The Assembly of Bacteria Living in Natural Environments Shapes Neuronal Integrity and Behavioral Outputs in Caenorhabditis elegans

Do behavioral choices depend on animals’ microbiota? To answer this question, we studied how different bacterial assemblies impact the life-history traits of the bacterivore nematode C. elegans using isolated bacteria found in association with wild nematodes in Chilean soil. We identified the first isolate, Iso1, as a novel species of Stenotrophomonas and isolate Iso2 as Bacillus pumilus. ABSTRACT Bacterivore nematodes are the most abundant animals in the biosphere, largely contributing to global biogeochemistry. Thus, the effects of environmental microbes on the nematodes’ life-history traits are likely to contribute to the general health of the biosphere. Caenorhabditis elegans is an excellent model to study the behavioral and physiological outputs of microbial diets. However, the effects of complex natural bacterial assemblies have only recently been reported, as most studies have been carried out with monoxenic cultures of laboratory-reared bacteria. Here, we quantified the physiological, phenotypic, and behavioral traits of C. elegans feeding on two bacteria that were coisolated with wild nematodes from a soil sample. These bacteria were identified as a putative novel species of Stenotrophomonas named Stenotrophomonas sp. strain Iso1 and a strain of Bacillus pumilus designated Iso2. The distinctive behaviors and developmental patterns observed in animals fed with individual isolates changed when bacteria were mixed. We studied in more depth the degeneration rate of the touch circuit of C. elegans and show that B. pumilus alone is protective, while the mix with Stenotrophomonas sp. is degenerative. The analysis of the metabolite contents of each isolate and their combination identified NAD+ as being potentially neuroprotective. In vivo supplementation shows that NAD+ restores neuroprotection to the mixes and also to individual nonprotective bacteria. Our results highlight the distinctive physiological effects of bacteria resembling native diets in a multicomponent scenario rather than using single isolates on nematodes. IMPORTANCE Do behavioral choices depend on animals’ microbiota? To answer this question, we studied how different bacterial assemblies impact the life-history traits of the bacterivore nematode C. elegans using isolated bacteria found in association with wild nematodes in Chilean soil. We identified the first isolate, Iso1, as a novel species of Stenotrophomonas and isolate Iso2 as Bacillus pumilus. We find that worm traits such as food choice, pharyngeal pumping, and neuroprotection, among others, are dependent on the biota composition. For example, the neurodegeneration of the touch circuit needed to sense and escape from predators in the wild decreases when nematodes are fed on B. pumilus, while its coculture with Stenotrophomonas sp. eliminates neuroprotection. Using metabolomics analysis, we identify metabolites such as NAD+, present in B. pumilus yet lost in the mix, as being neuroprotective and validated their protective effects using in vivo experiments.

[1]  V. Narayan,et al.  Host Preference of Beneficial Commensals in a Microbially-Diverse Environment , 2022, Frontiers in Cellular and Infection Microbiology.

[2]  Lin Zhang,et al.  Stenotrophomonas nematodicola sp. nov., isolated from Caenorhabditis elegans , 2021, Archives of Microbiology.

[3]  J. Xia,et al.  MetaboAnalyst 5.0: narrowing the gap between raw spectra and functional insights , 2021, Nucleic Acids Res..

[4]  B. Khatabi,et al.  Diversity and abundance of culturable nitrogen‐fixing bacteria in the phyllosphere of maize , 2020, Journal of applied microbiology.

[5]  M. Shapira,et al.  CeMbio - The Caenorhabditis elegans Microbiome Resource , 2020, G3.

[6]  R. Tauler,et al.  MCR-ALS analysis of 1H NMR spectra by segments to study the zebrafish exposure to acrylamide , 2020, Analytical and Bioanalytical Chemistry.

[7]  P. Sengupta,et al.  A neurotransmitter produced by gut bacteria modulates host sensory behaviour , 2020, Nature.

[8]  J. Ugalde,et al.  Bacterially produced metabolites protect C. elegans neurons from degeneration , 2020, PLoS biology.

[9]  M. Mattson,et al.  NAD+ in Brain Aging and Neurodegenerative Disorders. , 2019, Cell metabolism.

[10]  Diana H. Wall,et al.  Soil nematode abundance and functional group composition at a global scale , 2019, Nature.

[11]  Jan P. Meier-Kolthoff,et al.  TYGS is an automated high-throughput platform for state-of-the-art genome-based taxonomy , 2019, Nature Communications.

[12]  A. Spang,et al.  Symbiosis in the microbial world: from ecology to genome evolution , 2018, Biology Open.

[13]  Bernardo Pollak,et al.  Transgenerational Diapause as an Avoidance Strategy against Bacterial Pathogens in Caenorhabditis elegans , 2017, mBio.

[14]  Min Han,et al.  A vitamin-B2-sensing mechanism that regulates gut protease activity to impact animal’s food behavior and growth , 2017, eLife.

[15]  S. P. Tiwari NEMATODES AND SOIL HEALTH INDICATORS , 2017 .

[16]  J. Chun,et al.  A large-scale evaluation of algorithms to calculate average nucleotide identity , 2017, Antonie van Leeuwenhoek.

[17]  Erel Levine,et al.  Serotonin-dependent kinetics of feeding bursts underlie a graded response to food availability in C. elegans , 2017, Nature Communications.

[18]  Jie Kang,et al.  Microbial production of vitamin B12: a review and future perspectives , 2017, Microbial Cell Factories.

[19]  M. Mattson,et al.  NAD+ Replenishment Improves Lifespan and Healthspan in Ataxia Telangiectasia Models via Mitophagy and DNA Repair. , 2016, Cell metabolism.

[20]  Gary Ruvkun,et al.  Caenorhabditis elegans responses to bacteria from its natural habitats , 2016, Proceedings of the National Academy of Sciences.

[21]  P. Rosenstiel,et al.  The native microbiome of the nematode Caenorhabditis elegans: gateway to a new host-microbiome model , 2016, BMC Biology.

[22]  M. Shapira,et al.  Assembly of the Caenorhabditis elegans gut microbiota from diverse soil microbial environments , 2016, The ISME Journal.

[23]  M. Spraul,et al.  Precision high-throughput proton NMR spectroscopy of human urine, serum, and plasma for large-scale metabolic phenotyping. , 2014, Analytical chemistry.

[24]  Adam P. Rosebrock,et al.  Interspecies Systems Biology Uncovers Metabolites Affecting C. elegans Gene Expression and Life History Traits , 2014, Cell.

[25]  Adam P. Rosebrock,et al.  Interspecies Systems Biology Uncovers Metabolites Affecting C. elegans Gene Expression and Life History Traits , 2014, Cell.

[26]  A. Douglas Symbiosis as a general principle in eukaryotic evolution. , 2014, Cold Spring Harbor perspectives in biology.

[27]  Lihua Julie Zhu,et al.  Integration of Metabolic and Gene Regulatory Networks Modulates the C. elegans Dietary Response , 2013, Cell.

[28]  N. Metcalfe,et al.  Experimental demonstration of the growth rate–lifespan trade-off , 2013, Proceedings of the Royal Society B: Biological Sciences.

[29]  Bo-mi Song,et al.  Recognition of familiar food activates feeding via an endocrine serotonin signal in Caenorhabditis elegans , 2013, eLife.

[30]  L. Avery,et al.  The pharynx of the nematode C. elegans , 2013, Worm.

[31]  D. Raizen,et al.  Methods for measuring pharyngeal behaviors. , 2012, WormBook : the online review of C. elegans biology.

[32]  F. Court,et al.  Diapause Formation and Downregulation of Insulin-Like Signaling via DAF-16/FOXO Delays Axonal Degeneration and Neuronal Loss , 2012, PLoS genetics.

[33]  Jennifer K Pirri,et al.  The C. elegans Touch Response Facilitates Escape from Predacious Fungi , 2011, Current Biology.

[34]  F. Celico,et al.  Potential role of Bacillus endospores in soil amended by olive mill wastewater. , 2010, Water science and technology : a journal of the International Association on Water Pollution Research.

[35]  Aravinthan D. T. Samuel,et al.  Two size-selective mechanisms specifically trap bacteria-sized food particles in Caenorhabditis elegans , 2009, Proceedings of the National Academy of Sciences.

[36]  T. Ebbels,et al.  Recursive segment-wise peak alignment of biological (1)h NMR spectra for improved metabolic biomarker recovery. , 2009, Analytical chemistry.

[37]  Miron Livny,et al.  BioMagResBank , 2007, Nucleic Acids Res..

[38]  S. Glautier,et al.  The concentration-dependent effects of ethanol on Caenorhabditis elegans behaviour , 2007, The Pharmacogenomics Journal.

[39]  T. Ebbels,et al.  Metabolic profiling, metabolomic and metabonomic procedures for NMR spectroscopy of urine, plasma, serum and tissue extracts , 2007, Nature Protocols.

[40]  H. Senn,et al.  Probabilistic quotient normalization as robust method to account for dilution of complex biological mixtures. Application in 1H NMR metabonomics. , 2006, Analytical chemistry.

[41]  Leon Avery,et al.  Dietary choice behavior in Caenorhabditis elegans , 2006, Journal of Experimental Biology.

[42]  M. Chalfie,et al.  The MEC-4 DEG/ENaC channel of Caenorhabditis elegans touch receptor neurons transduces mechanical signals , 2005, Nature Neuroscience.

[43]  L. Avery,et al.  Food transport in the C. elegans pharynx , 2003, Journal of Experimental Biology.

[44]  W. Nicholson,et al.  Spore UV and acceleration resistance of endolithic Bacillus pumilus and Bacillus subtilis isolates obtained from Sonoran desert basalt: implications for lithopanspermia. , 2003, Astrobiology.

[45]  M. Labouesse [Caenorhabditis elegans]. , 2003, Medecine sciences : M/S.

[46]  S. Wold,et al.  Orthogonal projections to latent structures (O‐PLS) , 2002 .

[47]  Nektarios Tavernarakis,et al.  Molecular modeling of mechanotransduction in the nematode Caenorhabditis elegans. , 1997, Annual review of physiology.

[48]  P. Morgan,et al.  Mutations affecting sensitivity to ethanol in the nematode, Caenorhabditis elegans. , 1995, Alcoholism, clinical and experimental research.

[49]  Jh Thomas,et al.  Regulation of a periodic motor program in C. elegans , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[50]  N. Munakata [Genetics of Caenorhabditis elegans]. , 1989, Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme.

[51]  J. Sulston,et al.  Developmental genetics of the mechanosensory neurons of Caenorhabditis elegans. , 1981, Developmental biology.

[52]  S. Stearns Life-History Tactics: A Review of the Ideas , 1976, The Quarterly Review of Biology.