Episymbiotic Saccharibacteria induce intracellular lipid droplet production in their host bacteria

Author:

Dong Pu-Ting123,Tian Jing4,Kobayashi-Kirschvink Koseki J567,Cen Lujia1,McLean Jeffrey S8,Bor Batbileg123,Shi Wenyuan1,He Xuesong123

Affiliation:

1. Department of Microbiology, The ADA Forsyth Institute , Boston, MA 02142 , United States

2. Department of Oral Medicine , Infection, and Immunity, , Boston, MA 02115 , United States

3. Harvard School of Dental Medicine , Infection, and Immunity, , Boston, MA 02115 , United States

4. Department of Pediatric Dentistry, Peking University School and Hospital of Stomatology , Beijing 100081 , China

5. Klarman Cell Observatory, Broad Institute of MIT and Harvard , Cambridge, MA 02142 , United States

6. Laser Biomedical Research Center , G. R. Harrison Spectroscopy Laboratory, , Cambridge, MA 02139 , United States

7. Massachusetts Institute of Technology , G. R. Harrison Spectroscopy Laboratory, , Cambridge, MA 02139 , United States

8. Department of Periodontics, University of Washington , Seattle, WA 98195 , United States

Abstract

Abstract Saccharibacteria (formerly TM7) are a group of widespread and genetically diverse ultrasmall bacteria with highly reduced genomes that belong to Candidate Phyla Radiation, a large monophyletic lineage with poorly understood biology. Nanosynbacter lyticus type strain TM7x is the first Saccharibacteria member isolated from the human oral microbiome. With restrained metabolic capacities, TM7x lives on the surface of, and forms an obligate episymbiotic relationship with its bacterial host, Schaalia odontolytica strain XH001. The symbiosis allows TM7x to propagate but presents a burden to host bacteria by inducing stress response. Here, we employed super-resolution fluorescence imaging to investigate the physical association between TM7x and XH001. We showed that the binding with TM7x led to a substantial alteration in the membrane fluidity of XH001. We also revealed the formation of intracellular lipid droplets in XH001 when forming episymbiosis with TM7x, a feature that has not been reported in oral bacteria. The TM7x-induced lipid droplets accumulation in XH001 was confirmed by label-free Raman spectroscopy, which also unveiled additional phenotypical features when XH001 cells are physically associated with TM7x. Further exploration through culturing XH001 under various stress conditions showed that lipid droplets accumulation was a general response to stress. A survival assay demonstrated that the presence of lipid droplets plays a protective role in XH001, enhancing its survival under adverse conditions. In conclusion, our study sheds new light on the intricate interaction between Saccharibacteria and their host bacteria, highlighting the potential benefit conferred by TM7x to its host and further emphasizing the context-dependent nature of symbiotic relationships.

Funder

National Institute of Dental and Craniofacial Research

NIDCR

Forsyth Pilot

Publisher

Oxford University Press (OUP)

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