Editorial for Infectious Diseases - Drug Targets (in silico issue)
International audience Coming from Crimea, the Black Death spread to Western Europe and North Africa during the 1340s. From 1346 to 1352, the plague killed an estimated 25-40% of Europeans of all age-groups [1] , i.e., 30 to 60% of Europe population. One of the earliest and most widely accepted expl...
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ftunivparis:oai:HAL:inserm-00395256v1 2024-09-15T18:32:07+00:00 Editorial for Infectious Diseases - Drug Targets (in silico issue) de Brevern, Alexandre Protéines de la membrane érythrocytaire et homologues non-érythroides (U665) Université des Antilles et de la Guyane (UAG)-Institut National de la Transfusion Sanguine Paris (INTS)-Université Paris Diderot - Paris 7 (UPD7)-Université de La Réunion (UR)-Institut National de la Santé et de la Recherche Médicale (INSERM) 2009-06 https://inserm.hal.science/inserm-00395256 https://inserm.hal.science/inserm-00395256/document https://inserm.hal.science/inserm-00395256/file/editorial.pdf https://inserm.hal.science/inserm-00395256/file/inserm-00395256_edited.pdf en eng HAL CCSD info:eu-repo/semantics/altIdentifier/pmid/19519478 inserm-00395256 https://inserm.hal.science/inserm-00395256 https://inserm.hal.science/inserm-00395256/document https://inserm.hal.science/inserm-00395256/file/editorial.pdf https://inserm.hal.science/inserm-00395256/file/inserm-00395256_edited.pdf PUBMED: 19519478 info:eu-repo/semantics/OpenAccess Infectious disorders drug targets https://inserm.hal.science/inserm-00395256 Infectious disorders drug targets, 2009, 9 (3), pp.246-7 [SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular Biology [SDV.BIBS]Life Sciences [q-bio]/Quantitative Methods [q-bio.QM] [INFO.INFO-BI]Computer Science [cs]/Bioinformatics [q-bio.QM] info:eu-repo/semantics/article Journal articles 2009 ftunivparis 2024-07-04T23:36:27Z International audience Coming from Crimea, the Black Death spread to Western Europe and North Africa during the 1340s. From 1346 to 1352, the plague killed an estimated 25-40% of Europeans of all age-groups [1] , i.e., 30 to 60% of Europe population. One of the earliest and most widely accepted explanations was that God was punishing humanity for their sins. One remedy for the curse was to do penitence. Thus in 1348 there rapidly arose a mass movement of flagellation [2]. In fact flagellation could not really help against such threat. The Black Death or Bubonic plague is caused by Yersinia pestis, a Eubacteria discovered in 1894 by Alexandre Yersin. It is transmitted by the bite of the flea Xenopsylla cheopsis. This flea lives by feeding the blood of many species besides man but its most preferred relationship is with the black rat (Rattus rattus). Fossilized remains of the plague flea have been found in large numbers in Amarna, Egypt [3, 4] about 1350 BC, and thus could be directly linked to the events described in the Book of Samuel [5, 6]. During the epidemic of Bubonic plague in London in 1665-1666, the known treatments were made use of, e.g. the so-famous Theriac or Venice Treacle which is used from the time of ancient Rome as a remedy against poison [7]. Since then, more specialized and novel treatments have been developed. However, since the characterization of Yersinia pestis, numerous drugs have been developed against it, e.g. gentamicin or doxycycline [8]. These researches had been carried out using more elaborated biochemical, biophysical and biological approaches. Article in Journal/Newspaper Rattus rattus Université de Paris: Portail HAL |
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Université de Paris: Portail HAL |
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ftunivparis |
language |
English |
topic |
[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular Biology [SDV.BIBS]Life Sciences [q-bio]/Quantitative Methods [q-bio.QM] [INFO.INFO-BI]Computer Science [cs]/Bioinformatics [q-bio.QM] |
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[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular Biology [SDV.BIBS]Life Sciences [q-bio]/Quantitative Methods [q-bio.QM] [INFO.INFO-BI]Computer Science [cs]/Bioinformatics [q-bio.QM] de Brevern, Alexandre Editorial for Infectious Diseases - Drug Targets (in silico issue) |
topic_facet |
[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular Biology [SDV.BIBS]Life Sciences [q-bio]/Quantitative Methods [q-bio.QM] [INFO.INFO-BI]Computer Science [cs]/Bioinformatics [q-bio.QM] |
description |
International audience Coming from Crimea, the Black Death spread to Western Europe and North Africa during the 1340s. From 1346 to 1352, the plague killed an estimated 25-40% of Europeans of all age-groups [1] , i.e., 30 to 60% of Europe population. One of the earliest and most widely accepted explanations was that God was punishing humanity for their sins. One remedy for the curse was to do penitence. Thus in 1348 there rapidly arose a mass movement of flagellation [2]. In fact flagellation could not really help against such threat. The Black Death or Bubonic plague is caused by Yersinia pestis, a Eubacteria discovered in 1894 by Alexandre Yersin. It is transmitted by the bite of the flea Xenopsylla cheopsis. This flea lives by feeding the blood of many species besides man but its most preferred relationship is with the black rat (Rattus rattus). Fossilized remains of the plague flea have been found in large numbers in Amarna, Egypt [3, 4] about 1350 BC, and thus could be directly linked to the events described in the Book of Samuel [5, 6]. During the epidemic of Bubonic plague in London in 1665-1666, the known treatments were made use of, e.g. the so-famous Theriac or Venice Treacle which is used from the time of ancient Rome as a remedy against poison [7]. Since then, more specialized and novel treatments have been developed. However, since the characterization of Yersinia pestis, numerous drugs have been developed against it, e.g. gentamicin or doxycycline [8]. These researches had been carried out using more elaborated biochemical, biophysical and biological approaches. |
author2 |
Protéines de la membrane érythrocytaire et homologues non-érythroides (U665) Université des Antilles et de la Guyane (UAG)-Institut National de la Transfusion Sanguine Paris (INTS)-Université Paris Diderot - Paris 7 (UPD7)-Université de La Réunion (UR)-Institut National de la Santé et de la Recherche Médicale (INSERM) |
format |
Article in Journal/Newspaper |
author |
de Brevern, Alexandre |
author_facet |
de Brevern, Alexandre |
author_sort |
de Brevern, Alexandre |
title |
Editorial for Infectious Diseases - Drug Targets (in silico issue) |
title_short |
Editorial for Infectious Diseases - Drug Targets (in silico issue) |
title_full |
Editorial for Infectious Diseases - Drug Targets (in silico issue) |
title_fullStr |
Editorial for Infectious Diseases - Drug Targets (in silico issue) |
title_full_unstemmed |
Editorial for Infectious Diseases - Drug Targets (in silico issue) |
title_sort |
editorial for infectious diseases - drug targets (in silico issue) |
publisher |
HAL CCSD |
publishDate |
2009 |
url |
https://inserm.hal.science/inserm-00395256 https://inserm.hal.science/inserm-00395256/document https://inserm.hal.science/inserm-00395256/file/editorial.pdf https://inserm.hal.science/inserm-00395256/file/inserm-00395256_edited.pdf |
genre |
Rattus rattus |
genre_facet |
Rattus rattus |
op_source |
Infectious disorders drug targets https://inserm.hal.science/inserm-00395256 Infectious disorders drug targets, 2009, 9 (3), pp.246-7 |
op_relation |
info:eu-repo/semantics/altIdentifier/pmid/19519478 inserm-00395256 https://inserm.hal.science/inserm-00395256 https://inserm.hal.science/inserm-00395256/document https://inserm.hal.science/inserm-00395256/file/editorial.pdf https://inserm.hal.science/inserm-00395256/file/inserm-00395256_edited.pdf PUBMED: 19519478 |
op_rights |
info:eu-repo/semantics/OpenAccess |
_version_ |
1810473876981809152 |