Fatal Illnesses Associated with a New World Arenavirus
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X-Ray Structure of the Arenavirus Glycoprotein GP2 in Its Postfusion Hairpin Conformation
Corrections NEUROBIOLOGY Correction for “High-resolution structure of hair-cell tip links,” The authors note that Figure 3 appeared incorrectly. The by Bechara Kachar, Marianne Parakkal, Mauricio Kurc, Yi-dong corrected figure and its legend appear below. This error does not Zhao, and Peter G. Gillespie, which appeared in issue 24, affect the conclusions of the article. November 21, 2000, of Proc Natl Acad Sci USA (97:13336– 13341; 10.1073/pnas.97.24.13336). CORRECTIONS Fig. 3. Upper and lower attachments of the tip link. (A and B) Freeze-etch images of tip-link upper insertions in guinea pig cochlea (A) and (left to right) two from guinea pig cochlea, two from bullfrog sacculus, and two from guinea pig utriculus (B). Each example shows pronounced branching. (C and D) Freeze- etch images of the tip-link lower insertion in stereocilia from bullfrog sacculus (C) and guinea pig utriculus (D); multiple strands (arrows) arise from the stereociliary tip. (E) Freeze-fracture image of stereociliary tips from bullfrog sacculus; indentations at tips are indicated by arrows. (Scale bars: A = 100 nm, B = 25 nm; C–E = 100 nm.) www.pnas.org/cgi/doi/10.1073/pnas.1311228110 www.pnas.org PNAS | July 16, 2013 | vol. 110 | no. 29 | 12155–12156 Downloaded by guest on September 28, 2021 BIOCHEMISTRY BIOPHYSICS AND COMPUTATIONAL BIOLOGY, STATISTICS Correction for “X-ray structure of the arenavirus glycoprotein Correction for “Differential principal component analysis of GP2 in its postfusion hairpin conformation,” by Sébastien Igo- ChIP-seq,” by Hongkai Ji, Xia Li, Qian-fei Wang, and Yang net, Marie-Christine Vaney, Clemens Vonhrein, Gérard Bri- Ning, which appeared in issue 17, April 23, 2013, of Proc Natl cogne, Enrico A. -
MARBURG HEMORRHAGIC FEVER (Marburg HF)
MARBURG HEMORRHAGIC FEVER (Marburg HF) REPORTING INFORMATION • Class A: Report immediately via telephone the case or suspected case and/or a positive laboratory result to the local public health department where the patient resides. If patient residence is unknown, report immediately via telephone to the local public health department in which the reporting health care provider or laboratory is located. Local health departments should report immediately via telephone the case or suspected case and/or a positive laboratory result to the Ohio Department of Health (ODH). • Reporting Form(s) and/or Mechanism: o Immediately via telephone. o For local health departments, cases should also be entered into the Ohio Disease Reporting System (ODRS) within 24 hours of the initial telephone report to the ODH. • Key fields for ODRS reporting include: import status (whether the infection was travel-associated or Ohio-acquired), date of illness onset, and all the fields in the Epidemiology module. AGENT Marburg hemorrhagic fever is a rare, severe type of hemorrhagic fever which affects both humans and non-human primates. Caused by a genetically unique zoonotic RNA virus of the family Filoviridae, its recognition led to the creation of this virus family. The five species of Ebola virus are the only other known members of the family Filoviridae. Marburg virus was first recognized in 1967, when outbreaks of hemorrhagic fever occurred simultaneously in laboratories in Marburg and Frankfurt, Germany and in Belgrade, Yugoslavia (now Serbia). A total of 31 people became ill, including laboratory workers as well as several medical personnel and family members who had cared for them. -
1 Lujo Viral Hemorrhagic Fever: Considering Diagnostic Capacity And
1 Lujo Viral Hemorrhagic Fever: Considering Diagnostic Capacity and 2 Preparedness in the Wake of Recent Ebola and Zika Virus Outbreaks 3 4 Dr Edgar Simulundu1,, Prof Aaron S Mweene1, Dr Katendi Changula1, Dr Mwaka 5 Monze2, Dr Elizabeth Chizema3, Dr Peter Mwaba3, Prof Ayato Takada1,4,5, Prof 6 Guiseppe Ippolito6, Dr Francis Kasolo7, Prof Alimuddin Zumla8,9, Dr Matthew Bates 7 8,9,10* 8 9 1 Department of Disease Control, School of Veterinary Medicine, University of Zambia, 10 Lusaka, Zambia 11 2 University Teaching Hospital & National Virology Reference Laboratory, Lusaka, Zambia 12 3 Ministry of Health, Republic of Zambia 13 4 Division of Global Epidemiology, Hokkaido University Research Center for Zoonosis 14 Control, Sapporo, Japan 15 5 Global Institution for Collaborative Research and Education, Hokkaido University, Sapporo, 16 Japan 17 6 Lazzaro Spallanzani National Institute for Infectious Diseases, IRCCS, Rome, Italy 18 7 World Health Organization, WHO Africa, Brazzaville, Republic of Congo 19 8 Department of Infection, Division of Infection and Immunity, University College London, 20 U.K 21 9 University of Zambia – University College London Research & Training Programme 22 (www.unza-uclms.org), University Teaching Hospital, Lusaka, Zambia 23 10 HerpeZ (www.herpez.org), University Teaching Hospital, Lusaka, Zambia 24 25 *Corresponding author: Dr. Matthew Bates 26 Address: UNZA-UCLMS Research & Training Programme, University Teaching Hospital, 27 Lusaka, Zambia, RW1X 1 28 Email: [email protected]; Phone: +260974044708 29 30 2 31 Abstract 32 Lujo virus is a novel old world arenavirus identified in Southern Africa in 2008 as the 33 cause of a viral hemorrhagic fever (VHF) characterized by nosocomial transmission 34 with a high case fatality rate of 80% (4/5 cases). -
Past, Present, and Future of Arenavirus Taxonomy
Arch Virol DOI 10.1007/s00705-015-2418-y VIROLOGY DIVISION NEWS Past, present, and future of arenavirus taxonomy Sheli R. Radoshitzky1 · Yīmíng Bào2 · Michael J. Buchmeier3 · Rémi N. Charrel4,18 · Anna N. Clawson5 · Christopher S. Clegg6 · Joseph L. DeRisi7,8,9 · Sébastien Emonet10 · Jean-Paul Gonzalez11 · Jens H. Kuhn5 · Igor S. Lukashevich12 · Clarence J. Peters13 · Victor Romanowski14 · Maria S. Salvato15 · Mark D. Stenglein16 · Juan Carlos de la Torre17 © Springer-Verlag Wien 2015 Abstract Until recently, members of the monogeneric Arenaviridae to accommodate reptilian arenaviruses and family Arenaviridae (arenaviruses) have been known to other recently discovered mammalian arenaviruses and to infect only muroid rodents and, in one case, possibly improve compliance with the Rules of the International phyllostomid bats. The paradigm of arenaviruses exclu- Code of Virus Classification and Nomenclature (ICVCN). sively infecting small mammals shifted dramatically when PAirwise Sequence Comparison (PASC) of arenavirus several groups independently published the detection and genomes and NP amino acid pairwise distances support the isolation of a divergent group of arenaviruses in captive modification of the present classification. As a result, the alethinophidian snakes. Preliminary phylogenetic analyses current genus Arenavirus is replaced by two genera, suggest that these reptilian arenaviruses constitute a sister Mammarenavirus and Reptarenavirus, which are estab- clade to mammalian arenaviruses. Here, the members of lished to accommodate mammalian and reptilian the International Committee on Taxonomy of Viruses arenaviruses, respectively, in the same family. The current (ICTV) Arenaviridae Study Group, together with other species landscape among mammalian arenaviruses is experts, outline the taxonomic reorganization of the family upheld, with two new species added for Lunk and Merino Walk viruses and minor corrections to the spelling of some names. -
Study of Chikungunya Virus Entry and Host Response to Infection Marie Cresson
Study of chikungunya virus entry and host response to infection Marie Cresson To cite this version: Marie Cresson. Study of chikungunya virus entry and host response to infection. Virology. Uni- versité de Lyon; Institut Pasteur of Shanghai. Chinese Academy of Sciences, 2019. English. NNT : 2019LYSE1050. tel-03270900 HAL Id: tel-03270900 https://tel.archives-ouvertes.fr/tel-03270900 Submitted on 25 Jun 2021 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. N°d’ordre NNT : 2019LYSE1050 THESE de DOCTORAT DE L’UNIVERSITE DE LYON opérée au sein de l’Université Claude Bernard Lyon 1 Ecole Doctorale N° 341 – E2M2 Evolution, Ecosystèmes, Microbiologie, Modélisation Spécialité de doctorat : Biologie Discipline : Virologie Soutenue publiquement le 15/04/2019, par : Marie Cresson Study of chikungunya virus entry and host response to infection Devant le jury composé de : Choumet Valérie - Chargée de recherche - Institut Pasteur Paris Rapporteure Meng Guangxun - Professeur - Institut Pasteur Shanghai Rapporteur Lozach Pierre-Yves - Chargé de recherche - CHU d'Heidelberg Rapporteur Kretz Carole - Professeure - Université Claude Bernard Lyon 1 Examinatrice Roques Pierre - Directeur de recherche - CEA Fontenay-aux-Roses Examinateur Maisse-Paradisi Carine - Chargée de recherche - INRA Directrice de thèse Lavillette Dimitri - Professeur - Institut Pasteur Shanghai Co-directeur de thèse 2 UNIVERSITE CLAUDE BERNARD - LYON 1 Président de l’Université M. -
Genomic Diversity and Spatiotemporal Distributions of Lassa Virus Outbreaks in Nigeria
Genomic Diversity and Spatiotemporal Distributions of Lassa Virus Outbreaks in Nigeria Abdulwahid Abaukaka Yahaya Tehran University of Medical Sciences Yazdan Asgari ( [email protected] ) Tehran University of Medical Sciences https://orcid.org/0000-0001-6993-6956 Research article Keywords: Genomic, Lassa Virus, Phylogeography, Spatiotemporal and Nigeria Posted Date: October 28th, 2019 DOI: https://doi.org/10.21203/rs.2.16266/v2 License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License Page 1/20 Abstract Abstract Background Lassa virus (LASV) is a single-negative strand RNA Arenavirus (genus Mammarenavirus), oriented in both negative and positive senses. Due to the increase in the fatality rate of deadly disease LASV caused (Lassa fever), widespread LASV in Nigeria has been a subject of interest. Following the upsurge of LASV endemicity in 2012, another marked incidence recorded in Nigeria, 2018, with 394 conrmed cases in 19 states, and an estimated 25% cases led to death. This study aimed at acquiring the genetic variation of LASV ancestral evolution with the evolvement of new strains in different lineage and its geographical distributions within a specic time of outbreaks through Bayesian inference, using genomic sequence across affected states in Nigeria. Results From the result, we were able to establish the relationship of Lassa mamarenavirus and other arenaviruses by classifying them into distinct monophyletic groups, i.e., the old world arenaviruses, new world arenaviruses, and Reptarenaviruses. Corresponding promoter sites for genetic expression of the viral genome were analyzed based on Transcription Starting Site (TSS), the S_Segment (MK291249.1) is about 2917–2947 bp and L_Segment (MH157036.1), is about1863–1894 bp long. -
Identification of Novel Antiviral Compounds Targeting Entry Of
viruses Article Identification of Novel Antiviral Compounds Targeting Entry of Hantaviruses Jennifer Mayor 1,2, Giulia Torriani 1,2, Olivier Engler 2 and Sylvia Rothenberger 1,2,* 1 Institute of Microbiology, University Hospital Center and University of Lausanne, Rue du Bugnon 48, CH-1011 Lausanne, Switzerland; [email protected] (J.M.); [email protected] (G.T.) 2 Spiez Laboratory, Swiss Federal Institute for NBC-Protection, CH-3700 Spiez, Switzerland; [email protected] * Correspondence: [email protected]; Tel.: +41-21-314-51-03 Abstract: Hemorrhagic fever viruses, among them orthohantaviruses, arenaviruses and filoviruses, are responsible for some of the most severe human diseases and represent a serious challenge for public health. The current limited therapeutic options and available vaccines make the development of novel efficacious antiviral agents an urgent need. Inhibiting viral attachment and entry is a promising strategy for the development of new treatments and to prevent all subsequent steps in virus infection. Here, we developed a fluorescence-based screening assay for the identification of new antivirals against hemorrhagic fever virus entry. We screened a phytochemical library containing 320 natural compounds using a validated VSV pseudotype platform bearing the glycoprotein of the virus of interest and encoding enhanced green fluorescent protein (EGFP). EGFP expression allows the quantitative detection of infection and the identification of compounds affecting viral entry. We identified several hits against four pseudoviruses for the orthohantaviruses Hantaan (HTNV) and Citation: Mayor, J.; Torriani, G.; Andes (ANDV), the filovirus Ebola (EBOV) and the arenavirus Lassa (LASV). Two selected inhibitors, Engler, O.; Rothenberger, S. -
Serological Evidence of Multiple Zoonotic Viral Infections Among Wild Rodents in Barbados
pathogens Article Serological Evidence of Multiple Zoonotic Viral Infections among Wild Rodents in Barbados Kirk Osmond Douglas 1,*, Claire Cayol 2 , Kristian Michael Forbes 3, Thelma Alafia Samuels 4, Olli Vapalahti 5, Tarja Sironen 5 and Marquita Gittens-St. Hilaire 6,7 1 Centre for Biosecurity Studies, The University of the West Indies, Cave Hill, St. Michael BB11000, Barbados 2 Department of Wildlife, Fish, and Environmental Studies, Swedish University of Agricultural Sciences, Skogsmarksgränd 17, 901 83 Umeå, Sweden; [email protected] 3 Department of Biological Sciences, University of Arkansas, Fayetteville, AR 72701, USA; [email protected] 4 Epidemiology Research Unit, Caribbean Institute for Health Research (CAIHR), The University of the West Indies, Mona, Kingston 7, Jamaica; alafi[email protected] 5 Department of Virology, Faculty of Medicine, University of Helsinki, Medicum, Haartmaninkatu 3, 0290 Helsinki, Finland; olli.vapalahti@helsinki.fi (O.V.); tarja.sironen@helsinki.fi (T.S.) 6 Faculty of Medical Sciences, The University of the West Indies, Cave Hill, St. Michael BB11000, Barbados; [email protected] 7 Best–dos Santos Public Health Laboratory, Enmore #6, Lower Collymore Rock, St. Michael BB11155, Barbados * Correspondence: [email protected]; Tel.: +246-417-7468 Abstract: Background: Rodents are reservoirs for several zoonotic pathogens that can cause human infectious diseases, including orthohantaviruses, mammarenaviruses and orthopoxviruses. Evidence exists for these viruses circulating among rodents and causing human infections in the Americas, Citation: Douglas, K.O.; Cayol, C.; but much less evidence exists for their presence in wild rodents in the Caribbean. Methods: Here, Forbes, K.M.; Samuels, T.A.; we conducted serological and molecular investigations of wild rodents in Barbados to determine Vapalahti, O.; Sironen, T.; Gittens-St. -
Arenaviridae Astroviridae Filoviridae Flaviviridae Hantaviridae
Hantaviridae 0.7 Filoviridae 0.6 Picornaviridae 0.3 Wenling red spikefish hantavirus Rhinovirus C Ahab virus * Possum enterovirus * Aronnax virus * * Wenling minipizza batfish hantavirus Wenling filefish filovirus Norway rat hunnivirus * Wenling yellow goosefish hantavirus Starbuck virus * * Porcine teschovirus European mole nova virus Human Marburg marburgvirus Mosavirus Asturias virus * * * Tortoise picornavirus Egyptian fruit bat Marburg marburgvirus Banded bullfrog picornavirus * Spanish mole uluguru virus Human Sudan ebolavirus * Black spectacled toad picornavirus * Kilimanjaro virus * * * Crab-eating macaque reston ebolavirus Equine rhinitis A virus Imjin virus * Foot and mouth disease virus Dode virus * Angolan free-tailed bat bombali ebolavirus * * Human cosavirus E Seoul orthohantavirus Little free-tailed bat bombali ebolavirus * African bat icavirus A Tigray hantavirus Human Zaire ebolavirus * Saffold virus * Human choclo virus *Little collared fruit bat ebolavirus Peleg virus * Eastern red scorpionfish picornavirus * Reed vole hantavirus Human bundibugyo ebolavirus * * Isla vista hantavirus * Seal picornavirus Human Tai forest ebolavirus Chicken orivirus Paramyxoviridae 0.4 * Duck picornavirus Hepadnaviridae 0.4 Bildad virus Ned virus Tiger rockfish hepatitis B virus Western African lungfish picornavirus * Pacific spadenose shark paramyxovirus * European eel hepatitis B virus Bluegill picornavirus Nemo virus * Carp picornavirus * African cichlid hepatitis B virus Triplecross lizardfish paramyxovirus * * Fathead minnow picornavirus -
A Comparative Analysis of the West African Hemorrhagic Fevers Caused by the Lassa and Ebola Viruses Emiene E
Southeastern University FireScholars Selected Honors Theses Spring 4-28-2017 A Comparative Analysis of the West African Hemorrhagic Fevers Caused by the Lassa and Ebola Viruses Emiene E. Amali-Adekwu Southeastern University - Lakeland Follow this and additional works at: http://firescholars.seu.edu/honors Part of the Immune System Diseases Commons, Immunology of Infectious Disease Commons, Immunopathology Commons, Infectious Disease Commons, and the Virus Diseases Commons Recommended Citation Amali-Adekwu, Emiene E., "A Comparative Analysis of the West African Hemorrhagic Fevers Caused by the Lassa and Ebola Viruses" (2017). Selected Honors Theses. 70. http://firescholars.seu.edu/honors/70 This Thesis is brought to you for free and open access by FireScholars. It has been accepted for inclusion in Selected Honors Theses by an authorized administrator of FireScholars. For more information, please contact [email protected]. A COMPARATIVE ANALYSIS OF THE WEST AFRICAN HEMORRHAGIC FEVERS CAUSED BY THE LASSA AND EBOLA VIRUSES By Emiene E. Amali-Adekwu Submitted to the Honors Program Committee in partial fulfillment of the requirements for University Honors Scholars Southeastern University 2017 Amali-Adekwu 1 ©Copyright, Emiene E. Amali-Adekwu 2017 Amali-Adekwu 2 Abstract Lassa fever (LF) and Ebola Hemorrhagic Fever (EHF) are viral diseases endemic to West Africa.The etiological agent of Lassa fever is an enveloped virus from the Arenaviridae family and was first discovered in 1969 when two missionary nurses died of a mysterious illness in the town of Lassa in Borno state, Nigeria.1 This virus is animal-borne (zoonotic) and is carried by the animal vector Mastomys natalensis (multimammate rat). -
A Novel Experimental System Reveals Immunoregulatory Responses As Mediators Of
bioRxiv preprint doi: https://doi.org/10.1101/831214; this version posted November 5, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 A novel experimental system reveals immunoregulatory responses as mediators of 2 persistent orthohantavirus infections in a rodent reservoir host 3 4 Tomas Strandin1, Teemu Smura1, Paula Ahola1, Kirsi Aaltonen1,2, Tarja Sironen1,2, Jussi 5 Hepojoki1,3, Isabella Eckerle4, Rainer G. Ulrich5, Olli Vapalahti1,2, Anja Kipar2,3, Kristian M. 6 Forbes6 7 8 1) Zoonosis Unit, Department of Virology, Medicum, University of Helsinki, Helsinki, Finland 9 2) Department of Basic Veterinary Sciences, Faculty of Veterinary Medicine, University of 10 Helsinki, Helsinki, Finland 11 3) Laboratory for Animal Model Pathology, Institute of Veterinary Pathology, Vetsuisse 12 Faculty, University of Zurich, Zurich, Switzerland 13 4) Institute of Virology, University of Bonn Medical Centre, Bonn, Germany and present 14 address: Geneva Centre for Emerging Viral Diseases, University Hospital of Geneva & 15 Department of Microbiology and Molecular Medicine, University of Geneva, Geneva, 16 Switzerland 17 5) Institute of Novel and Emerging Infectious Diseases, Friedrich-Loeffler-Institut, Federal 18 Research Institute for Animal Health, Greifswald-Insel Riems, Germany 19 6) Department of Biological Sciences, University of Arkansas, Fayetteville, USA 20 Word count: abstract 250, text 6019 21 Corresponding author 22 Tomas Strandin 23 [email protected] 24 Running title: Persistence of Puumala orthohantavirus in bank voles 25 Keywords: immunity, Puumala orthohantavirus, rodent reservoir, spillover, vole, zoonoses 1 bioRxiv preprint doi: https://doi.org/10.1101/831214; this version posted November 5, 2019. -
Isolation and Identification of a Novel Phlebovirus, Hedi Virus
viruses Communication Isolation and Identification of a Novel Phlebovirus, Hedi Virus, from Sandflies Collected in China Ziqian Xu 1,†, Na Fan 1,†, Xin Hou 2,†, Jing Wang 2, Shihong Fu 1, Jingdong Song 1, Mang Shi 2,* and Guodong Liang 1,* 1 State Key Laboratory of Infectious Disease Prevention and Control, Key Laboratory for Medical Virology, National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing 100052, China; [email protected] (Z.X.); [email protected] (N.F.); [email protected] (S.F.); [email protected] (J.S.) 2 The Center for Infection & Immunity Study, School of Medicine, Sun Yat-sen University, Guangzhou 510006, China; [email protected] (X.H.); [email protected] (J.W.) * Correspondence: [email protected] (M.S.); [email protected] (G.L.) † These authors contribute equally to the work. Abstract: We report the isolation of a newly recognized phlebovirus, Hedi virus (HEDV), from Phlebotomus chinensis sandflies collected in Shanxi Province, China. The virus’ RNA is comprised of three segments. The greatest amino acid sequence similarity of the three gene segments between this virus and previously recognized phleboviruses is 40.85–63.52%, and the RNA-dependent RNA polymerase (RdRp) amino acid sequence has the greatest similarity (63.52%) to the Rift Valley fever virus (RVFV) ZH-548 strain. Phylogenetic analysis of the amino acid sequence of the virus RdRp indicated that HEDV is close to RVFV and distinct from other phleboviruses, forming its own evolutionary branch. We conclude that it is necessary to increase the monitoring of phleboviruses Citation: Xu, Z.; Fan, N.; Hou, X.; carried by sandflies in China.