A cross-sectional #study of avian #influenza virus in #poultry #markets of #Guangdong #China, 2025

 

Abstract

Background: 

Guangdong, China is a critical epicenter for avian influenza virus (AIV) emergence, where H5N1 and highly pathogenic H7N9 were first identified. Monitoring AIV genotype distribution and genetic diversity in this region is essential for providing early warnings and mitigating the risk of human infections.

Methods: 

In May 2025, a cross-sectional study was conducted across 4 representative cities in Guangdong. We collected 500 environmental swabs and 45 wastewater samples from 23 live poultry markets (LPMs). Samples were screened for influenza A virus (IAV) and subtyped for H5, H7, and H9. Next generation sequencing (NGS) and phylogenetic analyses were employed to characterize viral diversity and zoonotic potential.

Results: 

AIV was detected in 49.2% (246/500) of environmental samples. H9 was the dominant subtype (38.2%), followed by H5 (3.2%) and H7 (0.8%); 2.4% of positive samples showed multi-subtype co-occurrence. “Non-restricted zone” markets (80.0%) and “waste storage areas” (68.4%) were identified as primary contamination hotspots. Phylogenetic analysis revealed that H5 and H9 viruses are accumulating mutations linked to enhanced human-type receptor affinity. Notably, H5 and H6 sequences exhibited long internal branches and clustered with isolates from other Asian countries rather than domestic strains, highlighting a significant gap in current domestic molecular surveillance and a lack of continuous evolutionary data for these genotypes.

Conclusions: 

Widespread AIV contamination persists in Guangdong LPMs, dominated by H9 with low-level circulation of highly pathogenic subtypes. The identified surveillance gaps for H5/H6 and the presence of multi-subtype environments underscore the urgent need for strengthened, integrated molecular monitoring and stricter market regulation to mitigate public health risks.

Source: 

Link: https://www.frontiersin.org/journals/cellular-and-infection-microbiology/articles/10.3389/fcimb.2026.1914072/full

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Egyptian rousette #bat humoral #immunity to #H9 #influenza hemagglutinin

 

Abstract

In mammals, antibodies are central to antiviral defense, but they can also impose selective pressure that drives viral evolution. The interplay between viral antigenic variation and host antibody diversification constitutes a molecular arms race that influences pathogenicity, transmission, and spillover risk. Bats are reservoirs for zoonotic viruses with pandemic potential yet they appear to tolerate infection without overt disease. Although distinctive features of bat innate immunity have been described, the role of adaptive immunity, particularly antibody-mediated responses, remains largely undefined. Moreover, how antibody evolutionary pressure operates in bats is unknown, in part because tools to interrogate bat B cell responses at the monoclonal level are limited. Here, we developed a yeast surface display library of bat antibodies derived from splenic RNA of wild-caught Egyptian rousette bats to interrogate humoral responses to the bat-derived H9 influenza hemagglutinin. We isolated monoclonal antibodies recognizing the hemagglutinin (HA) antigen and defined their gene usage, somatic hypermutation frequency, binding affinities, and breadth. We then used cryo-EM to structurally characterize three bat antibodies in complex with HA engaging distinct antigenic sites. Together, these data enable direct comparison with human anti-influenza antibodies highlighting similarities in humoral immunity across mammals and provides a tool to examine bat antibody responses to other potential zoonotic viruses.

Competing Interest Statement

The authors have declared no competing interest.

Source: 

Link: https://www.biorxiv.org/content/10.64898/2026.06.04.730146v1

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#Replication and #Transmission of #Influenza A Virus in Farmed #Mink

 

Abstract

Farmed mink are frequently exposed to circulating influenza A viruses (IAVs), as confirmed by viral isolation and serological evidence. Previous work reveals that naïve mink serve as susceptible hosts for both avian and human influenza strains, highlighting their potential role in influenza ecology. In this study, we investigated whether farmed mink naturally pre-exposed to H9 retain the capacity to serve as “mixing vessels” for reassorting human and avian IAVs. Our results demonstrate that they remain fully susceptible and permissive to infection by both avian H6N6 and human H1N1 influenza strains. Notably, efficient transmission of these viruses occurred among farmed mink, confirming their potential to sustain viral exchange. These findings indicate that farmed mink represent highly permissive hosts capable of facilitating reassortment between circulating human and avian IAVs. Given this risk, current mink farming practices may substantially increase the likelihood of a pandemic emergence. We therefore urge immediate revision, stringent enhancement, and rigorous enforcement of biosecurity protocols and active surveillance systems in fur farming operations.

Source: 

Link: https://www.mdpi.com/1999-4915/18/1/9

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Divergent #antibody-mediated #population #immunity to #H5, #H7 and #H9 subtype potential #pandemic #influenza viruses

 

Abstract

Influenza continues to cause significant mortality globally and possesses substantial pandemic potential. Assessing pandemic risk requires a clear understanding of existing population immunity. Leveraging a unique large-scale cohort of human sera, we evaluated total and neutralising antibody-mediated immunity to multiple haemagglutinin (HA) proteins, including those from subtypes with high pandemic potential. Our analysis reveals that population immunity is heterogeneous, with distinct age-dependent differences in responses to H5, H7, and H9 avian influenza subtypes. These shifts align with historical circulation patterns of seasonal H1N1 and H3N2 human viruses. Notably, H7 viruses are primarily neutralised through head domain epitopes, while H5 viruses are targeted mainly via stem epitopes, although in both instances some neutralisation occurred via receptor binding site-adjacent epitopes. Furthermore, H7 responses were dominated by non-glycan-targeted IgG2 antibodies, whereas H5 responses were primarily IgG1-mediated. These findings highlight varying levels of susceptibility to influenza across the population, supporting vaccination approaches informed by exposure history.

Competing Interest Statement

CPT has received lecture fees from Moderna.

Funding Statement

J.S.B. was supported by funding from the Biotechnology and Biological Sciences Research Council (BBSRC) doctoral training programme grant [grant number BB/M011224/1]. R.S. is funded by a Medical Research Council Impact Accelerator Account grant [grant ref MR/X502674/1]. RG was funded by The Institute for Global Pandemic Planning at the University of Warwick, UK, as part of a philanthropically supported doctoral programme. K.C. was funded via the Medical Research Council doctoral training programme grant [MC_UP_A025_1011]. L.H. was funded by a Defence and Science Technology Laboratory grant [grant ref RQ31692]. U.O. and C.P.T. acknowledge funding from the British Council ISFP scheme [grant number 47650215]. N.C.R. is supported by a Royal Society Dorothy Hodgkin Research Fellowship [grant number DHR00620].

Source: MedRxIV, https://www.medrxiv.org/content/10.1101/2025.09.08.25335309v1

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