ライフサイエンスコーパス: Salmonella enteritidis

1 ria monocytogenes, Staphylococcus aureus and Salmonella enteritidis.

2 4% (9/203) of the isolates, 3 of which were Salmonella Enteritidis.

3 Salmonella Typhimurium and 1608 (15.8%) were Salmonella Enteritidis.

4 defined phage type (PT) reference strains of Salmonella enteritidis.

5 less numerous than the flagella observed on Salmonella enteritidis.

6 -fold), as did bacterial lipopolysaccharides Salmonella enteritidis (0.24 nmol/L, 5-fold) greater tha

7 incidence of cross-immunizing infection with Salmonella Enteritidis; (3) an increase in the duration

8 e consisted of 85 Salmonella Typhimurium, 58 Salmonella Enteritidis, 32 other nontyphoidal Salmonella

9 During a subsequent challenge with virulent Salmonella enteritidis a selection against lpf phase-on

10 351 NTS isolates serotyped, 160 (45.6%) were Salmonella Enteritidis and 152 (43.3%) were Salmonella T

11 Among NTS isolates, >/=80% (79.7% of Salmonella Enteritidis and 90.2% of Salmonella Typhimuri

12 eously exposed to an inoculum of inactivated Salmonella Enteritidis and a chronic heat stress (CHS).

13 ical analysis of a patient with disseminated Salmonella enteritidis and a homozygous splice acceptor

14 Bacillus cereus) and Gram-negative microbes (Salmonella enteritidis and Escherichia coli O157:H7).

15 aphylococcus aureus, Listeria monocytogenes, Salmonella enteritidis and Escherichia coli.

16 oxytoca strain M5a1, Salmonella eastbourne, Salmonella enteritidis and Salmonella gelsenkirchen, res

17 Salmonella Enteritidis and Salmonella Typhimurium are ma

18 important serovars of the Salmonella genus: Salmonella enteritidis and Salmonella typhimurium.

19 aphylococcus aureus, Listeria monocytogenes, Salmonella enteritidis, and Escherichia coli, and showed

20 cleared 90% of intracellular MRSA and 98% of Salmonella enteritidis at 2x the MIC.

21 rified recombinant His-tagged flagellin from Salmonella enteritidis bound to TLR5 in detergent lysate

22 e aged <5 years and case fatality was 20.3%; Salmonella Enteritidis case fatality (27.8%) was higher

23 Since 2010, Salmonella Enteritidis cases have risen and Salmonella T

24 Salmonella Enteritidis cells in a VBNC physiological sta

25 s and recent international travel by linking Salmonella Enteritidis data from the National Antimicrob

26 d, global scale, and extended protraction of Salmonella Enteritidis dissemination via centralized sou

27 rmed 2 hrs after an intravenous injection of Salmonella enteritidis endotoxin (10 mg/kg) or saline.

28 for 2 hrs after an intravenous injection of Salmonella enteritidis endotoxin (10 mg/kg).

29 Administration of 0.5 mg/kg Salmonella enteritidis endotoxin to male Fischer rats in

30 No interference/cross-reactivity from Salmonella enteritidis, Enterobacter agglomerans, Pseudo

31 molecule profiles of Listeria monocytogenes, Salmonella enteritidis, Escherichia coli, during growth

32 tty acids against some food-borne pathogens (Salmonella enteritidis, Escherichia coli, Listeria monoc

33 nd a mixture of related pathogens, including Salmonella enteritidis, Escherichia coli, Staphylococcus

34 immunized with native LT or with recombinant Salmonella enteritidis expressing LT-B.

35 A Tn10 insertion from a Salmonella enteritidis fimU mutant was transduced into S

36 We have analyzed the pathway by which Salmonella enteritidis flagellin (FliC) activates murine

37 n 3 epidemics of Salmonella BSI in Blantyre; Salmonella Enteritidis from 1999 to 2002, Salmonella Typ

38 By integrating over 30,000 Salmonella Enteritidis genomes from 98 countries during

39 The incidence of Salmonella Enteritidis has been falling since 1997, and

40 The lipopolysaccharide (LPS) of Salmonella enteritidis has been implicated as a virulenc

41 ex emerged as significant risk factors, with Salmonella Enteritidis identified as a major cause.

42 te cyclases from the Gram-negative bacterium Salmonella Enteritidis, identifying AdrA as the most pot

43 lmonella-associated food poisoning caused by Salmonella enteritidis in eggs because the avirulent S.

44 We report on a technology to reduce Salmonella enteritidis in poultry.

45 SPS phage can both prevent the spread of AMR Salmonella Enteritidis infection in chickens and shift t

46 cted an increase in the number of reports of Salmonella enteritidis infections.

47 ons of people each year and among pathogens, Salmonella Enteritidis is most widely found bacteria cau

48 in an IS3-type element with homology to the Salmonella enteritidis IS1351 element and Yersinia enter

49 of Salmonella Typhimurium and 30% (24/79) of Salmonella Enteritidis isolates tested were found to be

50 g method has been developed to differentiate Salmonella enteritidis isolates.

51 conjugated core polysaccharide-OPS (COPS) of Salmonella Enteritidis lipopolysaccharide (LPS) to flage

52 de repeating unit of the O-polysaccharide of Salmonella enteritidis lipopolysaccharide has been accom

53 Escherichia coli, Salmonella enteritidis, Listeria innocua, Pseudomonas ae

54 s after injection with a hypotensive dose of Salmonella enteritidis LPS.

55 /6 mice following injection of 300 microg of Salmonella enteritidis LPS.

56 d for 87% of the 687 NTS isolates, including Salmonella Enteritidis (n = 244 [35.5%]), Salmonella Typ

57 pathogens were S Typhimurium (n=154, 49.8%), Salmonella enteritidis (n=21, 6.8%), vaccinia virus (n=1

58 ected from a single culture-proven foodborne Salmonella enteritidis outbreak in 1994, Salmonella-indu

59 monitored a single culture-proven foodborne Salmonella enteritidis outbreak that involved 1811 patie

60 ained phylodynamic characteristics of global Salmonella Enteritidis populations that lend spatiotempo

61 s has been falling since 1997, and levels of Salmonella Enteritidis PT4 have fallen to preepidemic le

62 How Salmonella Enteritidis rapidly swept through continents

63 Salmonella Typhimurium and Salmonella Enteritidis represented 386 (49.2%) and 391 (

64 richia coli O157:H7, Salmonella typhimurium, Salmonella enteritidis, Salmonella arizonae, Shigella so

65 nd 23S rRNA genes of Salmonella typhimurium, Salmonella enteritidis, Salmonella arizonae, Shigella so

66 domonas aeruginosa, Pseudomonas fluorescens, Salmonella Enteritidis, Salmonella Typhimurium, Escheric

67 athogens including Escherichia coli O157:H7, Salmonella enteritidis, Salmonella typhimurium, Listeria

68 Intestinal carriage of Salmonella Enteritidis (SE) in the chicken host serves a

69 ckens from each treatment were challenged by Salmonella Enteritidis (SE), while fifteen from each tre

70 ild type fimbria genes were replaced both in Salmonella enteritidis (sefA, agfA and fimC) and Escheri

71 l and 82 (47.7%) from blood, 53 (30.8%) were Salmonella Enteritidis sequence type (ST) 11 and 62 (36.

72 l and 82 (47.7%) from blood, 53 (30.8%) were Salmonella Enteritidis ST11 and 62 (36.0%) Salmonella Ty

73 source of human infection by some clades of Salmonella Enteritidis ST11 in East Africa, but not of h

74 ource of human infection with some clades of Salmonella Enteritidis ST11 in East Africa, but not of h

75 We identified cgMLST clusters within Salmonella Enteritidis ST11, Salmonella Heidelberg ST15,

76 We identified cgMLST clusters within Salmonella Enteritidis ST11, Salmonella Heidelberg ST15,

77 microbial activity against Escherichia coli, Salmonella enteritidis, Staphylococcus aureus, and Mycob

78 of the trade in the geographic dispersal of Salmonella Enteritidis, suggesting that the centralized

79 against challenge with nontyphoidal serovar Salmonella Enteritidis than with another nontyphoidal se

80 ed compound is able to reduce the ability of Salmonella Enteritidis to kill A459 respiratory cells.

81 nance of the NTS serotypes also shifted from Salmonella Enteritidis to Salmonella Typhimurium.

82 vasion of chicken ovarian granulosa cells by Salmonella enteritidis was examined in vitro.

83 Salmonella Enteritidis was the most frequent isolate, wi

84 Highly specific DNA aptamers to Salmonella enteritidis were selected via Cell-SELEX tech