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Infect. Immun., 01 1995, 191-198, Vol 63, No. 1
RP Vanmaele, MC Finlayson and GD Armstrong
Enteropathogenic Escherichia coli (EPEC) O111:H2, O119:H6, or O142:H6
caused rapid detachment of Chinese hamster ovary (CHO) cell monolayers
within 2 to 4 h of cocultivation. CHO cell detachment was not promoted by
nonenteropathogenic E. coli (O125:H4, O126:H27, O157:H7, and O26:H11) and
could not be attributed to EPEC production of enterohemolysin or Shiga-like
toxins. In contrast, EPEC strains did not promote rapid detachment of Lec1,
Lec2, or Lec8 CHO cell monolayers. These CHO cell Lec mutants all express
abbreviated glycan sequences on membrane glycoproteins and glycolipids.
Although EPEC strains failed to alter the adherent properties of Lec2 cells
lacking only terminal sialic acid groups, EPEC adherence to the Lec2 mutant
was indistinguishable from that observed with wild-type CHO cells. There
was also no significant difference in EPEC-induced actin accumulation or
invasion of Lec2 cells. In contrast, EPEC localized adherence to Lec1 and
Lec8 mutants, lacking sialyllactosamine (Lec1) or sialic acid and galactose
(Lec8) sequences, was reduced by 84 and 93%, respectively. Our results
suggest that lactosamine sequences [beta Gal(1-4 or 1-3)beta GlcNAc] not
containing sialic acid are sufficient for EPEC adherence, actin
accumulation, and invasion of CHO cells. Sialic acid groups, however, may
be necessary for EPEC-mediated CHO cell detachment.
Copyright © 1995, American Society for Microbiology
Effect of enteropathogenic Escherichia coli on adherent properties of Chinese hamster ovary cells
Department of Medical Microbiology and Infectious Diseases, University of Alberta, Edmonton, Canada.
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