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1 phylococcus aureus, 27% Pseudomonas, and 10% extended-spectrum beta-lactamase-producing bacteria, wit
4 1 (AmpC), 2b (TEM-1, TEM-2, and SHV-1), 2be (extended spectrum beta-lactamases [ESBLs] and K1), and 2
6 icillin-resistant Staphylococcus aureus [5], extended-spectrum beta-lactamase-producing Klebsiella pn
8 ach of the three described isoenzymes and 69 extended-spectrum beta-lactamase-producing clinical isol
11 th N1MS exhibiting superior activity against extended spectrum beta lactamase producers, despite dimi
13 ctivity of ceftazidime and cefpirome against extended-spectrum cephalosporin and Sme-1 containing car
14 platforms identified susceptibility against extended-spectrum cephalosporins and carbapenems in >90%
16 of the strains were resistant to ampicillin, extended-spectrum cephalosporins, and aminoglycosides, i
17 ements for the hydrolysis of ceftazidime, an extended spectrum cephalosporin commonly used to treat s
20 The beta-lactamase of E. cloacae GC1, an extended spectrum mutant of the P99 enzyme, rapidly hydr
21 lelic mutations in KDSR are implicated in an extended spectrum of disorders of keratinization in whic
22 ch that uncovered the key role of IL-1 in an extended spectrum of immune dysregulatory conditions.
26 meolysin", ClyR, with robust activity and an extended-spectrum streptococcal host range against most
27 at are widely used in the clinic, such as an extended-spectrum beta-lactam antibiotic amoxicillin/cla
28 d urinary tract infection (UTI) caused by an extended-spectrum beta-lactamase (ESBL)-producing, multi
29 ized patients were more likely to develop an extended-spectrum beta-lactamase-producing Enterobacteri
30 atory have shown that the enzyme exhibits an extended-spectrum phenotype, with very high levels of pe
32 y in the Omega-loop may form the basis of an extended-spectrum activity of class C beta-lactamases ag
35 rovar Newport MDR-AmpC expressing TEM-1b and extended-spectrum beta-lactamase SHV-12 was isolated fro
37 , the test accurately distinguished AmpC and extended-spectrum beta-lactamase production and differen
38 , carbapenem-resistant Escherichia coli, and extended-spectrum beta-lactamase-producing Klebsiella pn
39 nem-nonsusceptible (excluding ertapenem) and extended-spectrum cephalosporin-resistant Escherichia co
40 pled with restriction of fluoroquinolone and extended-spectrum beta-lactam use to control both the ma
42 the implications of fluoroquinolone (FQ) and extended-spectrum cephalosporin plus cephamycin (AmpC) r
43 res, including complexes with inhibitors and extended-spectrum antibiotics, were determined by X-ray
44 and derepressed chromosomal beta-lactam and extended-spectrum beta-lactamase-producing Enterobacter
46 especially extended-spectrum macrolides and extended-spectrum fluoroquinolones (P<.001 for all trend
48 zed by resistant intestinal bacteria such as extended-spectrum beta-lactamase-producing Enterobacteri
50 ROs such as methicillin-resistant S. aureus, extended-spectrum beta-lactamase-producing, and carbapen
51 d by mixed resistant Gram-negative bacteria, extended-spectrum beta-lactamase-producing Enterobacteri
52 he benefits and safety of azithromycin-based extended-spectrum prophylaxis in women undergoing nonele
53 targeted pathogens (Acinetobacter baumannii, extended-spectrum beta-lactamase-producing Gram-negative
55 e primary treatment for infections caused by extended-spectrum beta-lactamase (ESBL)-producing Klebsi
56 The continued rise in infections caused by extended-spectrum beta-lactamase (ESBL)-producing pathog
57 ad ventilator-associated pneumonia caused by extended-spectrum beta-lactamase-producing Enterobacteri
58 the isolated bacteria, infections caused by extended-spectrum beta-lactamase-producing Enterobacteri
59 ment considerations for infections caused by extended-spectrum beta-lactamase-producing organisms, Am
60 ary broad-spectrum beta-lactams, mediated by extended-spectrum beta-lactamase (ESBL) enzymes, is an i
61 pound also inhibits irreversibly the class C extended-spectrum GC1 beta-lactamase (IC(50) = 6.2 nM).
62 stance against beta-lactams, cephalosporins (extended-spectrum beta-lactamase-producing type SHV-12),
63 ia coli strains producing well-characterized extended-spectrum, AmpC, or carbapenem-hydrolyzing beta-
64 bs on two selective culture media, CHROMagar extended-spectrum-beta-lactamase (ESBL) and vancomycin,
66 ncing of previously uncharacterized clinical extended-spectrum beta-lactamase (ESBL)-producing Escher
71 rbapenem-resistant Enterobacteriaceae (CRE), extended-spectrum beta-lactamase (ESBL)-producing Entero
72 performed to assess their ability to detect extended-spectrum beta-lactamases (ESBLs) in members of
73 Eight (21.0%) of 38 labs failed to detect extended-spectrum cephalosporin or aztreonam resistance
74 rd CLSI disk diffusion methods for detecting extended-spectrum beta-lactamases (ESBLs) and with cefep
75 ening and confirmation methods for detecting extended-spectrum beta-lactamases (ESBLs) apply only to
76 sistant enterococcus, Clostridium difficile, extended-spectrum beta-lactamase-producing gram-negative
78 Representative isolates from 10 distinct extended-spectrum beta-lactamase-producing strains of Kl
79 esistant Staphylococcus aureus) and ESBL-EC (extended-spectrum beta-lactamase-producing Escherichia c
80 increasingly associated with plasmid-encoded extended-spectrum beta-lactamases (ESBLs) and carbapenem
82 rizontal dissemination of the genes encoding extended spectrum beta-lactamases (ESBLs) via conjugativ
83 se of nonrecommended antibiotics, especially extended-spectrum macrolides and extended-spectrum fluor
87 ined using the revised CLSI breakpoints, for extended-spectrum-beta-lactamase (ESBL)-producing Escher
89 talization were independent risk factors for extended-spectrum beta-lactamase-producing Enterobacteri
90 As routine testing of clinical isolates for extended-spectrum beta-lactamase (ESBL) production (scre
91 ught to assess the interest of screening for extended-spectrum beta-lactamase-producing Enterobacteri
93 ts and used the double disk synergy test for extended-spectrum beta-lactamase-producing Enterobacteri
95 To determine whether confirmatory tests for extended-spectrum beta-lactamase (ESBL) production in Es
96 ic structure of the Enterobacter cloacae GC1 extended-spectrum class C beta-lactamase, inhibited by a
97 ta-lactamases are one of the fastest growing extended-spectrum beta-lactamase (ESBL) families found i
99 resistant gram-negative bacteria that harbor extended-spectrum beta-lactamases (ESBLs) are increasing
100 Escherichia coli, such as strains harboring extended-spectrum beta-lactamase (ESBL) genes, frequentl
102 utations that permit the enzyme to hydrolyze extended-spectrum cephalosporins or to avoid inactivatio
105 tiple antibiotic resistance genes, including extended spectrum beta-lactamases, for which therapeutic
106 t to at least nine antimicrobials (including extended-spectrum cephalosporins), known as serotype New
107 biotic resistance evolution, we investigated extended-spectrum mutants of class C beta-lactamases, wh
109 Currently, rising problems include CTX-M extended-spectrum beta-lactamases (ESBLs), plasmid-media
110 methoxy-ticarcillin) shows stability to most extended spectrum beta-lactamases, but is considered ina
111 ug-resistant Pseudomonas aeruginosa and most extended-spectrum beta-lactamase (ESBL)-producing Entero
113 d efficacy and safety of posaconazole, a new extended-spectrum triazole, as salvage therapy for IFIs
115 arisen multiple times in naturally occurring extended-spectrum TEM alleles, seven were recovered mult
118 ly of beta-lactamases constitutes a group of extended spectrum resistance enzymes that hydrolyze peni
120 cent study in Texas showed that up to 70% of extended-spectrum beta-lactamase (ESBL)-containing membe
121 mp inhibitors (PPIs) were rectal carriers of extended-spectrum beta-lactamase-producing Enterobacteri
123 ly significant for postintervention cases of extended-spectrum beta-lactamase-producing organisms (P
124 t technologies permit the rapid detection of extended-spectrum beta-lactamase (bla(ESBL)) and Klebsie
125 impact of preenrichment on the detection of extended-spectrum beta-lactamase-producing Enterobacteri
129 amase inhibitors has driven the evolution of extended-spectrum beta-lactamases (ESBLs) that possess t
130 iated with significantly higher frequency of extended-spectrum beta-lactamase-producing Enterobacteri
134 enzyme to provide an increased hydrolysis of extended-spectrum cephalosporins or an increased resista
137 y was to determine if the interpretations of extended-spectrum and advanced-spectrum cephalosporins (
139 LSI); and for isolates for which the MICs of extended-spectrum cephalosporins were > or =1 microg/ml
140 the pAmpC enzymes may yield similar MICs of extended-spectrum cephalosporins, many of which fall wit
142 in 23 states to determine the occurrence of extended-spectrum beta-lactamase (ESBL) and AmpC beta-la
143 timicrobial resistance and the occurrence of extended-spectrum beta-lactamases (ESBLs) modulated by f
144 obacteriaceae colonization as a predictor of extended-spectrum beta-lactamase-producing Enterobacteri
146 p. and Escherichia coli with the presence of extended-spectrum beta-lactamase (ESBL) and plasmid-medi
147 ceptibility testing revealed the presence of extended-spectrum beta-lactamase (ESBL) resistance.
150 t neonatal sepsis, with a high prevalence of extended-spectrum beta-lactamase-producing organisms.
151 ates included porin mutants and producers of extended-spectrum beta-lactamases (ESBLs), AmpCs, K1, an
152 rce of this resistance is from production of extended-spectrum (ES) beta-lactamases by bacteria.
153 20-week period were tested for production of extended-spectrum beta-lactamases (ESBLs) by the double-
159 cillin-tazobactam (PTZ) for the treatment of extended-spectrum beta-lactamase (ESBL) bacteremia is co
160 e exists with the detection and treatment of extended-spectrum beta-lactamase-producing organisms (Kl
161 producing CTX-M-15, the predominant type of extended-spectrum beta-lactamase (ESBL) associated with
162 ance have appeared in response to the use of extended-spectrum beta-lactam antibiotics (e.g., ceftazi
163 plant Patients) has provided pivotal data on extended-spectrum beta-lactamase (ESBL)-producing Entero
164 was defined by the isolation of at least one extended-spectrum beta-lactamase-producing Enterobacteri
165 roth microdilution (BMD) MIC of at least one extended-spectrum cephalosporin was >/=2 micro g/ml.
166 tance, defined as resistance to at least one extended-spectrum cephalosporin, one aminoglycoside, and
167 ally fluoroquinolone-resistant (FQ-R) and/or extended-spectrum beta-lactamase (ESBL)-producing, has e
168 o >128 micro g/ml and the MICs for the other extended-spectrum cephalosporins were highly variable.
170 lasmid-mediated quinolone resistance (PMQR), extended-spectrum beta-lactamases (ESBL) and AmpC beta-l
171 ia coli and Klebsiella pneumoniae possessing extended-spectrum class A beta-lactamases (ESBLs) contin
172 screened by the MicroScan system as possible extended-spectrum-beta-lactamase (ESBL)-producing organi
174 Strains of Klebsiella frequently produce extended-spectrum beta-lactamases, and infections with t
175 a, especially Klebsiella pneumoniae, produce extended-spectrum beta-lactamases (ESBLs) as an antibiot
178 trols consisted of 50 isolates that produced extended-spectrum beta-lactamases (ESBLs), AmpCs (includ
179 hia coli, Escherichia coli (ESBL) (producing extended spectrum beta-lactamases) and Morganella morgan
182 l receiving standard antibiotic prophylaxis, extended-spectrum prophylaxis with adjunctive azithromyc
187 robacteriaceae (CRE), blaNDM-1, and selected extended-spectrum beta-lactam (ESBL) resistant bacteria
189 nella enterica serovar Typhi isolate showing extended spectrum beta-lactamase (ESBL) production in th
190 herichia coli DH10B strains bearing bla(SHV) extended-spectrum and inhibitor-resistant beta-lactamase
191 of prior colonization to predict subsequent extended-spectrum beta-lactamase-producing Enterobacteri
192 teus mirabilis with an ertapenem-susceptible extended-spectrum-beta-lactamase (ESBL)-positive phenoty
193 r case, and literature review, suggests that extended-spectrum penicillins, tetracycline, and trimeth
195 These structural differences may explain the extended spectrum activity of GC1 against this class of
197 nother mutant of the P99 beta-lactamase, the extended spectrum GC1 enzyme, also has space available f
201 phalosporins, we found genes that encode the extended-spectrum beta-lactamases CTX-M-2, CTX-M-14, and
202 rolytic activity of the G238S enzyme for the extended-spectrum antibiotics cefotaxime and ceftazidime
203 wild-type level activity or greater for the extended-spectrum cephalosporin ceftazidime and the mono
209 tween the restriction digest patterns of the extended-spectrum beta-lactamase-encoding plasmids were
211 spergillus spp. was observed for each of the extended-spectrum triazoles and varied by species over t
213 producers and reported the results with the extended-spectrum cephalosporins and aztreonam as resist
215 rams antibiotic disks, the fraction of these extended-spectrum beta-lactamase (ESBL)-producing isolat
217 apbpF DeltaponA mutant and triple mutants to extended spectrum cephalosporins (ceftriaxone and cefepi
218 gonorrhoeae with decreased susceptibility to extended spectrum cephalosporins raises the prospect of
220 enes fell within the susceptible category to extended-spectrum cephalosporins, raising concern over c
221 ce of community-associated infections due to extended-spectrum beta-lactamase (ESBL)-producing Escher
222 ment of bloodstream infections (BSIs) due to extended-spectrum beta-lactamase-producing Enterobacteri
223 halosporin and monobactam antibiotics due to extended-spectrum beta-lactamases (ESBLs) has resulted i
224 nd categorize evidence for human exposure to extended-spectrum beta-lactamase-producing Enterobacteri
225 alence and dynamics of resistance markers to extended-spectrum cephalosporins, macrolides, and fluoro
229 robacter spp. and also mediate resistance to extended-spectrum cephalosporins and aztreonam in additi
232 (ESBL-type enzymes that confer resistance to extended-spectrum cephalosporins and carbapenems) presen
233 e in Enterococcus faecium, and resistance to extended-spectrum cephalosporins in Klebsiella pneumonia
235 Enterobacteriaceae can confer resistance to extended-spectrum cephalosporins, aztreonam, and penicil
236 and a control strain that was susceptible to extended-spectrum cephalosporins to 38 laboratories in C
237 ance to carbapenems, which are used to treat extended-spectrum beta-lactamase (ESBL)-producing bacter
238 well as the D49A and F142A mutants, with two extended spectrum beta-lactamases (the G238S and the E10
239 plasmid-borne AmpC gene (bla CMY-42) and two extended-spectrum beta-lactamase genes (bla CTX-M-15 and
240 oacae bloodstream isolates produced SHV-type extended-spectrum beta-lactamases (ESBLs) in addition to
241 In 45 isolates, 49 previously unrecognized extended-spectrum beta-lactamase or plasmid AmpC targets
243 ns of non-Salmonella Enterobacteriaceae with extended spectrum beta-lactamase (ESBL) or fluoroquinolo
244 vided data on ICU-acquired colonization with extended-spectrum beta-lactamase-producing Enterobacteri
245 etermine the risk of stool colonization with extended-spectrum cephalosporin-resistant gram-negative
246 ted pneumonia, 40 (6.8%) were colonized with extended-spectrum beta-lactamase-producing Enterobacteri
247 previously detected as being colonized with extended-spectrum beta-lactamase-producing Enterobacteri
249 italized patients colonized or infected with extended-spectrum beta-lactamase-producing Escherichia c
250 ization is a risk factor for infections with extended-spectrum beta-lactamase (ESBL)-producing organi
251 coli and Klebsiella pneumoniae isolates with extended-spectrum beta-lactamases (ESBLs) or AmpC cephal
252 ion at C12 led to 12-epi-pleuromutilins with extended-spectrum antibacterial activity, including acti
253 the colonization of the digestive tract with extended-spectrum beta-lactamase-producing Enterobacteri
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