Genome-scale fitness profile of Caulobacter crescentus grown in natural freshwater.


Journal

The ISME journal
ISSN: 1751-7370
Titre abrégé: ISME J
Pays: England
ID NLM: 101301086

Informations de publication

Date de publication:
02 2019
Historique:
received: 03 05 2018
accepted: 21 09 2018
revised: 18 09 2018
pubmed: 10 10 2018
medline: 30 7 2019
entrez: 10 10 2018
Statut: ppublish

Résumé

Bacterial genomes evolve in complex ecosystems and are best understood in this natural context, but replicating such conditions in the lab is challenging. We used transposon sequencing to define the fitness consequences of gene disruption in the bacterium Caulobacter crescentus grown in natural freshwater, compared with axenic growth in common laboratory media. Gene disruptions in amino-acid and nucleotide sugar biosynthesis pathways and in metabolic substrate transport machinery impaired fitness in both lake water and defined minimal medium relative to complex peptone broth. Fitness in lake water was enhanced by insertions in genes required for flagellum biosynthesis and reduced by insertions in genes involved in biosynthesis of the holdfast surface adhesin. We further uncovered numerous hypothetical and uncharacterized genes for which disruption impaired fitness in lake water, defined minimal medium, or both. At the genome scale, the fitness profile of mutants cultivated in lake water was more similar to that in complex peptone broth than in defined minimal medium. Microfiltration of lake water did not significantly affect the terminal cell density or the fitness profile of the transposon mutant pool, suggesting that Caulobacter does not strongly interact with other microbes in this ecosystem on the measured timescale. Fitness of select mutants with defects in cell surface biosynthesis and environmental sensing were significantly more variable across days in lake water than in defined medium, presumably owing to day-to-day heterogeneity in the lake environment. This study reveals genetic interactions between Caulobacter and a natural freshwater environment, and provides a new avenue to study gene function in complex ecosystems.

Identifiants

pubmed: 30297849
doi: 10.1038/s41396-018-0295-6
pii: 10.1038/s41396-018-0295-6
pmc: PMC6331620
doi:

Substances chimiques

Bacterial Proteins 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Pagination

523-536

Subventions

Organisme : NIGMS NIH HHS
ID : F32 GM122242
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM087353
Pays : United States
Organisme : NIGMS NIH HHS
ID : R25 GM066522
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM007183
Pays : United States

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Auteurs

Kristy L Hentchel (KL)

Department of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL, 60637, USA.

Leila M Reyes Ruiz (LM)

Department of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL, 60637, USA.

Patrick D Curtis (PD)

Department of Biology, University of Mississippi, University, MS, 38677, USA.

Aretha Fiebig (A)

Department of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL, 60637, USA. aretha@uchicago.edu.

Maureen L Coleman (ML)

Department of the Geophysical Sciences, University of Chicago, Chicago, IL, 60637, USA. mlcoleman@uchicago.edu.

Sean Crosson (S)

Department of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL, 60637, USA. scrosson@uchicago.edu.

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Classifications MeSH