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1 li DH5alpha) and halotolerant cells (such as Staphylococcus epidermidis).
2 r crRNA primary processing and maturation in Staphylococcus epidermidis.
3 n binding protein present in most strains of Staphylococcus epidermidis.
4 the Gram-positive device-associated pathogen Staphylococcus epidermidis.
5 ostridium subterminale, Escherichia coli, or Staphylococcus epidermidis.
6 /- 0.9-fold) on exposure to S aureus but not Staphylococcus epidermidis.
7 d b and strains of Staphylococcus aureus and Staphylococcus epidermidis.
8 timulate growth and formation of biofilms by Staphylococcus epidermidis.
9 ntration on killing of a clinical isolate of Staphylococcus epidermidis.
10 usceptibility to vancomycin in an isolate of Staphylococcus epidermidis.
11 well as Gram-positive Bacillus subtilis and Staphylococcus epidermidis.
12 phenol-soluble modulin, a factor secreted by Staphylococcus epidermidis.
13 also in whole blood cultures stimulated with Staphylococcus epidermidis.
14 is of prosthetic-device infections caused by Staphylococcus epidermidis.
15 gens were Staphylococcus aureus, followed by Staphylococcus epidermidis.
16 S) to type 35 well-characterized isolates of Staphylococcus epidermidis.
17 une responses with Staphylococcus aureus and Staphylococcus epidermidis.
18 a GT-B folded teichoic acid polymerase from Staphylococcus epidermidis.
19 formation is the primary virulence factor of Staphylococcus epidermidis.
20 y to the phenol-soluble modulins (PSMs) from Staphylococcus epidermidis.
21 ould confer protection against S. aureus and Staphylococcus epidermidis.
22 njected with viable Staphylococcus aureus or Staphylococcus epidermidis (1,000 or 500,000 colony-form
24 ant staphylococci, with S aureus (42.0%) and Staphylococcus epidermidis (20.0%) as the predominant sp
25 en biofilm formation and hemagglutination in Staphylococcus epidermidis, 20 skin isolates and 19 pros
26 am-positive bacteria were isolated in 78.5%; Staphylococcus epidermidis (28.6%) was the most common m
31 ity islands have been found in the genome of Staphylococcus epidermidis, a generally less virulent re
34 f all Gram-negative/fungal episodes) whereas Staphylococcus epidermidis accounted for only 1 death (0
35 izing filter (2.1%) became contaminated with Staphylococcus epidermidis after 1 month of treatment, w
36 .01 muM, while the truncated analogue of the Staphylococcus epidermidis AIP-1 (3) elicited an IC50 va
38 haride produced by Staphylococcus aureus and Staphylococcus epidermidis and is an effective target fo
39 esulted in a 1- to 2-log enhanced killing of Staphylococcus epidermidis and other microbes in vitro c
40 acteria, mostly normal skin bacteria such as Staphylococcus epidermidis and Propionibacterium acnes,
42 hic alpha-helix is inducible within hours by Staphylococcus epidermidis and slowly by another mechani
49 It also demonstrates potent activity against Staphylococcus epidermidis and Streptococcus spp. (MIC90
50 nce genes (mecA in Staphylococcus aureus and Staphylococcus epidermidis and vanA or vanB in Enterococ
52 nst gram-positive (Staphylococcus aureus and Staphylococcus epidermidis) and gram-negative (Escherich
53 in vitro >/= 90% reduction of Gram-positive (Staphylococcus epidermidis) and Gram-negative (Pseudomon
54 the upper airway (Staphylococcus aureus and Staphylococcus epidermidis) and intestinal microbiota (L
55 ates of Staphylococcus aureus, 2 isolates of Staphylococcus epidermidis, and 7 isolates of Staphyloco
57 nst Escherichia coli, Staphylococcus aureus, Staphylococcus epidermidis, and group B Streptococcus.
59 ections with the leading nosocomial pathogen Staphylococcus epidermidis are characterized by biofilm
62 coagulase-negative staphylococci, including Staphylococcus epidermidis, are often considered a conta
63 tive staphylococci, with the leading species Staphylococcus epidermidis, are the predominant cause of
64 and to pathogens Bacillus thuringiensis and Staphylococcus epidermidis, as by the survival rate of t
65 le cells of another Gram-positive bacterium, Staphylococcus epidermidis, as well as of the Gram-negat
66 t in in vitro antibacterial activity against Staphylococcus epidermidis at loadings of silver that ar
67 eudomonas aeruginosa, Bacillus subtilis, and Staphylococcus epidermidis at the single cell and popula
68 a KT2440, Salmonella Typhimurium ATCC 14028, Staphylococcus epidermidis ATCC 12228, Enterococcus faec
70 rt of the failure of linezolid treatment for Staphylococcus epidermidis bacteremia associated with a
72 s been implicated as an Escherichia coli and Staphylococcus epidermidis biofilm adhesin, the formatio
73 ucosamine (PNAG) is a major component of the Staphylococcus epidermidis biofilm extracellular matrix.
76 electrical current reduced the viability of Staphylococcus epidermidis biofilms in conjunction with
79 mediate-frequency alleles in an arcC gene of Staphylococcus epidermidis, but not in a homologous gene
80 ere also seen with PS/A-producing strains of Staphylococcus epidermidis, but not with transposon muta
81 lling of 10(3)-10(8) colony forming units/ml Staphylococcus epidermidis by 10(5)-10(8) human neutroph
82 trains of Escherichia coli and one strain of Staphylococcus epidermidis by hierarchy cluster analysis
83 d that N-deacetylation of beta-1,6-GlcNAc in Staphylococcus epidermidis by the PgaB homolog, IcaB, an
85 examined against Pseudomonas aeruginosa and Staphylococcus epidermidis by varying the dose, the time
86 lebsiella pneumoniae, Staphylococcus aureus, Staphylococcus epidermidis, Candida albicans, and K. kin
88 tant Staphylococcus aureus cultures, 9.2% of Staphylococcus epidermidis cultures, and 2.5% of P. aeru
89 ellular adhesin (PIA) in the pathogenesis of Staphylococcus epidermidis CVC-associated infection.
91 atment of experimental methicillin-resistant Staphylococcus epidermidis endophthalmitis was evaluated
92 llin-resistant Staphylococcus aureus (MRSA), Staphylococcus epidermidis, Enterococcus faecalis, Acine
93 strains that have been tested, B. subtilis, Staphylococcus epidermidis, Enterococcus faecalis, and E
94 d on surfaces, and belong to species such as Staphylococcus epidermidis, Enterococcus faecalis, Pseud
97 ort on an analysis of sequential isolates of Staphylococcus epidermidis from cultures of blood obtain
99 Here, we report the crystal structure of the Staphylococcus epidermidis glucose/H(+) symporter in an
101 rR, a DtxR homologue initially identified in Staphylococcus epidermidis, governs the expression of th
102 Typhimurium (all gram-negative bacteria) and Staphylococcus epidermidis (gram-positive) showed marked
103 hylococcus lugdunensis (groups I and II) and Staphylococcus epidermidis (groups I-III) were sequentia
110 ding clinical isolates of MRSA and MSSA) and Staphylococcus epidermidis identified one candidate that
111 The most common organisms identified were Staphylococcus epidermidis in 30.1% (135/448), Streptoco
112 The relationship of initial concentration of Staphylococcus epidermidis in blood cultures and time to
113 isolation of a strictly anaerobic strain of Staphylococcus epidermidis in pure culture from the site
114 es the selective and capacitive detection of Staphylococcus epidermidis in synthetic urine also conta
116 endophthalmitis and revealed the presence of Staphylococcus epidermidis in the vitreous of a culture-
117 factor (STF) and phenol-soluble modulin from Staphylococcus epidermidis induced HIV-LTR trans-activat
119 be effective at reducing both S. aureus and Staphylococcus epidermidis infections in a murine animal
120 nd show that the common blood-borne pathogen Staphylococcus epidermidis influences this in vitro mode
133 oteins whose secretion from stationary-phase Staphylococcus epidermidis is dependent on SPase activit
139 edical devices in hospitalized patients, and Staphylococcus epidermidis is the leading cause of infec
143 , we demonstrated that the saePQRS region in Staphylococcus epidermidis is transcriptionally regulate
145 s level from the OW (126) and ER (117), with Staphylococcus epidermidis isolates being the most commo
146 Similar proteolytic capacities were found in Staphylococcus epidermidis isolates but not in Staphyloc
147 the species level as containing 203 (73.3%) Staphylococcus epidermidis isolates, 10 (3.6%) Staphyloc
149 valuated whether the commensal microorganism Staphylococcus epidermidis may enhance production of ant
150 sibility, we report the crystal structure of Staphylococcus epidermidis MDD (1.85 A resolution) and,
154 y a normal microbial resident of human skin, Staphylococcus epidermidis, might also act as an antimic
155 us aureus (MSSA) (14), methicillin-resistant Staphylococcus epidermidis (MRSE) (17), methicillin-susc
156 endocarditis caused by methicillin-resistant Staphylococcus epidermidis (MRSE) and a rare linezolid-r
158 illin-resistant Stapylococcus aureus (MRSA), Staphylococcus epidermidis (MRSE), and Mycobacterium spp
159 ermidis (MRSE) (17), methicillin-susceptible Staphylococcus epidermidis (MSSE) (9), other coagulase-n
160 010, we recovered 38 methicillin-susceptible Staphylococcus epidermidis (MSSE) isolates from endophth
161 were 1 x 108 colony forming units of either Staphylococcus epidermidis (n = 100) or Enterobacter clo
163 = 99); 176 received tail vein injections of Staphylococcus epidermidis on postoperative day (POD) 10
166 cillus actinomycetemcomitans, skin commensal Staphylococcus epidermidis, or skin pathogen Streptococc
169 Therefore, we investigated the impact of the Staphylococcus epidermidis phenotype on colonization of
171 monstrates that quorum-sensing regulation in Staphylococcus epidermidis protects it from key mechanis
172 carditis due to Rhodotorula mucilaginosa and Staphylococcus epidermidis, proven by culture and histop
173 show here that d-lactate dehydrogenase from Staphylococcus epidermidis reduces a broad spectrum of 2
178 cnes, Staphylococcus aureus (S. aureus), and Staphylococcus epidermidis (S. epidermidis) with lauric
181 a significant reduction in viable counts of Staphylococcus epidermidis, Saccharomyces cerevisiae, an
182 DNA fragment was identified and cloned from Staphylococcus epidermidis (Se) using femA from S. aureu
183 ginosa [PA], Staphylococcus aureus [SA], and Staphylococcus epidermidis [SE]) was tested by using Kir
184 in commensal and leading nosocomial pathogen Staphylococcus epidermidis senses and efficiently inacti
185 ecreted polypeptides from the skin commensal Staphylococcus epidermidis, soluble tuberculosis factor
187 ng, and wound; the most common isolates were Staphylococcus epidermidis, Staphylococcus aureus, and C
188 gel surface is active against Gram-positive (Staphylococcus epidermidis, Staphylococcus aureus, and S
189 identification of 20 blood-borne pathogens (Staphylococcus epidermidis, Staphylococcus aureus, Bacil
191 s detected by radial diffusion assay against Staphylococcus epidermidis, Staphylococcus aureus, Esche
195 documented isolation of a strictly anaerobic Staphylococcus epidermidis strain, confirmed by rpoB gen
198 ve bacterial species (Staphylococcus aureus, Staphylococcus epidermidis, Streptococcus pneumoniae, En
199 lanB) which have substantial homology to the Staphylococcus epidermidis structural gene (epiA) and a
200 y expressed repeats of the AtlE amidase from Staphylococcus epidermidis suggest that the repeating se
201 y related accumulation-associated protein of Staphylococcus epidermidis, suggesting the possibility o
202 mmation initiated by a single application of Staphylococcus epidermidis supernatant, correlating with
204 SdrG is a cell wall-anchored adhesin from Staphylococcus epidermidis that binds to the Bbeta chain
205 the growth of both Staphylococcus aureus and Staphylococcus epidermidis, the latter were unable to el
206 ntified as Staphylococcus lugdunensis (one), Staphylococcus epidermidis (three), Staphylococcus haemo
207 ght to be a crucial factor in the ability of Staphylococcus epidermidis to produce a biomaterial-base
209 that transcription across the targets of the Staphylococcus epidermidis type III-A CRISPR-Cas system
211 inetobacter and Moraxella species (type II), Staphylococcus epidermidis (type III), Porphyromonas and
212 ms from the primary broth culture other than Staphylococcus epidermidis, viridans group streptococci,
213 oll-like receptors with Candida albicans and Staphylococcus epidermidis was 2.5- and 2.9-fold higher
214 hermic preservation by investigating whether Staphylococcus epidermidis was capable of growing in a s
215 miting the spread of conjugative plasmids in Staphylococcus epidermidis was first described in 2008.
218 ated catheters from studied patients against Staphylococcus epidermidis was used to determine the ant
219 ysiology of the leading nosocomial pathogen, Staphylococcus epidermidis, we analyzed the genome of bi
220 n beta-defensin 3 in the nosocomial pathogen Staphylococcus epidermidis, we discovered an antimicrobi
222 e ligands for E. coli, Citrobacter freundii, Staphylococcus epidermidis were 100%, 2.6% and 8.6% resp
223 Fibrin gels (1500 microm thick) containing Staphylococcus epidermidis were formed in Boyden-type ch
224 ein fractions from Staphylococcus aureus and Staphylococcus epidermidis, were able to distinguish bet
226 h of the pathogens Staphylococcus aureus and Staphylococcus epidermidis with comparable IC(50) to van
227 ynebacterium glutamicum, Microcuccus luteus, Staphylococcus epidermidis, Yersinia ruckeri, Escherichi
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