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PMID: 6408002 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

In vitro inhibition of lymphocyte proliferation by Pseudomonas aeruginosa phenazine pigments.

Infection and immunity ·Vol. 41 ·No. 1 ·1983-07-00 ·Pages 321-30

Sorensen RU, Klinger JD, Cash HA, Chase PA, Dearborn DG

Abstract

Human lymphocyte proliferation is inhibited in vitro in the presence of killed Pseudomonas aeruginosa or cell-free P. aeruginosa culture supernatants. A comparison of culture supernatants obtained under similar conditions from Staphylococcus aureus, Escherichia coli, P. aeruginosa, and Pseudomonas cepacia strains demonstrated that all P. aeruginosa supernatants were strongly inhibitory, whereas supernatants from other bacteria were mildly inhibitory or not inhibitory at all. These P. aeruginosa inhibitors prevent proliferative responses of resting cells upon mitogen activation and decrease [3H]thymidine uptake when added to human lymphocytes undergoing active proliferation in culture. The inhibitory effect is reversible and not due to cytotoxicity. Most of the inhibitory activity present in crude supernatants was detected in ultrafiltrates of molecular weights below 2,000. Purified P. aeruginosa pyocyanine, a low-molecular-weight phenazine pigment present in culture supernatant, was strongly inhibitory for lymphocyte proliferation. Extraction of pyocyanine and phenazine pigments from inhibitory P. aeruginosa supernatants eliminated their inhibitory activity. Inhibitors were recovered from reverse-phase chromatographic cartridges by both chloroform and methanol elution, indicating that pyocyanine and other phenazine pigments present in P. aeruginosa supernatants are responsible for the inhibition of lymphocyte proliferation. In addition to the identification of phenazine pigments as lymphocyte proliferation inhibitors, several criteria ruled out major contributions of P. aeruginosa polysaccharide, exotoxin A, and proteases to this phenomenon. P. aeruginosa strains selected for very low protease production or for very low exotoxin A production produced supernatants as inhibitory for lymphocyte proliferation as supernatants obtained from clinical P. aeruginosa isolates. Purified P. aeruginosa lipopolysaccharide and protease preparations failed to induce reversible lymphocyte proliferation inhibition. Finally, heat inactivation of P. aeruginosa supernatants at 100 degrees C for 60 min inactivates exotoxin A and proteases but produced only a moderate decrease of the inhibitory activity for lymphocyte proliferation.

MeSH Terms
Cell Division/drug effects Concanavalin A/pharmacology Hot Temperature Humans Lipopolysaccharides/pharmacology Lymphocyte Activation/drug effects Lymphocytes/cytology Peptide Hydrolases/pharmacology Phenazines/pharmacology Pigments, Biological/pharmacology Pseudomonas aeruginosa/analysis Pyocyanine/pharmacology Thymidine/metabolism
Chemicals
Lipopolysaccharides Phenazines Pigments, Biological Concanavalin A Pyocyanine Peptide Hydrolases Thymidine
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Sorensen R U
Klinger J D
Cash H A
Chase P A
Dearborn D G
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Article Info
Journal
Infection and immunity
Abbr.
Infect Immun
ISSN
0019-9567
Published
1983-07-00
Pages
321-30
Language
English
Region
United States
NLM ID
0246127
PMCID
PMC264781
Subset
IM
Grants
NIAID NIH HHS · AI-14862 · United States
NHLBI NIH HHS · HL-24244 · United States
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