#Coronavirus Disease Research #References (AMEDEO, June 13 '26)

 

Clin Infect Dis

1. BRITT NS, Khader K, He T, Prinzi AM, et al
   Clinical Impact of the BIOFIRE(R) FILMARRAY(R) Pneumonia Panel in the Veterans Affairs Healthcare System: A Difference-in-Differences Study.
   Clin Infect Dis. 2026 Jun 12:ciag328. doi: 10.1093.
   PubMed         Abstract available
   
   

   
   Infect Control Hosp Epidemiol

2. NERBY J, Berg W, McFarren M, Rhame F, et al
   Collaborative approaches to masking: statewide threshold development and performance across three respiratory seasons.
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   PubMed         Abstract available
   
   

   
   Int J Infect Dis

3. CHEN H, Manu EK
   Shifting patterns of acute respiratory infection mortality in Australia: Changing contributions of COVID-19, influenza and respiratory syncytial virus and persistent Indigenous inequalities.
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   PubMed         Abstract available
   
   

   
   Intensive Care Med

4. MEYBOHM P, Baron DM, Fries D, Lasocki S, et al
   Patient blood management in general intensive care patients.
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   PubMed         Abstract available
   
   

   
   J Infect

5. HARRIS R, Thirard R, McBrien C, Middleditch A, et al
   Immunogenicity and safety of co-administration of a recombinant shingles vaccine with an mRNA COVID-19 or adjuvanted influenza vaccine: a randomised controlled trial.
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   PubMed         Abstract available
   
   
6. WANG X, Yin J, Xu B, Guanhua X, et al
   Clinical epidemiological characteristics of hospitalized pediatric Mycoplasma pneumoniae pneumonia in China.
   J Infect. 2026 Jun 10:106793. doi: 10.1016/j.jinf.2026.106793.
   PubMed         Abstract available
   
   
7. TRUONG T, Radin JM, Li L, Ordonez-Mena JM, et al
   Burden and economic impact of RSV hospitalisations among English adults, 2023/24.
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   PubMed         Abstract available
   
   

   
   J Med Virol

8. USHIJIMA H, Onda-Shimizu Y, Kotaki T, Nishimura S, et al
   Co-Circulation and Mixed Infections of Classic and Melbourne Human Astroviruses Among Pediatric Acute Gastroenteritis Patients in Japan, 2018-2024.
   J Med Virol. 2026;98:e71002.
   PubMed         Abstract available
   
   
9. AYDIN U, Duzenci D, Akkoc RF, Karatas A, et al
   Serum Histatin Levels in COVID-19: Association With Disease Severity and Immune Status.
   J Med Virol. 2026;98:e71009.
   PubMed         Abstract available
   
   
10. CHEN R, Kong W, Li C, Zhang J, et al
    TXD-198 Exhibits Inhibitory Activity Against SARS-CoV-2 by Upregulating ANO1.
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    PubMed         Abstract available
    
    
11. DENG J, Lin Q, Zeng Z, Huang H, et al
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    PubMed         Abstract available
    
    
12. FU JYL, Lim SK, Jalalonmuhali M, Bador MK, et al
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    PubMed         Abstract available
    
    

    
    J Travel Med

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    Lancet Infect Dis

22. XIE Y, Choi T, Al-Aly Z
    Seasonal influenza versus COVID-19 hospitalisation risk during the 2025-26 influenza season.
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    PubMed        
    
    

    
    Travel Med Infect Dis

23. MIHAI I, Bonnaud L, Arregle F, Doudier B, et al
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    PubMed         Abstract available
    

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

 

Ann Intern Med

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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.
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   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.
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   PubMed         Abstract available
   
   
4. LIU C, Okoli GN, Chen R, Sullivan SG, et al
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   Infect Control Hosp Epidemiol

5. JURICA JM, Smith DM, Abeles S, Torriani FJ, et al
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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.
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   PubMed         Abstract available
   
   

   
   Int J Infect Dis

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9. LAW AHT, Wong JY, Lin Y, Cowling BJ, et al
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10. LIN Y, Wu P, Lau EHY, Blais J, et al
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    J Med Virol

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    J Thorac Oncol

12. XU X, Saad MB, Grippin A, Xu H, et al
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    J Virol

13. FAN L, Gao X, Feng W, Huang Q, et al
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    Lancet

14. KARIM SA, Mahomed S, Lewis L, Karim SSA, et al
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    Lancet Infect Dis

15. 
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    PubMed         Abstract available
    
    

    
    Science

16. EMANUEL N, Harrington E, Pallais A
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    PubMed         Abstract available

#SARS-CoV-2 #Omicron BA.2.86 and JN.1 expand #tropism in #human proximal #intestinal epithelium

 

Abstract

Omicron SARS-CoV-2 has diversified into multiple sub-lineages, complicating assessment of their intrinsic phenotypes due to background population immunity. We compare replication and biological characteristics of variants from BA.1 to JN.1 using human bronchial and lung explants, airway organoids, colon cells, and proximal intestinal enteroids. XBB.1.5 and EG.5.1 achieve higher replication titres in respiratory tissues than BA.2.86 and JN.1, indicating enhanced respiratory fitness. EG.5.1 displays dual cell-entry pathways and greater replication in alveolar epithelial cells, supporting increased lung tropism and pathogenicity. In contrast, BA.2.86 and JN.1 rely on TMPRSS2-mediated entry in airways. Notably, BA.2.86 and JN.1 replicate more efficiently than EG.5.1 in proximal intestinal enteroids in an ACE2- and TMPRSS2-dependent manner, but not in colon cells. JN.1 exhibits elevated intestinal tropism with limited proinflammatory cytokine induction, suggesting potential for faecal transmission. Here we show XBB.1.5 and EG.5.1 greater transmissibility and severity potential whereas BA.2.86 and JN.1 exhibit enhanced intestinal adaptation.

Source: 

Link: https://www.nature.com/articles/s41467-026-74111-y

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#Coronavirus Disease Research #References (AMEDEO, May 30 '26)

 

Antiviral Res

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    Radiology

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#Coronavirus Disease Research #References (AMEDEO, May 23 '26)

 

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   Ann Intern Med

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    Travel Med Infect Dis. 2026;72:102994.
    PubMed         Abstract available

#Coronavirus #diversity and #SARS-CoV-2 #exposure at the #wildlife – #human interface in Northern #Italy

 

Abstract

Background

Members of the Coronaviridae family infect humans as well as domestic and wild animals. Over the past three decades, three members of this family, all with zoonotic origins, have caused significant epidemics or pandemics (SARS, MERS, and COVID-19). Despite the spread of SARS-CoV-2 being primarily driven by human-to-human transmission, various animal species are susceptible to infection and may contribute to viral circulation. Aim of this work was to monitor coronavirus (CoV) infections in wild mammals in the Emilia-Romagna region (RER), Italy, using a combined approach of molecular screening for viral RNA detection and serological testing for anti-SARS-CoV-2 antibodies.

Methods

Respiratory and gastrointestinal tissue samples were collected from wild animal carcasses between 2022 and 2024. Samples were tested for SARS-CoV-2 using two RT-qPCR assays targeting the E and N genes, and for other CoVs using a nested pan-coronavirus RT-PCR followed by Sanger sequencing of positive samples. Additionally, serum samples obtained from blood, cardiac clot, or thoracic exudate were screened for antibodies against the SARS-CoV-2 nucleocapsid (N) protein, with positive samples subsequently confirmed by an ELISA targeting antibodies to the receptor-binding domain (RBD) of the Spike (S) protein, focused on variants circulating during the study period.

Results

Molecular analyses were performed on 2,238 animals, all of which tested negative for SARS-CoV-2, while 90 (79% hedgehogs) tested positive for CoVs. Among these, most sequences were consistent with coronaviruses typically reported in the respective host species. However, some exceptions – such as Betacoronavirus erinacei in fox, porcupine, hare, and roe deer, and EmbeCoV-related sequences in a porcupine – warrant further attention. Suitable serum samples were available from 1,751 animals. Overall, 65 animals tested positive for anti-N antibodies, 31 of which (22 foxes, 4 badgers, 2 hedgehogs, 1 roe deer, 1 wolf, 1 rat) were subsequently confirmed by an anti-RBD ELISA.

Conclusions

This study provides an overview of CoVs circulation among wild mammals in RER, supporting the role of hedgehogs as reservoirs and identifying some species with evidence of exposure to SARS-CoV-2. Certain unexpected findings highlight the need for further investigations to clarify the potential for cross-species transmission.

Source: 

Link: https://link.springer.com/article/10.1186/s12985-026-03193-3

____

#Coronavirus Disease Research #References (AMEDEO, May 16 '26)

 

Ann Intern Med

1. JOHNSON D, Quinn S, Algase LF, Watkins C Jr, et al
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   PubMed         Abstract available
   
   

   
   BMJ

2. SUMMERS C, Cook T, Suntharalingam G, Fong K, et al
   Covid Inquiry module 3 reveals critical gaps in UK health system resilience.
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   PubMed        
   
   

   
   Br J Anaesth

3. FRASER S, Syratt T, Bridson JD, Gilbert-Kawai N, et al
   Refusal of blood transfusion based on donor COVID-19 vaccination status: an emerging postpandemic challenge for perioperative care.
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   PubMed        
   
   

   
   Clin Infect Dis

4. PEREZ MA, Patel KA, Rasmy L, Yoshida H, et al
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   Infect Control Hosp Epidemiol

5. MENG L, Bell JM, Barbre K, Guthrie S, et al
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   Int J Infect Dis

6. KIM S, Chun BC
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7. WENG TP, Li MC, Tsai HP, Chen CJ, et al
   Viral Rebound and Clinical Outcomes in Hospitalized Patients with COVID-19.
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   PubMed         Abstract available
   
   
8. SHI R, Li Y, Liu L, Wang Y, et al
   Molecular epidemiology and genomic characterization of post-pandemic macrolide-resistant Mycoplasma pneumoniae in hospitalized children.
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9. MARTINEZ-DIAZ I, Nunez-Delgado S, Ortiz-Perez JT, Morales A, et al
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    J Med Virol

12. YAVUZ HC, Boysan SN, Tuna MM
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13. KIM DS, Kim U, Woo HM, Lee H, et al
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    PubMed         Abstract available
    
    

    
    J Virol

14. MCCABE M, Groves HE, Getty E, Campbell E, et al
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15. LI P, Zheng Y-M, Liu S-L
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    PubMed         Abstract available
    
    

    
    Lancet Infect Dis

16. HANSEN CH, Soborg B, Rasmussen M, Moustsen-Helms IR, et al
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    Lancet Infect Dis. 2026 May 13:S1473-3099(26)00236.
    PubMed        
    
    

    
    N Engl J Med

17. HAYDEN FG, Shinkai M, Clark TW, Luetkemeyer AF, et al
    Ensitrelvir for Covid-19 Postexposure Prophylaxis in Household Contacts.
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    PubMed         Abstract available
    
    

    
    Nature

18. DOLGIN E
    At last, a pill that can prevent COVID after exposure to infected people.
    Nature. 2026 May 13. doi: 10.1038/d41586-026-01546.
    PubMed        
    
    

    
    Science

19. LESSLER J, Christensen A
    From wastewater analysis to public health action.
    Science. 2026;392:692.
    PubMed         Abstract available
    
    
20. HILL DT, Schulman R, Caldas IV, Dunham C, et al
    Genetic variability of SARS-CoV-2 in wastewater and associations with community transmission.
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    PubMed         Abstract available
    

Sequencing of #Betacoronavirus erinacei from faeces of pet #hedgehogs demonstrates a continuity of #MERS-CoV like viruses in #European and Eurasian hedgehog species

 

Abstract

Hedgehogs have been recently identified as carriers of Betacoronavirus erinacei (also known as Erinaceus coronavirus, EriCoV) a virus closely related to B. cameli responsible for human Middle East Respiratory Syndrome (MERS), raising questions about the risk of hedgehog-to-human transmission and suggesting the need for coronavirus (CoV) surveillance in hedgehogs. This study investigated the presence of CoVs in fecal samples of hedgehogs kept as pets in Italy in 2021–2022. A pan-CoV nested RT-PCR targeting the RdRp gene was used for screening and positive samples were sequenced and phylogenetically analyzed. Two (6.2%) out of 30 hedgehogs analyzed were positive for B. erinacei represented by 2/3 (66.7%) long eared hedgehog (Hemiechinus auritus) while all the 27 tested African pygmy hedgehog (Atelerix albiventris) were negative. Whole genome sequence obtained from one B. erinacei-positive sample showed closest homology (85.7%) with B. erinacei previously detected in Erinaceus sp. from Eastern Russia. Phylogeny showed that the virus of this study formed a separate clade in the cluster with other B. erinacei identified in Europe and European Russia and did not cluster with other B. erinacei identified in China in Amur hedgehog (E. amurensis). No recombination events were observed. Analysis of the Spike protein revealed the presence of six out of the 11 key receptor binding residues, including two out of the three critical residues recently identified for the binding of Erinaceus europaeus receptor APN and B. erinacei. Results of this study suggest the presence of a long-eared hedgehog-specific strain of B. erinacei. Overall results support the circulation of coronaviruses along a phylogenetic continuum among different species of hedgehogs and geographic locations, suggesting the need for further CoV surveillance in both domestic and wild animals. There is also a need for studies on the affinity of EriCoV with the H. auritus APN specific receptor to confirm its involvement in the viral entry process.

Source: 

Link: https://www.sciencedirect.com/science/article/pii/S2352771426000960?via%3Dihub

____

#Coronavirus Disease Research #References (by AMEDEO, May 9 '26)

 

Clin Infect Dis

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   Int J Infect Dis

2. HIBINO M, Shintani A, Murayama H, Morikawa N, et al
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3. KURITA J, Mukasa K, Kawana Y, Kaneko M, et al
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4. LEWIS L, Mohammed D, Evans L, Patterson B, et al
   COVID-19 Hospitalisations in women of childbearing age and children during the Omicron period, January 2023 to September 2024.
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   J Med Virol

5. ANINAGYEI E, Ayivor-Djanie R, Boatey CA, Mateen AA, et al
   High SARS-CoV-2 Antibody Seroprevalence Amid COVID-19 Vaccine Hesitancy Among Unvaccinated Adults in Ghana.
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6. STONE S, Elsharkawy A, Patterson LD, Natekar JP, et al
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   J Virol

7. SUOMALAINEN M, Haenseler W, Kolibius J, Pluckthun A, et al
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8. ZHANG L, Hoffmann M, Pohlmann S
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   Lancet Infect Dis

9. RITCHIE AJ, Hassan O, Urasa N, Apanga PA, et al
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   PubMed         Abstract available
   
   

   
   Nature

10. BAO Z, Liu Z, Zhang Z, Wang X, et al
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    PubMed         Abstract available
    
    

    
    Science

11. COHEN J
    Arrest of Fauci aide for records violations decried as political.
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Loss of nsp14-exonuclease activity impairs the #replication, proofreading, fitness, and #pathogenesis of #SARS-CoV-2

 

ABSTRACT

Coronaviruses (CoVs) replicate their RNA genomes with a higher degree of fidelity than other RNA viruses, a mechanism mediated by the proofreading and recombination activities of the exoribonuclease domain of replicase nonstructural protein 14 (nsp14-ExoN). Both murine hepatitis virus (MHV) and SARS-CoV tolerate nsp14-ExoN loss-of-function mutations (ExoN−) (D90A and E92A), but have impaired replication fidelity and pathogenesis; yet identical substitutions in MERS-CoV and SARS-CoV-2 have been reported to be lethal. Here, we report a saturation mutagenesis approach facilitating the recovery and analysis of several constellations of SARS-CoV-2 nsp14 ExoN-inactivating, loss-of-function substitutions, including the canonical D90A and E92A. Biochemical assays with purified WT or ExoN-nsp10-14 fusion proteins confirmed that active site substitutions abolished ExoN activity (ExoN−). SARS-CoV-2 ExoN− viruses exhibited impaired replication, RNA synthesis, and recombination, as well as decreased replication fidelity and loss of fitness in vitro. ExoN− viruses were significantly attenuated for replication in human primary airway epithelial cells and were attenuated for replication and pathogenesis in WT mice, as well as the highly susceptible K18 transgenic mice. In the absence of interferon signaling in vivo, SARS-CoV and SARS-CoV-2 ExoN− viral replication could be partially restored. These results demonstrate that SARS-CoV-2 ExoN− viruses are viable but highly impaired for replication, fitness, and fidelity in vitro, as well as innate immune antagonism and pathogenesis in vivo. Collectively, our results solidify the multiple critical roles of nsp14-ExoN across CoV genera and establish new approaches for rescuing and analyzing loss-of-function substitutions in studies of CoV replication, pathogenesis, and evolution.

Source: 

Link: https://journals.asm.org/doi/10.1128/mbio.00073-26

____

#Coronavirus Disease Research #References (AMEDEO, May 2 '26)

 

Ann Intern Med

1. COTTON D
   "Never More Than 15 Feet From the Respirator": Housestaff Research During the 1955 Boston Polio Epidemic.
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   PubMed         Abstract available
   
   

   
   Clin Infect Dis

2. WALLS G, McGrath L, Herdman MT, Campbell AJ, et al
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3. SHAH AB, Lindsey KN, Zambrano LD, Free RJ, et al
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4. RAMACHANDRAN V, Onukwube Okaro J, Prasad N, Park S, et al
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   Int J Infect Dis

5. SHAH P, Pischel L, Sack B, Km AB, et al
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6. REICH S
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7. TERLIESNER N, Lesniowski D, Unterwalder N, von Bernuth H, et al
   RSV as an independent driver of a subsequent influenza epidemic in Berlin before and after the COVID-19 pandemic.
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8. YAO C, Dong Y, Zou X, Alhaskawi A, et al
   Severe acute limb ischemia in patients with COVID-19: a single-center case series.
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   Intensive Care Med

9. VENKATESAN N, Shah FA, Bain W, Yang Z, et al
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   J Infect

10. KIM HK, Jo S, Min KD, Cho SI, et al
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    J Med Virol

11. LARSEN L, Bistrup C, Sorensen SS, Jorgensen CS, et al
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12. WEISS JJ, Messina J, Saullo J, Li Y, et al
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    PubMed         Abstract available
    
    

    
    J Virol

13. GUO D, Yu S, Ma K, Tao H, et al
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14. NASIR A, Lee D, Avena LE, Berrueta DM, et al
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15. CHEN L, Su H, Shang W, Nie T, et al
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    PubMed         Abstract available
    
    
16. KOTANI N, Iwasa K, Amimoto T, Yamashita C, et al
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    PubMed         Abstract available
    
    

    
    JAMA

17. ANDERER S
    Most US Health Care Workers Vaccinated for Flu, Less Than Half for COVID-19.
    JAMA. 2026 May 1. doi: 10.1001/jama.2026.2126.
    PubMed        
    
    

    
    Lancet

18. SHANKAR-HARI M, Ming D, Mendelson M, Rupali P, et al
    The Lancet Commission on Sepsis: transforming sepsis care and outcomes.
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    PubMed        
    
    

    
    Science

19. BOHM R, Schneider A, Betsch C, Lilleholt L, et al
    CDC communication undermines trust in vaccines.
    Science. 2026;392:475-477.
    PubMed         Abstract available
    

Operational #zoonotic #containment of #MERS #coronavirus in #Saudi Arabia: An implementation-oriented #OneHealth genomic #framework

 

Abstract

Background and Aim: 

Middle East respiratory syndrome coronavirus (MERS-CoV) remains a persistent zoonotic threat more than a decade after its first detection, with Saudi Arabia continuing to be the global epicenter of human infections and the main reservoir interface through dromedary camels. Despite ongoing surveillance, advances in molecular diagnostics, and research on vaccines and therapeutics, sporadic zoonotic spillovers and healthcare-associated outbreaks still occur, showing that current prevention strategies are still not enough. This review compiles current evidence from epidemiological studies, camel reservoir research, genomic monitoring, and public health reports published between 2012 and April 2025 to identify the key gaps preventing effective containment. Special focus is given to recent genomic discoveries, including post-2022 clade B sublineages, recombination events, and spike protein changes that might affect transmission and the effectiveness of countermeasures. Available data suggest that MERS-CoV epidemiology is driven by repeated camel-to-human transmission, followed by occasional amplification in healthcare settings rather than sustained community spread. High seroprevalence and frequent detection of viral RNA in juvenile camels, seasonal gathering in markets, and extensive animal movement networks contribute to ongoing viral circulation at the animal–human interface. Genomic studies consistently show close phylogenetic relationships between camel and human isolates, confirming recurrent zoonotic transmissions. However, fragmented surveillance systems, delayed genomic data integration, inconsistent biosecurity practices, and limited field evidence for camel vaccination pose major barriers to control. Additionally, hospital outbreaks continue to occur due to delayed diagnosis, overcrowding, and incomplete adherence to infection-prevention protocols, underscoring the need for improved clinical preparedness. Based on the integrated synthesis of epidemiological, veterinary, and genomic evidence, this review proposes an implementation-focused One Health genomic framework tailored to the Saudi context. The proposed roadmap highlights real-time connection of human and camel surveillance, expands genomic sequencing capacity, targets vaccination strategies in camels and high-risk human populations, standardizes biosecurity measures in markets and abattoirs, and strengthens infection control systems in healthcare facilities. Alignment with national governance structures and Saudi Vision 2030 offers a practical pathway for coordinated multi-sectoral action. This review concludes that MERS-CoV is unlikely to be eradicated soon, but it can be effectively managed through a genomics-enabled, operational One Health approach that combines surveillance, vaccination, clinical preparedness, and policy coordination. The model outlined here provides a scalable way to reduce zoonotic spillover risk and strengthen readiness against future coronavirus and emerging zoonotic threats. 

Source: 

Link: https://veterinaryworld.org/Vol.19/March-2026/29.php

____

#Coronavirus Disease Research #References (by AMEDEO, April 25 '26)

 

Ann Intern Med

1. FRITZ JM, Skolasky RL, Brennan G, Minick K, et al
   Effectiveness of Nonpharmacologic Treatments for Chronic Low Back Pain : A Sequential, Multiple-Assignment, Randomized Trial.
   Ann Intern Med. 2026 Apr 21. doi: 10.7326/ANNALS-25-04645.
   PubMed         Abstract available
   
   

   
   Clin Infect Dis

2. BAKER JV, Siegel L, Losso M, Vasudeva S, et al
   Ensitrelvir for the treatment of hospitalized adults with COVID-19: an international phase 3 randomized placebo-controlled trial.
   Clin Infect Dis. 2026 Apr 22:ciag272. doi: 10.1093.
   PubMed         Abstract available
   
   

   
   Int J Infect Dis

3. ZHAO CY, Wang FS, Jiao YM
   SARS-CoV-2 infection disrupts the immune control status in a male HIV-1 elite controller.
   Int J Infect Dis. 2026 Apr 20:108713. doi: 10.1016/j.ijid.2026.108713.
   PubMed         Abstract available
   
   

   
   J Infect

4. BEHARIER O, Guedalia J, Sehtman-Shachar DR, Kerem L, et al
   Maternal SARS-CoV-2 Infection and Early Child Growth and Development: A Nationwide Cohort Study.
   J Infect. 2026 Apr 17:106749. doi: 10.1016/j.jinf.2026.106749.
   PubMed         Abstract available
   
   

   
   J Med Virol

5. HO SY, Liu YC, Ho SY, Chen SH, et al
   Emergence of Echovirus 11 in Severe and Neonatal Enterovirus Infections: A 9-Year Retrospective Study in Taiwan Before and After the COVID-19 Pandemic.
   J Med Virol. 2026;98:e70929.
   PubMed         Abstract available
   
   
6. AVILA JP, Park P, Singh Y, Amaral PP, et al
   Multiorgan Molecular Landscape of Severe COVID-19 Revealed by Consensus Gene Signatures and RAB8B Targeting.
   J Med Virol. 2026;98:e70932.
   PubMed         Abstract available
   
   
7. KESKIN S, Pavel STI, Sak R, Bahadori F, et al
   Modified mRNA Encoding the Crimean-Congo Hemorrhagic Fever Virus Nucleocapsid Protein Confers Robust Protection Against Lethal Challenge in Mice.
   J Med Virol. 2026;98:e70940.
   PubMed         Abstract available
   
   

   
   J Virol

8. SALISCH F, Muller-Ruttloff C
   Behind the membranous curtain-lipid dynamics and functions in coronaviral replication.
   J Virol. 2026 Apr 21:e0175325. doi: 10.1128/jvi.01753.
   PubMed         Abstract available
   
   
9. YANG M, Zhao Y, Guo W, Wang L, et al
   Development of a vaccine based on mRNA assembly of PEDV virus-like particle.
   J Virol. 2026 Apr 21:e0206025. doi: 10.1128/jvi.02060.
   PubMed         Abstract available
   
   
10. ZHANG K, Wang S, Kang X, Li F, et al
    Swine GBP1 restricts PDCoV replication via disrupting the replication and transcription complex formation.
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    PubMed         Abstract available
    
    
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