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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
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
12 s with fever and bloody diarrhea (indicating enteroinvasive bacterial etiology) showed little seasona
14 t mediator of an immune response against the enteroinvasive bacterium Shigella flexneri, both in vitr
18 oxigenic E coli, rotavirus, Shigella spp and enteroinvasive E coli, and Vibrio cholerae-the strength
19 otoxins (such as those produced by Shigella, enteroinvasive E coli, or Clostridium difficile) that da
20 coli (1.8%), enterotoxigenic E. coli (2.4%), enteroinvasive E. coli (1.2%), enterohemorrhagic E. coli
21 (AF, 18.4% [95% CI, 12.9%-21.9%]), Shigella/enteroinvasive E. coli (AF, 14.5% [95% CI, 10.2%-22.8%])
22 i (EPEC), enterohaemorrhagic E. coli (EHEC), enteroinvasive E. coli (EIEC) and enterotoxigenic E. col
24 nd Shiga-toxigenic E. coli [STEC]), Shigella/enteroinvasive E. coli (EIEC), protozoa (Cryptosporidium
25 targets from soils (E. coli: ybbW, Shigella/enteroinvasive E. coli (EIEC): ipaH, Giardia duodenalis:
26 18.0% and 8.3%, respectively), and Shigella/enteroinvasive E. coli (in 15.8% and 5.7%, respectively)
27 oli (OR: 1.55; 95% CI: 1.04, 2.33), Shigella/enteroinvasive E. coli (OR: 1.65; 95% CI: 1.10, 2.46), n
28 en proposed as an antivirulence mechanism in enteroinvasive E. coli and Shigella flexneri and as a fa
29 Representative strains of Shigella spp. and enteroinvasive E. coli displayed similar deletions of ca
34 (STEC), stx(1) and stx(2) for STEC, ipaH for enteroinvasive E. coli, and daaD for diffusely adherent
35 coli [EPEC], enterotoxigenic E. coli [ETEC], enteroinvasive E. coli, and Shiga toxin-producing E. col
36 ic detection of E. coli O157), Shigella spp./enteroinvasive E. coli, Cryptosporidium spp., Cyclospora
39 enic Escherichia coli, Campylobacter jejuni, enteroinvasive E. coli/Shigella spp., Salmonella spp., n
40 s 40/41 (around five times), Shigella spp or enteroinvasive Escherichia coli (EIEC) and Campylobactor
41 f 577 clinical isolates of Shigella spp. and enteroinvasive Escherichia coli (EIEC) from a variety of
42 detects enteric pathogens including Shigella/enteroinvasive Escherichia coli (EIEC) in about an hour.
45 mid library of DNA from colicin Js-sensitive enteroinvasive Escherichia coli (EIEC) strain O164 was m
47 i, Campylobacter coli, Salmonella, Shigella, enteroinvasive Escherichia coli (EIEC), Vibrio, and Yers
48 ase, was synthesized by Shigella species and enteroinvasive Escherichia coli and shown to be responsi
50 s with Salmonella enterica serovar Dublin or enteroinvasive Escherichia coli modestly upregulated LL-
51 present in all Shigella species and in most enteroinvasive Escherichia coli strains but not in any o
52 of nadA and nadB in 14 Shigella strains and enteroinvasive Escherichia coli versus E. coli showed th
53 up II, Cryptosporidium, and Shigella species/enteroinvasive Escherichia coli were significantly assoc
54 on for the detection of Salmonella, Shigella/Enteroinvasive Escherichia coli, Campylobacter, Shiga to
55 for expression of virulence in Shigella and enteroinvasive Escherichia coli, has been found to encod
56 dren, followed by adenovirus 40/41, Shigella/enteroinvasive Escherichia coli, norovirus GII, sapoviru
57 ular localizations (i.e., Salmonella dublin, enteroinvasive Escherichia coli, or Yersinia enterocolit
58 f the well-studied enteric bacteria, such as enteroinvasive Escherichia coli, Salmonella, Shigella, a
64 s unique to virulent strains of Shigella and enteroinvasive Escherichia coli; these known genes accou
70 This bacterium evolved from an ancestral enteroinvasive Yersinia pseudotuberculosis strain by gen