Bailey and Scott's Diagnostic Microbiology |
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Page 47
... growth . In the case of biphasic blood culture bottles , the bottles should be tipped daily so as to flow the blood - broth mixture over the surface of the agar slant . When a culture is positive , the broth may assume one of several ...
... growth . In the case of biphasic blood culture bottles , the bottles should be tipped daily so as to flow the blood - broth mixture over the surface of the agar slant . When a culture is positive , the broth may assume one of several ...
Page 263
... Growth on MacConkey agar SS agar Cetrimide agar Hydrogen sulfide Sign Percent 100 9 ( w ) * 0.8 0 0 0 0 ( 64 ) + TSI ... growth are evident : ( 1 ) a clear , moist , glistening central zone , ( 2 ) a highly refractile pearllike circle of ...
... Growth on MacConkey agar SS agar Cetrimide agar Hydrogen sulfide Sign Percent 100 9 ( w ) * 0.8 0 0 0 0 ( 64 ) + TSI ... growth are evident : ( 1 ) a clear , moist , glistening central zone , ( 2 ) a highly refractile pearllike circle of ...
Page 604
... Growth , green colony with black center Growth , orange colony ( or no growth ) Positive Negative Positive Negative Growth ( anaerobic ) Inhibited ( anaerobic ) Growth No growth Hippurate hydrolysis Indole Kanamycin - vancomycin blood ...
... Growth , green colony with black center Growth , orange colony ( or no growth ) Positive Negative Positive Negative Growth ( anaerobic ) Inhibited ( anaerobic ) Growth No growth Hippurate hydrolysis Indole Kanamycin - vancomycin blood ...
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