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Journal of Bacteriology, March 2004, p. 1785-1792, Vol. 186, No. 6
0021-9193/04/$08.00+0     DOI: 10.1128/JB.186.6.1785-1792.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Roles of Genes 44, 50, and 51 in Regulating Gene Expression and Host Takeover during Infection of Bacillus subtilis by Bacteriophage SPO1

Aruna Sampath{dagger} and Charles R. Stewart*

Department of Biochemistry and Cell Biology, Rice University, Houston, Texas 77251

Received 12 September 2003/ Accepted 5 December 2003

We show that the products of SPO1 genes 44, 50, and 51 are required for the normal transition from early to middle gene expression during infection of Bacillus subtilis by bacteriophage SPO1; that they are also required for control of the shutoff of host DNA, RNA, and protein synthesis; and that their effects on host shutoff could be accounted for by their effects on the regulation of gene expression. These three gene products had four distinguishable effects in regulating SPO1 gene expression: (i) gp44-50-51 acted to restrain expression of all SPO1 genes tested, (ii) gp44 and/or gp50-51 caused additional specific repression of immediate-early genes, (iii) gp44 and/or gp50-51 stimulated expression of middle genes, and (iv) gp44 and/or gp50-51 stimulated expression of some delayed-early genes. Shutoff of immediate-early gene expression also required the activity of gp28, the middle-gene-specific sigma factor. Shutoff of host RNA and protein synthesis was accelerated by either the 44- single mutant or the 50-51- double mutant and more so by the 44-50-51- triple mutant. Shutoff of host DNA synthesis was accelerated by the mutants early in infection but delayed by the 44-50-51- triple mutant at later times. Although gp50 is a very small protein, consisting almost entirely of an apparent membrane-spanning domain, it contributed significantly to each activity tested. We identify SPO1 genes 41 to 51 and 53 to 60 as immediate-early genes; genes 27, 28, and 37 to 40 as delayed-early genes; and gene 52 as a middle gene.

* Corresponding author. Mailing address: Department of Biochemistry and Cell Biology, Rice University, Houston, TX 77251. Phone: (713) 348-4926. Fax: (713) 348-5154. E-mail: crs{at}bioc.rice.edu.

{dagger} Present address: Novartis Institute for Tropical Diseases, Singapore 117528.

Journal of Bacteriology, March 2004, p. 1785-1792, Vol. 186, No. 6
0021-9193/04/$08.00+0     DOI: 10.1128/JB.186.6.1785-1792.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.



This article has been cited by other articles:

  • Klumpp, J., Dorscht, J., Lurz, R., Bielmann, R., Wieland, M., Zimmer, M., Calendar, R., Loessner, M. J. (2008). The Terminally Redundant, Nonpermuted Genome of Listeria Bacteriophage A511: a Model for the SPO1-Like Myoviruses of Gram-Positive Bacteria. J. Bacteriol. 190: 5753-5765 [Abstract] [Full Text]  


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