guinea pig as an in vivo transmission model, this study examined the susceptibility, viral shedding, and in-contact transmission of H5N1 virus isolate (A/duck/India/11TR05/2021) belonging to clade 2.3.4.4b. Six guinea pigs (infection subgroup) were given an intranasal dose of 106 EID50, and another six naive guinea pigs (transmission subgroup) were co-housed 24 hours post-infection. Specimens from nasal washing have been taken up to 14 dpi to evaluate viral transmission and shedding. Every day, clinical symptoms were evaluated, while viral RNA in nasal washing samples and seroconversion were evaluated by RT-qPCR and hemagglutination inhibition assay, respectively. All animals (infection and transmission subgroup) remained clinically stable with no visible disease symptoms. All directly inoculated guinea pigs supported efficient replication of virus, with high viral RNA loads between 1 and 6 dpi. One contact animal had evidence of in-contact transmission, which showed progressive viral replication and seroconversion, while the remaining contact animals exhibited low-level or transient viral RNA detection without detectable antibody responses. This study reveals that the wild-type A/duck/India/11TR05/2021 H5N1 virus isolate belonging to clade 2.3.4.4b replicates efficiently in guinea pigs and has a limited transmission capacity to in-contact animals without prior mammalian adaptation. Continued molecular surveillance and experimental transmission studies are essential to detect early indicators of increased mammalian transmissibility and pandemic risk.

Keywords

Highly Pathogenic Avian Influenza, In-contact Transmission, Mammalian Adaptation, Pandemic Risk, Viral Shedding

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© The Author(s) 2026. Open Access. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License which permits unrestricted use, sharing, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.