Saturday, September 6, 2025

#Coronavirus Disease Research #References (by AMEDEO, September 6 '25)

 


    Am J Obstet Gynecol

  1. ROSSEN LM, Hoyert DL, Horon I, Branum AM, et al
    Trends in Maternal Mortality Rates by State, United States, 2018-2023.
    Am J Obstet Gynecol. 2025 Aug 28:S0002-9378(25)00585.
    PubMed         Abstract available


    Antiviral Res

  2. BI W, Zhu T, Xu Y, Chen Y, et al
    An engineered chimeric ACE2-HR2 peptide exhibits potent and broad-spectrum activity against SARS-CoV-2 variants.
    Antiviral Res. 2025;242:106265.
    PubMed         Abstract available

  3. ICHIKAWA T, Tamura T, Nao N, Suzuki H, et al
    Characterization of remdesivir resistance mutations in COVID-19 patients with various immunosuppressive diseases.
    Antiviral Res. 2025;242:106264.
    PubMed         Abstract available

  4. TASHIMA R, Kuroda T, Nobori H, Miyagawa S, et al
    Ensitrelvir suppresses prolonged olfactory abnormalities derived from SARS-CoV-2 infection in hamsters.
    Antiviral Res. 2025 Sep 2:106270. doi: 10.1016/j.antiviral.2025.106270.
    PubMed         Abstract available

  5. ZHU C, Wang Z, Pan Z, Mai X, et al
    DMBT1 promotes SARS-CoV-2 infection and its SRCR-derived peptide inhibits SARS-CoV-2 infection.
    Antiviral Res. 2025 Sep 3:106269. doi: 10.1016/j.antiviral.2025.106269.
    PubMed         Abstract available


    BMJ

  6. DEWIDAR O, Shamseer L, Melendez-Torres GJ, Akl EA, et al
    Improving the reporting on health equity in observational research (STROBE-Equity): extension checklist and elaboration.
    BMJ. 2025;390:e083882.
    PubMed         Abstract available


    Clin Infect Dis

  7. DRAGHIA-AKLI R, Hill NM, Altevogt B, Bradley K, et al
    The Indispensable Value of Small-Molecule Antivirals in Epidemic and Pandemic Preparedness.
    Clin Infect Dis. 2025 Sep 1:ciaf476. doi: 10.1093.
    PubMed         Abstract available

  8. CHAICHANA U, Man KKC, Ju C, Makaronidis J, et al
    Effect of Metformin on the Risk of Post-coronavirus Disease 2019 Condition Among Individuals With Overweight or Obese: A Population-based Retrospective Cohort Study.
    Clin Infect Dis. 2025 Sep 1:ciaf429. doi: 10.1093.
    PubMed         Abstract available


    Int J Infect Dis

  9. FERNANDEZ-DE-LAS-PENAS C, Ruiz-Ruigomez M, Esparcia-Pinedo L, Colom-Fernandez B, et al
    Classical Pathway Persistent Complement Activation is Associated with Specific Symptoms in Individuals with Post-COVID-19 Condition: A Case-Control Study.
    Int J Infect Dis. 2025 Aug 28:108032. doi: 10.1016/j.ijid.2025.108032.
    PubMed         Abstract available

  10. SHANG L, Perniciaro S, Weinberger DM
    Changes in pneumococcal deaths in the United States following the COVID-19 pandemic.
    Int J Infect Dis. 2025 Aug 29:108020. doi: 10.1016/j.ijid.2025.108020.
    PubMed         Abstract available

  11. SIMONSEN L, Pedersen RK, Andreasen V, Krause TG, et al
    A Disease Suppression Strategy in Action: The Impact of Non-Pharmaceutical interventions in the COVID-19 pandemic in Denmark.
    Int J Infect Dis. 2025 Sep 2:108039. doi: 10.1016/j.ijid.2025.108039.
    PubMed         Abstract available

  12. SAGHAUG CS, Markussen DL, Knoop ST, Holvik BC, et al
    Diagnostic Accuracy of a Host Response Test in Suspected Community-Acquired Pneumonia During the COVID-19 Era.
    Int J Infect Dis. 2025 Sep 2:108045. doi: 10.1016/j.ijid.2025.108045.
    PubMed         Abstract available


    J Infect

  13. STANLEY J, Arnold D, Hamilton F
    Genetic evidence supports trialling IL-6 inhibition in influenza.
    J Infect. 2025 Aug 31:106606. doi: 10.1016/j.jinf.2025.106606.
    PubMed        

  14. PRITCHARD E, Vihta KD, Lipworth S, Pouwels KB, et al
    An Electronic Health Record-Wide Association Study to identify populations at increased risk of E. coli bloodstream infections.
    J Infect. 2025 Sep 3:106612. doi: 10.1016/j.jinf.2025.106612.
    PubMed         Abstract available


    J Med Virol

  15. MAK WA, Wapperom D, Redel AL, Koeleman JGM, et al
    Seasonal Coronavirus-Induced Immunological Imprinting and Previous Herpesvirus Infections in Patients With Long COVID.
    J Med Virol. 2025;97:e70582.
    PubMed         Abstract available


  16. Correction to "Modeling Antibody Kinetics Post-mRNA Booster Vaccination and Protection Durations Against SARS-CoV-2 Infection".
    J Med Virol. 2025;97:e70590.
    PubMed        

  17. HOSSEINI ST, Mahmanzar M, Rahimian K, Bayat S, et al
    Spatial Transcriptomics and Single Cell-RNASeq Reveals Cellular Heterogeneity of SARS-CoV-2 in Lung Tissues and Global Mutational Patterns in COVID-19 Patients.
    J Med Virol. 2025;97:e70586.
    PubMed         Abstract available


    J Virol

  18. GRACIE NP, Aggarwal A, Luo R, Spicer M, et al
    An RGD motif on SARS-CoV-2 Spike induces TGF-beta signaling and downregulates interferon.
    J Virol. 2025 Sep 4:e0043525. doi: 10.1128/jvi.00435.
    PubMed         Abstract available

  19. JOSEPH R, Marais G, Iranzadeh I, Alisoltani A, et al
    Intra-host SARS-CoV-2 diversity in immunocompromised people living with HIV provides insight into the evolutionary trajectory of SARS-CoV-2.
    J Virol. 2025 Sep 5:e0078025. doi: 10.1128/jvi.00780.
    PubMed         Abstract available


    JAMA

  20. SURIE D, Self WH, Yuengling KA, Lauring AS, et al
    RSV Vaccine Effectiveness Against Hospitalization Among US Adults Aged 60 Years or Older During 2 Seasons.
    JAMA. 2025 Aug 30:e2515896. doi: 10.1001/jama.2025.15896.
    PubMed         Abstract available

  21. ANDERER S
    Breaking From CDC, ACOG Continues Recommending COVID-19 Vaccine During Pregnancy.
    JAMA. 2025 Sep 5. doi: 10.1001/jama.2025.16943.
    PubMed        


    Lancet

  22. CHANG AY, Bolongaita S, Cao B, Castro MC, et al
    Epidemiological and demographic trends and projections in global health from 1970 to 2050: a descriptive analysis from the third Lancet Commission on Investing in Health, Global Health 2050.
    Lancet. 2025;406:940-949.
    PubMed         Abstract available


    Lancet Infect Dis

  23. VON LILIENFELD-TOAL M, Khawaja F, Compagno F, Robin C, et al
    Community-acquired respiratory virus infections in patients with haematological malignancies or undergoing haematopoietic cell transplantation: updated recommendations from the 10th European Conference on Infections in Leukaemia.
    Lancet Infect Dis. 2025 Aug 27:S1473-3099(25)00365.
    PubMed         Abstract available

  24. FOCOSI D, Maggi F
    Reassessing sotrovimab's role in COVID-19: insights and implications.
    Lancet Infect Dis. 2025 Aug 28:S1473-3099(25)00410.
    PubMed        


  25. Sotrovimab versus usual care in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial.
    Lancet Infect Dis. 2025 Aug 28:S1473-3099(25)00361.
    PubMed         Abstract available

#Influenza and Other Respiratory Viruses Research #References (by AMEDEO, September 6 '25)

 


    Antimicrob Agents Chemother

  1. YAMADA AY, de Souza AR, Madalosso G, de Assis DB, et al
    Emergence of carbapenem-resistant Acinetobacter baumannii clonal complex 2 in multiple hospitals in Sao Paulo state, Brazil.
    Antimicrob Agents Chemother. 2025 Jul 23:e0186524. doi: 10.1128/aac.01865.
    PubMed         Abstract available


    Biochemistry

  2. XIA H, Wei D, Guo Z, Chung LW, et al
    Machine Learning on the Impacts of Mutations in the SARS-CoV-2 Spike RBD on Binding Affinity to Human ACE2 Based on Deep Mutational Scanning Data.
    Biochemistry. 2025;64:3790-3800.
    PubMed         Abstract available


    Cell

  3. KONG W, Lu WJ, Dubey M, Suryawanshi RK, et al
    Neuroendocrine cells orchestrate regeneration through Desert hedgehog signaling.
    Cell. 2025;188:5020-5038.
    PubMed         Abstract available


    J Gen Virol

  4. POKHAREL BR, Majumdar N, Williams F, Dickerson A, et al
    SARS-CoV-2 infection of substantia nigra pars compacta induces expression of miR-330-5p at 10 days post-infection.
    J Gen Virol. 2025;106.
    PubMed         Abstract available

  5. BILLINGTON E, Di Genova C, Warren CJ, Thomas SS, et al
    Investigating factors driving shifts in subtype dominance within H5Nx clade 2.3.4.4b high pathogenicity avian influenza viruses.
    J Gen Virol. 2025;106:002150.
    PubMed         Abstract available


    J Infect

  6. STANLEY J, Arnold D, Hamilton F
    Genetic evidence supports trialling IL-6 inhibition in influenza.
    J Infect. 2025 Aug 31:106606. doi: 10.1016/j.jinf.2025.106606.
    PubMed        


    J Virol Methods

  7. LIM JY, Fiore A, Le B, Minzer C, et al
    Development and Validation of Novel Cell-free Direct Neutralization Assay for SARS-CoV-2.
    J Virol Methods. 2025;338:115201.
    PubMed         Abstract available

  8. WAGNER DD, Nabakooza G, Momin N, Marine RL, et al
    Illumina MiSeq and iSeq platforms yield comparable results for viral genomic sequencing.
    J Virol Methods. 2025;338:115202.
    PubMed         Abstract available

  9. LESCHINSKY G, Dexter WA, Leschinsky B, Trolinger J, et al
    Design and feasibility of a novel personal protection device against airborne pathogens for everyday use.
    J Virol Methods. 2025;338:115203.
    PubMed         Abstract available

  10. MORRISON EN, Harnden M, Boisvert E, Wilson AE, et al
    Towards efficient and targeted sampling of primary respiratory diseases from wastewater in congregate settings for seniors: Empowering high-risk demographics with prospective health threat data.
    J Virol Methods. 2025;338:115212.
    PubMed         Abstract available

  11. KATSANOVSKAJA K, Marchesin F, Ujetz J, Ijaz S, et al
    Beyond the limits of conventional 'endpoint' ELISA and rescuing the signal with lag k-ELISA.
    J Virol Methods. 2025;338:115231.
    PubMed         Abstract available

  12. ZENG L, Wang Y, Xiang B, Lin J, et al
    The dynamics of common respiratory pathogens in southern china under the context of COVID-19 pandemic and prediction of mycoplasma pneumonia (2018-2023).
    J Virol Methods. 2025;338:115240.
    PubMed         Abstract available

  13. GONZALEZ G S, Dias A, Reis R, Villalba S, et al
    Effective RNA extraction with readily available reagents: A comparative analysis of alternative protocols.
    J Virol Methods. 2025;338:115242.
    PubMed         Abstract available

  14. NAPOLITAN A, Mazzacan E, Fonti N, Tomasoni S, et al
    Cryopreservation of chicken and duck tracheal rings and precision-cut lung slices: A promising tool for the rapid characterization of avian influenza viruses.
    J Virol Methods. 2025;339:115257.
    PubMed         Abstract available


    Lancet

  15. ANDERSON CS, Hua C, Wang Z, Wang C, et al
    Influenza vaccination to improve outcomes for patients with acute heart failure (PANDA II): a multiregional, seasonal, hospital-based, cluster-randomised, controlled trial in China.
    Lancet. 2025 Aug 28:S0140-6736(25)01485-0. doi: 10.1016/S0140-6736(25)01485.
    PubMed         Abstract available

  16. BHATT AS, Vardeny O
    Influenza vaccination in heart failure: a shot worth taking?
    Lancet. 2025 Aug 28:S0140-6736(25)01679-4. doi: 10.1016/S0140-6736(25)01679.
    PubMed        


    MMWR Morb Mortal Wkly Rep

  17. TOBOLOWSKY FA, Morris E, Castro L, Schaff T, et al
    Highly Pathogenic Avian Influenza A(H5N1) Virus Infection in a Child with No Known Exposure - San Francisco, California, December 2024-January 2025.
    MMWR Morb Mortal Wkly Rep. 2025;74:522-527.
    PubMed         Abstract available


    N Engl J Med

  18. JOHANSEN ND, Modin D, Loiacono MM, Harris RC, et al
    High-Dose Influenza Vaccine Effectiveness against Hospitalization in Older Adults.
    N Engl J Med. 2025 Aug 30. doi: 10.1056/NEJMoa2509907.
    PubMed         Abstract available

  19. PARDO-SECO J, Rodriguez-Tenreiro-Sanchez C, Gine-Vazquez I, Mallah N, et al
    High-Dose Influenza Vaccine to Reduce Hospitalizations.
    N Engl J Med. 2025 Aug 30. doi: 10.1056/NEJMoa2509834.
    PubMed         Abstract available


    Pediatrics

  20. FREE RJ, Patel K, Taylor CA, Sachdev D, et al
    Hospitalization for COVID-19 and Risk Factors for Severe Disease Among Children: 2022-2024.
    Pediatrics. 2025;156:e2025072788.
    PubMed         Abstract available

  21. ALLEN AJ, Nguyen N, Lorman V, Maltenfort M, et al
    Respiratory and Other Infections Following COVID.
    Pediatrics. 2025;156:e2024068280.
    PubMed         Abstract available

  22. GOLDSTEIN LA, Michaels MG, Salthouse A, Toepfer AP, et al
    Human Metapneumovirus and Respiratory Syncytial Virus in Children: A Comparative Analysis.
    Pediatrics. 2025;156:e2024070218.
    PubMed         Abstract available

  23. BODY A, Lal L, Downie P, Anazodo A, et al
    Immune Response to COVID-19 Vaccination in Children With Cancer.
    Pediatrics. 2025 Aug 8:e2024070209. doi: 10.1542/peds.2024-070209.
    PubMed         Abstract available


    PLoS Biol

  24. HOLMES KE, Ferreri LM, Elie B, Ganti K, et al
    Viral expansion after transfer is a primary driver of influenza A virus transmission bottlenecks.
    PLoS Biol. 2025;23:e3003352.
    PubMed         Abstract available


    PLoS Comput Biol

  25. TORRES-FLOREZ S, Flores Anato JL, He JH, Portilla VG, et al
    Evaluating COVID-19 vaccination policy in Quebec (Canada) using a data-driven dynamic transmission model.
    PLoS Comput Biol. 2025;21:e1013207.
    PubMed         Abstract available

  26. REYNE B, Kamiya T, Djidjou-Demasse R, Alizon S, et al
    Leaky or polarised immunity: Non-Markovian modelling highlights the impact of immune memory assumptions.
    PLoS Comput Biol. 2025;21:e1013399.
    PubMed         Abstract available


    PLoS One

  27. HBID Y, Stanley K, Wolfe CDA, Bhalla A, et al
    Stroke care in the United Kingdom before, during, and after the COVID-19 lockdowns: A retrospective nationwide cohort study.
    PLoS One. 2025;20:e0330903.
    PubMed         Abstract available

  28. STOLARCZUK JE, Sosa M, Pike M, Baranoff A, et al
    Transplacental transfer of maternal SARS-CoV-2 antibodies in dichorionic and monochorionic twin pregnancies.
    PLoS One. 2025;20:e0328137.
    PubMed         Abstract available

  29. VISKUPIC F, Wiltse DL, Stenvig TE
    Nurses' attitudes about RSV vaccination for pregnant women and infants: Evidence from a cross-sectional survey.
    PLoS One. 2025;20:e0331326.
    PubMed         Abstract available

  30. ARIK A, Cairns AJG, Streftaris G
    Cancer disparities: Projection, COVID-19, and scenario-based diagnosis delay impact.
    PLoS One. 2025;20:e0330752.
    PubMed         Abstract available

  31. SONG J, Jeon J
    Deep momentum networks with market trend dynamics.
    PLoS One. 2025;20:e0331391.
    PubMed         Abstract available

  32. BI W, Shen Y, Ji Y, Du Y, et al
    Who continued travelling by bus in different periods of COVID-19? A data-driven analysis from Shanghai, China.
    PLoS One. 2025;20:e0328700.
    PubMed         Abstract available

  33. ATHA L, Ryde E, Burke L, Brady S, et al
    Investigating the use of a one-page infographic to improve recruitment and retention to the BASIL+ randomised controlled trial: A Study Within a Trial (SWAT).
    PLoS One. 2025;20:e0320821.
    PubMed         Abstract available

  34. SEMANCIK CS, Fantin R, Butt J, Abdelnour A, et al
    SARS-CoV-2 antibody and neutralization dynamics among persons with natural- and vaccine-induced exposures.
    PLoS One. 2025;20:e0331212.
    PubMed         Abstract available

  35. RITCHWOOD TD, Burton K, Wynn M
    Before the wave: Exploring early perspectives on COVID-19 self-testing among African Americans in Eastern North Carolina.
    PLoS One. 2025;20:e0330513.
    PubMed         Abstract available

  36. EVANS LV, Bonz JW, Buck S, Gerwin JN, et al
    An adaptive simulation intervention decreases emergency physician physiologic stress while caring for patients during COVID-19: A randomized clinical trial.
    PLoS One. 2025;20:e0331488.
    PubMed         Abstract available

  37. TAN C, Zhong J, Yang D, Huang W, et al
    Forecasting and analysing global average temperature trends based on LSTM and ARIMA models.
    PLoS One. 2025;20:e0330645.
    PubMed         Abstract available

  38. MULLER-POLYZOU R, Reuter-Oppermann M
    Radiotherapy continuity for cancer treatment: Lessons learned from natural disasters.
    PLoS One. 2025;20:e0308056.
    PubMed         Abstract available

  39. SHANKAR R, Wang L, Hoe HS, Fong LM, et al
    Cost-effectiveness of virtual emergency care models: A protocol for a systematic review.
    PLoS One. 2025;20:e0330946.
    PubMed         Abstract available

  40. CATES ZP, Facciuolo A, Scruten E, Kusalik A, et al
    Peptide immunoarrays for rationale development of vaccines with enhanced cross-reactivity.
    PLoS One. 2025;20:e0330741.
    PubMed         Abstract available

  41. OKYERE E, Marfoh K, Kabukeinamala D, Goundar R, et al
    Benefits and challenges: Qualitative exploration of women's experiences during the COVID-19 pandemic in Fiji.
    PLoS One. 2025;20:e0331794.
    PubMed         Abstract available

  42. KAMADA N, Hagiya H, Kutsuna S
    Impact of COVID-19 on the awareness and interest in infectious disease specialization among Japanese medical students.
    PLoS One. 2025;20:e0329451.
    PubMed         Abstract available

  43. NAGY A, Cernikova L, Sedlak K
    Genetic data and meteorological conditions suggesting windborne transmission of H5N1 high-pathogenicity avian influenza between commercial poultry outbreaks.
    PLoS One. 2025;20:e0319880.
    PubMed         Abstract available

  44. XIE F, Wei H
    Characteristics and dynamic evolution of inter-industry volatility spillovers in China's stock market.
    PLoS One. 2025;20:e0330599.
    PubMed         Abstract available

  45. SALAZAR-GRANIZO YE, Caparros-Gonzalez RA, Puente-Fernandez D, Hueso-Montoro C, et al
    Highly stressful global event affecting health sciences students: A longitudinal qualitative study.
    PLoS One. 2025;20:e0331694.
    PubMed         Abstract available

  46. HAN D, Choi CG
    The spatial dynamics of urban vegetation and housing prices: Insights from pre- and post-pandemic Chicago using OLS and MGWR models.
    PLoS One. 2025;20:e0330932.
    PubMed         Abstract available


    Proc Natl Acad Sci U S A

  47. ROWNTREE LC, Allen LF, Hagen RR, McQuilten HA, et al
    HLA-B*15:01-positive severe COVID-19 patients lack CD8(+) T cell pools with highly expanded public clonotypes.
    Proc Natl Acad Sci U S A. 2025;122:e2503145122.
    PubMed         Abstract available


    Vaccine

  48. IRVING SA, Groom HC, Belongia EA, Crane B, et al
    Differences in influenza vaccination coverage by race and ethnicity across age groups in the Vaccine Safety Datalink, 2017-18 through 2022-23 influenza seasons.
    Vaccine. 2025;64:127667.
    PubMed         Abstract available

  49. ZHOU Y, Wang H, Chu L, Chen K, et al
    Influenza vaccination hesitancy and decision between parental and grandparental caregivers of preschoolers: a comparative study.
    Vaccine. 2025;64:127696.
    PubMed         Abstract available

#Genetic data and #meteorological conditions suggesting #windborne #transmission of #H5N1 high-pathogenicity avian #influenza between commercial #poultry outbreaks

 


Abstract

Understanding the transmission routes of high-pathogenicity avian influenza (HPAI) is crucial for developing effective control measures to prevent its spread. In this context, windborne transmission, the idea that the virus could travel through the air over considerable distances, is a contentious concept, and documented cases have been rare. Here, though, we provide genetic evidence supporting the feasibility of windborne transmission. During the 2023−24 HPAI season, molecular surveillance identified identical H5N1 strains among a cluster of unrelated commercial farms about 8 km apart in the Czech Republic. The episode started with the abrupt mortality of fattening ducks on one farm. This was followed by disease outbreaks at two nearby high-biosecurity chicken farms. Using genetic, epizootiological, meteorological and geographical data, we reconstructed a mosaic of events strongly suggesting wind was the most probable mechanism of infection transmission between poultry in at least two independent cases. By aligning the genetic and meteorological data with critical outbreak events, we determined the most likely time window during which the transmission occurred and inferred the sequence of infected houses at the recipient sites. Our results suggest that the contaminated plume emitted from the infected fattening duck farm was the critical medium of HPAI transmission, rather than the dust generated during depopulation. Furthermore, our results also strongly implicate the role of confined mechanically-ventilated buildings with high population densities in facilitating windborne transmission and propagating virus concentrations below the minimum infectious dose at the recipient sites. These findings underscore the importance of considering windborne spread in future outbreak mitigation strategies.

Source: PLoS One, https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0319880

____

History of Mass Transportation: The FS ETR 460 Electric Multiple Unit

 


By Superalbs - Own work, CC BY-SA 4.0, https://commons.wikimedia.org/w/index.php?curid=93344176

Source: Wikipedia, https://en.wikipedia.org/wiki/FS_Class_ETR_460

____

Friday, September 5, 2025

#Ebola virus disease - #DRC (#WHO D.O.N., September 5 '25)

 


Situation at a glance

On 1 September 2025, WHO received an alert from the Ministry of Health of the Democratic Republic of the Congo (DRC) regarding suspected cases of Ebola virus disease (EVD) in the Bulape Health Zone, Kasai Province, DRC

The first known index case was a pregnant woman who presented at Bulape General Reference Hospital on 20 August 2025 with symptoms of high fever, bloody diarrhoea, haemorrhage and extreme weakness. She died on 25 August from multiple organ failure

On 4 September 2025, following confirmatory laboratory testing, the Ministry of Health declared an outbreak of EVD

Ebola virus disease is a serious, often fatal illness in humans. The virus is transmitted to humans through close contact with the blood or secretions of infected wildlife and then spreads through human-to-human transmission

As of 4 September 2025, 28 suspected cases, including 15 deaths (case fatality ratio (CFR): 54%), have been reported from three areas of the Bulape health zone (Bulape, Bulape Com and Dikolo) and Mweka health zone. 

Among the deaths, four are health-care workers

About 80% of the suspected cases are aged 15 years and older. Six samples were collected from five suspected cases and one probable death from Bulape health zone and arrived on 3 September at the National Public Health Laboratory (INRB) in Kinshasa for confirmation testing. All five samples tested positive for Ebola virus (EBOV) through GeneXpert and Polymerase Chain Reaction (PCR) assays on 3 September 2025. 

The Ministry of Health, with support from WHO and partners, is implementing public health response measures to contain the outbreak. WHO assesses the overall public health risk posed by the current EVD outbreak as high at the national level, moderate at the regional level and low at the global level.


Description of the situation

On 1 September 2025, WHO received an alert from the Ministry of Health of the Democratic Republic of the Congo (DRC) regarding suspected cases of EVD in the Bulape Health Zone, Kasai Province, DRC. 

The first known suspected index case was admitted to the Bulape General Reference Hospital on 20 August 2025. The patient was a pregnant woman at 34-weeks of gestation who presented with symptoms of fever, bloody diarrhoea,  haemorrhage, vomiting, asthenia, followed by multiple organ failure. She died on 25 August 2025. Two of the health-care workers that had initially been in contact with this first case also developed similar symptoms and died.

As of 4 September 2025, a total of 28 suspected cases, including 15 deaths, of which four are health-care workers (case fatality ratio (CFR): 54%) have been reported from three areas of the Bulape health zone (Bulape, Bulape Com and Dikolo) and Mweka health zone. 

About 80% of the suspected cases are aged 15 years and older. Five blood samples from five suspected cases and a  naso-pharyngeal swab from a probable death were collected from the three health areas and shipped to the National Public Health Laboratory (INRB) in Kinshasa for testing.

On 3 September 2025, the laboratory testing conducted at INRB confirmed Ebola virus (EBOV)[1] through GeneXpert and Polymerase Chain Reaction (PCR) assays.

The results obtained from whole genome sequencing suggest that the outbreak is a new zoonotic spillover event and is not directly linked to the 2007 Luebo or 2008/2009 Mweka EVD outbreaks.[2]

(...)


Epidemiology

Ebola virus disease is a severe disease caused by the Ebola virus (EBOV). The virus belongs to the species Orthoebolavirus Zairense. The virus is transmitted to humans through close contact with the blood or secretions of infected wildlife and then spreads through human-to-human transmission by direct contact with bodily fluids, organs, or contaminated surfaces and materials.

The incubation period, the time between infection with the virus and the onset of symptoms, ranges from 2 to 21 days, but typically is 7–11 days. People are not infectious during the incubation period; they become contagious with early symptoms, therefore, transmission risk begins at the onset of clinical signs and increases with disease severity.

The average case fatality ratio is 50%; case fatality ratios ranging from 25% to 90% have been reported in previous outbreaks. 

The disease is characterised by an acute onset of fever with non-specific symptoms/signs (e.g., abdominal pain, anorexia, fatigue, malaise, myalgia, sore throat) usually followed several days later by nausea, vomiting, diarrhoea, and occasionally a variable rash. 

Severe illness may include haemorrhagic manifestations (e.g., bleeding), encephalopathy, shock/hypotension, multi-organ failure, and spontaneous abortion in infected pregnant women. 

Individuals who recover may experience prolonged sequelae (e.g., arthralgia, neurocognitive dysfunction, uveitis, sometimes followed by cataract formation), and clinical and subclinical persistent infection may occur in immune-privileged compartments (e.g., central nervous system, eyes, testes). 

Family members, health and care providers, and participants in burial ceremonies with direct contact with the deceased are at particular risk. 


Public health response

Health authorities are implementing public health measures, including but not limited to the following:

-- A crisis committee was activated at both the local and provincial levels.

-- Risk communication and active surveillance activities are ongoing.

-- All cases are isolated, and Infection Prevention and Control (IPC) measures have been implemented.

-- Patients are receiving intravenous medication.

-- Contact isolation and tracing are continuing.

-- Investigations are ongoing. 

WHO is supporting the national authorities, including through:

-- Risk assessment and investigation.

-- Providing operational, financial and technical support to the Ministry of Health to ensure swift response.

-- Provision of essential supplies (Personal Protective Equipment (PPE), medical supplies and infrastructures support)

-- The approved Ervebo vaccine is available with a stock of 2000 doses located in Kinshasa expected to be shipped shortly to the affected area, to vaccinate contacts of confirmed or suspected cases,  frontline and health workers.


WHO risk assessment

This is the 16th EVD outbreak in the DRC since 1976. The current outbreak occurs after almost three years without a confirmed EVD outbreak in the country. The last EVD outbreak in the country was declared on 15 August 2022 in Beni city, North Kivu province, with one single case reported who later died, and the MoH declared the end of the outbreak on 27 September 2022. In the Bulape district, the epicentre of the current outbreak, the last EVD outbreak was recorded in 2007.  

This outbreak is occurring in a complex epidemiological and humanitarian context. The country is facing several outbreaks, including mpox, cholera, and measles. In addition, the country is experiencing a long-term economic and political crisis. The country's resources and capacity to effectively respond to the current outbreak are therefore limited. 

The epicentre of this outbreak is in the proximity of the Tshikapa city, the capital city of the Kasai province, and the Angolan border (approximately 100 to 200 kilometres, depending on the nearest border crossing point). 

Although the affected district is a hard-to-reach rural area relatively far from the two main urban centres of Mbuji Mayi and Kananga, population movements between different parts of the province are frequent, especially between Bulape and Tshikapa.

In addition, epidemiological investigations are ongoing with transmission chains, and the source of the outbreak has not yet been identified; therefore, additional infected people cannot be ruled out.  

The date of symptom onset for the first case is not yet known, as well as the therapeutic itinerary prior to health facility consultation, which further increases the likelihood of an ongoing community transmission with further risk of spread to other health districts.

WHO assesses the overall public health risk posed by the current EVD outbreak as high at the national level, moderate at the regional level and low at the global level. 


WHO advice

Effective outbreak control relies on the application of a set of interventions, namely clinical management, IPC & Water, sanitation and hygiene (WASH), surveillance and contact tracing, good laboratory service, safe and dignified burials, community engagement, and social mobilization. 

The Ebola virus can persist in some body fluids of people who have recovered from EVD. 

In a limited number of cases, secondary transmissions resulting from exposure to the body fluids of people who have recovered from EVD have been documented. Therefore, maintaining collaborative relationships with survivor associations while monitoring survivors is a priority to mitigate any potential risks.

Early diagnosis and initiation of optimized supportive clinical care can reduce mortality from EVD. 

In addition, monoclonal antibodies active against a 3-antibody combination of atoltivimab, maftivimab and odesivimab [Inmazeb®] or a single antibody ansuvimab [Ebanga®].  

Ebola treatment centres should be designed and managed to ensure safe care is provided with appropriate biosecurity and infection prevention and control intervention, and allow optimized care, allowing direct visualization of patients in the red zone as much as possible. WHO and partners have worked to develop these innovative solutions. 

There is a need to strengthen surveillance and other response activities, including at relevant points of entry and borders, to contain the possibility of exponential spread. 

Cases, contacts and individuals in affected areas who present signs and symptoms compatible with case definitions should be considered suspects and cared for and treated in designated treatment facilities with appropriate biosecurity, infection prevention and control and be offered testing in a timely fashion and advised not to travel. 

Collaboration with neighbouring countries should be enhanced to harmonize reporting mechanisms, conduct joint investigations, and share critical data in real time. 

Surrounding countries should enhance readiness activities to enable early case detection, isolation and treatment. 

Critical infection prevention and control measures should be implemented and/or strengthened in all health care facilities, per WHO's Infection prevention and control guideline for Ebola and Marburg disease.   

Health workers caring for patients with confirmed or suspected Ebola should apply transmission-based precautions in addition to standard precautions, including appropriate use of PPE and hand hygiene according to the WHO 5 moments to avoid contact with patients’ blood and other body fluids, and with contaminated surfaces and objects. 

Waste generated in health-care facilities must be safely segregated, safely collected, transported, stored, treated and finally disposed. National guidelines should be followed on rules and regulations for safe waste disposal or WHO’s guidelines on safe waste management.

Patient-care activities should be undertaken in a clean and hygienic environment that facilitates practices related to the prevention and control of health-care-associated infections, as outlined in Essential environmental health standards in health care. Safe water, adequate sanitation and hygiene infrastructure and services should be provided in healthcare facilities. For details on recommendations and improvement, follow the WASH FIT implementation Package.

In accordance with the recommendations of the Strategic Advisory Group of Experts on immunization, the Ervebo vaccine is recommended during an EVD outbreak due to EBOV for ring vaccination, for contacts and potential contacts of confirmed/suspected EVD cases, as well as for frontline workers. A global stockpile has been established and is being coordinated by the International Coordination Group for vaccine procurement.

WHO advises against any restrictions on travel and/or trade to the Democratic Republic of the Congo based on available information for the current outbreak.

(...)

Source: World Health Organization, https://www.who.int/emergencies/disease-outbreak-news/item/2025-DON580

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#Molnupiravir inhibits #Bourbon virus #infection and disease-associated #pathology in mice

 


ABSTRACT

Bourbon virus (BRBV) is an emerging tick-borne virus that can cause severe and fatal disease in humans. BRBV is vectored via the Amblyomma americanum tick, which is widely distributed throughout the central, eastern, and southern United States. Serosurveillance studies in Missouri and North Carolina identified BRBV-neutralizing antibodies in approximately 0.6% of tested individuals. To date, no specific antiviral therapy exists. As part of an initial screen, several nucleoside analogs were tested for their ability to inhibit BRBV replication in cell culture. Among the compounds assessed, molnupiravir, an antiviral drug with oral availability and broad spectrum antiviral activity against RNA viruses, showed antiviral activity against BRBV production in vitro. In vivo, pre-exposure administration of molnupiravir protected susceptible type I interferon receptor knockout (Ifnar1-/-) mice against lethal BRBV infection. The protection by molnupiravir was associated with lower virus burden in mouse tissues, improvement of T-cell (CD4+, CD8+) and B-cell (follicular) profiles in the spleen, improvement of severe thrombocytopenia, and reduced pathology in the spleen and liver of BRBV-infected mice. Finally, therapeutic administration of molnupiravir starting 24 or 48 hours after infection ameliorated weight loss, clinical signs of disease, and lethality associated with BRBV infection. Overall, our experiments suggest that molnupiravir is a potential antiviral therapy for evaluation in humans with BRBV infections.


IMPORTANCE

Bourbon virus (BRBV) is an emerging tick-borne pathogen that can cause severe and fatal illness in humans. Currently, there are no approved antiviral therapies or vaccines against this disease. In this study, we evaluated the efficacy of molnupiravir, a broad-spectrum antiviral drug that is approved in the United States for other RNA viruses, using a mouse model of lethal BRBV disease. Molnupiravir significantly inhibited virus replication, improved survival rates, and suppressed clinical signs of disease, including thrombocytopenia and liver and spleen pathology. These findings support further investigation of molnupiravir as a potential therapeutic candidate for treating BRBV infections in humans.

Source: Journal of Virology, https://journals.asm.org/doi/full/10.1128/jvi.00740-25?af=R

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#USA, #Wastewater #Data for Avian #Influenza #H5 (#CDC, September 5 '25)




{Summary}

Time Period: August 24, 2025 - August 30, 2025

-- H5 Detection3 sites (0.7%)

-- No Detection428 sites (99.3%)

-- No samples in last week31 sites




(...)

Source: US Centers for Disease Control and Prevention, https://www.cdc.gov/nwss/rv/wwd-h5.html

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#Influenza #vaccination to improve #outcomes for #patients with acute heart failure (PANDA II): a multiregional, seasonal, hospital-based, cluster-randomised, controlled trial in #China

 


Summary

Background

Influenza vaccination is widely recommended to prevent death and serious illness in vulnerable people, including those with heart failure. However, the randomised evidence to support this practice is limited and few people are vaccinated in many parts of the world. We aimed to determine whether influenza vaccination can improve the outcome of patients after an episode of acute heart failure requiring admission to hospital in China.

Methods

We undertook a pragmatic, multiregional, parallel-group, cluster (hospital)-randomised, controlled, superiority trial over three winter seasons in China. Participating hospitals were located in the counties of 12 provinces with the capability of establishing a point-of-care service to provide free influenza vaccination to a sufficient number of patients before their discharge, if allocated to the intervention group. No such service was used in hospitals allocated to usual care (control) but patients were informed of fee-for-service influenza vaccination being available at local community medical centres, as per usual standard of care. Hospitals were randomised (1:1) in each year, stratified by province and up to three times (ie, new randomisation for each season), to include eligible adult (aged ≥18 years) patients with moderate to severe heart failure (New York Heart Association class III or IV) and no contraindication to influenza vaccination. Patient enrolment was conducted over three consecutive winter seasons, from October in each year to March of the following year, between 2021 and 2024. All patients received usual standard of care and were followed up at 1, 3, 6, and 12 months after their hospital discharge by trained study personnel using a standardised protocol. The primary outcome was a composite of all-cause mortality or any hospital readmission over 12 months, excluding events that occurred within 30 days after hospital discharge at all sites and in the summer season only for sites in northern China. The effect of the intervention was assessed at an individual level in the modified intention-to-treat population (all randomly assigned patients with available information until the time of last follow-up, excluding censored events) with a two-level hierarchical logistic regression model that included study period (year) as a fixed effect, and hospital and hospital-period as random effects, with the censored events excluded. The trial is registered at the Chinese Clinical Trial Registry (ChiCTR2100053264).

Findings

Of 252 hospitals assessed for eligibility, 196 hospitals agreed to join and were randomised in three batches at the beginning of each winter season from October, 2021, but 32 hospitals subsequently withdrew before any patients were included. Overall, 7771 participants were enrolled at 164 hospitals in each winter season between Dec 3, 2021, and Feb 14, 2024, with 3570 assigned to the influenza vaccination group and 4201 to the usual care (control) group. The primary outcome occurred in 1378 (41·2%) of 3342 patients in the vaccination group and in 1843 (47·0%) of 3919 patients in the usual care group (odds ratio 0·83 [95% CI 0·72–0·97]; p=0·019). The result was consistent in the sensitivity analysis. The number of participants with a serious adverse event was significantly lower in the vaccination group (1809 [52·5%] of 3444) than the usual care group (2426 [59·0%] of 4110; odds ratio 0·82 [0·70–0·96]; p=0·013).

Interpretation

Influenza vaccination during a hospital admission in patients with acute heart failure can improve their survival and reduce likelihood of readmission to hospital over the subsequent 12 months. The integration of influenza vaccination into inpatient care could offer a widely applicable strategy for an underserved high-risk patient group, that is relevant to resource-limited and possibly resource-rich settings.

Funding

Sanofi and the Chinese Society of Cardiology.

Source: The Lancet, https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(25)01485-0/abstract?rss=yes

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Cross-reactive #human #antibody responses to #H5N1 #influenza virus #neuraminidase are shaped by immune history

 


Abstract

H5N1 highly pathogenic avian influenza viruses have spread globally and pose a risk for a human pandemic. Prior studies suggest that early life exposures to group 1 influenza viruses (H1N1 and H2N2) prime antibodies that cross-react to the hemagglutinin of H5N1, which is also a group 1 virus. Less is known about how immune history affects antibody responses against the neuraminidase (NA) of H5N1 viruses. Here, we measured NA inhibition antibodies against multiple H5N1 viruses using sera from 155 individuals born between 1927 and 2016. We found that individuals primed in childhood with H1N1 viruses were more likely to possess higher levels of antibodies that cross-react with the NA of H5N1 viruses compared to individuals primed in childhood with H2N2 or H3N2 viruses. While young children rarely possessed cross-reactive NA antibodies, we found that childhood infections with contemporary H1N1, but not H3N2, viruses can elicit them. These data suggest that immune history greatly impacts the generation of cross-reactive NA antibodies that can inhibit H5N1 viruses.


Competing Interest Statement

S.E.H. is a co-inventor on patents that describe the use of nucleoside-modified mRNA as a vaccine platform. S.E.H reports receiving consulting fees from Sanofi, Pfizer, Lumen, Novavax, and Merck. A.S.L. is now an employee of Sanofi but was affiliated with the Childrens Hospital of Pennsylvania when this work was completed. The authors declare no other competing interests.


Funding Statement

This project was funded in part with federal funds from the National Institute of Allergy and Infectious Diseases, National Institutes of Health, Department of Health and Human Services, under contract no. 75N93021C00015 (S.E.H., S.C.) and grant number R01AI08686 (S.E.H.).

Source: MedRxIV, https://www.medrxiv.org/content/10.1101/2025.09.02.25334929v1

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Thursday, September 4, 2025

Highly Pathogenic Avian #Influenza #H5N1 Virus #Infection in a #Child with No Known Exposure — San Francisco, #California, December 2024–January 2025

 


Summary

-- What is already known about this topic?

- As of January 1, 2025, 37 human cases of highly pathogenic avian influenza (HPAI) A(H5N1) had been detected in California, none of which occurred in San Francisco.

-- What is added by this report?

- On January 9, 2025, a case of HPAI A(H5N1) infection was identified in a school-aged child in San Francisco through enhanced surveillance (influenza A virus subtyping of a sample of specimens weekly). No source of exposure was identified, and investigations found no laboratory evidence of human-to-human transmission among close contacts.

-- What are the implications for public health practice?

- Enhanced surveillance and timely subtyping of a subset of influenza A–positive specimens, including specimens from persons without known A(H5N1) exposure, are important to detect avian influenza A virus infections. Public health investigations are critical to monitoring for human-to-human transmission.


Abstract

In response to a highly pathogenic avian influenza (HPAI) A(H5N1) outbreak in U.S. dairy cows detected in March 2024, with subsequent identification of human cases, the San Francisco Department of Public Health instituted enhanced influenza surveillance (influenza A virus subtyping of a sample of specimens weekly) in June 2024. As of January 1, 2025, 37 human cases of influenza A(H5N1) had been detected in California, none of which occurred in San Francisco. On January 9, 2025, enhanced surveillance detected a human influenza A(H5N1) virus genotype B3.13 infection in a school-aged child in San Francisco with mild illness. Case investigation and contact tracing were conducted to ascertain exposures and detect possible human-to-human transmission. Activities comprised a household visit that included an environmental assessment, close contact interviews and surveys, and molecular and serologic testing. Sixty-seven close contacts (household, school, and health care) were identified. Upper respiratory tract specimens collected from seven asymptomatic household contacts and four symptomatic school contacts all tested negative for influenza virus by real-time reverse transcription–polymerase chain reaction (rRT-PCR). Although antibodies against influenza A(H5N1) were detected in the index patient, serologic testing of a convenience sample of nine close contacts identified no detectable A(H5)-specific antibodies. Despite an extensive investigation, the infection source remains unknown; no human-to-human transmission was identified among close contacts by rRT-PCR and serologic testing. Continued enhanced surveillance and timely subtyping of a subset of influenza A–positive specimens are essential components of a comprehensive strategy to detect human novel influenza A virus infections, including among persons without known exposures to A(H5N1) viruses.

Source: US Centers for Disease Control and Prevention, MMWR, https://www.cdc.gov/mmwr/volumes/74/wr/mm7433a2.htm?s_cid=OS_mm7433a2_e&ACSTrackingID=USCDC_921-DM149891&ACSTrackingLabel=Week%20in%20MMWR%3A%20Vol.%2074%2C%20September%204%2C%202025&deliveryName=USCDC_921-DM149891

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#DRC declares #Ebola virus disease #outbreak in #Kasai Province (#WHO AFRO, September 4 '25)

 


Kinshasa – Health authorities in the Democratic Republic of the Congo have declared an outbreak of Ebola virus disease in Kasai Province where 28 suspected cases and 15 deaths, including four health workers, have been reported as of 4 September 2025.

The outbreak has affected Bulape and Mweka health zones in Kasai Province where health officials have been carrying out investigations after the cases and the deaths reported presented with symptoms including fever, vomiting, diarrhoea and haemorrhage. Samples tested on 3 September at the country’s National Institute of Biomedical Research in the capital Kinshasa confirmed the cause of the outbreak as Ebola Zaire caused by Ebola virus disease.   

A national Rapid Response Team joined by World Health Organization (WHO) experts in epidemiology, infection prevention and control, laboratory and case management has been deployed to Kasai Province to rapidly strengthen disease surveillance, treatment and infection prevention and control in health facilities. Provincial risk communication experts have also been deployed to reach communities and help them understand how to protect themselves.

Additionally, WHO is delivering two tonnes of supplies including personal protective equipment, mobile laboratory equipment and medical supplies. The area is difficult to reach, taking at least one day of driving from Tshikapa (the provincial capital of Kasai), with few air links.   

“We’re acting with determination to rapidly halt the spread of the virus and protect communities,” said Dr Mohamed Janabi, WHO Regional Director for Africa. “Banking on the country’s long-standing expertise in controlling viral disease outbreaks, we’re working closely with the health authorities to quickly scale up key response measures to end the outbreak as soon as possible.”   

Case numbers are likely to increase as the transmission is ongoing. Response teams and local teams will work to find the people who may be infected and need to receive care, to ensure everyone is protected as quickly as possible.    

The country has a stockpile of treatments, as well as 2000 doses of the Ervebo Ebola vaccine, effective to protect against this type of Ebola, already prepositioned in Kinshasa that will be quickly moved to Kasai to vaccinate contacts and frontline health workers.   

The Democratic Republic of the Congo’s last outbreak of Ebola virus disease affected the north-western Equateur province in April 2022. It was brought under control in under three months thanks to the robust efforts of the health authorities. In Kasai province, previous outbreaks of Ebola virus disease were reported in 2007 and 2008. In the country overall, there have been 15 outbreaks since the disease was first identified in 1976.    

Ebola virus disease is a rare but severe, often fatal illness in humans. It is transmitted to people through close contact with the blood, secretions, organs or other bodily fluids of infected animals such as fruit bats (thought to be the natural hosts). Human-to-human transmission is through direct contact with blood or body fluids of a person who is sick with or has died from Ebola, objects that have been contaminated with body fluids from a person sick with Ebola or the body of a person who died from Ebola.

Source: World Health Organization, Regional Office for Africa, https://www.afro.who.int/countries/democratic-republic-of-congo/news/democratic-republic-congo-declares-ebola-virus-disease-outbreak-kasai-province

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#Italy, Integrated #WNV & #USUV Viruses #Surveillance - Weekly #Bulletin No. 8, September 4 2025 (summary)



{Summary}

-- During current surveillance week (28 August - 3 September 2025): 

- 72 new confirmed human cases of West Nile Virus infection have been confirmed; 

-- The total number of cases since the beginning of epidemic season has risen to 502 (they were 430 in the last bulletin); of these: 

- 226 were West Nile Neuroinvasive Disease (WNND): 11 in Piedmont, 16 in Lombardy, 17 Veneto, 1 Friuli-Venezia Giulia, 1 Liguria, 15 Emilia-Romagna, 3 Tuscany, 71 Latium, 2 Molise, 72 Campania, 1 Apulia, 2 Basilicata, 5 Calabria, 1 Sicily, 8 Sardinia, 

- 40 were asymptomatic cases detected in blood donors

- 226 were West Nile Fever cases (one of them imported from Kenya),

- 5 asymptomatic cases, 

- 5 unspecified. 

-- So far there have been 33 fatal cases: 3 in Piedmont, 1 Lombardy, 1 Emilia-Romagna, 14 Latium, 12 Campania, 2 Calabria. 

- The Case-Fatality rate among WNND cases is thus far at 14.6% (in 2018 it was 20%, in 2024 14%). 

-- During current surveillance week, there have been 4 confirmed Usutu virus human infections: 2 in Piedmont, 1 Veneto, 1 Latium).

(...)

Source: High Institute of Health, https://www.epicentro.iss.it/westnile/bollettino/Bollettino_WND_2025_08.pdf

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Wednesday, September 3, 2025

Characterization of the first detected Avian #Influenza #H9N2 #human case in #Ghana

 


Abstract

Avian influenza A(H9N2) has been circulating in poultry across Asia, the Middle East, and Africa, posing human health risks. In Ghana, it has co-circulated among poultry with influenza A (H5N1). This report describes Ghana’s first confirmed human case of avian influenza A(H9N2) virus infection in a two-year-old boy from Upper East Region, identified through active respiratory surveillance. Molecular and genomic analyses confirmed the virus was of the G1 lineage, closely related to other West African strains, with mammalian adaptive mutations known to increase human infection potential. The child experienced mild symptoms, received outpatient care, and recovered. Health authorities conducted epidemiological investigations. No source was identified for the child’s infection; no additional human infections were detected. This case highlights the importance of robust avian influenza surveillance in animals and humans, particularly in regions with human-animal interactions. It underscores the importance of national and global collaboration using a One Health approach to detect and prevent zoonotic spillovers and potential pandemics.

Source: Emerging Microbes and Infections, https://www.tandfonline.com/doi/full/10.1080/22221751.2025.2556717

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#Bolivia - #Influenza A #H5 viruses of high pathogenicity (Inf. with) (non-poultry including wild birds) (2017-) - Immediate notification

 


Neurological-respiratory disease in backyard domestic birds raised in a farm with partial laboratory results of H5 avian influenza virus. Zoning was implemented for the control of the outbreak with stamping out measures for all affected and contact birds on the farm, and surveillance will be carried out in the perifocal and protection areas. A body of water representing a possible place of contact between domestic and wild birds is located on the premises.

Source: WOAH, https://wahis.woah.org/#/in-review/6755

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

 


A poultry farm in SantarĂ©m Region.

Source: WOAH, https://wahis.woah.org/#/in-review/6759

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

 


A poultry farm in Schleswig-Holstein State.

Source: WOAH, https://wahis.woah.org/#/in-review/6760

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The paradoxical #impact of #drought on #WNV #risk: insights from long-term ecological data

 


Abstract

Mosquito-borne diseases are deeply embedded within ecological communities, with environmental changes—particularly climate change—shaping their dynamics. Increasingly intense droughts across the globe have profound implications for the transmission of these diseases, as drought conditions can alter mosquito breeding habitats, host-seeking behaviours and mosquito–host contact rates. To quantify the effect of drought on disease transmission, we use West Nile virus as a model system and leverage a robust mosquito and virus dataset consisting of over 500 000 trap nights collected from 2010 to 2023, spanning a historic drought period followed by atmospheric rivers. We pair this surveillance dataset with a novel modelling approach that incorporates monthly changes in bird host community competence, along with drought conditions, to estimate the effect of drought severity on West Nile virus risk using panel regression models. Our results show that while drought decreases mosquito abundances, it paradoxically increases West Nile virus infection rates. This counterintuitive pattern probably stems from reduced water availability, which concentrates mosquitoes and pathogen-amplifying bird hosts around limited water sources, thereby increasing disease transmission risk. However, the magnitude of the effect depends critically on mosquito species, suggesting species-specific behavioural traits are key to understanding the effect of drought on mosquito-borne disease risk across real landscapes.

Source: Proceedings of the Royal Society B Biological Sciences, https://royalsocietypublishing.org/doi/full/10.1098/rspb.2025.1365?af=R

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Tuesday, September 2, 2025

#Azelastine Nasal #Spray for #Prevention of #SARS-CoV-2 Infections A Phase 2 #RCT

 


Key Points

-- Question: Is regular application of azelastine nasal spray associated with reduced risk of SARS-CoV-2 infections?

- Findings: In this randomized placebo-controlled clinical trial that included 450 participants, the incidence of laboratory-confirmed SARS-CoV-2 infections was significantly lower with application of azelastine nasal spray compared with placebo treatment.

-- Meaning: The use of azelastine nasal spray may help to reduce the risk of SARS-CoV-2 infections.



Abstract

Importance  

Limited pharmaceutical options exist for preexposure prophylaxis of COVID-19 beyond vaccination. Azelastine, an antihistamine nasal spray used for decades to treat allergic rhinitis, has in vitro antiviral activity against respiratory viruses, including SARS-CoV-2.

Objective  

To determine the efficacy and safety of azelastine nasal spray for prevention of SARS-CoV-2 infections in healthy adults.

Design, Setting, and Participants  

A phase 2, double-blind, placebo-controlled, single-center trial was conducted from March 2023 to July 2024. Healthy adults from the general population were enrolled at the Saarland University Hospital in Germany.

Interventions  

Participants were randomly assigned 1:1 to receive azelastine, 0.1%, nasal spray or placebo 3 times daily for 56 days. SARS-CoV-2 rapid antigen testing (RAT) was conducted twice weekly, with positive results confirmed by polymerase chain reaction (PCR). Symptomatic participants with negative RAT results underwent multiplex PCR testing for respiratory viruses.

Main Outcome  

The primary end point was the number of PCR-confirmed SARS-CoV-2 infections during the study.

Results  

A total of 450 participants were randomized, with 227 assigned to azelastine and 223 to placebo; 299 (66.4%) were female, 151 (33.6%) male, with a mean (SD) age of 33.0 (13.3) years. Most were White (417 [92.7%]), with 4 (0.9%) African, 22 (4.9%) Asian, and 7 (1.6%) of other ethnicity. In the intention-to-treat (ITT) population, the incidence of PCR-confirmed SARS-CoV-2 infection was significantly lower in the azelastine group (n = 5 [2.2%]) compared with the placebo group (n = 15 [6.7%]) (OR, 0.31; 95% CI, 0.11-0.87). As secondary end points, azelastine demonstrated an increase in mean (SD) time to SARS-CoV-2 infection among infected participants (31.2 [9.3] vs 19.5 [14.8] days), a reduction of the overall number of PCR-confirmed symptomatic infections (21 of 227 participants vs 49 of 223 participants), and a lower incidence of PCR-confirmed rhinovirus infections (1.8% vs 6.3%). Adverse events were comparable between the groups.

Conclusions and Relevance  

In this single-center trial, azelastine nasal spray was associated with reduced risk of SARS-CoV-2 respiratory infections. These findings support the potential of azelastine as a safe prophylactic approach warranting confirmation in larger, multicentric trials.


Trial registration  EudraCT number: 2022-003756-13

Source: JAMA Internal Medicine, https://jamanetwork.com/journals/jamainternalmedicine/fullarticle/2838335

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