Bluefin
tuna (Thunnus thynnus) is a species
strongly impacted in the western Atlantic Ocean and Mediterranean Sea and the
collapse of its recruitment put effort to develop methods for reproduction in
captivity. Improving the survival of the early developmental stage is one of
the major targets in larval hatchery. At the moment survival expectancy for
tuna larvae drops at 2-3 days after mouth opening. Although more studies are
required to understand the effect of environmental factors and nutritional
requirements, there is growing concern about the microbiota associated with tuna
larvae and their interactions.
Studies on the microbial communities structure of
captive reared marine fish are more abundant on cold water species (Atlantic
halibut and cod) than warm and temperate water species as tuna. Some studies on
halibut reveal similarities between larvae sampled from different geographical
regions. Other similarities in Bacterial Community Profiles (BCP) were found
over several years in the same batches of larvae. Also feeds and change of diet
can affect significantly BCP associated with larvae (this was reported in cod
larvae). If we consider that for cod larvae BCP varied as much between
individuals from the same tank as between different hatcheries.
Furthermore some studies demonstrate that the high
temperature (around 24°C) required by tuna larvae may promote potential
pathogen bacterial growth in the rearing tanks so “green water” system are
commonly used. Green and pseudo-green methods are rearing systems that use
microalgae to regulate microbial growth, and where light intensity, photoperiod
and feed supply are also regulated. Another system is mesocosm: large tanks
colonized by wild plankton populations and after the first phytoplankton bloom
bacteria proliferate and then remain constant. This system is combined with
regular addition of cultured feed as microalgae and rotifers.
The aim of this work was to compare BCPs of tuna
larvae reared with three methods commonly used in Mediterranean hatcheries:
clear water, pseudo green and mesocosm.
To evaluate how these three methods affected the bacterial colonization
of individual tuna larvae, BCPs of individual were compared within and between
rearing groups during two years using the PCR-DGGE method. The authors found
high individual variability of microbiota associated with larvae and this
result agree with previous result observed in cod larvae sampled from different
hatcheries. Unexpected result was high diversity and individual variability
after the mouth opening, when the larvae had not started exogenous feeding (in
many species this is a crucial point for microbial colonization). No regular
succession of bacterial communities after start feeding were found in this
study. An apparent shift was found after the introduction of live prey (yolk
sac sea bream larvae) but it was reported only in two individuals from one
hatchery. No significant effect of rearing systems was detected on the
bacterial communities composition. To explain these results authors do not
exclude the implication of any factors as physiological status of individual,
stochastic inoculation, effect of live feed. They point out the limited set of
experiments on this species and the need of many individuals to obtain
representative sample avoiding errors.
In my opinion this work lack of the identification of
at least some specific group of bacteria. Is knew that in Sarda sarda larvae (bonito, another Scombridae reared in the same condition as T. thynnus) the most two abundant groups of associated microbes are
Vibrionaceae and Rhodobacteriaceae. Should be interesting to see if these groups
match with that from tuna. Anyway the author mentioned that the sequencing of
band from the gel wasn’t possible for this work. Another point should be the
sampling of different larval tissues as skin and gut after mouth opening using
also in situ visualization methods. From this work seems that tuna larvae are stochastically colonized by bacteria and to clarify this, useful data in this work, should be the evaluation of BCPs of surrounding water. The
study of tuna hatchery and larvae associated microbial communities seems to be
a wide open field for the moment.
Gatesoupe, F. J., Covès, D., Ortega, A., Papandroulakis, N.,
Vadstein, O., & Gándara, F. (2013). A spatiotemporal study of bacterial
community profiles associated with Atlantic bluefin tuna larvae, Thunnus
thynnus L., in three Mediterranean hatcheries. Aquaculture Research, 44(10), 1511-1523.
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