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1 erococcus faecium, and beta-lactam-resistant Klebsiella pneumoniae).
2 carbapenemase OXA-48, in lysate samples from Klebsiella pneumoniae.
3 human pathogens Streptococcus pneumoniae and Klebsiella pneumoniae.
4 ococcus faecium, Acinetobacter baumannii and Klebsiella pneumoniae.
5 verlapping AR genes, and are correlated with Klebsiella pneumoniae.
6 Staphylococcus aureus, Escherichia coli and Klebsiella pneumoniae.
7 orbactam-nonsusceptible, ompK36 porin mutant Klebsiella pneumoniae.
8 cus faecium (VRE), and beta-lactam-resistant Klebsiella pneumoniae.
9 ssues of infected mice by the human pathogen Klebsiella pneumoniae.
10 are also active against MDR E. coli and MDR Klebsiella pneumoniae.
11 o lung infection by the major human pathogen Klebsiella pneumoniae.
12 richia coli O157:H7, and multidrug resistant Klebsiella pneumoniae.
13 t within 4 h for Acinetobacter baumannii and Klebsiella pneumoniae.
14 eptible to infection by Escherichia coli and Klebsiella pneumoniae.
15 a variety of bacterial pathogens, including Klebsiella pneumoniae.
16 the rapid dissemination of a single clone of Klebsiella pneumoniae.
17 h diverse KPC producers not limited to ST258 Klebsiella pneumoniae.
18 ntibiotic-resistant metallo-beta-lactamase 1 Klebsiella pneumoniae.
19 in pathogenesis during bacteremia caused by Klebsiella pneumoniae.
20 for the vaccine against the K2 sero group of Klebsiella pneumoniae.
21 (MDR) strains of Salmonella Typhimurium and Klebsiella pneumoniae.
22 cture of an assembled T2SS from the pathogen Klebsiella pneumoniae.
23 jirovecii (18.8%), cytomegalovirus (15.6%), Klebsiella pneumoniae (15.6%), and Streptococcus pneumon
24 g-resistant Acinetobacter baumannii (52.2%), Klebsiella pneumoniae (22.4%), and Staphylococcus aureus
27 d intention-to-treat population (n=355) were Klebsiella pneumoniae (37%) and Pseudomonas aeruginosa (
29 the most common contributory pathogens were Klebsiella pneumoniae (86 [31%]), Streptococcus pneumoni
30 coli (28%), Burkholderia pseudomallei (11%), Klebsiella pneumoniae (9%), and Staphylococcus aureus (6
31 thod was as follows; Escherichia coli, 100%; Klebsiella pneumoniae, 92.9%; Klebsiella oxytoca, 95.5%;
35 I agents, and multidrug-resistant strains of Klebsiella pneumoniae, a leading HAI agent, have caused
36 as historically largely been associated with Klebsiella pneumoniae, a predominant plasmid (pKpQIL), a
37 CutC GRE and the activating enzyme CutD from Klebsiella pneumoniae, a representative of the human mic
39 rum activity, encompassing Escherichia coli, Klebsiella pneumoniae, Acinetobacter baumanii, Pseudomon
40 beta-lactam resistance in Escherichia coli, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomo
41 Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomo
42 Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomo
43 p., Escherichia coli, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomo
44 Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomo
46 nterobacteriaceae isolates, 125 (94.7%) were Klebsiella pneumoniae and 74 harbored K. pneumoniae carb
47 ogens Escherichia coli, Salmonella enterica, Klebsiella pneumoniae and Acinetobacter baumannii agains
48 e Neisseria gonorrhoeae datasets, as well as Klebsiella pneumoniae and Acinetobacter baumannii datase
51 bly identified pathogenic bacteria (that is, Klebsiella pneumoniae and Enterobacter cloacae) and thei
54 ptococus pneumoniae, Pseudomonas aeruginosa, Klebsiella pneumoniae and Escherichia coli in Conjunctiv
55 on the occurrence of carbapenemase-producing Klebsiella pneumoniae and Escherichia coli in European h
57 terferes with their cognate function against Klebsiella pneumoniae and Escherichia coli; vi) MAIT cel
58 s were detected from NP/OP specimens whereas Klebsiella pneumoniae and Mycobacterium tuberculosis wer
59 (-/-) mice following airway exposure to LPS, Klebsiella pneumoniae and Mycobacterium tuberculosis.
60 sortium on Resistance Against Carbapenems in Klebsiella pneumoniae and Other Enterobacteriaceae) has
61 obacteriaceae, including multidrug-resistant Klebsiella pneumoniae and pathogenic Escherichia coli, r
62 ainst Enterococcus faecium, platinum against Klebsiella pneumoniae and platinum and silver against Ac
68 . aureus], 2 Stenotrophomonas maltophilia, 1 Klebsiella pneumoniae) and resulted in antimicrobial cha
70 n Escherichia coli, Pseudomonas syringae and Klebsiella pneumoniae, and endogenous CRISPR-Cas use was
72 omycin-resistant Enterococcus faecium (VRE), Klebsiella pneumoniae, and Escherichia coli in the intes
73 resistant Enterococcus, carbapenem-resistant Klebsiella pneumoniae, and Escherichia coli infection in
74 riggered by LPS from Pseudomonas aeruginosa, Klebsiella pneumoniae, and Escherichia coli Sixteen cyto
75 bacterium tuberculosis, Salmonella enterica, Klebsiella pneumoniae, and Escherichia coli We compare p
78 of Escherichia coli, Enterococcus faecalis, Klebsiella pneumoniae, and Pseudomonas aeruginosa We the
80 cies-Enterobacter cloacae, Escherichia coli, Klebsiella pneumoniae, and Pseudomonas aeruginosa-report
81 , Enterococcus faecalis, Klebsiella oxytoca, Klebsiella pneumoniae, and Staphylococcus aureus at age
82 ucosal challenge with the pulmonary pathogen Klebsiella pneumoniae, and substantially reduced epithel
84 DM)-producing strains of multidrug-resistant Klebsiella pneumoniae are a global public health threat
86 , Micrococcus luteus, Bacillus subtilis, and Klebsiella pneumoniae at a minimal inhibitory concentrat
87 trains, notably against multi-drug resistant Klebsiella pneumoniae ATCC 700603 while isolates LB4 and
88 922, E. coli ATCC 35218, E. coli NCTC 13353, Klebsiella pneumoniae ATCC 700603, and Pseudomonas aerug
90 ein A (TTPA) is a structural tail protein of Klebsiella pneumoniae bacteriophage KP32, and is respons
91 resistant (MDR) carbapenemase-producing (CP) Klebsiella pneumoniae, belonging to clonal group CG258,
92 oteins from E. coli, Salmonella enterica and Klebsiella pneumoniae bind c-di-GMP via the domain of un
93 t SPLUNC1 (rSPLUNC1) significantly inhibited Klebsiella pneumoniae biofilm formation on airway epithe
94 ridium perfringens, Ruminococcus gnavus, and Klebsiella pneumoniae, but also beneficial species, such
95 portant carbapenem-resistant human pathogen, Klebsiella pneumoniae, by B. bacteriovorus in human seru
97 CAZ-AVI displays in vitro activity against Klebsiella pneumoniae carbapenemase (KPC) enzyme produce
98 detection of ertapenem (ETP) resistance and Klebsiella pneumoniae carbapenemase (KPC) in 47 Klebsiel
100 ogy labs to perform confirmatory testing for Klebsiella pneumoniae carbapenemase (KPC) production or
102 n of serine carbapenemases, particularly the Klebsiella pneumoniae carbapenemase (KPC), with no inhib
106 tam antibiotics due to the production of the Klebsiella pneumoniae carbapenemase (KPC-2) class A beta
107 nce to their genotypic profiles, whereas all Klebsiella pneumoniae carbapenemase (KPC; n = 8) and GES
108 n with an Enterobacter sp. isolate producing Klebsiella pneumoniae Carbapenemase-4 and New Delhi Meta
110 the most common transmissible CPE worldwide, Klebsiella pneumoniae carbapenemase-producing K. pneumon
112 the emergence and clinical impact of a novel Klebsiella pneumoniae carbapenemase-producing K. pneumon
113 e performed on isolates to identify specific Klebsiella pneumoniae carbapenemases (KPC) and additiona
114 e, in contrast to metallo-beta-lactamases or Klebsiella pneumoniae carbapenemases (KPC), no specific
119 We investigated the possible transmission of Klebsiella pneumoniae carrying mcr-1 via duodenoscope an
126 cy, lung disease, baseline urine source, and Klebsiella pneumoniae, compared to the Escherichia coli
127 ial activity against E. coli, Salmonella and Klebsiella pneumoniae, comparing to the supercritical ex
128 am-negative bacteria on clinical isolates of Klebsiella pneumoniae, containing highly-resistant antim
129 istent with regional clinical concern, e.g., Klebsiella pneumoniae contigs containing KPC-2 within an
131 Infections caused by carpabenem-resistant Klebsiella pneumoniae (CR-Kp) are especially problematic
132 rgently needed to treat carbapenem-resistant Klebsiella pneumoniae (CR-Kp)-mediated infection, which
133 sortium on Resistance against Carbapenems in Klebsiella pneumoniae (CRACKLE) was constructed of patie
134 The rapid emergence of carbapenem-resistant Klebsiella pneumoniae (CRKP) represents a major public h
135 k of OXA-232-expressing carbapenem-resistant Klebsiella pneumoniae (CRKP) transmitted to 16 patients
136 e growing importance of carbapenem-resistant Klebsiella pneumoniae (CRKP), the clonal relationships b
138 nding global distribution of multi-resistant Klebsiella pneumoniae demands faster antimicrobial susce
140 te the antagonism between the microbiota and Klebsiella pneumoniae during colonization and transmissi
141 nterococcus faecium and carbapenem-resistant Klebsiella pneumoniae, emerge from the intestinal lumen
144 ta that produces SCFAs enhances clearance of Klebsiella pneumoniae, Escherichia coli, and Proteus mir
145 of antibiotic-resistant clinical isolates of Klebsiella pneumoniae, Escherichia coli, and Proteus mir
146 a, Proteus mirabilis, Enterococcus faecalis, Klebsiella pneumoniae, Escherichia coli, and Staphylococ
147 0.7%, respectively, caused by ESBL-producing Klebsiella pneumoniae, Escherichia coli, Klebsiella oxyt
148 scovery of a new enzyme, first identified in Klebsiella pneumoniae from a patient from New Delhi and
149 seudomonas aeruginosa, Escherichia coli, and Klebsiella pneumoniae from resin-containing BacT/Alert F
150 riable regions V3 and V6 were amplified from Klebsiella pneumoniae genomic DNA with blood in situ.
153 nst clinical isolates of Eschericia coli and Klebsiella pneumoniae harboring NDM-1 were reduced to su
156 idrug resistant (MDR) opportunistic pathogen Klebsiella pneumoniae has previously been shown to adapt
157 activity against Acinetobacter baumannii and Klebsiella pneumoniae; however, analogue 9 and 16 at 4 m
158 spiked with approximately 1,500 CFU bla(KPC) Klebsiella pneumoniae; however, the detection rate dropp
159 ly studied in some enteric bacteria, such as Klebsiella pneumoniae; however, their role in pathogenes
160 minant siderophore produced by hypervirulent Klebsiella pneumoniae (hvKP) and was previously shown to
165 lly track a clonal outbreak of blaKPC-pKpQIL-Klebsiella pneumoniae in a proof-of-principle study.
166 ogues with in vivo efficacy against MRSA and Klebsiella pneumoniae in animal models of infection.
168 the major uropathogens Proteus mirabilis and Klebsiella pneumoniae, in addition to UPEC, in humans.
169 lipopolysaccharide transporter LptB2FG from Klebsiella pneumoniae, in which both LptF and LptG are c
170 so show that expression of Gam in E. coli or Klebsiella pneumoniae increases sensitivity to fluoroqui
171 d in vivo during pneumoseptic infection with Klebsiella pneumoniae, indicating its regulatory role in
173 electin participates in host defense against Klebsiella pneumoniae-induced pulmonary inflammation is
174 reported that host defense against pulmonary Klebsiella pneumoniae infection requires IL-22, which wa
175 zone to induce Paneth cell loss, followed by Klebsiella pneumoniae infection to induce intestinal inj
196 esequencing of three plasmids in a reference Klebsiella pneumoniae isolate demonstrated approximately
199 Escherichia coli, Pseudomonas aeruginosa, or Klebsiella pneumoniae) isolated from clinical cases.
200 ion of long- and short-read sequence data of Klebsiella pneumoniae isolates (n = 1,717) from a Europe
201 0% of Escherichia coli isolates and 24.2% of Klebsiella pneumoniae isolates globally, with rates reac
202 ically-related NDM-1 carbapenemase producing Klebsiella pneumoniae isolates identified during an outb
203 bsiella pneumoniae carbapenemase (KPC) in 47 Klebsiella pneumoniae isolates using a novel automated m
206 prim-resistant clinical Escherichia coli and Klebsiella pneumoniae isolates, suggesting that they may
207 (1) urine cultures growing Escherichia coli, Klebsiella pneumoniae, K. oxytoca, or Proteus mirabilis
209 428) and 9,371 isolates of Escherichia coli, Klebsiella pneumoniae, Klebsiella oxytoca, and Proteus m
210 after this death phase, only three species, Klebsiella pneumoniae, Klebsiella oxytoca, and Providenc
211 (1) urine cultures growing Escherichia coli, Klebsiella pneumoniae, Klebsiella oxytoca, or Proteus mi
212 -/-) mice were infected intratracheally with Klebsiella pneumoniae (KP) and assessed for extrapulmona
219 Escherichia coli PI-7, blaCTX-M-15-positive Klebsiella pneumoniae L7, and blaOXA-48-positive E. coli
220 ei, Chlamydia trachomatis, Escherichia coli, Klebsiella pneumoniae, Legionella pneumophila, Pseudomon
221 Here, we show the increased prevalence of Klebsiella pneumoniae lipopolysaccharide O2 serotype str
229 ase genes were most frequently identified in Klebsiella pneumoniae (n = 1,127), Escherichia coli (n =
231 genes were detected by the Carba-R assay in Klebsiella pneumoniae (n = 236), Escherichia coli (n = 2
232 mmunities consisting of Escherichia coli and Klebsiella pneumoniae once antibiotics were removed.
233 1%) of 5332 E coli isolates, 13 (<1%) of 348 Klebsiella pneumoniae, one (<1%) of 890 Enterobacter clo
235 dministration of pathogenic bacteria, either Klebsiella pneumoniae or Salmonella enterica serovar Typ
236 ilis epsHIJK locus into pga-deleted E. coli, Klebsiella pneumoniae, or alginate-negative Pseudomonas
237 ter aerogenes, Enterobacter cloacae complex, Klebsiella pneumoniae, or Klebsiella oxytoca that were r
238 l isolates of either Pseudomonas aeruginosa, Klebsiella pneumoniae, or Staphylococcus aureus produces
239 (FMDV) veterinary outbreak in England and a Klebsiella pneumoniae outbreak in a Nepali neonatal unit
240 hese findings can help up better predict MDR Klebsiella pneumoniae outbreaks associated with specific
241 PS) of the multiresistant clinical strain of Klebsiella pneumoniae, PCM2713, and thus should be regar
242 radrenergic neurons improves survival during Klebsiella pneumoniae peritonitis (67 versus 23%, p < 0.
245 chia coli/Shigella spp., Klebsiella oxytoca, Klebsiella pneumoniae, Proteus spp., Pseudomonas aerugin
246 he Gram-negative pathogens Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, and Acine
247 pathogens including Acinetobacter baumannii, Klebsiella pneumoniae, Pseudomonas aeruginosa, and Esche
248 Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Pseudomonas aeruginosa, and Esche
249 f Escherichia coli, Acinetobacter baumannii, Klebsiella pneumoniae, Pseudomonas aeruginosa, Staphyloc
251 the current epidemic of carbapenem-resistant Klebsiella pneumoniae rely on a comprehensive understand
255 The extracellular polysaccharide capsule of Klebsiella pneumoniae resists penetration by antimicrobi
256 , Bacillus subtilis, Pseudomonas aeruginosa, Klebsiella pneumoniae, Salmonellae typhi, Candida albica
257 ed susceptibility to Escherichia coli K1 and Klebsiella pneumoniae sepsis in antibiotic-treated neona
259 t the capsular polysaccharide of a dominated Klebsiella pneumoniae serotype K2 is difficult to synthe
264 ATCC 25922, CM-13457, and CM-10455) and one Klebsiella pneumoniae strain (CM-11073) were grown overn
268 ence of mcr-1 was investigated in E coli and Klebsiella pneumoniae strains collected from five provin
270 raperitoneally (i.p.) with Escherichia coli, Klebsiella pneumoniae, Streptococcus pneumoniae, lipopol
271 wk and then challenged intratracheally with Klebsiella pneumoniae, Streptococcus pneumoniae, or lipo
272 ed as model pJHCMW1, a plasmid isolated from Klebsiella pneumoniae that includes two beta-lactamase a
273 o human pathogens, Staphylococcus aureus and Klebsiella pneumoniae, that utilize this metal nutrient
274 umonic sepsis using pulmonary infection with Klebsiella pneumoniae, the expression of MGL1 was upregu
275 ing the sequence type 258 (ST258) lineage of Klebsiella pneumoniae There was very little evidence of
276 to killing by serum enhances the capacity of Klebsiella pneumoniae to cause infection, but it is an i
277 1 hypomorphic (Hypo) mice were infected with Klebsiella pneumoniae to determine infectious burden, im
278 survey of clinical polymyxin-resistant (PR) Klebsiella pneumoniae to determine the molecular mechani
279 zontal gene transfer (HGT) of blaOXA-48 from Klebsiella pneumoniae to Escherichia coli in an infected
280 acheally inoculated with either live or dead Klebsiella pneumoniae to induce either lung infection or
281 -derived sepsis caused by the human pathogen Klebsiella pneumoniae to study the role of platelets in
282 , as well as in a model of lung infection by Klebsiella pneumoniae Transferring serum from Ig-deficie
283 cation of DNA from Staphylococcus aureus and Klebsiella pneumoniae, two pathogens commonly related to
285 ) mice with the common human sepsis pathogen Klebsiella pneumoniae via the airways to induce pneumoni
286 teria could reduce bacterial burden in vivo, Klebsiella pneumoniae was injected into the tail veins o
290 T CRE infection was identified in 59 (15.7%) Klebsiella pneumoniae was isolated in 83.2%; surgical si
291 sphoenolpyruvate carboxylase gene (ppc) from Klebsiella pneumoniae was overexpressed to access the on
292 netobacter baumannii and multidrug-resistant Klebsiella pneumoniae was treated with bacteriophages an
293 Enterococcus spp., Escherichia coli and Klebsiella pneumoniae were the common bacterial pathogen
294 studied the recovery of Escherichia coli and Klebsiella pneumoniae when exposed to meropenem, imipene
295 ndogenous endophthalmitis is associated with Klebsiella pneumoniae whereas Coagulase negative Staphyl
297 coccus faecalis, Pseudomonas aeruginosa, and Klebsiella pneumoniae, which are frequently implicated i
298 subjected to intra-abdominal infection with Klebsiella pneumoniae, which results in liver injury and
300 m negative bacteria (e.g., Escherichia coli, Klebsiella pneumoniae) with varying levels of antibiotic