ライフサイエンスコーパス: enteroinvasive

1 owever, pathogenic Escherichia coli strains (enteroinvasive and enterohemorrhagic E. coli) show low s

2 n intestinal epithelial cells can respond to enteroinvasive bacteria and induce an inflammatory respo

3 Pathogenic and enteroinvasive bacteria have been shown to trigger the I

4 ed that Nod1 is a crucial sensor for certain enteroinvasive bacteria that avoid TLR signaling.

5 that diverse signals, which are activated by enteroinvasive bacteria, can be integrated into a common

6 colon epithelial cell lines; infection with enteroinvasive bacteria, or stimulation with the proinfl

7 oxide synthase-2, ICAM-1) activated by those enteroinvasive bacteria.

8 tion with a spectrum of different strains of enteroinvasive bacteria.

9 stimulation or infection of those cells with enteroinvasive bacteria.

10 ell innate immune response to infection with enteroinvasive bacteria.

11 bowel disease, ischemia-reperfusion injury, enteroinvasive bacterial and parasitic infections.

12 The Gram-negative enteroinvasive bacterium Shigella flexneri is responsibl

13 t mediator of an immune response against the enteroinvasive bacterium Shigella flexneri, both in vitr

14 The enteroinvasive bacterium Shigella is a facultative intra

15 x)-producing E. coli (STEC) bacteria are not enteroinvasive but can cause hemorrhagic colitis.

16 oxigenic E coli, rotavirus, Shigella spp and enteroinvasive E coli, and Vibrio cholerae-the strength

17 otoxins (such as those produced by Shigella, enteroinvasive E coli, or Clostridium difficile) that da

18 coli (1.8%), enterotoxigenic E. coli (2.4%), enteroinvasive E. coli (1.2%), enterohemorrhagic E. coli

19 (AF, 18.4% [95% CI, 12.9%-21.9%]), Shigella/enteroinvasive E. coli (AF, 14.5% [95% CI, 10.2%-22.8%])

20 i (EPEC), enterohaemorrhagic E. coli (EHEC), enteroinvasive E. coli (EIEC) and enterotoxigenic E. col

21 ETEC), Shiga toxin-producing E. coli (STEC), enteroinvasive E. coli (EIEC), and Giardia lamblia.

22 nd Shiga-toxigenic E. coli [STEC]), Shigella/enteroinvasive E. coli (EIEC), protozoa (Cryptosporidium

23 oli (OR: 1.55; 95% CI: 1.04, 2.33), Shigella/enteroinvasive E. coli (OR: 1.65; 95% CI: 1.10, 2.46), n

24 en proposed as an antivirulence mechanism in enteroinvasive E. coli and Shigella flexneri and as a fa

25 Representative strains of Shigella spp. and enteroinvasive E. coli displayed similar deletions of ca

26 nella, and Yersinia species and Shigella and enteroinvasive E. coli in stool samples.

27 Of the 25 mismatches identified, 10 were enteroinvasive E. coli isolates that were misidentified

28 ve, diffusely adherent, enterotoxigenic, and enteroinvasive E. coli strains.

29 None of 55 enteroinvasive E. coli, 12 Yersinia enterocolitica, or 2

30 (STEC), stx(1) and stx(2) for STEC, ipaH for enteroinvasive E. coli, and daaD for diffusely adherent

31 ic detection of E. coli O157), Shigella spp./enteroinvasive E. coli, Cryptosporidium spp., Cyclospora

32 t located within SHI-2 in Shigella boydii or enteroinvasive E. coli.

33 s 40/41 (around five times), Shigella spp or enteroinvasive Escherichia coli (EIEC) and Campylobactor

34 f 577 clinical isolates of Shigella spp. and enteroinvasive Escherichia coli (EIEC) from a variety of

35 sed in epidemiologic studies of Shigella and enteroinvasive Escherichia coli (EIEC) infections.

36 Enteroinvasive Escherichia coli (EIEC) is a unique patho

37 mid library of DNA from colicin Js-sensitive enteroinvasive Escherichia coli (EIEC) strain O164 was m

38 i, Campylobacter coli, Salmonella, Shigella, enteroinvasive Escherichia coli (EIEC), Vibrio, and Yers

39 ase, was synthesized by Shigella species and enteroinvasive Escherichia coli and shown to be responsi

40 s with Salmonella enterica serovar Dublin or enteroinvasive Escherichia coli modestly upregulated LL-

41 present in all Shigella species and in most enteroinvasive Escherichia coli strains but not in any o

42 of nadA and nadB in 14 Shigella strains and enteroinvasive Escherichia coli versus E. coli showed th

43 up II, Cryptosporidium, and Shigella species/enteroinvasive Escherichia coli were significantly assoc

44 for expression of virulence in Shigella and enteroinvasive Escherichia coli, has been found to encod

45 ular localizations (i.e., Salmonella dublin, enteroinvasive Escherichia coli, or Yersinia enterocolit

46 f the well-studied enteric bacteria, such as enteroinvasive Escherichia coli, Salmonella, Shigella, a

47 ess susceptibility of the tissue segments to enteroinvasive Escherichia coli.

48 paB activation in response to infection with enteroinvasive Escherichia coli.

49 ive enteric pathogens, such as Salmonella or enteroinvasive Escherichia coli.

50 enic, enteroadherent, enterohemorrhagic, and enteroinvasive Escherichia coli.

51 s unique to virulent strains of Shigella and enteroinvasive Escherichia coli; these known genes accou

52 Listeria monocytogenes is an enteroinvasive intracellular bacterial pathogen that inf

53 Commensal and enteroinvasive microbes in the human gut release bacteri

54 ediated by endotoxin and was augmented by an enteroinvasive phenotype.

55 This bacterium evolved from an ancestral enteroinvasive Yersinia pseudotuberculosis strain by gen