Amongst the
several marine phytoplankton groups, there is a component of eukaryotes smaller
than 5 µm, accordingly called photosynthetic picoeukaryotes (PPEs). These PPEs
gained recognition over the past years for their role in the oceanic carbon cycle
by O2 fixation and their trophic role as bacterivores. This last feature
proves the mixotrophic character of some PPE’s, since these organisms act as
primary producers as well. In contrast to the relatively good understanding we
have on PPE’s in general, there is less knowledge on environmental factors
limiting these organism’s abundance. It’s already found that nutrient
concentrations don’t show a controlling effect, which implies PPE abundance and
carbon fixation regulation from higher levels in the trophic system. Lepère et
al. (2016) investigated associations between marine PPEs and eukaryotic
parasites, where the role for parasitic fungi was explored as well.
To evaluate
abundance of PPE classes and parasites and associations between them, tyramide
signal amplification-fluorescence in situ
hybridization (TSA-FISH) was used. The probing of potentionally infected
organisms could give new insights in the interactions between PPEs and
parasites, therefore two probes are used at the same time: one labelling the
potential parasite and one labelling the PPE host. The investigated potential
parasites are: Syndiniales, Perkinsozoa and a wide range of fungi. To measure
PPE abundance and composition, sea water samples were taken from the surface
mixed layer in the Atlantic Ocean, along a transect passing ten stations in the
southern subtropical gyre and the southern temperate region. The sampled
organisms were separated in two size fractions of 2 µm and 3.1 µm, named
‘small, plastidic eukaryotes’(Plast-S) and ‘large, plastidic
eukaryotes’(Plast-L), respectively.
Pelagophyceae
and Chrysophyceae were the dominating fractions for Plast-S at all stations,
while this was Prymnesiophyceae for the Plast-L PPE. Cryptophyceae was also
detected in some Plast-L samples, albeit with much lower concentrations. At
some stations, the dominating PPE classes were still measured in relatively low
concentrations, which implies occurrence of other clades. Lepère et al. (2013)
suggest some prasinophyceae clades could contribute at these stations as well,
as they showed to play an important role within the PPE community in some
oceanic regions. In our seminar two weeks ago, me and Eleni discussed the
article of dos Santos et al. (2016), in which this contribution is researched
for prasinophytes clade VII.
The
investigated Syndiales parasites showed generally low concentrations. At six
stations no Syndiales cells were found at all. However, these low numbers could
be an underestimation, since the probe used to stain Syndiales was only
specific for 75% of the described clades. Perkinsozoa is a phylum known to
comprise aquatic parasites infecting a wide range of organisms. Yet, the FISH
analysis barely gave any positive signals. This can be explained by the fact
that Perkinsozoa mainly occur in sediments. The last group of potential
parasites researched is separated by the use of three different FISH probes.
Each one staining a specific kind of fungal parasites: Eumyocota, Chytridiales
and some fungi within the Cryptomycota clade. The last two clades are known to
contain some freshwater parasites. Eumyocota and Chytridiales represented
respectively 9.3% and 3.5% of the total eukaryotic community, but no positive
signals were found for Cryptomycota. This latter suggests that Cryptomycota
don’t occur in the surface mixing layer of the Atlantic ocean.
Since it
was known before that parasitism by Syndiales shows a preference for larger
cells, it was not a surprise that there were no associations found between this
parasite and PPEs. As mentioned before, Perkinsozoa was barely present in the
surface mixing layer. The fungal organisms however, were the only group that
showed parasitism of PPEs at some of the sampling stations, albeit only with
the Plast-L fraction size. That is, Eumyocota and Chytridiales were associated
with a small fraction of Chrysophyceae and Prymnesiophyceae, varying from 2.4%
to 7.3% for the two PPE groups separately.
In the
conclusion the authors state a quantitave importance of free-living fungi in
the open ocean. However, to me it seems that the low percentages mentioned
before don’t show a particularly great
impact of eukaryotic parasitism on PPEs. Also it occurred to me that the depths
at which the PPE samples are taken, vary from five to 88 meters. I wonder if
this difference shows in the results for parasitic associations found per
station. In table 2 in the article, no associations – not even with fungal
parasites – were found at a depth of 88 meters. Nevertheless, this article gave innovative
insights into the topic, where it was largely unexplored with regards to marine
pelagic ecosystems before.
Article reviewed:
Lepère, C., Ostrowski, M., Hartmann, M., Zubkov, M. V., & Scanlan,
D. J. (2015). In situ associations between marine photosynthetic picoeukaryotes
and potential parasites–a role for fungi?. Environmental microbiology reports.
Further reading (article discussed in seminar
3, by me and Eleni):
dos Santos, A. L., Gourvil, P., Tragin, M., Noël, M. H., Decelle, J.,
Romac, S., & Vaulot, D. (2016). Diversity and oceanic distribution of
prasinophytes clade VII, the dominant group of green algae in oceanic waters. The ISME Journal.
Hi Thyrza, thanks for your review I was wondering if the authors mentions any other environmental factors besides nutrient availability or other ways higher tropic levels may affect PPE abundance?
ReplyDeleteIt also mentions how Perkinsozoa mainly occur in sediments. The samples were all collected in the water column do you think it would have also been useful for the authors to collect sediment samples to assess their abundance in sediment?
Thanks
Alisha
Hi Alisha,
ReplyDeleteAfter establishing that nutrient availability wasn't a limiting factor in CO2 fixation by PPEs, the authors directly concluded that top-down regulation would be the most likely limitation. However, I can imagine that certain species amongst the PPEs have a temperature or salinity preference for example (which would thus influence the PPE distribution over different oceans). However, since the authors considered the group of PPE species as a whole, I think they disregarded these preferences. It may be intersting to explore these differentation in further research ofcourse.
With regards to your question about the Perkinsozoa, I don't think that taking sediment samples would have been useful within the scope of this research. The article was about parasitism on PPEs, which are photosynthetic organisms and therefore only occur in the euphotic zone. We can expect that living PPEs won't be found in sediments of the ocean open, as there is no light.
I hope this answers your questions! Thyrza
Hi,
ReplyDeleteAlthough previous work has shown nutrients do not control PPE , do you think higher nutrient availability from areas of upwelling may affect the control of these organisms? I realise this is probably beyond the scope of this study, I'd just be interested to see if you think it could be a factor.
Chloe