Literature detail

Genomic signatures and host adaptation of H5N1 clade 2.3.4.4b: A call for global surveillance and multi-target antiviral strategies.

Guangxu Zhang1 Yuren Shi1 Haoyu Ge1 Yuanzhou Wang1 Lu Lu1 Shibo Jiang1 Qian Wang1
Affiliations 1 institutions
  1. Key Laboratory of Medical Molecular Virology (MOE/NHC/CAMS), Shanghai Institute of Infectious Disease and Biosecurity, School of Basic Medical Sciences, Shanghai Public Health Clinical Center, Fudan University, Shanghai, China.
PMID 40177627 2025 Curr Res Microb Sci eng epublish
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Article

Publication summary

The recent report of the first fatality associated with infection by influenza virus H5N1 clade 2.3.4.4b, identified as genotype D1.1, which is distinct from the B3.13 genotype, has sparked fears of a potential human pandemic. However, the genetic relationships between B3.13 and D1.1, as well as their origins, host adaptability, and antiviral resistance, remain poorly understood. Here we conducted a comprehensive phylogenetic and comparative analysis of H5N1 clade 2.3.4.4b across multiple species, in order to identify the molecular characteristics and frequency of resistance mutations in these two genotypes, elucidate their evolutionary trajectories, and assess their implications for public health. Our results demonstrate that B3.13 exhibits mammalian adaptability, while D1.1 retains avian adaptability. Importantly, both genotypes display limited occurrences of human-like signatures, which can help alleviate public anxiety. Additionally, the emergence of the resistance mutations in the clade 2.3.4.4b on the binding sites of antivirals calls for the development of multi-target antiviral strategies to mitigate the risk of resistant strain reassortment.

Antiviral resistance mutation Cross-species substitution Genomic signature H5N1 clade 2.3.4.4b Influenza virus

Structured evidence records

Evidence records

3 total
1 records
Extraction confidence 0.90
Key finding

Phylogenetic and comparative genomic analyses of H5N1 clade 2.3.4.4b revealed evolutionary differences between genotypes B3.13 and D1.1, showing mammalian versus avian adaptation patterns.

Virus
Host
Not specified
Location
Not specified
Supporting text

Here we conducted a comprehensive phylogenetic and comparative analysis of H5N1 clade 2.3.4.4b across multiple species, in order to identify the molecular characteristics and frequency of resistance mutations in these two genotypes, elucidate their evolutionary trajectories, and assess their implications for public health.

Analysis methods
phylogenetic analysis; comparative analysis
1 records
Extraction confidence 0.95
Key finding

Influenza virus H5N1 clade 2.3.4.4b genotype B3.13 shows molecular adaptation toward mammalian hosts, while genotype D1.1 remains adapted to avian hosts and both display resistance mutations affecting antiviral binding sites.

Virus
Host
Not specified
Location
Not specified
Supporting text

Our results demonstrate that B3.13 exhibits mammalian adaptability, while D1.1 retains avian adaptability. Additionally, the emergence of the resistance mutations in the clade 2.3.4.4b on the binding sites of antivirals calls for the development of multi-target antiviral strategies.

Mechanism types
host_adaptation; antiviral_resistance
1 records
Extraction confidence 0.70
Key finding

The study highlights a risk of resistant strain reassortment within H5N1 clade 2.3.4.4b genotypes, suggesting reassortment as a mechanism of potential viral emergence or altered host adaptation.

Virus
Host
Not specified
Location
Not specified
Supporting text

The abstract states that 'the emergence of the resistance mutations in the clade 2.3.4.4b on the binding sites of antivirals calls for the development of multi-target antiviral strategies to mitigate the risk of resistant strain reassortment.'

Event type
reassortment