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Methods

Fluorescence Tools Adapted for Real-Time Monitoring of the Behaviors of Streptococcus Species

R. C. Shields, J. R. Kaspar, K. Lee, S. A. M. Underhill, R. A. Burne
Donald W. Schaffner, Editor
R. C. Shields
aDepartment of Oral Biology, College of Dentistry, University of Florida, Gainesville, Florida, USA
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J. R. Kaspar
aDepartment of Oral Biology, College of Dentistry, University of Florida, Gainesville, Florida, USA
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K. Lee
aDepartment of Oral Biology, College of Dentistry, University of Florida, Gainesville, Florida, USA
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S. A. M. Underhill
bDepartment of Physics, University of Florida, Gainesville, Florida, USA
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R. A. Burne
aDepartment of Oral Biology, College of Dentistry, University of Florida, Gainesville, Florida, USA
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Donald W. Schaffner
Rutgers, The State University of New Jersey
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DOI: 10.1128/AEM.00620-19
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ABSTRACT

Tagging of bacteria with fluorescent proteins has become an essential component of modern microbiology. Fluorescent proteins can be used to monitor gene expression and biofilm growth and to visualize host-pathogen interactions. Here, we developed a collection of fluorescent protein reporter plasmids for Streptococcus mutans UA159 and other oral streptococci. Using superfolder green fluorescent protein (sfGFP) as a reporter for transcriptional activity, we were able to characterize four strong constitutive promoters in S. mutans. These promoter-sfgfp fusions worked both for single-copy chromosomal integration and on a multicopy plasmid, with the latter being segregationally stable in the absence of selective pressure under the conditions tested. We successfully labeled S. mutans UA159, Streptococcus gordonii DL1, and Streptococcus sp. strain A12 with sfGFP, DsRed-Express2 (red), and citrine (yellow). To test these plasmids under more challenging conditions, we performed mixed-species biofilm experiments and separated fluorescent populations using fluorescence-activated cell sorting (FACS). This allowed us to visualize two streptococci at a time and quantify the amounts of each species simultaneously. These fluorescent reporter plasmids add to the genetic toolbox available for the study of oral streptococci.

IMPORTANCE Oral streptococci are the most abundant bacteria in the mouth and have a major influence on oral health and disease. In this study, we designed and optimized the expression of fluorescent proteins in Streptococcus mutans and other oral streptococci. We monitored the levels of expression and noise (the variability in fluorescence across the population). We then created several fluorescent protein delivery systems (green, yellow, and red) for use in oral streptococci. The data show that we can monitor bacterial growth and interactions in situ, differentiating between different bacteria growing in biofilms, the natural state of the organisms in the human mouth. These new tools will allow researchers to study these bacteria in novel ways to create more effective diagnostic and therapeutic tools for ubiquitous infectious diseases.

FOOTNOTES

    • Received 14 March 2019.
    • Accepted 11 May 2019.
    • Accepted manuscript posted online 17 May 2019.
  • Supplemental material for this article may be found at https://doi.org/10.1128/AEM.00620-19.

  • Copyright © 2019 American Society for Microbiology.

All Rights Reserved.

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Fluorescence Tools Adapted for Real-Time Monitoring of the Behaviors of Streptococcus Species
R. C. Shields, J. R. Kaspar, K. Lee, S. A. M. Underhill, R. A. Burne
Applied and Environmental Microbiology Jul 2019, 85 (15) e00620-19; DOI: 10.1128/AEM.00620-19

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Fluorescence Tools Adapted for Real-Time Monitoring of the Behaviors of Streptococcus Species
R. C. Shields, J. R. Kaspar, K. Lee, S. A. M. Underhill, R. A. Burne
Applied and Environmental Microbiology Jul 2019, 85 (15) e00620-19; DOI: 10.1128/AEM.00620-19
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KEYWORDS

Streptococcus mutans
biofilm
fluorescence microscopy
green fluorescent protein
oral streptococci

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