Bailey and Scott's Diagnostic Microbiology |
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Page 48
... ture has incubated at least 6 hours . Subcultures are not indicated , of course , in the case of biphasic bottles . Recent studies indicate that there is little or nothing to be gained from rou- tine subculture of macroscopically ...
... ture has incubated at least 6 hours . Subcultures are not indicated , of course , in the case of biphasic bottles . Recent studies indicate that there is little or nothing to be gained from rou- tine subculture of macroscopically ...
Page 156
... ture incubated at 35 C ( Chapter 26 ) and incubate at 35 C for 24 hours in a candle jar or CO2 incubator , along with the original broth tube . Examine and identify as indi- cated in Chapter 26. If no listeriae are obtained from the 35 ...
... ture incubated at 35 C ( Chapter 26 ) and incubate at 35 C for 24 hours in a candle jar or CO2 incubator , along with the original broth tube . Examine and identify as indi- cated in Chapter 26. If no listeriae are obtained from the 35 ...
Page 299
... ture anthrax - type colonies . Both forms stain evenly and may show deeply stained granules . The organism is microaerophilic and faculta- tively anaerobic and grows best at 30 to 35 C. Hemolysis on blood agar occurs when 10 % horse ...
... ture anthrax - type colonies . Both forms stain evenly and may show deeply stained granules . The organism is microaerophilic and faculta- tively anaerobic and grows best at 30 to 35 C. Hemolysis on blood agar occurs when 10 % horse ...
Contents
Microorganisms encountered in the eye 26 Grampositive nonsporeforming | 14 |
Methods of obtaining pure cultures | 17 |
Collection and transport of specimens | 31 |
Copyright | |
18 other sections not shown
Common terms and phrases
acid activity addition agar agar plate agents agglutination amounts anaerobic antibiotics antibody antigen antimicrobial appear bacilli bacterial blood agar blood culture bottle broth caused cells Chapter characteristics Clin clinical collection colonies concentration containing described detection determined develop diagnosis differentiation dilution direct disease disk Distilled water drugs effective eggs examined fluid forms frequently genus glucose Gram gram-negative grow growth human identification important incubation indicated infection inoculated involved isolation laboratory less material medium meningitis method Microbiol Microbiology minutes mixed negative noted obtained occur organisms pathogenic patients placed plate pneumonia positive prepared present procedure produce rapid reaction reagents recommended reference reported resistant Salmonella selective serum slant slide smears sodium solution species specimens sputum stain sterile streptococci swab Table technique tion tissue tract tube urine usually various