Swarming Differentiation and Swimming Motility in Bacillus subtilis Are Controlled by swrA , a Newly Identified Dicistronic Operon

Author:

Calvio Cinzia1,Celandroni Francesco2,Ghelardi Emilia2,Amati Giuseppe1,Salvetti Sara2,Ceciliani Fabrizio3,Galizzi Alessandro1,Senesi Sonia2

Affiliation:

1. Dipartimento di Genetica e Microbiologia “A. Buzzati-Traverso” and Centro di Eccellenza in Biologia Applicata, Università degli Studi di Pavia, 27100 Pavia

2. Dipartimento di Patologia Sperimentale, Biotecnologie Mediche, Infettivologia ed Epidemiologia, Università di Pisa, 56127 Pisa

3. Dipartimento di Patologia Animale, Igiene e Sanità Pubblica Veterinaria, Università degli Studi di Milano, 20133 Milano, Italy

Abstract

ABSTRACT The number and disposition of flagella harbored by eubacteria are regulated by a specific trait successfully maintained over generations. The genes governing the number of flagella in Bacillus subtilis have never been identified, although the ifm locus has long been recognized to influence the motility phenotype of this microorganism. The characterization of a spontaneous ifm mutant of B. subtilis , displaying diverse degrees of cell flagellation in both liquid and solid media, raised the question of how the ifm locus governs the number and assembly of functional flagella. The major finding of this investigation is the characterization of a newly identified dicistronic operon, named swrA , that controls both swimming motility and swarming differentiation in B. subtilis . Functional analysis of the swrA operon allowed swrAA (previously named swrA [D. B. Kearns, F. Chu, R. Rudner, and R. Losick, Mol. Microbiol. 52: 357-369, 2004]) to be the first gene identified in B. subtilis that controls the number of flagella in liquid environments and the assembly of flagella in response to cell contact with solid surfaces. Evidence is given that the second gene of the operon, swrAB , is essential for enabling the surface-adhering cells to undergo swarming differentiation. Preliminary data point to a molecular interaction between the two gene products.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

Reference40 articles.

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2. Burkart, M., A. Toguchi, and R. M. Harshey. 1998. The chemotaxis system, but not chemotaxis, is essential for swarming motility in Escherichia coli. Proc. Natl. Acad. Sci. USA95:2568-2573.

3. Chen, J. C., P. H. Viollier, and L. Shapiro. 2005. A membrane metalloprotease participates in the sequential degradation of a Caulobacter polarity determinant. Mol. Microbiol.55:1085-1103.

4. Extracellular Proteolytic Activity Plays a Central Role in Swarming Motility in Bacillus subtilis

5. Dong, T. C., and S. M. Cutting. 2003. SpoIVB-mediated cleavage of SpoIVFA could provide the intercellular signal to activate processing of pro σK in Bacillus subtilis. Mol. Microbiol.49:1425-1443.

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