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Ciba Foundation Symposium 128 - Novel Diarrhoea Viruses PDF

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Preview Ciba Foundation Symposium 128 - Novel Diarrhoea Viruses

NOVEL DIARRHOEA VIRUSES The Ciba Foundation is an international scientific and educational charity. It was established in 1947 by the Swiss chemical and pharmaceutical company of ClBA LimitedMow CIBA-GEIGY Limited. The Foundation operates independently in London under English trust law. The Ciba Foundation exists to promote international cooperation in biological, medical and chemical research. It organizes about eight international multidisciplinary symposia each year on topics that seem ready for discussion by a small group of research workers. The papers and discussions are published in the Ciba Foundation symposium series. The Foundation also holds many shorter meetings (not published), organized by the Foundation itself or by outside scientific organizations. The staff always welcome suggestions for future meetings. The Foundation’s house at 41 Portland Place, London, W1 N 4BN, provides facilities for meetings of all kinds. Its Media Resource Service supplies information to journalists on all scientific and technological topics. The library, open seven days a week to any graduate in science or medicine, also provides information on scientific meetings throughout the world and answers general enquiries on biomedical and chemical subjects. Scientistsfrom any part of the world may stay in the house during working visits to London. Ciba Foundation Syrnposiurri 128 NOVEL DIARRHOEA VIRUSES A Wiley - lnterscience Publication 1987 JOHN WlLEY 8, SONS Chichester . New York . Brisbane . Toronto . Singapore 0C iba Foundation 1987 Published in 1987 by John Wiley & Sons Ltd, Chichester, UK Suggested series entry for library catalogues: Ciba Foundation Symposia Ciba Foundation Symposium 128 VIII + 272 pages, 58 figures. 22 tables British Library Cataloguing in Publication Data Novel diarrhoea viruses. - (CIBA Foundation symposium ; 128) 1. Diarrhea in animals 2. Veterinary virology I. Series 591.2'34 SF809.D5 ISBN 0 471 91094 5 Printed and bound in Great Britain Contents Symposium on Novel Diarrhoea Viruses, held at the Ciba Foundation, London, 15-17 July 1986 The subject of this symposium was proposed by Dr T.H . Flewett Editors: Gregory Bock (Organizer) (2nd Julie Whelan R. F. Bishop Introduction 1 J. C. Bridger Novel rotaviruses in animals and man 5 Discussion 15 M. A. McCrae Nucleic acid-based a.nalyses of non-group A rotaviruses 24 Discussion 37 T. Hung, G. M. Chen, C. A. Wang, K. Fan, R. Yong, J. Chang, R. Dan and M. H. Ng Seroepidemiology and molecular epidemiology of the Chinese rotavirus 49 Discussion 54 G. Wadell, A. Allard, M. Johansson, L. Svensson and I. Uhnoo Enteric adenoviruses 63 Discussion 84 J. B. Kurtz and T. W. Lee Astroviruses: human and animal 92 Discussion 102 H. Appleton Small round viruses: classification and role in food-borne infections 108 Discussion 120 W. D. Cubitt The candidate caliciviruses 126 Discussion 138 N. R. Blacklow, J. E. Herrmann and W. D. Cubitt Immunobiology of Norwalk virus 144 Discussion 153 vi Contents M. C. Horzinek, M. Weiss and J. Ederveen Toroviridae: a proposed new family of enveloped RNA viruses 162 Discussion 171 G. N. Woode Breda and Breda-like viruses: diagnosis, pathology and epidemiology 175 Discussion 183 G. A. Hall Comparative pathology of infection by novel diarrhoea viruses 192 Discussion 207 T. Vesikari, E. Isolauri, T. Ruuska and T. Rautanen Clinical trials of rotavirus vaccines 218 Discussion 23 1 T. H. Flewett, G. M. Beards, D. W. G. Brown and R. C. Saunders The diagnostic gap in diarrhoea1 aetiology 238 Discussion 245 Final general discussion Criteria for non-group A rotaviruses 250 Enteric adenoviruses 251 Small round viruses 252 Human coronaviruses 252 Comparative pathology of diarrhoea1 infections 255 Vaccination against rotavirus diarrhoea 256 R. F. Bishop Chairman’s closing remarks 261 Index of contributors 264 Subject index 266 Participants H. Appleton Virus Reference Laboratory, Central Public Health Laboratory, 61 Colindale Avenue, London NW9 5HT, UK R. F. Bishop (Chairman) Department of Gastroenterology, Royal Children’s Hospital, Flemington Road, Parkville, Melbourne, Victoria 3052, Australia N. R. Blacklow Division of Infectious Diseases, Department of Medicine, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA F. J. Bourne Department of Veterinary Medicine, University of Bristol, Langford House, Langford, Bristol, Avon BS18 7DU, UK J. C. Bridger AFRC Institute for .Animal Disease Research, Compton, Nr Newbury, Berkshire RG16 ONN, UK E. 0. Caul Public Health Laboratory, Myrtle Road, Kingsdown, Bristol, Avon BS2 8EL, UK S. Chiba Department of Paediatrics, Sapporo Medical College, S1, W.17, Chuo-Ku, Sapporo, Hokkaido 060, Japan W. D. Cubitt Public Health Laboratory & Department of Microbiology, Central Middlesex Hospital, Park Royal, London NWlO 7NS, UK T. H. Flewett Regional Virus Laboratory, East Birmingham Hospital, Bordesley Green East, Birmingham B9 5ST, UK H. B. Greenberg Division of Gastroenterology - S069, Department of Medicine, Stanford University School of Medicine, Medical Center, Stanford, California 94305, USA G. A. Hall AFRC Institute for Animal Disease Research. Compton, Nr Newbury, Berkshire RG16 ONN, UK I. H. Holmes Department of Microbiology, University of Melbourne, Parkville, Melbourne, Victoria 3052, Australia vii viii Participants M. C. Horzinek Veterinary Faculty, Institute of Virology, State University of Utrecht, Yalelaan 1, 3508 TD Utrecht, The Netherlands Hung Tao Department of Virus Morphology and Viral Diarrhoea, Institute of Virology, Chinese National Academy of Preventive Medicine, 100 Ying Xing Jie, Xuan Wu Qu, Beijing 100052, People’s Republic of China A. Z. Kapikian Epidemiology Section, Laboratory of Infectious Diseases National Institute of Allergy and Infectious Diseases, Bldg 7, Room 103, National Institutes of Health, Bethesda, Maryland 20205, USA J. B. Kurtz Department of Virology, John Radcliffe Hospital, Headington, Oxford OX3 9DU, UK M. A. McCrae Department of Biological Sciences, University of Warwick, Coventry CV4 7AL, UK M. S. McNulty Veterinary Research Laboratories, Stormont, Belfast BT4 3SD, Northern Ireland, UK M. M. Mathan Wellcome Research Unit , Christian Medical College Hospital, Vellore 632004, Tamil Nadu, India L. J. Saif Food Animal Health Research Program, Department of Veterinary Preventive Medicine, Ohio Agricultural Research & Development Center/Ohio State University, Wooster, Ohio 44691, USA D. R. Snodgrass Animal Diseases Research Association, Moredun Research Institute, 408 Gilmerton Road, Edinburgh EH17 7JH, UK L. Svensson (Ciba Foundation Bursar) Department of Virology, The National Bacteriological Laboratory, S-105 21, Stockholm, Sweden T. Vesikari Department of Clinical Sciences, University of Tampere, Teiskontie 35, SF-33520 Tampere, Finland G. Wadell Department of Virology, Ume5 University, S-901 85 Ume5, Sweden G. N. Woode Department of Veterinary Microbiology & Parasitology, College of Veterinary Medicine, Texas A & M University, College Station, Texas 77843-4467, USA Novartis Foundation Symposium Edited by Gregory Bock, Julie Whelm Copyright 0 1987 by Ciba Foundation Introduction Ruth Bishop Department of Gastroenterology, Royal Children’s Hospital, Flemington Road, Parkville, Melbourne, victoria 3052, Australia 1987 Novel diarrhoea viruses. Wiley. Chichester (Ciba Foundation Symposium 128) p. 1-4 The symposium on ‘Acute Diarrhoea in Childhood’, held in 1975 here at the Ciba Foundation, heralded a renewal of interest in the aetiology and pathophy- siology of acute diarrhoea, particularly in humans, which until early in the 1970s had been a rather neglected disease syndrome. There were several reasons for the renewed interest. Firstly, there was a slowly growing apprecia- tion in developed countries of the overwhelming problem posed by acute diarrhoea in developing countries; that there was a high morbidity, and an unnecessarily high mortality, in young children, with many millions dying each year in the acute stage of the disease. The survivors, as the result of repeated enteric infection, frequently failed to thrive and progressed to malnutrition and eventual death. Secondly, there had been rapid advances in the study of aetiology, with the hope that further advances lay ahead. New viruses had been identified by a relatively simple technique using the electron microscope; and new pathogene- tic mechanisms, such as the production of toxins by enteric bacteria, had begun to be investigated. The realization that a technique as simple as examination of diarrhoeal faeces by electron microscopy could identify viral pathogens revolu- tionized the diagnosis of viral diarrhoeal disease. Virologists working on hu- man disease were able to draw on considerable knowledge already available to veterinarians. Thirdly, developing countries had themselves begun to realize the extent of their problems and to want to do something about them. The World Health Organization, with its expressed goal of ‘health for all by the year 2000’, began to put a major effort into decreasing the morbidity and mortality of children in the developing countries. Primary health care networks were set up by de- veloping countries to educate mothers in recognizing the dangers of diarrhoea and to establish oral rehydration therapy in the home to reduce the mortality in young children. Overall, in both developing and developed countries, there was a shared realization of the size of the problem and of solutions in terms both of aetiology and of therapy. This concurrence of events galvanized laboratory 1 2 Bishop scientists into taking an interest in the problems of acute diarrhoea in veterin- ary and in human medicine. Since 1975 there have been rapid developments in diagnostic techniques (based on enzyme immunoassays), and in protein chemistry, molecular biology and immunology. All have been brought into the overall thrust to solve problems related to acute diarrhoea. There has been an understanding on the part of people working in human medicine of all that veterinary science has to offer, and much fruitful collaboration has been established between veterinary and medical microbiologists. Thus, since 1975, we have attempted to do what Jon Rohde and Rob Northrup then urged us to do, which was to take science ‘where the diarrhoea is’ (Rohde & Northrup 1976). In the 1975 symposium the emphasis as far as viruses were concerned was on Norwalk agent and on rotavirus. We mentioned adenoviruses briefly: Tom Flewett pointed out that they were often shed in large numbers in faeces from diarrhoeal children, and that they had the puzzling characteristic of being difficult to grow; but that was as far as our appreciation of the role of adenovir- uses went. Astroviruses had already been named, and small round viruses had been described, but there was caution about their relation to diarrhoeal dis- eases. (There was even the suggestion that, on morphological grounds, many of them could be phages derived from bacterial or yeast gut infections and bore no relation to diarrhoeal disease.) Coronaviruses were thought to be a possible new pathogen in human medi- cine. TGE virus (transmissible gastroenteritis virus) was being used as a model of physiological changes, by infecting piglets and studying the electrolyte and fluid fluxes resulting from infection of the pig gut. But it seems that the early promise held out by the study of coronaviruses has been either unfulfilled or held in a state of suspended animation. The present symposium is a timely one. It is deliberately restricted to the so-called ‘novel’ diarrhoea viruses and will not be concerned to any great extent with what have become the ‘classical’r otaviruses-the group A rotaviruses that were a major topic in the earlier symposium. We shall discuss what are collectively called the ‘novel rotaviruses’ (non-group A) that have emerged as important causes of diarrhoea in both human and animal medicine since 1975; then the enteric adenoviruses; the small round viruses; and the new group of Berne and Breda viruses, suggested as a new family, the Toroviridae. The novel rotaviruses were recognized almost simultaneously in animals and in humans, although publication of the observations was delayed. Particles, morphologically identical with the classical rotaviruses, had been seen in animals and humans with acute diarrhoea; however, these rotaviruses would not react in serological tests. It became apparent that they were rotaviruses, but serologically distinct ones; they were characterized by failure to react with group (A) antiserum; they had the further useful characteristic of having genomic patterns markedly different from those of the ‘classical’, group A

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