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Congo Red-mediated Regulation of Levels of Shigella Flexneri 2a Membrane Proteins

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Journal Infect Immun
Date 1989 Aug 1
PMID 2663721
Citations 12
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Abstract

The ability of Shigella spp. to bind Congo red from agar medium is generally correlated with their virulence properties. We used a metabolically active culture of Shigella flexneri 2a to determine the effect of Congo red on its membrane protein profiles. Virulent S. flexneri grown in the presence of Congo red at 37 degrees C showed increased levels of three proteins with Mrs of 43,000, 58,000, and 63,000 (43K, 58K, and 63K proteins) in the Sarkosyl-soluble membrane fractions. The observed phenomenon was temperature dependent. At 30 or 42 degrees C the protein levels remained unaffected by the presence of Congo red. Similar regulation of the levels of the 43K, 58K, and 63K membrane proteins was also observed with Shigella dysenteriae 1 and enteroinvasive Escherichia coli, but not with enteropathogenic E. coli. The cellular uptake of Congo red seemed to be essential, but not sufficient, for regulation. All three proteins reacted with human convalescent-phase sera in immunoblots of S. flexneri 2a Sarkosyl-soluble membrane fractions. Using the 43K-specific antiserum as the primary antibody, by indirect immunofluorescence studies, we detected an increase in the level of the 43K protein in S. flexneri which had invaded epithelial cells. These observations strongly indicate that the 43K, 58K, and 63K proteins are virulence associated. We propose that the observed regulatory effect of Congo red on membrane proteins of S. flexneri is mediated through induction. Since the same regulatory effect was also observed during the invasion of epithelial cells by S. flexneri, it is suggested that Congo red mimics some host tissue factor in vitro.

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References
1.
Laemmli U . Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970; 227(5259):680-5. DOI: 10.1038/227680a0. View

2.
Daskaleros P, Payne S . Cloning the gene for Congo red binding in Shigella flexneri. Infect Immun. 1985; 48(1):165-8. PMC: 261930. DOI: 10.1128/iai.48.1.165-168.1985. View

3.
Sansonetti P, Kopecko D, Formal S . Involvement of a plasmid in the invasive ability of Shigella flexneri. Infect Immun. 1982; 35(3):852-60. PMC: 351125. DOI: 10.1128/iai.35.3.852-860.1982. View

4.
Sasakawa C, Kamata K, Sakai T, Murayama S, Makino S, Yoshikawa M . Molecular alteration of the 140-megadalton plasmid associated with loss of virulence and Congo red binding activity in Shigella flexneri. Infect Immun. 1986; 51(2):470-5. PMC: 262355. DOI: 10.1128/iai.51.2.470-475.1986. View

5.
Hale T, Formal S . Genetics of virulence in Shigella. Microb Pathog. 1986; 1(6):511-8. DOI: 10.1016/0882-4010(86)90037-9. View