Prof. Anthony Peter "Tony" Waterson (born 1923)

[Prof. Anthony Peter "Tony" Waterson (born 1923)], left, a leading authority on viruses, holding a virus model with [Prof. Rudolf Rott (born 1926)] of Germany in the mid 1960s. They worked together on research.[HN01IP][GDrive]

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Biographies and Memorials

Royal College of Physicians (UK) - History profile of "Anthony Peter Waterson"

https://history.rcplondon.ac.uk/inspiring-physicians/anthony-peter-waterson

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b.23 December 1923 d.11 October 1983

MB BChir Cantab(1947) MRCP(1950) MD(1954) FRCP(1970) FRCPath(1973)

Tony Waterson died at the age of 59, having recently retired as professor of virology at the Royal Postgraduate Medical School, London. Academically his record was quite outstanding. He was an open entrance scholar at Epsom College and gained an open scholarship in classics at Emmanuel College, Cambridge, where he obtained a double first in Natural Sciences. He carried out his clinical studies at the London Hospital Medical College, qualifying in 1947. 

After house appointments at the London, Waterson served as medical officer in the RAF in Germany. He then returned to Cambridge, first as a house physician at Addenbrooke’s Hospital to Sir Lionel Whitby and Lawrence Martin, followed by an appointment as assistant pathologist in the clinical laboratories. In 1952, Waterson transferred to the University, first as Elmore research student in the department of medicine and then as university demonstrator and later lecturer in the department of pathology, where he stayed until his appointment to St Thomas’s Hospital in 1964. During this period, Waterson was able to combine and achieve distinction in his College and departmental activities. Thus, after being elected to a fellowship of Emmanuel College in 1954, he successfully became director of studies in medicine and assistant tutor and college lecturer in pathology. He was a member of the governing body of Emmanuel College and also served on the College council and tutorial committee. In the department of pathology, Waterson was involved in important discoveries, most of which were related to the fine structure of viruses in which the then newly recognized technique of negative contrast staining was used. His book, Introduction to Animal Virology, was designed specifically for students studying pathology for part II of the Natural Sciences Tripos in Cambridge; it was widely popular, not only in Cambridge but wherever basic virology was being taught. 

However, unlike most academic virologists during this time, he realized the potential of the clinical applications of virology, and actively encouraged research into the clinical aspects of virus diseases. When he moved to St Thomas’s Hospital in 1964, after a year’s sabbatical in the Max Planck Institute for Virus Research, Tübingen, he was amongst the foremost to develop clinical services and research into clinical virology. After three years Waterson moved to the Royal Postgraduate Medical School, where he also developed clinical services and continued to supervise research both in basic and clinical virology. His interests and activities covered a wide field and included viral hepatitis, slow virus infections, as well as various aspects of the fine structure, taxonomy and evolution of viruses. He threw himself with enthusiasm into a study of viral infection and cardiomyopathy. At Hammersmith, Tony Waterson was respected and admired for his distinctive approach to clinical virology. His clear, forthright, but unassuming contributions to staff rounds were always received with attention and remembered for their value. 

Like many people of high intellectual achievement he was reserved, and despite the breadth of scholarship, truly modest. He never thrust his opinions and views upon others, and was an admirable and imaginative collaborator in research. Those who worked with him appreciated his style, knowledge and competence as well as his capacity for tolerance and understanding. 

One of his major achievements was his bringing together of clinical virologists at first in small, but later in much larger groups for meetings at a time when there was no forum available. The large and flourishing clinical virology group, now incorporated into the Society for General Microbiology, provides a tribute to Waterson’s foresight and enthusiasm. Shortly after his retirement, a ‘Festschrift’ was arranged on his behalf at the Royal Postgraduate Medical School. Despite this coinciding with both a complete rail and London Transport strike, it was a measure of the high esteem in which Tony Waterson was held that a large number of his friends and former colleagues still managed to come, not only from the UK but also from abroad. 

Tony was a scholar in every sense of the word; he had a considerable knowledge of history, both ancient and modern, and the book he wrote with Lise Wilkinson on the History of Virology is a classic. Unknown, even to many of his closer friends, Waterson was a biblical scholar of some repute and had read the Bible in the original Greek. Those who came to know him well found him kind and considerate, and his behaviour that of a true gentleman; he was also a man of deep religious conviction. He was devoted to and obtained great pleasure from his family; he was survived by his wife, two daughters and a son.

JF Goodwin

[Brit.med.J., 1983, 287, 1386 & 2559; Lancet, 1983, 2, 1040; Times, 4 Nov 1983]

2021 (Feb 22) - Yorkshire Post : "The Yorkshireman who named the coronavirus and aided its discovery; A brilliant but modest Yorkshire scientist helped name the coronavirus and played a role in its discovery"

By Sharon Dale  /  Monday, 22nd February 2021, 12:51 pm  /   PDF at [HN01IN][GDrive]  

Mentioned : Prof. Anthony Peter "Tony" Waterson (born 1923)   /   Prof. Rudolf Rott (born 1926)   /  Dr. David Arthur John Tyrrell (born 1925)  /  Dr. June Dalziel Almeida (born 1930)  /  

[Prof. Anthony Peter "Tony" Waterson (born 1923)] who helped name the coronavirus in the 1960s[HN01IO][GDrive]
[Prof. Anthony Peter "Tony" Waterson (born 1923)], left, a leading authority on viruses, holding a virus model with [Prof. Rudolf Rott (born 1926)] of Germany in the mid 1960s. They worked together on research.[HN01IP][GDrive]

As Prime Minister Boris Johnson lay dangerously ill with Covid-19 in St Thomas’ Hospital in London, he was unaware that decades earlier, in that very same hospital, a Yorkshireman had helped facilitate the discovery of the virus type that caused the devastating world-wide pandemic.

It was in Professor Tony Waterson’s Microbiology Department at St Thomas’ that the coronavirus was first identified in 1964 by [Dr. June Dalziel Almeida (born 1930)], a brilliant, Scottish-born scientist he had headhunted from the Ontario Cancer Institute in Canada.

Hornsea-born [Prof. Anthony Peter "Tony" Waterson (born 1923)] and [Dr. David Arthur John Tyrrell (born 1925)], then head of the Common Cold Research Unit, then took on the task of naming the virus with help from a dictionary. This initial discovery was the crucial first building block in helping modern day scientists battle this latest deadly strain.

The story began when the Common Cold Research Unit in Salisbury identified an unusual virus strain in nostril swabs taken from schoolboys. They found that it caused cold-like symptoms but had properties that were quite distinct from the familiar cold viruses and they were keen to find out more. 

Dr David Tyrrell later wrote: “I decided to seek help from [Prof. Anthony Peter "Tony" Waterson (born 1923)], the new professor of virology at St Thomas’ Hospital. “He had just recruited an electron microscopist, [Dr. June Dalziel Almeida (born 1930)], who was seemingly extending the range of the electron microscope to new limits. She claimed that she would be able to find virus particles with her new, improved techniques.

“We were not too hopeful but felt it was worth a try. The results exceeded all our hopes and her pictures revealed their structure beautifully. June was confident that these three viruses were something quite new.”

The daughter of a Scottish bus driver who grew up in a Glasgow tenement and left school at 16 was right. Starting as a lab technician, she went on to study virology and became a leading light in virus imaging, identification, and diagnosis. What she saw that day 56 years ago was the first glimpse of a human coronavirus and she recognised that it was related to viruses in animals as she had seen similar particles while investigating mouse hepatitis and infectious bronchitis in chickens.

This new virus group needed a name and the circumstances of its coinage were recounted by [Dr. David Arthur John Tyrrell (born 1925)]: “We sat down in Waterson’s office to consider the implications of these results. We were quite certain that we had identified a previously unrecognized group of viruses. So what should we call them? “Influenza-like seemed a bit feeble, somewhat vague, and probably misleading. “We looked more closely at the appearance of the new viruses and noticed that they had a kind of halo surrounding them. Recourse to a dictionary produced the Latin equivalent, corona, and so the name coronavirus was born.”

It was in a short article in the journal Nature in November 1968 that [Dr. June Dalziel Almeida (born 1930)], [Dr. David Arthur John Tyrrell (born 1925)] and six other virologists first used the name “coronavirus” in print.

[Prof. Anthony Peter "Tony" Waterson (born 1923)] was a leading authority on viruses[HN01IQ][GDrive]

Prof. Waterson’s son Nicholas says that it was only after the start of the pandemic last year that the family became aware of their father’s involvement with the work, after looking through his papers and books. “We knew, of course, that he did something clever with viruses and we were even sometimes allowed to peer down the electron microscope on visits to his lab but we really had no idea what he got up to in any detail,” says Nicholas. “He died when I was only 18 and learning about this has made me feel closer to him again after so many years.”

Just over fifty years ago, in 1970, Prof. Tony Waterson wrote the following somewhat prescient words: “If a pathogenic micro-organism should break loose, which can spread not only from animals to man but also readily from man to man, a major and global disaster would happen.”

Dying prematurely in 1983, at the age of 59, he did not live to see the viruses he had named finally cause the global pandemic he had feared. Dr June Almeida passed away in 2007 and Dr David Tyrrell in 2005 but their work also lives on.

*A LIFE SCIENTIFIC: Professor Tony Waterson was born at the Old Hall in Hornsea on the East Yorkshire coast in 1923. His parents had just moved north from Kent after buying Hornsea College, a girl’s boarding school based in a rambling Jacobean manor house. Gladys, his mother, became the headmistress and it seems that she was a woman with enormous drive as she was still only in her twenties when she took on the role.

She set the bar very high not only for her pupils but also her own children., though Trevor’s son Edward Waterson who lives in York, says: “Tony and his older brother, Trevor, were very close and enjoyed a carefree seaside childhood in what was then a quiet little seaside town.”

The young Tony was enrolled at Hornsea College and then sent off to board at the age of only seven at Orleton Preparatory School up the coast in Scarborough. Though he missed his family and objected to cliff-top football in the bracing Yorkshire winds, he threw himself into his schoolwork and excelled academically.

When it came to his secondary schooling, Tony was sent south, winning a scholarship to Epsom College in Surrey and later won a classics scholarship to Emmanuel College, Cambridge in 1941. Despite his lifelong love of Latin and Greek, he chose to follow a more practical scientific path, graduating with a double first in Natural Sciences.

He had been due to be called up for military service in 1943 but according to College archivist Amanda Goode, Emmanuel fought successfully to keep him, arguing that he was one of the “very best” students. It was also at Cambridge that Tony discovered the Christian faith that would guide him through the rest of his life. After completing his medical studies at the London Hospital, he did National Service as an RAF Medical Officer in Germany, looking after servicemen and their families during the Berlin airlift.

His daughter Sarah says that there was always a caring side to him. She recently found a letter he wrote to his mother asking her to send a tin of cocoa from Yorkshire as there was none to be had in Germany and his German teacher wanted some for his elderly mother.

Following National Service, his scientific career took off fast. He returned to Cambridge to lecture and research in pathology, specialising in viruses, and after a sabbatical year back in Germany, he took up the post of Professor of Microbiology at St Thomas’s Hospital in London in 1964 at the age of 40. Later he would become the first Professor of Virology at the Royal Postgraduate Medical School at Hammersmith Hospital.

1983 (Nov) Obituary/Memorial for AP Waterson in British Medical Journal

Saved PDF : [HP00D3][GDrive

DOI :  10.1136/bmj.287.6402.1386   

 [HP00D4][GDrive

Professor A P Waterson, formerly professor of virology at the Royal Postgraduate Medical School, died at home on 17 October. He was 59.

Anthony Peter Waterson had an outstanding academic record: an open entrance to Epsom College was followed by an open scholarship in classics to Emmanuel College,Cambridge, where he obtained a double first in natural sciences. He graduated MB, BChir in 1947, carrying out his clinical studies at the London Hospital Medical College, where he was an open entrance scholar. After house officer appointments there and at Addenbrooke's and national service with the Royal Air Force he became successively Elmore research student in the department of medicine at Cambridge and in 1954 university demonstrator and then lecturer in the department of pathology, eventually with responsibility for the virus research laboratory. During this time he was also active in college affairs at Emmanuel, being a fellow, director of studies in medicine, and supervisor of pathology.

It was during his early days in the department of pathology that Tony Waterson's interest in virology was kindled, and within a short time he had made many important contributions in relation to the structure of viruses. In contrast with many academic virologists who at that time rarely ventured into the field of clinical virology, he predicted that this would soon be a rapidly developing specialty. Perhaps more than any other person he was responsible for bringing virology out of the research laboratory and into everyday use in clinical practice. When appointed to the chair of medical microbiology at St Thomas's Hospital in 1964 and when four years later he moved to the chair in virology at the Royal Postgraduate Medical School he encouraged the development of clinical services and research in clinical virology. Although not primarily an investigator, he made a remarkable contribution as a catalyst, coordinator of stimulating meetings, and editor. Thus within only a six year period he edited three editions of Recent Advances in Clinical Virology. His many review articles were widely read as they were not simply collections of facts pulled together from other sources but were works exhibiting considerable critical insight into aspects of disease that had sometimes escaped the notice of those who were more actively engaged in research. He brought clinical virologists together, at first in small, but later in much larger groups, for meetings at a time when there was no forum available. The large and flourishing clinical virology group now incorporated into the Society for General Microbiology provides a tribute to his foresight and enthusiasm.

Shortly after Professor Waterson's retirement a "Festschrift" was arranged on his behalf at the Royal Postgraduate Medical School. It was a tribute to the high esteem in which he was held that, despite this coinciding with a complete strike of both the railways and London Transport, a large number of his friends and former colleagues still managed to come - not only from the United Kingdom but also from abroad.

Professor Waterson was a scholar in every sense of the word; he had a considerable knowledge of history, both ancient and modern, and the book he wrote with Lise Wilkinson, An Introduction to the History of Virology (1978), is a classic. Unknown even to many of his closer friends, he was a biblical scholar of some repute and had read the Bible in the original Greek. As an individual he was reserved and, despite the breadth ofhis scholarship, truly modest. Those who came to know him well found him truly kind and in his behaviour a thorough gentleman; he was also a man of deep religious convictions. He was devoted to and obtained great pleasure from his family; he is survived by his wife Ellen, two daughters, and a son.-JEB.

mentioned in SVCP 

Green, M.: Oncogenic viruses. In: Modern Trends in Medical Virology II, (R.B. Heath and

A.P. Waterson, eds.), Butterworths, London, 1970, pp. 701–756.  

EVIDENCE TIMELINE

1959 (April)

DOI:10.1016/S0022-2836(59)80011-5Corpus ID: 83481661

The icosahedral form of an adenovirus

R. Horne, S. Brenner, +1 author P. Wildy

Published 1 April 1959

Chemistry

Journal of Molecular Biology

View via Publisher

horne1959.pdf  

With Sydney Brenner !!!   https://sites.google.com/housatonicits.com/home0003/research/sydney-brenner-b1927  

1961 (Nov)

DOI:10.1016/0042-6822(61)90370-1Corpus ID: 7283684

The nature of measles virus.

A. P. Waterson, J. G. Cruickshank, G. Laurence, A. Kanarek less

Published 1 November 1961

Biology, Medicine

Virology

View on PubMed

doi.org

waterson1961.pdf 

1963 (May)

The Components of Measles Virus and their Relation to Rinderpest and Distemper

Measles virus has been disintegrated by treatment with ether and Tween 80. This destroys the infectivity, and physically disintegrates the particle, with the release of an inner component structurally like the nucleoprotein of Newcastle disease virus (NDV), and another structure similar to the haemagglutinin (HA) of NDV. The preparation after ether-tween treatment has an enhanced HA activity. The two components are separable in a CsCl density gradient. The inner component is probably a nucleoprotein. The HA component could be adsorbed by monkey erythrocytes but not eluted from them. The action on it of sodium metaperiodate suggests that a carbohydrate may be involved. The ether-tween preparation could be used as an antigen in the CF-reaction with antisera to rinderpest and distemper. It could also be used in the HA-inhibition test as a sensitive indicator with antisera to rinderpest and distemper, as well as to measles, giving higher titres in the HA-inhibition test than when the untreated virus was used. Injection of the ether-tween preparation stimulated the production of neutralizing, HA-inhibiting and complement-fixing antibodies in the rabbit. Collapse

waterson1963-2.pdf  

1963 (Aug)

Home  Archiv für die gesamte Virusforschung  Article

Published: August 1963

The fine structure of influenza A, B and C viruses

A. P. Waterson, J. M. W. Hurrell & Keith E. Jensen 

Archiv für die gesamte Virusforschung volume 12, pages487–495 (1963)Cite this article

Summary

2. The particles of influenza B and influenza C are similar to those of influenza A, and different from those of the Newcastle disease-mumpsparainfluenza group.

3.  The treatment of particles of strains of influenza A and B with formalin enabled the internal structure to be resolved somewhat more clearly. Treatment with chloroform in addition to formalin made it possible to resolve the internal ribonucleoprotein (soluble antigen) lying coiled within the particle in a regular manner.

Waterson, A.P., Hurrell, J.M.W. & Jensen, K.E. The fine structure of influenza A, B and C viruses. Archiv f Virusforschung 12, 487–495 (1963). https://doi.org/10.1007/BF01242156

Received

11 August 1963

Issue Date

August 1963

DOI

https://doi.org/10.1007/BF01242156

waterson1963.pdf

1963 (August)

Arch Gesamte Virusforsch

. 1963 Aug 26;13:577-81. doi: 10.1007/BF01267799.

THE VIROMICROSOMES OF FOWL PLAGUE VIRUS. (BRIEF REPORT)

A P WATERSON, R ROTT


1963-08-26-arch-gesamte-virusfosch-viromicrosomes-of-fowl-plague-virus.pdf

1964 (June 04) - RECEIVED - 

DOI:10.1007/BF01241759  Corpus ID: 36221200

The significance of viral structure

A. P. Waterson

Published 2005

Biology, Medicine

Archiv für die gesamte Virusforschung

View on Springer

ncbi.nlm.nih.gov

waterson1965.pdf

1965 (June)

DOI:10.1038/2061125a0

Simulation of Viral Sub-Structure by Radiography of Models

esters as butyrylcholine24 , propionylcholine2', imidazole acrylylcholine26 and phosphorylcholine27 • All these esters would be hydrolysable by cholinesterase (specific and nonspecific), since it is now recognized that the cholinesterascs are a group of enzymes capable of hydrolysing a large series of choline and non-choline esters with variation in the aliphatic and aromatic hydrocarbon moieties 24 • 28 • It is thus possible thvt in those mammalian species in which cholinesterase is located in the marginal sinus, sub-marginal capillaries and post-capillary venulcs, the enzyme could bo concerned in the inactivation of any potentially toxic esters produced during mitosis in the various distinctive tissues • According to this view the cholinesterase located at the periphery of cortical nodules could carry out a similar function in those species in relation to esters produced in the germinal centres of such nodules. However, if the localization of cholinesterase in lymph nodes is interpreted in the wider perspective that lymphoid tissue normally plays a part in the regulation of tissue size • (a view which is entirely consistent with present knowledge concerning lymphoid tissue 3 •4 ), then cholinesterase in lymph nodes would be strategically placed to catabolize 'tissue-coding factors'• ITCF) which, it is postulated, normally reach lymph nodes along their afferent lymphatics. Cholincsterascs and 'or non-specific esterases (non-specific esterases are located in the marginal sinus, sub-marginal capillaries and post-capillary venulos of lymph nodes in a wide variety of marrnnals2 • 7 • 16) could 'strip' the lipid component from the TCF before the 'processed-TCF' is presented to the 'receptor' cells• of the lymphocyte series-perhaps mainly in the wall of the post-capillary venule, which, as Marchesi and Gowans29 have shown, is the site in lymph nodes through which small lymphocytes normally enter a node in their continuous re-circulation throughout the body (Fig. l). We thank Mr. R. K. Adkin and Mr. R. H. Nettleton for help. We also thank the Wellcome Research Laboratories for a gift of the anticholinesterase 62047h di-iodide. 1 Burwell, R. G., and Gowland, G. J., Bone Jt. Surg., 43, B, 820 (1961). Burwell, R. G., Bone Jt. Surg., 44, B, 688 (1962). 2 Burwell, R. G., .Ann. N.Y . .Acad. Sci., 99, 821 (1962). 'Burwell, R. G., Lancet, ii, 69 (1963). 'Burch, P.R . . T., and Burwell, R. G., Quart. Rev. Biol. (in the press). 'Mann, jun., L. T., Corson, J. M., and Dammin, G. J., Nature, 187, 77! (1960l. Brent, L., Medawar, P. B., and Ruskiewicz, M., Brit. J. Exp. Path., 42, 464 (1961). Herzenberg, L.A., and Herzenberg, L.A., Proc. U.S. Nat . .Acad. Sci., 47, 762 0961). 'Green, H. N., and Wilson, R., Nature, 182, 1054 (1958). Vogt, P., Nature, 182, 1807 (1958). Okada, T. S., Nature, 194, 306 (1962). 'Burwell, R. G., J . .A nat., 97, 629 (1963). Burwell, R. G., and Ballantyne, B. (in preparation). ','Coupland, R. E., and Holmes, R. L., Quart. J. Micro. Sci., 98,327 (1957). 'Koelle, G. B., J. Pharmacal. Exp. Therap., 100, 158 (1950). "Gerebtzoff, M. A., Cholinesterases, 4 (Pergamon Press, London, 1959). "Pearse, A. G. E., Histochemistry, Theoretical and .Applied, 462 (J. and.-\. Churchill, London, 1960). 12 Adams, C. W. M., Marples, E. A., and Trounce, J. R., Clin. Sci., 19, 473 (1960). "Dumont, L., C.R. Soc. Biol., Paris, 149, 960 (1955). "Gerebtzoff, M.A., Cholinesterases, p, 21 (Pergamon Press, Loudon, 1959). "Rogister, G., and Gerebtzoff, M. A., .Acta .Anat., 32, 39 (1958). 18 Ballantyne, B. (unpublished observations). "D'Agostini, N., and Rossatti, R., J . .A nat., 93, 354 (1959). "Moe, R. E., .A mer. J . .A nat., 112, 311 (1963). "Crooke, J. C., Nature, 199, 41 (1963). "Koelle, G. B., Biochem. J., 53, 217 (1953). 21 Smith, C. E., and Henan, B. K., .A nat. Rec., 135, 207 (1959). 22 Clitherow, J. W., Mitchard, M., and Hasper, N . . T., ~Nature, 199, 1000 (1963). " Ballantyne, B., J . .A nat., 98, 689 (1964). "Heath, D. F., Organophosphorus Poisons, 103 (Pergamon Press, Oxford, 1961). "Banister, J., Whittaker, V. P., and Wijesundera, S., J. Physiol., 115, 55P (1951). "Grelis, M. E., and Tabaehnick, I. I. A., Brit. J. Pharmacal., 12, 320 (1957). "Augustinsson, K.-B., in The Enzymes, edit. by Boyer, P. D., Lardy, H., and Myrback, K., 4, 521 (Academic Press, New York, 1960). "Lehmann, H., and Silk, E., Brit. Med. Bull., 17, 230 (1961). Mounter, L. D., and Cheatham, R. M., Enzymology, 25, 215 (1963). Bodansky, 0., .Ann. N.Y . .Acad. Sci., 47, 521 (1946). Chcssick, R. D., J. Histochem. Cytochem.,2, 258 (1954). Nachmansohn, D., and Wilson, I. B., in .Advances in Enzymology, edit. by Nord,.!!'. 1!'., 12 259 (Intcrscience Publishers, New York, 1951). Mendel, B., Mundell, D. B., and Rudney, H., Biochem. J., 37, 59 (1943). "Marchesi, V. T., and Gowans, J. L., Proc. Roy. Soc., B, 169, 283 (1964). Collapse

https://www.semanticscholar.org/paper/Simulation-of-Viral-Sub-Structure-by-Radiography-of-Almeida-Waterson/d31e0dc327953b80a6f4cb64b75cf63b9a41385b 

almeida1965.pdf 

1965 

Measles virus

Downloading the book in this website lists can give you more advantages. It will show you the best book collections and completed collections. So many books can be found in this website. So, this is not only this measles virus. However, this book is referred to read because it is an inspiring book to give you more chance to get experiences and also thoughts. This is simple, read the soft file of the book and you get it. 

waterson1965-2.pdf

1967 (Jan)

Volume 46, Issue 1

Research Article Free

Some Observations on the Envelope of an Influenza Virus 


Text - https://www.microbiologyresearch.org/content/journal/micro/10.1099/00221287-46-1-107  

SUMMARY Micrographs of the envelope of fowl-plague virus revealed an arrangement of subunits each one of which was surrounded by either five or six others. The similarity of this arrangement to that of a cubic virus capsid has led us to consider which components of morphologically different viruses fulfil similar functions.
 INTRODUCTION A virus particle consists of two parts, the essential nucleic acid and a means of protecting this from the environment. It was predicted that the protective covering would be built up of identical repeating subunits (Crick & Watson, 1956). Early X-ray diffraction studies suggested that these units would be arranged symmetrically (Hodgkin, 1949) and that the symmetry would be one of two types, helical or cubic. The application of negative-staining to virus particles shortly after this revealed pictorially both types of symmetry (Horne & Wildy, 1961). Viruses which had by previous techniques been considered to be spherical were now seen to be icosahedral, i.e. belonged to the cubic group, and particles which had been described as rod-shaped were now seen to have helically-arranged subunits. The cubic arrangement was found for DNA and for RNA viruses and can be found among bacterial, plant and animal viruses. The simple helical arrangement, on the other hand, seems to be confined mainly to RNA viruses, and, of even greater importance in the present connexion, has not been found in the simple form among animal viruses. Helical symmetry, however, is frequently present among animal viruses, the simple RNA and protein arrangement (ribonucleoprotein) being found enclosed within an additional lipo-protein envelope. The overall form of this outer envelope is usually irregular, and viruses such as influenza are usually described as being pleomorphic. The lipoprotein covering of such viruses seems to contain both viral and host material (Cruickshank, 1964). Until now it has not been looked on as conforming to the requirements of virus structure—that is, made up of identical repeating subunits identically arranged in a helical virus, or with each subunit surrounded by either six or five others in a cubic virus (Caspar & Klug, 1962).
 RESULTS While working with fowl-plague virus, an influenza A virus (Almeida, Himmelweit & Isaacs, 1966), we obtained micrographs which suggested that, although not conforming to the arrangement found in either helical or cubic viruses, the envelope of pleomorphic viruses such as the myxoviruses may bear a much closer resemblance to these arrangements than was previously suspected.
Plate 1, fig. 1., shows a negatively-stained fowl-plague virus particle with a completely regular array of subunits on the surface. Particles showing such complete regularity of arrangement were found only with difficulty and probably resulted from a fortunate combination of staining conditions and particle orientation. On the other hand, particles showing regular subunit arrangement over small areas could be found frequently and confirmed that the phenomenon was a real one and not an artifact formed by local conditions (Pl. 1, fig. 2). Like the cubic capsid (Pl. 1, fig. 3) the fowl-plague envelope illustrated in Pl. 1, fig. 1, is built up of subunits surrounded by either five or six other subunits. The difference between them lies in the fact that while the distribution of ‘fives’ and ‘sixes’ is fixed for the adenovirus capsid, it is random for the fowl-plague envelope. (Pl. 2, fig. 5)
This finding, that the envelope of a myxovirus resembles more closely than had been supposed the capsid of a cubic virus, led us to consider which components of morphologically distinct viruses—for example, measles and poliovirus—correspond most closely with regard to structure and function. Of course, there is no doubt that the helical ribonucleoprotein which constitutes the virion (the entire infective virus) in plant viruses, such as tobacco mosaic virus, bears a marked similarity to the internal component of a virus such as measles. They both consist of RNA and protein: in both the protein is arranged helically and the diameter of both is the same. The morphology of the ribonucleoprotein of measles, though usually seen as a herringbone pattern indicative of an extended helix, can nevertheless sometimes be seen in a much more straight and compressed form, very similar to the tobacco mosaic virus rod (Pl. 1, fig. 4).
However, when the two are compared biologically, the roles of the two proteins are markedly different The tobacco mosaic virus protein is in direct contact with the environment and is apparently capable of protecting the nucleic acid from it, whereas the measles helix is separated from the environment by the envelope, and it seems improbable that the ribonucleoprotein should be capable of survival in the environment as an infective entity when not surrounded by this envelope. Again, when compared in their capacity as antigens, the tobacco mosaic virus protein will cause the production of antibodies which neutralize the virus, but the internal myxovirus protein will not (Schäfer, 1957). This means that, when compared biologically, the simple cubic virus bears the same relationship to the helical protein of tobacco mosaic virus as it does to the outer envelope of animal viruses with an internal helical component.
It follows that that, in terms of biological function, if not of morphology alone, it is the coverings presented to the environment that correspond, and the flexible helical ribonucleoprotein of the myxoviruses, inside its envelope, corresponds with the contents of the simple cubic virus capsid. This leads to the question of whether cubic capsids contain an internal protein in association with the nucleic acid. The absence of such a protein is by no means certain, and its presence would of course heighten the resemblance. One virus with a regular capsid (vesicular stomatitis virus) has now been shown to contain within its capsid a ribonucleoprotein helix (Brown, Cartwright & Almeida, 1966) ; also, an arbovirus (Venezuelan equine encephalomyelitis), which may have a symmetrical cubic capsid, has been shown to contain a helix (Klimenko et al. 1965).
A further corollary is that the myxovirus envelope and the cubic capsid have more in common with each other than has been realized hitherto (Pl. 1, figs. 1, 3). Admittedly the myxovirus envelope contains lipid and carbohydrate, which are lacking from the cubic capsid, and is asymmetrical. On the other hand, this envelope is the basic means of protecting the internal nucleic acid, it is in contact with the environment, and it, rather than protein of the ribonucleoprotein, is the immunogen. In all of these respects the myxovirus envelope parallels the function of the cubic virus capsid.
It appears therefore that animal viruses may be regarded as having two components : first, the nucleic acid, which in some cases, e.g. the myxoviruses and vesicular stomatitis virus, has helically-arranged protein associated with it ; secondly, the capsid or envelope, which consists essentially of protein units arranged as hexamers or pentamers, and which surrounds and protects the contained nucleic acid or nucleoprotein. This protective apparatus of ‘fives’ and ‘sixes’ can be arranged in either a symmetrical or a pleomorphic manner and can be built solely of protein or may have additional lipid and carbohydrate. The term ‘nucleo-capsid’ (Caspar et al. 1962) used for both the virion of simple cubic viruses and the ribonucleoprotein of myxoviruses is therefore misleading, being applied to two functionally different entities. If this reasoning is valid, then the distinction into cubic and helical would not be as meaningful as a division into cubic and pleomorphic. This would then compare analogous structures that appear to be constructed in a similar manner.
 ACKNOWLEDGMENTS We are indebted to Dr H. G. Pereira for supplying us with the fowl-plague virus.
 REFERENCES Almeida J. D., Himmelweit F., Isaacs A. 1966; Studies on the intracellular haemagglutinin component of fowl plague virus and other myxoviruses. J. gen. Microbiol 45:153 [Google Scholar]Brown F., Cartwright B., Almeida J. D. 1966; The antigens of vesicular stomatitis virus. I. Separation and immunogenicity of three complement fixing components. J. Immunol 96:537 [Google Scholar]Caspar D. L. D., Dulbecco T., Klug A., Lwoff A., Stoker M. G. P., Tournier P., Wildy P. 1962; Proposals. Cold Spring Harb. Symp. quant. Biol 2749 [Google Scholar]Caspar D. L. D., Klug A. 1962; Physical principles in the construction of regular viruses. Cold Spring Harb. Symp. quant. Biol 271 [Google Scholar]Crick F. H. C., Watson J. D. 1956; Structure of small viruses. Nature, Lond 177:473 [Google Scholar]Cruickshank J. G. 1964; The structure of myxoviruses and its biological significance. In Cellular Biology of Myxovirus Infections Wolstenholme G. E. W., Knight J. 5 London: Churchill; [Google Scholar]Hodgkin D. C. 1949; X-ray analysis and protein structure. Cold Spring Harb. Symp. quant. Biol 1465 [Google Scholar]Horne R. W., Wildy P. 1961; Symmetry in virus architecture. Virology 15:348 [Google Scholar]Klimenko S. M., Yershow F. I., Gofman Y. P., Nabantikov A. P., Zhdanov V. M. 1965; Architecture of Venezuelan equine encephalomyelitis virus. Virology 27:125 [Google Scholar]Schäfer W. 1957; Units isolated after splitting fowl plague virus. In The Nature of Viruses Wolstenholme G. E. W., Millar E. C. P. 91 London: Churchill; [Google Scholar] EXPLANATION OF PLATE Plate 1Electron micrographs of negatively-stained preparations, all at × 415,000.
Fig. 1.An unusual micrograph of a fowl-plague virus particle, showing the arrangement of subunits on its surface. The majority of these subunits are surrounded by six others, but a small, randomly located number have only five others round them. The arrow points to a location where a subunit surrounded by five others can be clearly seen. The centre-to-centre spacing of the subunits, about 70 Å, in this particle is almost identical with that of the capsomeres of the adenovirus particle shown in fig. 3.Fig. 1.Click to view
 Fig. 2.Subunit arrangements of the kind shown here are frequently encountered in preparations of influenza-type viruses. Although not as regular as the subunit array in fig. 1, it is still possible to see a geometric arrangement on the surface.Fig. 2.Click to view
 Fig. 3.An adenovirus particle viewed along a two-fold axis. It is similar to fig. 1 inasmuch as the capsid is composed of subunits surrounded by either five or six others, but dissimilar in that the distribution of these is rigidly fixed.Fig. 3.Click to view
 Fig. 4.A length of the ribonucleoprotein component of measles virus. More usually, micrographs of this structure show a herringbone arrangement, but in this case the helix has remained compressed and shows a strong resemblance to helical plant viruses (e.g. tobacco mosaic virus).Fig. 4.Click to view
 Plate 2Fig. 5.Using 5- and 6-sleeve connectors, model (a) was built to fulfil icosahedral requirements, that is, a 5-sleeve connector at each apex and 6-sleeve connectors in between, to give a total of 92 subunits. Model (b) is built of randomly distributed 5- and 6-sleeve connectors. Although the overall appearance of the two models is quite different, the basic arrangement of each is the same and differs only in the presence or absence of symmetry.Fig. 5.Click to view
  © Society for General Microbiology 1967

1967 (July)

DOI:10.1016/S0140-6736(67)92302-1 Corpus ID: 84376978

MORPHOLOGICAL CHARACTERISTICS OF RUBELLA VIRUS

J. Best, J. Banatvala, +1 author A. P. Waterson

Published 29 July 1967

Biology

The Lancet

best1967.pdf

1968 (Nov 16)  - Nature : First article that introduces the new term "coronarviurs"; credit is attributed to Prof. Tony Waterson 

Nature volume 220, page 650  /  Published: 16 November 1968    /   doi : 10.1038/220650b0

Saved PDF: [HP00D5][GDrive]   

Mentioned :  Dr. June Dalziel Almeida (born 1930)  /  Dr. David Arthur John Tyrrell (born 1925)  /   Prof. Anthony Peter "Tony" Waterson (born 1923)   /  

Image of page 650:  [HP00D6][GDrive

VIROLOGY / CORONAVIRUSES

A NEW group of viruses with the name of coronaviruses has been recognized by an informal group of virologists who have sent their conclusions to Nature. (They are [Dr. June Dalziel Almeida (born 1930)]; D. M. Berry; C. H. Cunningham; D. Hamre; M. S. Hofstad; L. Mallucci; K. McIntosh; [Dr. David Arthur John Tyrrell (born 1925)].)

They point out that with negative staining, avian infectious bronchitis virus has a characteristic electron microscopic appearance resembling, but distinct from, that of myxoviruses. Particles are more or less rounded in profile; although there is a certain amount of polymorphism, there is also a characteristic "fringe" of projections 200 A long, which are rounded or petal shaped, rather than sharp or pointed, as in the myxoviruses. This appearance, recalling the solar corona, is shard by mouse hepatitis virus and several viruses recently recovered from man, namely strain B814, 229E and several others. These viruses also share a number of other properties as indicated in the table. (Anyone interested in the data on which the table is based may obtain a short bibliography on application to Dr D. A. J. Tyrrell at the Common Cold Research Unit, Salisbury, Wiltshire.)

[...]

Some other relevant properties should bc mentioned. There is an antigenic relationship between the human and murine strains, but none has been detected between avian strains and the others. A haemagglutinin has been detected by certain workers using avian infectious bronchitis virus and also antigens separable from the virus particle, but these have so far not been recorded for the human or murine strains.

In the opinion of the eight virologists these viruses are members of a previously unrecognized group which they suggest should be called the coronaviruses, to recall the characteristic appearance by which these viruses are identified in the electron microscope.

These suggestions have been received by members of the Myxovirus Study Group (chairman, [Prof. Anthony Peter "Tony" Waterson (born 1923)]) under the International Committee for the Nomenclature of Viruses (ICNV). The suggestions were found acceptable and are now to be considered by the Vertebrate Virus Committee of the ICNV.

1969 (Feb)

DOI:10.1016/S0140-6736(69)91243-4Corpus ID: 45793570

Structures associated with leptospires possibly relevant to the Marburg agent.

J. Almeida, A. P. Waterson, +1 author L. H. Turner

Published 1 February 1969

Medicine

Lancet

almeida1969-3.pdf

1969  - No paper available, but INTERSTING... 

Corpus ID: 88939551

Immune electron microscopy of the Australian-SH (serum hepatitis) antigen.

J. Almeida, A. Zuckerman, +1 author A. P. Waterson

Published 1969

Medicine

Microbios

No Paper Link Available

https://www.semanticscholar.org/paper/Immune-electron-microscopy-of-the-Australian-SH-Almeida-Zuckerman/5b7b559ed688ca1741a185c5c5e251b15e2b7d94 

1969 (June)

Virological aspects of neurological disease

Viruses are now known to consist of only two major components; the nucleic acid which is essential for infectivity and an external covering to protect this. Visualization of this external shell by electron microscopy has revealed that viruses display distinctive arrangements of sub-units by which they can be both recognized and characterized. This has made it possible to classify viruses according to their structural and chemical features and such a classification has superseded earlier and essentially biological classifications without contradicting them. The action of a virus upon a cell may take one of three forms. The virus in the process of replication may destroy the cell which it has infected (lytic action). A second possibility is that it may transform the cell to malignancy (oncogenic action). A third possibility is that the virus may remain latent within the cell for long periods with no obvious manifestations of its presence (symbiotic relationship). It is this last type of interaction between a virus and the host cell which appears to be of particular interest in the context of the nervous system. Collapse

351-full.pdf

1969 (Nov)

DOI:10.1016/S0140-6736(69)90540-6Corpus ID: 11740666

Immune complexes in hepatitis.

J. Almeida, A. P. Waterson

Published 8 November 1969

Medicine, Biology

Lancet

almeida1969-2.pdf

1969 (Dec)

DOI:10.1016/S0065-3527(08)60878-7Corpus ID: 42108265

The Morphology of Virus-Antibody Interaction

J. Almeida, A. P. Waterson

Published 31 December 1969

Biology

Advances in Virus Research

almeida1969.pdf

1971 (Oct)


. 1971 Oct 16;2(7729):849-50. doi: 10.1016/s0140-6736(71)90223-6.

Possible airborne spread of serum-hepatitis virus within a haemodialysis unit

J D Almeida, A E Kulatilake, D H Mackay, R Shackman, G D Chisholm, A B MacGregor, E P O'Donoghue, A P Waterson


almeida1971.pdf  

1976 (Feb)


Annu Rev Med




. 1976;27:23-35. doi: 10.1146/annurev.me.27.020176.000323.

Infectious particles in hepatitis

A P Waterson

https://sci-hub.ru/10.1146/annurev.me.27.020176.000323

waterson1976.pdf

1978 (July)

Virological investigations in congestive cardiomyopathy.

VIRUSES and other non-bacterial agents (rickettsiae and chlamydiae) can cause acute inflammatory infections in the heart, just as they can in other organs of the body. The pericardium, myocardium and endocardium can be attacked by viruses to varying degrees and in varying ways. The heart can be affected even before birth by rubella virus, with resulting congenital defects, and a direct infection of the heart membranes or muscle, or both can be caused by several viruses in childhood, adolescence and adult life (Table 1). Disease of the valves is associated particularly with the rickettsiae and chlamydiae, and involves, usually, a previously damaged valve. Acute myopericarditis is associated frequently, though not exclusively, with enteroviruses, particularly with the Coxsackie B group (Grist and Bell, 1974; Grist, 1977). Typically, the course of acute myopericarditis is a short one, progressing rapidly to recovery or death, although the natural history also includes the phenomenon of recurrence or recurrences, and progression to longterm cardiac disease. Curiously, the clinical endproduct seems rarely to be what may be defined as congestive (primary) cardiomyopathy (Goodwin, 1970; Olsen, 1972). Collapse

waterson1978.pdf 

1978 BOOK - 

An Introduction to the History of Virology

If you really want to be smarter, reading can be one of the lots ways to evoke and realize. Many people who like reading will have more knowledge and experiences. Reading can be a way to gain information from economics, politics, science, fiction, literature, religion, and many others. As one of the part of book categories, introduction to the history of virology always becomes the most wanted book. Many people are absolutely searching for this book. It means that many love to read this kind of book. 

ORDERD on EBAY

1979 (Sep)

DOI:10.1136/bmj.2.6190.564  Corpus ID: 42628239

Virus infections (other than rubella) during pregnancy.

A. P. Waterson

Published 8 September 1979

Medicine

British Medical Journal

waterson1979.pdf  

1979 (Sep)

DOI:10.1136/adc.54.9.670

Vertical transmission of hepatitis B surface antigen in carrier mothers in two west London hospitals.

126 children of 102 hepatitis B surface antigen (HBsAg) carrier mothers were delivered at Hammersmith Hospital and Queen Charlotte's Maternity Hospital, between 1971 and mid-1978. Blood tests on 110 of these children showed that 8 out of the 18 with Chinese mothers, but only 6 out of the 92 other children, have become HBsAg positive. The presence of maternal hepatitis B e antigen (HBeAg) is also significantly correlated with transmission of HBsAg to the children. The management of children whose mothers are carriers is discussed. Collapse

woo1979.pdf   

1982 (Feb)

Percival GH. An introduction to dermatology. Edinburgh: Livingstone, 1967. 2 Pillsbury DM, Shelley WB, Kligman AM. Dermatology. Philadelphia: W B Saunders, 1956. 3 Betterle C, Peserico A, Del Prete… Expand

View on BMJ

waterson1982.pdf

1983 (March)

DOI:10.1136/bmj.286.6367.743

Corpus ID: 31627211

Acquired immune deficiency syndrome.

A. P. Waterson

Published 5 March 1983

Law

British Medical Journal (Clinical research ed.)

consent to examination by a medical practitioner rather than the station sergeant falls a long way short of full, free, and informed consent. In the case of intimate body samples the Bill does provide that consent must be given and the sample has to be taken by a medical practitioner. Nevertheless, the Bill refers simply to "written consent," and this does not leave the doctor the discretion to satisfy himself that the suspect has given full, free, and informed consent to the sample being taken. This should be a required precondition to taking intimate body samples for the purpose of providing evidence for a criminal prosecution. The most unsettling aspect of the powers affecting the doctor-patient relationship in this Bill is that no case has been made out for their justification. No evidence has been provided that the police have experienced any serious difficulty in securing the cooperation of doctors when circumstances justify it. So far as the disclosure of confidential information is concerned, an informal agreement reached between the Association of Chief Police Officers and the BMA was in the process of being adopted nationwide and had already provided the police with important information in some well known cases. The procedure worked speedily and effectively. The possibilities of abuse of the powers provided in this Bill are considerable, and, as a joint letter to The Times from the secretaries of the BMA and Law Society pointed out recently,3 the police themselves are not adequately protected against the consequences. J D J HAVARD 

waterson1983.pdf