Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0348321 (Haemophilus)
 15,372 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Bacteria of the species B. parapertussis and B. bronchiseptica have proved to be identical in their fatty-acid composition with a high level (35.7-39%) of methylene-hexadecanoic acid, found to be absent in B. pertussis in experimental conditions. At the same time the total content of methylene-hexadecanoic acid and its biosynthetic precursor, hexadecenoic acid, in the first two Bordetella species is similar to the content of hexadecenoic acid in B. pertussis, which, along with the presence of common characteristics in the sign under consideration (the low level of C18:1), indicates the close relationship of these three Bordetella species. Bacteria of the species H. influenzae, H. parainfluenzae, H. aegyptius, H. aphrophilus have similar fatty-acid composition with the prevalence of hexadecanoic and hexadecenoic acids and the low level of fatty acids with 18 carbon atoms. The data on fatty-acid composition may suggest the presence of philogenetic links between the genera Bordetella and Haemophilus.
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PMID:[Taxonomic significance of the fatty acid composition of bacteria of the genera Bordetella and Haemophilus]. 632 84

Haemophilus influenzae type b remains the major cause of bacterial meningitis in infants and children. Serum antibodies against the capsular polysaccharide--polyribosylribitolphosphate (PRP)--are protective, but its immunogenicity is poor in children under two years of age. Clinical trials actually in progress concerning an association of PRP with Bordetella pertussis are presented. Other vaccinal preparations are possible, such outer membrane protein, but prospects offered by polysaccharide-protein conjugates appear as the most encouraging.
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PMID:[Prospects for the vaccinal prevention of Haemophilus influenzae type b meningitis]. 634 45

Microbicidal cationic proteins 1 and 2, peptides derived from rabbit lung macrophages, were tested for bactericidal activity against various bacterial species. Both were highly active against diverse gram-positive and gram-negative organisms under conditions of near-neutral pH (between 7 and 8) and relatively low ionic strength. Susceptible species included Staphylococcus aureus, Staphylococcus epidermidis, Streptococcus pneumoniae, Listeria monocytogenes, Pseudomonas aeruginosa, Klebsiella pneumoniae, Haemophilus influenzae, Escherichia coli, and Serratia marcescens. Streptococcus agalactiae, type 1A, was less susceptible than the aforementioned organisms or S. agalactiae, type 3. Bordetella bronchiseptica, a common commensal and pathogen of the rabbit respiratory tract, was completely resistant to both peptides.
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PMID:Antibacterial activity of microbicidal cationic proteins 1 and 2, natural peptide antibiotics of rabbit lung macrophages. 641 8

Cefpiramide (CPM, SM-1652) had broad-spectrum antibacterial activities against most of clinically isolated organisms to which are paid attention as pathogenic organism in the field of pediatrics. Antibacterial activities of CPM against Staphylococcus aureus, Streptococcus pyogenes, Haemophilus influenzae, Bordetella pertussis and Proteus mirabilis were almost the same as those of cefoperazone (CPZ). Antibacterial activities of CPM against Escherichia coli and Klebsiella pneumoniae were somewhat weaker than those of CPZ, but antibacterial activity of CPM against Pseudomonas aeruginosa was rather stronger than that of CPZ and almost the same as that of cefsulodin. Antibacterial activity of CPM has a tendency to decrease in beta-lactamase (PCase type) producing S. aureus, E. coli, K. pneumoniae, H. Influenzae, etc. It is suggestive that the determination of not only the antibacterial activity of CPM against pathogenic organisms but also the beta-lactamase producing activity of them is important on the occasion of clinical use of CPM.
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PMID:[Susceptibility of clinical isolates in pediatrics to cefpiramide]. 665 31

Porcine tracheal and bronchial explant cultures exposed to log-phase cultures of Bordetella, Candida, Corynebacterium, Haemophilus, Klebsiella, Mycoplasma, Pasteurella, Proteus, Saccharomyces, Staphylococcus and Streptococcus were examined for surface sequential changes by scanning electron and light microscopy. Infected tissues, observed microscopically, had diminution or cessation of ciliary activity, and histologically had exfoliation of cilia, ciliocytophthoria, elevation of cellular borders, and cellular detachment. Treatment of these tissues with sterile medium containing penicillin and streptomycin did not prevent death or alteration of cells with increasing periods of incubation. The potential value of using scanning electron microscopy with explant cultures for studying organization of cellular surfaces in association with microbial growth and pathogenesis was demonstrated.
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PMID:Effects of microbial isolates on porcine tracheal and bronchial explant cultures as observed by scanning electron microscopy. 675 Jul 64

At the Mayo Clinic, 56 patients with infective endocarditis caused by gram-negative bacteria were seen from 1958 through 1979, 35 of whom were seen from 1970 through 1979. The patients were categorized into two divisions: those with medical, naturally acquired valve infections (40 [71%]) and those with infective endocarditis after cardiac operation (16 [29%]). The overall cure rate was 82% (46 of 56 patients); 35 of 40 patients (88%) were cured in the medical group, and 11 of 16 patients (69%) were cured in the surgical group. The patients were further classified on the basis of organism: group 1 (33 patients)--infections caused by Haemophilus (18), Actinobacillus actinomycetemcomitans (4), Cardiobacterium hominis (6), Eikenella corrodens (2), Kingella kingii (2), and Bordetella bronchiseptica (1); 32 of these 33 patients (97%) were cured, and 6 of these infections were on prosthetic valves; group 2 (21 patients)--infections caused by enteric aerobic bacilli; 13 of the 21 patients (62%) were cured; group 3 (1 patient)--infection caused by anaerobes (Bacteroides fragilis); this patient died; and group 4 (1 patient)--infection caused by Neisseria gonorrhoeae; this patient was cured. The gram-negative bacteria in the survivors and nonsurvivors and the curative antibiotic regimens were tabulated. Among the 35 survivors in the medical group, a combined antibiotic regimen cured 21 patients (60%) and a single antibiotic agent cured 14 (40%). Among the 11 survivors in the surgical group, combined therapy was given to 8 (73%), a single drug was used once, and operation alone achieved a cure in 2 patients. Compared with past data, the current study indicates an increasing incidence of gram-negative bacterial endocarditis (approximately 10%) and an improving cure rate 82%).
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PMID:Symposium on infective endocarditis. III. Endocarditis due to gram-negative bacteria. Report of 56 cases. 706 78

Since its discovery in 1947, chloramphenicol has enjoyed a prominent place in the veterinarian's drug arsenal. Some of the reasons for its popularity are: (1) Antimicrobial activity--effective against a variety of infective pathogens, including staphylococci, salmonellae, pasturellae, Bordetella, Haemophilus, coliform organisms, chlamydiae, and rickettsiae, many of which may be resistant to other antimicrobial agents; (2) Kinetic properties--allowing production and maintenance of effective therapeutic concentrations in body fluids and tissues, with a practicable dosage schedule in most species; (3) Safety--toxic reactions to chloramphenicol encountered thus far in animals have not warranted any serious limitations on its use in veterinary medicine.
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PMID:Pharmacotherapeutics of chloramphenicol in veterinary medicine. 721 74

Nasopharyngeal cultures from 180 children aged 1 to 9 were examined. All children were suffering from cough for at least 10 days. The findings were compared to those from 67 non-coughing children. Bordetella pertussis was isolated from 12.2% of the children in the study group but from none of the control children. Branhamella catarrhalis was isolated from 66.1% of the children in the study group and from 28.3% in the control group (p less than 0.01). Br. catarrhalis was more common in pure cultures from sick children than from control children. Pneumococci were isolated from 20% of the sick children and 28% of the control children. Haemophilus influenzae was isolated from 15% in each group. Some possible interpretations of the findings are discussed.
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PMID:Branhamella catarrhalis and other bacteria in the nasopharynx of children with longstanding cough. 731 64

In addition to Ipa proteins and IcsA, which are involved in entry into epithelial cells and intercellular spread, respectively, Shigella secretes a 110 kDa protein, designated SepA. We report the identification, cloning, and nucleotide sequence determination of the sepA gene, analysis of SepA secretion, and construction and characterization of a sepA mutant. The sepA gene is carried by the virulence plasmid and codes for a 150 kDa precursor. Upon secretion, which does not involve accessory proteins encoded by the virulence plasmid, the precursor is converted to a mature protein of 110 kDa by two cleavages removing an N-terminal signal sequence and a C-terminal fragment. Extensive similarities were detected between the sequence of the first 500 residues of mature SepA and the N-terminal region of IgA1 proteases from Neisseria gonorrhoeae and Haemophilus influenzae, the Tsh haemagglutinin of an avian pathogenic Escherichia coli, and the Hap protein involved in adhesion and penetration of H. influenzae. The C-terminal domain of the SepA precursor, which is not present in the secreted protein, exhibits sequence similarity with pertactin of Bordetella pertussis and the ring-forming protein of Helicobacter mustelae. Construction and phenotypic characterization of a sepA mutant indicated that SepA is required neither for entry into cultured epithelial cells nor for intercellular dissemination. However, in the rabbit ligated ileal loop model, the sepA mutant exhibited an attenuated virulence, which suggests that SepA might play a role in tissue invasion.
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PMID:SepA, the major extracellular protein of Shigella flexneri: autonomous secretion and involvement in tissue invasion. 747 98

A murine monoclonal antibody, MAHI 3 (immunoglobulin G2b), that is broadly reactive with Haemophilus influenzae lipopolysaccharides (LPSs) but nonreactive with all enterobacterial LPSs tested was generated by fusing mouse myeloma cells with spleen cells of BALB/c mice immunized with azide-killed H. influenzae RM.7004. MAHI 3 bound to all H. influenzae, all other human Haemophilus spp., all Bordetella pertussis and Bordetella parapertussis, and all Aeromonas spp. tested but not to any Neisseria or Moraxella catarrhalis strains, as determined by enzyme immunoassay, colony dot immunoblotting, and immunoblotting. In an inhibition enzyme immunoassay, MAHI 3 reacted with all 45 H. influenzae LPSs tested but not with the LPS from the rough mutant I69 Rd-/b+, which has only 3-deoxy-D-manno-octulosonic acid (P) [Kdo(P)] and lipid A. The antibody was not inhibited by H. influenzae lipid A or lipid-free polysaccharide isolated after mild acid hydrolysis. Only native LPSs show positive inhibitory activity, indicating that part of lipid A is involved in the binding of MAHI 3. From the results, it is indicated that the structural element recognized by MAHI 3 is Hep alpha 1-->2Hep alpha 1-->3Hep alpha 1-->Kdo together with part of lipid A, including the phosphate.
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PMID:The tetrasaccharide L-alpha-D-heptose1-->2-L-alpha-D-heptose1--> 3-L-alpha-D-heptose1-->(3-deoxy-D-manno-octulosonic acid) and phosphate in lipid A define the conserved epitope in Haemophilus lipopolysaccharides recognized by a monoclonal antibody. 754 87


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