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1.
Microbiol Immunol ; 60(5): 303-11, 2016 May.
Article in English | MEDLINE | ID: mdl-26970508

ABSTRACT

Multilocus sequence analysis based on hypervariable housekeeping proteins was utilized to differentiate closely related species in the family Enterobacteriaceae. Of 150 housekeeping proteins, the top 10 hypervariable proteins were selected and concatenated to obtain distance data. Distances between concatenated proteins within the family were 0.9-41.2%, whereas the 16S rRNA and atpD-gyrB-infB-rpoB concatenated sequence (4MLSA) distances were 0.8-6.0% and 0.9-22.1%, respectively. These data indicate that phylogenetic analysis by concatenation of hypervariable proteins is a powerful tool for discriminating species in the family Enterobacteriaceae. To confirm the discriminatory power of the 10 chosen concatenated hypervariable proteins (C10HKP), phylogenetic trees based on C10HKP, 4MLSA, and the 16S rRNA gene were constructed. Comparison of average bootstrap values among C10HKP, 4MLSA and 16S rRNA genes indicated that the C10HKP tree was the most reliable. Location via the C10HKP tree was consistent with existing assignments for almost all species in the family Enterobacteriaceae. However, the C10HKP tree suggested that several species (including Enterobacter massiliensis, Escherichia vulneris, Escherichia hermannii, and Salmonella subterranea) should be reassigned to different clusters than those defined in previous analyses. Furthermore, E. hermannii and S. subterranea appeared to fall onto a branch independent from those occupied by the other Enterobacteriaceae. Therefore, we propose Atlantibacter gen. nov., such that E. hermannii and S. subterranea would be transferred to genus Atlantibacter as Atlantibacter hermannii, comb. nov. and Atlantibacter subterranea. comb. nov., respectively.


Subject(s)
Enterobacteriaceae/classification , Enterobacteriaceae/genetics , Multilocus Sequence Typing , Phylogeny , Bacterial Proteins/genetics , Cluster Analysis , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , DNA, Ribosomal/chemistry , DNA, Ribosomal/genetics , Genes, Essential , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNA
2.
Jpn Hosp ; (34): 55-65, 2015 Jul.
Article in English | MEDLINE | ID: mdl-26373188

ABSTRACT

The "Social Healthcare Corporation" system was established on 1 April 2007 as a result of the revised Japanese Medical Care Law. As of 1 October 2014, 234 corporations are certified Social Healthcare Corporations. These corporations are allowed to issue public bonds. However, to this day (1 December 2014), no bonds have been issued. In this paper, we focus on cost analysis with respect to issuing public bonds.


Subject(s)
Delivery of Health Care/economics , Investments/economics , Organizations, Nonprofit , Costs and Cost Analysis , Hospital Administration , Japan
3.
J Antimicrob Chemother ; 56(5): 861-8, 2005 Nov.
Article in English | MEDLINE | ID: mdl-16172105

ABSTRACT

OBJECTIVES: Chlamydiae are obligate intracellular bacteria, causing a variety of diseases, i.e. pneumonia, sexually transmitted disease, conjunctivitis and zoonosis. Tryptophan depletion by interferon-gamma (IFN-gamma) is the most important host defence system against chlamydial infection. Thus chlamydial tryptophan metabolism is thought to play key roles for IFN-gamma resistance, persistent infection and host/tissue tropisms. We tested tryptophan derivatives for activity against chlamydia-infected cells. METHODS: Rates of chlamydial infection and sizes of the inclusions were evaluated by in vitro infection using three Chlamydiaceae species, Chlamydia trachomatis, Chlamydophila pneumoniae and Chlamydophila felis, which show significant divergence of tryptophan synthesis genes and different susceptibilities to IFN-gamma. RESULTS: Melatonin and serotonin, which are recognized as neural hormones for maintenance of organism homeostasis, reduced chlamydial infection but not other bacterial growth tested here. Unlike IFN-gamma, melatonin limited infection of all three chlamydiae and the effects were not recovered by tryptophan supplementation. Melatonin treatment only of host cells could diminish infection and the infection reduction was neutralized by a pertussis toxin, an inhibitor of G proteins. Ligands of melatonin and serotonin receptors also hampered infection. CONCLUSIONS: Inhibition mechanisms of chlamydial infection by melatonin and serotonin appear to be different from those of IFN-gamma and involve specific G-protein-coupled receptors. Melatonin is deemed to inhibit early progression of the chlamydial development cycle, such as establishment of intracellular infection and/or conversion from elementary body to reticulate body. Utilization of melatonin, serotonin or their derivatives may be advantageous for harmless prevention of chlamydial infection.


Subject(s)
Anti-Bacterial Agents/pharmacology , Chlamydia/drug effects , Melatonin/pharmacology , Serotonin/pharmacology , Cell Line, Tumor , Chlamydia/growth & development , Chlamydia trachomatis/drug effects , Chlamydia trachomatis/growth & development , Chlamydophila pneumoniae/drug effects , Chlamydophila pneumoniae/growth & development , Humans , Inclusion Bodies , Interferon-gamma/pharmacology , Pertussis Toxin/toxicity , Receptors, G-Protein-Coupled/drug effects , Receptors, G-Protein-Coupled/physiology , Tryptophan/biosynthesis
4.
Respir Med ; 97(8): 933-8, 2003 Aug.
Article in English | MEDLINE | ID: mdl-12924521

ABSTRACT

It has been argued whether bronchiectasis is truly caused by MAC infection or just a predisposed condition in which MAC colonizes. Our present study was designed to evaluate the pathological findings of bronchiectases caused by Mycobacterium avium intracellulare complex (MAC) lung infection and to demonstrate MAC in the lesion of bronchiectases. A retrospective study was performed in nine cases with positive cultures for MAC in whom lung resections were performed. A determination of whether or not MAC caused pulmonary disease was made using the 1997 criteria required by the American Thoracic Society. In addition, MAC were cultured from all nine lung specimens. Pathological findings of bronchiectases were evaluated in these nine patients. Destruction of bronchial cartilage and smooth muscles layer, obstruction of airway by granulomas, and ulceration of bronchial mucosa were frequently observed. Our present study demonstrates that destruction of fundamental bronchial structure due to extensive granuloma formation throughout the airways was likely the main cause of bronchiectases in MAC infection.


Subject(s)
Bronchiectasis/pathology , Mycobacterium avium-intracellulare Infection/pathology , Adult , Aged , Bronchiectasis/microbiology , Cartilage/microbiology , Female , Humans , Male , Middle Aged , Muscle, Smooth/microbiology , Mycobacterium avium Complex , Mycobacterium avium-intracellulare Infection/complications , Retrospective Studies
5.
Am J Respir Crit Care Med ; 166(7): 994-7, 2002 Oct 01.
Article in English | MEDLINE | ID: mdl-12359660

ABSTRACT

Microscopic examination of tissue sections of mycobacterial lesions frequently results in few or no bacilli seen, even if the lesions appear active histologically. This might be due to the effects of the fixative fluid and/or organic solvent, both of which are conventionally used to make tissue sections for histopathology, on the acid-fast staining of bacteria. The present study was performed to examine how formalin and xylene lower the sensitivity of acid-fast staining for Mycobacterium tuberculosis and to clarify the meaning of the staining result in tissue sections. Microscopic observation of mycobacteria smeared on glass slides revealed that both of these agents greatly reduced the sensitivity of acid-fast staining. Moreover, the number of bacilli was calculated in 30 samples of paraffin-embedded granulomatous lesions using acid-fast microscopy and real-time polymerase chain reaction. The numbers of bacilli present that were estimated by real-time polymerase chain reaction were considerably higher than those counted with a microscope. These results suggest that the bacilli are frequently missed or underestimated with acid-fast microscopy on formalin-fixed, paraffin-embedded tissue.


Subject(s)
Acids , Fixatives/pharmacology , Formaldehyde/pharmacology , Mycobacterium tuberculosis/drug effects , Staining and Labeling , Tissue Fixation , DNA, Bacterial/analysis , Drug Therapy, Combination , Humans , Mycobacterium tuberculosis/genetics , Polymerase Chain Reaction , Sensitivity and Specificity , Tuberculosis/microbiology , Xylenes/pharmacology
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