Читайте также: |
|
A. Staining according to Leffler’s technique
B. Staining according to Gram’s technique
C. *By «hanging» drop technique
D. By electron microscope
E. By «lying» drop technique
A. Bacillus cereus
B. Bacillus subtilis
C. Clostridium perfringens
D. Clostridium difficile
E. *Clostridium sporogenes
A. Bacillus cereus
B. Bacillus subtilis
C. Clostridium perfringens
D. Clostridium difficile
E. *Bacillus steatothermophilus
A. forceps
B. bacteriological loops
C. *tampons for material collection
D. slide glasses
E. cover slip
A. Morphological identification
B. Biological identification
C. Biochemical identification
D. *Serological identification
E. All answer are correct
A. not before, than in 10-15 min
B. not before, than in 15-20 min
C. not before, than in 20-30 min
D. *not before, than in 30-45 min
E. not before, than in 60-90 min
A. Reactions of hybridization of DNK and RNK (reaction of gene probes)
B. Polymerase chain reaction
C. Immunofluorescence test
D. *Right answers A and B
E. Right answers A, B and C
A. *In the passing light at the small increase of microscope
B. In an electron microscope
C. By a "hanging" drop technique
D. By a phase-contrast microscope
E. By the immersion system of microscope
A. simple MPA
B. simple MPB
C. Endo’s medium
D. *blood MPA
E. serum MPA
A. simple MPA
B. simple MPB
C. Endo’s medium
D. *blood MPA
E. serum MPA
A. MPA
B. Endo’s medium
C. Ru’s medium
D. % alkaline peptone water
E. *MPB
A. °С during 5-10 min
B. °С during 30 min
C. °С during 60 min
D. °С during 30 min
E. *80 °С during 5-10 min
A. *70 °С during 30 min
B. °С during 60 min
C. °С during 90 min
D. °С during 30 min
E. °С during 60 min
A. single sterilization during 10 min.
B. single sterilization during 20 min.
C. fractional sterilization – three times one after the other during one day, 30 min.
D. fractional sterilization – 2 days one after the other, 30 min.
E. *fractional sterilization – 3 days one after the other, 30 min.
A. °С during 20 minutes
B. °С during 20 minutes
C. °С during 40 minutes
D. *120 °С during 20 minutes
E. °С during 20 minutes
A. Meat-peptone agar
B. Sugar MPA
C. Coagulated serum
D. *Meat-peptone broth
E. gelatin
A. liquid nutrient media
B. physiological solution
C. *forceps
D. solid nutrient media
E. catheters
A. destruction of cellular lipids.
B. *Interaction with protein amino groups and their denaturation
C. destruction of cellular endotoxin
D. destruction of cellular polysaccharides.
E. Cell dehydration
A. *smooth, convex surface
B. gyrose surface
C. fibred consistency
D. edges are rosette-like
E. have capsules
A. *solution of dexon on 45 min at 18 °С
B. solution of dexon on 25 min at 18 °С
C. solution of dexon on 15 min at 18 °С
D. solution of dexon on 45 min at 56 °С
E. solution of dexon on 25 min at 56 °С
A. Bacteria staining
B. *agglutinating sera
C. laboratory animals
D. biochemical signs
E. character of growth on/in nutrient media
A. *0 аtm.
B.,5 аtm.
C. аtm.
D.,5 аtm.
E. аtm.
A. аtm.
B. *0,5 аtm.
C. аtm.
D.,5 аtm.
E. аtm.
A. аtm.
B.,5 аtm.
C. *1 аtm.
D.,5 аtm.
E. аtm.
A. аtm.
B.,5 аtm.
C. аtm.
D. *1,5 аtm.
E. аtm.
A. аtm.
B.,5 аtm.
C. аtm.
D.,5 аtm.
E. *2 аtm.
A. Inoculation of material in the melted sugar agar
B. *Inoculation of material in Kitt-Tarozzi’s medium
C. Inoculation of material in a coagulated serum
D. Inoculation of material on the Zeissler’s blood-sugar agar
E. Inoculation of material on Endo’s medium
A. Macroscopic examination of material and its inoculation in liquid nutrient medium
B. Macro- and microscopic verification of culture purity
C. Serological identification
D. *Macro- and microscopic study of colonies and their inoculation on slant agar
E. Biochemical identification
A. *In the passing light, small objective of microscope
B. In an electronic microscope
C. By a "hanging" drop technique
D. In a phase-contrast microscope
E. By the immersion system of microscope
A. character of growth
B. *character of bacterial staining
C. presence of flagella
D. antigen properties
E. all answers are correct
A. mechanical
B. *chemical
C. biological
D. pasteurization
E. in a heat oven
A. % hydrogen peroxide, 6 hours at 18 °С
B. % hydrogen peroxide, 12 hours at 18 °С
C. % hydrogen peroxide on 1 hour at 18 °С
D. *6 % hydrogen peroxide on 6 hours at 18 °С
E. % hydrogen peroxide on 2 hour at 18 °С
A. single sterilization by water bath at 98-100 °С during 30 minutes
B. *sterilization by water bath at 58-60 °С during a hour 5-6 day one after the other
C. sterilization by water bath at 98-100 °С during a hour 5-6 day one after the other
D. sterilization by water bath 58-60 °С during a hour 2-3 days one after the other
E. sterilization by water bath at 98-100 °С during a hour 5-6 days one after the other
A. Escherichia coli
B. Salmonella typhi
C. *Serratia mаrcescens
D. Clostridium perfringens
E. Corynebacterium xerosis
A. O
B. H
C. K
D. *All answers are correct
E. All answers are wrong
A. Features of bacterial staining
B. Features of growth of bacteria in the column of agar
C. Features of chemical composition of bacteria
D. *Features of bacterial growth on/in nutrient media
E. It is a manifestation of tinctorial signs
A. *Dilute material from Kitt-Tarozzi’s medium in tubes with melted sugar meat-peptone agar, their cultivation then
B. Dilute material from Kitt-Tarozzi’s medium in tubes with MPB, their cultivation then
C. Dilute material from 1 % alkaline peptone water in tubes with melted sugar MPA, their cultivation then
D. Dilute material from 1 % alkaline peptone water in tubes with MPB, their cultivation then
E. Transfer material in a test tube with melted sugar MPA, its cultivate then
A. Macroscopic examination of tested material and its inoculation in Kitt-Tarozzi’s medium and milk
B. Microscopic examination of tested material and its inoculation in Kitt-Tarozzi’s medium and milk
C. Macroscopic and microscopic examination of tested material and its inoculation on the slant agar and in milk
D. Macroscopic and microscopic examination of tested material and its inoculation in MPB and on MPA
E. *Macroscopic and microscopic examination of tested material and its inoculation in the Kitt-Tarozzi’s medium and milk
A. Medium which is inoculated with bacteria, where different microorganisms grow
B. Growth of microbes of one species on different nutrient medium
C. *Macroscopically visible growth of microbes (posterity of one bacterial cell) on a solid nutrient medium
D. Visible growth of bacteria in a liquid nutrient medium
E. Visible growth of bacteria on the slant meat-peptone agar
A. Isolation and analysis
B. Physical and chemical
C. Biochemical and serum
D. Quantitative and qualitative
E. *Mechanical and biological
A. Type of respiration
B. Motility
C. Spore formation
D. *Type of reproduction
E. Acid resistance
A. *wrinkled
B. gyrose
C. warty
D. rosette-shaped
E. all answers are correct
A. Coons’s test
B. Coombs’s test
C. Ouchterloni’s test
D. Manchini’s test
E. *Gruber’s test
A. Formation of diffuse turbidity
B. Formation of pellicle
C. *Dissolution of casein clot
D. Formation of sediment
E. Formation of pellicle and turbidity
A. Formation of diffuse turbidity
B. Formation of pellicle
C. Dissolution of casein clot
D. Formation of sediment
E. *Gelatin liquefacience
A. Features of antigen composition of bacteria
B. Features of chemical composition of bacteria
C. *Features of bacterial staining
D. Features of susceptibility to phages
E. Features of manifestation of antibiotics susceptibility
A. Enable to study biochemical properties of bacteria
B. Enable to study antigen properties of bacteria
C. Enable to obtain a pure culture
D. *Enable to obtain the isolated colonies
E. Right answer is not present
A. Material from Kitt-Tarozzi’s medium is inoculated consistently in test tubes with a sugar-blood agar by bacteriological loop, then they are placed in the jar and incubator
B. Material from the Kitt-Tarozzi’s medium is inoculated consistently on MPA in by a spatula, then they are placed in the jar and in a thermostat
C. Material from Kitt-Tarozzi’s medium is inoculated consistently on serum agar by a spatula, then it is placed in the jar and in a thermostat
D. *Material from Kitt-Tarozzi’s medium is inoculated consistently in the Petry’s plates with sugar-blood agar by a spatula, then they are placed in the jar and in the thermostat
E. Material from Kitt-Tarozzi’s medium is inoculated consistently in test tubes with serum broth by a loop, then they are placed in the jar and in a thermostat
A. *Use of melted nutrient media (gelatin) for obtaining the isolated colonies
B. Use of liquid nutrient media for obtaining the isolated colonies
C. Use of blood agar for examination of hemolysines types
D. Use of solid nutrient media for examination of antibiotics susceptibility
E. Use liquid nutrient media for examination of antibiotics susceptibility
A. Dilution of tested material in gelatin
B. *Dilution of tested material in a liquid nutrient medium
C. Dilution of tested material in MPA
D. Dilution of tested material in the AGV nutrient medium
E. Dilution of tested material in a solid nutrient medium
A. Inoculation of colonies on the proper nutrient medium
B. Examination of tinctorial properties of bacteria
C. *Checking the culture purity and its identification
D. Examination of serologic features of bacteria which form colonies by precipitation test
E. Right answer is absent
A. Medium which is inoculated with bacteria, where different microorganisms grow
B. Growth of microbes of one species on different nutrient medium
C. *Macroscopically visible growth of microbes (posterity of one bacterial cell) on a solid nutrient medium
D. Visible growth of bacteria in a liquid nutrient medium
E. Visible growth of bacteria on the slant meat-peptone agar
A. Verification of bacteria according to their ability to produce dehydrogenases
B. *Verification of bacteria according to their biochemical properties
C. Verification of bacteria according to their ability to produce hemolysines
D. Verification of bacteria according to their tinctorial properties
E. Verification of bacteria according to their reduce properties
A. *Verification of bacteria according to changes which they cause in the organism of laboratory animals
B. Verification of bacteria according to their tinctorial properties
C. Verification of bacteria according to their biochemical properties
D. Verification of bacteria according to their antigen properties
E. Verification of bacteria according to their cultural properties
A. Verification of bacteria according to their tinctorial properties
B. Verification of bacteria according to their ability to form S- and R-forms of colonies
C. Verification of bacteria according to their capacity to form slime layer
D. Verification of bacteria according to their capacity to produce hydrogen sulfide
E. *Verification of bacteria according to their features of growth on/in nutrient media
A. *Complex of measures for complete, partial or selective elimination of potentially pathogenic for human causative agents on the different objects of medium for warning transmission of causative agents from the source of infection to the receptive organism
B. Complex measures for complete, partial or selective elimination of potential pathogens for human in the air for warning transmission of causative agents from the source of infection to the receptive organism
C. Complex of measures for complete, partial or selective elimination of potential pathogens for human in his body for warning transmission of causative agents from the source of infection to the receptive organism
D. Complex of measures which prevent spread of potential pathogens from human body in an medium
E. Complex of measures for complete, partial or selective elimination of potential pathogens for human in the water for warning transmission of causative agents from the source of infection to the receptive organism
A. verification of culture purity
B. inoculation of Giss’ media, slide agglutination
C. examination of the antibiotics susceptibility
D. Phage typing
E. *all answers are correct
A. Study the features of colonies
B. Make a smear from colonies
C. Inoculation onto slant agar
D. *All answers are correct
E. All answers are not correct
A. Verification of bacteria according to their ability to form a capsule
B. Verification of bacteria according to their ability to form flagella
C. *Verification of bacteria according to their morphological signs
D. Verification of bacteria according to their capacity to spore formation
E. Verification of bacteria according to their ability to transform into L-forms
A. Verification of bacteria according to their capacity to form of lipopolysaccharide
B. Verification of bacteria according to their ability to producе bacteriocines
C. *Verification of bacteria according to their antigen properties
D. Verification of bacteria according to their capacity to produce antibodies
E. Right answer is not present
A. Examination of bacterial species according to biochemical properties
B. Examination of bacterial species according to ability to utilize a coagulated serum
C. *Examination of bacterial species according to their antigen structure
D. Examination of bacterial species according to ability to reduce some dyes
E. Examination of bacterial species according to gene composition of bacterial nucleoid
A. *Microbes of the only species isolated from different sources, or from the same source, but at different times
B. Microbes of different species isolated from different sources
C. Microbes of different species isolated from the only source
D. Microbes of different species isolated in different times
E. Microbes of different species isolated from different sources, or from the same source, but in different times
A. Examination the isolated colonies
B. Examination bacterial growth in the column of agar
C. Bacterial phage typing
D. *Identifications of the unknown bacteria
E. Examination of ability for bacteriocine production
A. To be solid
B. To be liquid
C. *To be sterile
D. To contain vitamins
E. To contain growth factors
A. Examination of features of pure culture and its identification
B. *Examination of features of colonies, preparing the smear from them, inoculation of colonies into Kitt-Tarozzi’s medium for obtaining the pure culture
C. Examination of features of colonies, preparing the smear from them, inoculation of colonies on slant MPA for obtaining the pure culture
D. Examination of features of colonies, preparing the smear from them, inoculation of colonies in MPB for obtaining the pure culture
E. Examination of features of colonies, inoculation of colonies in Kitt-Tarozzi’s medium for obtaining the pure culture
A. Guinea pigs
B. White mice
C. White rats
D. *All answers are correct
E. Right answer is not present
A. White rats
B. *Guinean pigs
C. Rabbits
D. Syrian hamsters
E. White mice
A. White rats
B. Guinean pigs
C. Rabbits
D. Syrian hamsters
E. *White mice
A. To study tested material
B. To choose nutrient medium for inoculation
C. *To obtain the isolated colonies
D. To study the morphological features of possible causative agent
E. To study the antigen features of causative agent
A. Leffler’s method
B. Grey’s method
C. *Streak’s method
D. Buchin’s method
E. Nemchinov’s method
A. “Roche”
B. “API”
C. “Enterotest”
D. *All answers are correct
E. All answers are wrong
A. Endo’s medium
B. Olkenitsky’s medium
C. MPB
D. *Milk
E. Levenshtein-Yensen’s medium
A. Morphological
B. Signs of growth in/on nutrient media
C. Biochemical
D. Toxigenic
E. *All answers are correct
A. Shape, color
B. Character of edges
C. Character of surface of colonies
D. A right answer is not present
E. *All answers are correct
A. some amino acids
B. tweens
C. active carbon
D. *all answers are correct
E. all answers are wrong
A. *For cultivation of anaerobes according to Veinberg’s technique
B. For cultivation of anaerobes according to Zeissler’s technique
C. For cultivation of aerobes according to Ziehl–Neelsen’s technique
D. For cultivation of aerobes according to Leffler’s technique
E. In bacteriology they are not used
A. for prescribing the treatment
B. *for revealing the etiological factor illness
C. for prophylaxis
D. for examination of phages susceptibility
E. for examination of antibiotics susceptibility
A. *1 % sodium bicarbonate
B. % potassium permanganate
C. % magnesium sulfate
D. % ether
E. % alcohol
A. fractional sterilization
B. sterilization by pressed steam
C. boiling
D. *by dry heat
E. ionizing radiation
A. ether
B. hydrochloric acid
C. formalin
D. chloroform
E. *Chloraminum
A. Enables to examine antibiotics susceptibility
B. Enables to examine biochemical properties of microbes
C. *Enables to obtain the isolated colonies
D. Enables to examine antigen properties of microbes
E. Has no substantial advantage
A. C, 15-30 minutes
B. 1C, 120 minutes
C. *180 1, 45-60
D. 1, 45-60 minutes
E. 1, 15-30
A. Leffler’s medium
B. *Kitt-Tarozzi’s medium
C. Petrov’s medium
D. Makkoy-Chepin’s medium
E. Petranyani’s medium
A. *Formation of colorless or pinky colonies on Endo’s and Ploskirev’s nutrient media
B. Formation of red colonies with metallic hue on Endo’s medium
C. Formation of colorless colonies on Bismuth-sulfite agar
D. Formation of haemolysis on a blood agar
E. Formation of tender pellicle on alkaline peptone water
A. *liquefacience of gelatin column
B. compression of gelatin column
C. discoloration of gelatin column
D. appearance of dark precipitate in gelatin column
E. brightening of gelatin column.
A. Bacillus cereus
B. *Bacillus subtilis
C. Clostridium perfringens
D. Clostridium difficile
E. Proteus vulgaris
A. *all will become red
B. appearance of red precipitate in the column of agar
C. appearance of greenish precipitate in the column of agar
D. to fix the urease production in this medium is impossible
E. appearance of brightly-violet precipitate in the column of agar
A. *Pseudomonas aeruginosa
B. Salmonella schottmuelleri
C. Staphylococcus aureus
Дата добавления: 2015-07-25; просмотров: 162 | Нарушение авторских прав
<== предыдущая страница | | | следующая страница ==> |
Text test questions 6 страница | | | Text test questions 8 страница |