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1 S. marcescens does not normally colonize human skin, but
2 S. marcescens expresses prodigiosin, a bright red and ce
3 S. marcescens facilitates arboviral infection through a
4 S. marcescens induced neutrophil recruitment to the corn
5 S. marcescens induces corneal inflammation by activation
6 S. marcescens isolates were compared using restriction-e
7 S. marcescens oxyR mutants were severely impaired in bio
8 S. marcescens was identified from a pharmacy water fauce
9 isolates, 5 Enterobacter cloacae isolates, 2 S. marcescens isolates, 1 Proteus mirabilis isolate, and
10 ene knockout mice was abraded, and 1 x 10(7) S. marcescens were added in the presence of a silicone h
11 Here, the development and evaluation of a S. marcescens cgMLST scheme is reported with the goal of
13 example, for growth on N-acetylglucosamine, S. marcescens exhibits high pentose phosphate pathway ac
15 tic (R)-(-)-mellein and micromolide, against S. marcescens and a Gram-positive bacterium, Staphylococ
17 tion of bronchoscopes with P. aeruginosa and S. marcescens and possible infection of patients at a co
18 ducted an investigation of P. aeruginosa and S. marcescens isolates related to bronchoscopy at a comm
20 with Acinetobacter spp., P. aeruginosa, and S. marcescens, 5/6 with Citrobacter spp., 13/14 with Ent
22 nce birth, but gut colonization with GBS and S. marcescens occurred closer to time of bloodstream inf
26 its transporter ShlB resulted in attenuated S. marcescens strains that failed to cause profound weig
27 eement was observed, excluding A. baumannii, S. marcescens, and S. pneumoniae, for which >/=4-fold di
28 n foreskin fibroblasts was also inhibited by S. marcescens secretomes indicating that the effect is n
30 , that is located upstream of NucC-dependent S. marcescens promoters and the late promoters of P2-rel
31 f multiple members of the recently described S. marcescens complex causing hospital- or community-ass
36 individuals exhibited reduced preference for S. marcescens, and dauers from some strains preferred E.
38 there is no standardized analytic scheme for S. marcescens core genome multilocus sequence typing (cg
42 haracterise the tripartite SmhABC toxin from S. marcescens and propose a mechanism of pore assembly.
44 ication methods are insufficient to identify S. marcescens complex and laboratory reporting should be
45 nd interleukin-1 receptor type 1 (IL-1R1) in S. marcescens-induced corneal inflammation and infection
49 expectedly, fliR but not flhD is involved in S. marcescens-mediated damages of the intestinal epithel
52 extracellular polysaccharides production in S. marcescens and provides important clues for future st
56 characterize the iron acquisition systems in S. marcescens isolate UMH9, which was recovered from a c
57 etermined that the addition of a chi-induced S. marcescens cell lysate to an uninfected culture cause
58 tic screen for loss of virulence of ingested S. marcescens and identified FliR, a structural componen
63 less, the temperature response of the native S. marcescens ATCase suggests a strong entropic effect t
64 fection and in infections with Gram-negative S. marcescens or Gram-positive E. faecalis bacteria, whi
67 opic bacteriophage chi (Chi) to a culture of S. marcescens stimulates a greater than fivefold overpro
68 ase treatments abrogated the cytotoxicity of S. marcescens culture filtrates towards HeLa cells, sugg
69 29 was refined by integrating RNAseq data of S. marcescens growth on three different carbon sources (
71 Despite multiple clinical descriptions of S. marcescens nosocomial pneumonia, little is known rega
72 ective means to control the dissemination of S. marcescens, an in-depth analysis of the population st
74 x strains, 89% of K. pneumoniae, and half of S. marcescens had an extended-spectrum B-lactamase pheno
83 was to characterize the metabolic profile of S. marcescens to provide insight for metabolic engineeri
85 in which OxyR contributes to early stages of S. marcescens biofilm formation by influencing fimbrial
86 first reports applying PFGE to the study of S. marcescens, and this method was a useful marker of st
88 istant clones suggests that the treatment of S. marcescens infections will become increasingly diffic
89 estigation, allowing better understanding of S. marcescens genomic epidemiology and facilitating inte
91 marcescens, but not from Escherichia coli or S. marcescens strains with mutations in the waaG and waa
93 for Fis are 100% identical in K. pneumoniae, S. marcescens, E. coli, and S. typhimurium and 96 to 98%
95 ematic collection of antimicrobial-resistant S. marcescens associated with bloodstream infections in
96 the clinically isolated multidrug-resistant S. marcescens strain and found that the sdeXY deletion m
97 what is observed in other bacterial species, S. marcescens OxyR is required for oxidative stress resi
98 he genomic sequence of NCBI reference strain S. marcescens Db11 (NZ_HG326223.1) as a starting point-a
99 eal aspiration model of lethal and sublethal S. marcescens pneumonia in BALB/c mice and extensively c
100 ability of the tigecycline Etest for testing S. marcescens, Acinetobacter spp., and S. pneumoniae is
102 or in vitro cytotoxic activity revealed that S. marcescens mutant strains that are deficient in produ
107 ight putative RND efflux system genes in the S. marcescens Db10 genome that included the previously c
109 CTP stimulates the catalytic activity of the S. marcescens ATCase and CTP/UTP inhibitory synergism ha
113 93-r97) of the regulatory polypeptide of the S. marcescens enzyme have been replaced with their E. co
114 ) retained 455 out of 460 amino acids of the S. marcescens enzyme, it possessed characteristics simil
115 ajority of the K. pneumoniae and half of the S. marcescens isolates were resistant to both cefotaxime
117 proteins are the original substrates of the S. marcescens T6SS, before horizontal acquisition of oth
118 yperthermophile Sulfolobus solfataricus, the S. marcescens structure shows similar subunit structures
120 ues of E. coli have been replaced with their S. marcescens counterpart, lost both heterotrophic and h
123 and phenoloxidase activity and resistance to S. marcescens in both sexes, but these relationships wer
126 (-/-), and TLR4/5(-/-) corneas infected with S. marcescens had significantly increased CFU, indicatin
127 itis of the chest wall due to infection with S. marcescens that initially manifested as bilateral bre
129 ording to univariate analysis, patients with S. marcescens bacteremia stayed in the surgical intensiv
131 tify risk factors, we compared patients with S. marcescens bacteremia with randomly selected controls