ライフサイエンスコーパス: Actinomyces naeslundii

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1 regulated in response to coaggregation with Actinomyces naeslundii.

2 n of KB cells by other oral streptococci and Actinomyces naeslundii.

3 ion with only group A and group E strains of Actinomyces naeslundii.

4 eponema denticola, Tannerella forsythia, and Actinomyces naeslundii.

5 us gordonii but was required for adhesion of Actinomyces naeslundii.

6 sitive coaggregations of these bacteria with Actinomyces naeslundii.

7 uman erythrocytes, and to the oral bacterium Actinomyces naeslundii.

8 monas gingivalis, Peptostreptococcus micros, Actinomyces naeslundii, Actinomyces israelii, Streptococ

9 Only the Sg/Actinomyces naeslundii (An)/Fn multispecies biofilms eli

10 Actinomyces naeslundii, an early colonizer of the oral c

11 The oral bacteria Actinomyces naeslundii and Actinomyces viscosus are know

12 he Orange-Blue cluster score (which included Actinomyces naeslundii and Eubacterium nodatum) was inve

13 al pathogens including Streptococcus mutans, Actinomyces naeslundii and Prevotella intermedia.

14 Actinomyces naeslundii and Streptococcus gordonii, oral

15 Biofilms of S. mutans, alone or mixed with Actinomyces naeslundii and Streptococcus oralis, were in

16 hogen Streptococcus mutans UA159, as well as Actinomyces naeslundii ATCC 12104 and Streptococcus oral

17 y in vitro on streptococcal biofilms than on Actinomyces naeslundii biofilms.

18 increased the ability of enterococci to bind Actinomyces naeslundii cells.

19 sequence of the chromosomal DNA flanking the Actinomyces naeslundii (formerly A. viscosus) T14V type

20 eptococcus sanguis, Haemophilus aphrophilus, Actinomyces naeslundii, Fusobacterium nucleatum, and A.

21 tobacillus acidophilus, Lactobacillus casei, Actinomyces naeslundii genospecies (gsp) 1 and 2, total

22 immune response in saliva to colonization by Actinomyces naeslundii genospecies 1 and 2 was studied i

23 These species included Actinomyces naeslundii II, Actinomyces israelii, Actinom

24 d of species found in healthy oral biofilms (Actinomyces naeslundii, Lactobacillus casei, Streptococc

25 eponema denticola, Streptococcus oralis, and Actinomyces naeslundii levels.

26 hydroxyapatite and did not coaggregate with Actinomyces naeslundii PK606.

27 Actinomyces naeslundii, Prevotella spp., and Porphyromon

28 in the presence of Streptococcus oralis and Actinomyces naeslundii steadily formed exopolysaccharide

29 brial gene clusters present in the genome of Actinomyces naeslundii strain MG-1.

30 he oral key pathogens Enterococcus faecalis, Actinomyces naeslundii, Streptococcus mutans, and Aggreg

31 ive with antibody against type 2 fimbriae of Actinomyces naeslundii T14V (anti-type-2) were much less

32 saliva of two human oral commensal bacteria, Actinomyces naeslundii T14V and Streptococcus oralis 34,

33 The type 1 fimbriae of Actinomyces naeslundii T14V mediate adhesion of this gra

34 The nucleotide sequence of the Actinomyces naeslundii T14V type 2 fimbrial structural s

35 s gordonii DL1, Streptococcus oralis 34, and Actinomyces naeslundii T14V).

36 The ability of Actinomyces naeslundii to convert sucrose to extracellul

37 organisms such as Streptococcus gordonii and Actinomyces naeslundii to the saliva-coated tooth surfac

38 When the main fimbrial subunit of Actinomyces naeslundii type I fimbriae, FimA, is express

39 ide to support fimbriae-mediated adhesion of Actinomyces naeslundii was explained by the position of

40 Streptococcus sanguis and type 2 fimbriated Actinomyces naeslundii, which bound terminal sialic acid

41 and characterized the urease gene cluster of Actinomyces naeslundii, which is one of the pioneer orga

42 A gene encoding FTF was isolated from Actinomyces naeslundii WVU45; the deduced amino acid seq

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