ライフサイエンスコーパス: CFU

1 CFU counts on BHI-V4 and BHI-V3 plates were stratified a

2 CFU cutoffs that best predict VISA and hVISA were determ

3 CFU inferred from qPCR analysis were positively correlat

4 imit of the detection of the assay, 0.01-1.0 CFU/ml.

5 ion on surfaces with a sensitivity (limit, 0 CFU) greater than that which is otherwise possible.

6 Bacterial growth of more than 0 CFU was noted in 16.1% duodenoscopes in the sHLD group,

7 ited microbial growth (from 1.4 x 10(7) to 0 CFU/mL) and hindered biodegradation.

8 ith starting concentrations as low as 10(0) CFU, from 100 or 250 mL of culture broth within similar

9 nd nonpathogenic E. coli isolates and (10(0) CFU/mL) E. faecalis and E. faecium strains were detected

10 mean residual lung fungal burdens of <1,000 CFU from an otherwise lethal C. posadasii intranasal inf

11 ropathogen, high-level candiduria (>/=50 000 CFU/mL), and any bacteriuria with uropathogens.

12 = 50) vaccination and inoculated with 80,000 CFU/100 mul of Streptococcus pneumoniae (6B) per naris.

13 nge from 5 to 100 CFU/mL with a LOD of 0.093 CFU/mL.

14 The detection limit are 1 CFU/mL and 10 CFU/mL correspondingly.

15 voltammetry (DPV) response from as low as 1 CFU of Mtb bacilli DNA input material, having shown its

16 er limit of detection was determined to be 1 CFU/mul.

17 It has a potential detection limit below 1 CFU/chamber and a total assay time of less than 1 h.

18 agalactiae and detection of bacteremia at <1 CFU/ml were unreliable.

19 The limit of detection was 1 CFU/mL for C. tropicalis and C. krusei, 2 CFU/mL for C.

20 a limit of quantification (LOQ) of 1 x 10(1) CFU mL(-1) and a limit of detection (LOD) of 6 CFU mL(-1

21 n of inoculated (2.3 x 10(2) and 3.1 x 10(1) CFU/mL or g of E. coli and E. faecium, respectively) spr

22 Low concentrations (10(1) CFU/mL) of pathogenic and nonpathogenic E. coli isolates

23 with values ranging from 10.5 to 0.5 x 10(1)CFU g(-1) and the species most found were Fusarium grami

24 ere 5 genome equivalents per reaction and 10 CFU/ml blood for both the B. anthracis Sterne and V1B st

25 The detection limit are 1 CFU/mL and 10 CFU/mL correspondingly.

26 genome equivalents (GE) per reaction and 10 CFU/ml F. tularensis in both human and macaque blood.

27 limit of 0.1 ng of the extracted DNAs and 10 CFU/test, can be achieved.

28 and high detection sensitivity (as low as 10 CFU mL(-1)).

29 pyranoside (IPTG), we were able to detect 10 CFU.mL(-1) in drinking water after 6 h of pre-enrichment

30 ly low concentration of E. coli O157:H7 (~10 CFU/mL) could be detected within 1h and 3h from both pur

31 performance with a limit of detection of 10 CFU mL(-1) in standard buffer and 100 CFU mL(-1) in bott

32 contamination below a detection limit of 10 CFU/25 cm(2) (0.4 CFU/cm(2)).

33 At 1 to 10 CFU/ml, Escherichia coli, Staphylococcus epidermidis, St

34 The detection limit was 10 CFU/mL for both E. coli and N. gonorrhoeae, while commer

35 stically significant impedance change was 10 CFU/mL.

36 tracheal instillation of E. coli (1.5-2 x 10 CFU/kg).

37 ins (Lactobacillus + Lactococcus (6 x 10(10) CFU/g), Bifidobacterium (1 x 10(10)/g), Propionibacteriu

38 (6)/g)) at a dose of 140 mg/kg (1.4 x 10(10) CFU/kg).

39 of 10 CFU mL(-1) in standard buffer and 100 CFU mL(-1) in bottled water and milk.

40 wed detection limits as low as 7, 40 and 100 CFU/mL for S. aureus in pure broth culture, and inoculat

41 low bacterium concentration, i.e., below 100 CFU/mL, blood samples show a random nature.

42 with a limit of quantification (LOQ) of 100 CFU mL(-1) and a limit of detection (LOD) of 3 CFU mL(-1

43 The optimized method provided LOD of 100 CFU.mL(-1) with linear range up to 10(6) CFU.mL(-1).

44 chieve a low limit of detection (LOD) of 100 CFU/mL.

45 inically relevant linear range from 5 to 100 CFU/mL with a LOD of 0.093 CFU/mL.

46 olony-forming units (CFU) in vitro and <1000 CFU in the lungs of mice.

47 08 CFU/mL yielded greater IL-10 than did 103 CFU/mL (4.4 +/- 1.8 vs 1.0 +/- 0.6 pg/mL; P < .01).

48 achieved following challenge with 1-5 x 103 CFU (group 1), which resulted in an attack rate of 12 of

49 Paratyphi A at a dose of 1-5 x 103 CFU was well tolerated and associated with an acceptable

50 forming units [CFU] and group 2: 0.5-1 x 103 CFU).

51 Ex vivo studies showed that 108 CFU/mL yielded greater IL-10 than did 103 CFU/mL (4.4 +/

52 e specificity was lowered to 89.5% with a 12-CFU cutoff.

53 a seeded concentration of approximately 150 CFU.

54 distinguish VISA from hVISA, a cutoff of 16 CFU provided 83.3% sensitivity and 94.7% specificity; th

55 racts were determined to be 57 CFU/mL and 17 CFU/mL for E. coli and 7.4 x 10(3) CFU/mL and 11.7 x 10(

56 Detection limits of 21 CFU/mL and 18 CFU/mL were achieved in stool and blood, respectively, c

57 to draining lymph nodes (controls median 183 CFU per node [IQR 8-5800] vs trauma group 20 000 [1875-6

58 1 CFU/mL for C. tropicalis and C. krusei, 2 CFU/mL for C. albicans and C. glabrata, and 3 CFU/mL for

59 A detection limit (DL) of 2 CFU mL(-1) was reached after 120 min of solar exposure f

60 For VISA screening on BHI-V4, a cutoff of 2 CFU/droplet provided 100% sensitivity and 97.7% specific

61 This assay had a detection limit of 10(2) CFU mL(-1) for S. typhimurium, providing an instrument-f

62 tion of S. typhimurium was found to be 10(2) CFU mL(-1) in culturing solution without any pre-enrichm

63 cs, we determined a detection limit of 10(2) CFU mL(-1).

64 ation ( approximately 10(0), 10(1), or 10(2) CFU of spores) from test surfaces (a bed rail, a stainle

65 an initial bacterial concentration of 10(2) CFU.mL(-1).

66 mL in these aqueous samples in 3 h and 10(2) CFU/mL after 7 h.

67 hetic urine at low concentrations (1 x 10(2) CFU/ml) was detected in FCDI cell lysates using real-tim

68 lony growth at 24 h from as few as 1 x 10(2) CFU/ml.

69 ection for bacterial detection equal to 10(2)CFU (colony formation unit) for live bacteria detection

70 ial pathogens with a detection limit of 10(2)CFU/mL for four bacterial strains including Escherichia

71 bition, selectivity, sensitivity (10(1)-10(2)CFU/mL) and reproducibility (below 12.5%).

72 10(7)CFU/ml and LOD is calculated as 9x10(2)CFU/ml.

73 For detecting hVISA/VISA on BHI-V3, a 2-CFU/droplet cutoff provided 98.5% sensitivity and 93.8%

74 These results suggest that 2-CFU/droplet cutoffs on BHI-V4 and BHI-V3 best approximat

75 Detection limits of 21 CFU/mL and 18 CFU/mL were achieved in stool and blood, r

76 FU/mL for C. albicans and C. glabrata, and 3 CFU/mL for C. parapsilosis.

77 lotype, were infected with a lower dose of 3 CFU M. tuberculosis All animals mounted similar T-cell r

78 U mL(-1) and a limit of detection (LOD) of 3 CFU mL(-1).

79 etection limits of 10(5) CFU g(-1) and 10(3) CFU mL(-1), respectively, and this is the first publishe

80 mL and 17 CFU/mL for E. coli and 7.4 x 10(3) CFU/mL and 11.7 x 10(3)CFU/mL for Salmonella sp., respec

81 mits of detection at 1 x 10(3) to 10 x 10(3) CFU/ml or as few as 50 CFU per assay.

82 t medium, an inoculum size of 1 to 3 x 10(3) CFU/ml, and an incubation time and temperature of 96 h a

83 With the detection limit of 10(3) CFU/mL, crn-1 and crn-2 based platforms detected target

84 or Staphylococcus saprophyticus at >/=10(3) CFU/ml.

85 The lower limit of detection was 10(3) CFU/mL.

86 le detection limit of the biosensor is 10(3) CFU/mL.

87 coli and 7.4 x 10(3) CFU/mL and 11.7 x 10(3)CFU/mL for Salmonella sp., respectively.

88 ase in sensitivity enabled us to detect 10(3)CFU/mL of Escherichia coli in broth after 7h, and by add

89 The LOD was 300 CFU of Mycobacterium tuberculosis in 1 ml sputum.

90 Detection limits (LOD) of 148, 457 and 309 CFU/mL were obtained in buffer solution, minced beef and

91 el sensor has a detection limit of around 32 CFU/mL for C. albicans.

92 1, there was a >12-fold decrease (23 and 331 CFU/mL, respectively; P < .0001).

93 n promoted an increase of approximately 3log CFU/g cycles of the microorganisms and the storage proce

94 ow a detection limit of 10 CFU/25 cm(2) (0.4 CFU/cm(2)).

95 , could be detected with LODs of approx. 2-4 CFU mL(-1) in an assay time of approx. 140 min.

96 m with the limit of detection (LOD) of 10(4) CFU.mL(-1) and the analysis time of 10 min.

97 tect E. coli at a concentration of 1 x 10(4) CFU.mL(-1) within 2.5 h.

98 es for Gram-negative bacteriuria at >/=10(4) CFU/ml and >/=10(5) CFU/ml were 96% and 99%, respectivel

99 nced beef and tap water with 10(3) and 10(4) CFU/mL were 94.7 and 90.4 (in beef) and 91.3 and 94.8% (

100 aureus with starting concentration of 10(4) CFU/mL were removed from 5 mL blood in a few hours.

101 f 0-100ng/ml (R(2)=0.992) and log10 (1-10(4) CFU/ml) (R(2)=0.9918), respectively.

102 strains of heterologous genera (all at 10(4) CFU/ml), or tissue samples from mice infected with MRSA,

103 with gold nanoparticle probes and 10(2)-10(4)CFU for typing bacteria by an on-chip polymerase chain r

104 The LODs of the system were 2.5 x 10(4)CFU/ml and 2.5 x 10(5)CFU/ml for cells spiked into water

105 la detection, a limit of detection of 8x10(4)CFU/mL is achieved within a total assay time of 3h.

106 5.90 CFU/cm(2)), toilet floor (1.87 +/- 2.40 CFU/cm(2)), and chair arm (1.33 +/- 4.69 CFU/cm(2)).

107 type were bronchoscopically infected with 41 CFU of the M. tuberculosis Erdman strain.

108 um pellets, the limit of detection was 1,478 CFU/ml (95% confidence interval [CI], 1,211 to 1,943) at

109 -1) are capable of detecting approximately 5 CFU in 7 hours.

110 in, with high selectivity and sensitivity (5 CFU/mL and 10 microg/g for bacteria and meat, respective

111 nd whole milk with detection limits of 10(5) CFU g(-1) and 10(3) CFU mL(-1), respectively, and this i

112 l strains (E. coli and E. faecalis, at 10(5) CFU mL(-1)) were spiked in real WW.

113 teria concentrations ranging from 10 - 10(5) CFU mL(-1).

114 Volunteers ingested approximately 1 x 10(5) CFU of wild-type V. cholerae O1 El Tor Inaba strain N169

115 and egg samples with 10(3), 10(4) and 10(5) CFU/mL E. coli O157:H7 were 106.98, 96.52 and 102.65 (in

116 with a broad detection range of 10(2)-10(5) CFU/mL in all cases.

117 at the concentration of approximately 10(5) CFU/mL in these aqueous samples in 3 h and 10(2) CFU/mL

118 bacteriuria at >/=10(4) CFU/ml and >/=10(5) CFU/ml were 96% and 99%, respectively.

119 ow the clinical diagnostic criterion (>10(5) CFU/mL) for UTI.

120 respectively, yielding a LOD of 1.0 x 10(5) CFU/ml.

121 2 survive a dose of C. albicans (2.5 x 10(5) CFU/mouse) that is uniformly lethal to wild-type mice wi

122 that the limit of quantitation is 1.9x10(5) CFU/mL with this simple device, which is more than 10,00

123 teria with a detection limit of >/= 5 x 10(5)CFU.

124 system were 2.5 x 10(4)CFU/ml and 2.5 x 10(5)CFU/ml for cells spiked into water and sputum, respectiv

125 0.978 and R(2)=0.992, in range of 10(2)-10(5)CFU/mL.

126 x 10(3) to 10 x 10(3) CFU/ml or as few as 50 CFU per assay.

127 he sensitivity of biosensor was as few as 50 CFU/ml and it showed no responses to other entric bacter

128 in 20min) even at a low concentration of 50 CFU mL(-1), rapid antibacterial rate (100% killing in 30

129 gle specimen spiked with approximately 1,500 CFU bla(KPC) Klebsiella pneumoniae; however, the detecti

130 cells at weeks 1 and 3 after high-dose (500 CFU) M. tuberculosis infection exhibited significantly l

131 hamburger extracts were determined to be 57 CFU/mL and 17 CFU/mL for E. coli and 7.4 x 10(3) CFU/mL

132 U mL(-1) and a limit of detection (LOD) of 6 CFU mL(-1).

133 her group B streptococcus (GBS) at 1 x 10(6) CFU (n = 5) or saline (n = 5) in the choriodecidual spac

134 n spiked (1 x 10(2), 1 x 10(4) and 1 x 10(6) CFU mL(-1)) apple juice samples.

135 infected via the footpad with 10(3) to 10(6) CFU of Brucella spp. display neutrophil and monocyte inf

136 wed by intratracheal Escherichia coli (10(6) CFU) in wild-type mice or those lacking hepatocyte STAT3

137 allenged with a sublethal dose (<2.0 x 10(6) CFU) rapidly lost weight, had diminished lung compliance

138 Lethal challenge (>4.0 x 10(6) CFU) was characterized by fulminate hemorrhagic pneumoni

139 100 CFU.mL(-1) with linear range up to 10(6) CFU.mL(-1).

140 In contrast, after exposure to 10(6) CFU/ml of methicillin-sensitive S. aureus (MSSA) attenua

141 was able to detect luminescence from 10(6) CFU/mL of the bio-reporter, which corresponds to 10(7)

142 st strip also had a detection limit of 10(6) CFU/mL, but this method is not antibody-based and thus n

143 rapid kit showed a detection limit of 10(6) CFU/mL.

144 c detection of S. aureus cells as low as 682 CFU in whole blood.

145 mean CFUs per milliliter (90 596 and 114 683 CFU/mL for serogroup B and C strains, respectively; P <

146 .40 CFU/cm(2)), and chair arm (1.33 +/- 4.69 CFU/cm(2)).

147 nd blood, respectively, corresponding to 2-7 CFUs immobilized on the detecting electrode.

148 el, in which we used 25 mug of CRP and 10(7) CFU of pneumococci, both wild-type and mutant CRP protec

149 l, in which we used 150 mug of CRP and 10(7) CFU of pneumococci, mutant CRP was as protective as wild

150 in which we used 25 mug of CRP and 5 x 10(7) CFU of pneumococci, mutant CRP was not protective while

151 yeast transformation efficiency up to 10(7) CFU per mug plasmid DNA and per 10(8) cells with a 13.8

152 reus with a starting concentration of 10(7) CFU/mL and 95.4 +/- 1.0% of Methicillin-resistant Staphy

153 nd the linear range of the assay up to 10(7) CFU/mL.

154 ith plate counting at a range of 10(3)-10(7) CFU/mL.

155 ntrations ranging from ~10(5) to 3.2 x 10(7) CFUs/mL in phosphate buffered saline (PBS) and peritonea

156 d out within the range of 1.0x10(2)-1.0x10(7)CFU/mL.

157 ures with populations ranging from 1 to 10(7)CFU/10mL were detected in a single step without any prep

158 the sensitivity range is from 10(1) to 10(7)CFU/ml and LOD is calculated as 9x10(2)CFU/ml.

159 eria, even at concentrations as high as 10(7)CFU/mL.

160 llin provided significant reduction (1.73log CFU/g) in yeast-mold growth.

161 nucleic acid fragments of Ebola virus, and 8 CFU of Escherichia coli carrying Ebola virus-derived pla

162 ration was carried out using 10(7) and 10(8) CFU mL(-1) Pseudomonas fluorescens to study the effects

163 urium in the concentration range 10(2)-10(8) CFU mL(-1) with high selectivity over other model pathog

164 he lateral tail vein), and muscle (1 x 10(8) CFU per mouse intramuscularly) at three timepoints after

165 Apc(Min/+) mice were infected with CR (10(8) CFU); BLT1(-/-)Apc(Min/+) mice, azoxymethane (AOM)/dextr

166 ised in a wide range between 10(4) and 10(8) CFU/mL, where linear relation was found between conducti

167 acteria concentration between 10(1) to 10(8) CFU/mL.

168 he concentration range 1 x 10(1) to 1 x 10(8)CFU mL(-1), with a limit of quantification (LOQ) of 1 x

169 constitute an obstacle to L. casei 01 (>10(8)CFU/g) during storage.

170 more bacteria than the estimated ID50 (2.83 CFU g(-1)), consistent with a soil-borne reservoir emerg

171 o 1,943) at a 3:1 ratio and decreased to 832 CFU/ml (95% CI, 671 to 1,134) at 2:1.

172 s contaminated ( approximately 1.34 +/- 6.88 CFU/cm(2) C. difficile spores).

173 imalis VKB) at a dose of 50 mg/kg (5 x 10(9) CFU/kg) (g) (intragastrically).

174 nt: a dirty utility room sink (2.26 +/- 5.90 CFU/cm(2)), toilet floor (1.87 +/- 2.40 CFU/cm(2)), and

175 sor cells that give rise to plastic-adherent CFU-Fs.

176 rming units [CFUs]) increased from 4% of all CFUs at week 4 to 16% at week 12, indicating transductio

177 ositivity rates of 0%, 0%, 30%, and 100% and CFU detection of blood culture at 0%, 0%, 0%, and 10% po

178 he correlations among ALDH(br), CD34(+), and CFU content of 3908 segments over a 5-year period.

179 and erythroid colony-forming unit (BFU-E and CFU-E) colonies, the clonogenic assays that quantify ear

180 st-forming unit-erythroid/CFU-erythroid, and CFU-granulocyte/erythroid/macrophage/MK) irrespective of

181 dard incubator at 37 degrees C, with TTD and CFU being monitored for up to 72 h.

182 f the standard regimen based by both TTP and CFU/mL over 28 days of treatment.

183 reased abscess severity, MRSA viability, and CFU density in skin.

184 The circulating WBCs and LSKs, and CFUs were reduced in both models with a shorter duration

185 nto individual PCR mixtures and B. anthracis CFU into human blood.

186 Bacteriuria with any CFU/mL was also reduced in men in the universal decoloni

187 committed Mk and E progenitors identified as CFU-Mk and burst forming unit-E.

188 d by increases in bioluminescence, S. aureus CFU in tissue, and death within the first 7 days.

189 d the biofilm bacterial burden of S. aureus (CFU cm(-2)) by three logs with no statistically signific

190 In MS-WF-exposed mice CV-3988 reduced BALF CFU values.

191 tently high correlation coefficients between CFU and relative bioluminescence; P. aeruginosa ATCC9027

192 ishes or on collagen membrane and assayed by CFU, live-dead staining using confocal microscopy, trans

193 lular M. tuberculosis growth (as measured by CFU count).

194 silosis for at least 28 days, as measured by CFU.

195 g agents (EDTA formulations) reduced E. coli CFU but were ineffective at disrupting preformed biofilm

196 ed kitchen floors (Beta: -0.65 log10 E. coli CFU/900 cm(2); 95% CI: -1.15, -0.16).

197 n and dirt floors (Beta: -1.18 log10 E. coli CFU/900 cm(2); 95% confidence interval [CI]: -1.77, -0.6

198 The relationship between culturable counts (CFU) and quantitative PCR (qPCR) cell equivalent counts

199 Between 4 h and 10 days, CFU numbers increased to numbers comparable to the inocu

200 B-infected mice could significantly decrease CFU counts in the lung and spleen.

201 Notably, MET-1 did not decrease CFUs of Salmonella in the intestine.

202 by reduced abscess severities and decreased CFU densities compared to those in naive controls.

203 idal activity, demonstrated by the decreased CFU recovery of internalized yeasts, with comparable pha

204 ve detection of Shigella on the single-digit CFU level suggests the feasibility of the direct detecti

205 stool and blood matrixes at the single-digit CFU level.

206 [tdT+] BM cells), circulating and splenic EC-CFUs were BM-derived (tdT+), whereas cells positive for

207 ssing markers of EC colony-forming units (EC-CFUs) were detected.

208 in the E. coli numbers determined as either CFU or gene copies during the summer for the field-expos

209 yte/macrophage, burst-forming unit-erythroid/CFU-erythroid, and CFU-granulocyte/erythroid/macrophage/

210 d with serotype Enteritidis received 10 exp7 CFU intramuscularly.

211 orally to serotype Kentucky received 10 exp9 CFU, and hens injected with serotype Enteritidis receive

212 to generate colony-forming unit-fibroblasts (CFU-Fs) on plastic and the large cell numbers required f

213 portional to the bacterial concentrations in CFU/ml.

214 ll density, indicating that the reduction in CFU number is explained by cells entering into a Viable

215 rain LH128-GFP showed about 99% reduction in CFU while microscopic counts of GFP-expressing cells wer

216 solates were observed to have a reduction in CFU, and minimal effects were observed for P. aeruginosa

217 ed were unaffected except for an increase in CFUs in the colon.

218 ferentiates down both the Mk and E lineages (CFU-Mk/E), which allowed development and validation of a

219 t 9 log CFU/g, ranging from 7.11 to 9.21 log CFU/g, respectively.

220 rvival, with presented values of about 9 log CFU/g, ranging from 7.11 to 9.21 log CFU/g, respectively

221 vo, single-dose phage therapy killed 2.5 log CFUs/g of vegetations in 6 hours (P < .001 vs untreated

222 ions were highly synergistic, killing >6 log CFUs/g of vegetations in 6 hours and successfully treati

223 counts to the limit of detection (2.0 log10 CFU/g), whereas metronidazole was associated with mean C

224 nterally in a daily dose of 8.2 to 9.2 log10 CFU; the placebo was dilute infant formula alone.

225 Second, stable necrotic granulomas with low CFU counts and limited inflammation are characterized by

226 MazFsa in the cshA mutant resulted in lower CFU per milliliter accompanied by a precipitous drop in

227 bronchoalveolar lavage fluid (BALF) and lung CFU values were determined.

228 pores and led to a 26-fold reduction in lung CFU by 6 d postinfection versus nondepleted mice.

229 time frame that correlated with reduced lung CFU.

230 neumococci developed significantly more lung CFUs at 48 h.

231 re was a >22-fold increase in geometric mean CFUs per milliliter (90 596 and 114 683 CFU/mL for serog

232 patients with low IL-10 (35.5 vs 0.5 median CFU/mL; P = .044).

233 ble HPCs (colony-forming unit-megakaryocyte [CFU-MK], CFU-granulocyte/macrophage, burst-forming unit-

234 ng both colony-forming units per milliliter (CFU/mL) and time to positivity (TTP).

235 e 10(0) colony forming units per milliliter (CFU/mL) with a detection limit of 9.4 x 10(-12) mol L(-1

236 (colony-forming unit-megakaryocyte [CFU-MK], CFU-granulocyte/macrophage, burst-forming unit-erythroid

237 was 1.2 x 10(2) colony-forming-units per mL (CFU/mL), which is well below the clinical diagnostic cri

238 d at just 10(1) colony forming units per mL (CFU/mL).

239 und to be 2.17x10(2) colony forming unit/ml (CFU/ml).

240 Bacterial growth or 10 or more CFU was noted in 2.3% of duodenoscopes in the sHLD group

241 ably, comparative evaluation showed that MTB CFU counts in BBD-treated mice were lower than those in

242 umococcal infection increased the numbers of CFU recovered from an intranasal mouse model of infectio

243 rence was most prominent at lower numbers of CFU/ml.

244 at 2:1 than at 3:1 for almost all numbers of CFU/ml; this difference was most prominent at lower numb

245 nt, which resulted in an increased number of CFUs in the lung.

246 F. tularensis DNA in buffer or CFU of F. tularensis was spiked into human or macaque bl

247 e number of colony-forming unit osteoblasts (CFU-Os), a surrogate marker of undifferentiated mesenchy

248 onan production (mucoid colonies 200 mug per CFU and no detectable capsule production in the non-muco

249 ion and increased BALF and lung pneumococcal CFU values.

250 e colony-forming unit erythroid progenitors (CFU-Es) that respond to Epo are either too few in number

251 We reviewed the growth results (CFU) during population analysis profile-area under the c

252 and enhances the formation of Epo-sensitive CFU-E progenitors.

253 e sensitive measure of bacterial burden than CFU/mL.

254 The CFU of recoverable P. aeruginosa and K. pneumoniae isola

255 iesis failure occurs in these animals at the CFU-E/proerythroblast stage, a point at which the transf

256 rupting preformed biofilms or decreasing the CFU of P. aeruginosa and K. pneumoniae within a biofilm.

257 From the CFU-E/proerythroblast (CD71(+) Ter119(-) cells) stage on

258 However, the CFU assay is difficult to standardize and requires 2 wee

259 e veterinary practice was able to reduce the CFU and biofilm biomass of all three Gram-negative speci

260 ecreased the biofilm biomass and reduced the CFU of E. coli isolates, K. pneumoniae isolates were obs

261 U) per reaction for L. pneumophila and three CFU per reaction for S. typhimurium and S. aureus.

262 )CD105(+)CD36(+) cells as LEP giving rise to CFU-E, in a hierarchical fashion.

263 ily fall in log10 Mycobacterium tuberculosis CFU per milliliter sputum estimated by joint nonlinear m

264 an daily rate of reduction in M tuberculosis CFUs per mL overnight sputum collected once a week, with

265 ion functional in vitro colony-forming unit (CFU) assay for single cells that differentiates down bot

266 (+) (LSK) cells, and by colony forming unit (CFU) assay.

267 ation and comparison of colony forming unit (CFU) counting and optical density (OD) measurements.

268 ells), proliferation by colony forming unit (CFU) counts, and differentiation by staining for the pre

269 detection (LOD) of 150 colony forming unit (CFU)mL(-1) of C. jejuni in solution.

270 tween bioluminescence, colony-forming units (CFU) count and fluorescence were obtained for BKC concen

271 her than 6.5 and 7 log colony-forming units (CFU) g(-1) of cheese at the 1st and 28th days of storage

272 0 is approximately 100 colony-forming units (CFU) in vitro and <1000 CFU in the lungs of mice.

273 than 0 and 10 or more colony-forming units (CFU) of aerobic bacterial growth on either sampling loca

274 PCR assay achieved two colony-forming units (CFU) per reaction for L. pneumophila and three CFU per r

275 a dramatic decrease in Colony Forming Units (CFU) upon soil inoculation but this behavior is not well

276 lture and expressed as colony-forming units (CFU).

277 ring 20 years were 507 colony forming units (CFU)/5 plate every year.

278 ining a total of 10(7) colony-forming units (CFU)/g of Bifidobacterium bifidum, Bifidobacterium breve

279 concentration of 10(2) colony forming units (CFU)/mL and -88.1+/-6.3mV/pH over a pH range of 1-13) an

280 it of detection of 300 colony forming units (CFU)/mL for C. trachomatis and 1500CFU/mL for N. gonorrh

281 of genomic DNA and 10 colony-forming units (CFU)/ml of bacterial cells with dynamic ranges of 0-100n

282 the LPG-ISAM to 10(2) colony forming units (CFU)/ml of MR S. aureus (MRSA) for 50 min., light transm

283 ns starting from 10(1) colony forming units (CFU)mL(-1) in KCl and from 10(2) CFUmL(-1) in artificial

284 sence of inhibitors, colony formation units (CFUs) per milliliter in blood from all 12 immunized subj

285 es higher fibroblastic colony-forming units (CFUs) and mesensphere capacity, criteria for assessing s

286 Colony-forming units (CFUs) have been previously shown to predict CBU potency,

287 ples were analyzed for colony forming units (CFUs) of E. coli, and households were evaluated for thei

288 ned as the decrease in colony forming units (CFUs) of Mycobacterium tuberculosis in the sputum of pat

289 aused the reduction in colony forming units (CFUs) substantially for almost 3 orders of magnitude.

290 fection as measured by colony-forming units (CFUs).

291 e therapy killed 7 log colony-forming units (CFUs)/g of fibrin clots in 6 hours.

292 rations from <1 to 100 colony-forming units (CFUs)/mL for 5 different Candida species.

293 ls (group 1: 1-5 x 103 colony-forming units [CFU] and group 2: 0.5-1 x 103 CFU).

294 challenge of 1 x 10(7) colony forming units [CFU] per mouse), intravenous (1 x 10(7). per mouse via t

295 10 C. difficile count (colony-forming units [CFU]) of 6.7 +/- 2.0 at study entry; vancomycin treatmen

296 pproximately 5 x 10(8) colony-forming units [CFU]) or placebo in double-blind fashion.

297 bacteriuria (>/=50 000 colony forming units [CFU]/mL) with any uropathogen, high-level candiduria (>/

298 uria (ie, at least 105 colony-forming units [CFUs] per milliliter of 1 or 2 microorganisms in urine c

299 e progenitor colonies (colony-forming units [CFUs]) increased from 4% of all CFUs at week 4 to 16% at

300 CI, 0.22-0.28), was strongly correlated with CFU content as well as ALDH(br) content of the CBU.