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Table 2 Evaluation of single phenotypic identification tests for Gram-positive, catalase-negative cocci

From: Phenotypic and genotypic identification of streptococci and related bacteria isolated from bovine intramammary infections

Bacterium

n

α H1

CAMP1

ESC1

KM1

NACL1

INU1

HIP1

LAP1

PYR1

Streptococcus uberis

58

3%

9%

100%

8%a

0%a

100%a

92%a

100%a

68%a

Streptococcus dysgalactiae

20

100%

0%

0%

0%b

0%b

0%b

0%b

100%b

0%b

Streptococcus agalactiae

9

0%

100%

0%

0%

0%

0%

100%

100%

0%

Viridans streptococci

17

88%

0%

53%

47%

0%

24%

24%

88%

6%

Enterococcus spp

3

1/3

0/3

3/3

3/3

1/3

2/3

1/3

2/3

1/3

Aerococcus viridans

30

87%

0%

100%

3%

73%

13%

100%

3%

27%

Lactococcus garvieae

12

67%

0%

100%

0%

0%

17%

92%

100%

83%

Lactococcus lactis

2

0/2

0/2

2/2

1/2

0/2

2/2

2/2

2/2

1/2

  1. All strains were isolated from milk of cows with intrammamary infection and previously identified by 16S rRNA sequencing. Data is expressed as percentage (%) of strains showing a positive reaction in the corresponding phenotypic tests.
  2. 1Alpha-hemolysis (α H); CAMP reaction (CAMP); esculin hydrolysis (ESC); growth on kanamycin esculin azide agar (KM); growth on sodium chloride agar (NACL); inulin fermentation (INU); hippurate hydrolysis (HIP); leucine aminopeptidase activity (LAP); pyrrolidonyl peptidase activity (PYR).
  3. aFor these analyses, 25 strains of Streptococcus uberis were used.
  4. bFor these analyses, 13 strains of Streptococcus dysgalactiae were used.