FIELD: medicine.
SUBSTANCE: identifying a yersiniosis agent is enabled by using the intestinal yersinia pague FK-100 stripped on a double-layer grass lower layer of which represents an agar medium (pH 7.1) with added ampicillin in the concentration of 50 mcg/ml, while an upper layer of which is produced of the strain being tested cultivated on 1.5% Hottinger's agar at 28°C during one day and inoculated in 4 ml of Hottinger's broth, incubated at temperature 28°C to the final concentration n·108 m.c./ml; thereafter 0.3 ml of the prepared culture is mixed with 4.5 ml of 0.7% Hottinger's agar melted and cooled to 45°C with 50 mcg/ml of ampicillin and poured as a second layer on the agar plates. The inoculation is incubated at 28°C for 20-24 hours. Yersinia enterocolitica in the sample being tested is identified from the other types of yiersinia by the presence of phagolysis on the growth culture.
EFFECT: method provides complete identification effectiveness.
1 tbl, 3 ex
Title | Year | Author | Number |
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METHOD FOR IDENTIFYING THE PATHOGEN OF INTESTINAL YERSINIOSIS BY THE YERSINIA ENTEROCOLITICA 2021 BACTERIOPHAGE (FC-115) | 2021 |
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STRAIN OF BACTERIUM YERSINIA ENTEROCOLITICA SEROVARA 037 USED FR PREPARATION OF DIAGNOSTIC AGGLUTINATING MONOVARIC SERUM | 0 |
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AVIRULENT STRAIN OF Vibrio cholerae KM 263 BACTERIA OF SEROVAR INABA OF BIOVAR ELTOR - PRODUCER OF PROTECTIVE O1 ANTIGEN | 2010 |
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RU2425867C1 |
PHAGUM PESTIS M-1 STAIN USED FOR INTERSPECIES DIFFERENTIATION OF PLAGUE | 0 |
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SU1106834A1 |
RECOMBINANT PLASMIDE DNA FOR INDENTIFICATION OF STRAIN OF PLAGUE MICROBE | 0 |
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SU1615181A1 |
STRAIN OF BACTERIUM VIBRIO CHOLERAE 2414 OF CLASSICAL BIOVARA SEROVARA OHAVA AS PRODUCER OF CHOLERAIC TOXIN AND TOXIN-COREGULATED ADHESION PILES | 2000 |
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RU2169187C1 |
Authors
Dates
2012-09-10—Published
2011-04-11—Filed