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The frequency of expression of pyelonephritis-associated pili is under regulatory control
Authors:D Low  E N Robinson  Z A McGee  S Falkow
Institution:Department of Pathology, University of Utah School of Medicine. Salt Lake City. Utah 84132, USA.;Center for Infectious Diseases. Diagnostic Microbiology and Immunology, Division of Infectious Diseases, Department of Medicine, University of Utah School of Medicine, Salt Lake City, Utah 84132, USA.;Department of Medical Microbiology, Stanford University School of Medicine, Stanford, California 94305, USA.
Abstract:The Bscherfchia coli urinary tract Isolate C1212 contains two pyelonephritis-associated pili (pap) DNA sequences designated here as pap-17 and pap-21. Each of these pap sequences encodes antigenically-distinct pilin monomers, pllin-17 and pilin-21, respectively. Most individual strain C1212 cells isolated from a single bacterial colony expressed pilin-21. Only a small fraction (5%) of strain C1212 cells expressed pilin-17. Most of the latter population simultaneously expressed pilin-21, but a low percentage of cells expressed pill composed of pilin-17 alone. In contrast, almost every E. coli K-12 cell containing multicopy pap-17 expressed pilin-17 at the ceil surface. These results Indicated that the regulation of pilin-17 expression observed for strain C1212 was lost when pap-17 was in the multicopy state. Transfer of pap-17 to a single copy vector resulted in a pilin-17 expression frequency lower than strain C1212 (1%). Using E. coli K-12 containing single copy pap-17, we found that the frequency of piiin-17 expression increased about 15-foid when pap-21 was present in multiple copies in trans. Subcloning of pap-21 showed that a 2.2 kilobase-pair DNA sequence adjacent to, but not including, the pilin-21 structural gene was sufficient for activation of pilin-17 expression.
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