GSBS Student Publications

Title

A surface protease and the invasive character of plague

UMMS Affiliation

Graduate School of Biomedical Sciences; Department of Molecular Genetics and Microbiology

Date

11-6-1992

Document Type

Article

Medical Subject Headings

Amino Acid Sequence; Animals; *Bacterial Proteins; Colony Count, Microbial; Escherichia coli; Injections, Intravenous; Kinetics; Liver; Mice; Molecular Sequence Data; Mutation; Plague; Plasmids; Plasmin; Plasminogen Activators; Recombinant Proteins; Spleen; Tissue Plasminogen Activator; Urinary Plasminogen Activator; Yersinia pestis

Disciplines

Life Sciences | Medicine and Health Sciences

Abstract

A 9.5-kilobase plasmid of Yersinia pestis, the causative agent of plague, is required for high virulence when mice are inoculated with the bacterium by subcutaneous injection. Inactivation of the plasmid gene pla, which encodes a surface protease, increased the median lethal dose of the bacteria for mice by a millionfold. Moreover, cloned pla was sufficient to restore segregants lacking the entire pla-bearing plasmid to full virulence. Both pla+ strains injected subcutaneously and pla- mutants injected intravenously reached high titers in liver and spleen of infected mice, whereas pla- mutants injected subcutaneously failed to do so even though they establish a sustained local infection at the injection site. More inflammatory cells accumulated in lesions caused by the pla- mutants than in lesions produced by the pla+ parent. The Pla protease was shown to be a plasminogen activator with unusual kinetic properties. It can also cleave complement C3 at a specific site.

Rights and Permissions

Citation: Science. 1992 Nov 6;258(5084):1004-7.

Related Resources

Link to Article in PubMed

Journal Title

Science (New York, N.Y.)

PubMed ID

1439793