Saturday, June 27, 2026

#Pixavir Marboxil: First Approval

 


Abstract

Pixavir marboxil (Yilikang®; 壹立康®) is an oral cap-snatching endonuclease inhibitor being developed by TaiGen Biotechnology for the treatment of influenza virus infections. Pixavir marboxil recently received approval in China for the treatment of uncomplicated influenza A and B in previously healthy adults and adolescents aged ≥ 12 years. This article summarizes the milestones in the development of pixavir marboxil leading to this first approval for uncomplicated influenza A and B infections.

Source: 


Link: https://link.springer.com/article/10.1007/s40265-026-02320-2

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#Coronavirus Disease Research #References (AMEDEO, June 27 '26)

 


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    PubMed         Abstract available

#Influenza and Other Respiratory Viruses Research #References (AMEDEO, June 27 '26)

 


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    PubMed        

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    PubMed         Abstract available

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    Impact of SARS-CoV-2 variants and vaccination on pediatric febrile seizures: a retrospective cohort study.
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    PubMed        


    Cell

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    Drugs

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    Pixavir Marboxil: First Approval.
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    J Virol Methods

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    Pediatrics

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    Concordance Between Maternal and Infant COVID-19 and Influenza Vaccination Status.
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    PLoS Comput Biol

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    TCRBinder: Unified pre-trained language model with paired-chain synergy for predicting T-cell receptor binding specificity.
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    PLoS Med

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    Comparisons of core component delivery in cardiac rehabilitation programs by country income classification and decade based on the 2025 Global Audit Update: A survey study.
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    PLoS One

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  15. BETTIO F, Tavares FF, Ticci E
    Intimate partner violence during lockdown in Tuscany, Italy: Economic or confinement-related shocks?
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    Will there be new trends in the public's attention to express services in the post-COVID-19 era?
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  18. KEITA NY, Onywera H, Abdou M, Dicko Z, et al
    A tale of SARS-CoV-2 genomic surveillance in Mali: Variants introductions and transmission dynamics.
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  19. RAVINDRARAJAH R, Gittins M, Paterson L, Rogers G, et al
    Clinical and cost-effectiveness of the digital intervention, MyWay Diabetes, in people with type 2 diabetes living in Greater Manchester during the COVID-19 pandemic.
    PLoS One. 2026;21:e0349232.
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  20. MAJEWSKA M, Mazdziarz MA, Lepiarczyk E, Lipka A, et al
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  25. CHANG YS, Jones J, Hong SA, Chien LY, et al
    Factors associated with multiple births in the United Kingdom during COVID-19: A cross-sectional survey.
    PLoS One. 2026;21:e0352340.
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  26. BIACKOVA N, Laskov O, Adamova A, Piorecka V, et al
    Transcranial direct current stimulation in affecting neuropsychiatric symptoms of post-COVID syndrome: No change in microstates and functional connectivity.
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  27. LAMB D, Scott H, Carr E, Stevelink SAM, et al
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    Proc Natl Acad Sci U S A

  28. KIM T, Biswas A, Kandel S, Kuroda M, et al
    Extra gene coding capacity of SARS-CoV-2 provides a virus engineering platform for in vitro and in vivo applications.
    Proc Natl Acad Sci U S A. 2026;123:e2532920123.
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    Vaccine

  29. MAGNUSSON AC, Lim S, Niemi C, Wolf N, et al
    Intranasal influenza vaccination using an outer membrane vesicle platform.
    Vaccine. 2026;89:128876.
    PubMed         Abstract available

  30. CHEN S, Fang Y, Yu FY, Ding L, et al
    Systematic review and meta-analysis of digital seasonal influenza vaccination promotion in people aged >/=50 ?years.
    Vaccine. 2026;88:128865.
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  31. LEVATI E, Calvani R, Cacciatore S, Tosato M, et al
    Influenza, pneumococcal, and herpes zoster vaccination in Italy: Knowledge, uptake, and determinants across the adult life course.
    Vaccine. 2026;88:128853.
    PubMed         Abstract available

  32. COUTO MONIZ M, Luo S, Krokhin A, Egorov A, et al
    Purified gamma-irradiated influenza A vaccine demonstrates high immunogenicity and protection against a drifted H1N1 strain.
    Vaccine. 2026;88:128872.
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  33. SHINJOH M, Furuichi M, Sugimoto R, Kawakami C, et al
    Effectiveness of inactivated and live-attenuated influenza vaccines in children during the 2025-2026 influenza season with genetically distinct influenza A and B viruses.
    Vaccine. 2026;88:128869.
    PubMed         Abstract available


    Virology

  34. CHOWDHURY D, Vanderven HA, Wangchuk P, Sarker S, et al
    Mechanistic insights into flavonoid-mediated regulation of human influenza virus replication.
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  35. HEREMIA L, Langsbury H, Treece J, Miller AK, et al
    Rapid GeneXpert surveillance of influenza A virus in seabirds and the environment provides early warning for wildlife health in Aotearoa New Zealand.
    Virology. 2026;623:111014.
    PubMed         Abstract available

Detection of #H5N1-Related #PB1 Sequences in a Low Pathogenic #H11N2 Virus from South #American Migratory #Shorebirds

 


Abstract

Highly pathogenic avian influenza (HPAI) A(H5N1) viruses of clade 2.3.4.4b have recently spread across the Americas, prompting intensified surveillance efforts in Brazil aimed at early detection in wild birds. As part of these efforts, we identified a low pathogenic avian influenza A(H11N2) virus in a white-rumped sandpiper (Calidris fuscicollis) sampled at Lagoa do Peixe National Park (PNLP) in southern Brazil. Whole-genome sequencing revealed that seven of the eight gene segments shared high nucleotide similarity (approximately 98.8%) with viruses previously detected in shorebirds from Delaware Bay, North America. In contrast, the PB1 segment showed high nucleotide similarity (approximately 99%) to the PB1 lineage associated with clade 2.3.4.4b A(H5N1) genotype B3.2 viruses circulating in the Americas. Phylogenetic, nucleotide identity, and molecular clock analyses indicated that this lineage shares a recent common ancestor with North American LPAI viruses and was subsequently detected in distinct viral genetic backgrounds. Although no HPAI virus was identified in this study, the presence of a PB1 segment related to H5N1-associated lineages suggests that genetic components linked to these viruses were circulating among low pathogenic avian influenza viruses in South America. These findings highlight the importance of continued surveillance in migratory bird populations to improve understanding of avian influenza virus diversity and support epidemiological monitoring.

Source: 


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The #NK Cell #Landscape in the Natural History of #Hantavirus Cardiopulmonary Syndrome in a Chilean Cohort

 


Abstract

Hantavirus cardiopulmonary syndrome (HCPS) caused by Andes Orthohantavirus (ANDV) carries case-fatality rates up to 40%; however, the innate immune determinants of disease severity remain poorly defined. Natural killer (NK) cells are central mediators of early antiviral immunity, but their landscape during the earliest phase of ANDV infection has not been characterized. Using multiparameter flow cytometry and unsupervised UMAP-based clustering in PBMCs from 13 HCPS patients stratified by severity and nine healthy donors, we show that severe HCPS is characterized by a coordinated disruption of the CD56dim NK cell compartment, encompassing reduced subset frequencies, specific reduction in the terminally differentiated NKG2C+CD57+ adaptive-like pool, and intrinsic impairment of IFN-γ production and degranulation, deficits that were absent in mild patients and persisted in part beyond clinical recovery. Furthermore, CD56dimCD16+ NK cell frequencies correlated negatively with viral load across all acute patients, independent of clinical severity. These findings establish severe HCPS not merely as a state of NK cell depletion, but as one of selective functional impairment of the most cytotoxically competent NK cell population during the critical early acute phase of ANDV infection.

Source: 


Link: https://www.mdpi.com/1999-4915/18/7/712

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Systemic #atopy and upper - #airway disease define susceptibility to incident #asthma after #COVID19 in #Korea

 


Abstract

Incident asthma is an important respiratory sequela after COVID-19, but it is unclear which allergic phenotypes amplify risk. Using a linked nationwide Korean database of 3,987,182 individuals with confirmed severe acute respiratory syndrome coronavirus 2 infection, we compare claims-based incident asthma in those with pre-existing systemic atopy and/or upper-airway disease (allergic rhinitis, chronic rhinosinusitis, atopic dermatitis or food allergy) versus those without after 1:1 propensity score matching. During follow-up to 31 December 2022, participants with pre-existing disease have higher asthma incidence than matched controls (3.55 vs 2.13 per 1,000 person-years), with a hazard ratio of 1.66 (95% confidence interval 1.58–1.75). Asthma risk is elevated for each condition and increases with greater disease burden. These findings show that pre-existing allergic and upper-airway phenotypes stratify post-COVID incident asthma risk on a national scale, supporting targeted surveillance in high-risk subgroups.

Source: 


Link: https://www.nature.com/articles/s41467-026-74860-w

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History of Mass Transportation: The Class 86 Diesel Shunter of Romania Railways

 


{Click on Image to Enlarge}

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By Stefan Puscasu - http://cfr.stfp.net/?class=86&veh=23&all=Y&ppr=5, Public Domain, https://commons.wikimedia.org/w/index.php?curid=8459449

Source: 


Link: https://en.wikipedia.org/wiki/Rolling_stock_of_the_Romanian_Railways#/media/File:Locomotiva_CFR_clasa_86.jpg

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Friday, June 26, 2026

TAG-TP #statement on #immunomodulators and host-directed #therapies for #Bundibugyo virus disease (WHO, June 26 '26)



    In the context of prioritization of therapeutics to be included in clinical research for Bundibugyo virus disease (BVD) the Technical Advisory Group on Therapeutics Prioritization (TAG-TP) has begun examining the landscape of immunomodulatory and host-directed new or repurposed agents

    Currently, there are no studies in patients characterizing the downstream pathogenesis that follows infection with Bundibugyo virus (BDBV). 

    The available evidence derives mainly from data collected with Ebola virus, specifically Zaire ebolavirus (EBOV) that provides relevant information from animal models and patients, but not sufficient to allow a proper assessment for the selection of immunomodulatory and host-directed candidates for clinical trials in BVD. 

    In addition, it is noted that even corticosteroids have never been tested in a stringent filovirus animal model

    For other infectious diseases leading to sepsis or other severe disease evolutions, it is also noted that immunomodulators can be beneficial or detrimental depending on the timing of the administration.

    To allow for a proper scientific evaluation of the different potential interventions, the appropriate timing of administration and the appropriate patient selection for inclusion in large clinical trials, it is imperative to generate quality data on the natural history of BVD from people infected with BDBV. 

    This would likely need to occur at select clinical sites that are adequately equipped to collect and analyze samples from patients with BVD. 

    Suggested data for collection include immune makers associated with inflammation and innate/adaptive immunity, correlative viral load and clinical features, markers of coagulation perturbation and organ/tissue damage. 

    This will help identify biomarkers pertaining to a pro-inflammatory status with co-relation to clinical phenotypes and organ dysfunction.

    Only in this way will it be possible to identify and/or confirm potential pharmacological targets and related potential interventions. 

    Collecting further evidence is paramount to minimizing risks to participants in clinical trials, as, depending on individual patient phenotypes and the status of disease evolution, the administration of some immunomodulatory agents may result in detrimental effects (e.g. on viral replication).

    In addition, some of these clinical investigations may have to be tailored to specific immune phenotypes based on the pharmacological activity of the investigational candidate, but sophisticated biomarker testing should be avoided to ensure implementation of clinical trials at BDBV Treatment Units.

    Lastly, timely availability of data from animal models would also provide evidence to facilitate the identification of the most promising therapies for inclusion in clinical trials.

Source: 


Link: https://www.who.int/news/item/26-06-2026-tag-tp-statement-on-immunomodulators-and-host-directed-therapies-for-bundibugyo-virus-disease

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#USA, #Wastewater Data for Avian #Influenza #H5 (US CDC, June 26 '26)

 


{Excerpt}

(...)

Time Period: June 14, 2026 - June 20, 2026

    -- A(H5) Detection4 site(s) (0.9%)

    -- No Detection:  455 site(s) (99.1%)

    -- No samples32 site(s)


{Click on Image to Enlarge}




(...)

Source: 


Link: https://www.cdc.gov/wastewater/emerging-viruses/h5.html?

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Avian #influenza #overview March–May 2026 (ECDC, Summary, June 26 '26)



26 June 2026

Publication series: Avian influenza overview

    

    Between 28 February and 4 June 2026, 949 highly pathogenic avian influenza (HPAI) A(H5) virus detections were reported in domestic (186) and wild (763) birds in 30 countries in Europe.


Abstract

    The downward trend in the number of detections observed at the end of the previous reporting period continued and is expected to persist throughout the summer. 

    While the number of HPAI A(H5N1) outbreaks in domestic birds remained at a low level, except in a few countries, A(H9N2) virus of clade G5.5 was detected in poultry in Europe for the first time

    Following the intense circulation of HPAI viruses in waterfowl in recent months, sporadic detections were reported in mammals, particularly in wild carnivores, including the detection of A(H5N5) virus in a polar bear and a walrus in Norway

    Outside Europe, the focus of HPAI virus detections shifted from North to South America, where a large number of outbreaks and mortality events in swans were reported. 

    Between 28 February and 4 June 2026, 19 cases of avian influenza virus infection were publicly reported in humans (including three fatal cases) in six countries and territories: Bangladesh (two cases with A(H5N1), one fatal), Cambodia (three cases with A(H5N1), one fatal), India (one case with A(H5N1)), Italy (one imported case with A(H9N2)), China (10 A(H9N2) cases and one fatal A(H5N6) case), and Taiwan (one A(H7N7) case). 

    Most human cases reported exposure to poultry or a poultry environment prior to detection or onset of illness. 

    Human infections with avian influenza viruses remain rare and no sustained human-to-human transmission has been documented. 

    The risk posed by avian influenza A(H5N1) clade 2.3.4.4b viruses currently circulating in Europe remains low for the general public in the European Union/European Economic Area (EU/EEA) and low-to-moderate for those occupationally or otherwise exposed to infected animals or contaminated environments.

Source: 


Link: https://www.ecdc.europa.eu/en/publications-data/avian-influenza-overview-march-may-2026

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Surveillance for West NileVirus Infections in Humans in Europe, Weekly Report: Week 26, 2026 (ECDC, summary)

 


{Excerpt}

Epidemiological summary

    Since the beginning of 2026, and as of 24 June, two countries in Europe reported three human cases{1} of West Nile virus (WNV) infection: Italy (two cases) and North Macedonia (one case).

    The current report in Table 1 includes the number of probable and confirmed cases of WNV infections per NUTS3 region. However, these figures are preliminary and should be interpreted with caution as they may be revised by the countries as more information becomes available. For further details on case numbers, please refer to the joint monthly report, which offers a more detailed analysis.

    Please note: The table and map in this report contain countries and areas where human West Nile virus infection cases were reported to EpiPulse Cases.

(...)

#) Country

    ° Affected area*

        § Newly affected area**

            - Number of probable cases - Number of confirmed cases - Total cases 

1) Italy

    ° Caserta

        § No

            - 0 / 1 /1 

    ° Firenze

         § No

            - 0 / 1 /1 

2) North Macedonia

    ° Vardarski

        § No

            - 0 / 1 / 1

__

{*} An ‘affected area’ or ‘risk area’ is defined as ‘a risk area with ongoing transmission of WNV to humans’. This means that at least one autochthonous human case of WNV has been reported as a result of local transmission in the area according to the agreed, standardised and disease-specific case definition. In exceptional circumstances, a probable case can be used to determine transmission, however, this should only apply in specific and agreed situations when a case cannot be confirmed within a reasonable time.

{**} Compared to the previous weekly report.

(...)

Source: 


Link: https://wnv-weekly.ecdc.europa.eu/

____

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

 


{Click on Image to Enlarge}

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By Benjamint444 - Own work, GFDL 1.2, https://commons.wikimedia.org/w/index.php?curid=26540141

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Late in the afternoon of Thursday, June 18 of this year, officials from the National System of Conservation Areas (SINAC) of the Ministry of Environment and Energy (MINAE) found a blue-footed booby at Espadilla Beach in Manuel Antonio, Quepos city. The bird was transferred to the quarantine area of an animal rescue center in Quepos, where it was euthanized on Friday, June 19, and a necropsy was performed to collect samples. These samples were transported by official SENASA personnel to the National Laboratory of Veterinary Services (LANASEVE) on Monday, June 22, and a positive result for highly pathogenic avian influenza type A, H5, was obtained on June 24. As complementary measures, public-private coordination strategies have been established to strengthen epidemiological surveillance, promote the reporting of suspected cases nationwide, and reinforce biosecurity measures. To date, there is no evidence of disease transmission to domestic birds.

Source: WOAH, https://wahis.woah.org/#/home


Link: https://wahis.woah.org/#/in-review/7657

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Effectiveness of #baloxavir marboxil in nonhuman #primates infected with highly pathogenic avian #influenza #H7N9 virus

 


Summary

Background

Highly pathogenic avian influenza (HPAI) A(H7N9) virus poses a potential public health threat, underscoring the need for effective antiviral options for outbreak preparedness. Baloxavir marboxil (BXM) is a cap-dependent endonuclease inhibitor approved for seasonal influenza, but its in vivo efficacy against HPAI A(H7N9) virus has not been fully evaluated.

Methods

We evaluated the efficacy of BXM in cynomolgus macaques infected with a reverse genetics-generated HPAI A(H7N9) virus. Animals received either low- or high-dose BXM, single-dose oseltamivir, or vehicle at 4 or 48 h post-infection (hpi). BXM administration was designed to mimic human pharmacokinetics. Viral titres, body temperature, body weight, lung pathology, and treatment-emergent viral substitutions were analysed.

Findings

Early treatment (4 hpi) with BXM significantly reduced viral titres in nasal and tracheal swabs, lessened weight loss, and decreased pulmonary inflammation and alveolar damage compared to untreated or oseltamivir-treated animals. Virus pathogenicity was relatively mild; no animals died. Delayed treatment (48 hpi) showed limited benefit. The PA-I38T (83.8%) and PA-E23G (78.6%) substitutions associated with BXM resistance were detected in one animal, and a PA-K34R (85.4%) substitution was detected in another animal. These substitutions reduce BXM susceptibility and were detected at low titres.

Interpretation

Although the dosing regimen used in this study involved repeat dosing to achieve the plasma drug concentrations after a single dose in humans, these findings highlight the importance of early antiviral intervention and support BXM use as a potential countermeasure against HPAI A(H7N9) virus infection, as resistance-associated substitutions remained limited in the macaque model. BXM may be a valuable therapeutic option for HPAI A(H7N9) virus infections.

Funding

Supported by the Japan Agency for Medical Research and Development (JP20wm0125002, JP223fa627001) and Shionogi & Co., Ltd.

Source: 


Link: https://www.thelancet.com/journals/ebiom/article/PIIS2352-3964(26)00233-1/fulltext

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Size of the 2026 #Ebola #outbreak and #risk of cross-border #spillover from #Bundibugyo virus in Ituri Province, #DRC, and its implications for #preparedness: a recalibrated stochastic modelling study

 


Summary

Background

On May 15, 2026, WHO declared a Bundibugyo virus (BDBV) outbreak in Ituri Province, DR Congo with an estimated index case on April 1, 2026 (6-week pre-declaration interval). By May 24, DR Congo reported 906 suspected cases (105 confirmed and ten confirmed deaths) across three provinces. Uganda reported seven confirmed cases (three imported; four locally acquired including three health-care workers; case-fatality ratio 14%). WHO declared a Public Health Emergency of International Concern on May 17, 2026; Africa Centres for Disease Control and Prevention declared a Public Health Emergency of Continental Security on May 18, 2026. The study aimed to establish a short-term trajectory of the BDBV outbreak and probability of cross-border spillover into countries with elevated risk of importation to guide preparedness priorities.

Methods

We calibrated a stochastic SEIRD (susceptible, exposed, infectious, recovered, and dead) ensemble model to the laboratory-confirmed case series, anchoring on 598 cumulative confirmed cases on June 8, 2026 (day 68) using simulation filtering (calibration window ±30%; reporting fraction 1·0 for laboratory-confirmed cases). The case-fatality ratio was drawn from a previous value centred on the observed confirmed-case ratio of approximately 19% (115 of 598). A linked daily-hazard spillover model estimated importation probability for Uganda, South Sudan, Rwanda, and Burundi over a 12-week horizon. The early suspected-case series, which peaked at 1077 on May 26, 2026, before being substantially revised downward by laboratory reclassification, is reported for context but was not used for calibration.

Findings

Laboratory-confirmed DR Congo cases rose from 33 on May 18, 2026, to 598 by June 8, 2026. Calibrated to the confirmed-case anchor (598 on June 8, 2026; central basic reproduction number [R0]=1·71), the confirmed-case trajectory is most consistent with the central scenario. Under the central scenario the ensemble projected a median of 990 cumulative confirmed cases by week 12 (June 24, 2026; 90% prediction interval [PI] 709–1293) and 174 deaths; the low scenario projected 870 confirmed cases (90% PI 641–1133) and 160 deaths. The early suspected-case count (peak 1077 on 26 May 2026) was substantially revised by laboratory reclassification and is reported for context only. Cross-border spillover remained material: Uganda 94·2% importation probability (19 confirmed cases as of June 4, 2026, including five health-care worker infections and two deaths); South Sudan 69·3%; Rwanda 8·6%; and Burundi 2·0%. As of June 22, 2026, DR Congo has 1048 confirmed cases and 267 confirmed deaths and Uganda has 20 confirmed cases, two confirmed deaths, and one probable death. These numbers are changing daily and are likely to align with what is predicted in the central scenario.

Interpretation

From the most recent laboratory-confirmed data, the outbreak is closer to what is predicted by the central scenario, even with the intensified response within DR Congo. However, uncertainty remains around reported case numbers due to low rate of contact tracing. Sustained control nonetheless remains the primary determinant of regional risk: importation into Uganda is already established, and South Sudan must continue to reinforce infection prevention and control, rapid response capacity, and cross-border surveillance under International Health Regulations 2005. These projections should be interpreted as exploratory preparedness-oriented estimates derived from a stochastic scenario-based modelling framework, rather than predictions generated from formally fitted epidemiological models using comprehensive parameter estimation and identifiability analyses.

Funding

None.

Translations

For the French and Swahili translations of the abstract see Supplementary Materials section.

Source: 


Link: https://www.thelancet.com/journals/laninf/article/PIIS1473-3099(26)00320-8/fulltext

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Thursday, June 25, 2026

#Nipah virus disease - #India (WHO D.O.N., June 25 '26)

 


Situation at a glance

    On 11 June 2026, the Kerala State Health Department confirmed one laboratory confirmed case of Nipah virus (NiV) infection in Kozhikode district, Kerala State, India

    The case is an adult male who developed symptoms on 30 May 2026 and was hospitalized on 10 June 2026. 

    He presented with neurological manifestations and at the time of reporting is on ventilatory support in an intensive care unit (ICU). 

    As of 18 June 2026, a total of 104 contacts had been identified and were under monitoring, including health and care workers, with no reported secondary cases to date. 

    NiV is a zoonotic disease transmitted to humans through infected animals, or through consumption of fruits or fruit products, such as raw date palm juice contaminated with the saliva, urine, or excreta of infected bats, as well as close contact with infected individuals

    The current event involves a single confirmed case, with no secondary transmission identified to date. 

    Public health measures are in place, including isolation, contact tracing, and enhanced surveillance. 

    However, as the source of infection has not yet been identified and given the known presence of animal reservoirs, additional cases cannot be excluded.


Description of the situation

    On 11 June 2026, WHO was informed of a laboratory-confirmed case of Nipah virus infection reported in Kozhikode district, Kerala State

    Initial positive results were obtained through PCR testing at local laboratories and were subsequently confirmed by RT‑PCR at the National Institute of Virology, Pune.

    The case is an adult male resident of Kozhikode district. He developed symptoms on 30 May 2026 and was admitted to hospital on 10 June 2026. The clinical presentation was primarily neurological, without reported respiratory symptoms prior to intubation. The patient is on ventilatory support in the ICU.

    Following confirmation of the case, extensive contact tracing was initiated. As of 18 June 2026, a total of 104 contacts had been identified, including four very high-risk, 14 high-risk, and 86 low-risk contacts. Among these, 45 are health and care workers. All contacts are under active monitoring with regular follow-up, and no secondary cases have been reported to date.

    This event follows a pattern of recurrent Nipah virus outbreaks in Kerala, including in Kozhikode district, since the first outbreak was reported in 2018. Additional outbreaks occurred in 2019, 2021, 2023, 2025, and 2026 according to the NCDC Communicable Disease Alert.


Epidemiology

    NiV infection is a zoonotic disease transmitted to humans through infected animals (such as bats), or fruit or fruit products contaminated with saliva, urine, and excreta of infected bats.  

    Fruit bats or flying foxes (Pteropus species) are the natural hosts for the virus.  

    It can also be transmitted directly from person to person through close contact with an infected person.

    The incubation period ranges from 3 to 14 days. In some rare cases, an incubation period of up to 45 days has been reported. 

    Laboratory diagnosis of a patient with a clinical history of NiV infection can be made during the acute and convalescent phases of the disease by using a combination of tests. 

    The main tests used are RT-PCR from bodily fluids and antibody detection via ELISA. 

    Human infections range from asymptomatic infection to acute respiratory infection (mild, severe), neurological symptoms, and fatal encephalitis (brain swelling). 

    Infected people initially develop symptoms including fever, headaches, myalgia (muscle pain), vomiting and sore throat. This can be followed by dizziness, drowsiness, altered consciousness, and neurological signs that indicate acute encephalitis (brain swelling). Some people can also experience atypical pneumonia and severe respiratory complications, including acute respiratory distress. Encephalitis and seizures occur in severe cases, progressing to coma within 24 to 48 hours. 

    The case fatality ratio (CFR) in outbreaks across Bangladesh, India, Malaysia, and Singapore range from 40% to 75%, depending on local capabilities for early detection and clinical management.  

    Intensive supportive care is recommended to treat severe respiratory and neurologic complications.  

    There are currently no licensed medicines or vaccines specific for NiV infection.  

    Henipavirus nipahense (Nipah virus) is considered a priority pathogen for the accelerated development of medical countermeasures (MCMs) to respond to epidemics and pandemics as part of the WHO R&D Blueprint for Epidemics.  

    Further information about NiV infection can be found here. 


Public health response

    National and State authorities have implemented a range of coordinated response measures, including surveillance, case management, contact tracing, risk communication, and One Health investigations.

    Immediate initiation of response measures upon preliminary positive laboratory results prior to national confirmation. Ongoing monitoring and coordination by State and Central health authorities, including the activation of Rapid Response Teams and coordination meetings at district level. 

    Deployment of central expert teams: a National Centre for Disease Control (NCDC) team and an Indian Council of Medical Research (ICMR) expert team both visited Kozhikode on 13 June 2026 to evaluate the situation and provide technical support for ongoing response activities.

    Establishment of a State High-Power Committee for Epidemic Control: the Kerala State Health Department has constituted a multi-sectoral expert committee to study recurrent seasonal outbreaks in Kerala and develop evidence-based preventive recommendations. Membership includes government and private-sector clinicians, One Health experts, representatives from Animal Husbandry, Food Safety, Ayurveda, Yoga and Naturopathy, Unani, Siddha, and Homoeopathy (AYUSH), and local government bodies.

    Identification and monitoring of 104 contacts, with twice-daily follow-up.

    Establishment of isolation wards and dedicated quarantine facilities at Kozhikode Government Medical College Hospital. Provision and stockpiling of personal protective equipment (PPE) and essential medical supplies.

    Establishment of a control room for risk communication and public queries.

    Systematic community surveillance: door-to-door surveys completed across all 320 households (1047 residents) in Ramanattukara Municipality Division 5. No Nipah-compatible symptoms were identified among surveyed residents.

    Psychosocial support: a district mental health programme is providing psychological support to contacts under quarantine, with 125 contacts reached by 18 June 2026.

    One Health and environmental investigation: Animal Husbandry Department conducted specimen collection within a 5 km radius of the epicentre, including bat specimens (collected with Forest Department assistance) and faecal samples from bat roosting sites along with samples from other animals. All samples have been dispatched to the National Institute of High Security Animal Diseases (NIHSAD), Bhopal, for Nipah virus testing; results are pending.

    WHO continues to monitor the evolving situation and support risk assessment and coordination efforts as needed.


WHO risk assessment

    Nipah virus (NiV) (Henipavirus nipahense) is a rare zoonotic pathogen with a high case fatality rate (40–75%) and no licensed vaccine or specific antiviral treatment. 

    Its natural reservoirs are fruit bats (Pteropus spp.), which are widely distributed across India, South and Southeast Asia, and parts of Oceania. 

    Transmission to humans can occur through direct contact with infected animals, including bats and domestic animals, via contaminated food products such as raw date palm sap, or through close and prolonged contact with infected individuals, particularly in healthcare settings.

    Since its first identification in 1998, NiV outbreaks have been reported in Bangladesh, India, Malaysia, the Philippines, and Singapore

    In India, outbreaks have been recurrent but relatively limited in scale, with the highest numbers reported in 2001 (66 cases) and 2018 (18 cases). 

    Over the past five years, approximately a dozen confirmed cases have been reported, all in Kerala State. Kerala has experienced NiV events since 2018 and has established surveillance systems, laboratory capacity, and rapid response mechanisms, including Rapid Response Teams at central and state levels. Ecological conditions, including those in districts such as Kozhikode, support fruit bat populations, facilitating repeated spillover events. Seasonal patterns are observed and locally, April to September is recognized as a Nipah high‑alert period.

    The current event involves a single confirmed case with no evidence of secondary transmission as of 23 June 2026. The case has been isolated, and public health measures, including contact tracing, enhanced surveillance, and strengthened infection prevention and control in healthcare settings, have been rapidly implemented. The event appears to be geographically limited, with no evidence of international spread reported.

    However, as the source of infection has not yet been identified and given the presence of known animal reservoirs and ongoing seasonal risk, additional cases, including sporadic zoonotic spillover, cannot be excluded.

    This event represents the second notification of NiV infection in India in 2026, following the earlier two epidemiologically linked cases reported in West Bengal state in January 2026. There is an ongoing moderate sub-national risk, driven by recurrent zoonotic spillover, limited clinical specificity during the early stages of disease, and the absence of licensed vaccines or specific therapeutics, with potential for transmission among close contacts and in healthcare settings

    At the regional and global levels, the risk remains low, given the absence of cross-border or international spread and the geographically contained nature of the outbreak.


WHO advice

    In the absence of a licensed vaccine or specific therapeutic treatment for Nipah virus disease, reducing or preventing infection in people relies on raising awareness of the risk factors. 

    This includes providing guidance on and reinforcing risk communication messages about the measures that people can take to reduce exposure to the Nipah virus. 

    Patient management should focus on delivering timely supportive care, supported by an effective laboratory system and adequate infection prevention and control measures in health facilities. 

    Intensive supportive care is recommended for treatment of severe respiratory and neurologic complications.  

    Public health educational messages should focus on

        ° Reducing the risk of bat-to-human transmission 

            Efforts to prevent transmission should first focus on decreasing bat access to date palm sap and other fresh food products

            Freshly collected date palm juice should be boiled, and fruits should be thoroughly washed and peeled before consumption. 

            Fruits with signs of bat bites should be discarded. 

            Areas where bats are known to roost should be avoided. 

        ° Reducing the risk of human-to-human transmission

            Close unprotected physical contact with NiV-infected people should be avoided. 

            Regular hand washing should be carried out after caring for or visiting sick people along other preventive measures. 

            People experiencing Nipah-like symptoms should be referred to a health facility, as early supportive care is key in the absence of treatment. 

            Contact tracing and monitoring are also key to mitigate human-to-human transmission.  

        ° Controlling infection in health care settings 

            Health and care workers caring for patients with suspected or confirmed infection, or handling specimens from them, should always implement standard precautions for infection prevention and control at all times, for all patients. 

            When caring for patients with suspected or confirmed NiV, WHO advises the use of contact and droplet precautions including a well-fitting medical mask, eye protection, a fluid-resistant gown, and examination gloves

            Airborne precautions should be implemented during aerosol-generating procedures, including placing the patient in an airborne-infection isolation room and the use of a fit-tested filtering facepiece respirator instead of a medical mask. 

            Suspected or confirmed cases of NiV should be placed in a single-patient room. 

            Samples taken from people and animals with suspected NiV infection should be handled by trained staff working in suitably equipped laboratories. 

Based on the currently available information, WHO does not recommend any travel and/or trade restrictions

(...)

Source: 


Link: https://www.who.int/emergencies/disease-outbreak-news/item/2026-DON609

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