WikiJournal of Medicine/History of penicillin
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Kholhring Lalchhandama (22 October 2021). "History of penicillin". WikiJournal of Medicine 8 (1): 3. doi:10.15347/WJM/2021.003. Wikidata Q107303937. ISSN 2002-4436. https://upload.wikimedia.org/wikiversity/en/1/1c/History_of_Penicillin.pdf.
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Penicillin (Figure 1) is the second antibiotic and the first naturally-occurring antibiotic discovered. The first antibiotic discovered was arsphenamine, marketed as Salvarsan, by German physician Paul Ehrlich and his Japanese assistant Sahachiro Hata in 1909. It was a modified compound of a highly toxic chemical arsenic that was used for the treatment of sexually transmitted bacterial (Treponema pallidum) infection or syphilis, and became the most commonly prescribed drug in the early 20th century. However, it was overshadowed by penicillin, a safer and more efficacious antibiotic, that was effective against a wide range of Gram-positive bacteria, as well as Gram-negative T. pallidum.
Traditional curative practices preceded the discovery of penicillin as a component of the mould Penicillium (from the Latin word penicillum, meaning "painter's brush"). Ancient Egypt, Greece and India were aware of the curative properties of fungi and plants in treating bacterial infections, as shown by the 16th-century BCE record of a Greek king of the use of bread moulds by a woman healer to treat wounded soldiers. Around the same time, Chinese traditional practitioners used moulds from soya bean for wound infections.
In 17th-century Poland, wet bread was mixed with spider webs (which often contained fungal spores) to treat wounds, a technique mentioned by Henryk Sienkiewicz in his 1884 book With Fire and Sword. In 1640, the idea of using mould as a form of medical treatment was recorded by English apothecaries such as John Parkinson, royal botanist to Charles I, who described the use of certain mould (possibly Penicillium) in his book on pharmacology Theatrum Botanicum (The Botanical Theatre). One of the common practices for treating impetigo (an infection due to the bacterium Staphylococcus aureus) was mould therapy using moulds obtained from bread and porridge. A Canadian biologist A. E. Cliffe provided a vivid description:
It was during a visit through central Europe in 1908 that I came across the fact that almost every farmhouse followed the practice of keeping a mouldy loaf on one of the beams in the kitchen. When I asked the reason for this I was told that this was an old custom and that when any member of the family received an injury such as a cut or bruise, a thin slice from the outside of the loaf was cut off, mixed into a paste with water and applied to the wound with a bandage. It was assumed that no infection would result from such a cut.
One of the most detailed medical narratives was how Brenda Ward (née Whitnear) was cured of her facial impetigo in 1929. After treating an eight-year-old Brenda with all possible medications available, the family physician James Twomey resorted to traditional practice and advised the mother to prepare a starch paste. The paste was was left in the pantry kept at the cellar head for several days until it became very mouldy. It was then applied on the girl's face as an ointment for over a week until she was completely healed. There is no written record of the treatment except for the receipt of the consultation fee. Ward recalled that the mould initially appeared yellow in colour, grew into bronze colour, and finally turned into blue-green colonies, which indicates it was either Penicillium or Aspergillus. Based on Ward's description, in 1989, British microbiologist Milton Wainright concluded that most likely the mould was Penicillum due the growth pattern and antibacterial activity.
Traditional treatments often worked because numerous organisms, including many species of moulds, naturally produce antibiotic substances. However, it was not until recently that practitioners were able to identify or isolate the active components in these organisms.
Early scientific evidence
The modern history of penicillin research began in earnest in the 1870s in the United Kingdom. Sir John Scott Burdon-Sanderson, physiologist and lecturer at St. Mary's Hospital, observed that culture fluid covered with mould inhibited bacterial growth in his experiments on spontaneous generation in 1870. His reports in 1871 described:
On October 10 glass a was turbid, and was found on microscopical examination to be teeming with bacteria; a thick whitish scum had formed on its surface. Glass h was perfectly clear; there were, however, great numbers of torula [a type of yeast] cells on its surface, but no bacteria. On October 12 6 exhibited numerous tufts of penicillium, but the liquid still remained limpid and free from bacteria.[a]
From his experiments, Burdon-Sanderson believed that decomposition or putrefaction was caused by bacteria, and not by moulds. He applied the Penicillium mould on dissected thigh muscles from a guinea pig and left them in bell jars. After two weeks tissues in sterilised jars and with Penicillium mould did not show signs of rotting. These experiments indicate that the mould had antibacterial activity, but Burdon-Sanderson failed to notice the importance of this finding.
Burdon-Sanderson's discovery prompted Joseph Lister, an English surgeon and the father of modern antisepsis, to discover in 1871 that urine samples contaminated with mould also prevented the growth of bacteria. Lister identified the mould as Penicillium glaucum and found that most bacteria could not grow alongside this mould. He also described the antibacterial action of the mould on human tissue. In 1877, he treated Ellen Jones, a nurse at King's College Hospital, whose wounds did not respond to any traditional antiseptic. The nurse was cured when a crude extract of P. glaucum culture was applied to her wounds. Uncertain of the nature and effect of the mould, Lister did not published his observations.
In 1873, Welsh physician William Roberts, who later coined the term "enzyme", also conducted experiments on spontaneous generation and observed that glass tubes were easily contaminated by airborne bacteria and moulds. In his 1874 report in the Philosophical Transactions of the Royal Society, he stated: "I have repeatedly observed that liquids in which the Penicillum glaucum was growing luxuriantly could with difficulty be artificially infected with Bacteria; it seemed, in fact, as if this fungus played the part of the plants in an aquarium, and held in check the growth of Bacteria, with their attendant putrefactive changes." This is regarded as "the first unequivocal published statement" on antibacterial activity of any substance.
John Tyndall, professor of physics at the Royal Institution of Great Britain, followed up on Roberts's work on refutation of spontaneous generation and demonstrated in 1875 the antibacterial action of the P. glaucum. His report, read before the Royal Society in 1876 (and published as a monograph in 1881), stated:
[The] two most actively charged tubes were in part crowned by beautiful tufts of Penicilllum Glaucum. This expanded gradually until it covered the entire surface with a thick tough layer, which must have seriously intercepted the oxygen necessary to the Bacterial life. The bacteria lost their translatory power, fell to the bottom, and left the liquid between them and the superficial layer clear.
In 1876, German biologist Robert Koch discovered that Bacillus anthracis was the causative pathogen of anthrax; it was the first time a specific bacterium was proved to cause a specific disease, and the first direct evidence of the germ theory of diseases. A year later, French biologists Louis Pasteur and Jules Francois Joubert observed that, when contaminated with moulds, cultures of the anthrax bacilli could be successfully inhibited. They reported their findings in the Comptes Rendus de l'Académie des Sciences:
Neutral or slightly alkaline urine is an excellent medium for the bacteria... But if when the urine is inoculated with these bacteria an aerobic organism, for example one of the "common bacteria," is sown at the same time, the anthrax bacterium makes little or no growth and sooner or later dies out altogether. It is a remarkable thing that the same phenomenon is seen in the body even of those animals most susceptible to anthrax, leading to the astonishing result that anthrax bacteria can be introduced in profusion into an animal, which yet does not develop the disease; it is only necessary to add some "common 'bacteria" at the same time to the liquid containing the suspension of anthrax bacteria. These facts perhaps justify the highest hopes for therapeutics.
The phenomenon was described by Pasteur and Koch as antibacterial activity and was named as "antibiosis" by French biologist Jean Paul Vuillemin in 1877 (the term antibiosis, meaning "against life", was adopted as "antibiotic" by American biologist and later Nobel laureate Selman Waksman in 1947). It has also been asserted that Pasteur identified the mould as Penicillium notatum. However, Paul de Kruif's 1926 Microbe Hunters disagrees, describing this incident as contamination by other bacteria rather than by mould. Ten years later, in 1887, Swiss physician Carl Alois Philipp Garré developed a test method using glass plate to see bacterial inhibition and found similar results. Using a gelatin-based culture plate, he grew two different bacteria and found that their growths were inhibited differently; and reported:
I inoculated on the untouched cooled [gelatin] plate alternate parallel strokes of B. fluorescens [Pseudomonas fluorescens] and Staph. pyogenes [Streptococcus pyogenes ]... B. fluorescens grew more quickly... [This] is not a question of overgrowth or crowding out of one by another quicker-growing species, as in a garden where luxuriantly growing weeds kill the delicate plants. Nor is it due to the utilization of the available foodstuff by the more quickly growing organisms, rather there is an antagonism caused by the secretion of specific, easily diffusible substances which are inhibitory to the growth of some species but completely ineffective against others.
At the University of Naples, in 1895, physician Vincenzo Tiberio published his research about moulds initially found in a water well in Arzano. He noticed that whenever the moulds on the wall of the well was cleaned, many people had abdominal pain due to infection (enteritis), which was unheard of when the well was mouldy. He believed that there was a link between the infection and the mould. After identifying different moulds from the well, he found that Penicilium and Aspergillus could kill certain bacteria including Vibrio cholerae, and some staphylococci strains. From his observations, he concluded that these moulds contained soluble substances having antibacterial action. However, his findings did not receive any attention until the discovery of penicillin.
French medical student Ernest Duchesne at École du Service de Santé Militaire (Military Service Health School) in Lyon independently discovered the healing properties of P. glaucum. He was able to grow the mould on pieces of moist food. When he mixed the mould with the bacterium Escherichia coli, he found that the bacteria did not grow, and when he injected the mould juice into guinea pigs experimentally inoculated with typhoid bacteria (Salmonella enterica), the animals never developed the disease. He described the experiment in his 1897 doctoral dissertation titled Contribution à l'étude de la concurrence vitale chez les microorganismes (Contribution to the study of vital competition between microorganisms: antagonism between moulds and microbes) submitted to the Pasteur Institute. Unfortunately, his discovery was ignored by the institute and soon forgotten. It was not until 50 years later when a librarian found the thesis, once penicillin had already been discovered.
Duchesne could not continue his experiments due to a severe illness (believed to be tuberculosis) he contracted five years later. He died in 1912 while serving in the French Army. He was himself using moulds to treat horses, a method learned from Arab stable boys to cure animals' sores; but he did not claim that the mould contained any antibacterial substance, only that it somehow protected the animals. His conclusion was nonetheless prognostic, stating that competition between bacteria and moulds could be useful in the medical management of infections. Penicillin does not cure typhoid as it is ineffective against most Gram-negative bacteria and so it remains unknown which substance might have been responsible for Duchesne's cure.[b] A similar antibiotic effect of Penicillium was recorded in 1923 by Costa Rican Clodomiro Picado Twight, a Pasteur Institute scientist. In these early stages of penicillin research, most species of Penicillium were non-specifically referred to as P. glaucum, so that it is impossible to know the exact species and that it was really penicillin that prevented bacterial growth.
The first to discover and isolate an antibiotic compound from Penicillium was an Italian physician Bartolomeo Gosio. Gosio was investigating pellagra, which at the time was a common disease in southern Europe and America. It was known that the staple food of people having the disease was corn, and fungal contamination of corn was regarded as the source (American biochemist Conrad Elvehjem would identify in 1937 its aetiology as the deficiency of niacin or vitamin B3.) In 1893, Gosio identified the mould Penicillium brevicompactum as one possible cause, developed a simple culture method to make pure culture extract in crystalline form. In 1896, he tested the substance on anthrax bacillus and found that it was highly potent against the bacteria. Nonetheless, his discovery was largely forgotten as the substance was found not to be the cause of pellagra, and its medicinal potential was not obvious. American scientists, Carl Alsberg and Otis Fisher Black resynthesized Gosio's substance in 1912 giving it the name mycophenolic acid, which is now used as an immunosuppressant.
In 1924, Andre Gratia and Sara Dath at the Free University of Brussels, Belgium, found that dead Staphylococcus aureus cultures were contaminated by a mould, a streptomycete. On further experimentation, they showed that the mould extract could kill not only S. aureus, but also Pseudomonas aeruginosa, Mycobacterium tuberculosis and Escherichia coli. Gratia called the antibacterial agent "mycolysate" (killer mould). The next year they found another killer mould that could inhibit anthrax bacterium (B. anthracis). Reporting in Comptes Rendus Des Séances de La Société de Biologie et de Ses Filiales, they identified the mould as Penicillium glaucum. In 1927, Gratia reported its medical use:
A poor patient who during three years had suffered from furuncles [infection by S. aureus], in spite of all treatments, was sent to us in despair. Jaumain did not hesitate to continue the treatment by a series of injections of the mycolysat. The result was remarkable. Not only was the recovery rapid, but it is now three years that [sic] this recovery continues without the slightest relapse. Since that time we have given the mycolysat to a very large number of cases. It is the most effective treatment even of the most resistant types of staphylococcic diseases.
Unfortunately, as in the case of Duchesne, these findings received little attention as the antibacterial agent and its medical values were not fully understood; moreover, Gratia's samples were lost.
The breakthrough discovery
Penicillin as we know it today was "accidentally" discovered by the Scottish physician Alexander Fleming in 1928. While working at St Mary's Hospital, London, Fleming was investigating the pattern of variation in S. aureus (Figures 2 and 3). He was inspired by the recent discovery by the Irish physician Joseph Warwick Bigger and his two students C.R. Boland and R.A.Q. O’Meara at the Trinity College, Dublin, Ireland, in 1927. Bigger and his students found that a particular strain of S. aureus (designated "Y") that they isolated a year before from the pus of an axillary abscess (boil on the armpit) from one individual grew into a variety of strains. They published their discovery as "Variant colonies of Staphylococcus aureus" in The Journal of Pathology and Bacteriology, by concluding:
We were surprised and rather disturbed to find, on a number of plates, various types of colonies which differed completely from the typical aureus colony. Some of these were quite white; some, either white or of the usual colour were rough on the surface and with crenated margins.
Fleming and his research scholar Daniel Merlin Pryce pursued this experiment but Pryce was transferred to another laboratory in early 1928. Their experiment had been successful and Fleming was planning and agreed to write a report in the compendium A System of Bacteriology to be published by the Medical Research Council at the end of that year.
In August, Fleming spent a vacation with his family at his country home The Dhoon at Barton Mills, Suffolk. Before leaving his laboratory (Figures 3 & 4), he inoculated several culture plates with S. aureus. He kept the plates aside on one corner of the table away from direct sunlight to allow proper growth of the bacteria. There are two versions of the reason he returned to his laboratory during the vacation. According to some sources, he was appointed Professor of Bacteriology at the St Mary's Hospital Medical School and had to officially join on Saturday 1 September 1928. The next Monday he visited the laboratory. Alternative sources say that he went to London "on a flying visit" to help a colleague with the treatment of haemolytic bacillus. It was while waiting for the colleague that he visited the laboratory. At the laboratory, Pryce paid him a visit and found him sorting out the Petri dishes. He and Pryce noticed one culture plate with an open lid and the culture contaminated with a blue-green mould. In the contaminated plate the bacteria around the mould did not grow, while those farther away grew normally, meaning that the mould killed the bacteria. Fleming commented as he watched the plate: "That's funny." Pryce remarked to Fleming: "That's how you discovered lysozyme."
Fleming went off to resume his vacation and returned to his laboratory late in September. He collected the original mould and grew it in culture plates. After four days he found that the plates developed large colonies of the mould. He repeated the experiment with the same bacteria-killing results. He later recounted his experience:
When I woke up just after dawn on September 28, 1928, I certainly didn't plan to revolutionize all medicine by discovering the world's first antibiotic, or bacteria killer. But I suppose that was exactly what I did.
He concluded that the mould was releasing a substance that was inhibiting bacterial growth, and he produced a culture broth of the mould and subsequently concentrated the antibacterial component. After testing against different bacteria, he found that the mould could kill only specific bacteria. For example, Gram-positive bacteria such as Staphylococcus, Streptococcus, and diphtheria bacillus (Corynebacterium diphtheriae) were easily killed; but there was no effect on Gram-negative species like typhoid bacterium (Salmonella typhimurium) and influenza bacillus (Haemophilus influenzae). He prepared a large-culture method from which he could obtain large amounts of the mould juice. On 7 March 1929, he coined the name "penicillin" for the mould extract, explaining the reason as "to avoid the repetition of the rather cumbersome phrase 'Mould broth filtrate', the name 'penicillin' will be used." In his Nobel lecture, he gave a further explanation:
I have been frequently asked why I invented the name "Penicillin". I simply followed perfectly orthodox lines and coined a word which explained that the substance penicillin was derived from a plant of the genus Penicillium just as many years ago the word "Digitalin" was invented for a substance derived from the plant Digitalis.
Fleming had no training in chemistry so that he left all the chemical works to his new research scholar Stuart Craddock, who joined him in December; he once remarked: "I am a bacteriologist, not a chemist." In January 1929, Fleming recruited his former research scholar Frederick Ridley, who had studied biochemistry, to study the chemical properties of the mould. However, both Craddock and Ridley left Fleming for other jobs before completing the experiments and isolating penicillin. Their failure to isolate the compound resulted in Fleming practically abandoning further research on the chemical aspects of penicillin. Nonetheless, he continued doing biological tests up to 1939.
Identification of the mould
The source of the fungal contamination in Fleming's experiment remained a matter of speculation for several decades. The Royal Society of Chemistry believed that it came from a cup of coffee which Fleming left on the table. In 1945, Fleming himself suggested that the fungal spores came through the window facing Praed Street. This story was regarded as a reliable explanation and was popularised in the literature, starting with George Lacken's 1945 book The Story of Penicillin. But it was later disputed by his co-workers, particularly Pryce, who testified much later that Fleming's laboratory window was kept shut all the time. Ronald Hare also agreed in 1970 that the window remain locked as a large table in front of it made it difficult to open. In 1966, Charles John Patrick La Touche told Hare that he had given Fleming 13 specimens of fungi (10 from his lab) and only one from his lab was showing penicillin-like antibacterial activity. It was therefore concluded that Fleming's mould came from La Touche's lab, located a floor below, and the spores had drifted in the air through the open doors.
After a structural comparison with different species of Penicillium, Fleming believed that his specimen was Penicillium chrysogenum, a species described by the American microbiologist Charles Thom in 1910. He was fortunate as Charles John Patrick La Touche, an Irish botanist, had just recently joined as a mycologist at St Mary's to investigate fungi as the cause of asthma. La Touche identified the specimen as Penicillium rubrum, the identification used by Fleming in his publication of the discovery.
In 1931, Thom re-examined different species of Penicillium including that of Fleming's specimen. He came to a confusing conclusion, stating: "Ad. 35 [Fleming's specimen] is P. notatum WESTLING. This is a member of the P. chrysogenum series with smaller conidia than P. chrysogenum itself." From then on, Fleming's mould was synonymously referred to as P. chrysogenum and P. notatum, a species discovered by Swedish chemist Richard Westling in 1811. But Thom adopted and popularised the use of P. chrysogenum. Adding to the controversial taxonomy, newly discovered species such as P. meleagrinum and P. cyaneofulvum were recognised as members of P. chrysogenum in 1977. To resolve the confusion, in 2005, the Seventeenth International Botanical Congress held in Vienna, Austria, formally adopted the name P. chrysogenum as the conserved name (nomen conservandum) for all related Penicilium species. In 2011, whole genome sequence and phylogenetic analysis revealed that Fleming's mould belongs to P. rubens (Figure 5), a species described by Belgian microbiologist Philibert Biourge in 1923, and that P. chrysogenum is a different species.
Reception and publication
Initially, Fleming's discovery was not considered important, and as he showed to his his colleagues, all he received was an indifferent response. He described the discovery on 13 February 1929 before the Medical Research Club but his presentation titled "A medium for the isolation of Pfeiffer's bacillus" did not receive any particular attention.
In May 1929, Fleming reported his findings to the British Journal of Experimental Pathology whch published them in the next month's issue. It failed to attract any serious attention. Fleming himself was quite unsure of the medical application and was more concerned about the application for bacterial isolation, as he concluded:
In addition to its possible use in the treatment of bacterial infections penicillin is certainly useful to the bacteriologist for its power of inhibiting unwanted microbes in bacterial cultures so that penicillin insensitive bacteria can readily be isolated. A notable instance of this is the very easy, isolation of Pfeiffers bacillus of influenza when penicillin is used...It is suggested that it may be an efficient antiseptic for application to, or injection into, areas infected with penicillin-sensitive microbes.
G. E. Breen, a fellow member of the Chelsea Arts Club, once asked Fleming: "I just wanted you to tell me whether you think it will ever be possible to make practical use of the stuff [penicillin]. For instance, could I use it?" Fleming gazed vacantly for a moment and then replied: "I don't know. It's too unstable. It will have to be purified, and I can't do that by myself." Even as late as in 1941, the British Medical Journal reported that "the main facts emerging from a very comprehensive study [of penicillin] in which a large team of workers is engaged... does not appear to have been considered as possibly useful from any other point of view."[c]
In 1933, Ernst Boris Chain, a chemist of Jewish-German origin, joined Australian scientist Howard Florey (later Baron Florey) at the Sir William Dunn School of Pathology at the University of Oxford in 1936 to investigate antibiotics. Florey assigned him to work on lysozyme, an antibacterial enzyme discovered by Fleming in 1922. In 1938, he came across Fleming's 1929 paper while writing a research report and informed his supervisor of the potential medical benefits of penicillin. Although a year before, Florey had concentrated on pyocyanase (a pigment from the bacterium Bacillus pycyaneus, now called Pseudomonas aeruginosa), he agreed with Chain that penicillin was medically more promising. In 1939, Florey and Chain obtained a research grant of $25,000 from the Rockefeller Foundation to study antibiotics, which allowed them to assemble a research team composed of Edward Abraham, Arthur Duncan Gardner, Norman Heatley, Margaret Jennings, J. Orr-Ewing and G. Sanders.
The Oxford team soon prepared a concentrated extract of P. rubens as "a brown powder" that "has been obtained which is freely soluble in water". They found that the powder was not only effective in vitro against bacterial cultures but also and in vivo against bacterial infection in mice. On 5 May 1939, they injected a group of eight mice with a virulent strain of S. aureus, and then injected four of them with the penicillin solution. After one day, all the untreated mice died while the penicillin-treated mice survived; "a miracle" in Chain's view. The team published its findings in The Lancet in 1940.
The team reported details of the isolation method in 1941 with a scheme for large-scale extraction. They also found that penicillin was most abundant as a yellow concentrate from the mould extract, but it was able to produce only small quantities. By the early 1942, they could prepare highly purified compound, and derived the empirical chemical formula as C24H32O10N2Ba. In the June 1942 issue of the British Journal of Experimental Pathology, Chain, Abraham and E. R. Holiday reported the production of the pure compound concluding that:
The penicillin preparation described in this paper is the most powerful antibacterial agent with predominantly bacteriostatic action so far known. Though it has not yet been obtained crystalline there are indications that it possesses a considerable degree of purity... The unusual biological properties of penicillin are linked with an exceptionally unstable chemical configuration. Inactivation by acid, alkali, and by boiling at any pH has been shown to be accompanied by definite chemical changes.
First medical use
In January 1929, Fleming performed the first clinical trial with penicillin on his assistant Craddock. Craddock had developed a severe infection of the nasal antrum (sinusitis) for which he had undergone surgery. Fleming made use of the surgical opening of the nasal passage and started injecting penicillin on 9 January. Craddock showed no sign of improvement, probably because the infection was caused by influenza bacillus (Haemophilus influenzae), the bacterium which he had found not susceptible to penicillin. It seems that Fleming gave some of his original penicillin samples to his colleague-surgeon Arthur Dickson Wright for clinical test in 1928. Although Wright reportedly said that it: "seemed to work satisfactorily," there are no records of its specific use.
In November 1930, Cecil George Paine, a pathologist at the Royal Infirmary in Sheffield, was the first to use penicillin for medical treatment successfully. He was a former student of Fleming who, after learning about penicillin, requested a sample from Fleming. He initially attempted to treat sycosis (eruptions in beard follicles). On 25 November, he then tried it successfully with four patients (one adult, the others infants) who had ophthalmia neonatorum, an inflammation of the eye due to infection. Thus, penicillin first worked on an eye infection.
Nine years later, the Oxford team showed that Penicillium extract killed different bacteria (Streptococcus pyogenes, Staphylococcus aureus, and Clostridium septique) in culture and effectively cured Streptococcus infection in mice. Thus, they reported their findings in the 24 August 1940 issue of The Lancet under the title "Penicillin as a chemotherapeutic agent" concluding:
The results are clear cut, and show that penicillin is active in vivo against at least three of the organisms inhibited in vitro. It would seem a reasonable hope that all organisms in high dilution in vitro will be found to be dealt with in vivo. Penicillin does not appear to be related to any chemotherapeutic substance at present in use and is particularly remarkable for its activity against the anaerobic organisms associated with gas gangrene.
The following year, the Oxford team treated a policeman, Albert Alexander, who had a severe facial infection; his condition improved, but he eventually died as the researchers ran out of penicillin. Subsequently, several other patients were treated successfully, among them the survivors of the Cocoanut Grove fire in Boston (December 1942) who were the first burn patients to be successfully treated with penicillin.
The most important clinical test took place in August 1942 when Fleming cured Harry Lambert (a work associate of Robert, Fleming's brother) of a fatal infection of the nervous system (streptococcal meningitis). Fleming asked Florey for a purified penicillin sample, which he immediately injected into Lambert's spinal canal. Lambert showed signs of improvement the next day, and completely recovered within a week. Fleming reported his findings in The Lancet in 1943. It was on this medical evidence that the British War Cabinet set up the Penicillin Committee on 5 April 1943 formed by Cecil Weir, Director General of Equipment, as Chairman, Fleming, Florey, Sir Percival Hartley, Allison and representatives from pharmaceutical companies as members. The establishment of the committee opened the door to the mass production of penicillin the next year.
Knowing that large-scale production for medical use was futile in a confined laboratory, the Oxford team tried to persuade the war-torn British government and private companies to undertake mass production, but in vain. Florey and Heatley travelled to the United States (US) in June 1941 to persuade the American government and pharmaceutical companies there. Ton ensure safe transportation of the sample, they smeared their coat pockets with the mould instead of taking it in a vial. In July, they met with Andrew Jackson Moyer and Robert D. Coghill at the USDA Northern Regional Research Laboratory (NRRL, now the National Center for Agricultural Utilization Research) in Peoria, Illinois, where large-scale fermentations were done. The Americans showed great interest and were able to make a Penicillium culture by the end of July but realised that Fleming's mould was not efficient enough to produce large quantities of penicillin.
With the help of US Army Transport Command, NRRL mycologist Kenneth Bryan Raper was able to locate similar but better moulds from Chungkin (China), Bombay (Mumbai, India) and Cape Town (South Africa). However, the single-best sample was obtained in 1943 from cantaloupe (a type of melon) sold in the Peoria fruit market. The mould was identified to be P. chrysogenum and designated as "NRRL 1951" or "cantaloupe strain" (Figure 6). There is a popular story that Mary K. Hunt (or Mary Hunt Stevens), a staff member at NRRL, collected the mould; for which she was popularised as "Mouldy Mary." However, Raper remarked that this story was "folklore" and that the fruit was delivered to the laboratory by a woman from the local fruit market.
Between 1941 and 1943, Moyer, Coghill and Raper developed methods for industrialized penicillin production and isolated higher-yielding strains of the Penicillium mould. Simultaneous research by Jasper H. Kane and other Pfizer scientists in Brooklyn developed the practical, deep-tank fermentation method for production of large quantities of pharmaceutical-grade penicillin.
When production first began, one-litre containers had a yield of less than 1%, but improved to a yield of 80–90% in 10,000 gallon containers. This increase in efficiency happened between 1941 and 1945 as the result of continuous process innovation (Figure 7 shows one of the first mass applications). Orvill May, director of the Agricultural Research Service, had Coghill use his experience with fermentation to increase the efficiency of extracting penicillin from the mould. When Moyer and Coghill replaced sucrose with lactose in the growth media, penicillin yield was increased. An even larger increase occurred when they added corn steep liquor.
The inefficiency of growing the mould on the surface of their nutrient baths, rather than having it submerged was a major challenge to the scientists. Although a submerged process of growing the mould was more efficient, the strain used was not suitable for the required conditions. With the improved fermentation, the cantaloupe strain could produced six times as much penicillin per millilitre of the culture filtrate. To improve on the cantaloupe strain, researchers subjected it to X-rays to facilitate mutations in its genome. The new mutant strain, designated "X-1612", made in in 1946 produced twice as much penicillin as the original strain. Another mutant strain, named "Q176", made in 1947 from ultraviolet irradiation further doubled the penicillin productivity.
Now scientists had a mould that grew well submerged and produced an acceptable amount of penicillin. The next challenge was to provide the air required by the mould to grow. This problem was solved using an aerator but, due to the use of corn steep, aeration caused severe foaming. The addition of an anti-foaming agents such as arachis oil, lard oil and other fatty acids solved this problem. These anti-foaming agents further enhanced penicillin production.
The chemical structure of penicillin was first proposed by Edward Abraham in 1942, and three years later, Dorothy Hodgkin, working at Oxford, determined the correct chemical structure using X-ray crystallography. The same year, chemical analyses done at different universities, pharmaceutical companies and government research departments was published jointly by the US Committee on Medical Research and the British Medical Research Council in the journal Science. The report announced the existence of different forms of penicillin compounds that shared the same structural component called β-lactam. In the United Kingdom the penicillins were called penicillin I, II, III, and IV (Roman numerals were used according to the order of their discovery) while in the US scientists used letters such as F, G, K, and X that referred to their origins or sources as shown below:
|UK nomenclature||US nomenclature||Chemical name|
|Penicillin I||Penicillin F||2-Pentenylpenicillin|
|Penicillin II||Penicillin G||Benzylpenicillin|
|Penicillin III||Penicillin X||p-Hydroxybenzylpenicillin|
|Penicillin IV||Penicillin K||n-Heptylpenicillin|
The use of two different names for each penicillin caused confusion. As the chemical structures came to be known, the chemical names (based on the side chains of the compounds) further complicated their identification and application. Thus, penicillin literature became a mixture of three naming systems. Chemists mostly adhered to the chemical names, while biologists preferred the classic numbered or lettered names. To resolve the confusion, in 1948, Chain introduced the chemical names as standard nomenclature, remarking: "To make the nomenclature as far as possible unambiguous it was decided to replace the system of numbers or letters by prefixes indicating the chemical nature of the side chain R."
Further developments took place. In Austria, Hans Margreiter and Ernst Brandl of Biochemie (now Sandoz) developed the first acid-stable penicillin for oral administration, penicillin V in 1952. American chemist John C. Sheehan at the Massachusetts Institute of Technology (MIT) completed the first chemical synthesis of penicillin in 1957. Sheehan had started his studies into penicillin synthesis in 1948, and during these investigations developed new methods for the synthesis of peptides, as well as new protecting groups—groups that mask the reactivity of certain functional groups. Although the initial synthesis developed by Sheehan was not appropriate for mass production of penicillins, one of the intermediate compounds in his synthesis was 6-aminopenicillanic acid (6-APA), the nucleus of penicillin.
An important moment in the history of penicillin was the discovery of 6-APA itself. In 1957, researchers at Surrey's Beecham Research Laboratories (now the Beecham Group) isolated 6-APA from the culture media of P. chrysogenum. As published in Nature (1959), 6-APA was found to constitute the core 'nucleus' of penicillin (in fact, all β-lactam antibiotics) and was easily chemically modified by attaching side chains through chemical reactions. This discovery paved the way for new and improved drugs as all semi-synthetic penicillins are produced from chemical manipulation of 6-APA.
The second-generation semi-synthetic β-lactam antibiotic methicillin, designed to counter first-generation-resistant penicillinases, was introduced in the United Kingdom in 1959. It is likely that methicillin-resistant forms of Staphylococcus aureus already existed at the time.
Penicillin patents became a matter of concern and conflict. Chain had wanted to apply for a patent but Florey and his teammates had objected arguing that penicillin should benefit all. He sought the advice of Sir Henry Hallett Dale (Chairman of the Wellcome Trust and member of the Scientific Advisory Panel to the Cabinet of British government) and John William Trevan (Director of the Wellcome Trust Research Laboratory). On 26 and 27 March 1941, Dale and Trevan met at Sir William Dunn School of Pathology to discuss the issue. Dale specifically advised that patenting penicillin would be unethical. Not giving up, Chain approached Sir Edward Mellanby, then Secretary of the Medical Research Council, who also objected on ethical grounds. As Chain later admitted, he had "many bitter fights" with Mellanby, but Mellanby's decision was accepted as final.
In 1945, Moyer patented the methods for production and isolation of penicillin. Moyer could not obtain a patent in the US as an employee of the NRRL, and filed his patent at the British Patent Office (now the Intellectual Property Office). He gave the license to a US company, Commercial Solvents Corporation. Although completely legal, his colleague Coghill felt it was an injustice for outsiders to have the royalties for the "British discovery." A year later, Moyer asked Coghill for permission to file another patent based on the use of phenylacetic acid that increased penicillin production by 66%, but as the principal researcher, Coghill refused.
When Fleming learned of the American patents on penicillin production, he was infuriated and commented:
I found penicillin and have given it free for the benefit of humanity. Why should it become a profit-making monopoly of manufacturers in another country?
Fleming, Florey and Chain shared the 1945 Nobel Prize in Physiology or Medicine "for the discovery of penicillin and its curative effect in various infectious diseases." Hodgkin received the 1964 Nobel Prize in Chemistry "for her determinations by X-ray techniques of the structures of important biochemical substances."
Development of penicillin-derivatives
The narrow range of treatable diseases of the penicillins prompted further search for derivatives of penicillin. The isolation of 6-APA allowed preparation of semisynthetic penicillins, with various improvements in terms of bioavailability, spectrum, stability, tolerance. The first major development was the production of ampicillin by the Beecham Research Laboratories in London in 1961. Ampicillin had advantages over the original penicillin as it showed activity against both Gram-positive and Gram-negative bacteria. Further development yielded β-lactamase-resistant penicillins, including flucloxacillin, dicloxacillin, and methicillin, which were specifically active against β-lactamase-producing bacterial species, but not against the methicillin-resistant Staphylococcus aureus strains that subsequently emerged.
Another development in penicillin synthesis was the antipseudomonal penicillins, such as carbenicillin, ticarcillin, and piperacillin, useful for their activity against Gram-negative bacteria. The penicillins and related β-lactams have become the most widely used antibiotics in the world. Amoxicillin, a semisynthetic penicillin developed by Beecham Research Laboratories in 1970, is the single-most commonly used. However, the usefulness of these penicillins and later developed antibiotics, including the mecillinams, the carbapenems and, most important, the cephalosporins, is limited by the common structure, the β-lactam ring, which is not only the antibiotic active part of the chemical compound, but also the target site of bacteria in drug resistance.
In his Nobel lecture, Fleming warned of the possibility of penicillin resistance in clinical conditions:
The time may come when penicillin can be bought by anyone in the shops. Then there is the danger that the ignorant man may easily underdose himself and by exposing his microbes to non-lethal quantities of the drug make them resistant.
In 1940, Chain and Abraham reported the first indication of antibiotic resistance to penicillin, an E. coli strain that produced the penicillinase enzyme, which was capable of breaking down penicillin and completely negating its antibacterial effect. They worked out the chemical nature of penicillinase which they reported in Nature:
The conclusion that the active substance is an enzyme is drawn from the fact that it is destroyed by heating at 90° for 5 minutes and by incubation with papain activated with potassium cyanide at pH 6, and that it is non-dialysable through 'Cellophane' membranes.
By 1942, some strains of Staphylococcus aureus had developed a strong resistance to penicillin. Eighteen years later, most of the strains were resistant to penicillin. In 1967, Streptococcus pneumoniae was also reported to be penicillin resistant. Many other strains of bacteria have eventually developed, and continue to develop a resistance to penicillin.
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- ↑ Unlike his predecessor scientists such as Francesco Redi and Louis Pasteur who had experimentally rebutted spontaneous generation, Burdon-Sanderson went further by specifically identifying the types of microbes as bacteria, microzyme, fungi, torula, and Penicillium, including the differences in their growth pattern. His experiment on 11 November 1870 reads: "At the same date all the glasses showed tufts of penicillium; those on 3 and 5 were more advanced than the rest... the liquid in 5 was found to be perfectly limpid and free from microzymes (referring to bacteria)."
- ↑ At the time, the term Penicillium glaucum was used as a catch-all phrase for a variety of different fungi, though not for Penicillium notatum. Duchesne's specific mold was unfortunately not preserved, which makes it impossible to be certain today which fungus might have been responsible for the cure and, consequently, even less certain which specific antibacterial substance was responsible.
- ↑ The statement "does not appear to have been considered as possibly useful from any other point of view" seems to be later deleted, but is still apparent from Fleming's response (BMJ, 1941, 2 (4210): 386–386).
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- ↑ "Methicillin-Resistant Staphylococci in a General Hospital". Lancet 1 (7385): 595–7. March 1965. doi:10.1016/S0140-6736(65)91165-7. PMID 14250094.
- ↑ de Sousa Coelho, F.; Mainardi, J.-L. (2021-01-05). "The multiple benefits of second-generation β-lactamase inhibitors in treatment of multidrug-resistant bacteria". Infectious Diseases Now online. doi:10.1016/j.idnow.2020.11.007. PMID 33870896. https://pubmed.ncbi.nlm.nih.gov/33870896.
- ↑ Croydon, E. A.; Sutherland, R. (1970). "α-amino-p-hydroxybenzylpenicillin (BRL 2333), a new semisynthetic penicillin: absorption and excretion in man". Antimicrobial Agents and Chemotherapy 10: 427–430. PMID 5521362. https://pubmed.ncbi.nlm.nih.gov/5521362.
- ↑ Sutherland, R.; Rolinson, G. N. (1970). "α-amino-p-hydroxybenzylpenicillin (BRL 2333), a new semisynthetic penicillin: in vitro evaluation". Antimicrobial Agents and Chemotherapy 10: 411–415. doi:10.1128/AAC.10.3.411. PMID 5000265. https://pubmed.ncbi.nlm.nih.gov/5000265.
- ↑ Burch, D. G. S.; Sperling, D. (2018). "Amoxicillin-current use in swine medicine". Journal of Veterinary Pharmacology and Therapeutics 41 (3): 356–368. doi:10.1111/jvp.12482. http://doi.wiley.com/10.1111/jvp.12482.
- ↑ Aberer, Werner; Macy, Eric (2017). "Moving toward optimizing testing for penicillin allergy". The Journal of Allergy and Clinical Immunology. In Practice 5 (3): 684–685. doi:10.1016/j.jaip.2017.03.020. PMID 28483319. https://pubmed.ncbi.nlm.nih.gov/28483319.
- ↑ James, C.W.; Gurk-Turner, C. (2001). "Cross-reactivity of beta-lactam antibiotics". Proceedings 14 (1): 106–7. doi:10.1080/08998280.2001.11927741. PMID 16369597. PMC 1291320. //www.ncbi.nlm.nih.gov/pmc/articles/PMC1291320/.
- ↑ Lima, Lidia Moreira; Silva, Bianca Nascimento Monteiro da; Barbosa, Gisele; Barreiro, Eliezer J. (2020). "β-lactam antibiotics: An overview from a medicinal chemistry perspective". European Journal of Medicinal Chemistry 208: 112829. doi:10.1016/j.ejmech.2020.112829. PMID 33002736. https://pubmed.ncbi.nlm.nih.gov/33002736.
- ↑ Abraham, E.P.; Chain, E. (1940). "An enzyme from bacteria able to destroy penicillin". Nature 10 (4): 677–8. doi:10.1038/146837a0. PMID 3055168. http://www.nature.com/articles/146837a0.
- ↑ Lowy, F.D. (2003). "Antimicrobial resistance: the example of Staphylococcus aureus". The Journal of Clinical Investigation 111 (9): 1265–73. doi:10.1172/JCI18535. PMID 12727914. PMC 154455. //www.ncbi.nlm.nih.gov/pmc/articles/PMC154455/.
- ↑ Davies, J; Davies, D (2010). "Origins and evolution of antibiotic resistance". Microbiology and Molecular Biology Reviews 74 (3): 417–33. doi:10.1128/MMBR.00016-10. PMID 20805405. PMC 2937522. //www.ncbi.nlm.nih.gov/pmc/articles/PMC2937522/.