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1 ight mass spectrometry (MALDI-TOF MS) (e.g., Streptococcus oralis).
2 udopneumoniae, Streptococcus pneumoniae, and Streptococcus oralis.
3 ayers of Streptococcus gordonii Blackburn or Streptococcus oralis 10557 on enamel chips were placed o
4 burn, 10558, Streptococcus mitis 10712, 903, Streptococcus oralis 10557, 9811, and Streptococcus sang
5 e tooth surface (Streptococcus gordonii DL1, Streptococcus oralis 34, and Actinomyces naeslundii T14V
6 al bacteria, Actinomyces naeslundii T14V and Streptococcus oralis 34, is dependent upon production of
9 streptococci examined, except one strain of Streptococcus oralis (35037), rapidly induced up-regulat
10 cluding Streptococcus sanguinis (3 strains), Streptococcus oralis (4 strains), and Streptococcus muta
11 ical blood cultures with Streptococcus mitis/Streptococcus oralis and 1/3 blood cultures spiked with
12 mutans grown with sucrose in the presence of Streptococcus oralis and Actinomyces naeslundii steadily
13 ggregation receptor polysaccharides (RPS) of Streptococcus oralis and related species are recognized
14 stant to cleavage by the IgA1 proteases from Streptococcus oralis and Streptococcus mitis biovar 1 st
15 , Tannerella forsythia, Treponema denticola, Streptococcus oralis, and Actinomyces naeslundii levels.
16 s yielded a mutant defective in adherence to Streptococcus oralis, and revealed the essential role of
17 A within typical and atypical S. pneumoniae, Streptococcus oralis, and Streptococcus mitis strains.
18 unts and proportions of Streptococcus mitis, Streptococcus oralis, and Streptococcus mutans, whereas
21 ell as Actinomyces naeslundii ATCC 12104 and Streptococcus oralis ATCC 9811, grown on machine-etched
22 e species or together with initial colonizer Streptococcus oralis but showed mutualistic growth when
23 aggregation receptor polysaccharide (RPS) of Streptococcus oralis C104 have distinct ecological roles
26 ombinant blocks identified originated from a Streptococcus oralis isolate, demonstrating for the firs
28 Streptococcus gordonii 38 and type 2G RPS of Streptococcus oralis J22 are composed of heptasaccharide
29 rides (RPS) of Streptococcus gordonii 38 and Streptococcus oralis J22 was eliminated by replacement o
31 treptococcal species Streptococcus mitis and Streptococcus oralis on the basis of three differentiati
35 ggregation receptor polysaccharides (RPS) of Streptococcus oralis strains C104 and SK144 mediate reco
36 ers of the mitis group (Streptococcus mitis, Streptococcus oralis, Streptococcus gordonii, Streptococ
37 ability of C. albicans to form biofilms with Streptococcus oralis, Streptococcus sanguinis, or Strept
38 results indicated that PC-bearing strains of Streptococcus oralis, Streptococcus sanguis, Haemophilus
39 g the coaggregation of Actinomyces oris with Streptococcus oralis that helps to seed biofilm developm
40 a previously identified gene (i.e., wefM) of Streptococcus oralis that is associated with alpha1-1 tr
41 second set of genetic elements imported from Streptococcus oralis, the choline-independent streptococ
42 treptococci Streptococcus mitis biovar 1 and Streptococcus oralis, the late oral colonizer Streptococ
43 nnerella forsythia, Treponema denticola, and Streptococcus oralis were measured with real-time polyme
45 one or mixed with Actinomyces naeslundii and Streptococcus oralis, were initially formed onto saliva-
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