Tuesday, January 13, 2026

Humoral #immunity after #LP81 monovalent #vaccines against a broad range of #SARS-CoV-2 #variants including #XEC, LP.8.1, NB.1.8.1, #XFG, and #BA32

 


{Excerpt}

In the spring of 2025, multiple SARS-CoV-2 Omicron JN.1 subvariants were circulating, with LP.8.1 among the major variants. Pharmaceutical companies, such as Pfizer–BioNTech, Moderna, and Novavax–Takeda, adopted monovalent LP.8.1 for their 2025–26 season vaccines, following recommendations issued by WHO in May, 2025. As of November, 2025, SARS-CoV-2 variants including LP.8.1, XEC, NB.1.8.1, and XFG—all designated as variants under monitoring—were circulating. In terms of the spike gene, these variants, as well as LP.8.1, are derived from JN.1. Moreover, BA.3.2, a BA.3 descendant bearing multiple mutations in its spike gene, has potentially been spreading and exhibiting robust immune evasion. In Japan, the roll-out of the LP.8.1-based vaccination has progressed since the end of September, 2025. We previously reported the humoral immunity induced by the XBB.1.5-based monovalent vaccine in 2023,6 and the JN.1-based monovalent vaccine in 2024 in the Japanese population. We investigated the efficiency of humoral immunity induced by two LP.8.1-based vaccines, the mRNA vaccine from Pfizer–BioNTech and the recombinant protein-based vaccine from Novavax–Takeda, in Japan. Of note, the Novavax SARS-CoV-2 vaccine strain was updated to LP.8.1 only in Japan in 2025, whereas the formulation remains unchanged from JN.1 globally outside of Japan.

(...)

Source: 


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Intranasal #replicon #vaccine establishes mucosal #immunity and protects against #H5N1 and #H7N9 #influenza

 


Abstract

Seasonal and pandemic influenza viruses are continuous threats to human health, requiring rapid development of vaccines to multiple evolving viral strains. RNA vaccine technologies have the adaptability and manufacturability to facilitate pandemic preparedness but have limited flexibility in their route of administration, reducing the ability to establish local protective immune responses such as respiratory mucosal immunity. Here, we describe monovalent and bivalent replicon vaccines against A/Vietnam/1203/2004 H5N1 and A/Anhui/PA-1/2013 H7N9. These replicon vaccines express either H5 or H7 hemagglutinin and are formulated with a nanostructured lipid carrier (NLC) that permits both intramuscular (IM) and intranasal (IN) dosing. In mice, IM vaccination established systemic humoral and cellular responses but no detectable mucosal response, while IN administration induced robust systemic and mucosal immunity. The replicon-NLC vaccines protected against morbidity and mortality in ferret challenge models, establishing this intranasally-administered replicon-NLC vaccine platform as a potential pandemic response tool.

Source: 


Link: https://www.nature.com/articles/s41467-025-64829-6

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Monday, January 12, 2026

Novel recombinant H5-based #vaccine provides effective protection against #H5N1 #influenza virus in #cats

 


Abstract

The emergence and broad circulation of highly pathogenic avian influenza (HPAI) H5N1 virus in wild birds and its spillover into dairy cows with sustained transmission in this species pose a major risk to felines, which are highly susceptible and often succumb to the infection. Here, we developed a novel recombinant hemagglutinin H5-based vaccine and evaluated its safety, immunogenicity, and protective efficacy against HPAI H5N1 virus in domestic cats. Immunization of cats with H5-vaccine candidate elicited robust levels of neutralizing antibodies against H5N1 virus and protection against disease, mortality, and infection upon H5N1 virus challenge. The vaccine-elicited immunity significantly reduced virus shedding and viremia, limiting systemic spread and disease severity in immunized animals. Importantly, beyond protecting susceptible felids, vaccinating cats against the H5N1 virus could also reduce the risk of human exposure - underscoring the One Health impact of implementing such a vaccination strategy in feline populations.

Source: 


Link: https://www.nature.com/articles/s41541-025-01369-6

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#Iraq - High pathogenicity avian #influenza #H5N1 viruses (Inf. with) (#poultry) - Immediate notification

 


A layer poultry farm (located near small rivers, ponds, and migratory birds) began showing clinical signs of an outbreak of highly pathogenic avian influenza in its hens. These signs included pale combs and wattles, followed by increased mortality. The farm owner contacted the veterinary clinic in Taji, near Baghdad. A team of veterinarians was formed, samples were taken, and sent to the central laboratory for PCR testing. Control measures were initiated, including a ban on the movement of poultry. The entire flock will be culled in accordance with the procedures stipulated in Animal Health Law No. 32 of 2013, which mandates the culling of poultry infected with highly pathogenic avian influenza.

Source: 


Link: https://wahis.woah.org/#/in-review/7181

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#Hungary - High pathogenicity avian #influenza #H5N1 viruses (Inf. with) (#poultry) - Immediate notification

 


A breeding goose holding in NĂ³grĂ¡d Region.

Source: 


Link: https://wahis.woah.org/#/in-review/7185

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#Latvia - #Influenza A #H5N2 viruses of high pathogenicity (Inf. with) (non-poultry including wild birds) (2017-) - Immediate notification



Mallards in Saldus Region.

 Birds tested in frame of EFSA call project for Establishing capacities for active surveillance of highly pathogenic avian influenza in wild birds in Europe.

Source: 


Link: https://wahis.woah.org/#/in-review/7187

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Broadly neutralizing monoclonal #antibodies against #influenza A viruses: current #insights and future directions

 


Abstract

Monoclonal antibodies (mAbs) have become attractive tools for both the treatment and prevention of influenza A viruses due to their ability to target several viral components, which confers broad therapeutic potential. Advances in biotechnology, such as hybridoma technology, phage display technology, B cell immortalization, and artificial intelligence (Al)-driven antibody design, have significantly accelerated the development of effective mAbs. Clinical trials have shown that mAbs can improve clinical outcomes particularly in high-risk and immunocompromised populations by lowering viral loads and reducing disease severity. However, high production costs, the need for intravenous administration, and the risk of viral escape mutations are some of the obstacles to widespread clinical adoption. Post-marketing surveillance serves as a valuable source of information regarding safety, real-world effectiveness, and patterns of resistance. Broadly neutralizing antibodies (bnAbs), particularly those directed against conserved regions of the virus’s surface proteins, such as hemagglutinin (HA) and neuraminidase (NA), have demonstrated efficacy against antigenic drift-derived variants. Nevertheless, the emergence of escape mutants underscores the need for careful monitoring of mAb candidates and combination therapy. Monitoring genomic shifts requires a careful focus on the targeted regions affected by combination therapy. Challenges in accessibility are compounded by financial barriers, emphasizing the importance of large-scale production and alternative delivery methods, such as inhaled mAbs. To ensure that future mAb-based therapies for influenza A are both effective and accessible, it is critical to integrate resistance surveillance tools, monitoring AI, and advanced computational modeling in therapeutic strategies. This comprehensive review discusses the potential of mAbs to enhance influenza A treatment by offering precise and adaptable alternatives to traditional antivirals. It also examines recent technological advances, clinical performance, and scalability that may redefine future therapeutic strategies.

Source: 


Link: https://www.frontiersin.org/journals/microbiology/articles/10.3389/fmicb.2025.1738181/full

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Sunday, January 11, 2026

The Tribute Money, Titian (1516)

 


Public Domain.

Source: 


Link: https://www.wikiart.org/en/titian/the-tribute-money-1516

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#Clinical Features and #Management of a Critical #Human Case of #H10N3 Avian #Influenza: A Case Report and Literature Review

 


Highlights

• Nonspecific early signs hinder prompt diagnosis of H10N3 infection.

• H10N3 human infection remains rare but with high clinical severity.

• All patients had bird exposure and developed fever, cough, and dyspnoea.

• Diagnosis was confirmed by sequencing; imaging revealed viral pneumonia.


Abstract

Background

Since the first human case of H10N3 Avian Influenza in Jiangsu, China (April 2021), three cases have been reported globally. However, clinical and treatment data remain limited. Therefore, we describe the fourth patient’s epidemiology, clinical manifestations, diagnostics, treatment.

Case presentation

A 23-year-old woman, previously well, presented on 12 Dec 2024 with fever, dry cough and breathlessness after pig and chicken contact. CT showed bilateral pneumonia. Despite high-flow oxygen and broad-spectrum antibiotics she deteriorated, requiring intubation, lung-protective ventilation and VV-ECMO. Bronchoalveolar lavage isolated H10N3 influenza virus. Treatment with oseltamivir and baloxavir plus prone-position ventilation led to clinical improvement.

Conclusion

Due to its nonspecific early symptoms, H10N3 is difficult to diagnose promptly, increasing the risk. Early recognition, antiviral therapy, and aggressive support are essential in managing severe infections.

Source: 


Link: https://www.ijidonline.com/article/S1201-9712(26)00002-0/fulltext

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#Coronavirus Disease Research #References (by AMEDEO, Jan. 11 '26)

 


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    PubMed        

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    Target Trial Emulation of Oral Antivirals for B-Cell-Depleted COVID-19 Patients-Reply to Chen et al.
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    Macrolide-Resistant Mycoplasma pneumoniae in Children, Ohio, USA.
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    SARS-CoV-2 infection rates among home dialysis patients and patients receiving hemodialysis at outpatient centers, January 2021-May 2023, United States.
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    J Infect

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    Humoral and cellular immunogenicity of COVID-19 vaccine boosters in participants with advanced HIV disease.
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    J Med Virol

  9. HUANG CY, Cheng CC, Chen SH, Cheng D, et al
    SARS-CoV-2 Spike Protein-Mediated Cardiac Dysfunction: Structural Abnormalities, Impaired Calcium Dynamics, and Gene Expression Changes in Human Stem Cell-Derived Cardiomyocytes.
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    J Virol

  10. ZHANG Z, Zeng Y, Lv Y, Li X, et al
    Salvianolic acid A exerts antiviral effects by targeting the S protein, a virulence factor of porcine epidemic diarrhea virus.
    J Virol. 2026 Jan 8:e0204325. doi: 10.1128/jvi.02043.
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  11. MASTERS PS
    Coronavirus genome packaging and nucleocapsid assembly.
    J Virol. 2026 Jan 8:e0133025. doi: 10.1128/jvi.01330.
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  12. HAZELL NC, Reyna RA, Adam A, Bonam SR, et al
    mRNA-delivered neutralizing antibodies confer protection against SARS-CoV-2 in animal models.
    J Virol. 2026 Jan 7:e0189725. doi: 10.1128/jvi.01897.
    PubMed         Abstract available


    JAMA

  13. PRASAD V, Makary MA
    FDA Labeling Change for mRNA COVID-19 Vaccines-Reply.
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    PubMed        

  14. MEYEROWITZ EA
    FDA Labeling Change for mRNA COVID-19 Vaccines.
    JAMA. 2026 Jan 7. doi: 10.1001/jama.2025.21752.
    PubMed        


    Science

  15. KUPFERSCHMIDT K
    New conflicts erupt over key virus database.
    Science. 2026;391:116-117.
    PubMed         Abstract available

  16. CAVANAGH PE, Xue AG, Dai SA, Qiang A, et al
    Computational design of conformation-biasing mutations to alter protein functions.
    Science. 2026 Jan 8:eadv7953. doi: 10.1126/science.adv7953.
    PubMed         Abstract available

#Influenza and Other Respiratory Viruses Research #References (by AMEDEO, Jan. 11 '26)

 


    Ann Intern Med

  1. TERAN-PLASENCIA JM, Kalil AC
    In adults hospitalized with acute HF, predischarge influenza vaccination reduced a composite of mortality or readmission at 1 y.
    Ann Intern Med. 2026 Jan 6. doi: 10.7326/ANNALS-25-04799.
    PubMed         Abstract available

  2. TONG SYC, Gibney KB
    In older adults, high- vs. standard-dose influenza vaccine reduced hospitalization for influenza or pneumonia.
    Ann Intern Med. 2026 Jan 6. doi: 10.7326/ANNALS-25-05209.
    PubMed         Abstract available


    Arch Virol

  3. YAN Y, Pan Z, Mao L, Niu P, et al
    Genome surveillance of SARS-CoV-2 Omicron XBB subvariants in Wuhan in June 2023.
    Arch Virol. 2026;171:38.
    PubMed         Abstract available


    Biochem Biophys Res Commun

  4. HUANG A, Li C, Wu H, Sun W, et al
    Development of human single-domain antibodies against influenza based on NA-targeting IgG.
    Biochem Biophys Res Commun. 2026;798:153238.
    PubMed         Abstract available

  5. PARLAYAN C, Saadat KASM, Tekayev M, Barez SR, et al
    Leveraging genomic conservation in emerging SARS-CoV-2 variants for precision diagnostics, vaccines, and RNAi therapeutics.
    Biochem Biophys Res Commun. 2026;797:153176.
    PubMed         Abstract available


    BMC Pediatr

  6. MOREIRA RRB, Pereira HMD, Bernardes ALF, Altafini DD, et al
    Surveillance of bloodstream infections in pediatric patients for 11 years: what was the COVID-19 impact?
    BMC Pediatr. 2025;26:11.
    PubMed         Abstract available


    Cell

  7. REFFSIN S, Miller J, Ayyanathan K, Dunagin MC, et al
    Single-cell susceptibility to viral infection is driven by variable cell states.
    Cell. 2026;189:179-195.
    PubMed         Abstract available


    Epidemiol Infect

  8. CAMPOS MENA S, Perez-Gimeno G, Lorusso N, Alvarez Rio V, et al
    Monitoring effectiveness of nirsevimab immunization against RSV hospitalization using surveillance data: a test-negative case-control study, Spain, October 2024-March 2025.
    Epidemiol Infect. 2025;154:e5.
    PubMed         Abstract available

  9. JARRATT R, Clough H, Wilkinson E, Vivancos R, et al
    The Eat-Out-to-Help-Out incentive: A trigger for gastrointestinal infections in England, 2020?
    Epidemiol Infect. 2025;154:e3.
    PubMed         Abstract available

  10. JIMENEZ-RICO MA, Novelo-Perez DF, Puch-Magana CI, Manrique-Puch RA, et al
    Respiratory virus dynamics in a tropical region: Insights from Yucatan, Mexico (2018-2024).
    Epidemiol Infect. 2026;154:e7.
    PubMed         Abstract available

  11. MURAKAMI M, Yamagata M, Miura A
    The impact of COVID-19 infection experience on risk perception and preventive behaviour: a cohort study.
    Epidemiol Infect. 2026;154:e4.
    PubMed         Abstract available


    J Epidemiol Community Health

  12. CAMACHO C, Bower P, Webb RT, Munford L, et al
    Assessing the relationship between community resilience and health outcomes: an observational local-authority level study in England.
    J Epidemiol Community Health. 2026;80:73-79.
    PubMed         Abstract available

  13. FONG WLE, Beale S, Nguyen V, Kovar J, et al
    Estimating the risk of post-COVID condition in deprived communities, migrants and ethnic minorities in England: findings from Virus Watch-a prospective community cohort study.
    J Epidemiol Community Health. 2026;80:114-121.
    PubMed         Abstract available


    J Infect

  14. YUE M, Lee S, Tao S, Tomazetto G, et al
    Upper airway transcriptomics early after SARS-CoV-2 infection to identify individuals likely to develop symptomatic infection.
    J Infect. 2025;92:106664.
    PubMed         Abstract available

  15. KELLY E, Greenland M, de Whalley P, Macaulay GC, et al
    Reactogenicity and Immunogenicity following Heterologous and Homologous Third Dose COVID-19 vaccination in UK Adolescents (Com-COV3): A Randomised Controlled Non-Inferiority Trial.
    J Infect. 2025 Dec 1:106663. doi: 10.1016/j.jinf.2025.106663.
    PubMed         Abstract available


    J Virol

  16. DALY RE, Feng CY, Hesser CR, Myasnikov I, et al
    N-terminal acetylation controls multiple functional aspects of the influenza A virus ribonuclease PA-X.
    J Virol. 2026 Jan 9:e0199925. doi: 10.1128/jvi.01999.
    PubMed         Abstract available

  17. PRASAI K, Yang Z, Guan M, Li T, et al
    Intrahost HA polymorphisms and culture adaptation shape antigenic profiles of H3N2 influenza viruses.
    J Virol. 2026 Jan 7:e0177525. doi: 10.1128/jvi.01775.
    PubMed         Abstract available

  18. BI Z
    Adaptation differences and mechanisms of influenza viruses to ANP32 proteins across species.
    J Virol. 2026 Jan 5:e0190025. doi: 10.1128/jvi.01900.
    PubMed         Abstract available


    J Virol Methods

  19. WANG J, Li R, Liu L, Yu J, et al
    Development and application of a real-time RT-PCR assay for the specific detection of influenza D virus.
    J Virol Methods. 2026;342:115338.
    PubMed         Abstract available


    N Engl J Med

  20. LASSEN MCH, Johansen ND, Christensen SH, Aliabadi N, et al
    RSV Prefusion F Vaccine for Prevention of Hospitalization in Older Adults.
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    Pediatrics

  21. HAYEK H, Noble EK, Stewart LS, Sahni LC, et al
    Influenza Vaccine Effectiveness Among Children With and Without Underlying Conditions.
    Pediatrics. 2026 Jan 9:e2025072184. doi: 10.1542/peds.2025-072184.
    PubMed         Abstract available


    PLoS Biol

  22. EALES O, McCaw JM, Shearer FM
    Modeling of H5N1 influenza virus kinetics during dairy cattle infection suggests the timing of infectiousness.
    PLoS Biol. 2026;24:e3003586.
    PubMed         Abstract available


    PLoS Comput Biol

  23. DAVIS CN, Hill EM, Jewell CP, Rysava K, et al
    A modelling assessment of the impact of control measures on highly pathogenic avian influenza transmission in poultry in Great Britain.
    PLoS Comput Biol. 2026;22:e1013874.
    PubMed         Abstract available

  24. WU SX, Davis CN, Arnold M, Tildesley MJ, et al
    The role of ducks in detecting Highly Pathogenic Avian Influenza in small-scale backyard poultry farms.
    PLoS Comput Biol. 2026;22:e1013357.
    PubMed         Abstract available


    PLoS One

  25. VALDIVIA-GAGO A, Garcia PJ, Harper SL, Soria A, et al
    "What's the point, when we're already dead?" Implementation challenges of COVID-19 public policies for indigenous peoples in the Peruvian Amazon: A sequential multi-method qualitative study.
    PLoS One. 2026;21:e0340774.
    PubMed         Abstract available

  26. WAGNER F, Kolanisi U, Wagner RG, Makuapane LP, et al
    Effect of returning home on university student hunger during South African COVID-19 lockdown.
    PLoS One. 2026;21:e0340350.
    PubMed         Abstract available

  27. BAGULEY E, Knaub M, VanDyke J, Hirschfield G, et al
    Evaluating the clinical care, quality of life and overall experiences of patients with primary biliary cholangitis (PBC) during the pandemic: A Canadian mixed-methods study.
    PLoS One. 2026;21:e0340475.
    PubMed         Abstract available

  28. TALBOT Q, Batung E, Yusuf I, Omorodion F, et al
    Stigma and labelling of immigrant personal support workers during COVID-19 pandemic in Ontario: Implications for policy.
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    PubMed         Abstract available

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    Aetiology and impact of bacterial bloodstream infections in mechanically ventilated COVID-19 patients: A prospective Swedish multicenter cohort study.
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  30. ABBAS S, Nasir JA, Sherwani RAK
    Estimating the economic burden of COVID-19 survivors in Punjab, Pakistan.
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    PubMed         Abstract available

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    Elevated mortality and upregulated SARS-CoV-2-associated pathways in innate and adaptive immune cells from individuals with Down syndrome.
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    PubMed         Abstract available


    Proc Natl Acad Sci U S A

  33. ZHANG R, Deng R, Liu S, Yao Q, et al
    Reconstructing the early spatial spread of pandemic respiratory viruses in the United States.
    Proc Natl Acad Sci U S A. 2026;123:e2518051123.
    PubMed         Abstract available

  34. VERMA AK, Tan L, Schuster N, Moye SL, et al
    Combination antiviral and anti-inflammatory therapy mitigates persistent neurological deficits in mice post SARS-CoV-2 infection.
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    PubMed         Abstract available

  35. ZHANG Y, Silvestre-Roig C, Fu H, Alimohamadi H, et al
    SARS-CoV-2 peptide fragments selectively dysregulate specific immune cell populations via Gaussian curvature targeting.
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    PubMed         Abstract available


    Vaccine

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    A systematic review of the impact of vaccine reactogenicity on willingness to accept influenza vaccination in adults.
    Vaccine. 2026;74:128195.
    PubMed         Abstract available

  37. YOKOYAMA Y, Yao S, Cozza R, Gil F, et al
    A novel calcium influx inducer and a TLR7 agonist are synergistic co-adjuvants that enhance cross-reactive immunity against influenza in young and aged mice.
    Vaccine. 2026;74:128189.
    PubMed         Abstract available

Saturday, January 10, 2026

#Haemagglutinin 162-164 #deletions enhance #influenza B/Victoria virus #fitness and #virulence in vivo

 


Abstract

Influenza B viruses cause substantial respiratory disease and seasonal outbreaks. Despite decades of circulation in humans, only the B/Victoria lineage persisted after the COVID-19 pandemic. Continual evolution has generated hemagglutinin deletion variants at residues 162-164 that drive successive epidemics, yet their functional consequences remain poorly understood. Using integrated phylodynamics and reverse genetics, we show that Clade V1A.1 viruses carrying a two-amino acid deletion exhibit enhanced replication and increased virulence compared with ancestral viruses lacking deletions. The recently prevailing Clade V1A.3, which harbors a three-amino acid deletion together with the K136E substitution, has completely displaced V1A.1 and causes more severe disease in mice. Both clades bound efficiently to alpha 2-3 and 2-6 sialylated glycans and exhibited broad tolerance to acidic pH and elevated temperatures. These findings reveal that specific combinations of HA deletions and substitutions confer pronounced fitness advantages to emerging variants, driving global selective sweeps, evolutionary success and long-term persistence of B/Victoria lineage, and posing challenges for vaccine efficacy and influenza control.


Competing Interest Statement

The authors have declared no competing interest.


Funder Information Declared

National Institutes of Health, 75N93021C00016

Ministry of Health Singapore, CS-IRG/MOH-000374

Ministry of Health Singapore, OF-LCG/MOH-000505-05

Source: 


Link: https://www.biorxiv.org/content/10.64898/2026.01.08.698527v1

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History of Mass Transportation: The Fiat FS ETR.401 Electric Multiple Unit

 


Di maurizio messa - Flickr: FS ETR401, CC BY-SA 2.0, https://commons.wikimedia.org/w/index.php?curid=20276434

Source: 


Link: https://it.wikipedia.org/wiki/Fiat_Ferroviaria

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Friday, January 9, 2026

#Pathogenesis and #Research #Models of Acute #Influenza-Associated #Encephalitis / #Encephalopathy: An Update

 


Abstract

Influenza-associated encephalitis/encephalopathy (IAE) is a severe neurological complication characterized by central nervous system dysfunction and structural damage following influenza virus infection. Predominantly affecting infants and young children, IAE exhibits its highest incidence in those under five years of age. Key clinical manifestations of IAE include acute seizures, sudden high fever, and impaired consciousness, frequently progressing to coma. Neuroimaging, particularly magnetic resonance imaging (MRI), often reveals multifocal brain lesions involving multiple brain regions, including the cerebellum, brainstem, and corpus callosum. The prognosis of IAE is poor, with a mortality rate reaching 30%. Current diagnosis relies heavily on clinical presentation and characteristic neuroimaging findings, as the precise pathogenesis of IAE remains elusive. While various research models, including cell lines, brain organoids, and animal models, have been developed to recapitulate IAE features, significant limitations persist in modeling the core clinical pathophysiology observed in pediatric patients, necessitating further model refinement. This review synthesizes the clinical spectrum of IAE, summarizes progress in understanding its pathogenesis, and critically evaluates existing research models. We aim to provide a foundation for utilizing experimental approaches to elucidate IAE mechanisms and identify potential therapeutic strategies.

Source: 


Link: https://www.mdpi.com/1999-4915/18/1/95

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#USA, #Wastewater Data for Avian #Influenza #H5 (#CDC, Jan. 8 '26)

 


{Excerpt}

Time Period: December 28, 2025 - January 03, 2026

-- H5 Detection3 site(s) (0.7%)

-- No Detection428 site(s) (99.3%)

-- No samples in last week111 site(s)




(...)

Source: 


Link: https://www.cdc.gov/nwss/rv/wwd-h5.html

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#Sweden - #Influenza A #H5N1 viruses of high pathogenicity (Inf. with) (non-poultry including wild birds) (2017-) - Immediate notification

 


{A barnacle goose} By Andreas Trepte - Own work, CC BY-SA 2.5, https://commons.wikimedia.org/w/index.php?curid=32487518

___

In accordance with the WOAH Terrestrial Animal Health Code, Article 10.4.1, point 4, this outbreak does not change the disease-free status of Sweden as these are wild birds or birds kept in a single household, and therefore do not fall within the WOAH definition of poultry.

{Sjöbo Region} A barnacle goose was killed. It was sent to the Swedish Veterinary Agency for laboratory analysis as part of the national surveillance program for avian influenza.

Source: 


Link: https://wahis.woah.org/#/in-review/7180

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#Philippines - High pathogenicity avian #influenza #H5 viruses (#poultry) (Inf. with) - Immediate notification

 


Affected avian species were grazing ducks in Davao del Sur Region.

Source: 


Link: https://wahis.woah.org/#/in-review/7105

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Thursday, January 8, 2026

One confirmed and one potential #human case of #influenza #H5N1 detected through an expanded subtyping protocol

 


ABSTRACT

Current U.S. surveillance for highly pathogenic avian influenza A(H5N1) in humans prioritizes individuals with known animal exposures, potentially missing community-acquired infections. To address this gap, we implemented universal H5 subtyping of all influenza A-positive respiratory samples collected within our hospital system, regardless of patient exposure history. Between August 2024 and April 2025, we subtyped 4,488 influenza A-positive samples and identified two cases positive for H5 RNA in Alameda County, California, USA. The first case was a 14-month-old girl with mild respiratory symptoms and no H5N1 exposure risks; sequencing of the sample revealed an H5 gene closely related to clade 2.3.4.4b, genotype B3.13 viruses circulating in U.S. dairies. The second case was a 79-year-old male, also with no known exposures, whose sample reproducibly tested positive with a high cycle threshold value but could not be confirmed by public health laboratories. Both patients had evidence of co-infection with other common respiratory viruses. These findings, while requiring cautious interpretation due to low virus levels and the presence of potential confounding factors, highlight limitations in exposure-based testing and demonstrate the potential for cryptic H5N1 circulation. This report underscores that broader, geographically targeted surveillance may be a critical tool for early detection of potential community transmission of pandemic-capable pathogens.

Source: 


Link: https://journals.asm.org/doi/10.1128/asmcr.00165-25

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Within-host adaptive #evolution is limited by genetic #drift in experimental #human #influenza A virus #infections

 


Abstract

Selection of advantageous mutations drives the emergence of dominant variants during seasonal influenza epidemics. However, within-host detection of such variants remains rare, limiting our understanding of how selection operates at the scale of individual hosts. In this study, we used a controlled human infection model to examine the within-host evolutionary dynamics in thirteen participants intranasally infected with a seasonal H3N2 influenza A virus. Although this clinical trial is ongoing, our work represents a pre-planned, interim, exploratory analysis. Results in this system were contrasted with those observed in a ferret model of infection. The inoculum, used in both humans and ferrets, carried standing diversity that enabled evaluation of variant trajectories during infection. Although the dynamics were variable among participants, in humans, the minor variants in the PA and NP gene segments tended to increase in frequency as infection progressed. Variant dynamics were more consistent among ferrets but showed differences from humans in the fate of the minor NP allele. Based on these observations, we fit a population genetic model to longitudinal measurements of variant frequencies. Estimates of variant selection coefficients and effective viral population sizes indicated that in humans the two minor variants had a selective advantage over the major variants, but genetic drift was strong, limiting the efficiency of selection. In ferrets, the PA minor variant also was estimated to have a selective advantage, while the NP minor variant was estimated to have a selective disadvantage. Moreover, effective viral population sizes were estimated to be considerably higher in ferrets than in humans, indicating that genetic drift was weaker in ferrets. Our analyses reveal differing selective environments acting on influenza viruses in human and ferret hosts and indicate that selection at the within-host level is weakened by genetic drift.


Competing Interest Statement

The authors have declared no competing interest.

Source: 


Link: https://www.biorxiv.org/content/10.64898/2026.01.07.698006v1

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#Poland - High pathogenicity avian #influenza #H5N1 viruses (Inf. with) (#poultry) - Follow up report 2

 


Poultry farms in Podlaskie Region.

Source: 


Link: https://wahis.woah.org/#/in-review/7177

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