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Items: 1 to 20 of 106

1.

Laboratory adapted Escherichia coli K-12 becomes a pathogen of Caenorhabditis elegans upon restoration of O antigen biosynthesis.

Browning DF, Wells TJ, França FL, Morris FC, Sevastsyanovich YR, Bryant JA, Johnson MD, Lund PA, Cunningham AF, Hobman JL, May RC, Webber MA, Henderson IR.

Mol Microbiol. 2013 Mar;87(5):939-50. doi: 10.1111/mmi.12144. Epub 2013 Jan 28.

2.

Escherichia coli O157:H7 LPS O-side chains and pO157 are required for killing Caenorhabditis elegans.

Youn M, Lee KM, Kim SH, Lim J, Yoon JW, Park S.

Biochem Biophys Res Commun. 2013 Jul 5;436(3):388-93. doi: 10.1016/j.bbrc.2013.05.111. Epub 2013 Jun 6.

PMID:
23747730
3.

Paralysis and killing of Caenorhabditis elegans by enteropathogenic Escherichia coli requires the bacterial tryptophanase gene.

Anyanful A, Dolan-Livengood JM, Lewis T, Sheth S, Dezalia MN, Sherman MA, Kalman LV, Benian GM, Kalman D.

Mol Microbiol. 2005 Aug;57(4):988-1007.

4.

Giardia duodenalis-induced alterations of commensal bacteria kill Caenorhabditis elegans: a new model to study microbial-microbial interactions in the gut.

Gerbaba TK, Gupta P, Rioux K, Hansen D, Buret AG.

Am J Physiol Gastrointest Liver Physiol. 2015 Mar 15;308(6):G550-61. doi: 10.1152/ajpgi.00335.2014. Epub 2015 Jan 8.

5.

Conversion of commensal Escherichia coli K-12 to an invasive form via expression of a mutant histone-like protein.

Koli P, Sudan S, Fitzgerald D, Adhya S, Kar S.

MBio. 2011 Sep 6;2(5). pii: e00182-11. doi: 10.1128/mBio.00182-11. Print 2011. Erratum in: MBio. 2011;2(6). doi: 10.1128/mBio.00263-11.

6.
7.

Yersinia enterocolitica infection and tcaA-dependent killing of Caenorhabditis elegans.

Spanier B, Starke M, Higel F, Scherer S, Fuchs TM.

Appl Environ Microbiol. 2010 Sep;76(18):6277-85. doi: 10.1128/AEM.01274-10. Epub 2010 Jul 16.

8.

Enhanced protection of pathogenic Escherichia coli ingested by a soil nematode Caenorhabditis elegans against sanitizer treatments.

Park MR, Oh S, Yun HS, Kim SH, Ko YH, Ryu JH, Rhee MS, Shin OS, Kim Y.

Biosci Biotechnol Biochem. 2014;78(11):1917-22. doi: 10.1080/09168451.2014.940830. Epub 2014 Jul 23.

PMID:
25052260
9.

The global regulator Ler is necessary for enteropathogenic Escherichia coli colonization of Caenorhabditis elegans.

Mellies JL, Barron AM, Haack KR, Korson AS, Oldridge DA.

Infect Immun. 2006 Jan;74(1):64-72.

10.

A gene (wbbL) from Serratia marcescens N28b (O4) complements the rfb-50 mutation of Escherichia coli K-12 derivatives.

Rubirés X, Saigi F, Piqué N, Climent N, Merino S, Albertí S, Tomás JM, Regué M.

J Bacteriol. 1997 Dec;179(23):7581-6.

11.

Restoring de novo coenzyme Q biosynthesis in Caenorhabditis elegans coq-3 mutants yields profound rescue compared to exogenous coenzyme Q supplementation.

Gomez F, Saiki R, Chin R, Srinivasan C, Clarke CF.

Gene. 2012 Sep 10;506(1):106-16. doi: 10.1016/j.gene.2012.06.023. Epub 2012 Jun 23.

12.

Lack of the RNA chaperone Hfq attenuates pathogenicity of several Escherichia coli pathotypes towards Caenorhabditis elegans.

Bojer MS, Jakobsen H, Struve C, Krogfelt KA, Løbner-Olesen A.

Microbes Infect. 2012 Oct;14(12):1034-9. doi: 10.1016/j.micinf.2012.06.002. Epub 2012 Jun 17.

PMID:
22713744
13.

Functional analysis of antigen 43 in uropathogenic Escherichia coli reveals a role in long-term persistence in the urinary tract.

Ulett GC, Valle J, Beloin C, Sherlock O, Ghigo JM, Schembri MA.

Infect Immun. 2007 Jul;75(7):3233-44. Epub 2007 Apr 9.

14.
15.

Genetic characterization of the Escherichia coli O66 antigen and functional identification of its wzy gene.

Cheng J, Liu B, Bastin DA, Han W, Wang L, Feng L.

J Microbiol. 2007 Feb;45(1):69-74.

16.

O acetylation of the enterobacterial common antigen polysaccharide is catalyzed by the product of the yiaH gene of Escherichia coli K-12.

Kajimura J, Rahman A, Hsu J, Evans MR, Gardner KH, Rick PD.

J Bacteriol. 2006 Nov;188(21):7542-50. Epub 2006 Aug 25.

17.

Effect of iclR and arcA knockouts on biomass formation and metabolic fluxes in Escherichia coli K12 and its implications on understanding the metabolism of Escherichia coli BL21 (DE3).

Waegeman H, Beauprez J, Moens H, Maertens J, De Mey M, Foulquié-Moreno MR, Heijnen JJ, Charlier D, Soetaert W.

BMC Microbiol. 2011 Apr 11;11:70. doi: 10.1186/1471-2180-11-70.

18.

Genotype and phenotypes of an intestine-adapted Escherichia coli K-12 mutant selected by animal passage for superior colonization.

Fabich AJ, Leatham MP, Grissom JE, Wiley G, Lai H, Najar F, Roe BA, Cohen PS, Conway T.

Infect Immun. 2011 Jun;79(6):2430-9. doi: 10.1128/IAI.01199-10. Epub 2011 Mar 21.

19.

Relationship between O-antigen subtypes, bacterial surface structures and O-antigen gene clusters in Escherichia coli O123 strains carrying genes for Shiga toxins and intimin.

Beutin L, Wang Q, Naumann D, Han W, Krause G, Leomil L, Wang L, Feng L.

J Med Microbiol. 2007 Feb;56(Pt 2):177-84.

PMID:
17244797
20.

Escherichia coli serogroup O2 and O28ac O-antigen gene cluster sequences and detection of pathogenic E. coli O2 and O28ac by PCR.

Fratamico PM, Yan X, Liu Y, DebRoy C, Byrne B, Monaghan A, Fanning S, Bolton D.

Can J Microbiol. 2010 Apr;56(4):308-16. doi: 10.1139/w10-010.

PMID:
20453897
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