ライフサイエンスコーパス: Peptostreptococcus

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1 gilis group, Fusobacterium, Clostridium, and Peptostreptococcus.

2 rium (12), Leptotrichia (8), Mobiluncus (8), Peptostreptococcus (16), and Propionibacterium (24).

3 Peptostreptococcus, Actinomyces, and Peptostreptococcace

4 0.01), Anaerococcus tetradius (P < 0.05) and Peptostreptococcus anaerobius (P < 0.05) and lower level

5 Gardnerella vaginalis, Prevotella bivia, and Peptostreptococcus anaerobius, acidified their growth me

6 omonas asaccharolytica, Mobiluncus curtisii, Peptostreptococcus anaerobius, and Gardnerella vaginalis

7 toid cells, whereas Bacteroides ureolyticus, Peptostreptococcus anaerobius, and Lactobacillus acidoph

8 ptococcus micros, Peptostreptococcus magnus, Peptostreptococcus anaerobius, Porphyromonas gingivalis,

9 erous of which were gram positive, including Peptostreptococcus and Filifactor.

10 Peptostreptococcus asaccharolyticus and Prevotella bivia

11 negative than the corresponding clusters of Peptostreptococcus asaccharolyticus ferredoxin and relat

12 Oral Peptostreptococcus isolates tentatively identified by co

13 vo immunobiologic properties of protein L of Peptostreptococcus magnus (PpL), a microbial Ig-binding

14 rotein L (PpL) is a B-cell superantigen from Peptostreptococcus magnus known to bind to mammalian Vka

15 0(-6) M to protein L, a cell-wall protein of Peptostreptococcus magnus, independent of the IgH, indic

16 terium nucleatum, Peptostreptococcus micros, Peptostreptococcus magnus, Peptostreptococcus anaerobius

17 pecies (7.9%), Campylobacter species (2.2%), Peptostreptococcus micros (3.4%), and Candida albicans (

18 es of Bacteroides forsythus (P = 0.0006) and Peptostreptococcus micros (P = 0.0001) than the AnaeroPa

19 Total microbial counts and the percentage of Peptostreptococcus micros and Capnocytophaga species at

20 tans; Actinomyces meyeri was coisolated with Peptostreptococcus micros and was the only species other

21 studies provide strong evidence implicating Peptostreptococcus micros in the pathogenesis of various

22 he AP group for Parvimonas micra (previously Peptostreptococcus micros or Micromonas micros) (7.7 x 1

23 rium nucleatum, Parvimonas micra [previously Peptostreptococcus micros or Micromonas micros], Campylo

24 cterium nucleatum, Porphyromonas gingivalis, Peptostreptococcus micros, Actinomyces naeslundii, Actin

25 cocci, capnocytophagae, Veillonella parvula, Peptostreptococcus micros, and Fusobacterium nucleatum.

26 votella intermedia, Fusobacterium nucleatum, Peptostreptococcus micros, and Streptococcus intermedius

27 votella intermedia, Fusobacterium nucleatum, Peptostreptococcus micros, and Streptococcus intermedius

28 us intermedius, Fusobacterium nucleatum, and Peptostreptococcus micros, and teeth were sealed to prev

29 hyromonas gingivalis, Fusobacterium species, Peptostreptococcus micros, Bacteroides forsythus, and mo

30 ate with strains of Fusobacterium nucleatum, Peptostreptococcus micros, Peptostreptococcus magnus, Pe

31 Prevotella heparinolytica, Prevotella spp., Peptostreptococcus micros, Streptococcus milleri group,

32 um nucleatum, Streptococcus intermedius, and Peptostreptococcus micros.

33 lobacter species, Fusobacterium species, and Peptostreptococcus micros.

34 e of anaerobic, proteolytic bacteria such as Peptostreptococcus, Porphyromonas and Prevotella.

35 as, Desulfovibrio, Leptotrichia, Mobiluncus, Peptostreptococcus, Porphyromonas, Provetella, Propionib

36 rium, Fusobacterium, Gemella, Mogibacterium, Peptostreptococcus, Prevotella, Propionibacterium, Selen

37 mble those of the NADH-dependent enzyme from Peptostreptococcus productus and the NADPH-dependent enz

38 Streptococcus avium, Eubacterium contortum, Peptostreptococcus productus, and B. vulgatus [DESEP-B])

39 us protein G (SpG), and Finegoldia (formerly Peptostreptococcus) protein L (PpL).

40 = .008), Lactobacillus (r = 0.45, P = .001), Peptostreptococcus (r = 0.37, P = .008), and Capnocytoph

41 One such mucin utilizer, Peptostreptococcus russellii, reduces susceptibility to

42 phyromonas sp., Fusobacterium nucleatum, and Peptostreptococcus sp.

43 were Bacteroides fragilis group (n = 9) and Peptostreptococcus sp. (n = 6) isolates.

44 factor alocis, A. actinomycetemcomitans, and Peptostreptococcus sp. human oral taxon 113 (HOT-113).

45 m spp., Filifactor alocis, Parvimonas micra, Peptostreptococcus sp. OT113, Fusobacterium sp. OT203, P

46 trichia (Sneathia) spp., a Bergeyella sp., a Peptostreptococcus sp., Bacteroides spp., and a species

47 Several Peptostreptococcus species contain a gene cluster enabli

48 tes were anaerobic gram-negative bacilli and Peptostreptococcus spp.

49 s: Bacteroides fragilis group (85 isolates), Peptostreptococcus spp. (72 isolates), Prevotella spp. (

50 86% agreement) or in cases of light growth (Peptostreptococcus spp., 86% agreement).

51 eus, coagulase-negative staphylococci (CNS), Peptostreptococcus spp., Bacteroides fragilis, Escherich

52 nce and prevalence of Leptotrichia wadei and Peptostreptococcus stomatis were higher in tongue coatin

53 the genera Corynebacterium, Staphylococcus, Peptostreptococcus, Streptococcus, and Escherichia.

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