US2014242051A1PendingUtilityA1

Probiotic, Lactic Acid-Producing Bacteria and Uses Thereof

Assignee: GANEDEN BIOTECH INCPriority: Aug 24, 1998Filed: Feb 26, 2014Published: Aug 28, 2014
Est. expiryAug 24, 2018(expired)· nominal 20-yr term from priority
Inventors:Sean Farmer
A61P 43/00A61P 31/12A61P 31/10A61P 31/00A61P 33/00A61P 31/04A61K 31/704A61K 35/742A61K 31/65A61K 38/14A61K 35/747A61P 1/04A61K 31/545A61P 1/00A61K 31/7048A61K 31/496A61K 31/43A61K 35/745A61K 45/06C12R 2001/07C12N 1/205Y02A50/30
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Claims

Abstract

The present invention discloses compositions and methodologies for the utilization of probiotic organisms in therapeutic compositions. More specifically, the present invention relates to the utilization of one or more species or strains of lactic acid-producing bacteria, preferably strains of Bacillus coagulans , for the control of gastrointestinal tract pathogens, including antibiotic-resistant gastrointestinal tract pathogens, and their associated diseases by both a reduction in the rate of colonization and the severity of the deleterious physiological effects of the colonization of the antibiotic-resistant pathogen.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method for reducing gastrointestinal colonization by a pathogenic  Clostridium  bacterium, comprising identifying a mammalian subject having an infection with said pathogenic  Clostridium  bacterium, and orally administering a therapeutically-effective concentration of  Bacillus coagulans  bacteria within a pharmaceutically-acceptable carrier suitable for administration to the gastrointestinal tract of said subject, and further comprising the administration of an antibiotic, wherein the  Bacillus coagulans  bacteria reduce colonization of the pathogenic  Clostridium  bacteria. 
     
     
         2 . The method of  claim 1 , wherein the  Clostridium  bacterium is selected from the group consisting of  C. difficile, C. perfringes, C. sporogenes, C. botulinum , and  C. tributrycum.    
     
     
         3 . The method of  claim 1 , wherein the bacteria are resistant to the antibiotic. 
     
     
         4 . The method of  claim 1 , wherein the antibiotic is selected from the group consisting of a macrolide antibiotic, a cephalosporin antibiotic, a penicillin antibiotic, a fluoroquinolone antibiotic, and a vancomycin antibiotic. 
     
     
         5 . The method of  claim 1 , wherein the antibiotic is selected from the group consisting of gentamicin, vancomycin, oxacillin, a tetracyclines, nitroflurantoin, chloramphenicol, clindamycin, trimethoprim-sulfamethoxasole, cefaclor, cefadroxil, cefixime, cefprozil, ceftriaxone, cefuroxime, cephalexin, loracarbef, ampicillin, amoxicillin/clavulanate, bacampicillin, cloxicillin, penicillin VK, ciprofloxacin, grepafloxacin, levofloxacin, lomefloxacin, norfloxacin, ofloxacin, sparfloxacin, trovafloxacin, azithromycin, and erythromycin. 
     
     
         6 . The method of  claim 1 , wherein the bacteria are in the form of spores. 
     
     
         7 . The method of  claim 1 , wherein the  Bacillus coagulans  is  B. coagulans  Hammer strain deposited under ATCC accession number 31284. 
     
     
         8 . The method of  claim 1 , wherein approximately 2.5×10 8  to approximately 1×10 10  viable  Bacillus coagulans  bacteria or spores are administered per day. 
     
     
         9 . The method of  claim 1 , wherein said mammalian subject is a human.

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