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30 results about "Moraxella species" patented technology

The organisms are short rods, coccobacilli, or as in the case of Moraxella catarrhalis, diplococci in morphology, with asaccharolytic, oxidase-positive, and catalase-positive properties. M. catarrhalis is the clinically most important species under this genus.

High molecular weight major outer membrane protein of moraxella

An isolated and purified outer membrane protein of a Moraxella strain, particularly M. catarrhalis, has a molecular mass of about 200 kDa. The about 200 kDa outer membrane protein as well as nucleic acid molecules encoding the same are useful in diagnostic applications and immunogenic compositions, particularly for in vivo administration to a host to confer protection against disease caused by a bacterial pathogen that produces the about 200 kDa outer membrane protein or produces a protein capable of inducing antibodies in a host specifically reactive with the about 200 kDa outer membrane protein.
Owner:AVENTIS PASTUER LTD

DNA encoding a transferrin receptor of Moraxella

Purified and isolated nucleic acid molecules are provided which encode transferrin receptor proteins of Moraxella, such as M. catarrhalis or a fragment or an analog of the transferrin receptor protein. The nucleic acid sequence may be used to produce recombinant transferrin receptor proteins Tbp1 and Tbp2 of the strain of Moraxella free of other proteins of the Moraxella strain for purposes of diagnostics and medical treatment. Furthermore, the nucleic acid molecule may be used in the diagnosis of infection.
Owner:CONNAUGHT LAB

Nucleic acids encoding 3-ketoacyl-ACP reductase from Moraxella catarrahalis

InactiveUS6632636B1Extended half-lifeIncrease intracellular stabilitySugar derivativesBacteriaPDAT enzymeOpen reading frame
The present invention provides the genomic sequences of a library of purified nucleic acid molecules, or their complements, comprising the genome of <HIL><PDAT>Moraxella catarrhalis< / ITALIC><PDAT>. The invention also provides the identification of open reading frames contained within the nucleic acid molecules of the library. The present invention further provides for the use of the nucleic acid molecules, their complements or fragments, and proteins or portions thereof for identifying ligands and useful diagnostic and therapeutic compositions. In addition the invention provides for vectors, host cells and methods for producing <HIL><PDAT>M. catarrhalis < / ITALIC><PDAT>proteins or portions thereof.< / PTEXT>
Owner:MERCK & CO INC

High molecular weight major outer membrane protein of moraxella

InactiveUS20020068070A1Improving immunogenicitySlow and sustained releaseAntibacterial agentsVirusesDiseaseIn vivo
An isolated and purified outer membrane protein of a Moraxella strain, particularly M. catarrhalis, having a molecular mass of about 200 kDa, is provided. The about 200 kDa outer membrane protein as well as nucleic acid molecules encoding the same are useful in diagnostic applications and immunogenic compositions, particularly for in vivo administration to a host to confer protection against disease caused by a bacterial pathogen that produces the about 200 kDa outer membrane protein or produces a protein capable of inducing antibodies in a host specifically reactive with the about 200 kDa outer membrane protein.
Owner:AVENTIS PASTEUR LTD

Transferrin receptor protein of moraxella

An isolated and purified non-denatured transferrin receptor protein of a Moraxella strain, particularly M. catarrhalis, has an apparent molecular mass of about 80 to about 90 kDa, as determined by SDS-PAGE. The transferrin receptor protein or a fragment analog thereof is useful in diagnostic applications and immunogenic compositions, particularly for in vivo administration to a host to confer protection against disease caused by a strain of Moraxella. The transferrin receptor protein is isolated from strains of Moraxella catarrhalis by a procedure including extraction of agent soluble proteins of a cell mass produced by cultivating the strain under iron-starved conditions. The transferrin receptor protein is selectively solubilized from the extracted cell mass and purified.
Owner:AVENTIS PASTUER LTD

Lactoferrin receptor protein

An isolated and purified lactoferrin receptor protein is isolated and purified from bacterial pathogens, including Moraxella and Neisseria, and has a molecular weight of between about 70,000 and about 90,000, as determined by SDS-PAGE. Such lactoferrin receptor protein may be provided in combination with a lactoferrin receptor protein from the bacterial pathogen of a molecular weight of about 100,000 to about 105,000 daltons. The lactoferrin receptor protein may be produced by providing a solubilized membrane preparation from the bacterial pathogen containing lactoferrin receptor proteins, non-lactoferrin receptor proteins and other contaminants, complexing the lactoferrin receptor proteins with lactoferrin and purifying the resulting complexes substantially free from the non-lactoferrin receptor proteins and the other contaminants, and separating the novel lactoferrin receptor protein from the complexes. The lactoferrin receptor protein is useful in diagnostic applications and immunogenic compositions, particularly for in vivo administration to a host to confer protection against disease caused by a bacterial pathogen that produces the lactoferrin receptor protein or produces a protein capable of inducing antibodies in a host specifically reactive with the lactoferrin receptor protein.
Owner:AVENTIS PASTEUR LTD

Lactoferrin receptor protein

An isolated and purified lactoferrin receptor protein is isolated and purified from bacterial pathogens, including Moraxella and Neisseria, and has a molecular weight of between about 70,000 and about 90,000, as determined by SDS-PAGE. Such lactoferrin receptor protein may be provided in combination with a lactoferrin receptor protein from the bacterial pathogen of a molecular weight of about 100,000 to about 105,000 daltons. The lactoferrin receptor protein may be produced by providing a solubilized membrane preparation from the bacterial pathogen containing lactoferrin receptor proteins, non-lactoferrin receptor proteins and other contaminants, complexing the lactoferrin receptor proteins with lactoferrin and purifying the resulting complexes substantially free from the non-lactoferrin receptor proteins and the other contaminants, and separating the novel lactoferrin receptor protein from the complexes. The lactoferrin receptor protein is useful in diagnostic applications and immunogenic compositions, particularly for in vivo administration to a host to confer protection against disease caused by a bacterial pathogen that produces the lactoferrin receptor protein or produces a protein capable of inducing antibodies in a host specifically reactive with the lactoferrin receptor protein.
Owner:CONNAUGHT LAB

Lipooligosaccharide-based vaccine for prevention of i(moraxella) i(branhamella) i (catarrhalis) infections in mammals

A conjugate vaccine for Moraxella (Branhamella) catarrhalis comprising isolated lipooligosaccharide from which esterified fatty acids have been removed, to produce a detoxified lipooligosaccharide (dLOS), or from which lipid A has been removed, to produce a detoxified oligosaccharide (OS), which is linked to an immunogenic carrier. The vaccine is useful for preventing otitis media and respiratory infections caused by M. catarrhalis in mammals, including humans.
Owner:UNITED STATES OF AMERICA

Moraxella bovis cytotoxin, cytotoxin gene, antibodies and vaccines for prevention and treatment of Moraxella bovis infections

InactiveUS7220421B2Bacterial antigen ingredientsPeptide/protein ingredientsInfectious bovine keratoconjunctivitisNucleotide sequencing
Moraxella bovis cytotoxin and a gene encoding Moraxella bovis cytotoxin. Identification, isolation, cloning and identification of nucleotide sequence of the Moraxella bovis genes mbxA, mbxB, mbxC and mbxD, partial purification of the native cytotoxin, preparation of partially purified native and a recombinant Moraxella bovis cytotoxin, identification of an amino acid sequence of the cytotoxin, preparation of antibodies against the Moraxella bovis cytotoxin, preparation of vaccines against Moraxella bovis. Method for prevention and treatment of infectious bovine keratoconjunctivitis caused by Moraxella bovis.
Owner:RGT UNIV OF CALIFORNIA

Lactoferrin receptor genes of Moraxella

Purified and isolated nucleic acid molecules are provided which encode lactoferrin receptor proteins of Moraxella, such as M. catarrhalis, or a fragment or an analog of the lactoferrin receptor protein. The nucleic acid sequence may be used to produce recombinant lactoferrin receptor proteins Lbp1, Lbp2 and ORF3 of the strain of Moraxella free of other proteins of the Moraxella strain for purposes of diagnostics and medical treatment. Furthermore, the nucleic acid molecule may be used in the diagnosis of infection.
Owner:AVENTIS PASTUER LTD

Vaccine antigens of Moraxella

The present invention relates to antigens of Moraxella, in particular, Moraxella bovis, nucleic acid sequences encoding these antigens and formulations for use in raising an immune response against Moraxella.
Owner:COMMONWEALTH SCI & IND RES ORG +1

Benzimidazole derivatives and use thereof as peptide deformylase inhibitors

Benzimidazole compounds of the general formula (I) and pharmaceutically acceptable salts or esters thereof are peptide deformylase inhibitors useful in the treatment or prevention of infections and other diseases in which peptide deformylases are involved, especially in the treatment of bacterial and parasitic infections, for example infections fully or partly caused by microorganisms belonging to Staphylococcus, Enterococcus, Streptococcus, Haemophilus, Moraxella, Escherichia, Mycobacterium, Mycoplasma, Pseudomonas, Chlamydia, Rickettsia, Klebsiella, Shigella, Salmonella, Bordetella, Clostridium, helicobacter, Campylobacter, Legionella, or Neisseria.
Owner:ARPIDA AG

Isoxazoles as peptide deformylase inhibitors

Isoxazole compounds of formula (I) and pharmaceutically acceptable salts or esters thereof are peptide deformylase inhibitors useful in the treatment or prevention of infections and other disease in which peptide deformylases are involved, especially in the treatment of bacterial and parasitic infections, for example infections fully or partly caused by microorganisms belonging to Staphylococcus, Enterococcus, Streptococcus, Haemophilus, Moraxella, Escherichia, Mycobacterium, Mycoplasma, Pseudomonas, Chlamydia, Rickettsia, Klebsiella, Shigella, Salmonella, Bordetella, Clostridium, Helicobacter, Campylobacter, Legionella or Neisseria.
Owner:ARPIDA AG

Recombinant high molecular weight major outer membrane protein of Moraxella

An isolated and purified outer membrane protein of a Moraxella strain, particularly M. catarrhalis, having a molecular mass of about 200 kDa, is provided by recombinant means. The about 200 kDa outer membrane protein as well as nucleic acid molecules encoding the same are useful in diagnostic applications and immunogenic compositions, particularly for in vivo administration to a host to confer protection against disease caused by a bacterial pathogen that produces the about 200 kDa outer membrane protein or produces a protein capable of inducing antibodies in a host specifically reactive with the about 200 kDa outer membrane protein.
Owner:LOOSMORE SHEENA +3

Moraxella bovis cytotoxin, cytotoxin gene, antibodies and vaccines for prevention and treatment of moraxella bovis infections

Moraxella bovis cytotoxin, cytotoxin gene, antibodies and vaccines for prevention and treatment of Moraxella bovis infections Moraxella bovis cytotoxin and a gene encoding Moraxella bovis cytotoxin. Identification, isolation, cloning and identification of nucleotide sequence of the Moraxella bovis genes mbxA, mbxB, mbxC and mbxD, partial purification of the native cytotoxin, preparation of partially purified native and a recombinant Moraxella bovis cytotoxin, identification of an amino acid sequence of the cytotoxin, preparation of antibodies against the Moraxella bovis cytotoxin, preparation of vaccines against Moraxella bovis. Method for prevention and treatment of infectious bovine keratoconjunctivitis caused by Moraxella bovis.
Owner:RGT UNIV OF CALIFORNIA

Peptide Deformylase Inhibitors

Benzothiazine compounds of the general formula (I) and pharmaceutically acceptable salts or esters thereof are peptide deformylase inhibitors useful in the treatment or prevention of infections and other diseases in which peptide deformylases are involved, especially in the treatment of bacterial and parasitic infections, for example infections fully or partly caused by microorganisms belonging to Staphylococcus, Enterococcus, Streptococcus, Haemophilus, Moraxella, Escherichia, Mycobacterium, Mycoplasma, Pseudomonas, Chlamydia, Rickettsia, Klebsiella, Shigella, Salmonella, Bordetella, Clostridium, Helicobacter, Campylobacter, Legionella or Neisseria.
Owner:ARPIDA AG

Moraxella (Branhamella) catarrhalis antigens

InactiveUS7410645B2Antibacterial agentsFungiMedicineBranhamella
The present invention relates to polypeptides of Moraxella(Branhamella) catarrhalis which may be useful for prophylaxis, diagnosis and / or therapy purposes.1ATGGACACTG ACATGAAACA TTTAACAAAA CATCGCCTAT51CATTGGCGTT TTATTATTCA TTAGCCCATC AGTGCAAGCA101ACCATCACAC GCTAACCAGT AGCGAGCTTA AACTTGCTGATGATAGTATT151ATTGATAGTA TCAATCAATT GGGTGAGCTG ACCGTCAATATTCCAAATAC201ACAATATTTT CAAACCAACA ACGGTGTGAG CGTTGCTTTTACGCCATTAC251ATGAGCTGCC TATTGTCGAT ATCAGCTTGT ATTTTAATGCAGGGTCAGCG301TATCACCATC AGGTTGGCAA ATCAGGCACG GCTAACATGGTTGCAACCAT351GCTCACCCAA GGAACTGACA GCCTTTCTGA AGATGAGTTTGTTGCTGCCA401AAGAGCGTCT TCGCATTCAT TTTACCAGTA CAGCAAATAAGGATAACTTA451ACTTTATCAT TAAGAAGCTT GTCTGATCAA TCATTATTAAATCAAGCCGC501CGATTTAATG GTCGATGCTG TCACTCAACC TGCTTTTGATGATAAGACTC551TACAACGCAA CAAAAATCAG CTCATCACCA GTTTAAAACAAAAAAAGCAA601AACCCTTATC ATGTAGCTTC TGTTGCTTAT CATCAAGCCGTATATGAAAA651TCATCCTTAT GCACACGCAA CCACAGGCGA TGAAGATAGTATTGCCAAAA701TTGATCGTGA TGAGCTGCTT AATTTTTGGC ATACTTTTATTAATGCAAAT751AATGCGACAC TGCTGATTAC AGGTGATATG ACCGCCGAGCAAGCCAAATC801ACTTGCCAAC CATCTGACCG CCAAATTACC CACAGGCAAGTCGTATAAAA851ATACGCTGGA TTTGACAAAA CCAGTTAAGG CTCGTCATATCCATATTCCT901CACAACAGTA GTCAAACCCA AATCATCATC GGTCATCCCACCAGTAAAGT951ACGCACGGAC AAAGCAGGTC GTCAAGAGTT CAGCGATTTTTCATTAGCTA1001ATGAAATTTT GGCAGGTGGT GATTTTAATG CCAGATTGATGAAAACCATT1051CGAGAGCAAA AAGGCTACAC TTATGGCATT TATGGCGGTATGGAACGCCT1101CAGAGCAGGT GGTAATTATG TGGTTGAATT TTCAACCGATGGCGATAAAG1151CAGCCGATGC CATTTTAGAG ACGCTACACA TCATTAATCAGTCGCTGAAT1201GAAGGCATAA CCCAAGAAGA GCTTGAGTTG GTGCGTTTGGGCAATAAAAA1251TGGTTTTGCC AATATTTTTT CAAGCAATGC CAGTATTCATCGTGTCATTC1301GTGCTTTATT TGTTGCCGAT TATCCAAAAG ATCATCTTAACCATACGCTC1351AATCGCTTGG ATAATGCCAC GATAAATAGT GTTAATACCGCACTGAACTT1401GCGTATCAAG CCTGATGAAT TTATCATCAT CACCGTGGGTAAAACTAAGC1451CAAATTTGGA CAAATAA
Owner:ID BIOMEDICAL
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