Marburg and Ebola Viruses – Marking 50 Years Since Their Discovery
Notice bibliographique
Résumé
In 1967, a mysterious infectious disease was described in patients at the University Hospital in Marburg, Germany. Most patients had come into contact with a shipment of African green monkeys from Uganda. Additional patients were noted in Frankfurt, Germany and Belgrade, now Serbia. The etiological agent was identified as a virus and named after the city of Marburg – Marburg virus. Nine years later, a similar clinical infectious syndrome was described in patients in rural areas in southern Sudan (now South Sudan) and northern Zaire (now the Democratic Republic of Congo, DRC). The pathogen was identified as a virus similar to Marburg virus and named Ebola virus after a river in the northern DRC. Today we have a family of viruses, Filoviridae, comprising the genera Marburgvirus (single species), Ebolavirus (five species), and Cuevavirus (single species; no virus isolates) and a few unclassified sequences from bats. Until the mid-‘90s, filoviruses were neglected tropical pathogens, classified as high-containment viruses and of little research, infectious disease, and public health interest. This situation changed with the Ebola outbreak in Kikwit, DRC in 1995 and the classification as biothreat pathogens around the millennium switch. Research into filoviruses increased, mainly funded by governments concerned about bioterrorism seeking countermeasures such as diagnostics, vaccines, and therapies. Despite several smaller outbreaks with passing interest from regional public health groups, the interest in filoviruses from a public health perspective did not really change until recently when faced with an unprecedented outbreak in West Africa (2013–2016) that caused approximately 30,000 infections and more than 11,000 deaths. This devastating public health disaster finally also awakened the interest of the pharmaceutical industry in countermeasure development. Today, we have a vibrant research community with interest in all aspects of filoviruses as our knowledge had and still has tremendous gaps caused by the past lack of interest, lack of funding, limited involvement of scientific disciplines, and biocontainment constraints. Excitingly, efforts over the years have resulted in the implementation of rapid mobile diagnostics including bed-side tests, improved case patient management and multiple experimental therapeutic and vaccines candidates in clinical trials. The change in research activities and achievements over this time is nicely reflected by the increasing interest in attending the International Filovirus Symposium. This young meeting series was launched in 2000 in Marburg, Germany and founded based on the International Colloquium on Ebola Virus Research held in Antwerp in 1996. Symposia followed in Bethesda, USA (2003); Winnipeg, Canada (2006); Libreville, Gabon (2008); Tokyo, Japan (2010); Galveston, USA (2014); Washington, USA (2015), Antwerp; Belgium (2016), and Marburg, Germany (2017). The last two meetings were dedicated to the 40th and 50th Anniversary of Ebola virus and Marburg virus, respectively. Several of these meetings have been complemented by a Supplement Issue of the Journal of Infectious Diseases, a series that has been highly successful with articles being well cited in the fields of filoviruses, infectious diseases, and public health. As the current organizers of the meeting, we hope to continue in the short tradition of holding the International Filovirus Symposium every three years unless circumstances call for ad hoc meetings in shorter intervals, such as during the West African outbreak. The next symposium is scheduled for 2020 in La Jolla, USA and we hope to welcome the filovirus community to this future event.
Récupéré en direct depuis OpenAlex et désinversé. Les résumés ne sont pas conservés dans cette base de données : les index inversés représentent 8,6 Go des 9,3 Go de texte de la base, et le serveur dispose de 13 Go libres.
Comment cette classification a été obtenuedéplier
Prédiction machine sur la base complète
Imitation des enseignantsNi prévalence calibrée, ni vérité terrain. Validation humaine à venir. Le volet Gemma est une étiquette directe du modèle pour chaque travail de la base, lue sur la notice réduite au titre. Le volet Codex est un classifieur appris des 10 348 étiquettes directes de Codex et calibré sur les taux pondérés de l'échantillon; les champs sans appui suffisant ne portent aucun appel Codex. Le mode candidate est l'union des deux volets; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont pas des étiquettes humaines.
Scores du classifieur distillé par catégorie (deux têtes)
| Catégorie | Codex | Gemma |
|---|---|---|
| Métarecherche | 0,001 | 0,003 |
| Méta-épidémiologie (sens strict) | 0,001 | 0,000 |
| Méta-épidémiologie (sens large) | 0,000 | 0,000 |
| Bibliométrie | 0,001 | 0,001 |
| Études des sciences et des technologies | 0,001 | 0,002 |
| Communication savante | 0,003 | 0,003 |
| Science ouverte | 0,000 | 0,002 |
| Intégrité de la recherche | 0,001 | 0,002 |
| Charge utile insuffisante (le modèle a refusé de juger) | 0,002 | 0,001 |
Scores machine (provisoires)
Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.
Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.
score_only:v0-immature-baseline · tel quel depuis la passe de notation : score_only signifie que le nombre peut ordonner les travaux, et qu'aucune étiquette de catégorie n'en découleClassification
machine, non validéePrédiction automatique; un appel candidat d’une seule source (Gemma direct ou Codex distillé), pas un consensus.
Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».