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Biomedical subjects

G Sato

Publications and source records attributed to G Sato.

At least 73 records · Page 4Linked to original sources
PubMed1985

Nucleotide sequence of the gene determining plasmid-mediated citrate utilization.

The citrate utilization determinant from transposon Tn3411 has been cloned and sequenced, and its polypeptide products have been characterized in minicell experiments. The nucleotide sequence was determined for a 2,047-base-pair BglII restriction endonuclease fragment that includes the citrate determinant. This region contains an open reading frame that would encode a 431-amino-acid very hydrophobic polypeptide and which is preceded by a reasonable ribosomal binding site. However, the single polypeptide found in minicell experiments had an apparent molecular weight of 35,000 on sodium dodecyl sulfate-polyacrylamide gel electrophoresis.

Amino Acid Sequence↗
PubMed1985

Plasmid DNA relatedness among different serogroups of Yersinia pseudotuberculosis.

Thirteen different serogroup strains of Yersinia pseudotuberculosis and two strains of Yersinia enterocolitica O:3 were examined for the presence of plasmids and plasmid-mediated properties, calcium growth dependency, and autoagglutination. Two Y. enterocolitica strains and eight serogroup (IA, IIA, IIC, III, IVA, VB, VI, and VIII) strains, except for five serogroups (IB, IIB, IVB, VA, and VII), of Y. pseudotuberculosis harbored plasmids ranging in molecular size from 27 to 115 kilobases. Filter hybridization of restriction endonuclease-digested plasmid DNA from different serogroup strains indicated that all plasmid DNAs conferring calcium growth dependency and autoagglutination shared a high degree of DNA sequence homology, regardless of the different serogroups of Y. pseudotuberculosis and Y. enterocolitica.

DNA, Bacterial↗
PubMed1985

[An outbreak of staphylococcal dermatitis in laboratory mice].

An epizootic of dermatitis with erosion, ulcer and crust broke out in an experimental colony of JCL-ICR mouse over a period from December 1975 to June 1976. The disease was detected in 592 of a total of 1831 mice of 3-24 months old, especially in males of 7-24 months old (517/821). At the beginning of December 1975, only a few males of 12 months old were found to have the lesion on the back skin, and thereafter the dermatitis prevailed gradually among the mice. Histopathologic examinations showed the loss of the epidermis, necrosis and/or collapse of the corium, accumulation of serous exudate with neutrophilic cell infiltration and a few cocci scattered on the surface. In chronic cases, fibrous granulation tissues with neutrophilic cell infiltration were formed in the corium. Staphylococcus aureus was isolated in pure culture from the skin lesions in all of the mice examined. Skin disease similar to that of the field case was reproduced in mice inoculated subcutaneously with 10(7) viable organisms of the fresh isolate. By giving chlortetracycline in drinking water for 7 days, treatment of the affected mice was efficacious in mild cases, but not in severe cases.

Aging↗
PubMed1985

[Biological properties, phage typing and antimicrobial susceptibility of Staphylococcus aureus isolated from dermatitis in laboratory mice].

The characteristics of 167 isolates of S. aureus from 106 mice suffering dermatitis were examined. All 167 isolates coagulated both rabbit and human plasmas and 161 of them also coagulated bovine plasma. All the isolates produced heat-stable and heat-labile DNase, phosphatase and yellow pigment, reduced nitrate, hydrolysed egg yolk, Tween 80, and hippurate, and grew on crystal violet agar in colonies of the negative type C and on medium with 10% NaCl. The majority of them produced fibrinolysin, protease and acetoin. Fifty-three percent were gelatinase positive. In hemolysis tests, 25, 57 and 45 isolates showed alpha-, beta-, alpha beta-hemolysis, respectively. Forty isolates did not produce hemolysins in the rabbit and sheep blood agar. All of 75 isolates tested produced acid from fructose, galactose, glucose, glycerol and mannose, but did not from arabinose, dextrin, inulin, raffinose, salicin, sorbitol and xylose. Most of these isolates produced acid from lactose, mannitol, sucrose and trehalose. All of the 75 isolates were highly sensitive to penicillin, methylphenylisoxazolyl penicillin, erythromycin, spiramycin, lincomycin, chloramphenicol, tetracycline, kanamycin, gentamicin and cephaloridine, but were resistant to sulfisoxazole. With phages of human set, all 167 isolates were typable at 100 X RTD. All but one of the typable isolates belonged to mixed lytic groups. These were I + III (35 isolates), I + M (1), I + III + M (124) and I + II + III + M (6), with long phage patterns. When the 167 isolates were biotyped as described by Hájek and Marsálek [7, 8], 5 belonged to biotype A, 1 to biotype B and 60 to biotype C.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMed1984

The chick oviduct in tissue culture. I. Initial characterization of growing primary oviduct tissue cultures.

A simple three-enzyme treatment of collagenase, dispase and hyaluronidase on finely minced chick oviduct yields clumps of 50-150 cells. These cells attach to collagen-treated dishes and survive in culture for at least 2 weeks without subculturing. Oviduct cell cultures can also be induced to grow. Estradiol or epidermal growth factor (EGF) induce a 40% increase in cells in 4 days when cultures are grown in serum levels that do not support growth. Serum from estrogen-stimulated chicks promotes rapid cellular proliferation (doubling times of 1-2 days). Sera from estrogen withdrawn chicks, laying hen or horse do not support as rapid proliferation. The oviduct growth-promoting factors in serum from estrogen-stimulated chicks are not steroids or fibroblast growth factors (FGF). Removal of steroids from these sera by charcoal treatment or delipidization does not decrease the rate of growth. The addition of 1-100 nM estradiol does not increase a serum's ability to promote growth. Purified FGF or platelet-derived growth factor (PDGF) do not induce oviduct proliferation. These results were reproduced in oviduct cell cultures started from estrogen-stimulated and withdrawn chicks as well as laying hens. Thus the factors in serum from estrogen-stimulated chicks that promote rapid oviduct growth are induced by estrogen treatments in vivo, but do not seem to be only steroids.

Animals↗
PubMed1984

Polypeptide involved in the Escherichia coli plasmid-mediated citrate transport system.

A genetic determinant conferring on Escherichia coli the ability to utilize citrate as a sole source of carbon and energy was subcloned into pBR322 from a naturally occurring, citrate utilization (Cit+) plasmid, pOH30221, and was localized to a 1.6-kilobase region by cloning and subsequent deletion analysis. Genetic expression of the Cit+ determinant in E. coli minicells revealed that the Cit+ determinant encoded a single, membrane-associated polypeptide with an apparent molecular weight of 35,000, as determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. This polypeptide seemed not to be synthesized as a precursor with an amino-terminal signal sequence.

Base Sequence↗
PubMed1984

Spontaneous deletion of citrate-utilizing ability promoted by insertion sequences.

The citrate utilization (Cit+) transposon Tn3411 was shown to be flanked by directly repeated sequences (IS3411L and IS3411R) by restriction enzyme analysis and electron microscope observation. Cit- deletion mutants were frequently found to be generated in pBR322::Tn3411 by intramolecular recombination between the two copies of IS3411. The flanking IS3411 elements of Tn3411 were shown to be functional insertion sequences by Tn3411-mediated direct and inverse transposition. Tn3411-mediated inverse transposition from pBR322::Tn3411 to the F-plasmid derivative pED100 occurred more efficiently than that of direct transposition of the Cit+ determinant. This was thought to be due to the differential transposability of IS3411L and IS3411R in the transposition process. The frequency of transposition of IS3411 marked with a chloramphenicol resistance determinant was much higher than IS3411-mediated cointegrate formation, suggesting that replicon fusions are not essential intermediates in the transposition process of Tn3411 or IS3411. Spontaneous deletions occurred with high frequency in recA hosts. The spontaneous deletion promoted by homologous recombination between two IS3411 elements in Tn3411 was examined with deletion mutants.

Chromosome Deletion↗
PubMed1984

Growth inhibition of human tumor cells in athymic mice by anti-epidermal growth factor receptor monoclonal antibodies.

Monoclonal antibodies (MoAbs) were raised against epidermal growth factor (EGF) receptors on a human epidermoid carcinoma cell line, A431. Administration of anti-EGF receptor MoAbs inhibited tumor formation in athymic mice by A431 cells and by another epidermal carcinoma cell line, T222. When one of the same MoAbs was used in therapy against Li-7 (a human hepatoma) and HeLa cells (a cervical carcinoma), tumor growth was not affected. The number of EGF receptors on A431 cells was about 100-fold higher than on T222, Li-7, and HeLa cells, suggesting that the number of EGF receptors may not be an important determinant in suppressing tumor growth. Three anti-EGF receptor MoAbs were used in the present studies. MoAbs 528 (immunoglobulin G2a) and 225 (immunoglobulin G1) are capable of competing with EGF for receptor binding and inhibit proliferation of A431 cells in culture. The other MoAb, 455 (immunoglobulin G1), is incapable of blocking the binding of EGF to its receptors and has no effect on the proliferation of cultured A431 cells. All three MoAbs inhibited A431 tumor growth in athymic mice, indicating that the antibody isotype and the site of binding on the EGF receptor are not the determinants of antiproliferative activity in vivo. The observation that MoAb against the receptor for EGF is cytostatic rather than cytocidal in vitro against A431 cells, yet completely prevents tumor growth in vivo, suggests that some host animal responses also may be involved in the antitumor effect. MoAbs against growth factor receptors could provide useful immunotherapeutic agents.

Animals↗
PubMed1983

Comparative sequence analysis of the inverted terminal repetition in the genomes of animal and avian adenoviruses.

The nucleotide sequences at the inverted terminal repetitions from two animal adenoviruses, infectious canine hepatitis virus and equine adenovirus, and from one avian adenovirus, CELO, were analyzed. DNAs from infectious canine hepatitis virus and equine adenovirus contain a homologous region which is 23 nucleotides long from the terminus. The first 17 nucleotides of this region are identical to the ones in human adenovirus type 2 DNA. The striking homologous sequence of 14 nucleotides, conserved in the inverted terminal repetitions of several human adenovirus strains and in simian adenovirus type 7, is only partially conserved in the two animal and one avian adenoviruses reported here.

Adenoviridae↗
PubMed1983

Electromyographic assessment of fatiguability and recovery of orbicularis oculi in myasthenia gravis.

Orbicularis oculi fatiguability following maximal voluntary contraction and its recovery after administration of Tensilon (edrophonium chloride) were studied in 13 patients with myasthenia gravis (MG) and 8 normal controls. The number of EMG pulses per sec (C) was calculated using an experimentally manufactured EMG pulse counting system and the mean amplitude of the motor unit potentials per sec (A) was measured using the action potential analysis module (Medelec APA-6 MK-1) during maximal voluntary contraction of the orbicularis oculi muscle. Fatiguability was estimated as percentage change of C, the pre-exercise value being taken as 100%. It was 74.4 +/- 18.2% (mean +/- S.D.) in patients and was significantly different from 110.8 +/- 8.4% found in the controls (p less than 0.01). Recovery following intravenous injection of Tensilon was estimated as percentage change in C and A, the values before Tensilon injection being taken as 100%. The change in EMG pulse per sec (C) was 360.0 +/- 90.0% in MG and 113.0 + 21.2% in controls (p less than 0.005). The mean amplitude of the motor unit potential per sec (A) increased by 180.0 +/- 95.0% in MG and 120.0 +/- 42.0% in controls (p less than 0.01). This technique is thought to be valuable to confirm the diagnosis of MG when routine electrophysiological tests fail to demonstrate abnormalities in neuromuscular transmission.

Adolescent↗
PubMed1983

Genetic properties of conjugative R plasmids in Escherichia coli and Salmonella isolated from feral and domestic pigeons, crows and kites.

A total of 62 conjugative R plasmids detected in 48 Escherichia coli and 19 conjugative R plasmids in 16 Salmonella strains from domestic (carrier and emerald) and feral pigeons, crows (Japanese jungle crows and carrion crows) and black kite, were examined for genetic properties. Out of the 62 E. coli R plasmids examined for fertility inhibition (Fi), 29 (46.8%) were Fi+, and the remainder were Fi-. Among the 62 R plasmids, 16 (25.8%) were classified into incompatibility (Inc) group FII, 15 (24.2%) into I alpha, 7 (11.3%) into H1 and 2 (3.2%) into N. The remaining 23 R plasmids could not be classified in this study. Among the 19 Salmonella R plasmids, 4 showed thermosensitive (ts) transfer. Out of the 18 plasmids tested, 13 (72.2%) including 4 ts-R plasmids were Fi-, and the remaining 5 (27.8%) were Fi+. Five R plasmids containing 4 Fi- were IncI alpha, while 4 ts-R plasmids belonged to IncH1 (1 R plasmid) and H2 (3 R plasmids). The remainings were not tested. In E. coli strains, IncFII and I alpha were widely (4 of 6 lots of birds, respectively) distributed, followed by N (2 lots) and H1 (1 lot). IncN R plasmid was detected from domestic pigeons and crows, but not from feral pigeons. In Salmonella strains from 5 lots of birds, IncFII and N plasmids which were detected from E. coli were not found, but IncH2 was detected from domestic pigeons (1 lot) and kite (1 lot). IncI alpha was detected from feral pigeons (1 lot) and kite (1 lot). The potential transfer of R plasmids between Salmonella and E. coli, and of dissemination of the plasmids among the free-flying birds, animals and humans is discussed.

Animals↗