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Composition and Stability of the Microbial Community inside the Digestive Tract of the Aquatic Crustacean Daphnia magna

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Abstract

Small filter-feeding zooplankton organisms like the cladoceran Daphnia spp. are key members of freshwater food webs. Although several interactions between Daphnia and bacteria have been investigated, the importance of the microbial communities inside Daphnia guts has been studied only poorly so far. In the present study, we characterised the bacterial community composition inside the digestive tract of a laboratory-reared clonal culture of Daphnia magna using 16S rRNA gene libraries and terminal-restriction length polymorphism fingerprint analyses. In addition, the diversity and stability of the intestinal microbial community were investigated over time, with different food sources as well as under starvation stress and death, and were compared to the community in the cultivation water. The diversity of the Daphnia gut microbiota was low. The bacterial community consisted mainly of Betaproteobacteria (e.g. Limnohabitans sp.), few Gammaproteobacteria (e.g. Pseudomonas sp.) and Bacteroidetes that were related to facultatively anaerobic bacteria, but did not contain typical fermentative or obligately anaerobic gut bacteria. Rather, the microbiota was constantly dominated by Limnohabitans sp. which belongs to the Lhab-A1 tribe (previously called R-BT065 cluster) that is abundant in various freshwaters. Other bacterial groups varied distinctly even under constant cultivation conditions. Overall, the intestinal microbial community did not reflect the community in the surrounding cultivation water and clustered separately when analysed via the Additive Main Effects and Multiplicative Interaction model. In addition, the microbiota proved to be stable also when Daphnia were exposed to bacteria associated with a different food alga. After starvation, the community in the digestive tract was reduced to stable members. After death of the host animals, the community composition in the gut changed distinctly, and formerly undetected bacteria were activated. Our results suggest that the Daphnia microbiota consists mainly of an aerobic resident bacterial community which is indigenous to this habitat.

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References

  1. Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ (1990) Basic local alignment search tool. J Mol Biol 215:403–410

    Article  CAS  PubMed  Google Scholar 

  2. Azam F, Fenchel T, Field JG, Gray JS, Meyer-Reil LA, Thingstad F (1983) The ecological role of water-column microbes in the sea. Mar Ecol Prog Ser 10:257–263

    Article  Google Scholar 

  3. Ben Ami E, Yuval B, Jurkevitch E (2010) Manipulation of the microbiota of mass-reared Mediterranean fruit flies Ceratitis capitata (Diptera: Tephritidae) improves sterile male sexual performance. ISME J 4:28–37

    Article  PubMed  Google Scholar 

  4. Brune A (1998) Termite guts: the world’s smallest bioreactors. Trends Biotechnol 16:16–21

    Article  CAS  Google Scholar 

  5. Buck U, Grossart HP, Amann R, Pernthaler J (2009) Substrate incorporation patterns of bacterioplankton populations in stratified and mixed waters of a humic lake. Environ Microbiol 11:1854–1865

    Article  CAS  PubMed  Google Scholar 

  6. Chou JH, Sheu SY, Lin KY, Chen WM, Arun AB, Young CC (2007) Comamonas odontotermitis sp. nov., isolated from the gut of the termite Odontotermes formosanus. Int J Syst Evol Microbiol 57:887–891

    Article  CAS  PubMed  Google Scholar 

  7. Culman S, Bukowski R, Gauch H, Cadillo-Quiroz H, Buckley D (2009) T-REX: software for the processing and analysis of T-RFLP data. BMC Bioinformatics 10:171

    Article  PubMed  PubMed Central  Google Scholar 

  8. de Cambiaire JC, Otis C, Lemieux C, Turmel M (2006) The complete chloroplast genome sequence of the chlorophycean green alga Scenedesmus obliquus reveals a compact gene organization and a biased distribution of genes on the two DNA strands. BMC Evol Biol 6:37

    Article  PubMed  PubMed Central  Google Scholar 

  9. Degans H, Zollner E, Van der Gucht K, De Meester L, Jürgens K (2002) Rapid Daphnia-mediated changes in microbial community structure: an experimental study. FEMS Microbiol Ecol 42:137–149

    Article  CAS  PubMed  Google Scholar 

  10. Dillon RJ, Dillon VM (2004) The gut bacteria of insects: nonpathogenic interactions. Annu Rev Entomol 49:71–92

    Article  CAS  PubMed  Google Scholar 

  11. Drake HL, Horn MA (2007) As the worm turns: the earthworm gut as a transient habitat for soil microbial biomes. Annu Rev Microbiol 61:169–189

    Article  CAS  PubMed  Google Scholar 

  12. Ducklow HW, Purdie DA, Williams PJL, Davies JM (1986) Bacterioplankton: a sink for carbon in a coastal marine plankton community. Science 232:865–867

    Article  CAS  PubMed  Google Scholar 

  13. Dunbar J, Ticknor LO, Kuske CR (2001) Phylogenetic specificity and reproducibility and new method for analysis of terminal restriction fragment profiles of 16S rRNA genes from bacterial communities. Appl Environ Microbiol 67:190–197

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  14. Egert M, Wagner B, Lemke T, Brune A, Friedrich MW (2003) Microbial community structure in midgut and hindgut of the humus-feeding larva of Pachnoda ephippiata (Coleoptera: Scarabaeidae). Appl Environ Microbiol 69:6659–6668

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Felsenstein J (1985) Confidence limits on phylogenies—an approach using the bootstrap. Evolution 39:783–791

    Article  Google Scholar 

  16. Green J (1974) Parasites and epibionts of Cladocera. Trans Zool Soc Lond 32:417–515

    Article  Google Scholar 

  17. Grossart HP, Dziallas C, Tang KW (2009) Bacterial diversity associated with freshwater zooplankton. Environ Microbiol Rep 1:50–55

    Article  CAS  PubMed  Google Scholar 

  18. Guarner F, Malagelada JR (2003) Gut flora in health and disease. Lancet 361:512–519

    Article  PubMed  Google Scholar 

  19. Haglund AL, Törnblom E, Boström B, Tranvik L (2002) Large differences in the fraction of active bacteria in plankton, sediments, and biofilm. Microb Ecol 43:232–241

    Article  CAS  PubMed  Google Scholar 

  20. Hall TA (1999) Bioedit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symp Ser 41:95–98

    CAS  Google Scholar 

  21. Harris JM (1993) The presence, nature, and role of gut microflora in aquatic invertebrates—a synthesis. Microb Ecol 25:195–231

    Article  CAS  PubMed  Google Scholar 

  22. Haynes S, Darby AC, Daniell TJ, Webster G, van Veen FJF, Godfray HCJ, Prosser JI, Douglas AE (2003) Diversity of bacteria associated with natural aphid populations. Appl Environ Microbiol 69:7216–7223

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  23. Hentschel U, Usher KM, Taylor MW (2006) Marine sponges as microbial fermenters. FEMS Microbiol Ecol 55:167–177

    Article  CAS  PubMed  Google Scholar 

  24. Hongoh Y, Ohkuma M, Kudo T (2003) Molecular analysis of bacterial microbiota in the gut of the termite Reticulitermes speratus (Isoptera; Rhinotermitidae). FEMS Microbiol Ecol 44:231–242

    Article  CAS  PubMed  Google Scholar 

  25. Hornák K, Jezbera J, Nedoma J, Gasol JM, Šimek K (2006) Effects of resource availability and bacterivory on leucine incorporation in different groups of freshwater bacterioplankton, assessed using microautoradiography. Aquat Microb Ecol 45:277–289

    Article  Google Scholar 

  26. Huber I, Spanggaard B, Appel KF, Rossen L, Nielsen T, Gram L (2004) Phylogenetic analysis and in situ identification of the intestinal microbial community of rainbow trout (Oncorhynchus mykiss, Walbaum). J App Microbiol 96:117–132

    Article  CAS  Google Scholar 

  27. Jiang Y, Xie CX, Yang GG, Gong XL, Chen XJ, Xu LX, Bao BL (2011) Cellulase-producing bacteria of Aeromonas are dominant and indigenous in the gut of Ctenopharyngodon idellus (Valenciennes). Aquacult Res 42:499–505

    Article  CAS  Google Scholar 

  28. Jürgens K (1994) Impact of Daphnia on planktonic microbial food webs—a review. Mar Microbial Food Webs 8:295–324

    Google Scholar 

  29. Jüttner F, Leonhardt J, Mohren S (1983) Environmental-factors affecting the formation of mesityloxide, dimethylallylic alcohol and other volatile compounds excreted by Anabaena cylindrica. J Gen Microbiol 129:407–412

    Google Scholar 

  30. Kasalicky V, Jezbera J, Šimek K, Hahn MW (2010) Limnohabitans planktonicus sp. nov., and Limnohabitans parvus sp. nov., two novel planktonic Betaproteobacteria isolated from a freshwater reservoir and emended description of the genus Limnohabitans. Int J Syst Evol Microbiol 60:2710–2714

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. Kassen R, Rainey PB (2004) The ecology and genetics of microbial diversity. Annu Rev Microbiol 58:207–231

    Article  CAS  PubMed  Google Scholar 

  32. Kirchman DL, Dittel AI, Findlay SEG, Fischer D (2004) Changes in bacterial activity and community structure in response to dissolved organic matter in the Hudson River, New York. Aquat Microb Ecol 35:243–257

    Article  Google Scholar 

  33. Kostanjšek R, Štrus J, Avguštin G (2002) Genetic diversity of bacteria associated with the hindgut of the terrestrial crustacean Porcellio scaber (Crustacea: Isopoda). FEMS Microbiol Ecol 40:171–179

    Article  PubMed  Google Scholar 

  34. Kovacs A, Ben Jacob N, Tayem H, Halperin E, Iraqi F, Gophna U (2011) Genotype is a stronger determinant than sex of the mouse gut microbiota. Microb Ecol 61:423–428

    Article  PubMed  Google Scholar 

  35. Lampert W (1991) The dynamics of Daphnia in a shallow lake. Verh Int Ver Limnol 24:795–798

    Google Scholar 

  36. Lane DJ (1991) 16S/23S rRNA sequencing. In: Stackebrandt E, Goodfellow M (eds) Nucleic acid techniques in bacterial systematics. Wiley, Chichester, pp 115–175

    Google Scholar 

  37. Langenheder S, Jürgens K (2001) Regulation of bacterial biomass and community structure by metazoan and protozoan predation. Limnol Oceanogr 46:121–134

    Article  Google Scholar 

  38. Lee HG, Kim SG, Im WT, Oh HM, Lee ST (2009) Pedobacter composti sp. nov., isolated from compost. Int J Syst Evol Microbiol 59:345–349

    Article  CAS  PubMed  Google Scholar 

  39. Lehman R, Lundgren J, Petzke L (2009) Bacterial communities associated with the digestive tract of the predatory ground beetle, Poecilus chalcites, and their modification by laboratory rearing and antibiotic treatment. Microb Ecol 57:349–358

    Article  PubMed  Google Scholar 

  40. Li K, Guan W, Wei G, Liu B, Xu J, Zhao L, Zhang Y (2007) Phylogenetic analysis of intestinal bacteria in the Chinese mitten crab (Eriocheir sinensis). J Appl Microbiol 103:675–682

    Article  CAS  PubMed  Google Scholar 

  41. Liu WT, Marsh TL, Cheng H, Forney LJ (1997) Characterization of microbial diversity by determining terminal restriction fragment length polymorphisms of genes encoding 16S rRNA. Appl Environ Microbiol 63:4516–4522

    CAS  PubMed  PubMed Central  Google Scholar 

  42. Martin-Creuzburg D, Beck B, Freese HM (2011) Food quality of heterotrophic bacteria for Daphnia magna: evidence for a limitation by sterols. FEMS Microbiol Ecol. doi:10.1111/j.1574-6941.2011.01076.x:

  43. Moré MI, Herrick JB, Silva MC, Ghiorse WC, Madsen EL (1994) Quantitative cell lysis of indigenous microorganisms and rapid extraction of microbial DNA from sediment. Appl Environ Microbiol 60:1572–1580

    PubMed  PubMed Central  Google Scholar 

  44. Murtaugh PA (1985) The influence of food concentration and feeding rate in the gut residence time of Daphnia. J Plankton Res 7:415–420

    Article  Google Scholar 

  45. Newton RJ, Jones SE, Eiler A, McMahon KD, Bertilsson S (2011) A guide to the natural history of freshwater lake bacteria. Microbiol Mol Biol Rev 75:14–49

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  46. Pérez MT, Sommaruga R (2006) Differential effect of algal- and soil-derived dissolved organic matter on alpine lake bacterial community composition and activity. Limnol Oceanogr 51:2527–2537

    Article  Google Scholar 

  47. Pester M, Brune A (2007) Hydrogen is the central free intermediate during lignocellulose degradation by termite gut symbionts. ISME J 1:551–565

    Article  CAS  PubMed  Google Scholar 

  48. Peter H, Sommaruga R (2008) An evaluation of methods to study the gut bacterial community composition of freshwater zooplankton. J Plankton Res 30:997–1006

    Article  Google Scholar 

  49. Peters RH, de Bernardi R (1987) Daphnia. Mem Ist Ital Idrobiol 45:1–502

    Google Scholar 

  50. Peterson BJ, Hobbie JE, Haney JF (1978) Daphnia grazing on natural bacteria. Limnol Oceanogr 23:1039–1044

    Article  Google Scholar 

  51. Proulx D, Lésel R, de la Noüe J (1984) Growth of Daphnia magna in axenic, monoxenic and holoxenic conditions. Rev Franc Sci l’Eau 3:83–91

    Google Scholar 

  52. Qi W, Nong G, Preston J, Ben Ami F, Ebert D (2009) Comparative metagenomics of Daphnia symbionts. BMC Genomics 10:172

    Article  PubMed  PubMed Central  Google Scholar 

  53. Salcher MM, Pernthaler J, Zeder M, Psenner R, Posch T (2008) Spatio-temporal niche separation of planktonic Betaproteobacteria in an oligo-mesotrophic lake. Environ Microbiol 10:2074–2086

    Article  CAS  PubMed  Google Scholar 

  54. Šimek K, Hornák K, Jezbera J, Mašín M, Nedoma J, Gasol JM, Schauer M (2005) Influence of top-down and bottom-up manipulations on the R-BT065 subcluster of beta-proteobacteria, an abundant group in bacterioplankton of a freshwater reservoir. Appl Environ Microbiol 71:2381–2390

    Article  PubMed  PubMed Central  Google Scholar 

  55. Šimek K, Kasalický V, Jezbera J, Jezberová J, Hejzlar J, Hahn MW (2010) Broad habitat range of the phylogenetically narrow R-BT065 cluster, representing a core group of the betaproteobacterial genus Limnohabitans. Appl Environ Microbiol 76:631–639

    Article  PubMed  Google Scholar 

  56. Simon M, Grossart HP, Schweitzer B, Ploug H (2002) Microbial ecology of organic aggregates in aquatic ecosystems. Aquat Microb Ecol 28:175–211

    Article  Google Scholar 

  57. Stief P, Poulsen M, Nielsen LP, Brix H, Schramm A (2009) Nitrous oxide emission by aquatic macrofauna. Proc Natl Acad Sci USA 106:4296–4300

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  58. Tamura K, Dudley J, Nei M, Kumar S (2007) MEGA4: molecular evolutionary genetics analysis (MEGA) software version 4.0. Mol Biol Evol 24:1596–1599

    Article  CAS  PubMed  Google Scholar 

  59. Tamura K, Nei M, Kumar S (2004) Prospects for inferring very large phylogenies by using the neighbor-joining method. Proc Natl Acad Sci USA 101:11030–11035

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  60. Tang KW, Bickel SL, Dziallas C, Grossart HP (2009) Microbial activities accompanying decomposition of cladoceran and copepod carcasses under different environmental conditions. Aquat Microb Ecol 57:89–100

    Article  Google Scholar 

  61. Tang KW, Turk V, Grossart HP (2010) Linkage between crustacean zooplankton and aquatic bacteria. Aquat Microb Ecol 61:261–277

    Article  Google Scholar 

  62. Yarza P, Richter M, Peplies J, Euzeby J, Amann R, Schleifer KH, Ludwig W, Glöckner FO, Rosselló-Móra R (2008) The All-Species Living Tree project: a 16S rRNA-based phylogenetic tree of all sequenced type strains. Syst Appl Microbiol 31:241–250

    Article  CAS  PubMed  Google Scholar 

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Acknowledgements

We thank S. Wiechmann for technical assistance, A. Held for experimental assistance and E. Hespeler (chair Prof. Meyer) for help with the Genetic Analyzer for T-RFLP analysis. We are grateful to Dr D. Martin-Creuzburg and T. Basen (Limnology department) for sharing their expertise in the cultivation of Daphnia magna and Scenedesmus obliquus. We also want to thank Dr D. Ebert, Basel, who kindly provided the bacterial 16S rRNA gene shotgun sequences from intact Daphnia. This study was supported by research grants of the University of Konstanz.

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Correspondence to Heike M. Freese.

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Supplementary Table 1

Relative fluorescence values of T-RFs from Msp1 digested bacterial 16S rRNA genes amplified from DNA extracts of Daphnia magna microbiota incubated with Scenedesmus obliquus in different experiments (E1–3; E3_30: double amount of dissected guts), with xenic Cryptomonas sp., and incubated without food in comparison to respective cultivation water and the algal culture used for feeding. T-RFs identified via clones were named after these clones; if T-RFs were identified via bacterial isolates from the gut, the name was placed in brackets. (DOC 26 kb)

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Freese, H.M., Schink, B. Composition and Stability of the Microbial Community inside the Digestive Tract of the Aquatic Crustacean Daphnia magna . Microb Ecol 62, 882–894 (2011). https://doi.org/10.1007/s00248-011-9886-8

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