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Results for “pathogen identification”

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At least 181 records · Page 10Linked to original sources
PubMed1981

Detection of lysozyme production using modified technique as an aid for the identification of pathogenic staphylococci causing some animal and human diseases.

Lysozyme production is an essential character of the potentially pathogenic staphylococci. In the present work 88 strains of animal origin and 40 strains of human origin were tested. Of 103 strains isolated from pathogenic cases of human and animal origin 89 (86.4%) were lysozyme producers and 86 (83.5%) were coagulase positive. Out of 75 strains isolated from pathogenic cases of animal origin 75 (100%) were lysozyme producers and 71 (94.6%) were coagulase positive. On the other hand out of 28 strains isolated from pathogenic human cases 14 (50%) were lysozyme producers and 15 (53.6%) were coagulase positive. This indicates that lysozyme production could be a better index of pathogenic staphylococci than the coagulase measurement specially in cases of animal origin strains. The method used in this work for the determination of the lysozyme production seems to be a simple one if compared with other used methods.

Animals↗
PubMed1995

[Identification of pathogenic and nonpathogenic leptospires by recombinant DNA probe].

A gene bank of L. interrogans serovar lai strain 017 was constructed with plasmid vector pUC 18. Recombinant plasmids designated pDJ 6 and pDJ 8 were screened from the gene bank. Inserted fragments of them are 1.9kb and 2.2kb respectively. Diglabelled 1.9kb inserted fragment of pDJ 6. Results showed that the probe had hybridization with pathogenic leptospires, but it did not have hybridization with nonpathogenic leptospires such as L. biflexa strain Patoc I and Leptonema illini. The probe did not have hybridization with nonhomologous DNA (e.g. human leucocyte and E. coli JM 103), either. So, the recombinant probe is a good tool for distinguishing and identifying genus, species, pathogenic leptospires and nonpathogenic leptospires.

DNA Probes↗
PubMed1994

Identification of pathogenic leptospires by recombinant DNA probes.

Early diagnosis of leptospirosis of pulmonary diffuse hemorrhage type (PDH) is of crucial importance in saving patients. To develop a sensitive and specific method for diagnosis, a genomic library of the main pathogen of PDH, L. interrogans serovar lai strain 017, was constructed with the plasmid vector pUC9. Recombinant plasmids which have homologous fragments of pathogenic leptospires were screened from the bank. A recombinant plasmid, designated pCX7, could detect 1.7 kb fragment of strain 017, 9.0 kb of strain 601 and 30.0 kb of strain Hebdomadis, respectively, without cross hybridization with nonpathogenic leptospires such as L. biflexa strain Patoc I and Leptonema illini. The recombinant plasmid pCX7 could detect pathogenic leptospires which are the main pathogens endemic to Sichuan Province.

Blotting, Southern↗
PubMed1995

[A new zoonosis--investigation of Gardnerella vaginalis disease of fox. II. Identification of pathogenic bacteria].

16 strains isolated from aborted foetus and vaginal exeretions of foxes were used for examination of cell morphology including fine structure of the cell wall and septa, test for homolysis, biochemical reactions and analysis of G+C content of the bacterial DNA. The cells are pleomorphic bacilli and coccobacilli, Gram stain reaction appear positive to variable, catalse and oxidase-negative, with a fermentative type of glucose metabolism, giving acetic and lactic acid as the major end products of fermentation. It's differentiated from the human strains of G. vaginalis by its less fastidious in growth requirements and being facultatively anaerobic to aerobic. We propose the name: a new subspecies--Gardnerella vaginalis subsp. fox, the type strain is U80.

Animals↗