Literature DB >> 14273631

EFFECT OF ENZYMES ON THE INTERACTION OF ENTEROVIRUSES WITH LIVING HELA CELLS.

I ZAJAC, R L CROWELL.   

Abstract

Zajac, Ihor (Hahnemann Medical College, Philadelphia, Pa.), and Richard L. Crowell. Effect of enzymes on the interaction of enteroviruses with living HeLa cells. J. Bacteriol. 89:574-582. 1965.-Eight crude enzyme preparations and two crystalline enzymes were tested for ability to inactivate coxsackie group B and poliovirus receptors on living HeLa cells. Receptor-destroying enzyme, erepsin, lysozyme, collagenase, proteinase, and cobra venom did not alter attachment of coxsackie B3 or poliovirus T1 to cells, whereas elastase prevented attachment of both viruses tested. Treatment of live cells with pancreatin or chymotrypsin rendered cells unable to attach group B coxsackie viruses, whereas cells treated with trypsin failed to attach poliovirus T1. In addition, chymotrypsin was found to release coxsackie B3 and poliovirus T1 from cell surfaces, whereas trypsin was unable to dissociate virus-cell union. These results indicate that cellular receptors for polioviruses differ from those for group B coxsackie-viruses. The finding that 1% solutions of enzymes will inactivate differentially the enteroviral receptors of HeLa cells, without altering cell viability, provides a useful approach for study of enterovirus receptors of live host cells.

Entities:  

Keywords:  CHYMOTRYPSIN; CLONE CELLS; COXSACKIE VIRUSES; ENZYME REPRESSION; ENZYMES; EXPERIMENTAL LAB STUDY; HELA CELLS; MURAMIDASE; PANCREATIC EXTRACTS; PEPTIDE HYDROLASES; PEPTIDE PEPTIDOHYDROLASES; PHARMACOLOGY; POLIOVIRUS; SNAKES; TISSUE CULTURE; TRYPSIN; VENOMS; VIRUS CULTIVATION

Mesh:

Substances:

Year:  1965        PMID: 14273631      PMCID: PMC277505          DOI: 10.1128/jb.89.3.574-582.1965

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  18 in total

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  21 in total

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Authors:  I ZAJAC; R L CROWELL
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2.  Studies on the attachment of herpes simplex virus. Effect of trypsin treatment.

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9.  Mechanism of resistance to enteroviruses of some primate cells in tissue culture.

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10.  Plaque enhancement of enteroviruses by magnesium chloride, cysteine, and pancreatin.

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