scholarly journals Repeated Phenotypic Evolution by Different Genetic Routes in Pseudomonas fluorescens SBW25

2019 ◽  
Vol 36 (5) ◽  
pp. 1071-1085 ◽  
Author(s):  
Jenna Gallie ◽  
Frederic Bertels ◽  
Philippe Remigi ◽  
Gayle C Ferguson ◽  
Sylke Nestmann ◽  
...  

Abstract Repeated evolution of functionally similar phenotypes is observed throughout the tree of life. The extent to which the underlying genetics are conserved remains an area of considerable interest. Previously, we reported the evolution of colony switching in two independent lineages of Pseudomonas fluorescens SBW25. The phenotypic and genotypic bases of colony switching in the first lineage (Line 1) have been described elsewhere. Here, we deconstruct the evolution of colony switching in the second lineage (Line 6). We show that, as for Line 1, Line 6 colony switching results from an increase in the expression of a colanic acid-like polymer (CAP). At the genetic level, nine mutations occur in Line 6. Only one of these—a nonsynonymous point mutation in the housekeeping sigma factor rpoD—is required for colony switching. In contrast, the genetic basis of colony switching in Line 1 is a mutation in the metabolic gene carB. A molecular model has recently been proposed whereby the carB mutation increases capsulation by redressing the intracellular balance of positive (ribosomes) and negative (RsmAE/CsrA) regulators of a positive feedback loop in capsule expression. We show that Line 6 colony switching is consistent with this model; the rpoD mutation generates an increase in ribosomal gene expression, and ultimately an increase in CAP expression.

2018 ◽  
Author(s):  
Jenna Gallie ◽  
Frederic Bertels ◽  
Philippe Remigi ◽  
Gayle C Ferguson ◽  
Sylke Nestmann ◽  
...  

ABSTRACTRepeated evolution of functionally similar phenotypes is observed throughout the tree of life. The extent to which the underlying genetics are conserved remains an area of considerable interest. Previously, we reported the evolution of colony switching in two independent lineages of Pseudomonas fluorescens SBW25 (Beaumont et al., 2009). The phenotypic and genotypic bases of colony switching in the first lineage (Line 1) have been described elsewhere (Beaumont et al., 2009; Gallie et al., 2015). Here, we deconstruct the evolution of colony switching in the second lineage (Line 6). We show that, as for Line 1, Line 6 colony switching results from an increase in the expression of a colanic acid-like polymer (CAP). At the genetic level, nine mutations occur in Line 6. Only one of these - a non-synonymous point mutation in the housekeeping sigma factor rpoD - is required for colony switching. In contrast, the genetic basis of colony switching in Line 1 is a mutation in the metabolic gene carB (Beaumont et al., 2009). A molecular model has recently been proposed whereby the carB mutation increases capsulation by redressing the intracellular balance of positive (ribosomes) and negative (RsmAE/CsrA) regulators of a positive feedback loop in capsule expression (Remigi et al., 2018). We show that Line 6 colony switching is consistent with this model; the rpoD mutation generates an increase in ribosome expression, and ultimately an increase in CAP expression.


2013 ◽  
Vol 7 (1) ◽  
pp. 19 ◽  
Author(s):  
Sven EF Borgos ◽  
Sergio Bordel ◽  
Håvard Sletta ◽  
Helga Ertesvåg ◽  
Øyvind Jakobsen ◽  
...  

2007 ◽  
Vol 20 (5) ◽  
pp. 581-588 ◽  
Author(s):  
Xue-Xian Zhang ◽  
Paul B. Rainey

The genome of the plant-colonizing bacterium Pseudomonas fluorescens SBW25 possesses a putative copper-transporting P1-type ATPase (CueA) that is induced on the plant surfaces. Using a chromosomally-integrated cueA-'lacZ fusion, we show that transcription of cueA can be induced (in vitro) by ions of copper, silver, gold, and mercury. To investigate the biological significance of cueA, a nonpolar cueA deletion mutant (SBW25ΔcueA) was constructed. This mutant strain displayed a twofold reduction in its tolerance to copper compared with the wild-type strain; however, no change was observed in the sensitivity of the mutant strain to silver, gold, or mercury ions. To obtain insight into the ecological significance of cueA, the competitive ability of SBW25ΔcueA was determined relative to wild-type SBW25 in three environments (none contained added copper): minimal M9 medium, the root of sugar beet (Beta vulgaris), and the root of pea (Pisum sativum). Results showed that the fitness of SBW25ΔcueA was not different from the wild type in laboratory medium but was compromised in the two plant environments. Taken together, these data demonstrate a functional role for CueA in copper homeostasis and reveal an ecologically significant contribution to bacterial fitness in the plant rhizosphere. They also suggest that copper ions accumulate on plant surfaces.


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