The human mouth is colonized by a microbial community of enormous complexity that plays a key role in human health and disease. Increasingly, it is recognized that the spatial organization of microbial communities in unique micro-niches may have to be explored at fine resolution to provide the basis for elucidating the rules of community assembly and function and to understand their role in disease. Although next-generation DNA sequencing technology and metagenomics have revolutionized the analysis of microbial communities, a major gap in our understanding is the lack of spatial information at the micron level,--information necessary to better characterize the interrelationships between members of a microbial community and with host tissue. We propose to fill this gap through a novel collaboration between the Borisy lab at the Marine Biological Laboratory and the Dewhirst lab at the Forsyth Institute and Harvard School of Dental Medicine. The Borisy lab has recently developed a Combinatorial Labeling and Spectral Imaging (CLASI) strategy for the simultaneous identification of tens of microbial taxa in a single microscopic image. The Dewhirst lab has carried out ground-breaking microbiomic studies of the human oral microbiota. An initial collaboration between the two laboratories, supported by an ARRA Challenge Grant, applied the CLASI strategy to the analysis of human dental plaque, a microbial biofilm, and led to a proof-of-principle publication that characterized the proximity relationshis of 15 oral taxa. Building on this foundation, our proposed research will visualize and define the micron-scale biogeography of the oral microbiome for 9 oral niches: subgingival plaque, supragingival plaque, keratinized gingivae, hard palate, tongue dorsum, buccal mucosa, palatine tonsils, throat, and saliva. Employing an automated tile- scanning capability, it will document the architecture for subgingival microbes in periodontal disease, demonstrating the utility of the approach for examining other oral diseases. It will produce a validated set of FISH probes for the oral research community. By revealing the precise, micron-scale structure of the oral microbiome, this research will address fundamental mechanisms and principles of community dynamics. It will provide an unprecedented systems-level understanding for how members of the human oral microbiota are organized and it will lay the foundation for future studies examining the role of the normal microbial flora in both healthy and diseased mouths. It will impact the broader oral and microbial research communities by developing methods, analysis tools and probes. This project should lead to the identification of key bacterial interactions that may serve as novel targets for therapeutic intervention.

Public Health Relevance

The human mouth is colonized by a microbial community of enormous complexity that plays a key role in human health and disease. Increasingly, it is being recognized that the architecture of microbial communities in unique micro-niches may have to be explored at fine (micron-scale) resolution to provide the basis for elucidating the rules of community assembly and function and to understand their role in disease. This is a project designed to use innovative fluorescence imaging techniques to determine the spatial organization of the oral microbiome. It has the potential to reveal key bacterial interactions that may serve as novel targets for therapeutic intervention.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
5R01DE022586-05
Application #
8970560
Study Section
Oral, Dental and Craniofacial Sciences Study Section (ODCS)
Program Officer
Lunsford, Dwayne
Project Start
2012-12-03
Project End
2017-11-30
Budget Start
2015-12-01
Budget End
2016-11-30
Support Year
5
Fiscal Year
2016
Total Cost
Indirect Cost
Name
Forsyth Institute
Department
Type
DUNS #
062190616
City
Cambridge
State
MA
Country
United States
Zip Code
Mark Welch, Jessica L; Hasegawa, Yuko; McNulty, Nathan P et al. (2017) Spatial organization of a model 15-member human gut microbiota established in gnotobiotic mice. Proc Natl Acad Sci U S A 114:E9105-E9114
Mark Welch, Jessica L; Rossetti, Blair J; Rieken, Christopher W et al. (2016) Biogeography of a human oral microbiome at the micron scale. Proc Natl Acad Sci U S A 113:E791-800
Utter, Daniel R; Mark Welch, Jessica L; Borisy, Gary G (2016) Individuality, Stability, and Variability of the Plaque Microbiome. Front Microbiol 7:564
Valm, Alex M; Oldenbourg, Rudolf; Borisy, Gary G (2016) Multiplexed Spectral Imaging of 120 Different Fluorescent Labels. PLoS One 11:e0158495
Eren, A Murat; Borisy, Gary G; Huse, Susan M et al. (2014) Oligotyping analysis of the human oral microbiome. Proc Natl Acad Sci U S A 111:E2875-84
Mark Welch, Jessica L; Utter, Daniel R; Rossetti, Blair J et al. (2014) Dynamics of tongue microbial communities with single-nucleotide resolution using oligotyping. Front Microbiol 5:568
Kojima, Shin-Ichiro; Borisy, Gary G (2014) An image-based, dual fluorescence reporter assay to evaluate the efficacy of shRNA for gene silencing at the single-cell level. F1000Res 3:60
Dejea, Christine M; Wick, Elizabeth C; Hechenbleikner, Elizabeth M et al. (2014) Microbiota organization is a distinct feature of proximal colorectal cancers. Proc Natl Acad Sci U S A 111:18321-6
Valm, Alex M; Mark Welch, Jessica L; Borisy, Gary G (2012) CLASI-FISH: principles of combinatorial labeling and spectral imaging. Syst Appl Microbiol 35:496-502