Pseudomonas aeruginosa: bacteriophage and uses thereof
AssigneeIntralytix, Inc.
InventorsAlexander Sulakvelidze, Gary R. Pasternack
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Abstract
The present invention is directed to isolated bacteriophage having strong lytic activity against strains of Pseudomonas aeruginosa, and methods of using that bacteriophage, and/or progeny or derivatives derived therefrom, to control the growth of Pseudomonas aeruginosa in various settings.
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Claims4
An isolated bacteriophage PAML-2, PAML-14, PAML-20, PAML22, PAML31-1, PAML-73, or PAML-75 deposited under ATCC accession Nos. PTA-8358, PTA-8359, PTA-8360, PTA-8361PTA-8362, PTA-8363, and PTA-8364 respectively and variants thereof, wherein said variants have the same phenotypic characteristics of said bacteriophage and said bacteriophage and variants thereof have the same lytic activity against Pseudomonas aeruginosa strains.
18 Jun 2027Estimated · howhide20 years from earliest known nonprovisional domestic filing plus recorded patent term adjustment. Maintenance-fee lapses, terminal disclaimers and statutory extensions have not been checked. The continuity chain may be incomplete; this is not an enforceability determination.
About 8 months of term left · ends 18 Jun 2027 (estimated)
Priority18 Jun 2007
Granted24 Nov 2009
Today12 Oct 2026
Term ends18 Jun 2027
Priority18 Jun 2007
Granted24 Nov 2009
Term ends18 Jun 2027
Application filedUS 11/764,608
Assigned to Intralytix, Inc.assignment of assignor's interest
PublishedUS 2008/0311643 A1
GrantedUS 7,622,293 B2
TodayWithin its term
Term endsEstimated
Description7,917 words
Summary997 words
#The present invention relates to a novel bacteriophage designated PAML-2, PAML-14, PAML-20, PAML-22, PAML-31-1, PAML-73 AND PAML-75 (the “Deposited bacteriophage”), and compositions and preparations corresponding thereto. More specifically, isolated bacteriophage preparations possessing lytic activity against strains of Psuedomonas aeruginosa (the “Targeted Bacteria”) are provided in order to control the growth of the Targeted Bacteria, which will reduce their ability to contaminate and colonize various environments, including but not limited to (i) raw, unprocessed food products, (ii) equipment used to process or manufacture various food products, (iii) various food products processed or manufactured with equipment contaminated with the Targeted Bacteria, (iv) animals contaminated with the Targeted Bacteria, and (v) animal environments contaminated with the Targeted Bacteria. The invention also provides methods for detecting the presence of the Targeted Bacteria in processed or unprocessed food products, and in equipment used to process or manufacture the food products. In addition, the invention provides methods of using the Deposited bacteriophage to remove the Targeted Bacteria from medical, veterinary, animal husbandry, and other environments where they may be passed to humans or animals. Also, the invention additionally provides methods of using the bacteriophage to prevent and treat animal and human diseases caused by the Targeted Bacteria.
#Bacteriophages are bacterial viruses that attach to their specific hosts and kill them by internal replication and bacterial lysis involving a complex lytic cycle involving several structural and regulatory genes. Phages are very specific in that they only attack their targeted bacterial hosts. They cannot infect human or other eukaryotic cells. Bacteriophages were first identified, in the early part of the 20th century by Frederick Twort and Felix D'Herelle who called them bacteriophages or bacteria-eaters (from the Greek phago meaning to eat or devour) (Duckworth, D. H. (1976). Who discovered bacteriophage? Bacteriol Rev 40(4): 793-802; Summers, W. C. (1999). Bacteriophage discovered. Felix d'Herelle and the origins of molecular biology. New Haven, Conn., Yale University Press: 47-59). At that time, with the age of antibiotics still in the future, bacteriophages were considered to be a potentially powerful cure for bacterial infections, and they were therapeutically utilized throughout the world during the pre-antibiotic era. The use of phages in humans was found to be very safe; however, phage therapy did not always work and, with the advent of antibiotics that were effective against a broad spectrum of pathogenic bacteria, it gradually fell out of favor in the United States and Western Europe. Several factors (reviewed in more detail in Sulakvelidze, A., Z. Alavidze, et al. (2001). Bacteriophage therapy. Antimicrob Agents Chemother 45(3): 649-659; Summers, W. C. (2001). Bacteriophage therapy. Ann Rev Microbiol 55: 437-51), including the lack of a broad understanding of phage biology and inadequate diagnostic bacteriology techniques, contributed to the failure of some of the early phage therapy studies and to the associated decline of interest in phage therapy in the West. At the same time, phage therapy continued to be utilized in the former Soviet Union and Eastern Europe, where phage therapy still is being used to treat a wide range of bacterial diseases ranging from intestinal infections to septicemia. Comprehensive information about human and veterinary applications of bacteriophages has been recently reviewed by several investigators (Alisky, J., K. Iczkowski, et al. (1998). Bacteriophages show promise as antimicrobial agents. J Infect 36(1): 5-15; Summers, W. C. (2001). Bacteriophage therapy. Annu Rev Microbiol 55: 437-51; Merril, C. R., D. Scholl, et al. (2003). “The prospect for bacteriophage therapy in Western medicine.” Nat Rev Drug Discov 2(6): 489-497; Sulakvelidze, A. and P. Barrow (2005). Phage therapy in animals and agribusiness. Bacteriophages: Biology and Applications. E. Kutter and A. Sulakvelidze. Boca Raton, Fla., CRC Press: 335-380; Sulakvelidze, A. and E. Kutter (2005). Bacteriophage therapy in humans. Bacteriophages: Biology and Application. E. Kutter and A. Sulakvelidze. Boca Raton, Fla., CRC Press: 381-436).
#Despite the use of bacteriophage in various practical settings, including the treatment of diseases in various animals, there remains in the art a need for the discovery of novel bacteriophages, selection of optimal bacteriophages for specific practical applications, and identifying methods for using these bacteriophages in several critical areas, including clinical applications, food safety-related uses and environmental decontamination. For example, one significant need concerns the treatment of processed or unprocessed food products to reduce, eliminate or prevent colonization with undesirable bacteria such as pathogens responsible for food-borne illness and food spoilage organisms. A second critical area of need concerns the removal of undesirable bacteria from industrial environments such as food processing facilities to prevent colonization thereof. A third critical area of need concerns the removal of antibiotic resistant organisms from environments where they may be passed to susceptible humans and animals, such as hospitals, nursing homes, veterinary facilities, and other such environments. Additionally, new bacteriophage and methods of using the same are needed for the prevention or treatment of animal and human bacterial disease, particularly those diseases caused by antibiotic-resistant organisms.
#FIG. 1 shows a Restriction Fragment Length Polymorphism (RFLP) profile of the PAML-2, PAML-14, PAML-20, PAML-22, PAML-31-1, PAML-73 AND PAML-75 bacteriophage in comparison to four other bacteriophages also specific for the Targeted Bacteria.
Detailed description6,886 words
#Table 1 shows the lytic specificity of the bacteriophage for Pseudomonas aeruginosa, the Targeted Bacteria.
#As used herein, “isolated” will mean material removed from its original environment in which it naturally occurs, and thus is altered by the hand of man from its natural environment. Isolated material may be, for example, foreign nucleic acid included in a vector system, foreign nucleic acid contained within a host cell, or any material which has been removed from its original environment and thus altered by the hand of man. Isolated material further encompasses bacteriophage specific for the Targeted Bacteria or particular Targeted Bacteria isolates, isolated and cultured separately from the environment in which it was located, where these isolates are present in purified compositions that do not contain any significant amount of other bacteriophage or bacterial strains, respectively.
#As used therein, “Deposited bacteriophage” will mean isolated bacteriophage PAML-2, PAML-14, PAML-20, PAML-22, PAML-31-1, PAML-73 AND PAML-75 deposited with the ATCC on Apr. 19, 2007, and receiving ATCC Deposit Accession Nos. PTA-8358, PTA-8359, PTA-8360, PTA-8361, PTA-8362, PTA-8363 and PTA-8364.