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PRESENTED BY,
ARNAB GUPTA KABIRAJ
M.Sc. MICROBIOLOGY SEMESTER – III
ROLL NO – BURMICRO 2016/002
REGISTRATION NO. – 001765 OF 2013-14
THE UNIVERSITY OF BURDWAN
HISTORY OF
THE
FORGOTTEN
CURE
1
PHAGE
Definition - Bacterial viruses that invade bacterial
cells, infect bacteria by injecting genetic material
& causes lysis.
Highly specific, has its own specific shape and size,
consists of ssDNA/dsDNA or ssRNA/dsRNA molecule
encapsulated inside a protein coat, ubiquitous, obligate
parasites, causes lysis or lysogeny of bacterial cell.
The term “Bacteriophage” is derived from two word….
Bacteria & the Greek word - Phagein which means to eat
or devour.
2
PHAGE THERAPY
Phage therapy - The therapeutic use of bacteriophages to treat
pathogenic bacterial infections.
Involves the use of phages or their products for the treatment of bacterial
infectious diseases.
Can be administered orally and topically on infected wounds
3
HISTORY
a. 1896 – Ernest Hankin ,a English bacteriologist, reported presence of antibacterial activity
(against Vibrio cholerae ) in waters of Ganges and Jamuna rivers in India and he
suggested that an unidentified substance was responsible for this phenomenon and for
limiting the spread of cholera epidemics.
4
Ernest Hankin
CONTD……
b. 1915 – Frederick Twort discovered entities capable
of destroying bacterial culture and of
producing small clear zone on bacterial lawns
but did not pursue his discovery.
c. 1917 – Félix d'Herelle independently
discovered the similar entities, he named
these as bacteriophage, investigated it the
and explored their ability to function as
therapeutic agents.
d. 1921 – First administration of phages was
given at the Hospital in Paris.
e. 1927 – An epidemic of Asiatic cholera was
impacting on the Punjab, and Félix d'Herelle
was able to treat 74 gravely ill patients with
his phage therapy.
f. 1940s – The Eli Lilly Company produced seven phage products for human use,
thus commercial production began. 5
Félix d'Herelle
Frederick Twort
REASONS FOR DECLINE
i. Fall of the Soviet Union.
ii. Subsequent displacement of its use after World War II by antibiotics.
iii. The beginning of a new era in Western countries with the golden age of antibiotics(1945).
iv. Technological limitations.
v. Inadequate scientific methodologies used by practitioners at that time.
vi. Initial problems like host range ,bacterial debris present in phage preparations & side effect.
6
REDISCOVERY & DEVELOPMENT OF THE
FORGOTTEN CURE
1) 1980 – Phage therapy was “rediscovered” by the work of Smith and Huggins.
2) 1990s – Western phage therapy gained momentum.
3) 2000 – The field finally began maturing.
4) 2004 – Levin and Bull suggested that phage therapy only needs to decrease the numbers of
infecting bacteria to a level where the host defences can take care of the remaining bacteria.
5) Latest era of phage therapy research as well as it’s application is continuing to this day.
7
REASON FOR REDISCOVERY
1)Antibiotic Resistance-
•Abusive use of antibiotics over the past twenty years.
•The resistance phenomenon represents an important healthcare issue.
•Return of the pre-antibiotic Era of untreatable infections and epidemics.
8
2)Advantages of phages over antibiotics
9
Issue Phage Antibiotics
Fate of the “drug”
molecule
Exponential growth in numbers, so that the
“drug” makes more of itself at the site of
infection, where it is needed.
Metabolic destruction of the
molecule, as it works.
Concentration of the
“drug” required to kill a
given bacterium
One phage particle is sufficient to kill a
given bacterium.
Numerous molecules of the
antibiotic are needed
to kill a given bacterium.
Ability to overcome
bacterial resistance
Phages are “living” organisms that undergo
mutations, some of which can overcome
bacterial mutations.
Antibiotics are fixed & cannot
adapt to a bacterial mutation.
Bacteria that have resisted them
can pass along the resistance
trait within and between species.
CONTD…..
10
Issue Phage Antibiotics
Spread of bacterial resistance Phages tend not to cross
species boundaries. Thus even
though the targeted bacterial
species may become resistant
to the phage, it is unlikely that
other species will.
The antibiotics in use tend to be
broad spectrum, thereby
provoking resistance in several
species and genera of bacteria.
Specificity Very specific.
Affect only the targeted bacterial
species so secondary infections
doesn't occur.
Antibiotics target both
pathogenic microorganisms and
normal microflora. Thus the the
microbial balance in the patient
is affected, which may lead to
serious secondary infections.
 Problem 1 - Host range
The solution
1. Screening of phages against infecting bacteria to ensure lysis.
2. Develop “multivalent” phages.
 Problem 2 - Bacterial debris present in the phage preparations
The solution
Use of modern technology for purification – centrifugation.
Problems with phage therapy and solution to overcome
the problems
11
CONTD….
 Problem 3 - Attempts to remove host bacteria from therapeutic preparations
The solution
1. Sterile filtration
2. Titration of preparations more than once over time to ensure that the
phage remain viable if chemical are used.
 Problem 4 - Lysogeny
The solution
Use only phages that replicate using the lytic cycle.
12
CONTD….
 Problem 5 - Anti-phage antibodies
The solution
1. Administering a higher dose of phage.
2. Study of titers of antibodies that develop in humans.
13
USES OF PHAGE THERAPY
1. Destruction of biofilm .
2. Enzymes produced by phages used as enzybiotics.
3. In food industry for control of bacterial loads on food & to control the presence of
biofilms in the food processing environment.
4. Candidate for co-therapy with antibiotics – prevent the emergence of bacterial
resistance to antibiotic.
5. PhagoBioDerm - used to treat recurrent leg ulcer and infections in burn
victims.
6. Future application – Phage Particles as Vaccine Delivery Vehicles
14
CONCLUSION
15
The need for alternatives to antibiotics such as phage therapy is
essential due to increase of resistance of bacteria towards
antibiotics. Thus revisiting the exploitation & research on
therapeutic property of phages are needed. Though this approach
has been neglected by the western world in the past but due to
antibiotic resistance, it has been recently stressed by the WHO.
Thus knowing the history of this therapy helps us to understand
and develop it further for future use.
REFERENCES
•d’Herelle F. Sur le rôle du microbe filtrant bactériophage dans la dysentérie bacillaire. CR Acad Sci, Paris 1918;167:970–2.
•d’Herelle F. Sur le microbe bactériophage. CR Acad Biol 1919;82:1123–237.
•Loc-Carrillo C, Abedon ST. Pros and cons of phage therapy. Bacteriophage2011;1:111–4.Lohans CT, Vederas JC
•O’Flaherty S, Coffey A, Meaney W, Fitzgerald GF, Ross RP. The recombinant phagelysin LysK has a broad spectrum of lytic activity
against clinically relevantstaphylococci including methicillin-resistant Staphylococcus aureus. J Bacteriol2005;187:7161–4.
•Lorch A. Bacteriophages. An alternative to antibiotics? Biotechnol Dev Monitor1999;39:14–7.
•Thiel K (2004) Old dogma, new tricks—21st Century phage therapy Nat Biotechnol 22:31-36
•V]AN HKELVOORT T. (1992): Bacteriological and physiological research styles in the early controversy on the nature of the
Nbacteriophage phenomenon. Med. Hist., 36, 243–270.
•Sulakvelidze A, Kutter E. Bacteriophage therapy in humans. In: Kutter E, Sulakvelidze A, eds.Bacteriophages: Biology and
Application. Boca Raton,FL: CRC Press, 2005:381-436.
•Brussow H. Phage therapy: the western perspective.In: Mc Grath S, van Sinderen D, eds. Bacteriophage:Genetics and
Microbiology. Norfolk, UK: Caister Academic Press, 2007:159-92.
•Twort FW. An investigation on the nature of ultramicroscopic viruses. Lancet 1915; 186:1241-3; DOI:10.1016/S0140-
6736(01)20383-3.
•d’Herelle F. On an invisible microbe antagonistic to dysentery bacilli. Comptes Rendus Academie des Sciences 1917; 165:373-5.
•Eaton MD, Bayne-Jones S. Bacteriophage therapy: Review of the principles and results of the use of bacteriophage in the treatment
of infections (I). J Am Med Assoc 1934; 103:1769-76.
•Eaton MD, Bayne-Jones S. Bacteriophage therapy: Review of the principles and results of the use of bacteriophage in the treatment
of infections (II). J Am Med Assoc 1934; 103:1847-53.
16
CONTD……
• Eaton MD, Bayne-Jones S. Bacteriophage therapy: Review of the principles and results of the use of bacteriophage in the
treatment of infections (III). J Am Med Assoc 1934; 103:1934-9.
• Smith HW, Huggins MB, Shaw KM. The control of experimental Escherichia coli diarrhoea in calves by means of bacteriophages.
J Gen Microbiol 1987; 133:1111-26. PMID: 3309177.
• Smith HW, Huggins MB, Shaw KM. Factors influencing the survival and multiplication of bacteriophages in calves and in their
environment. J Gen Microbiol 1987; 133:1127-35; PMID: 3309178.
• Smith HW, Huggins MB. Effectiveness of phages in treating experimental Escherichia coli diarrhoea in calves, piglets and lambs.
J Gen Microbiol 1983;129:2659-75; PMID: 6355391.
• Smith HW, Huggins MB. Successful treatment of experimental Escherichia coli infections in mice using phage: Its general
superiority over antibiotics. J Gen Microbiol 1982; 128:307-18; PMID: 7042903.
• Summers WC. History of phage research and phage therapy. In: Waldor M, Friedman D, Adhya S, eds. Phages: Their Role in
Bacterial Pathogenesis and Biotechnology. Washington DC: ASM Press, 2005.
• Kutter E. Phage Therapy: Bacteriophages as naturally occurring antimicrobials. In: Goldman E, Green LH,eds. Practical
Handbook of Microbiology. Boca Raton,FL: CRC Press, 2008:713-30.
• Summers WC. In the beginning. Bacteriophage 2011;1:50-1; DOI:10.4161/bact.1.1.14070.
• Duckworth DH. Who discovered bacteriophage? Bacteriol Rev 1976; 40:793-802; PMID: 795414.
• Summers WC. Felix d’Herelle and the Origins of Molecular Biology. New Haven, CT: Yale University Press, 1999.
• Summers WC. Bacteriophage therapy. Annu Rev Microbiol 2001; 55:437-51; PMID: 11544363;
DOI:10.1146/annurev.micro.55.1.437.
• Summers WC. Bacteriophage research: early research. In: Kutter E, Sulakvelidze A, eds. Bacteriophages:Biology and
Application. Boca Raton, FL: CRC Press,2005:5-28
• Hausler T. Viruses vs. Superbugs: A Solution to the Antibiotic Crisis.Macmillan, 2006.
17
18

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History of the Forgotten Cure - Phage therapy

  • 1. PRESENTED BY, ARNAB GUPTA KABIRAJ M.Sc. MICROBIOLOGY SEMESTER – III ROLL NO – BURMICRO 2016/002 REGISTRATION NO. – 001765 OF 2013-14 THE UNIVERSITY OF BURDWAN HISTORY OF THE FORGOTTEN CURE 1
  • 2. PHAGE Definition - Bacterial viruses that invade bacterial cells, infect bacteria by injecting genetic material & causes lysis. Highly specific, has its own specific shape and size, consists of ssDNA/dsDNA or ssRNA/dsRNA molecule encapsulated inside a protein coat, ubiquitous, obligate parasites, causes lysis or lysogeny of bacterial cell. The term “Bacteriophage” is derived from two word…. Bacteria & the Greek word - Phagein which means to eat or devour. 2
  • 3. PHAGE THERAPY Phage therapy - The therapeutic use of bacteriophages to treat pathogenic bacterial infections. Involves the use of phages or their products for the treatment of bacterial infectious diseases. Can be administered orally and topically on infected wounds 3
  • 4. HISTORY a. 1896 – Ernest Hankin ,a English bacteriologist, reported presence of antibacterial activity (against Vibrio cholerae ) in waters of Ganges and Jamuna rivers in India and he suggested that an unidentified substance was responsible for this phenomenon and for limiting the spread of cholera epidemics. 4 Ernest Hankin
  • 5. CONTD…… b. 1915 – Frederick Twort discovered entities capable of destroying bacterial culture and of producing small clear zone on bacterial lawns but did not pursue his discovery. c. 1917 – Félix d'Herelle independently discovered the similar entities, he named these as bacteriophage, investigated it the and explored their ability to function as therapeutic agents. d. 1921 – First administration of phages was given at the Hospital in Paris. e. 1927 – An epidemic of Asiatic cholera was impacting on the Punjab, and Félix d'Herelle was able to treat 74 gravely ill patients with his phage therapy. f. 1940s – The Eli Lilly Company produced seven phage products for human use, thus commercial production began. 5 Félix d'Herelle Frederick Twort
  • 6. REASONS FOR DECLINE i. Fall of the Soviet Union. ii. Subsequent displacement of its use after World War II by antibiotics. iii. The beginning of a new era in Western countries with the golden age of antibiotics(1945). iv. Technological limitations. v. Inadequate scientific methodologies used by practitioners at that time. vi. Initial problems like host range ,bacterial debris present in phage preparations & side effect. 6
  • 7. REDISCOVERY & DEVELOPMENT OF THE FORGOTTEN CURE 1) 1980 – Phage therapy was “rediscovered” by the work of Smith and Huggins. 2) 1990s – Western phage therapy gained momentum. 3) 2000 – The field finally began maturing. 4) 2004 – Levin and Bull suggested that phage therapy only needs to decrease the numbers of infecting bacteria to a level where the host defences can take care of the remaining bacteria. 5) Latest era of phage therapy research as well as it’s application is continuing to this day. 7
  • 8. REASON FOR REDISCOVERY 1)Antibiotic Resistance- •Abusive use of antibiotics over the past twenty years. •The resistance phenomenon represents an important healthcare issue. •Return of the pre-antibiotic Era of untreatable infections and epidemics. 8
  • 9. 2)Advantages of phages over antibiotics 9 Issue Phage Antibiotics Fate of the “drug” molecule Exponential growth in numbers, so that the “drug” makes more of itself at the site of infection, where it is needed. Metabolic destruction of the molecule, as it works. Concentration of the “drug” required to kill a given bacterium One phage particle is sufficient to kill a given bacterium. Numerous molecules of the antibiotic are needed to kill a given bacterium. Ability to overcome bacterial resistance Phages are “living” organisms that undergo mutations, some of which can overcome bacterial mutations. Antibiotics are fixed & cannot adapt to a bacterial mutation. Bacteria that have resisted them can pass along the resistance trait within and between species.
  • 10. CONTD….. 10 Issue Phage Antibiotics Spread of bacterial resistance Phages tend not to cross species boundaries. Thus even though the targeted bacterial species may become resistant to the phage, it is unlikely that other species will. The antibiotics in use tend to be broad spectrum, thereby provoking resistance in several species and genera of bacteria. Specificity Very specific. Affect only the targeted bacterial species so secondary infections doesn't occur. Antibiotics target both pathogenic microorganisms and normal microflora. Thus the the microbial balance in the patient is affected, which may lead to serious secondary infections.
  • 11.  Problem 1 - Host range The solution 1. Screening of phages against infecting bacteria to ensure lysis. 2. Develop “multivalent” phages.  Problem 2 - Bacterial debris present in the phage preparations The solution Use of modern technology for purification – centrifugation. Problems with phage therapy and solution to overcome the problems 11
  • 12. CONTD….  Problem 3 - Attempts to remove host bacteria from therapeutic preparations The solution 1. Sterile filtration 2. Titration of preparations more than once over time to ensure that the phage remain viable if chemical are used.  Problem 4 - Lysogeny The solution Use only phages that replicate using the lytic cycle. 12
  • 13. CONTD….  Problem 5 - Anti-phage antibodies The solution 1. Administering a higher dose of phage. 2. Study of titers of antibodies that develop in humans. 13
  • 14. USES OF PHAGE THERAPY 1. Destruction of biofilm . 2. Enzymes produced by phages used as enzybiotics. 3. In food industry for control of bacterial loads on food & to control the presence of biofilms in the food processing environment. 4. Candidate for co-therapy with antibiotics – prevent the emergence of bacterial resistance to antibiotic. 5. PhagoBioDerm - used to treat recurrent leg ulcer and infections in burn victims. 6. Future application – Phage Particles as Vaccine Delivery Vehicles 14
  • 15. CONCLUSION 15 The need for alternatives to antibiotics such as phage therapy is essential due to increase of resistance of bacteria towards antibiotics. Thus revisiting the exploitation & research on therapeutic property of phages are needed. Though this approach has been neglected by the western world in the past but due to antibiotic resistance, it has been recently stressed by the WHO. Thus knowing the history of this therapy helps us to understand and develop it further for future use.
  • 16. REFERENCES •d’Herelle F. Sur le rôle du microbe filtrant bactériophage dans la dysentérie bacillaire. CR Acad Sci, Paris 1918;167:970–2. •d’Herelle F. Sur le microbe bactériophage. CR Acad Biol 1919;82:1123–237. •Loc-Carrillo C, Abedon ST. Pros and cons of phage therapy. Bacteriophage2011;1:111–4.Lohans CT, Vederas JC •O’Flaherty S, Coffey A, Meaney W, Fitzgerald GF, Ross RP. The recombinant phagelysin LysK has a broad spectrum of lytic activity against clinically relevantstaphylococci including methicillin-resistant Staphylococcus aureus. J Bacteriol2005;187:7161–4. •Lorch A. Bacteriophages. An alternative to antibiotics? Biotechnol Dev Monitor1999;39:14–7. •Thiel K (2004) Old dogma, new tricks—21st Century phage therapy Nat Biotechnol 22:31-36 •V]AN HKELVOORT T. (1992): Bacteriological and physiological research styles in the early controversy on the nature of the Nbacteriophage phenomenon. Med. Hist., 36, 243–270. •Sulakvelidze A, Kutter E. Bacteriophage therapy in humans. In: Kutter E, Sulakvelidze A, eds.Bacteriophages: Biology and Application. Boca Raton,FL: CRC Press, 2005:381-436. •Brussow H. Phage therapy: the western perspective.In: Mc Grath S, van Sinderen D, eds. Bacteriophage:Genetics and Microbiology. Norfolk, UK: Caister Academic Press, 2007:159-92. •Twort FW. An investigation on the nature of ultramicroscopic viruses. Lancet 1915; 186:1241-3; DOI:10.1016/S0140- 6736(01)20383-3. •d’Herelle F. On an invisible microbe antagonistic to dysentery bacilli. Comptes Rendus Academie des Sciences 1917; 165:373-5. •Eaton MD, Bayne-Jones S. Bacteriophage therapy: Review of the principles and results of the use of bacteriophage in the treatment of infections (I). J Am Med Assoc 1934; 103:1769-76. •Eaton MD, Bayne-Jones S. Bacteriophage therapy: Review of the principles and results of the use of bacteriophage in the treatment of infections (II). J Am Med Assoc 1934; 103:1847-53. 16
  • 17. CONTD…… • Eaton MD, Bayne-Jones S. Bacteriophage therapy: Review of the principles and results of the use of bacteriophage in the treatment of infections (III). J Am Med Assoc 1934; 103:1934-9. • Smith HW, Huggins MB, Shaw KM. The control of experimental Escherichia coli diarrhoea in calves by means of bacteriophages. J Gen Microbiol 1987; 133:1111-26. PMID: 3309177. • Smith HW, Huggins MB, Shaw KM. Factors influencing the survival and multiplication of bacteriophages in calves and in their environment. J Gen Microbiol 1987; 133:1127-35; PMID: 3309178. • Smith HW, Huggins MB. Effectiveness of phages in treating experimental Escherichia coli diarrhoea in calves, piglets and lambs. J Gen Microbiol 1983;129:2659-75; PMID: 6355391. • Smith HW, Huggins MB. Successful treatment of experimental Escherichia coli infections in mice using phage: Its general superiority over antibiotics. J Gen Microbiol 1982; 128:307-18; PMID: 7042903. • Summers WC. History of phage research and phage therapy. In: Waldor M, Friedman D, Adhya S, eds. Phages: Their Role in Bacterial Pathogenesis and Biotechnology. Washington DC: ASM Press, 2005. • Kutter E. Phage Therapy: Bacteriophages as naturally occurring antimicrobials. In: Goldman E, Green LH,eds. Practical Handbook of Microbiology. Boca Raton,FL: CRC Press, 2008:713-30. • Summers WC. In the beginning. Bacteriophage 2011;1:50-1; DOI:10.4161/bact.1.1.14070. • Duckworth DH. Who discovered bacteriophage? Bacteriol Rev 1976; 40:793-802; PMID: 795414. • Summers WC. Felix d’Herelle and the Origins of Molecular Biology. New Haven, CT: Yale University Press, 1999. • Summers WC. Bacteriophage therapy. Annu Rev Microbiol 2001; 55:437-51; PMID: 11544363; DOI:10.1146/annurev.micro.55.1.437. • Summers WC. Bacteriophage research: early research. In: Kutter E, Sulakvelidze A, eds. Bacteriophages:Biology and Application. Boca Raton, FL: CRC Press,2005:5-28 • Hausler T. Viruses vs. Superbugs: A Solution to the Antibiotic Crisis.Macmillan, 2006. 17
  • 18. 18