Tuesday, June 9, 2026

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

 


Abstract

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


Competing Interest Statement

The authors have declared no competing interest.

Source: 


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

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Avian #Influenza #Report - May 31 – June 6 '26 (Wk 23) (#HK CHP, June 9 '26): 2 new human #H5N1 virus cases in #Bangladesh, #India; 1 new case of H9N2 virus in #China



(...)

    -- Bangladesh

        ° Avian influenza A(H5N1) 

            ° Sylhet Division

                - The case involved a child with symptom onset on March 27, 2026.  

                - The patient was admitted to a hospital on March 28 for treatment of measles with bronchopneumonia, and was discharged on March 30. 

                - Epidemiological investigations revealed the case had exposure to household poultry.   

                - No additional cases were reported among the identified contacts.  

    -- India

        ° Avian influenza A(H5N1)

            - The case involved a child who developed symptoms and was admitted to a hospital on March 19, 2026. 

            - The patient was discharged on March 23.  

            - Epidemiological investigations revealed the case likely had indirect exposure to poultry. 

            - No additional cases were reported among the identified contacts. 

        -- China

            ° Avian influenza A(H9N2)

                ° Yunnan Province

                    - A 4-year-old boy with onset on May 17, 2026. 

(...)


Link: https://www.chp.gov.hk/files/pdf/2026_avian_influenza_report_vol22_wk23.pdf

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

 


{Click on Image to Enlarge}

By Charles J. Sharp - Own work, from Sharp Photography, sharpphotography.co.uk, CC BY-SA 4.0, https://commons.wikimedia.org/w/index.php?curid=129540572

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    On June 3, 2026, the Regional Office of the National Agri-Food Health and Safety Services (SENASA) was notified of an unusual mortality event among wild birds in the community of El Higuito, Talgua, in the department of Lempira, an area bordering the department of Copán

    Following the official reception of the notification and the collection of samples, the Central Laboratory (IHIMV) confirmed on June 5, 2026, via RT-PCR, the presence of Avian Influenza Type A Subtype H5

    The event involved the mortality of black vultures (Coragyps atratus), which poses a potential risk to small-scale and commercial poultry farming in the area. 

    As an immediate response, the contingency team was activated, carrying out the collection, incineration, and sanitary burial of 136 wild birds found dead, with the aim of reducing the environmental viral load and limiting the spread of the pathogen. 

    Additionally, coordination with poultry sector authorities was strengthened to implement preventive and biosecurity measures. 

    Epidemiological surveillance has been intensified both in the outbreak zone of the event and around the outbreak. 

    Through door-to-door monitoring conducted in six surrounding communities, 14,282 backyard birds were inspected without identifying clinical signs compatible with avian influenza or mortality events. 

    These findings indicate that, to date, there is no evidence of transmission to domestic poultry

    Given the epidemiological risk associated with the circulation of the virus in wildlife, active surveillance will continue in neighbouring communities and municipalities, along with the strengthening of biosecurity measures and risk communication directed at producers and the general public. 

    Follow-up reports will be submitted to provide periodic updates.

Source: 


Link: https://wahis.woah.org/#/in-review/7612

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Could #bradykinin #pathway inhibition change the course of severe #hantavirus disease?

 


Highlights

    • Hantavirus triggers the kallikrein–kinin system, driving severe capillary leak.

    • In vitro data show that bradykinin directly disrupts endothelial barrier function.

    • Two clinical cases support targeting the bradykinin pathway with icatibant.


Abstract

A recent multi-country hantavirus outbreak associated with a cruise ship underscores the urgent need to understand the mechanisms driving severe vascular leakage and multi-organ failure. While disease severity is largely attributed to a dysregulated host immune response and intense cytokine surge, the precise molecular mediators remain incompletely defined. Laboratory evidence indicates that hantavirus infection activates the factor XII–dependent kallikrein–kinin system, leading to elevated bradykinin production and subsequent endothelial barrier dysfunction. This translational mechanism is tentatively supported by two clinical case reports where severe hantavirus infections were successfully treated with the bradykinin receptor antagonist icatibant. We hypothesize that exaggerated bradykinin signalling drives the vascular leak phenotype, making the kallikrein–kinin pathway a compelling therapeutic target. Ultimately, effectively combating hantavirus-induced vascular permeability may require a multi-faceted approach combining targeted bradykinin inhibition with broader immunomodulatory strategies.

Source: 


Link: https://www.sciencedirect.com/science/article/abs/pii/S016524782600074X?via%3Dihub

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#Taiwan reported a rise in domestic #COVID19 cases, public is invited to wear masks as needed (CDC, June 9 '26)

 


    The Taiwan Centers for Disease Control (CDC) stated today (June 9th) that, according to monitoring data, the domestic COVID-19 epidemic has been rising from its low point

    In the 22nd week (May 31st - June 6th), there were 1,000 outpatient and emergency room visits related to COVID-19, a 4.1% increase compared to the previous week. 

    Last week (June 2nd - June 8th), there were 5 new local cases of severe COVID-19 complications, with no new local deaths. 

    Since October 2025, there have been a cumulative total of 90 local cases of severe COVID-19 complications, of which 14 have died

    The majority of severe cases are among those aged 65 and above (72.2%) and those with a history of chronic diseases (81.1%), and 93.3% have not received the COVID-19 vaccine this season.

    The Centers for Disease Control (CDC) pointed out that the global COVID-19 positivity rate has recently risen slightly from its low point. 

    The predominant circulating variants are BA.3.2 and XFG, followed by NB.1.8.1. 

    Among all regions, Southeast Asia has seen a significant increase

    The epidemic in neighboring countries is rising in India, the epidemic in Singapore is fluctuating from its peak, the epidemic in China is rising slightly from its low point, and the epidemic in Japan is flat from its low point.

    The Taiwan Centers for Disease Control (CDC) reminds the public that with the rise of COVID-19 cases in Taiwan, it urges the public to strengthen their self-protection awareness, practice hand hygiene and respiratory etiquette

    To protect their own health and the health of others, if they experience respiratory symptoms such as fever, cough, runny nose, or sore throat, or when visiting healthcare facilities, in crowded places where social distancing is difficult or poorly ventilated, or in close contact with the elderly or immunocompromised individuals, it is recommended to wear a mask

    If you have a fever or respiratory symptoms, it is advised to stay home and avoid unnecessary outings. 

    Those with severe risk factors and who meet the criteria for publicly funded antiviral medication should seek medical attention as soon as possible if they experience suspected symptoms. 

    A doctor will assess the symptoms and prescribe antiviral medication to reduce the risk of serious complications or death after infection. 

    Furthermore, the CDC urges those who have not yet received this season's COVID-19 vaccine within the past six months to get vaccinated as soon as possible.

    The Centers for Disease Control (CDC) emphasizes that there are currently sufficient reserves of COVID-19 vaccines and antiviral drugs. 

    For inquiries about vaccination sites, contracted hospitals for publicly funded oral antiviral drugs, and the latest epidemic prevention policies, the public can visit the CDC website (https://www.cdc.gov.tw) or call the toll-free epidemic prevention hotline 1922 (or 0800-001922).

Source: 


Link: https://www.cdc.gov.tw/Bulletin/Detail/gyc9j6zazoe_7nR9FqdFYQ?typeid=9

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Monday, June 8, 2026

#Ebola disease caused by #Bundibugyo virus, #DRC & #Uganda (#WHO D.O.B., June 8 '26): 515 confirmed cases and 95 deaths in DRC

 


Situation at a glance

    The Bundibugyo virus disease (BVD) outbreak in the Democratic Republic of the Congo continues to evolve rapidly, with increasing case numbers, geographic spread, and cross-border transmission to Uganda

    As of 6 June, a total of 515 confirmed cases, with 91 deaths among these confirmed cases, have been reported from the Democratic Republic of the Congo; Uganda has reported 19 confirmed cases including two deaths, as well as one probable case who has died

    In Uganda, the outbreak remains epidemiologically linked to transmission originating in the Democratic Republic of the Congo, with evidence of both imported infections and secondary transmission among contacts and healthcare workers

    National authorities, in collaboration with WHO and partners, are undertaking a wide-ranging package of response measures

    On 5 June, the Africa Centres for Disease Control and Prevention (Africa CDC) and WHO, together with partners, launched a joint Ebola continental preparedness and response plan, with an ask of US$ 518 million to support African countries to prepare for, rapidly detect and respond to the outbreak.


Description of the situation

    Since the last Disease Outbreak News was published on 29 May 2026, the number of confirmed cases and deaths have increased rapidly in the Democratic Republic of the Congo and Uganda

    In total, 534 confirmed cases including 93 deaths (case fatality rate [CFR] 17.4%) have been reported from both countries, while at least 17 people have recovered from the disease.

(...)


Democratic Republic of the Congo

    Since 29 May, an additional 390 confirmed cases including 74 confirmed deaths have been reported from the Democratic Republic of the Congo. 

    The increase is in part due to the scale up of testing and diagnostic capacities, enabling testing of the backlog of previously collected samples

    As of 6 June 2026, a total of 515 confirmed cases including 91 deaths (CFR 17.7%) have been reported from the Democratic Republic of Congo. 

    The reported CFR is likely an underestimation as many deaths that occurred before the outbreak declaration remain under investigation. 

    So far, 12 patients have recovered

    Cases have been reported from 25 health zones (HZ) from Ituri (17/36 HZ), North Kivu (7/35 HZ) and South Kivu Provinces (1/34 HZ)[1]. 

    Sixteen confirmed cases have been reported among health and care workers to date.

    The outbreak remains concentrated in Ituri Province, which accounts for 94% (487) of confirmed cases. 

    The CFR in Ituri is 15% (74/487); significantly lower than the CFR in North Kivu which is 64% (16/25). 

    The highest confirmed case numbers in Ituri Province are reported from Bunia (142 cases), Rwampara (98 cases), Mongbwalu (92 cases), and Nyankunde (24 cases) HZ.

    As of 6 June, 5040 contacts had been identified and were under follow-up across Ituri (4118), North Kivu (699), and South Kivu (223) provinces. 

    Of these, 2535 contacts were followed up in the last 24 hours, corresponding to follow-up rates of 43.2% in Ituri, 82.5% in North Kivu, and 80.3% in South Kivu.

    Increasing security-related incidents affecting health facilities have posed additional operational challenges in affected provinces. These conditions are constraining access for the response, disrupting surveillance and response activities, and increasing the risk of undetected transmission. Such incidents underline the challenges of the context and the importance of working closely with local leaders and communities. 


Figure 2: Number of confirmed cases (n = 515), including deaths,  in the Democratic Republic of the Congo, by date of reporting and as of 6 June 2026




{Click on Image to Enlarge}

NB: Newly reported confirmed cases/deaths may be part of the back log of samples and therefore not necessarily newly acquired infections. 


Uganda

    Since the last update dated 29 May, an additional 10 confirmed cases and one death have been reported from Uganda. 

    As of 6 June 2026, a total of 19 confirmed cases including two deaths in imported cases, and one probable case who has died, have been reported. 

    Five recoveries have been reported

    Of the total cases, 14 cases are imported and five are Ugandans

    The cases were reported from two districts Kampala and Wakiso

    To date, all cases in Uganda can be linked to travelers from the Democratic Republic of the Congo, or secondary infections linked to them; there has been no documented community transmission in Uganda. 

    Exposure risks are associated with healthcare settings and cross-border movements.

    About 70% of the cases are Congolese nationals who came to Uganda to seek medical care. 

    This includes a Congolese national who travelled from the Democratic Republic of the Congo, via Uganda, to the United Arab Emirates and then back to Uganda. 

    WHO is working with public health authorities in the United Arab Emirates and Uganda to gather additional information to assess the risk of exposure and facilitate contact tracing through the National International Health Regulations (IHR) Focal Point mechanism. 

    Based on the information available to date, there is no evidence that the case exhibited clearly recognized symptoms consistent with BVD during travel to or from the United Arab Emirates. 

    Following notification of the case, UAE authorities rapidly implemented risk assessment, contact tracing activities, follow-up of identified contacts, public health investigations, enhanced preparedness measures at points of entry, and coordination with relevant national and international partners. 

    Epidemiological investigations to date have not identified any secondary cases, local transmission, or evidence of onward spread in the. The findings support the conclusion that the risk of transmission associated with this event in the United Arab Emirates was very low.

    As of 2 June, a total of 668 contacts linked to the cases have been identified and are under follow-up. These include close residential contacts and hospital contacts where the cases were hospitalized. 


Figure 3: Number of confirmed cases (n = 19), including deaths, in Uganda by date of reporting and as of 6 June 2026  Number of confirmed cases and deaths in Uganda


{Click on Image to Enlarge}


Epidemiology

    Bundibugyo virus disease (BVD) is a severe and often fatal form of Ebola disease caused by the Bundibugyo virus, one of the Orthoebolavirus species

    It is a zoonotic disease, with fruit bats suspected to be the natural reservoir. 

    Human infection is thought to occur through close contact with the blood or secretions of infected wildlife, such as bats or non-human primates, and it subsequently spreads from person to person through direct contact with the blood, secretions, organs, or other bodily fluids of infected individuals or contaminated surfaces or items. 

    Transmission is particularly amplified in health-care settings when infection prevention and control (IPC) measures are inadequate, and during unsafe burial practices involving direct contact with the deceased.

    The incubation period for BVD ranges from two to 21 days, and individuals are not infectious until symptom onset

    Early symptoms such as fever, fatigue, muscle pain, headache, and sore throat, are non-specific, which complicates clinical diagnosis and can delay detection. 

    These symptoms then progress to gastrointestinal symptoms, organ dysfunction, and in some cases haemorrhagic manifestations. 

    Case fatality rates in the past two BVD outbreaks, reported in Uganda and in the Democratic Republic of the Congo in 2007 and 2012 were 30% and 50% respectively.

    Differentiating BVD from other endemic febrile illnesses such as malaria is challenging without laboratory confirmation using PCR or antigen/antibody-based assays. 

    Control relies on rapid case identification, isolation and care, contact tracing, safe burials, and strong community engagement, as no approved vaccines or specific treatments currently exist for BVD.


Public health response

    Health authorities in the Democratic Republic of the Congo and Uganda, in collaboration with WHO and partners, are implementing comprehensive public health measures including implementing the continental response plan, engaging donors and mobilizing additional resources to address critical funding gaps and sustain response operations across affected and at-risk areas.

    Key response activities also include interagency coordination and deployment of field teams, delivery of medical supplies, strengthening surveillance, increasing laboratory capacity, infection prevention and control, the set-up of safe and optimized treatment centers, risk communication and community engagement, and research on potential medical countermeasures.

    For further information about public health response actions by the respective Ministry of Health, WHO, and partners, please refer to the latest situation reports published by the WHO Regional Office for Africa:  Ebola Bundibugyo Virus Disease Outbreak Democratic Republic of the Congo | Uganda Weekly External Situation Report 03, Data as of 31 May 2026 | WHO | Regional Office for Africa


WHO risk assessment

    On 6 June 2026, WHO reassessed the risk of the outbreak of BVD to incorporate newly available information and the WHO Temporary Recommendations. 

    The risk for countries sharing land borders with countries with documented Bundibugyo virus (BVDV) detection, as of this report Democratic Republic of the Congo and Uganda, has been separated out from the risk for other countries in the African Region.

    The risk in the Democratic Republic of the Congo remains assessed as very high due to ongoing transmission and the continued expansion of the outbreak into new health zones, increasing the potential for further national and regional spread.

    The risk in Uganda is still assessed as high due to confirmed cross-border spread through imported cases and ongoing epidemiological links along the eastern Democratic Republic of the Congo–western Uganda corridor, historically affected by Ebola outbreaks, including Bundibugyo and Sudan virus disease outbreaks.

    The risk for countries with land borders adjoining countries with documented BDBV detection, is assessed as high due to sustained population mobility linked to cross-border trade and mining activities, variation in capacities and experience of BVD response and variable levels of readiness.

    The risk for the rest of the Africa region and at the global level is assessed as low.


WHO advice

    WHO advises against any restriction of travel to, or trade with, the Democratic Republic of the Congo or Uganda based on the currently available information. WHO continues to closely monitor and, where necessary, verify travel and trade measures in relation to this event.

    For further information on the considerations for implementing border health and international travel-related temporary recommendations, please see the relevant technical note issued on 26 May 2026

    The temporary recommendations issued to State Parties on 22 May 2026 underscore the importance of coordinated outbreak control, enhanced cross‑border collaboration, and sustained surveillance and preparedness to prevent further regional spread and ensure an effective public health response.

    WHO has convened several technical advisory groups, including the Strategic Advisory group of Experts (SAGE) to assess candidate vaccines and therapeutics for BVD. Key recommendations made are available in the news release published on 28 May 2026.

(...)

Source: 


Link: https://www.who.int/emergencies/disease-outbreak-news/item/2026-DON606

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Sunday, June 7, 2026

Indian encampment on Lake Huron, Paul Kane (1850)

 


{Click on Image to Enlarge}

Public Domain.

Source: 


Link: https://www.wikiart.org/en/paul-kane/indian-encampment-on-lake-huron-1850

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#Taiwan, #NZ #passenger of the cruise #ship MV #Hondius tested negative four times and released from self-health management on June 7 (CDC, edited)

 


    The Taiwan Centers for Disease Control (CDC) announced today (June 7) that following the Hantavirus Andean cluster outbreak on the Dutch cruise ship MV Hondius, and after notification through the World Health Organization (WHO) and the International Health Regulations (IHR) mechanism, Taiwan has identified one New Zealand passenger who had traveled on the cruise ship and entered Taiwan on May 7. 

    Following expert advice, the CDC arranged for the case to undergo enhanced self-health management and health monitoring in a single-person hospital room until midnight on June 6. 

    The enhanced self-health management was lifted on June 7, and Taiwan's IHR office notified the WHO and New Zealand's IHR office.

    The Taiwan Centers for Disease Control (CDC) stated that the passenger did not exhibit fever, cough, difficulty breathing, or other symptoms suspected to be related to Hantavirus infection during the monitoring period. 

    The passenger underwent four tests on May 14, May 20, May 27, and June 3, including PCR testing for Hantavirus Andes strain and serum IgM and IgG antibody tests, all of which were negative

    The passenger's health condition is stable

    The CDC emphasized that the passenger has completed a 42-day enhanced self-health monitoring period after testing negative and poses no risk of community transmission in Taiwan.

    The Taiwan Centers for Disease Control (CDC) explained that the Hantavirus Andean strain cluster on the Dutch cruise ship "MV Hondius" has reported a total of 13 cases as of June 2 (11 confirmed cases and 2 probable cases), with 3 deaths, resulting in a case fatality rate of 23%. 

    International contact tracing is ongoing; as of May 22, over 600 contacts have been traced, 53% of whom are high-risk contacts. 

    The WHO assesses this outbreak as low-risk globally

    The CDC will continue to monitor the outbreak through international cooperation mechanisms such as the WHO and IHR, and will adjust relevant prevention and control measures as needed based on the development of the epidemic.

Source: 


Link: https://www.cdc.gov.tw/Bulletin/Detail/kNW6ZgmX0N8DQepCuX63xg?typeid=9

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Saturday, June 6, 2026

#Bundibugyo virus disease #outbreak in #DRC: current #trajectory and potential #risk for a Pandemic Emergency

 


{Excerpt}

On May 15, 2026, DR Congo declared the 17th orthoebolavirus disease outbreak—the third in the country in two decades caused by the Bundibugyo virus variant (Orthoebolavirus bundibugyoense)—in the conflict affected north-eastern province of Ituri.1 The next day, the WHO Director-General determined this event a Public Health Emergency of International Concern (PHEIC) and on May 18, the Africa Centres for Disease Control and Prevention (CDC) declared a Public Health Emergency of Continental Security.2 10 days earlier, WHO received an alert about a cluster of unexplained deaths, including deaths among health workers, in the Mongbwalu Health Zone. Initial laboratory results were negative for orthoebolavirus and reagents from Ituri were reasonably provisioned for Ebola virus.1

(...)

Source: 


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#Human ACE2‑specific benzothiazole-based allosteric #inhibitor against pan ‑ #sarbecoviruses

 


Abstract

Emerging SARS‑CoV‑2 variants and related zoonotic sarbecoviruses rely on ACE2 for cell entry, motivating host‑directed antivirals that block spike-ACE2 interaction. Here, we characterize MB‑32, a benzothiazole small molecule that binds ACE2, selectively disrupts binding of SARS‑CoV‑2 spike receptor‑binding domain to ACE2, and preserves ACE2 enzymatic activity across species. MB‑32 potently inhibits entry of SARS‑CoV‑2 variants, SARS‑CoV‑1 and diverse bat/pangolin sarbecoviruses in ACE2‑expressing cells, while sparing vesicular stomatitis virus and authentic MERS‑CoV, indicating non‑virucidal, ACE2‑focused activity. Biochemical and biophysical analyses, supported by ACE2 mutagenesis, support a model in which MB‑32 engages a non‑catalytic surface pocket on the ACE2 N‑terminal helix to allosterically disrupt spike attachment. Intranasal MB‑32 achieves high airway concentrations, protects male ACE2‑transgenic mice and hamsters from SARS‑CoV‑2 disease, and prevents contact transmission of Omicron‑lineage viruses without detectable cardiovascular toxicity. These findings establish MB‑32 as a host‑targeted ACE2 entry inhibitor and provide a framework for small‑molecule ACE2‑directed antivirals against current and future sarbecovirus spillovers.

Source: 


Link: https://www.nature.com/articles/s41467-026-73944-x

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Cross-reactive #Bundibugyo #antibody responses after licensed #Ebola #vaccines

 


Abstract

Background 

The ongoing Bundibugyo virus disease (BDBV) outbreak in Central Africa highlights the absence of approved vaccines specifically targeting BDBV. Whether licensed Zaire ebolavirus (EBOV) vaccines induce cross-reactive immunity against BDBV remains largely unknown.

Methods 

We performed an immunogenicity analysis using serum samples from participants enrolled in the PREVAC randomized clinical trial evaluating licensed Ebola vaccine strategies in West Africa. Samples collected at day 28 (D28) and month 3 (M3) following vaccination with rVSVΔG-ZEBOV-GP or Ad26.ZEBOV/MVA-BN-Filo were assessed using a multiplex Luminex assay against glycoproteins from multiple filoviruses, including EBOV Kikwit, EBOV Mayinga, BDBV, Sudan virus, Reston virus, and Marburg virus.

Results 

A total of 179 samples were analysed. Detectable cross-reactive antibody responses against BDBV were observed across vaccine groups, timepoints, and age categories. However, BDBV responses remained substantially lower than homologous EBOV responses. In rVSV recipients, median BDBV responses (net MFI) reached 282 (IQR 164–644) at D28 compared with 1788 (832–3311) against the homologous Kikwit antigen. Similar patterns were observed following rVSV booster vaccination and Ad26.ZEBOV/MVA-BN-Filo vaccination. The heterologous Ad26/MVA regimen demonstrated increasing BDBV responses between D28 and M3.

Conclusions 

Licensed EBOV vaccines induced detectable but quantitatively reduced cross-reactive antibody responses against BDBV. Although no direct assessment of vaccine efficacy against BDBV disease was possible, these findings support the plausibility of partial heterologous immunity following EBOV vaccination. In the absence of approved BDBV-specific vaccines, these data support the urgent evaluation of currently available Ebola vaccines during BDBV outbreaks and reinforce the importance of developing broadly protective pan-filovirus vaccines.


Competing Interest Statement

The authors have declared no competing interest.


Clinical Trial

NCT02876328

Source: 


Link: https://www.medrxiv.org/content/10.64898/2026.05.27.26354223v1

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The #canine respiratory #epithelium is a permissive #ecosystem for #influenza interspecies #transmission and emergence

 


Abstract

The outcome of virus spillover ranges from dead-end infections to pandemics and is underpinned by host-pathogen interactions as well as evolutionary and epidemiological processes. The emergence of novel influenza A viruses (IAVs) has been associated with reassortment events involving multiple species, highlighting the importance of reservoir and intermediate hosts in viral emergence. Highly pathogenic H5N1 IAVs of the 2.3.4.4b genotype have caused a panzootic affecting a broad range of mammals. The role of dogs -arguably the most popular companion animal and a natural host of IAVs- in the ecology of IAVs under this new zooepidemiological scenario is unknown. To address this, we characterised the glycome of the dog respiratory epithelium, infected canine tracheal explants with multiple IAVs (including canine H3N2 and H3N8, equine H3N8, avian H3N8 and H5N1, swine H1N1, human H1N1 and H3N2, and bovine H5N1 viruses), and determined their cellular tropism. We show that the respiratory tract of dogs presents abundant sialylated glycans known to act as IAV receptors. Further, most IAVs (including 2.3.4.4b viruses) infected and replicated in dog tracheas, targeting mainly ciliated cells. Serological testing showed evidence of influenza spillover infections in dogs from the UK. Overall, our results show that the canine respiratory tract can provide a suitable environment for the generation of new IAVs. Given the multi-host contact networks of dogs in nature, they could act as recipients, bridging hosts, and/or mixing vessels for multiple IAV lineages, playing a central role in the ecology of influenza emergence.


Competing Interest Statement

The authors have declared no competing interest.


Funder Information Declared

Medical Research Council, https://ror.org/03x94j517, MR/Y03368X/1, MC_UU_0034/2, MC_UU_0034/3

Biotechnology and Biological Sciences Research Council, BB/Y007093/1, BB/Y007298/1, BBS/E/PI/230001A, BBS/E/PI/230002A, BBS/E/PI/230002B, BBS/E/PI/230001C

Source: 


Link: https://www.biorxiv.org/content/10.64898/2026.06.04.730051v1

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History of Mass Transportation: The Diesel Shunter Class 89 of the Romanian Railways in Pitesti

 


{Click on Image to Enlarge}


By Dr2005 - Wk Ro, http://ro.wikipedia.org/wiki/Imagine:89-0585-3-Pitesti-002.jpg, CC BY-SA 3.0, https://commons.wikimedia.org/w/index.php?curid=3553605

Source: 


Link: https://en.wikipedia.org/wiki/Rolling_stock_of_the_Romanian_Railways

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#Coronavirus Disease Research #References (AMEDEO, June 6 '26)

 


    Ann Intern Med

  1. KOUTOURATSAS T, Dammad T, Mylonakis E
    In outpatients with COVID-19 during Omicron variant circulation, some antivirals reduce time to recovery.
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    PubMed         Abstract available


    Clin Infect Dis

  2. BONTEN M, Essink B, Hanning N, Leroux-Roels I, et al
    Immunogenicity and safety of co-administration of AS01E-adjuvanted respiratory syncytial virus prefusion F protein vaccine and a COVID-19 mRNA vaccine in adults aged >/=50 years: a phase 3, randomized, non-inferiority trial.
    Clin Infect Dis. 2026 Jun 4:ciag344. doi: 10.1093.
    PubMed         Abstract available

  3. BRAMANTE CT, Stewart TG, Boulware DR, McCarthy MW, et al
    Metformin on the Presence of COVID-19 Symptoms 6 Months after Infection: The ACTIV-6 Randomized Clinical Trial.
    Clin Infect Dis. 2026 Jun 4:ciag335. doi: 10.1093.
    PubMed         Abstract available

  4. LIU C, Okoli GN, Chen R, Sullivan SG, et al
    SARS-CoV-2 vaccination and attenuation of breakthrough infection severity: A systematic global review and meta-analysis.
    Clin Infect Dis. 2026 Jun 1:ciag346. doi: 10.1093.
    PubMed         Abstract available


    Infect Control Hosp Epidemiol

  5. JURICA JM, Smith DM, Abeles S, Torriani FJ, et al
    Discontinuing contact precautions for COVID-19: the science says its time.
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    PubMed         Abstract available

  6. ALSOUBANI M, Andujar G, Campion M
    Socioeconomic and racial review of COVID-19 antiviral prescriptions: a large health system cohort.
    Infect Control Hosp Epidemiol. 2026 Jun 1:1-6. doi: 10.1017/ice.2026.10473.
    PubMed         Abstract available


    Int J Infect Dis

  7. VEIJER C, van Asselt ADI, van Zon SKR, Rosmalen JGM, et al
    Healthcare Resource Use and Costs under Pandemic Circumstances in The Netherlands: Results from the Lifelines COVID-19 Cohort.
    Int J Infect Dis. 2026 Jun 3:108854. doi: 10.1016/j.ijid.2026.108854.
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  8. ABU-RADDAD LJ, Ayoub HH, Coyle P, Tang P, et al
    Routine SARS-CoV-2 Testing Frequency and Risk of Severe COVID-19: A Nationwide Population-Based Study.
    Int J Infect Dis. 2026 Jun 2:108851. doi: 10.1016/j.ijid.2026.108851.
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  9. LAW AHT, Wong JY, Lin Y, Cowling BJ, et al
    Sex differences in COVID-19 infection and mortality in Hong Kong.
    Int J Infect Dis. 2026 Jun 2:108852. doi: 10.1016/j.ijid.2026.108852.
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  10. LIN Y, Wu P, Lau EHY, Blais J, et al
    SARS-CoV-2 viral shedding and vaccination?modified effects of oral antivirals in older COVID-19 patients: a retrospective cohort study in Hong Kong.
    Int J Infect Dis. 2026 Jun 1:108848. doi: 10.1016/j.ijid.2026.108848.
    PubMed         Abstract available


    J Med Virol

  11. CHEN Y, Lan Y, Zhao A, Zhang Y, et al
    Anti-Zika Virus Activity of Azvudine via Inhibition of RNA Replication by Its Active Triphosphate Form.
    J Med Virol. 2026;98:e71000.
    PubMed         Abstract available


    J Thorac Oncol

  12. XU X, Saad MB, Grippin A, Xu H, et al
    Brief Report: SARS-CoV-2 mRNA Vaccination Improved Survival in NSCLC Treated with Radiotherapy.
    J Thorac Oncol. 2026 Jun 1:103956. doi: 10.1016/j.jtho.2026.103956.
    PubMed         Abstract available


    J Virol

  13. FAN L, Gao X, Feng W, Huang Q, et al
    SARS-CoV-2 ORF3a suppresses host antiviral interferon responses by promoting STUB1-mediated PTEN proteasomal degradation.
    J Virol. 2026 Jun 2:e0018626. doi: 10.1128/jvi.00186.
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    Lancet

  14. KARIM SA, Mahomed S, Lewis L, Karim SSA, et al
    Urgent need for a reliable rapid diagnostic test for the Ebola epidemic caused by Bundibugyo virus in Africa.
    Lancet. 2026 Jun 2:S0140-6736(26)01093-7. doi: 10.1016/S0140-6736(26)01093.
    PubMed        


    Lancet Infect Dis


  15. Global burden of enteric infectious diseases, diarrhoeal diseases, and corresponding aetiologies, 1990-2023: a systematic analysis for the Global Burden of Disease Study 2023.
    Lancet Infect Dis. 2026 Jun 2:S1473-3099(26)00194.
    PubMed         Abstract available


    Science

  16. EMANUEL N, Harrington E, Pallais A
    Home alone: Remote work, isolation, and mental health.
    Science. 2026;392:eaec7671.
    PubMed         Abstract available

#Influenza and Other Respiratory Viruses Research #References (AMEDEO, June 6 '26)

 


    Arch Virol

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    In vitro efficacy of anti-influenza active compounds against clinical isolates with high growth capability.
    Arch Virol. 2026;171:200.
    PubMed         Abstract available


    Biochem Biophys Res Commun

  2. SHAO S, Dong ZY, Kang ZY, Zhang H, et al
    Dynamic regulation-based stabilizing mutations are highly effective for designing RSV pre-fusion F mRNA vaccines.
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  3. SANE J
    Rebuilding trust in public health: Beyond polarization.
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  4. HASSELL K, Andrews N, Dabrera G, Kall M, et al
    Acute COVID-19 mortality in England in the omicron era: a national-level matched cohort study.
    Epidemiol Infect. 2026;154:e70.
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    J Infect Dis

  5. PRASERT K, Praphasiri P, Ditsungnoen D, Naosri S, et al
    Risk of hospitalization related to influenza A(H3N2) virus subclade K, Thailand, June-December 2025.
    J Infect Dis. 2026 May 31:jiag283. doi: 10.1093.
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    J Neurosurg Pediatr

  6. ANDERSON MG, Pindrik J, Michelow IC, Anuar A, et al
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    J Virol


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    Pediatrics

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Friday, June 5, 2026

Modeled #Scenario #Projections for the #Ebola Disease #Outbreak Caused by #Bundibugyo Virus, 2026 (MMWR)

 


Summary

    -- What is already known about this topic?

        ° An outbreak of Bundibugyo virus disease (BVD), a type of Ebola disease, is currently ongoing, centered in the Ituri province of the Democratic Republic of the Congo (DRC).

    -- What is added by this report?

        ° CDC used a transmission model to project outbreak growth over 3 months, by using different assumptions about the number of deaths as of May 24, 2026, and by varying the percentages of persons with BVD who are successfully identified and isolated to prevent ongoing transmission. Assuming 50 cumulative deaths as of May 24, 2026, if 70% of patients were to enter isolation, only approximately one in 20 simulations projected an outbreak exceeding 10,000 cases within 3 months.

    -- What are the implications for public health practice?

        ° Large-scale, rapid public health action is needed to control the current outbreak, already the largest known BVD outbreak, from becoming one of the largest Ebola epidemics in history.


Abstract

On May 15, 2026, the Ministries of Health in the Democratic Republic of the Congo and Uganda declared outbreaks of Bundibugyo virus disease (BVD), a type of Ebola disease. In response to reports of high numbers of suspected cases and deaths in these outbreaks, CDC simulated scenario projections to understand possible future morbidity and mortality. A branching process model with the capacity to model transmission-reducing nonpharmaceutical interventions was calibrated to three putative cumulative death counts and projected for four possible intervention scenarios ranging from poor (20%) to extremely high (95%) levels of isolation and treatment of symptomatic persons. The analysis suggested a plausible spillover event (i.e., the transmission of a virus from its natural animal reservoir to humans) in mid to late February 2026. With poor isolation levels of patients with BVD (20%) and no other interventions, the likelihood of an outbreak that exceeds 20,000 cases within 3 months is 65%. If, however a high proportion of patients were to enter isolation (70%), only a one in 20 chance is projected for an outbreak with ≥10,000 cases within 3 months. These results underscore the importance of strong public health interventions, because the current outbreak is already the largest known BVD outbreak and has the potential to quickly become one of the largest Ebola disease outbreaks ever recorded.

Source: 


Link: https://www.cdc.gov/mmwr/volumes/75/wr/mm7522e1.htm?s_cid=mm7522e1_e&ACSTrackingID=USCDC_921-DM155686&ACSTrackingLabel=Early%20Release%20%E2%80%93%20Vol.%2075%2C%20June%205%2C%202026&deliveryName=USCDC_921-DM155686

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#Assessment of #Risk to the #US #Population from the #Ebola Disease #Outbreak Caused by #Bundibugyo Virus, 2026 (MMWR)

 


Summary

    -- What is already known about this topic?

        ° An outbreak of Bundibugyo virus disease (BVD), a type of Ebola disease, is currently occurring, centered in the Ituri province of the Democratic Republic of the Congo (DRC).

    -- What is added by this report?

        ° CDC assessed the risk posed by this ongoing outbreak to the U.S. population during the next 3 months as low.

    -- What are the implications for public health practice?

        ° Ensuring sufficient public health resources to control the outbreak in DRC will be necessary for maintaining a low risk to the U.S. population. If cases arise in the United States, there is public health capacity to contain and control an outbreak, and CDC guidance for U.S. clinicians and public health practitioners can help prevent the potential spread.


Abstract

On May 15, 2026, the ministries of health in the Democratic Republic of the Congo and Uganda declared outbreaks of Bundibugyo virus disease (BVD), a type of Ebola disease. In response to reports of high numbers of suspected cases and deaths in the affected countries, CDC assessed the risk posed by the BVD outbreak to the U.S. population during the next 3 months. This analysis used a standardized risk assessment approach that included epidemiologic data from the ongoing outbreak and historical data from previous Ebola outbreaks; the overall risk was determined by taking into account independent assessments of the likelihood of infection and the impact of infection. The assessment found that the overall risk to the U.S. population posed by the current BVD outbreak during the next 3 months is low, based on the extremely low likelihood of transmission, despite the high impact that potential infection could have and the resources that would be required to respond to the outbreak. Limitations to this assessment included uncertainties around the epidemiology of BVD as well as the current and future scope and geographic spread of the outbreak. CDC continues to monitor factors that could change this risk assessment.

Source: 


Link: https://www.cdc.gov/mmwr/volumes/75/wr/mm7522e2.htm?s_cid=mm7522e2_e&ACSTrackingID=USCDC_921-DM155686&ACSTrackingLabel=Early%20Release%20%E2%80%93%20Vol.%2075%2C%20June%205%2C%202026&deliveryName=USCDC_921-DM155686

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