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PMID: 3553000 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Congo red binding phenotype is associated with hemin binding and increased infectivity of Shigella flexneri in the HeLa cell model.

Infection and immunity ·Vol. 55 ·No. 6 ·1987-06-00 ·Pages 1393-8

Daskaleros PA, Payne SM

Abstract

Wild-type isolates of Shigella flexneri bind the dye Congo red from solid media, thus producing red (Crb+) colonies. Mutants which fail to bind the dye produce white colonies (Crb-) and are avirulent in a variety of systems. In S. flexneri the ability to bind Congo red correlates with the ability to bind hemin and protoporphyrin IX. Binding of hemin by Crb+ S. flexneri was observed both in solid media and in liquid assays. Results of competition experiments suggest that Congo red and hemin bind to the same site on the bacterial cell and are retained on the cell surface. Binding of hemin by Crb+ S. flexneri is independent of hemin transport since both Crb+ and Crb- cells can utilize hemin as a sole source of iron. Both Crb- and Crb- organisms were able to grow in HeLa cell lysates, indicating that the gene(s) that is responsible for Congo red binding does not play a role in the acquisition of intracellular heme iron. By using the HeLa cell invasion system, the effect of hemin prebinding on the invasiveness of Crb+ S. flexneri was determined. Crb+ cells which had prebound hemin exhibited increased invasiveness, indicating a possible role for the crb gene product in the initial stages of invasion by S. flexneri.

MeSH Terms
Congo Red Dysentery, Bacillary/microbiology HeLa Cells Heme/analogs & derivatives Hemin/metabolism Humans Phenotype Shigella flexneri/pathogenicity
Chemicals
Congo Red Heme Hemin
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Daskaleros P A
Payne S M
References (17)
17 references, click to expand
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Article Info
Journal
Infection and immunity
Abbr.
Infect Immun
ISSN
0019-9567
Published
1987-06-00
Pages
1393-8
Language
English
Region
United States
NLM ID
0246127
PMCID
PMC260526
Subset
IM
Grants
NIAID NIH HHS · AI16935 · United States
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