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Query: UMLS:C0026936 (Mycoplasma)
 14,761 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Two mycoplasma strains isolated from the nasopharynx of guinea-pigs in two separate colonies were biochemically and serologically identical, and distinct from 80 Mycoplasma and Acholeplasma spp. One of them, strain 117C (NCTC 11700), is designated the type strain of a new species Mycoplasma cavipharyngis.
J Gen Microbiol 1984 Dec
PMID:Mycoplasma cavipharyngis, a new species isolated from the nasopharynx of guinea-pigs. 652 Jun 3

Mycoplasma spp. were isolated from five wild raccoon dogs (Nyctereutes procyonoides viverrinus). On the basis of biochemical properties and serological tests, nine isolates were identified as Mycoplasma edwardii and four were similar to a possibly new Mycoplasma sp. represented by strain LM2 which is negative for both glucose fermentation and arginine hydrolysis. In addition, ureaplasmas were detected from these animals. Ureaplasmas were compared serologically with ureaplasma strains isolated from human, monkey, cattle, goat, sheep, cat, chicken and dog and cross-reacted with one of four serological groups of canine ureaplasmas.
J Gen Microbiol 1983 Aug
PMID:Isolation of Mycoplasma and Ureaplasma species from raccoon dogs (Nyctereutes procyonoides viverrinus). 663 16

Cultures of the Mollicutes (mycoplasma) Acholeplasma laidlawii B, Acholeplasma morum, Mycoplasma bovis, Mycoplasma arginini, Mycoplasma fermentans and Mycoplasma gallisepticum, representing four metabolic groups, were sampled at intervals over a 40 to 50 h period and assayed for the numbers of c.f.u., changes in pH and glucose concentration, and concentrations of ATP, ADP, AMP, lactate and pyruvate. The adenylate energy charge (ECA), the mean generation time, and the number of nmol of ATP (mg dry weight)-1 were calculated for cultures in the mid-exponential growth phase. The maximum cell concentrations ranged from 0.2 X 10(10) to 5.0 X 10(10) c.f.u. ml-1. Doubling times ranged from 0.34 to 3.29 h. The fermentative, nonarginine-requiring A. laidlawii B, A. morum, and M. gallisepticum, as well as the fermentative, arginine-requiring M. fermentans, utilized glucose and produced lactate and pyruvate. The non-fermentative, non-arginine-requiring M. bovis neither utilized glucose nor produced lactate or pyruvate. The non-fermentative, arginine-requiring M. arginini utilized glucose, but did not produce lactate or pyruvate. At mid-exponential growth phase, the average ECA of A. laidlawii B was 0.90, a value similar to that reported for Spiroplasma citri and other bacteria. In contrast, the average ECA of A. morum and the four Mycoplasma species was 0.70. In A. laidlawii B at mid-exponential growth phase, ATP accounted for 97% of the total adenylate nucleotide pool.(ABSTRACT TRUNCATED AT 250 WORDS)
J Gen Microbiol 1983 Oct
PMID:Synthesis of adenylate nucleotides by Mollicutes (mycoplasmas). 665 57

A mycoplasma, designated strain 486, was isolated from the oviduct of an adult chicken. On the basis of its morphological, physical and cultural characteristics the organism was assigned to the class Mollicutes, order Mycoplasmatales. The guanine plus cytosine content of its DNA was estimated to be 27.5 mol%. The organism was inhibited by digitonin and it showed a growth response to sterol, although its minimal requirement was low. It neither showed helical forms nor hydrolysed urea and was hence assigned to the family Mycoplasmataceae, genus Mycoplasma. Strain 486 fermented glucose and reduced tetrazolium under anaerobic conditions. It did not hydrolyse arginine, aesculin or arbutin, nor did it produce films and spots or digest serum. Phosphatase activity was negative or very weak, and the organism adsorbed turkey but not chicken red blood cells. Serological tests (growth inhibition, indirect fluorescent antibody, double immunodiffusion and metabolism inhibition) with 75 currently accepted Mycoplasma species or serovars failed to identify the isolate. Thus strain 486 appears to represent a new species, for which the name Mycoplasma glycophilum is proposed. (NCTC 10194, ATCC 35277).
J Gen Microbiol 1984 Mar
PMID:Mycoplasma glycophilum, a new species of avian origin. 672 79

An easy, rapid tissue culture method for detection of Mycoplasma hyorhinis is described. The organism induces morphological changes in mink S + L - cells. This effect was not observed in eight other animal cell lines infected by M. hyorhinis and it did not occur in the mink cells infected with six other strains of mycoplasma. This cell system should be useful in research laboratories which do not have other standard techniques available for monitoring the presence of M. hyorhinis.
J Gen Microbiol 1982 Nov
PMID:Rapid tissue culture method for detection of Mycoplasma hyorhinis. 675 18

The whole cell proteins and the ribosomal proteins of Mycoplasma capricolum ATCC 27343 have been analyzed by two-dimensional polyacrylamide gel electrophoresis. The M. capricolum cell is relatively rich in basic proteins. The number of total protein spots detected was approximately 355, which is less than one-third of that of Escherichia coli or Bacillus subtilis. In contrast, the number (30 and 20 protein species have been found to be present in the 50S and 30S ribosomal subunits, respectively) and the size of the ribosomal proteins in the M. capricolum do not seem to be significantly different from those of typical eubacteria.
Mol Gen Genet 1982
PMID:The protein composition of Mycoplasma capricolum. 696 Feb 28

Representatives of groups of mycoplasmas which have antigens in common with Mycoplasma mycoides (as demonstrated by different serological tests) were compared by nucleic acid hybridization. Determinations of DNA homology were performed by filter hybridization as well as hybridization in solution; no differences were revealed between the two methods. Genetic relatedness was not demonstrated between M. primatum and strain F38. The antigenic similarities between strain F38 and the type strain of M. primatum (HRC292) may be due to common epitopes. DNA from strain F38 hybridized with DNA from M. capricolum (California kid) to 80%, but only to about 40% with the two M. mycoides subspecies, a result which can justify the classification of the F38 group as a variant of M. capricolum. The representative strain of bovine serogroup 7 of Leach was equally distant from F38, M. capricolum and the two subspecies of M. mycoides (approximately 60% hybridization).
J Gen Microbiol 1982 Nov
PMID:Classification of the F38 group of caprine Mycoplasma strains by DNA hybridization. 715 57

Several Mycoplasma and Acholeplasma species chosen at random and solubilized with sodium dodecyl sulphate showed a common periodic acid-Schiff positive band with an apparent molecular weight of about 64 000, when examined by polyacrylamide gel electrophoresis. Another more cathodic minor band was detected in M. hyopneumoniae and M. flocculare. The common periodic acid-Schiff positive band appeared when a precipitate of serum constituents of the uninoculated growth medium after incubation was examined. The minor band was identified as a serum glycoprotein contaminating mycoplasmas grown in the presence of swine serum. We draw attention to the compounds as a possible source of error in serological tests or in the lymphocyte stimulation response. After lithium diiodosalicylate solubilization and aqueous phenol extraction, polyacrylamide gel electrophoresis showed a periodic acid-Schiff positive band in membranes from M. hyopneumoniae (molecular weight 75 000) and M. hyorhinis (molecular weight 80 000), suggesting the presence of a membrane glycoprotein. Such a glycoprotein was absent from A. granularum. Since the common periodic acid-Schiff positive band was not extracted by aqueous phenol, this growth medium constituent did not contaminate the preparations of membrane glycoproteins. However, the minor band was present in glycoprotein preparations of M. hyopneumoniae grown in the presence of swine serum.
J Gen Microbiol 1980 Jul
PMID:Growth medium constituents contaminating mycoplasma preparations and their role in the study of membrane glycoproteins in porcine mycoplasmas. 719 Sep 98

The nucleotide sequence relationships between 18 species of Mycoplasma and 3 species of Acholeplasma were examined by solution DNA hybridization. Radiolabeled DNAs from strains representing 13 Mycoplasma and 2 Acholeplasma species were used as hybridization probes. The mycoplasmas were heterogeneous but displayed a low degree of conserved information of the order of 3 to 5% of the genome. However, several species within each genus showed 13 to 15% homology. There was no detectable homology between species from the two genera, and M. pneumoniae and M. neurolyticum appeared to be unrelated to any of the other Mycoplasma species or to each other. These results suggest that it may be possible to isolate genes common to most, if not all, Mycoplasma and Acholeplasma species.
J Gen Microbiol 1980 Dec
PMID:Partial nucleotide sequence similarity within species of Mycoplasma and Acholeplasma. 726 1

Colonies of Mycoplasma hominis, Acholeplasma laidlawii (three strains) and Ureaplasma urealyticum were examined by light and electron microscopy and their characteristic morphology, ultrastructure and morphogenesis are described. Mycoplasma hominis and A. laidlawii, PG8 and oral strains, developed typical 'fried-egg' colonies which were remarkably heterogeneous in size. The colonies of A. laidlawii strain NCTC 10116 were more homogeneous and grew mainly on the surface of the agar showing a fine granular appearance. Ureaplasma urealyticum produced smaller, granular colonies which grew deeply embedded in the agar and generally without much surface growth. The cellular ultrastructure in these colonies was also examined. The results indicate that several aspects of colony morphogenesis and ultrastructure varied for each of the three species examined.
J Gen Microbiol 1980 Feb
PMID:Colony morphology, ultrastructure and morphogenesis in Mycoplasma hominis, Acholeplasma laidlawii and Ureaplasma urealyticum. 737 81


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