Saturday 15 October 2016

First come, first provide: On microbial biofilms and metazoan colonisation at deep-sea hydrothermal vents



At deep-sea hydrothermal vents, temperature and chemical gradients lead to the formation of complex ecosystems. Previous studies have shown that newly-formed diffuse-flow hydrothermal vents are first colonised by chemoautotrophic microbes, which form biofilms. Subsequently metazoan larvae settle in the habitat. The larvae respond to the composition, texture and the chemicals produced by the biofilm. The biofilm might even induce the metamorphosis to the sessile adult stage. Thus, chemoautotrophic biofilms may indicate habitat suitability for metazoans as well as provide them fixed carbon. 

In their paper, O’Brien et al. (2015) combined the study of early microbial colonists, fluid chemistry and metazoan colonisation. A volcanic seafloor eruption in the East Pacific Rise in late 2005/early 2006 destroyed the pre-existing habitats and created more than 20 diffuse-flow vents. The studied area was divided into active eruption sites (in-flow) and no apparent eruption sites (no-flow). Temporal Autonomous Multi-Disciplinary Substrates (TAMS) were installed at each site, to serve as experimental colonisation substrates. The samples were collected in two cruises, in 2006 and 2007. Clonal libraries of the chemoautotrophs were assembled using extracted DNA and processing with PCR and DGGE. Voltametry and Microscopy were used to study in-situ fluid chemistry and metazoan colonists respectively

At in-flow sites the measured sulfide concentrations and temperatures were higher than at the no-flow sites. The average oxygen levels were higher at no-flow sites. In general, temperature was correlated with sulfide concentration and both were inversely correlated with oxygen levels.
The TAMS at in-flow sites were dominated by ε-Proteobacteria (on average 90,6%), while the biofilms on no-flow TAMS showed mostly γ-Proteobacteria (on average 84,7%). Unidentified bacterial sequences, α- and δ-Proteobacteria were also detected but only at low levels. The dominance of ε-Proteobacteria could be explained by their adaption to sulfidic habitats, allowing them to be omnipresent in marine geothermal environments. As they use reduced chemical compounds as energy resources, they are dependent on active hydrothermal vents. O’Brien et al. conclude that the chemical and thermal characteristics of the vent seem to control the composition of the biofilm communities. However, they also acknowledge that the experimental assembly has its limitations. 

The analysis of the megafauna at the TAMS showed that siboglinid tubeworms occurred only at in-flow sites. Most of the observed tubeworms were of the species Tevnia jerichonana. The authors assume that the early colonisation of T. jerichonana indicates an adaption to microaerobic conditions and a higher resistance to sulfide than other siboglinidae.

In conclusion the authors state that while they present a first study of the correlation between fluid chemistry, microbial diversity and metazoan colonisation, our knowledge about the role of biofilms in larval settlement is still limited. 

Since its publication in November 2015 the paper doesn’t seem to have gained much online impact and the results themselves don’t appear particularly surprising. However, the authors provide a template of methodology for the study of biofilms at hydrothermal vents. Thus, it would be interesting to see if future papers reported similar findings in other areas of the world. 

Reviewed Paper:

O’Brien, C. E., Giovannelli, D., Govenar, B., Luther, G. W., Lutz, R. A., Shank, T. M., & Vetriani, C. (2015). Microbial biofilms associated with fluid chemistry and megafaunal colonization at post-eruptive deep-sea hydrothermal vents. Deep Sea Research Part II: Topical Studies in Oceanography, 121, 31-40. Link: http://www.sciencedirect.com/science/article/pii/S0967064515002805

4 comments:

  1. Hi Johanna,

    Thanks for your review. Which abiotic factor do you think is responsible for gammaproteobacteria being dominant in the biofilms on no-flow TAMS? You've given a reason for the dominance of E-proteobacteria for TMAS at in-flow sites, so I wonder what the reason for the dominance of gammaproteobacteria would be.

    Thanks,
    Amy

    ReplyDelete
  2. Hi Amy,
    The reason for the dominance of γ-proteobacteria was not elaborated upon in this paper, but I was able to find another article by Yamamoto & Takai (2011). They state that ε- and γ-proteobacteria rely on two different sulfur metabolic pathways. Ε-proteobacteria use sulfur compounds as electron-donors and -aceptors, whereas γ-proteobacteria use two different sulfur oxidization pathways that generally require O2 as a terminal electron acceptor. As oxygen-levels seem to be negatively correlated with sulfur concentration, the lack of electron-acceptors at in-flow TAMS would be limiting for γ-proteobacteria.
    My guess would be that, as Ε-proteobacteria need active vents for their metabolism they wouldn’t compete with γ-proteobacteria for the sulfur compounds at no-flow TAMS. Moreover, no-flow TAMS could perhaps provide the ideal ration of sulfur to oxygen for the γ-proteobacteria. So, I think that the level of oxygen is the most influential abiotic factor here.

    Hope this answers your question.
    Thanks,
    Johanna

    Yamamoto, M., & Takai, K. (2011). Sulfur Metabolisms in Epsilon- and Gamma-Proteobacteria in Deep-Sea Hydrothermal Fields. Frontiers in Microbiology, 2, 192. http://doi.org/10.3389/fmicb.2011.00192
    Link: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3176464/

    ReplyDelete
  3. Hi Johanna,

    Thanks for the post, that study is quite intriguing. Some research has been conducted which suggests that quorum sensing autoinducers may act as a settlement cue for shallow water polychaete worms (as reviewed by Dobretsov et al, 2009). Although little is known about QS at hydrothermal vents, a fascinating recent ISME paper (Perez-Rodriguez et al, 2015) suggests that the luxS QS system is ancestral in the ε-proteobacteria (originating from a thermophilic ancestor) and present in deep-sea ε-proteobacteria from hydrothermal events. Could it be that QS molecules play a role in metazoan larval settlement at hydrothermal vents, as they may do in mesophilic habitats? I think this is a fascinating area that desperately needs further research!

    Thanks again,
    Davis

    Dobretsov, S., Teplitski, M., & Paul, V. (2009). Mini-review: quorum sensing in the marine environment and its relationship to biofouling. Biofouling, 25(5), 413-427. http://www.tandfonline.com/doi/abs/10.1080/08927010902853516

    Pérez-Rodríguez, I., Bolognini, M., Ricci, J., Bini, E., & Vetriani, C. (2015). From deep-sea volcanoes to human pathogens: a conserved quorum-sensing signal in Epsilonproteobacteria. The ISME journal, 9(5), 1222-1234. http://www.nature.com/ismej/journal/v9/n5/abs/ismej2014214a.html

    ReplyDelete
  4. Hi Davis,

    Thank you for your contribution.
    The hypothesis you present is very interesting and seems reasonable to me. In any case, more research is always needed!

    Thanks,
    Johanna

    ReplyDelete

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