Investigation Into the Link Between Water Quality and Microbiological Safety of Selected Fruit and Vegetables from Farming to Processing Stages (Volume 1)
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The Viruses of Wild Pigeon Droppings
The Viruses of Wild Pigeon Droppings Tung Gia Phan1,2, Nguyen Phung Vo1,3,A´ kos Boros4,Pe´ter Pankovics4,Ga´bor Reuter4, Olive T. W. Li6, Chunling Wang5, Xutao Deng1, Leo L. M. Poon6, Eric Delwart1,2* 1 Blood Systems Research Institute, San Francisco, California, United States of America, 2 Department of Laboratory Medicine, University of California San Francisco, San Francisco, California, United States of America, 3 Pharmacology Department, School of Pharmacy, Ho Chi Minh City University of Medicine and Pharmacy, Ho Chi Minh, Vietnam, 4 Regional Laboratory of Virology, National Reference Laboratory of Gastroenteric Viruses, A´ NTSZ Regional Institute of State Public Health Service, Pe´cs, Hungary, 5 Stanford Genome Technology Center, Stanford, California, United States of America, 6 Centre of Influenza Research and School of Public Health, University of Hong Kong, Hong Kong SAR Abstract Birds are frequent sources of emerging human infectious diseases. Viral particles were enriched from the feces of 51 wild urban pigeons (Columba livia) from Hong Kong and Hungary, their nucleic acids randomly amplified and then sequenced. We identified sequences from known and novel species from the viral families Circoviridae, Parvoviridae, Picornaviridae, Reoviridae, Adenovirus, Astroviridae, and Caliciviridae (listed in decreasing number of reads), as well as plant and insect viruses likely originating from consumed food. The near full genome of a new species of a proposed parvovirus genus provisionally called Aviparvovirus contained an unusually long middle ORF showing weak similarity to an ORF of unknown function from a fowl adenovirus. Picornaviruses found in both Asia and Europe that are distantly related to the turkey megrivirus and contained a highly divergent 2A1 region were named mesiviruses. -
Desenvolvimento E Avaliação De Uma Plataforma De Diagnóstico Para Meningoencefalites Virais Por Pcr Em Tempo Real
DANILO BRETAS DE OLIVEIRA DESENVOLVIMENTO E AVALIAÇÃO DE UMA PLATAFORMA DE DIAGNÓSTICO PARA MENINGOENCEFALITES VIRAIS POR PCR EM TEMPO REAL Orientadora: Profa. Dra. Erna Geessien Kroon Co-orientador: Dr. Gabriel Magno de Freitas Almeida Co-orientador: Prof. Dr. Jônatas Santos Abrahão Belo Horizonte Janeiro de 2015 DANILO BRETAS DE OLIVEIRA DESENVOLVIMENTO E AVALIAÇÃO DE UMA PLATAFORMA DE DIAGNÓSTICO PARA MENINGOENCEFALITES VIRAIS POR PCR EM TEMPO REAL Tese de doutorado apresentada ao Programa de Pós-Graduação em Microbiologia do Instituto de Ciências Biológicas da Universidade Federal de Minas Gerais, como requisito à obtenção do título de doutor em Microbiologia. Orientadora: Profa. Dra. Erna Geessien Kroon Co-orientador: Dr. Gabriel Magno de Freitas Almeida Co-orientador: Prof. Dr. Jônatas Santos Abrahão Belo Horizonte Janeiro de 2015 SUMÁRIO LISTA DE FIGURAS .......................................................................................... 7 LISTA DE TABELAS ........................................................................................ 10 LISTA DE ABREVIATURAS ............................................................................. 11 I. INTRODUÇÃO .............................................................................................. 17 1.1. INFECÇÕES VIRAIS NO SISTEMA NERVOSO CENTRAL (SNC) ....... 18 1.2. AGENTES VIRAIS CAUSADORES DE MENINGOENCEFALITES .......... 22 1.2.1. VÍRUS DA FAMÍLIA Picornaviridae ........................................................ 22 1.2.1.1.VÍRUS DO GÊNERO Enterovirus ....................................................... -
Evidence to Support Safe Return to Clinical Practice by Oral Health Professionals in Canada During the COVID-19 Pandemic: a Repo
Evidence to support safe return to clinical practice by oral health professionals in Canada during the COVID-19 pandemic: A report prepared for the Office of the Chief Dental Officer of Canada. November 2020 update This evidence synthesis was prepared for the Office of the Chief Dental Officer, based on a comprehensive review under contract by the following: Paul Allison, Faculty of Dentistry, McGill University Raphael Freitas de Souza, Faculty of Dentistry, McGill University Lilian Aboud, Faculty of Dentistry, McGill University Martin Morris, Library, McGill University November 30th, 2020 1 Contents Page Introduction 3 Project goal and specific objectives 3 Methods used to identify and include relevant literature 4 Report structure 5 Summary of update report 5 Report results a) Which patients are at greater risk of the consequences of COVID-19 and so 7 consideration should be given to delaying elective in-person oral health care? b) What are the signs and symptoms of COVID-19 that oral health professionals 9 should screen for prior to providing in-person health care? c) What evidence exists to support patient scheduling, waiting and other non- treatment management measures for in-person oral health care? 10 d) What evidence exists to support the use of various forms of personal protective equipment (PPE) while providing in-person oral health care? 13 e) What evidence exists to support the decontamination and re-use of PPE? 15 f) What evidence exists concerning the provision of aerosol-generating 16 procedures (AGP) as part of in-person -
Virus Kit Description List
VIRUS –Complete list and description CONTENTS – italics names are the common names you might be more familiar with. ADENOVIRUS 46. Cytomegalovirus 98. Parapoxvirus 1. Atadenovirus 47. Muromegalovirus 99. Suipoxvirus 2. Aviadenovirus 48. Proboscivirus 100. Yatapoxvirus 3. Ichtadenovirus 49. Roseolovirus 101. Alphaentomopoxvirus 4. Mastadenovirus 50. Lymphocryptovirus 102. Betaentomopoxvirus 5. Siadenovirus 51. Rhadinovirus 103. Gammaentomopoxvirus ANELLOVIRUS 52. Misc. herpes REOVIRUS 6. Alphatorquevirus IFLAVIRUS 104. Cardoreovirus 7. Betatorquevirus 53. Iflavirus 105. Mimoreovirus 8. Gammatorquevirus ORTHOMYXOVIRUS 106. Orbivirus 9. Deltatorquevirus 54. Influenzavirus A 107. Phytoreovirus 10. Epsilontorquevirus 55. Influenzavirus B 108. Rotavirus 11. Etatorquevirus 56. Influenzavirus C 109. Seadornavirus 12. Iotatorquevirus 57. Isavirus 110. Aquareovirus 13. Thetatorquevirus 58. Thogotovirus 111. Coltivirus 14. Zetatorquevirus PAPILLOMAVIRUS 112. Cypovirus ARTERIVIRUS 59. Papillomavirus 113. Dinovernavirus 15. Equine arteritis virus PARAMYXOVIRUS 114. Fijivirus ARENAVIRUS 60. Avulavirus 115. Idnoreovirus 16. Arena virus 61. Henipavirus 116. Mycoreovirus ASFIVIRUS 62. Morbillivirus 117. Orthoreovirus 17. African swine fever virus 63. Respirovirus 118. Oryzavirus ASTROVIRUS 64. Rubellavirus RETROVIRUS 18. Mamastrovirus 65. TPMV~virus 119. Alpharetrovirus 19. Avastrovirus 66. Pneumovirus 120. Betaretrovirus BORNAVIRUS 67. Metapneumovirus 121. Deltaretrovirus 20. Borna virus 68. Para. Unassigned 122. Epsilonretrovirus BUNYAVIRUS PARVOVIRUS -
A Potential Drug Target for Inhibiting Virus Replication
Old Dominion University ODU Digital Commons Chemistry & Biochemistry Theses & Dissertations Chemistry & Biochemistry Winter 2018 Structure of the Picornavirus Replication Platform: A Potential Drug Target for Inhibiting Virus Replication Meghan Suzanne Warden Old Dominion University, [email protected] Follow this and additional works at: https://digitalcommons.odu.edu/chemistry_etds Part of the Biochemistry Commons, Chemistry Commons, Epidemiology Commons, and the Physiology Commons Recommended Citation Warden, Meghan S.. "Structure of the Picornavirus Replication Platform: A Potential Drug Target for Inhibiting Virus Replication" (2018). Doctor of Philosophy (PhD), Dissertation, Chemistry & Biochemistry, Old Dominion University, DOI: 10.25777/wyvk-8b21 https://digitalcommons.odu.edu/chemistry_etds/22 This Dissertation is brought to you for free and open access by the Chemistry & Biochemistry at ODU Digital Commons. It has been accepted for inclusion in Chemistry & Biochemistry Theses & Dissertations by an authorized administrator of ODU Digital Commons. For more information, please contact [email protected]. STRUCTURE OF THE PICORNAVIRUS REPLICATION PLATFORM: A POTENTIAL DRUG TARGET FOR INHIBITING VIRUS REPLICATION by Meghan Suzanne Warden B.S. May 2011, Lambuth University A Dissertation Submitted to the Faculty of Old Dominion University in Partial Fulfillment of the Requirements for the Degree of DOCTOR OF PHILOSOPHY CHEMISTRY OLD DOMINION UNIVERSITY December 2018 Approved by: Steven M. Pascal (Director) Lesley H. Greene (Member) Hameeda Sultana (Member) James W. Lee (Member) John B. Cooper (Member) ABSTRACT STRUCTURE OF THE PICORNAVIRUS REPLICATION PLATFORM: A POTENTIAL DRUG TARGET FOR INHIBITING VIRUS REPLICATION Meghan Suzanne Warden Old Dominion University, 2018 Director: Dr. Steven M. Pascal Picornaviruses are small, positive-stranded RNA viruses, divided into twelve different genera. -
Guía Docente
FACULTAD DE VETERINARIA Curso 2020/21 GUÍA DOCENTE DENOMINACIÓN DE LA ASIGNATURA Denominación: MICROBIOLOGÍA E INMUNOLOGÍA Código: 101463 Plan de estudios: GRADO DE VETERINARIA Curso: 2 Denominación del módulo al que pertenece: FORMACIÓN BÁSICA COMÚN Materia: MICROBIOLOGÍA E INMUNOLOGÍA Carácter: BASICA Duración: ANUAL Créditos ECTS: 12.0 Horas de trabajo presencial: 120 Porcentaje de presencialidad: 40.0% Horas de trabajo no presencial: 180 Plataforma virtual: Uco-Moodle DATOS DEL PROFESORADO Nombre: GARRIDO JIMENEZ, MARIA ROSARIO (Coordinador) Departamento: SANIDAD ANIMAL Área: SANIDAD ANIMAL Ubicación del despacho: Tercera planta del edificio de Sanidad Animal. Campus Rabanales E-Mail: [email protected] Teléfono: 957218718 Nombre: CANO TERRIZA, DAVID Departamento: SANIDAD ANIMAL Área: SANIDAD ANIMAL Ubicación del despacho: Tercera planta del edificio de Sanidad Animal. Campus Rabanales E-Mail: [email protected] Teléfono: 957218718 Nombre: GÓMEZ GASCÓN, LIDIA Departamento: SANIDAD ANIMAL Área: SANIDAD ANIMAL Ubicación del despacho: Tercera planta del edificio de Sanidad Animal. Campus Rabanales E-Mail: [email protected] Teléfono: 957218718 Nombre: CABALLERO GÓMEZ, JAVIER MANUEL Departamento: SANIDAD ANIMAL Área: SANIDAD ANIMAL Ubicación del despacho: Tercera planta del edificio de Sanidad Animal. Campus Rabanales E-Mail: [email protected] Teléfono: 957218718 REQUISITOS Y RECOMENDACIONES Requisitos previos establecidos en el plan de estudios Ninguno Recomendaciones Ninguna especificada COMPETENCIAS CE23 Estudio de los microorganismos que afectan a los animales y de aquellos que tengan una aplicación industrial, biotecnológica o ecológica. CE24 Bases y aplicaciones técnicas de la respuesta inmune. INFORMACIÓN SOBRE TITULACIONES www.uco.es DE LA UNIVERSIDAD DE CORDOBA facebook.com/universidadcordoba @univcordoba uco.es/grados MICROBIOLOGÍA E INMUNOLOGÍA PÁG. 1 / 14 Curso 2020/21 FACULTAD DE VETERINARIA Curso 2020/21 GUÍA DOCENTE OBJETIVOS Los siguientes objetivos recogen las recomendaciones de la OIE para la formación del veterinario: 1. -
Evidence to Support Safe Return to Clinical Practice by Oral Health Professionals in Canada During the COVID- 19 Pandemic: A
Evidence to support safe return to clinical practice by oral health professionals in Canada during the COVID- 19 pandemic: A report prepared for the Office of the Chief Dental Officer of Canada. March 2021 update This evidence synthesis was prepared for the Office of the Chief Dental Officer, based on a comprehensive review under contract by the following: Raphael Freitas de Souza, Faculty of Dentistry, McGill University Paul Allison, Faculty of Dentistry, McGill University Lilian Aboud, Faculty of Dentistry, McGill University Martin Morris, Library, McGill University March 31, 2021 1 Contents Evidence to support safe return to clinical practice by oral health professionals in Canada during the COVID-19 pandemic: A report prepared for the Office of the Chief Dental Officer of Canada. .................................................................................................................................. 1 Foreword to the second update ............................................................................................. 4 Introduction ............................................................................................................................. 5 Project goal............................................................................................................................. 5 Specific objectives .................................................................................................................. 6 Methods used to identify and include relevant literature ...................................................... -
Formation and Working Mechanism of the Picornavirus Vpg Uridylylation
Available online at www.sciencedirect.com ScienceDirect Formation and working mechanism of the picornavirus VPg uridylylation complex 1,2,6 3,6 2,4,5 Yuna Sun , Yu Guo and Zhiyong Lou The initiation of picornavirus replication is featured by the initiated by a protein primer is the most unique one, in uridylylation of viral protein genome-linked (VPg). In this which the virus encodes a protein, that is, viral protein process, viral RNA-dependent RNA polymerase (RdRp) genome-linked (VPg), that acts as the primer to initiate catalyzes two uridine monophosphate (UMP) molecules to the replication. hydroxyl group of the third tyrosine residue of VPg. 0 Subsequently, the uridylylated VPg (VPg-pUpU) functions as VPg was first discovered to be covalently linked to the 5 the protein primer to initiate the replication of the viral genome. end of viral genomes extracted from mature virions of Although a large body of functional and structural works has several single-stranded positive-sense RNA (+ssRNA) been performed to define individual snapshots for particular viruses and subsequently was demonstrated to be stages of the VPg uridylylation process, the formation, encoded by the viral genome [1 ,2]. So far, VPg has only dynamics and mechanism of the whole VPg uridylylation been experimentally demonstrated in the Picornaviridae complex still requires further elucidation. We would like to [3 ,4,5] and Caliciviridae [2] families, and its existence provide an overview of the current knowledge of the been computationally predicted in Astroviridae [6,7 -
Genome Characterization of a Novel Chicken Picornavirus Distantly Related to the Members of Genus Avihepatovirus with a Single 2
Brief Report Arch Virol (2017) 162:2781–2789 DOI 10.1007/s00705-017-3403-4 https://link.springer.com/article/10.1007/s00705-017-3403-4 Genome characterization of a novel megrivirus-related avian picornavirus from a carnivorous wild bird Western Marsh-harrier (Circus aeruginosus) Ákos Borosa,b, Péter Pankovicsa,b, Róbert Máticsc,d, Ádám Adonyia, Nóra Bolbaa,b, Tung Gia Phane,f, Eric Delwarte,f, Gábor Reutera,b*, a Regional Laboratory of Virology, National Reference Laboratory of Gastroenteric Viruses, ÁNTSZ Regional Institute of State Public Health Service, Pécs, Hungary b Department of Medical Microbiology and Immunology, Medical School, University of Pécs, Pécs, Hungary c Hungarian Nature Research Society, (HuNaReS), Ajka, Hungary d Department of Pathophysiology, University of Pécs Medical Center, Hungary e Blood Systems Research Institute, San Francisco, CA, USA and f University of California, San Francisco, CA, USA Running title: Novel harrier picornavirus in Hungary 1 * Address for correspondence: Dr Gábor Reuter Department of Medical Microbiology and Immunology University of Pécs H-7624 Szigeti út 12. Pécs, Hungary Telephone: +36 (72) 536 252 Fax: +36 (72) 536 253 Email: [email protected] 1 The GenBank[/EMBL/DDBJ] accession number for the study sequence: KY488458 1 Abstract In this study, the complete genome of novel picornavirus called harrier picornavirus 1 (HaPV-1) strain harrier/MR-01/HUN/2014 (KY488458) was sequenced and analysed from a cloacal sample of a threatened, carnivorous wild bird Western Marsh-harrier (Circus aeruginosus). HaPV-1 was detectable from 2 of the 3 samples from harriers. HaPV-1 is phylogenetically related to the megriviruses (genus Megrivirus) from domestic chicken, turkey and duck showing similar genome organization pattern and has an avian picornavirus- like “Unit A” motif in 3’ UTR. -
Virus Metagenomics in Farm Animals: a Systematic Review
viruses Review Virus Metagenomics in Farm Animals: A Systematic Review Kirsty T. T. Kwok , David F. Nieuwenhuijse , My V. T. Phan and Marion P. G. Koopmans * Department of Viroscience, Erasmus MC, 3015 Rotterdam, The Netherlands; [email protected] (K.T.T.K.); [email protected] (D.F.N.); [email protected] (M.V.T.P.) * Correspondence: [email protected] Received: 21 December 2019; Accepted: 14 January 2020; Published: 16 January 2020 Abstract: A majority of emerging infectious diseases are of zoonotic origin. Metagenomic Next-Generation Sequencing (mNGS) has been employed to identify uncommon and novel infectious etiologies and characterize virus diversity in human, animal, and environmental samples. Here, we systematically reviewed studies that performed viral mNGS in common livestock (cattle, small ruminants, poultry, and pigs). We identified 2481 records and 120 records were ultimately included after a first and second screening. Pigs were the most frequently studied livestock and the virus diversity found in samples from poultry was the highest. Known animal viruses, zoonotic viruses, and novel viruses were reported in available literature, demonstrating the capacity of mNGS to identify both known and novel viruses. However, the coverage of metagenomic studies was patchy, with few data on the virome of small ruminants and respiratory virome of studied livestock. Essential metadata such as age of livestock and farm types were rarely mentioned in available literature, and only 10.8% of the datasets were publicly available. Developing a deeper understanding of livestock virome is crucial for detection of potential zoonotic and animal pathogens and One Health preparedness. -
Metagenomic Characterisation of Avian Parvoviruses And
www.nature.com/scientificreports OPEN Metagenomic characterisation of avian parvoviruses and picornaviruses from Australian wild ducks Jessy Vibin1,2*, Anthony Chamings1,2, Marcel Klaassen3, Tarka Raj Bhatta1,2 & Soren Alexandersen1,2,4* Ducks can shed and disseminate viruses and thus play a role in cross-species transmission. In the current study, we detected and characterised various avian parvoviruses and picornaviruses from wild Pacifc black ducks, Chestnut teals, Grey teals and Wood ducks sampled at multiple time points from a single location using metagenomics. We characterised 46 diferent avian parvoviruses belonging to three diferent genera Dependoparvovirus, Aveparvovirus and Chaphamaparvovirus, and 11 diferent avian picornaviruses tentatively belonging to four diferent genera Sicinivirus, Anativirus, Megrivirus and Aalivirus. Most of these viruses were genetically diferent from other currently known viruses from the NCBI dataset. The study showed that the abundance and number of avian picornaviruses and parvoviruses varied considerably throughout the year, with the high number of virus reads in some of the duck samples highly suggestive of an active infection at the time of sampling. The detection and characterisation of several parvoviruses and picornaviruses from the individual duck samples also suggests co-infection, which may lead to the emergence of novel viruses through possible recombination. Therefore, as new and emerging diseases evolve, it is relevant to explore and monitor potential animal reservoirs in their natural habitat. Birds and other animals can be reservoirs for zoonotic viruses that may have serious implications for human health and agriculture, for example, avian infuenza A virus1 or severe acute respiratory syndrome coronavirus2. Among birds, notably wild ducks constitute a signifcant reservoir for viruses including, but not limited to, infu- enza viruses3,4 and coronaviruses5,6. -
Taxonomy Bovine Ephemeral Fever Virus Kotonkan Virus Murrumbidgee
Taxonomy Bovine ephemeral fever virus Kotonkan virus Murrumbidgee virus Murrumbidgee virus Murrumbidgee virus Ngaingan virus Tibrogargan virus Circovirus-like genome BBC-A Circovirus-like genome CB-A Circovirus-like genome CB-B Circovirus-like genome RW-A Circovirus-like genome RW-B Circovirus-like genome RW-C Circovirus-like genome RW-D Circovirus-like genome RW-E Circovirus-like genome SAR-A Circovirus-like genome SAR-B Dragonfly larvae associated circular virus-1 Dragonfly larvae associated circular virus-10 Dragonfly larvae associated circular virus-2 Dragonfly larvae associated circular virus-3 Dragonfly larvae associated circular virus-4 Dragonfly larvae associated circular virus-5 Dragonfly larvae associated circular virus-6 Dragonfly larvae associated circular virus-7 Dragonfly larvae associated circular virus-8 Dragonfly larvae associated circular virus-9 Marine RNA virus JP-A Marine RNA virus JP-B Marine RNA virus SOG Ostreid herpesvirus 1 Pig stool associated circular ssDNA virus Pig stool associated circular ssDNA virus GER2011 Pithovirus sibericum Porcine associated stool circular virus Porcine stool-associated circular virus 2 Porcine stool-associated circular virus 3 Sclerotinia sclerotiorum hypovirulence associated DNA virus 1 Wallerfield virus AKR (endogenous) murine leukemia virus ARV-138 ARV-176 Abelson murine leukemia virus Acartia tonsa copepod circovirus Adeno-associated virus - 1 Adeno-associated virus - 4 Adeno-associated virus - 6 Adeno-associated virus - 7 Adeno-associated virus - 8 African elephant polyomavirus