Phage Therapy

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Introduction

Figure 1. Electron micrograph of a bacteriophage. Source: Molecular Tool http://www.bio.davidson.edu/Courses/Molbio/MolStudents/spring2003/Keogh/plasmids.html.

Bacteriophages are viruses that infect bacteria. Bacteriophages have many potential applications in biotechnology that are currently being explored such as being used as delivery vehicles for vaccines and gene therapy, detecting bacterial pathogens, and screening libraries of peptides or antibodies. Phage therapy takes advantage of this particular group of viruses in a relatively simple way; it aims to treat bacterial infections through the application of such phages. Though for some time people did not consider this use of bacteriophages feasible, since the emergence of many antibiotic-resistant pathogens, the field is again on the rise (Inal 2003). Recent WHO figures suggest that 14,000 people die in the US alone every year due to multidrug-resistant bacteria acquired in hospitals. Luckily, bacteriophages are found in all bacteria so there is at least a theoretical possibility that therapies can be developed for all species of bacteria (Inal 2003). Because humans are unlikely to be able to come up with novel antibiotics forever and bacteria will probably continue to evolve resistances, from the human perspective it is important that new ways of thwarting infection are discovered.

It seems that bacteriophages may be the knight in shining armor for the treatment of bacterial infections. They are specific to their bacterial host and therefore do not harm humans or plants, they can grow in numbers as long as the bacteria are present, and they are self-limiting in that once they kill all of the target bacteria they no longer have a place to live and they die off too (Summers 2001; Clark and March 2006).

History

Early research

Felix d'Herelle is usually credited with the first cogent description of bacteriophages (Summers 2001). He was studying dysentery and described certain "invisible microbes" that he found in some of his patients without bacteria in their stool, and he correctly attributed this to the action of the virus as some kind of recovery agent. Phage therapy was first attempted soon after the discovery of bacteriophages as d'Herelle tested out their therapeutic effectiveness on first animals (chickens and cows, to good success) and then humans. Later, a group in India began studying the usefulness of bacteriophages in the treatment of cholera and found that symptoms were reduced in severity and length when the patient was treated with phage, which is indicative of many other positive results from treatment with bacteriophages that were also seen around that time (Summers 2001). William Summers has divided the history of phage therapy into four periods: early enthusiasm, critical skepticism, abandonment, and recent interest and reappraisal. Though there was a fair amount of positive findings on the effectiveness of phage therapy, there were also some negative findings. As research interest waned in the West due to World War II, the rise in the use of antibiotics, and some early inconsistent and unsuccessful results, phage therapy was still being used on the battlefront by both the Russians and the Germans. For economic and cultural reasons research on phage therapy grew and expanded in the Soviet Union while the West separated itself and spent more time and money on discovering novel antibiotics. Therefore the countries with the richest history of phage research are Russia and Georgia (Summers 2001).

Early issues

There are several reasons why the early trials in bacteriophage therapy were unsuccessful (Weld et al 2004). For one, phage biology was poorly understood, and therefore the wrong phage or the wrong concentration of phage may have been given to treat an infection. Another limiting factor to the success of early therapeutic uses of phage is that the preparations of phage to be administered were all too commonly contaminated or did not contain enough viable viruses to be effective (Weld et al 2004). The biology of the bacteriophage was not well-understood and so many of the tests that showed inconsistent effectiveness of phage therapy were due to the fact that what was administered was not what was needed to do the job. By the time the underlying biology of bacteriophages was better understood, interest had waned and there were few who cared to go back and make new experimental treatments with the new information as a foundation (Summers 2001). Lastly, early attempts were not consistently effective because sometimes the wrong phage would be employed or they would choose phage-resistant bacteria to study. Current thinking to avoid this issue involves using cocktails of slightly different bacteriophages to target all of the pathogenic bacteria, even those with mutations or plasmids protecting them from certain phage. Though it is less likely that these same mistakes will be encountered in current use of bacteriophages in a therapeutic setting, there still needs to be significant research programs undertaken before phage therapy will be fit for widespread use (Weld et al 2004).

Current research and potential problems

Though current research appears promising and it seems that phage therapy may be a good solution to the problem of multidrug resistant bacteria, there is a long way to go before the therapy is ready to be applied on a widespread basis. One current issue is that many of the experiments that are done are in vitro, meaning that the same things that are observed may not be seen when ones goes to a larger and more complicated environment (Weld et al 2004). New growth models are needed that can be extrapolated to in vivo growth. In vitro studies are done in a lab in an artificial environment that often does not translate to the body (in vivo). Invivo, the environment is much more complicated and there are many barriers that a phage must pass through so that it can get in contact with the targeted bacteria. Weld et al (2004) attempted to make new models for phage growth, but quickly found that bacteriophages have a far more complicated growth cycle in vivo. They found not only that it was difficult to extrapolate from in vitro to in vivo, but also that it was hard to make generalizations about all in vivo situations from observing one (Weld et al 2004).

It is clear that before phage therapy can be used clinically there must be many more studies that can pinpoint more fully how to best make and administer phages. One potential problem is that just as bacteria are able to become resistant to antibiotics, they may also be able to develop resistances to phages (Inal 2003). There may be development of antibodies if phages are administered multiple times. This is easy to overcome by using instead of one type of phage, a cocktail of different ones. Another more significant potential issue is the possibility that the spleen will take up and deactivate the phages before they have the opportunity to reach their targets. This again reflects the need for more in vivo studies that can elucidate how phages actually react the the body and vice versa (Inal 2003).

Application

Delivery to targeted bacteria

When phages were first discovered and applied in a clinical setting for the treatment of diseases, they were injected in the vicinity of the infection. Later mechanisms of delivery included topical administration 3 times a day, eye drops, or orally before meals (Inal 2003). Phages, unlike many antibiotic molecules, are not diffusible across membranes and must therefore have a method of delivery to the target cells. Some researchers believe that the best delivery mechanism may lie in using other nonpathogenic species of bacteria to bring the phage to its pathogenic target.

Figure 2. The effect of treatment of Mycobacterium avium infected macrophages with Mycobacterium smegmatis 48 hours after infection (with and without the TM4 lytic phage) on number of intracellular M. avium. Coinfection with M. smegmatis alone did not result in significant destruction of M. avium cells. Coinfection with M. smegmatis and the TM4 phage resulted in a 100-fold decrease in the number of intracellular M. avium. Source: Broxmeyer et al 2002.

A study by Broxmeyer et al (2002) investigated the effectiveness of phage treatment of an intracellular human pathogen by using a mouse model. The study tested the ability of a mycobacteriophage delivered by a nonvirulent mycobacterium to kill Mycobacterium avium and Mycobacterium tuberculosis. These disease are common in sufferers of acquired immunodeficiency syndrome (AIDS), and though there have been some advancements in treatment in recent years, their effectiveness is limited by drug resistance and the fact that most of their modes of action require that the target is not in a dormant period. The researchers used vacuoles within macrophages to deliver the phage and found that treatment of M. avium-infected and to an even greater extent M. tuberculosis- infected cells with the phage resulted in decreased bacterial numbers (Figure 2). They capitalized on the fact that infecting macrophages with both M. avium and Mycobacterium smegmatis (the delivery bacteria for the TM4 lytic phage) leads to fusion of the vacuoles of the two, which in turn results in delivery of the phage to the target pathogenic bacteria. A decrease in M. avium number was seen when treated with the delivery bacteria, but a far greater decrease was seen when it was coinfected with the delivery bacteria plus the TM4 phage (Figure 2). (Broxmeyer et al 2002). This study provides promising support to the potential for the use of other bacteria as a delivery mechanism for bacteriophages to treat pathogenic diseases.

Some researchers have categorized different delivery modes as 'passive' and 'active'. Passive delivery is achieved by administering large doses of phage that likely exceed how many bacteria are present. Active delivery, on the other hand, involves making sure that the phage lives long enough to generate progeny cells which will then kill the bacterial cells. This latter category has the advantage that it can act over a longer period, but it may be difficult to realize fully because new doses must be administered at key time intervals. A study by Platt et al (2003) tried to employ a lysogenic life cycle such that cells would burst periodically and release phage into the environment. They used a non-pathogenic strain of E. coli that was lysogenic for a lytic mutant. They suggest that this is the best way to constantly release phage into the environment. They also say that this system may get around the issue of phage-resistant mutants by including different lysogens for different receptors on the target pathogen (Platt et al 2003).

Effectiveness

Figure 3. Venous leg ulcers infected with drug-resistant Pseudomonas and treated with bacteriophages over 5 months. Source: Clark and March 2006

Many of the recent studies that have looked at the effectiveness of phage therapy (in vitro and in vivo) have found that it can be very helpful in killing bacteria. One study by Huff et al (2003) found that treating chickens suffering from severe respiratory infections cause by E. coli was very helpful in clearing up symptoms. They found that the application of bacteriophage was most useful very soon after the chickens had been exposed to the bacteria and that, if treated early, multiple doses are better than a single dose. Interestingly, if treatment starts later, there is no difference between single or multiple doses, but treatment is still very helpful. Overall, this study found that phage therapy does seem to have a promising future and is very effective as an alternative to antibiotics. However, it is important to point out that phage therapy is the same as antibiotics in the necessity to catch the disease early (Huff et al 2003).

One clinic in the United States has begun using phages in some limited applications, for example to treat antibiotic-resistant infections. They have found that this method can be very effective. For example, one woman had venous leg ulcers infected with multidrug-resistant Pseudomonas. Within two weeks of phage application the wounds began improving and within a few months the wound had vastly improved (Figure 3). (Clark and March 2006).

Using phage therapy to treat MRSA

Figure 4. Staphylococcus aureus. Source: http://microbewiki.kenyon.edu/index.php/Hospital-acquired_Methicillin_Resistant_Staphylococcus_Aureus_%28MRSA%29

Meticillin-resistant Staphlococcus aureas or MRSA is a strain of Staphlococcus aureas that is resistant to the antibiotic methicillin (Barnes and Jinks 2008). Many MRSA strains are resistant to all but the most contemporary antibiotics, making MRSA infections very difficult to treat (Barnes and Jinks 2008). Luckily MRSA is an opportunistic pathogen, meaning it does not normally infect healthy individuals (Carnicer-Pont et al 2006). MRSA is a problem in hospitals where many of their patients have compromised immune systems, and thus are susceptible to MRSA infections (Carnicer-Pont et al 2006). To make matters worse, surgery and other invasive techniques create artificial entrances that allow MRSA to infect the patient (Barnes and Jinks 2008). Treating these patients is usually very costly and can greatly extend their stay in the hospital (Rubinovitch and Pittet 2001). This is because most of the antibiotics that are still effective in treating MRSA are much slower in cleaning the infection than methicillin, and other antibiotics that MRSA has already become resistant to (Rubinovitch and Pittet 2001). Although MRSA does not affect healthy individuals, it is becoming more common in the non-medical community (Barnes and Jinks 2008). These individuals don’t get sick, however they carry the pathogen and can introduce it to someone through direct or indirect contact (Barnes and Jinks 2008). This allows the pathogen to circulate throughout the community and find its way back into hospitals and medical centers where it can infect patients with a compromised immune system (Barnes and Jinks 2008).

Clearly MRSA is a problem in the medical community, resulting in lengthy and expensive antibiotic therapies. However phage therapy could provide a potential solution to this problem (Kvachadze et al 2011). To account for the natural diversity of MRSA, multiple phages with slightly different specificity need to be combined into a mixture or cocktail (Kutter et al 2012). This will increase the chance that one of the phages present in the cocktail will be able to destroy the strain of MRSA present in the patient (Kutter et al 2012). Phages with wider host ranges tend to be sought after, as they can be used against a broader range of MRSA strains (VinodKumar et al 2010). It is possible for MRSA to develop resistance to certain phages, in which case new phages can be created to target and destroy the new strain of MRSA. However, it should be noted that this is a very rare event, and most phage resistant MRSA strains tend to revert back to a non-phage resistant state once the phage is removed from the patient (Kvachadze et al 2011).

Figure 5. Graph of the percentage of MRSA strains, isolated from hospitalized diabetic patients, that are resistant to various antibiotics and therapies. Source: modified from data presented by Kvachadze et al. (2011)

In Georgia, phage therapy has been used for many years to treat patients infected with antibiotic resistant bacteria (Kutter et al 2012). Particularly the bacteriophage Sb-1 was found to be quite effective in eliminating MRSA infections (Kvachadze et al 2011). The Sb-1 bacteriophage was found to be effective against MRSA strains and in a case study involving a young cystic fibrosis patient infected with MRSA, treatment with the Sb-1 bacteriophage reduced MRSA levels below the limit of detection (Kvachadze et al 2011). In another study, MRSA was isolated from several hospitalized diabetic patients, and tested with a novel bacteriophage, bacteriophage Ø SH-56, isolated from a sewage treatment plant (VinodKumar et al 2010). Bacteriophage Ø SH-56 proved effective against 74% of the MRSA strains while most antibiotics had little to no effect (VinodKumar et al 2010).

With MRSA becoming ever more common in our population and the number of antibiotics capable of treating an MRSA infection quickly running out, phage therapy is becoming a very more tantalizing option for hospitals all over the world.

Comparison to antibiotics

Though phage therapy aims to do the same thing as antibiotics in treating bacterial infections, they have different mechanisms and therefore different associated advantages and disadvantages.

Advantages

Figure 6. A variety of prescribed antibiotics. Source: The GT Report http://gtreport.wordpress.com/2007/01/

One advantage of phage therapy is that phages cannot grow without their target bacteria. Therefore, once they have fulfilled their purpose and killed the pathogen, they too will die. Another advantage is they would be easy to administer orally, intravenously, or topically. Phages are also more host-specific than antibiotics, so it is less likely that there will be "collateral damage" relating to killing normal and healthy gut flora along with the pathogen (Clark and March 2006). This high specificity is also important because it reduces the potential for secondary infections to develop (Inal 2003). If administered intravenously, it is easy for the bacteriophages to spread rapidly throughout the body and they can also multiply on their own in vivo, which is important because repeated doses are therefore unlikely to be needed. This proliferation of progeny in vivo would also help in topical applications because they would be more able than antibiotics to infiltrate wounds and reach more of the bacteria (Clark and March 2006). Phages also work quickly. One study of mice infected with Vancomycin-resistant Enterococcus faecium found that if phage was injected 45 minutes after infection, 100% of the mice were saved, and after just one day all were almost back to full health (Biswas et al 2002, Figure 7).

Figure 7. Health state in Vancomycin-resistant Enterococcus faecium-infected mice treated with heat-killed phage, normal phage, and no phage over 4 days. 80% of mice treated with phage survived, while only 10% of each of the other categories survived. Source: Biswas et al 2002

The specificity of phages makes them less toxic than some antibiotics such as Vancomycin used to treat MRSA (Kutter et al 2012, Farber and Moellering 1983). Usually the levels of these antibiotics in the patient’s system are closely monitored to prevent toxicity (Farber and Moellering 1983). As a result, dosage can’t be varied to handle more resilient infections (Kutter et al 2012). These higher concentrations are occasionally required to eliminate certain bacterial infections (Kutter et al 2012). Antibiotics also kill many of the bacteria that normally live on the human body (normal flora) (Clark and March 2006). These bacteria provide us with specific vitamins and protect us from some bacterial infections. Since phages are highly specific they will not harm our cells or the normal flora, which allows us to use them in much higher concentrations (Kutter et al 2012). Since phages are viruses they are readily cleared out of our bodies by our immune system (Kutter et al 2012). This prevents them from accumulating in our bodies and possibly causing any long lasting toxicity, making phages even less toxic to our cells (Kutter et al 2012). This also presents the problem that phages can be prevented from doing their job by being cleared out by our immune system (Kutter et al 2012). This is why the majority of phage cocktails are applied directly to wounds so they won’t enter the blood stream and activate the immune system (Kutter et al 2012).

Antibiotics often have a problem reaching bacterial targets, especially if those targets have formed a biofilm that the antibiotics cannot penetrate. Some bacteriophages synthesize enzymes that allow the breakdown of these biofilms so that the interior cells can be reached and lysed (Clark and March 2006). Bacterial resistance to phages is also less of a concern than resistance to antibiotics (Inal 2003). Even if resistance develops to a bacteriophage, finding a phage that will still work against that bacteria would only take a couple of days. Phages mutate just as much or more than bacteria, so they can better keep up with the bacteria evolving resistances. This ability to continue to grow and multiply in the body is another advantage of phage therapy because while antibiotics are broken down by the body and then excreted, bacteriophages are able to continue to keep their populations up and even grow in number as long as the target bacteria is present. Another major advantage is that bacteriophages are cheap to produce and the years of experimentation in Russia and Georgia have shown almost no side effects at all (Inal 2003).

Disadvantages

There are also some disadvantages to phage therapy. For example, though they would be easy to administer orally, this may lead to a need to neutralize the stomach acid before ingesting in order to minimize damage to the phage or to the delivery bacteria, which may not be able to survive at such a low pH. For the intravenous application of bacteriophages, they may be cleared by the human immune system which would recognize tham as foreign and a possible threat. The phage would also need to be highly purified so that there is no dangerous contaminant or toxin going into the patient's circulatory system. Topical application of bacteriophages to treat infection may also have disadvantages again because of interference by the immune system and topical treatment may also require continuous treatment (Clark and March, 2006). The fact that bacteriophages are so strongly specified for their bacterial target, though in some ways an advantage, can also serve as a disadvantage (Inal 2003). This is because the exact bacteria must be diagnosed in order to use the right kind of phage. Antibiotics, on the other hand, affect a wider range of bacteria, so an exact diagnosis is not essential (Inal 2003).

A more non-scientific downside to the use of phage therapy is that due to intellectual property laws and the fact that currently its use is public, the technique of phage therapy would not be patentable. The development of drugs is very expensive and larger pharmaceutical companies have no motivation to go through the complicated and costly process is there is no patent protection on the products they may create.

The future of phage therapy

Possible novel uses

Bacteriophages can be used in many applications related to therapy besides pathogens alone (Inal 2003). For example, it may be possible to use the products of phages rather than the whole viral organism. Besides simplifying the questions related to whether the bacteriophage could survive in the complex in vivo environment of the human body, this would also be very specific to the bacterial hosts. If peptides such as lysins could be isolated from phages that do things like break down the peptidoglycan in the bacterial cell wall, then it may be possible to administer the protein alone. This would be good because many of these peptides are specific up the the subspecies level, and it has been found that the mutations that the bacteria would require to resist this lysis would also kill the bacteria (Inal 2003).

Figure 8. Representation of a T4 bacteriophage. Source: Bacteriophages and Biotechnology http://www.pharmainfo.net/luckypharmacist/bacteriophages-biotechnology

Another possible use of bacteriophages is against bacteria in agriculture and fisheries (Inal 2003). Early on, a likely application of phage therapy will be to control the outbreaks of bacterial infections in crops. Another application may be in fisheries to limit infections of the fish, crustaceans, etc. In fact, the control of fish pathogens through phage therapy is already in practice today and has been very successful. This is probably due to the fact that the liquid environments that they are placed in to be close to the fish are very close to the liquid environments where they were found. This skirts much of the issue relating to the in vivo difficulty of environment and mediates contact between the phage and the host (Inal 2003).

There is a company, OmniLytics, devoted to making products from phages that can be used in many contexts. They target bacteria in agriculture, they make products to improve food and water safety, they treat industrial equipment, they experiment with pharmaceuticals, and they even prepare for biohazard attacks such as those caused by biological weapons. This one company has been able to take the concept of bacteriophages and apply it to a variety of areas to come up with some specific and helpful innovations in many fields. For example, they received permission from the USDA to treat live poultry with bacteriophage products before butchering to cut down on Salmonella contamination (Walbeck 2008).

Obstacles

One obstacle to the widespread use of phage therapy is the public view of viruses. Since they have such a negative connotation in many cultures, it would take some education to cross that "psychological barrier" (Inal 2003). However, while there may initially be qualms about using a virus, it would probably be easy to move past once it was explained how many things actually use live viruses. For example, many of the routine vaccines given to people consist of live viruses. Additionally, viruses are everywhere, and most importantly, not all of them (indeed, most of them), will not cause people harm (Inal 2003). For example, the tagline of the company discussed previously, OmniLytics, is "Bacteriophage: The Good Virus", probably because of the negative connotation that viruses have (Walbeck 2008).

Conclusion

Bacterial resistance to antibiotics is a growing threat in our world. Though early studies of phage therapy did not produce consistently favorable results, there is reason to believe that with the enhanced understanding that we have of viral biology it is likely that bacteriophages can be a helpful therapeutic tool. Though many believe that phages will not replace antibiotics right away or maybe ever, there is definite potential for their use in conjunction with antibiotics (Clark and March 2006).

References

Barnes T., and Jinks A. "Meticillin-Resistant Staphylococcus Aureus: the Modern-Day Challenge" British Journal of Nursing,i/>, 2008, Volume 17, No 16.

Biswas, B., Adhya, S., Washart, P., Paul, B. Trostel, A.N., Powell, B., Carlton, R., and Merril, C. "Bacteriophage Therapy Rescues Mice Bacteremic from a Clinical Isolate of Vancomycin-Resistant Enterococcus faecium. Infection and Immunity. 2002. Volume 70, Number 1. p. 204-210.

Broxmeyer, L., Sosnowska, D., Miltner, E., Chacon, O., Wagner, D., McGarvey, J., Barletta, R.G., and Bermudez, L.E. "Killing of Mycobacterium avium and Mycobacterium tuberculosis by a Mycobacteriophage Delivered by a Nonvirulent Mycobacterium: A Model for Phage Therapy of Intracellular Bacterial Pathogens". The Journal of Infectious Diseases. 2002. Volume 186, Number 8. p. 1155-1160.

Carnicer-Pont, D., Bailey, K.A., Mason, B.W., Walker, A.M., Evans, M.R., Salmon, R.L. "Risk Factors for Hospital-acquired Methicillin-Resistant Staphylococcus aureus Bacteraemia:a Case-Control Study." Epidemiology and Infection. 2006. Volume 134. p. 1167-1173

Clark, J.R. and March, J.B. "Bacteriophages and biotechnology: vaccines, gene therapy and antibacterials". TRENDS in Biotechnology. 2006. Volume 24, Number 5. p. 212-218.

Enright M.C., Robinson D.A., Randle G., Feil E.J., Grundmann H., Spratt B.G. The Evolutionary History of Methicillin-Resistant Staphylococcus aureus (MRSA)” Proceedings of the National Academy of Sciences of the United States of America, 2002, Volume 99, p.7687-7692.

Farber B.F., Moellering R.C. “Retrospective Study of the Toxicity of Preparations of Vancomycin from 1974 to 1981.” Antimicrob Agents Chemother, 1983, Volume 23, Issue 1, p.138-141.

Huff, W.E., Huff, G.R., Rath, N.C., Balog, J.M., and Donoghue, A.M. "Bacteriophage Treatment of a Severe Escherichia coli Respiratory Infection in Broiler Chickens". Avian Diseases. 2003. Volume 47. p. 1399-1405.

Inal, J.M. "Phage Therapy: a Reappraisal of Bacteriophages as Antibiotics". Archivum Immunologiae et Therapiae Experimentalis. 2003. Volume 51. p. 237-244.

Kutter E., Vos D., Gvasalia G., Alavidze Z., Gogokhia L., Kuhl S., and Abedon S. "Phage Therapy in Clinical Practice: Treatment of Human Infections" Current Pharmaceutical Biotechnology, 2012, Volume 11, p.69-86.

Kvachadze L., Balarjishvili N., Meskhi T., Tevdoradze E., Skhirtladze N., Pataridze T., Adamia R., Topuria T., Kutter E., Rohde C., and Kutateladze M. "Evaluation of lytic Activity of Staphylococcal Bacteriophage Sb-1 Against Freshly Isolated Clinical Pathogens" Microbial Biotechnology, 2011, Volume 4, Issue 5, p.643-650.

"Molecular Tool: Plasmids and Phages Combine for pBluescript". http://www.bio.davidson.edu/Courses/Molbio/MolStudents/spring2003/Keogh/plasmids.html (5/14/10).

Platt, R., Reynolds, D.L., and Phillips, G.J. "Development of a novel method of lytic phage delivery by use of a bacteriophage P22 site-specific recombination system". FEMS Microbiology Letter. 2003. Volume 223. p. 259-265.

Rubinovitch B., and Pittet D. "Screening for Methicillin-Resistant Staphylococcus Aureus in the Endemic Hospital: What Have we Learned?" Journal of hospital Infection, 2001, Volume 47. p. 9-18.

Summers, W.C. "Bacteriophage Therapy". Annual Review of Microbiology. 2001. Volume 55. p. 437-451.

Untwal, Lakshya. 2008. "Bacteriophages and Biotechnology". http://www.pharmainfo.net/luckypharmacist/bacteriophages-biotechnology (5-14-10).

VinodKumar C.S., Srinivasa H., Basavarajappa K.G., Bandekar N. “Isolation of Bacteriophages for MRSA Obtained from Diabetic Foot – A Possible Treatment Option in Infections” International Journal of Biotechnology and Biochemistry, 2010, Volume 6, p.801-809.

Walbeck, Alan. 2008. "OmniLytics Announces USDA/FSIS Allowance of Bacteriophage Treatment of Salmonella on Poultry". http://www.omnilytics.com/news/news021.html (5/13/10).

Weld, R.J., Butts, C., and Heinemann, J.A. "Models of phage growth and their applicability to phage therapy". Journal of Theoretical Biology. 2004. Volume 227. p. 1-11.