A color-based competition assay for studying bacterial stress responses in Micrococcus luteus.


Journal

FEMS microbiology letters
ISSN: 1574-6968
Titre abrégé: FEMS Microbiol Lett
Pays: England
ID NLM: 7705721

Informations de publication

Date de publication:
01 03 2019
Historique:
received: 20 12 2018
accepted: 12 03 2019
pubmed: 14 3 2019
medline: 28 12 2019
entrez: 14 3 2019
Statut: ppublish

Résumé

Competition assays measure differences between populations of bacteria after stress adaptation, populations of different bacteria and mutations in antibiotic resistance genes. We have developed a competition-based assay to evaluate if genes upregulated under starvation are important for bacterial survival. Stress responses are critical for survival in non-pathogenic and pathogenic bacteria alike including Mycobacterium tuberculosis, Enterococcus fecaelis, Escherichia coli and Staphylococcus aureus. Unfortunately, most stress-survival proteins are poorly understood because suitable model bacteria and techniques are limited. To address this problem, we have engineered Micrococcus luteus NCTC 2665 (M. luteus) for competition assays by inactivating the sarcinaxanthin biosynthesis gene crtE (ΔcrtE), changing M. luteus colonies from yellow to white. This change allows easy identification in mixed cultures. The crtE knockout is relatively neutral for growth in complex and minimal acetate media and shows a measured fitness of one in competition with yellow wild-type bacteria. The ΔcrtE M. luteus competition assay identified a competition defect in a M. luteus strain when a specific universal stress protein was inactivated, suggesting a negative survival phenotype for this protein. We anticipate this competition assay can identify defects in other gene knockouts and mutational studies in M. luteus and will enhance our understanding of bacterial survival mechanisms.

Identifiants

pubmed: 30865770
pii: 5379281
doi: 10.1093/femsle/fnz054
pii:
doi:

Substances chimiques

Acetates 0
Bacterial Proteins 0
Culture Media 0
Xanthophylls 0
sarcinaxanthin 11031-47-3

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© FEMS 2019.

Auteurs

Spencer Havis (S)

Department of Biology and Biochemistry, The University of Houston, Houston, TX, USA.

Jonathan Rangel (J)

Department of Biology and Biochemistry, The University of Houston, Houston, TX, USA.

Sujina Mali (S)

Department of Biology, Washington University, St. Louis, MO, USA.

Abiodun Bodunrin (A)

Department of Biology and Biochemistry, The University of Houston, Houston, TX, USA.

Zina Housammy (Z)

University of North Texas Health Sciences Center, Fort Worth, TX, USA.

Rene Zimmerer (R)

Department of Biology and Biochemistry, The University of Houston, Houston, TX, USA.

Jesse Murphy (J)

Department of Biology and Biochemistry, The University of Houston, Houston, TX, USA.

William R Widger (WR)

Department of Biology and Biochemistry, The University of Houston, Houston, TX, USA.

Steven J Bark (SJ)

Department of Biology and Biochemistry, The University of Houston, Houston, TX, USA.

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Classifications MeSH