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. 2002 Sep;40(9):3146–3154. doi: 10.1128/JCM.40.9.3146-3154.2002

TABLE 1.

Relevant phenotypes of the strains used in this study

Strain or isolate Source or reference Colony morphologya
Hemolysis
Motilityb
Expression of FHAc Ureased Oxidased Citrated Nitrated Browninge
BG BG mod BG BG mod SS SS mod
RB50 8 sm/do la/fl + + 256 + + NDf ND
814 PR1g sm/do la/fl + + 256 + + + +
222 PR2g sm/do la/fl + + 256 + + + +
629 PR2g sm/do la/fl + + 256 ND ND ND ND ND
RB54 8 la/fl la/fl + + <2 + + ND ND ND
12822 33 sm/do la/fl + ND + +
Fr107 33 sm/do la/fl + ND + +
a

Colony morphology (sm/do, small and domed; la/fl, large and flat) and hemolytic activity were determined on BG blood agar without or with modulating (mod) agents (nicotinic acid and MgSO4).

b

Motility was determined in SS soft agar medium.

c

FHA expression was determined in supernatants by hemagglutination (the titer is expressed as the maximal dilution at which positive hemagglutination was detected).

d

Activities were determined with miniature bacterial identification strips (API 20E).

e

Browning activity was assessed on tyrosine agar plates.

f

ND, not done.

g

PR1 and PR2, patients 1 and 2 described in the present report, respectively.