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Microorganisms constitute more than 90% of the biomass in the sea. It is estimated that viruses kill approximately 20% of this biomass each day and that there are fifteen times as many viruses in the oceans as there are bacteria and archaea. Viruses are the main agents responsible for the rapid destruction of harmful [[algal bloom]]s, which often kill other marine life. <ref name="pmid16163346">{{cite journal |author=Suttle CA |title=Viruses in the sea |journal=Nature |volume=437 |issue=7057 |pages=356–61 |year=2005 |month=September |pmid=16163346 |doi=10.1038/nature04160}}</ref>
Microorganisms constitute more than 90% of the biomass in the sea. It is estimated that viruses kill approximately 20% of this biomass each day and that there are fifteen times as many viruses in the oceans as there are bacteria and archaea. Viruses are the main agents responsible for the rapid destruction of harmful [[algal bloom]]s, which often kill other marine life. <ref name="pmid16163346">{{cite journal |author=Suttle CA |title=Viruses in the sea |journal=Nature |volume=437 |issue=7057 |pages=356–61 |year=2005 |month=September |pmid=16163346 |doi=10.1038/nature04160}}</ref>


The [[Human Genome Project]] has revealed the presence of numerous viral DNA sequences scattered throughout human DNA.<ref name="pmid19795446">{{cite journal |author=Kurth R, Bannert N |title=Beneficial and detrimental effects of human endogenous retroviruses |journal=Int. J. Cancer |volume=126 |issue=2 |pages=306–14 |year=2010 |month=January |pmid=19795446 |doi=10.1002/ijc.24902}}</ref> They make up between 8–12% of human DNA,<ref>Shors p. 60</ref> and are the remains of ancient [[retrovirus]] infections of human ancestors. These pieces of DNA have firmly established themselves in human DNA. Most of this DNA is no longer functional and a few might occasionally cause harm. The remainder, however, seem beneficial having brought with them novel genes that are important to human development.<ref>Dimmock pp.426–430</ref>
The [[Human Genome Project]] has revealed the presence of numerous viral DNA sequences scattered throughout human DNA.<ref name="pmid19795446">{{cite journal |author=Kurth R, Bannert N |title=Beneficial and detrimental effects of human endogenous retroviruses |journal=Int. J. Cancer |volume=126 |issue=2 |pages=306–14 |year=2010 |month=January |pmid=19795446 |doi=10.1002/ijc.24902}}</ref> They make up between 8–12% of human DNA,<ref>Shors p. 60</ref> and are the remains of ancient [[retrovirus]] infections of human ancestors.<ref name="pmid18818874">{{cite journal |author=Blikstad V, Benachenhou F, Sperber GO, Blomberg J |title=Evolution of human endogenous retroviral sequences: a conceptual account |journal=Cellular and Molecular Life Sciences : CMLS |volume=65 |issue=21 |pages=3348–65 |year=2008 |month=November |pmid=18818874 |doi=10.1007/s00018-008-8495-2}}</ref> These pieces of DNA have firmly established themselves in human DNA.<ref name="pmid19795446">{{cite journal |author=Kurth R, Bannert N |title=Beneficial and detrimental effects of human endogenous retroviruses |journal=International Journal of Cancer. Journal International Du Cancer |volume=126 |issue=2 |pages=306–14 |year=2010 |month=January |pmid=19795446 |doi=10.1002/ijc.24902}}</ref> Most of this DNA is no longer functional and a few might occasionally cause harm. The remainder, however, seem beneficial having brought with them novel genes that are important to human development.<ref>Dimmock pp.426–430</ref>
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Revision as of 12:17, 5 December 2010

Electron micrograph of the rod-shaped particles of the tobacco mosaic virus that are too small to be seen using a light microscope

The history of viruses – or rather our understanding of them – began in the closing years of the nineteenth century. At this time many infectious diseases of plants and animals had been shown to be caused by bacteria and other microorganisms. Bacteria from many different types of infections could now be easily isolated and grown on synthetic media and observed by the light microscope. However, no cause could be found for some infections – such as smallpox – that had been recognised for over a thousand years.

The first evidence for the existence of infectious agents much smaller than bacteria came from experiments with filters. These Chamberland filters, which were designed for sterilising fluids, and had been used by Louis Pasteur, were made of porcelain with pores smaller than bacteria. In 1892, Dmitry Ivanovsky in Saint Petersburg, Russia, used one of these filters to show that sap from a diseased tobacco plant remained infectious to healthy tobacco plants despite having been filtered.

In 1898, ignorant of Ivanovsky's studies, Martinus Beijerinck in Delft in The Netherlands, made the same discovery. But he also showed that the infectious agent could diffuse through agar gel and concluded that the infectious agent was not a small bacterium, but a "contagious living liquid" (contagium vivum fluidum). He showed that the "fluid" could reproduce in otherwise healthy tobacco plants and called it a "virus". This discovery is considered to be the beginning of virology – the study of viruses and viral infections.

It is now known that viruses are the most abundant biological entity on Earth. They infect organisms from all of the three domains of life and have origins that date back millions of years to the time of the last universal common ancestor. Although scientists' initial interest in them arose because of the diseases they sometimes cause, most viruses are beneficial. They have driven evolution by transferring genes across species, play important roles in ecosystems, and are essential to life.

Origins

Viruses are ancient,Cite error: The <ref> tag has too many names (see the help page). they infect all forms of life and they are the most abundant biological entity on Earth.[1] Studies using molecular methods have revealed surprising relationships between viruses that infect organisms from the three domains of life and that some viral proteins pre-date the divergence of life and thus the last universal common ancestor. It is now thought that viruses existed before the emergence of modern cells.Cite error: The <ref> tag has too many names (see the help page).

There are three classical hypotheses on the origins of viruses: Viruses may have once been small cells that parasitised larger cells. This is called the degeneracy hypothesis,[2][3] or reduction hypothesis.[4] Some viruses may have evolved from bits of DNA or RNA that "escaped" from the genes of a larger organism. This is called the vagrancy hypothesis,[2][5] or the escape hypothesis.[4] The virus-first hypothesis proposes viruses could have evolved from complex molecules of protein and nucleic acid at the same time as cells first appeared on earth.[4]

Historically, none of these hypotheses were fully accepted: The regressive hypothesis did not explain why even the smallest of cellular parasites do not resemble viruses in any way. The escape hypothesis did not explain the complex capsids and other structures on virus particles. And, the virus-first hypothesis contravened the definition of viruses in that they require host cells and was quickly dismissed.[4] However, viruses are now recognised as ancient and to have origins that pre-date the divergence of life and virologists are beginning to reconsider and re-evaluate all three theories.[6][7]

Evolution

Viruses evolve and some rapidly. This follows changes in their DNA (or RNA) and the best adapted mutants quickly outnumber their less fit counterparts. In this sense their evolution is Darwinian just like their host organisms.[8] An enormous variety of genomic structures can be seen among viruses and they show more genomic diversity than plants, animals, archaea, or bacteria. Viruses are everywhere and it has been estimated that there are 1031 viruses on earth. Most of these are bacteriophages found in the oceans.[9] Although some species of viruses are ancient, many are relatively new and have only recently evolved from earlier species.[10] Modern viruses are not primitive but are highly adapted to thrive in their host species.[11] Viruses do not form fossils, they are infinitely smaller than the grains of sedimentary rocks that fossilize plants and animals. So the evolution of viruses has had to be traced by other methods. Of these DNA sequencing has been the most powerful and has provided unexpected insights. Most species of viruses are now known to have common ancestors and although the first virus hypothesis has yet to gain full acceptance, there is little doubt that the thousands of species of modern viruses have evolved from less numerous ancient species.[12]

The way viruses reproduce in their host cells makes them particularly susceptible to genetic changes that helps drive their evolution.[13] The RNA viruses are especially prone to mutations.[14] These viruses have genes made from RNA not DNA. In host cells there are mechanisms for correcting mistakes when DNA replicates and these kick in whenever cells divide.[14] These important mechanisms prevent potentially lethal mutations from being passed on to offspring. However, these mechanisms do not work for RNA and when an RNA virus replicates in its host cell numerous changes in their genes are introduced in error. Many of these are "silent" and do not result in any obvious changes to the progeny viruses. Others are lethal, but some confer advantages that increases the fitness of the viruses in the environment. These could be changes to the virus particles that disguise and are not identified by the cells of the immune system or changes that make antiviral drugs less effective. Both of these changes occur with alarming frequency with HIV.[15]

Many viruses can "shuffle" there genes with other viruses when two similar but unrelated strains infect the same cell. Influenza virus does this and gives rise to a phenomenon called genetic shift, which is often the cause of new and more virulent strains appearing. Other viruses change more slowly as mutations in their genes gradually accumulate over time, and this is called genetic drift.[16]

Through these mechanisms, new viruses are constantly emerging and present a continuing challenge to attempts to control the diseases they cause.[17][18]

Viruses in prehistory

The Neanderthals were a species of hominid that lived in Europe for about 200,000 years but became extinct about 28,000 years ago. The cause of their extinction has not been proven, but an hypothesis published in 2010 suggests that herpes virus infections, which had been brought to Europe from Africa by modern humans (Homo sapiens) might have been responsible.[19]

The Neolithic age, which began in the Middle East around 9500 BC, was a time when humans became farmers. This agricultural revolution embraced the development of monoculture and presented an opportunity for the rapid spread of plant viruses. The divergence and spread of sobemoviruses – southern bean mosaic virus – date from this time.[20]

Human virus infections also began to spread rapidly. Smallpox, which was one of the most lethal and devastating viral infections, emerged first among agricultural communities in Africa around 10,000 BC.[21] The virus, which only infected humans, probably descended from the poxviruses that infected rodents that lived in Africa thousands of years ago.[22] It is probable that early humans hunted these rodents and some people became infected by the viruses that they carried. When viruses cross this so called "species barrier" their effects can be severe[23] and humans may have had little natural resistance. At the time, humans lived in small communities and those who succumbed to infection either died or developed immunity. In humans, this acquired immunity is only passed down to offspring temporarily through breast milk and the antibodies that cross the placenta from the mother's blood to the unborn child's. So, sporadic outbreaks probably occurred in each generation. Around 9000 BC, when many people began to settle on the fertile flood plains of the River Nile, the population became dense enough for the virus to maintain a constant presence owing to the high concentration of susceptible people.[24]

Other, more ancient, viruses are less of a threat. Humans have lived with herpes virus infections since our species first came into being. The virus passed to us from other mammals over 80 million years ago.[25] Humans have developed a tolerance to these viruses, and most of us are infected with a least one species of them without being aware of it. Records of these milder virus infections are understandably rare. But, there is no reason to doubt that early hominids suffered from colds, 'flu and diarrhoea caused by viruses just as humans do today. It is the younger viruses that cause epidemics and pandemics – and it is these that history records.[26]

Viruses in antiquity

An Egyptian stele thought to depict a poliovirus victim, 18th Dynasty (1580–1350 BC)

Among the earliest records of a viral infection is an Egyptian stele thought to depict an Egyptian priest from the 18th Dynasty (1580–1350 BC) with a foot drop deformity characteristic of a poliovirus infection.[27] The mummy of Siptah – a ruler during the 19th Dynasty – also shows signs of poliomyelitis and that of Ramesses V, and other Egyptian mummies buried over 3000 years ago, show evidence of smallpox.[28] The Americas and Australia remained free of smallpox until the arrival of European colonists between the fifteenth and eighteenth centuries. The consequences were devastating and fatality rates reached 90% among the indigenous peoples.[29]

One of the earliest descriptions of a virus-infected plant can be found in a poem by written by the Japanese Empress Kōken (718 –770) in which she describes a plant in Summer with yellowing leaves. The plant, later identified as Eupatorium lindleyanum, is often infected with Tomato yellow leaf curl virus.[30]

The Middle Ages

The Middle Ages were times of plagues and pestilences. The rapidly growing population of Europe and the rising concentrations of people in its towns and cites became a fertile ground for many infectious and contagious diseases. The Black Death – a bacterial infection – is probably the most notorious of these.[31] Apart from smallpox and influenza, documented outbreaks of infections now known to be caused by viruses are rare. Rabies, a disease that had been recognised for over 4000 years,Cite error: The <ref> tag has too many names (see the help page). was rife in Europe,[32] and continued to be until the development of a vaccine by Louis Pasteur in 1886.[33] The average life-expectancy in the Middle Ages was 35 years and 60% of children died before the age of sixteen, many of them during the first six years of life. Among the plethora of diseases common at the time were influenza, measles and smallpox.[34]

Pioneers

An old, bespectacled man wearing a suit and sitting at a bench by a large window. The bench is covered with small bottles and test tubes. On the wall behind him is a large old-fashioned clock below which are four small enclosed shelves on which sit many neatly labelled bottles.
Martinus Beijerinck in his laboratory in 1921

Despite his other successes, Louis Pasteur (1822–1895) was unable to find a causative agent for rabies and speculated about a pathogen too small to be detected using a microscope.[35] In 1884, the French microbiologist Charles Chamberland (1851–1931) invented a filter – known today as the Chamberland filter – that had pores smaller than bacteria. Thus, he could pass a solution containing bacteria through the filter and completely remove them from the solution.[36]

In 1892, the Russian biologist Dmitry Ivanovsky (1864–1920) used this filter to study what is now known as the tobacco mosaic virus. His experiments showed that crushed leaf extracts from infected tobacco plants remain infectious after filtration. Ivanovsky suggested the infection might be caused by a toxin produced by bacteria, but did not pursue the idea.[37]

In 1898, the Dutch microbiologist Martinus Beijerinck (1851–1931) repeated the experiments and became convinced that the filtered solution contained a new form of infectious agent.[38] He observed that the agent multiplied only in cells that were dividing and he called it a contagium vivum fluidum (soluble living germ) and re-introduced the word virus.[37] Beijerinck maintained that viruses were liquid in nature, a theory later discredited by the American biochemist and virologist Wendell Meredith Stanley (1904–1971), who proved they were particles.[37] In the same year Friedrich Loeffler (1852–1915) and Paul Frosch (1860–1928) passed the first animal virus through a similar filter and discovered the cause of foot-and-mouth disease.[30]

By 1928 enough was known about viruses to enable Thomas Milton Rivers (1888–1962) to write the first book about all known viruses and his Filtrable Viruses was published in 1928. Rivers, who survived typhoid fever at the age of twelve, went on to have a distinguished career in virology. He was born in Jonebro, Georgia USA, was awarded a BA degree form Emory College in 1909 and graduated in medicine at John Hopkins University in 1915. In 1926, he was invited to speak at a meeting organised by the Society of American Bacteriology where he said for the first time, "Viruses appear to be obligate parasites in the sense that their reproduction is dependent on living cells."[39]

That viruses were particles was not considered unnatural and fitted in nicely with the germ theory. It is assumed that Dr. J. Buist of Edinburgh was the first person to see virus particles in 1886, when he reported seeing "micrococci" in vaccine lymph. But he had probably seen clumps of vaccinia virus.[40] In the years that followed, as optical microscopes were improved "inclusion bodies" were seen in many virus-infected cells, but these aggregates of virus particles were still too small to reveal any detailed structure. It was not until the invention of the electron microscope in 1931 by the German engineers Ernst Ruska (1906–1988) and Max Knoll (1887–1969),[41] that virus particles, especially bacteriophages, were shown to have a complex structure. The sizes of viruses determined using this new microscope fitted in well with those estimated by filtration experiments. Viruses were expected to be small, but the range of sizes came as a surprise. Some were only a little smaller than the smallest known bacteria, and the smaller viruses were of similar sizes to complex organic molecules.[42]

In 1935, Wendell Stanley examined the tobacco mosaic virus and found it was mostly made of protein.[43] In 1939, Stanley and Max Lauffer (1914) separated the virus into protein and RNA parts.[44] The discovery of RNA in the particles was important because in 1928, Fred Griffith (c.1879–1941) provided the first evidence that its "cousin", DNA, formed genes.[45]

In Pasteur's day, and for many years after his death the word "virus" was used to describe any cause of infectious disease. Painstaking work, by many bacteriologists, soon discovered the cause of numerous infections. However, some infections remained, many of them horrendous, but for which no bacterial cause could be found. These agents were invisible and could only be grown in living animals. The discovery of viruses was the key that unlocked the door that withheld the secrets of the cause of these mysterious infections. And, although Koch's postulates could not be fulfilled for many of these infections, this did not stop the pioneer virologists from looking for viruses in infections for which no other cause could be found.[46]

Bacteriophages

Bacteriophage

Discovery

Bacteriophages are the viruses that infect and reproduce in bacteria. They were discovered in the early 20th century, by the English bacteriologist Frederick Twort (1877–1950).[47] But before this time, in 1896, the bacteriologist Ernest Hanbury Hankin (1865–1939) reported that something in the waters of the River Ganges could kill Vibrio cholera – the cause of cholera. Whatever it was in the water could be passed through filters that remove bacteria but was destroyed by boiling.[48] Twort discovered the action of bacteriophages on staphylococci bacteria. He noticed that when grown on nutrient agar some colonies of the bacteria became watery or "glassy". He collected some of these watery colonies and passed them through a Chamberland filter to remove the bacteria and discovered that when the filtrate was added to fresh cultures of bacteria, they in turn became watery.[47] He proposed that the agent might be "an amoeba, an ultramicroscopic virus, a living protoplasm, or an enzyme with the power of growth".[48]

The antagonistic microbe can never be cultivated in media in the absence of the dysentery bacillus. It does not attack heat-killed dysentery bacilli, but is cultivated perfectly in a suspension of washed cells in physiological saline. This indicates that the anti dysentery microbe is an obligate bacteriophage.

Felix d'Herelle An invisible microbe that is antagonistic to the dysentery bacillus (1917)[49]

Félix d'Herelle (1873–1949) was a mainly self-taught French-Canadian microbiologist. In 1917 he discovered that "an invisible antagonist", when added to bacteria on agar, would produce areas of dead bacteria.[50] The antagonist, now known to be a bacteriophage could pass through a Chamberland filter. He accurately diluted a suspension of these viruses and discovered that the highest dilutions (lowest virus concentrations), rather than killing all the bacteria, formed discrete areas of dead organisms. Counting these areas and multiplying by the dilution factor allowed him to calculate the number of viruses in the original suspension.[51] He realised that he had discovered a new form of virus and later coined the term "bacteriophage".[52] Between 1918 and 1921 d'Herelle discovered different types of bacteriophages that could infect several other species of bacteria including Vibrio cholera.[53] Bacteriophages were heralded as a potential treatment for diseases such as typhoid and cholera, but their promise was forgotten with the development of penicillin.[54] Since the early 1970s, bacteria have continued to develop resistance to antibiotics such as penicillin, and this has led to a renewed interest in the use of bacteriophages to treat serious infections.[55]

Early research 1920–1940

File:Felix d'Herelle.png
Felix d'Herelle

D'Herelle travelled widely to promote the use of bacteriophages in the treatment of bacterial infections. In 1928, he became professor of biology at Yale and founded several research institutes.[56] He was convinced that bacteriophages were viruses despite opposition from established bacteriologists such as the Nobel Prize winner Jules Bordet (1870–1961). Bordet argued that bacteriophages were not viruses but just enzymes released from "lysogenic" bacteria. He said "the invisible world of d'Herelle does not exist".[57] But in the 1930s, the proof that bacteriophages were viruses was provided by Christopher Andrews (1896–1988) and others. They showed that these viruses differed in size and in their chemical and serological properties. In 1940, the first electron micrograph image of a bacteriophage was published and this silenced sceptics who had argued that bacteriophages were relatively simple enzymes and not viruses.[58] Numerous other types of bacteriophages were quickly discovered and were shown to infect bacteria wherever they are found. But this early research was interrupted by World War II. Even d'Herelle was silenced. Despite his Canadian citizenship, he was interned by the Vichy Government until the end of the war.[59]

Modern era

Knowledge of bacteriophages increased in the 1940s following the formation of the Phage Group by scientists throughout the US. Among the members were Max Delbrück (1906–1981) who founded a course on bacteriophages at Cold Spring Harbor Laboratory.[55] He showed that bacterial resistance to infection by bacteriophages was caused by random genetic mutations and not by adaptation.[60] Other key members of the Phage Group included Salvador Luria (1912–1991) and Alfred Hershey (1908–1997). During the 1950s, Hershey and Chase made important discoveries on the replication of DNA during their studies on a bacteriophage called T2. Together with Delbruck they were jointly awarded the 1969 Nobel Prize in Physiology or Medicine "for their discoveries concerning the replication mechanism and the genetic structure of viruses".[61] Since then, the study of bacteriophages has provided insights into the switching on and off of genes, and a useful mechanism for introducing foreign genes into bacteria and many other fundamental mechanisms of molecular biology.[62]

Plant viruses

Ambrosius Bosschaert (1573–1620) "Still Life

Many paintings can be found in the museums of Europe that depict tulips with attractive coloured stripes. Most of these, such as the still life studies of Johannes Bosschaert, were painted in the seventeenth century. These flowers were particularly popular and became sought after by those who could afford them. It was not known at the time that these attractive – and very expensive – stripes were caused by a virus that was accidentally transferred by humans to tulips from jasmine.[63]

In 1882, Adolf Mayer (1843–1942) described a condition of tobacco plants, which he called "mosaic disease" ("mozaïkziekte"). The diseased plants had variegated leaves that were mottled.[64] He excluded the possibility of a fungal infection and could not detect any bacterium and speculated that "soluble, enzyme-like infectious principle was involved".[65] He did not pursue his idea any further, and it was the filtration experiments of Ivanovsky and Beijerinck that suggested the cause was a previously unrecognised infectious agent. After tobacco mosaic was recognized as a virus disease, virus infections of many other plants were discovered.[65]

The importance of tobacco mosaic virus in the history of viruses cannot be overstated. It was the first virus to be discovered, and the first to be crystallised and its structure shown in detail. The first X-ray diffraction pictures of the crystallised virus were obtained by Bernal and Fankuchen in 1941. On the basis of her pictures, Rosalind Franklin discovered the full DNA structure of the virus in 1955.[66] In the same year, Heinz Fraenkel-Conrat and Robley Williams showed that purified tobacco mosaic virus RNA and its coat protein can assemble by themselves to form functional viruses, suggesting that this simple mechanism was probably the means through which viruses were created within their host cells.[67]

By 1935 many plant diseases were thought to be caused by viruses. In 1922, John Kunkel Small (1869–1938) discovered that insects could act as vectors and transmit virus to plants. In the following decade many diseases of plants were shown to be caused by viruses that were carried by insects and in 1939, Francis Holmes, a pioneer in plant virology,[68] described 129 viruses that caused disease of plants.[69] In 1970, the Russian plant virologist Joseph Atabekov discovered that many plant viruses only infect a single species of host plant.[68] Today, the International Committee on Taxonomy of Viruses recognises over 900 plant viruses.[70]

Vertebrate viruses

Discovery of vaccination

Edward Jenner

Humanity owes a great debt to Lady Mary Wortley Montagu (1689–1762). She was an aristocrat, a writer and the wife of a Member of Parliament. In 1716, her husband, Edward Wortley Montagu was appointed British Ambassador in Istanbul. She followed him there and two weeks after her arrival discovered the local practice of protection against smallpox by variolation, the injection of pus from smallpox victims into the skin.[24] Her younger brother had died of smallpox, and she too had had the disease but survived. Determined to spare her five-year-old son Edward from similar suffering, she ordered the embassy surgeon, Charles Maitland to variolate him. On her return to London, she asked Maitland to variolate her four-year-old daughter in the presence of the King's physicians.[24] Later, Montagu persuaded the Prince and Princess of Wales to sponsor a public demonstration of the procedure. Six men who had been condemned to death and were awaiting execution at Newgate Prison were offered a full pardon for serving as the subjects of the public experiment. They accepted, and in 1721 were variolated. All the prisoners recovered from the procedure and to test its protective effect one of them, a nineteen-year-old woman, was ordered to sleep in the same bed as a ten-year old smallpox victim for six weeks. She did not contract the disease.Cite error: The <ref> tag has too many names (see the help page). The experiment was repeated on six orphan children who survived the ordeal and by 1722, even King George I's grandchildren had been inoculated. But the practice was not entirely safe and caused many deaths. Although the number of lives saved far outweighed those lost, the practise was not widely adopted.[71]

Edward Jenner (1749–1823), a British rural physician, was variolated as a boy. He had suffered greatly from the ordeal but survived fully protected from smallpox. Jenner knew of a local belief that those who had suffered from a relatively mild infection called cowpox, which was common at the time in dairy workers, were immune to smallpox. Although probably not the first to do so, he decided to test the "theory". On May 14 1796 he selected "a healthy boy, about eight years old for the purpose of inoculation for the Cow Pox".Cite error: The <ref> tag has too many names (see the help page). The boy was James Phipps (1788–1853) who survived the experiment and suffered only a mild fever. On July 1 1796, Jenner took some "smallpox matter" (probably infected pus) and repeatedly inoculated Phipp's arms with it. Fortunately, Phipps survived, and was later inoculated with smallpox over twenty times without succumbing to the disease. Vaccination – the word is derived from the Latin vacca meaning "cow" – had been invented.[72]

Louis Pasteur and rabies

A cartoon from 1826 depicting a rabid dog on a London street

Rabies is an often fatal disease caused by the infection of mammals with rabies virus. Today it is mainly a disease that affects wild mammals such as foxes and bats, but it is one of the oldest known virus diseases: rabies is a Sanskrit word (rabhas) that dates from 3000 BC, [73] which means "madness" or "rage"[74] and the disease has been known for over 4000 years.[29] The ancient Greeks called it "lyssa" or "lytta" also meaning madness.[74] Although not a cause of epidemics, the infection was greatly feared because of its horrendous symptoms that include insanity, hydrophobia and death.[29] The disease had been known since antiquity and references to rabies can be found in the Laws of Eshnunna, which date from 2300 BC. Aristotle (384 BC–322 BC) wrote one of earliest undisputed descriptions of the disease and how it was passed to humans. Celsus in the first century AD first recorded the symptom called hydrophobia and suggested that the saliva of infected animals and humans contained a slime or poison – to describe this he used the word "virus".[29]

In France, in the time of Louis Pasteur, there were only a few hundred infections in humans each year but cures were desperately sought. Aware of the extreme danger, Pasteur worked on what he knew would be a challenge and he began to look for the "microbe" in the saliva of mad dogs.[71]

A member of Pasteur's team, Emile Roux (1853–1933), studied how long the spinal cords of dogs that had died from the disease remained infectious. Roux invented an ingenious glass bottle in which he hung the spinal cords to dry them. Pasteur was impressed with Roux's invention and ordered more bottles to be made. Pasteur never credited Roux for his invention and Roux considered his idea stolen. Roux never worked on rabies again. After fourteen days of drying, Pasteur showed that when the dried spinal cords were crushed and injected into healthy dogs they did not become infected. He repeated the experiment several times on the same dog with tissue that had been dried for fewer and fewer days, until the dog survived after injections of fresh rabies infected spinal tissue. Pasteur had immunised the dog against rabies as he later did with 50 more.[71]

Although he had little idea how his method worked, he went on to test it on a boy. Joseph Meister (1876–1940) was bought to Pasteur by his mother on July 6, 1885. He was covered in bites, having been set upon by a mad dog. A brick layer had defended the boy from the dog with an iron bar, but only after the salivating dog had bitten the boy fourteen times. Meister's mother begged Pasteur to help her son. Pasteur was a scientist, not a physician, and he was well aware of the consequences to him if things were to go wrong. Pasteur decided to help the boy and injected him with increasingly virulent rabid rabbit spinal cord over the following ten days.[71]

The date set for the final inoculation using undried tissue was July 16. Pasteur's assistant Grancher was given the task, but accidentally jabbed himself with the infected needle, and thus became the second guinea pig to receive Pasteur's new treatment. Later in an argument about the ethics of what they had done, Pasteur's whole team, including Pasteur, clandestinely inoculated one another. Although still angry with Pasteur, Roux discovered what was going on and, as he was the only qualified physician on the team, took charge of the dangerous situation. It was too late for the men to stop. Fortunately, they all lived to tell the tale and Meister returned home with his mother on July 27. But the full truth was kept a secret for many years.[71] Pasteur's method of treatment remained in use for over fifty years.[75]

Not much was known about the cause of the disease until in 1903, Adelchi Negri (1876–1912) first saw microscopic lesions in the brains of rabid animals now called Negri bodies.[76] He wrongly thought they were protozoan parasites. However Paul Remlinger (1871–1964) soon showed by filtration experiments that they were much smaller than protozoa and even smaller than bacteria. Thirty years later, Negri bodies were shown to be accumulations of particles 100–150 nanometres long, now known to be the size of rhabdovirus particles – the virus that causes rabies.[29]

20th century

A woman working during the 1918–1919 influenza epidemic – the face mask probably afforded minimal protection.

The discovery of viruses, and the control and treatment of the diseases they cause, is one of the great achievements of science in the 20th century.[77] By the end of the 19th century, viruses were defined in terms of their infectivity, their ability to be filtered, and their requirement for living hosts. Viruses had been grown only in plants and animals. In 1906, Ross Granville Harrison (1870–1959) invented a method for growing tissue in lymph,[78] and, in 1913, E. Steinhardt, C. Israeli, and R. A. Lambert used this method to grow vaccinia virus in fragments of guinea pig corneal tissue.[79] In 1928, H. B. Maitland and M. C. Maitland grew vaccinia virus in suspensions of minced hens' kidneys.[80] Their method was not widely adopted until the 1950s, when poliovirus was grown on a large scale for vaccine production.[81]

1918 Influenza pandemic

A short time after his victory at the Battle of Bosworth on 22 August 1485, Henry Tudor's army suddenly went down with "the English sweat", and observers of the events described it as something new. [82] References to influenza infections date from the late 15th and early 16th centuries,[82] but influenza infections almost certainly occurred long before this time.[83] Records from the time when medicine was not a science can be unreliable. The language used to describe diseases in these sources is often vague and colloquial. We read of "plagues of mice", "changes in the direction of the wind" and the "influence of comets". This makes retrospective diagnosis difficult. As medicine became a science, the descriptions of disease became less vague and the sources became more reliable. Although the influenza virus that caused the 1918–1919 influenza pandemic was not discovered until the 1930s, the descriptions of the disease and subsequent research has proved it was to blame.[84]

The pandemic killed 40–50 million people in less than a year,[85] but the proof that it was caused by a virus was not obtained until 1933.[86] Influenza viruses are relatively large and are difficult to pass through a Chamberland filter and this led many scientists, including the eminent German bacteriologist Richard Pfeiffer (1858–1945), to conclude that the cause was a bacterium.[87] A major breakthrough came in 1931, when the American pathologist Ernest William Goodpasture grew influenza and several other viruses in fertilised chickens' eggs.[88]

Poliomyelitis

In 1949, John F. Enders (1897–1985) Thomas Weller (1915–2008), and Frederick Robbins (1916–2003) grew polio virus for the first time in cultured human embryo cells, the first virus to be grown without using solid animal tissue or eggs. Infections by poliovirus most often cause the mildest of symptoms. This was not known until the virus was isolated in cultured cells and many people were shown to have had mild infections that did not lead to poliomyelitis. But, unlike other viral infections, the incidence of polio – the rarer severe form of the infection – increased in the 20th century and reached a peak around 1952. The invention of a cell culture system for growing the virus enabled Jonas Salk (1914–1995) to make an effective polio vaccine.[89]

Epstein-Barr virus

Denis Parsons Burkitt (1911–1993) was born in Enniskillen, County Fermanagh, Ireland. He was the first to describe a type of cancer that now bears his name Burkitt's lymphoma. This type of cancer was endemic in equatorial Africa and was the commonest malignancy of children in the early 1960s.[90] In an attempt to find a cause for the cancer, Burkitt sent cells from the tumour to Anthony Epstein (b. 1921) a British virologist, who along with Yvonne Barr and Bert Achong (1928–1996), and after may failures, discovered viruses that resembled herpes virus in the fluid that surrounded the cells. The virus was later shown to be a previously unrecognised herpes virus, which is now called Epstein-Barr virus.[91] Surprisingly, Epstein-Barr virus is a very common but relatively mild infection of Europeans. Why it can cause such a devastating illness in Africans is not fully understood, but reduced immunity to virus caused by malaria might be to blame.[92] Epstein-Barr virus is important in the history of viruses for being the first virus shown to cause cancer.[93]

Smallpox eradication

In 1979, the World Health Organisation declared smallpox eradicated, but it had still managed to kill 300 million people since 1900.[94] The erdication followed years of coordinated disease surveillance and vaccination campaigns throughout the world.[95] The main weapon used was vaccinia virus, which was used as the vaccine. No one seems too sure where vaccinia virus came from,[96] it is not the strain of cowpox that Edward Jenner had used and it is not a weakened form of smallpox,[97] but it was a highly successful vaccine.[98]

The eradication campaign was not without casualties. Most notable was the death of Janet Parker (c.1938–1978) and subsequent suicide of virologist Henry Bedson (1930–1978).[99] Before the September 11 attacks on America in 2001, it was planned to destroy all the remaining stocks of smallpox virus that were kept in laboratories in US and Russia. Had this plan gone ahead, smallpox virus would have been to first one to be made extinct by human intervention.[100]

Late 20th century

A rotavirus particle

The second half of the 20th century was the golden age of virus discovery and most of the 2,000 recognised species of animal, plant, and bacterial viruses were discovered during these years.[60][101] In 1957, equine arterivirus and the cause of Bovine virus diarrhea (a pestivirus) were discovered.[102] In 1963, the hepatitis B virus was discovered by Baruch Blumberg (b. 1925),[103] and in 1965, Howard Temin (1934–1994) described the first retrovirus.[104] Reverse transcriptase, the key enzyme that retroviruses use to translate their RNA into DNA, was first described in 1970, independently by Howard Martin Temin and David Baltimore (b. 1938).[105] In 1983 Luc Montagnier (b. 1932) and his team at the Pasteur Institute in France, first isolated the retrovirus now called HIV.[106]

Friendly viruses

Sir Peter Medewar (1915–1987) defined a virus as "a piece of bad news wrapped in a protein coat".[107] He might have had is tongue firmly in his cheek, but this summed-up the view of most virologists in the mid-20th century. With the exception of the bacteriophages, viruses had a well-deserved reputation for being nothing but the cause diseases and death. But, the discovery of the abundance of viruses and their overwhelming presence in many ecosystems has led modern virologists to consider them in a new light.[108]

Microorganisms constitute more than 90% of the biomass in the sea. It is estimated that viruses kill approximately 20% of this biomass each day and that there are fifteen times as many viruses in the oceans as there are bacteria and archaea. Viruses are the main agents responsible for the rapid destruction of harmful algal blooms, which often kill other marine life. [109]

The Human Genome Project has revealed the presence of numerous viral DNA sequences scattered throughout human DNA.[110] They make up between 8–12% of human DNA,[111] and are the remains of ancient retrovirus infections of human ancestors.[112] These pieces of DNA have firmly established themselves in human DNA.[110] Most of this DNA is no longer functional and a few might occasionally cause harm. The remainder, however, seem beneficial having brought with them novel genes that are important to human development.[113]

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  113. ^ Dimmock pp.426–430

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