ライフサイエンスコーパス: bacterial count

1 d the expiry period showed no marked drop in bacterial count.

2 sive care unit-acquired pneumonia and higher bacterial count.

3 ly at different time points for quantitative bacterial counts.

4 er standardization of IL-8 concentrations to bacterial counts.

5 l one associated with higher intraperitoneal bacterial counts.

6 USA300 strains caused reduced pathology and bacterial counts.

7 r system (in vivo imaging system [IVIS]) and bacterial counts.

8 only moderately larger with minimally higher bacterial counts.

9 ntal endocarditis infections by target organ bacterial counts.

10 ng compared to wild-type 104, as assessed by bacterial counts.

11 cterial cells directly from samples with low bacterial counts (10(4) cfu/mL) using a custom-designed

12 Infection, defined as a bacterial count above 50,000 cfu/ml, was present in 27 C

13 stigations demonstrate a >5-log reduction in bacterial counts after 5 minutes of AMF exposure.

14 Bacterial counts after decontamination confirmed that th

15 ctions in corneal pathology and also lowered bacterial counts after infection with six different labo

16 In the test group, 71.25% of the bacterial count analyses for the eight different periodo

17 te (IA3902) resulted in significantly higher bacterial counts and a significantly longer duration of

18 Lungs were processed for leukocyte and bacterial counts and cytokine measurements.

19 WT mice, which was associated with increased bacterial counts and elevated inflammatory cytokine and

20 ented milks, such as acidification kinetics, bacterial counts and fatty acid content.

21 1alpha, developed larger lesions with higher bacterial counts and had decreased neutrophil recruitmen

22 in was accompanied by a >50-fold increase in bacterial counts and higher numbers of viable intracellu

23 ubstantially larger skin lesions with higher bacterial counts and impaired neutrophil recruitment com

24 any of the subsequent time points, except in bacterial counts and MPO activity.

25 Bacterial counts and neutrophil counts were significantl

26 Associations between preterm birth and bacterial counts and percentages were tested using multi

27 c FasL(-/-) exhibited significantly elevated bacterial counts and polymorphonuclear leukocyte numbers

28 mBD2 silencing also increased bacterial counts and polymorphonuclear neutrophil infilt

29 Changes in bacterial counts and proportions during pregnancy also w

30 topathology, myeloperoxidase (MPO) activity, bacterial counts, and ELISA analysis were used to assess

31 the number of infected pancreatic specimens, bacterial counts, and identified species at 1 week.

32 assessed by electroretinography, histology, bacterial counts, and myeloperoxidase ELISAs.

33 increased corneal opacity, PMN infiltration, bacterial counts, and perforated infected corneas.

34 ry reaction, abscess wall formation, abscess bacterial counts, and peritoneal bacterial counts, were

35 decreased the number of perforated corneas, bacterial counts, and PMNs.

36 Clinical score, slit lamp, histopathology, bacterial counts, and polymorphonuclear neutrophil (PMN)

37 tion, slit lamp examination; clinical score; bacterial counts; and myeloperoxidase (MPO), RT-PCR, ELI

38 In the present study, bacterial counts around single implants in periodontally

39 M1 showed decreased survival and higher lung bacterial counts, as well as increased dissemination of

40 metry and microscopy and by determining live bacterial counts associated with B cells both in vivo an

41 fewer vitreous exudates, and higher vitreous bacterial counts at 24 hours (P < 0.05).

42 There was no consistent difference in bacterial counts at any of the time points when comparin

43 ase chain reaction was used to measure total bacterial counts, Bacteroides/Prevotella (herein referre

44 rial adherence is insufficient to reduce the bacterial counts below that which elicits disease.

45 was demonstrated in animal models, reducing bacterial counts by six orders of magnitude, and contrib

46 s, we found that G. vaginalis and M. hominis bacterial counts, Candida vaginitis, and herpes simplex

47 early inflammation and a delayed increase in bacterial counts compared to animals infected with NTHi

48 y E. coli had significantly higher pulmonary bacterial counts compared with animals that received E.

49 xhibited lower mortality and decreased brain bacterial counts compared with mice infected with the co

50 ice display persistently elevated peritoneal bacterial counts compared with wild-type mice, reduced p

51 t mice were substantially larger with higher bacterial counts compared with wild-type mice.

52 o approximately 7.6 log(10) by 18 hours, but bacterial count declined to approximately 6.4 log(10) CF

53 Differential bacterial counts demonstrated that motile bacteria outco

54 Quantitative bacterial counts for lactobacilli and M. hominis are bet

55 revealed rapid and significant decreases in bacterial counts for protegrin-1-treated groups compared

56 ifferences occurred despite the finding that bacterial counts for the strain pairs were indistinguish

57 Based on bacterial counts from excised tissue, the liver density

58 Utilizing all three log(10) bacterial counts (G. vaginalis, M. hominis, and lactobac

59 hoc exploratory analyses of UTIs with higher bacterial counts (>/=10(5) colony-forming units per mL),

60 sera were collected after each challenge for bacterial counts, histological evaluation, cytokine prof

61 tes (HCTLR4KO) and then determined survival, bacterial counts, host inflammatory responses, and organ

62 ameliorated corneal disease and reduced the bacterial count in the eye.

63 PVL(+) strains also had significantly higher bacterial counts in abscesses compared with mice given n

64 helial and lymphocyte apoptosis and systemic bacterial counts in animals given iron supplementation a

65 Animals receiving I-IgG had lower bacterial counts in blood samples and lower bacterial de

66 .5% of positive sample pairs had significant bacterial counts in both lungs.

67 e had a six- to eight-fold increase in total bacterial counts in comparison with sham and control mic

68 Bacterial counts in homogenized lungs and bronchoalveola

69 IL-6 treatment reduced total and liver bacterial counts in HS/IL-6 mice by 62% and 69%, respect

70 ory CD8+ T cells can reduce spleen and liver bacterial counts in IFN-gamma-deficient mice 3 d after L

71 th no attractant showed no increase in total bacterial counts in low permeability regions.

72 stant C57BL/6 mice, the mutant achieved high bacterial counts in lung and spleen that persisted in ti

73 (TNF) and interferon (IFN)-gamma, increased bacterial counts in lungs and blood, and early lethality

74 ed lung levels of TNF and IFN-gamma, reduced bacterial counts in lungs and plasma 40 h after the inoc

75 Decreased bacterial counts in mice infected with a cydC mutant (de

76 Among infected animals, bacterial counts in middle ear fluid specimens 7 days po

77 For example, bacterial counts in middle-ear fluids and the severity o

78 resulted in significantly lower total viable bacterial counts in moderate-to-deep pockets when compar

79 tiserum to mice produced significantly lower bacterial counts in organs than did normal rabbit serum

80 At late phase of infection, enhanced bacterial counts in PFOS treated mice were accompanied b

81 d was quantified in terms of change in total bacterial counts in pore throats in low permeability reg

82 n resulted in elevated PMN levels and viable bacterial counts in the cornea 3 and 5 days after infect

83 e susceptible to L. pneumophila, with higher bacterial counts in the lung.

84 We show that the viable and total bacterial counts in the lungs of chronically infected mi

85 nt (MyD88(-/-)) mice had dramatically higher bacterial counts in the lungs, with decreased neutrophil

86 r CFTR peptide 108-117 resulted in increased bacterial counts in the lungs.

87 and led to a substantial reduction of viable bacterial counts in the lungs.

88 ility to fluorescein isothiocyanate dextran, bacterial counts in the mesenteric lymph nodes complex,

89 sociated with, and perhaps due to, increased bacterial counts in the peritoneal cavity.

90 A large increase in bacterial counts in the pore throats just outside the lo

91 When mastitis occurred, the milk bacterial counts in the probiotic group were significant

92 erleukin-12 (IL-12) antibodies, resulting in bacterial counts in the spleens and livers of anti-IL-12

93 cholera toxin (CT), had significantly lower bacterial counts in their kidneys ( P = 0.001) and splee

94 e that lacked both T-cell subsets had higher bacterial counts in their livers 15 to 18 days after inf

95 d no significant effect on individual plaque bacterial counts in unadjusted models or those adjusted

96 mice, serum levels of IL-6 and TNF-alpha and bacterial counts in various organs were significantly re

97 Body weight, bacterial count, inflammation, and lung pathology were e

98 se (i.e., cachexia, diarrhea, and high fecal bacterial counts) is preceded by a lengthy subclinical s

99 s developed an inflammatory lesion with high bacterial counts, marked neutrophil infiltration, and hi

100 Finally, a loss of bacterial counts occurs after the first round of growth.

101 rs were recorded, and total and quantitative bacterial counts of Aggregatibacter actinomycetemcomitan

102 marcescens, 3 Acps significantly reduced the bacterial counts of infected females, suggesting a prote

103 Bacterial counts of the middle ear effusions were lower

104 There was no change in the total aerobic bacterial count or total mould count as a result of trea

105 ts (P=.006; inverse association), M. hominis bacterial counts (P=.0001; positive association), Candid

106 In multivariate analysis, only lactobacilli bacterial counts (P=.006; inverse association), M. homin

107 In vivo, lung bacterial count, pulmonary immune response (neutrophil m

108 An increase in total bacterial counts, ranging from 1.09 to 1.74 times, was o

109 he control sites indicated that 90.6% of the bacterial counts remained the same, 6% increased, and 3%

110 se of recombinant IL-17 had lesion sizes and bacterial counts resembling those of WT mice, demonstrat

111 GBS) showed 100% detection, but at the lower bacterial counts, SBCB and IGLB were more sensitive than

112 However, bacterial counts subsequently increased and by 15 hrs an

113 as associated with a significant decrease in bacterial counts, suppressed bacterial production of PVL

114 nt, proteolytic activities and psychrophilic bacterial count than did samples treated with soybean an

115 ceptibility more rapidly, with lower initial bacterial counts than existing commercial systems, and p

116 ontal diseases sites, as well as lower total bacterial count, than all the other groups at 180 days.

117 This phenotype was accompanied by higher bacterial counts, the formation of extracellular bacteri

118 By relating bacterial count to infectiousness and fitting dynamic ep

119 1 by 24-48 hours of infection, and increased bacterial counts up to 5 days after infection, compared

120 g 173 positive BAL sample pairs, significant bacterial counts were detected exclusively in 6.4% of le

121 aerodynamics were evaluated; neutrophil and bacterial counts were determined in bronchoalveolar lava

122 sted and levels of cytokines, defensins, and bacterial counts were determined.

123 Bacterial counts were done, and the MIC of each mouthwas

124 Very high bacterial counts were found in the ileum and cecal conte

125 In contrast, blood bacterial counts were greatest in deficient mice.

126 Bacterial counts were higher in the AP group for Parvimo

127 acterial counts, were all similar, but blood bacterial counts were higher.

128 in CapG(+/+) mice at days 5 to 9, while the bacterial counts were identical on day 5 for Salmonella-

129 d tailings pH and neutrophilic heterotrophic bacterial counts were observed.

130 rviving animals were sacrificed at 72 h, and bacterial counts were performed on their kidneys, livers

131 Total bacterial counts were significantly reduced by doxycycli

132 on, abscess bacterial counts, and peritoneal bacterial counts, were all similar, but blood bacterial

133 WT mice, Kit(W-sh/W-sh) mice showed reduced bacterial counts with less bacterial dissemination to di

134 Total viable bacterial count, yeast and mould count, colour, essentia