IP Library Granted Patent US 8,361,772
Granted Patent B2
US 8,361,772 · App. 13/192,150 · Granted Jan 29, 2013

Specific lysis of staphylococcal pathogens by bacteriophage phi11 endolysin

Inventor: David M. Donovan (Baltimore, MD)
Assignee: The United States of America as Represented by the Secretary of Agriculture
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Quick Facts
Patent No.
US 8,361,772
App. No.
13/192,150
Granted
Jan 29, 2013
Kind
B2
Abstract

The Staphylococcus aureus bacteriophage phi11 endolysin has two peptidoglycan hydrolase domains (endopeptidase and amidase) and a SH3b cell wall-binding domain. In turbidity reduction assays, the purified protein can lyse untreated staphylococcal mastitis-causing pathogens, S. aureus and coagulase negative staphylococci ( S. chronogenes, S. epidermis, S. hyicus, S. simulans, S. warneri , and S. xylocus ), making it a strong antimicrobial protein and an effective candidate for treating multidrug-resistant staphylococci. Lytic activity is maintained at the pH (6.7) and the ‘free’ calcium concentration (3 mM) of milk. Truncated endolysin-derived proteins, containing just the endopeptidase domain, also lyse staphylococci, in the absence of the SH3b-binding domain.

Claims (8)

1. An isolated antimicrobial peptidogiycan hydrolase protein wherein said protein is a truncated phi11 peptidoglycan hydrolase having an endopeptidase domain and an amidase domain and lacking a SH3b binding domain, and said truncated phi11 peptidoglycan hydrolase has the sequence set forth in SEQ ID NO 5.

2. An isolated antimicrobial peptidoglycan hydrolase protein wherein said protein is a truncated phi11 peptidoglycan hydrolase having an endopeptidase domain and lacking a SH3b binding domain, and said truncated phi11 peptidoglycan hydrolase has the sequence set forth in SEQ ID NO: 6.

3. A composition useful for the treatment of a disease caused by multidrug-resistant staphylococci, wherein said composition comprises the protein of claim 1 and a pharmaceutically acceptable carrier.

4. A composition useful for the treatment of a disease caused by muitidrug-resistant staphylococci, wherein said composition comprises the protein of claim 2 and a pharmaceutically acceptable carrier.

5. A method of treating infection end disease caused by multidrug-resistant staphylococci in an individual comprising:

administering to said individual an effective dosage of a composition of claim 3 or claim 4 , wherein said composition comprises an isolated peptidoglycan hydrolase protein having specificity and exolytic activity for the peptidoglycan cell wall of untreated staphylococci and wherein said administration is effective for the treatment of said multidrug-resistant staphylococci.

6. A method of treating mastitis in an animal comprising:

administering to said animal an effective dosage of a composition of claim 3 or claim 4 , wherein said composition comprises an isolated peptidoglycan hydrolase protein having specificity and exolytic activity for the peptidoglycan cell wall of mastitis-causing bacteria wherein said mastitis-causing bacteria are untreated Staphylococcus aureus and coagulase negative staphylococci (CNS), said CNS comprising S. chronogenes, S. epidermis, S. hyicus, S. simulans. S. wameri , and S. xyiocus and wherein said administration is effective for reducing the severity of said mastitis.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 18, 2013
From: DONOVAN, DAVID M.
To: THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY OF AGRICULTURE
Reel/Frame 029655/0126 →
Continuity (2)
Division 11511848 · Aug 29, 2006
Related Publication 20110318328A1 · Dec 29, 2011