Abstract
The infectivity of trachoma-inclusion conjunctivitis (TRIC) organisms (TW-5) was enhanced by pretreatment of HeLa cell monolayers before inoculation with diethylaminoethyl (DEAE)-dextran (30 mug/ml) and poly-l-lysine (10 mug/ml) and inhibited by dextran sulphate (250 mug/ml), fetuin (4%), ovomucoid (5%), N-acetyl neuraminic acid (0.5%), and Cholera vibrio neuraminidase (100 U/ml). The infectivity of lymphogranuloma venereum organisms (434) was not affected by DEAE-dextran, fetuin, and neuraminidase, was slightly inhibited by poly-l-lysine, and was inhibited by dextran-sulphate, ovomucoid, and N-acetyl neuraminic acid. The study suggested that sialic acid residues on the cell surface may be specific receptors for TRIC organisms. The receptors for TRIC organisms (TW-5 and TW-3) could be specifically blocked with inactivated (56 C for 30 min) TRIC organisms at the ratio of one live to 100 inactivated TRIC organisms, but not by inactivated lymphogranuloma venereum (434) or influenza virus (A(2)/Jap 305).
MeSH Terms
Binding Sites
Cations, Divalent/pharmacology
Chlamydia/drug effects,pathogenicity
Conjunctivitis, Inclusion/microbiology
Cytopathogenic Effect, Viral/drug effects
HeLa Cells/drug effects
Humans
Ion Exchange Resins/pharmacology
Lymphogranuloma Venereum/microbiology
Neuraminic Acids
Neuraminidase/pharmacology
Trachoma/microbiology
Virulence
Chemicals
Cations, Divalent
Ion Exchange Resins
Neuraminic Acids
Neuraminidase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Kuo C C
Wang S P
Grayston J T
References (19)
19 references, click to expand
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