{"title":"Les vaccinations antirabiques en France en 1987","authors":"A. Strady, G. Rémy, C. Rouger, J. Deville","doi":"10.1016/S0769-2617(88)80049-2","DOIUrl":"10.1016/S0769-2617(88)80049-2","url":null,"abstract":"","PeriodicalId":77667,"journal":{"name":"Annales de l'Institut Pasteur. Virology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1988-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0769-2617(88)80049-2","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"98610111","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Eléments de biologie relationnelle l'homme. Interrelations des êtres humains","authors":"","doi":"10.1016/S0769-2617(88)80025-X","DOIUrl":"https://doi.org/10.1016/S0769-2617(88)80025-X","url":null,"abstract":"","PeriodicalId":77667,"journal":{"name":"Annales de l'Institut Pasteur. Virology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1988-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0769-2617(88)80025-X","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136815511","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Lectin affinity of Junin virus glycoproteins","authors":"S.E. Mersich, V. Castilla, E.B. Damonte","doi":"10.1016/S0769-2617(88)80040-6","DOIUrl":"10.1016/S0769-2617(88)80040-6","url":null,"abstract":"<div><p>We studied the binding of Junin virus (<em>Arenaviridae</em>) glycoproteins, G1 and G2, to two insolubilized lectins. The results showed that mannose, N-acetyl-glucosamine and galactose residues were exposed on G2, while only the latter predominated on G1. Heterogeneity of carbohydrate chains was found in G2, the only glycoprotein that was iodinated by the lactoperoxidase method.</p></div><div><p>On étudie l'interaction des glycoprotéines (G1 et G2) du virus Junín, appartenant à la famille des <em>Arenaviridae</em>, avec deux lectines insolubilisées. Les résultats montrent la présence de mannose, de N-acétyl-glucosamine et de galactose dans G2, alors que dans G1 le galactose est prédominant.</p><p>On observe une hétérogénéité dans la composition des oligosides de l'unique protéine d'enveloppe, G2, que l'on peut iodiner avec la lactoperoxydase.</p></div>","PeriodicalId":77667,"journal":{"name":"Annales de l'Institut Pasteur. Virology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1988-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0769-2617(88)80040-6","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13988211","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Sequence and analysis of bovine enteritic coronavirus (F15) genome","authors":"C. Crucière , J. Laporte","doi":"10.1016/S0769-2617(88)80012-1","DOIUrl":"10.1016/S0769-2617(88)80012-1","url":null,"abstract":"<div><p>Sequences encoding the N protein of the bovine enteritic coronavirus-F15 strain (BECV-F15) have been cloned in PBR322 plasmid using cDNA produced by priming with oligo-dT on purified viral genomic RNA. Some 265 insert-containing clones were studied. Hybridization of these inserts with poly(A)<sup>+</sup> RNA extracted from infected cells led to the conclusion that they were located at the 3′-end of the genome.</p><p>After subcloning in M13 phage DNA, clones were sequenced by the Sanger technique. A 1,710-nucleotide sequence corresponding to the gene coding for the viral N-protein was established. It shows 2 overlapping open reading frames (ORF). The 3′-non-coding end of the gene has an 8-nucleotide sequence in common with the homologous genome areas of MHV, TGE and IBV viruses. This sequence may represent the polymerase RNA binding site.</p><p>An upstream sequence surrounding the first AUG of the smaller ORF corresponds to a potentially functional initiation codon. The sequence of the primary translation product deduced from the DNA sequence predicts a polypeptide of 207 amino acids (22.9 Kd) with a high leucine (19.8%) content, possessing a hydrophobic N-terminal end.</p><p>The larger ORF has a coding capacity of 448 amino acids (49.4 Kd), corresponding to the N-protein molecular weight. The deduced protein possesses 43 serine residues (9.6% of the total amino acid content) which may be phosporylated and involved in N-protein/RNA binding. N-protein also has 5 regions with a high basic amino acid content. One of them is also serine-rich and has a strong homology site with MHV, TGE and IBV viruses. In the first part of the N-terminal, a 12-amino-acid sequence (PRWYFYYLGTGP) is highly conserved for BECV-F15, JHM, TGE and IBV viruses. BCV Mebus strain and BECV-F15 have only minor differences in their N-protein sequence.</p></div><div><p>Nous avons cloné l'ARN génomique du coronavirus entéritique bovin F15 (BECV-F15), dans le plasmide PBR322 après avoir préparé le cDNA correspondant à l'aide d'une amorce oligo-dT: 265 clones ont été étudiés. Leur hybridation avec les ARN poly(A)<sup>+</sup> extraits des cellules infectées nous a permis de les localiser à l'extrémité 3′-terminale du génome.</p><p>Ces clones ont été séquencés par la technique de Sanger, après sous-clonage dans l'ADN du phage M13. Nous avons déterminé une séquence de 1.710 nucléotides correspondant au gène codant pour la protéine N virale. Elle présente deux cadres ouverts de lecture (ORF) chevauchants. On observe à l'extrémité 3′-terminale non codante du génome une séquence de 8 nucléotides observée également dans la région homologue des virus MHV, GET et IBV. Cette séquence pourrait être le site de fixation de l'ARN polymérase.</p><p>Le premier AUG du plus petit ORF possède en amont une séquence nucléotidique qui en fait un site d'initiation potentiellement fonctionnel. La séquence du produit primaire de traduction que l'on en déduit est un polypeptide de 207 acides aminés (22","PeriodicalId":77667,"journal":{"name":"Annales de l'Institut Pasteur. Virology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1988-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0769-2617(88)80012-1","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"14337071","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Cauliflower mosaic virus ORF VII is not required for aphid transmissibility","authors":"L. Givord , L. Dixon , I. Rauseo-Koenig , T. Hohn","doi":"10.1016/S0769-2617(88)80020-0","DOIUrl":"10.1016/S0769-2617(88)80020-0","url":null,"abstract":"<div><p>Des mutants du virus de la mosaïque du chou-fleur ont été construits <em>in vitro</em>. La transmissibilité de ces mutants par les pucerons a été testée. Pour que la transmission par pucerons soit possible il faut un ORF II intact, alors que l'ORF VII n'est pas nécessaire.</p></div>","PeriodicalId":77667,"journal":{"name":"Annales de l'Institut Pasteur. Virology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1988-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0769-2617(88)80020-0","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"14337970","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
M. Guillaud , B. Le Guenno , M.L. Wilson , D. Desoutter , J.P. Gonzalez , J.P. Digoutte
{"title":"Prévalence en anticorps contre le virus de la fièvre de la vallée du rift chez les petits ruminants du Sénégal","authors":"M. Guillaud , B. Le Guenno , M.L. Wilson , D. Desoutter , J.P. Gonzalez , J.P. Digoutte","doi":"10.1016/S0769-2617(88)80082-0","DOIUrl":"10.1016/S0769-2617(88)80082-0","url":null,"abstract":"<div><p>A total of 1,715 randomly selected sheep and goat sera from Senegal were tested for antibodies against Rift Valley fever virus using an enzyme-linked immunosorbent assay. The results showed that Rift Valley fever is enzootic. The prevalence is highly heterogeneous, depending on the aera. Sheep and goats expressed comparable antibody prevalence, suggesting that both are involved equally in the virus cycle.</p></div><div><p>Une enquête de prévalence en anticorps contre le virus de la fièvre de la vallée du Rift a été réalisée sur un échantillon représentatif du cheptel ovin et caprin du Sénégal. La répartition des anticorps montre l'état enzootique de la fièvre de la vallée du Rift dans ce cheptel. Les prévalences en anticorps chez les ovins et caprins sont comparables mais réparties de façon très hétérogène selon les zones étudiées.</p></div>","PeriodicalId":77667,"journal":{"name":"Annales de l'Institut Pasteur. Virology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1988-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0769-2617(88)80082-0","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"14344177","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"The Annales de l'Institut Pasteur, one hundred years later…","authors":"C. Hannoun","doi":"10.1016/S0769-2617(88)80002-9","DOIUrl":"10.1016/S0769-2617(88)80002-9","url":null,"abstract":"","PeriodicalId":77667,"journal":{"name":"Annales de l'Institut Pasteur. Virology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1988-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0769-2617(88)80002-9","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37831885","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}