Coastal
pollution is a major problem creating worldwide negative impacts on ecosystems
from the deep ocean, water columns, sediment communities and holobiont species.
As well as ocean acidification, pollutants change eukaryote, archaea, bacteria
and fungi microbial communities allowing opportunistic pathogenic bacteria to
dominate, increasing disease. The resulting nutrient type and pH increase or decrease,
with environmental fluctuations, influences microbes persisting however, few microbial
communities are not affected. The Mediterranean sponge (Crambe crambe) exhibits stable communities, with Proteobacteria dominating, across
habitats from a polluted harbour in Blanes, Spain, up to a distance of <1km (Gantt
et al., 2017). However, most
microbial communities studied are affected by pollution. The Boulder star coral
(Montastraea annularis), depth
distribution of 0-25m, is environmentally sensitive with high disease
susceptibility in polluted shallow coastal habitats. Its microbial community
was studied with proximity to the urban centre and seaport of Willemstad,
Netherlands Antilles (Klaus et al.,
2007).
Klaus et al., 2007 sampled tissue, coral mucus
and small colony fragments from 36 colonies, at depths 5, 10 and 20m (control).
Bacteria and zooxanthellae were collected from the top 2cm of the highest
branch. The 16SrRNA was analysed in PCR and sequences classified using clone
libraries and GenBank primers, with monosaccharide and amino-acid composition
of healthy mucus determined, visualising the microbial community’s potential
role. The authors recorded data on light availability, temperature, seawater
pollution, symbiotic algae’s community structure and photosynthetic activity
levels, by measuring 𝛿13C and 𝛿 15N of the upper growing 25cm2 branch, for reef
classification. Nitrogen levels also determined the amount of sewage-derived
compounds absorbed, via mass spectrometry and microbial communities were compared
using similarity matrix. They studied only one species, therefore, including multiple
corals could have enhanced understanding of the microbial pool and pathogenic
microbe distribution. Looking into behaviour of dominant bacteria, rather than
stating other studies findings, to see possible causes for disease at 5m, could
have also enhanced documented studies.
Results showed light intensity varied with
depth: 5m (33-36%), 10m (18-22%) and 20m (9-11%) with temperatures consistently
27.5±0.5°C. Coral tissue 𝛿 15N was 1.75‰ heavier at 5-10m, showing greater sewage uptake and 𝛿 13C was 1.0‰ lighter at
5m than 20m due to increased light. No significant difference between amino
acid or monosaccharide composition was found with location. However, variation
of the symbiotic algae genus Symbiodinium
and enzymes associated with each of its clades was seen, clade B at 5m, C at 10
and 20m. Bacterial communities also showed patterns within polluted and
controlled localities; CAB-1 decreased abundance whereas clones of plastids,
Cyanobacteria and Firicutes showed increasing abundance with depth. Terminal
restriction fragments showed a difference between 5-20m but not between 5-10m
or 10-20m suggesting importance in polluted areas, when the disease
cyanobacterium clone CD1C11 and CAB-1 had greater abundance on healthy corals
<10m.
This was the first study to identify the
importance of each bacterial abundance on this species providing comprehensive
analysis of potential issues but, further work is required for CAB-1. It
interested me as it demonstrated the effect of pollutants spreading and acted
on the understanding of how host and mucus microbiota are important in pathogen
inhibition and coral health. This study enhances knowledge of the susceptibility
of microbes to pollution, tolerance and environmental change, allowing us to
predict future microbial fluctuation and disease incidences potentially
occurring in areas not yet affected by pollution for similar genus. Finding
ways to inhibit the disease would be a main focus for future research
investment. Another future focus is to decrease pollution, sewage discharge and
underwater seepage, into our waters and find solutions to stop it spreading to
extensive coral reefs.
Reviewed
Article
Klaus, J. S., Janse, I., Helkoop, J. M.,
Sanford, R. A & Fouke, B. W. (2007). Coral microbial communities,
zooxanthellae and mucus along gradients of seawater depth and coastal pollution.
Environmental Microbiology, 9(5),
1291-1305
Extra
Reading
Gantt, S. E., López-Legentil, S &
Erwin, P. M. (2017). Stable microbial communities in the sponge Crambe crambe from inside and outside a
polluted Mediterranean harbour. FEMS
Microbiology Letters, 364 http://www.imesalab.com/iMESA/Erwin_files/Gantt_etal_2017.pdf
Hi,
ReplyDeleteReally interesting read , I was just curious if they identified what the most harmful pollutants on this ecosystem were or why/if individual components or properties of the pollutants allowed certain groups of bacteria to increase and caused the others to decrease?
Thanks for another interesting read,
Pippa
Hi Pippa,
ReplyDeleteThey did not specify what was the most harmful nutrients just that this area was prone to sewage discharge and groundwater seepage which gave the elevated nutrient concentrations. The only nutrients they studied was delta 15N uptake by the sewage discharge by each of the 36 colonies sampled and delta 13C. They did not specify what specific properties caused each to increase or decrease, they just stated the community composition within the different environments correlating to the environmental variables changing. This could have been very interesting for them to have done to enhance the understanding of predicting future community changes.
Thank you for you questions, they were interesting.
Sophie,