Literature DB >> 20472802

The genetic basis of laboratory adaptation in Caulobacter crescentus.

Melissa E Marks1, Cyd Marie Castro-Rojas, Clotilde Teiling, Lei Du, Vinayak Kapatral, Theresa L Walunas, Sean Crosson.   

Abstract

The dimorphic bacterium Caulobacter crescentus has evolved marked phenotypic changes during its 50-year history of culture in the laboratory environment, providing an excellent system for the study of natural selection and phenotypic microevolution in prokaryotes. Combining whole-genome sequencing with classical molecular genetic tools, we have comprehensively mapped a set of polymorphisms underlying multiple derived phenotypes, several of which arose independently in separate strain lineages. The genetic basis of phenotypic differences in growth rate, mucoidy, adhesion, sedimentation, phage susceptibility, and stationary-phase survival between C. crescentus strain CB15 and its derivative NA1000 is determined by coding, regulatory, and insertion/deletion polymorphisms at five chromosomal loci. This study evidences multiple genetic mechanisms of bacterial evolution as driven by selection for growth and survival in a new selective environment and identifies a common polymorphic locus, zwf, between lab-adapted C. crescentus and clinical isolates of Pseudomonas aeruginosa that have adapted to a human host during chronic infection.

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Year:  2010        PMID: 20472802      PMCID: PMC2897358          DOI: 10.1128/JB.00255-10

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  35 in total

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Journal:  FEBS Lett       Date:  2007-07-03       Impact factor: 4.124

3.  A transducing bacteriophage for Caulobacter crescentus uses the paracrystalline surface layer protein as a receptor.

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4.  Genome evolution and adaptation in a long-term experiment with Escherichia coli.

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Authors:  M Evinger; N Agabian
Journal:  J Bacteriol       Date:  1977-10       Impact factor: 3.490

Review 6.  The molecular genetics of crop domestication.

Authors:  John F Doebley; Brandon S Gaut; Bruce D Smith
Journal:  Cell       Date:  2006-12-29       Impact factor: 41.582

Review 7.  The caulobacters: ubiquitous unusual bacteria.

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8.  Adaptations of Pseudomonas aeruginosa to the cystic fibrosis lung environment can include deregulation of zwf, encoding glucose-6-phosphate dehydrogenase.

Authors:  Laura Silo-Suh; Sang-Jin Suh; Paul V Phibbs; Dennis E Ohman
Journal:  J Bacteriol       Date:  2005-11       Impact factor: 3.490

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Journal:  Environ Microbiol       Date:  2009-05       Impact factor: 5.491

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  74 in total

1.  Genome sequence and phenotypic characterization of Caulobacter segnis.

Authors:  Sagar Patel; Brock Fletcher; Derrick C Scott; Bert Ely
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2.  The LovK-LovR two-component system is a regulator of the general stress pathway in Caulobacter crescentus.

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Review 3.  Virulence strategies of the dominant USA300 lineage of community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA).

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Journal:  FEMS Immunol Med Microbiol       Date:  2012-03-05

4.  Global methylation state at base-pair resolution of the Caulobacter genome throughout the cell cycle.

Authors:  Jennifer B Kozdon; Michael D Melfi; Khai Luong; Tyson A Clark; Matthew Boitano; Susana Wang; Bo Zhou; Diego Gonzalez; Justine Collier; Stephen W Turner; Jonas Korlach; Lucy Shapiro; Harley H McAdams
Journal:  Proc Natl Acad Sci U S A       Date:  2013-11-11       Impact factor: 11.205

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Authors:  Jared M Schrader; Lucy Shapiro
Journal:  J Vis Exp       Date:  2015-04-08       Impact factor: 1.355

6.  Flagellar Mutants Have Reduced Pilus Synthesis in Caulobacter crescentus.

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Journal:  J Bacteriol       Date:  2019-08-22       Impact factor: 3.490

7.  Dynamic translation regulation in Caulobacter cell cycle control.

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8.  In vivo biochemistry in bacterial cells using FRAP: insight into the translation cycle.

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Journal:  Biophys J       Date:  2012-11-07       Impact factor: 4.033

9.  The cloning, expression, purification, characterization and modeled structure of Caulobacter crescentus β-Xylosidase I.

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10.  Microfluidic device for automated synchronization of bacterial cells.

Authors:  Seth M Madren; Michelle D Hoffman; Pamela J B Brown; David T Kysela; Yves V Brun; Stephen C Jacobson
Journal:  Anal Chem       Date:  2012-10-03       Impact factor: 6.986

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