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C. elegans Behavior of Preference Choice on Bacterial Food

  • Abada, Emad Abd-elmoniem (Brain Korea 21 Life Science for Global Warming Team, Department of Life Science, Hanyang University) ;
  • Sung, Hyun (Brain Korea 21 Life Science for Global Warming Team, Department of Life Science, Hanyang University) ;
  • Dwivedi, Meenakshi (Brain Korea 21 Life Science for Global Warming Team, Department of Life Science, Hanyang University) ;
  • Park, Byung-Jae (Department of Life Science, Bio-NURI, Hallym University) ;
  • Lee, Sun-Kyung (Brain Korea 21 Life Science for Global Warming Team, Department of Life Science, Hanyang University) ;
  • Ahnn, Joohong (Brain Korea 21 Life Science for Global Warming Team, Department of Life Science, Hanyang University)
  • 투고 : 2009.06.22
  • 심사 : 2009.07.20
  • 발행 : 2009.09.30

초록

Caenorhabditis elegans is a free living soil nematode and thus in its natural habitat, C. elegans encounters many different species of soil bacteria. Although some soil bacteria may be excellent sources of nutrition for the worm, others may be pathogenic. Thus, we undertook a study to understand how C. elegans can identify their preferred food using a simple behavioral assay. We found that there are various species of soil bacteria that C. elegans prefers in comparison to the standard laboratory E. coli strain OP50. In particular, two bacterial strains, Bacillus mycoides and Bacillus soli, were preferred strains. Interestingly, the sole feeding of these bacteria to wild type animals results in extended lifespan through the activation of the autophagic process. Further studies will be required to understand the precise mechanism controlling the behavior of identification and selection of food in C. elegans.

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과제정보

연구 과제 주관 기관 : Hanyang University

참고문헌

  1. Anderson, G.H., and Li, E.T.S. (1987). Protein and amino acids in the regulation of quantitative and qualitative aspects of food intake. Int. J. Obes. 11, 97-108
  2. Anderson, H.L., Benevenga, N.J., and Harper, A.E. (1968). Associations among food and protein intake, serine dehydratase, and plasma amino acids. Am. J. Physiol. 214, 1008-1013
  3. Avery, L., and Horvitz, B. (1989). Pharyngeal pumping continues after laser killing of the pharyngeal nervous system of C elegans. Neuron 3, 473-485 https://doi.org/10.1016/0896-6273(89)90206-7
  4. Avery, L., and Thomas, J.H. (1997). Feeding and defecation. In C. elegans II, D.L. Riddle, T. Blumenthal, B.J. Meyer, J.R. Priess, eds. (Cold Spring Harbor: Cold Spring Harbor Laboratory Press), pp. 679-716
  5. Dwivedi, M., and Ahnn, J. (2009). Autophagy-Is it a preferred route for lifespan extension? BMB Rep. 42, 65-71 https://doi.org/10.5483/BMBRep.2009.42.2.065
  6. Harper, A.E. (1967). Effects of dietary protein content and amino acid pattern on food intake and preference. In Handbook of physiology, Section 6, The Alimentary Canal, Vol. 1, (Washington: American Physiological Society), pp. 399-410
  7. Kenyon, C., Chang, J., Gensch, E., Rudner, A., and Tabtiang, R. (1993). A C. elegans mutant that lives twice as long as wild type. Nature 366, 461-464 https://doi.org/10.1038/366461a0
  8. Leung, P.M.B., Gamble, M.A., and Rogers, Q.R. (1981). Effect of prior protein ingestions on dietary choice of protein and energy in the rat. Nutr. Rep. Int. 24, 257-266
  9. Melendez, A., Talloczy, Z., Seaman, M., Eskelinen, E.L., Hall, D.H., and Levine, B. (2003). Autophagy genes are essential for dauer development and life-span extension in C.elegans Science 301, 1387-1391 https://doi.org/10.1126/science.1087782
  10. Sanahuja, J.C., and Harper, A.E. (1962). Effect of amino acid imbalance on food intake and preference. Am. J. Physiol. 202, 165-170

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  1. Fatal attraction: Bacterial bait lures worms to their death vol.107, pp.38, 2010, https://doi.org/10.1073/pnas.1011935107
  2. Reproductive Fitness and Dietary Choice Behavior of the Genetic Model Organism Caenorhabditis elegans under Semi-Natural Conditions vol.30, pp.4, 2010, https://doi.org/10.1007/s10059-010-0125-9
  3. ANK repeat-domain of SHN-1 Is indispensable for in vivo SHN-1 function in C. elegans vol.31, pp.1, 2009, https://doi.org/10.1007/s10059-011-0007-9
  4. Changes in Caenorhabditis elegans Exposed to Vibrio parahaemolyticus vol.21, pp.10, 2011, https://doi.org/10.4014/jmb.1102.02006
  5. GPA‐9 is a novel regulator of innate immunity against Escherichia coli foods in adult Caenorhabditis elegans vol.10, pp.2, 2009, https://doi.org/10.1111/j.1474-9726.2010.00655.x
  6. Secondary Metabolites of Pseudomonas fluorescens CHA0 Drive Complex Non-Trophic Interactions with Bacterivorous Nematodes vol.61, pp.4, 2011, https://doi.org/10.1007/s00248-011-9821-z
  7. Increased responsiveness in feeding behaviour of Caenorhabditis elegans after experimental coevolution with its microparasite Bacillus thuringiensis vol.8, pp.2, 2009, https://doi.org/10.1098/rsbl.2011.0684
  8. Host-Microbe Interactions in Caenorhabditis elegans vol.2013, pp.None, 2013, https://doi.org/10.1155/2013/356451
  9. Gene-environment and protein-degradation signatures characterize genomic and phenotypic diversity in wild Caenorhabditis elegans populations vol.11, pp.None, 2009, https://doi.org/10.1186/1741-7007-11-93
  10. Identification, Nomenclature, and Evolutionary Relationships of Mitogen-Activated Protein Kinase (MAPK) Genes in Soybean vol.9, pp.None, 2013, https://doi.org/10.4137/ebo.s12526
  11. Evolutionary history of mitogen-activated protein kinase (MAPK) genes inLotus,Medicago, andPhaseolus vol.8, pp.11, 2009, https://doi.org/10.4161/psb.27189
  12. Attraction and preference of bacteriophagous and plant-parasitic nematodes towards different types of soil bacteria vol.48, pp.25, 2009, https://doi.org/10.1080/00222933.2013.873088
  13. Feeding behaviour of Caenorhabditis elegans is an indicator of Pseudomonas aeruginosa PAO1 virulence vol.2, pp.None, 2009, https://doi.org/10.7717/peerj.521
  14. Gut microbiota–generated metabolites in animal health and disease vol.10, pp.6, 2009, https://doi.org/10.1038/nchembio.1535
  15. The metabolite α-ketoglutarate extends lifespan by inhibiting ATP synthase and TOR vol.510, pp.7505, 2009, https://doi.org/10.1038/nature13264
  16. The functionality of the gastrointestinal microbiome in non-human animals vol.3, pp.1, 2015, https://doi.org/10.1186/s40168-015-0113-6
  17. Elucidating the Mechanism of Weissella -dependent Lifespan Extension in Caenorhabditis elegans vol.5, pp.None, 2009, https://doi.org/10.1038/srep17128
  18. Bacterial Respiration and Growth Rates Affect the Feeding Preferences, Brood Size and Lifespan of Caenorhabditis elegans vol.10, pp.7, 2009, https://doi.org/10.1371/journal.pone.0134401
  19. Disentangling nematode-bacteria interactions using a modular soil model system and biochemical markers vol.18, pp.4, 2009, https://doi.org/10.1163/15685411-00002965
  20. Controlling the Microbiome: Microhabitat Adjustments for Successful Biocontrol Strategies in Soil and Human Gut vol.7, pp.None, 2016, https://doi.org/10.3389/fmicb.2016.01079
  21. FLP-4 neuropeptide and its receptor in a neuronal circuit regulate preference choice through functions of ASH-2 trithorax complex in Caenorhabditis elegans vol.6, pp.None, 2009, https://doi.org/10.1038/srep21485
  22. Dairy Propionibacterium extends the mean lifespan of Caenorhabditis elegans via activation of the innate immune system vol.6, pp.None, 2009, https://doi.org/10.1038/srep31713
  23. NAD + Is a Food Component That Promotes Exit from Dauer Diapause in Caenorhabditis elegans vol.11, pp.12, 2009, https://doi.org/10.1371/journal.pone.0167208
  24. Micro-Food Web Structure Shapes Rhizosphere Microbial Communities and Growth in Oak vol.10, pp.1, 2009, https://doi.org/10.3390/d10010015
  25. Interactions among competing nematode species affect population growth rates vol.187, pp.1, 2018, https://doi.org/10.1007/s00442-018-4109-3
  26. Pseudomonas donghuensis HYS virulence towards Caenorhabditis elegans is regulated by the Cbr/Crc system vol.9, pp.None, 2009, https://doi.org/10.1038/s41598-019-45145-8
  27. Ascaroside Signaling in the Bacterivorous Nematode Caenorhabditis remanei Encodes the Growth Phase of Its Bacterial Food Source vol.21, pp.15, 2009, https://doi.org/10.1021/acs.orglett.9b01914
  28. Multivariate Analysis of Increase in Life Span of Caenorhabditis elegans Through Intestinal Colonization by Indigenous Probiotic Strains vol.11, pp.3, 2019, https://doi.org/10.1007/s12602-018-9420-0
  29. Physiological and Metabolite Alterations Associated with Neuronal Signals of Caenorhabditis elegans during Cronobacter sakazakii Infections vol.12, pp.22, 2009, https://doi.org/10.1021/acschemneuro.1c00559