A surface protease and the invasive character of plague
Biochemistry & Molecular Pharmacology
Graduate School of Biomedical Sciences; Department of Molecular Genetics and Microbiology
Life Sciences | Medicine and Health Sciences
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.
DOI of Published Version
Science. 1992 Nov 6;258(5084):1004-7.
Science (New York, N.Y.)
Sodeinde OA, Subrahmanyam Y, Stark K, Quan T, Bao Y, Goguen JD. (1992). A surface protease and the invasive character of plague. GSBS Student Publications. https://doi.org/10.1126/science.1439793. Retrieved from https://escholarship.umassmed.edu/gsbs_sp/1137