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1.
Int J Syst Evol Microbiol ; 50 Pt 1: 83-89, 2000 Jan.
Article in English | MEDLINE | ID: mdl-10826790

ABSTRACT

A new Pseudomonas species, for which the name Pseudomonas plecoglossicida is proposed, was isolated from cultured ayu (Plecoglossus altivelis) with bacterial haemorrhagic ascites. The causative agent was similar to Pseudomonas putida biovar A in its phenotypic characteristics and on the basis of 16S rRNA gene sequence analysis, but it reduced nitrate to nitrite. Furthermore, it was distinguished phenotypically from Pseudomonas putida biovar A by utilization of D-malate, L-(+)-tartrate, m-tartrate and nicotinate. The levels of DNA-DNA hybridization between the isolate strain FPC 951T and other reference strains of Pseudomonas species, including Pseudomonas putida, were less than 50%. The G+C content of the DNA of FPC 951T was 62.8 mol%. Strain FPC 951T (= ATCC 700383T) is designated the type strain of the new species.


Subject(s)
Fish Diseases/microbiology , Pseudomonas Infections/veterinary , Pseudomonas/classification , Animals , Ascites/microbiology , Ascites/veterinary , Base Composition , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , DNA, Ribosomal/chemistry , DNA, Ribosomal/genetics , Fishes , Genes, rRNA , Hemorrhage/microbiology , Hemorrhage/veterinary , Molecular Sequence Data , Nucleic Acid Hybridization , Phenotype , Phylogeny , Pseudomonas/genetics , Pseudomonas/physiology , Pseudomonas Infections/microbiology , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNA
2.
J Periodontal Res ; 33(4): 196-204, 1998 May.
Article in English | MEDLINE | ID: mdl-9689615

ABSTRACT

This study examined the efficacy of YM175 [disodium dihydrogen (cycloheptylamino) methylene-1, 1-bisphosphonate] in reducing alveolar bone loss caused by experimental periodontitis in beagle dogs. Thirty-six dogs were used and divided into 6 groups. Periodontitis was induced in 30 dogs (groups 2-6) by ligating the bilateral mandibular third and fourth premolar teeth with silk ligatures and by feeding a soft diet. Six dogs were sham-operated (group 1). Saline (placebo), flurbiprofen (0.02 mg/kg) and YM175 (0.01, 0.1 and 1.0 mg/kg) were administered to the dogs (groups 2-6) 5 d/wk for 25 wk. Radiographic and morphometric analyses were performed. In placebo-treated animals (group 2), the ligation caused a significant decrease in the alveolar bone height by 0.57 and 1.91 mm at 2 and 25 wk, respectively. YM175 (1.0 mg/kg) prevented the decrease in bone height by 47 and 31% at 2 and 25 wk. YM175 (0.1 mg/kg) and flurbiprofen tended to prevent bone loss after 15 wk. Although the ligation elicited no significant change in bone mineral density, it significantly decreased bone volume. YM175 (1.0 mg/kg) and flurbiprofen tended to increase the bone volume. The number of formative or resorptive Haversian canals and the bone turnover through the periosteal bone surface were increased by the ligation, indicating the increased turnover of the cortical bone. YM175 (1.0 mg/kg) reduced the increased bone turnover. The gingival index was maximally increased at 2 wk and was suppressed by YM175. These results suggest that YM175 prevents alveolar bone loss by reducing the increased alveolar bone turnover in dogs with periodontitis.


Subject(s)
Alveolar Bone Loss/prevention & control , Diphosphonates/therapeutic use , Periodontitis/drug therapy , Alveolar Bone Loss/diagnostic imaging , Alveolar Bone Loss/metabolism , Alveolar Bone Loss/physiopathology , Alveolar Process/diagnostic imaging , Alveolar Process/drug effects , Alveolar Process/metabolism , Analysis of Variance , Animals , Anti-Inflammatory Agents, Non-Steroidal/administration & dosage , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Bicuspid , Bone Density , Diphosphonates/administration & dosage , Disease Progression , Dogs , Female , Flurbiprofen/administration & dosage , Flurbiprofen/therapeutic use , Haversian System/drug effects , Haversian System/metabolism , Mandible , Osteogenesis/drug effects , Periodontitis/diagnostic imaging , Periodontitis/metabolism , Periodontitis/physiopathology , Periosteum/drug effects , Periosteum/metabolism , Placebos , Radiography , Sodium Chloride
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