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The
softshell clam (Mya arenaria), which occurs along the Atlantic
coast of North America, is a commercially important bivalve with a wide
distribution. Particular species of dinoflagellates (such as Alexandrium),
sometimes referred to as red tide, bloom off the Maine and Canadian coast
starting in early spring and throughout the summer. These dinflagellates
produce paralytic shellfish toxins (PSTs), which in high concentrations,
are capable of blocking nerve function, leading to paralysis. While these
toxins typically aren’t present in threatening concentrations, Mya
arenaria can collect them in their body tissue at higher concentrations
via filter feeding the toxic algae.
Paralytic shellfish poisoning (PSP) in humans results from the ingestion
of shellfish which have been recently feeding on the toxic algae. This
resulting PSP constitutes a large public health hazard and is the cause
for severe economic losses in the shellfish industry on both coasts of
North America.
The Connell Lab has discovered a mutation in the gene responsible for
the voltage gated sodium channel in certain populations of softshell clams.
This mutation allows for a greatly increased resistance to PSTs and is
found most often in clam populations residing in an area with a history
of red tide blooms. While this resistance protects the clams against paralysis,
it also allows them to continue feeding during a bloom of toxic algae
which leads to a much higher biomagnification of the toxin. This directly
affects the shellfish industry as it can increase the severity of possible
poisoning and force us to close clam beds for a longer period of time.
We are currently undergoing further investigation on the scale of this
mutation in the wild and the dynamics of resistance development. Currently
we are tracking survival and growth of both sensitive and resistant bred
clams as a means of understanding how quickly a clam population would
shift towards resistance following the onset of regular blooms of toxic
algae.
Publications:
- Scott Hamilton and Laurie Connell (2009) Improved methodology for
tracking and genetically identifying the softshell clam, Mya arenaria.
Journal of Shellfish Research, Vol. 28, No. 4, 747–750.[ABSTRACT]
[VIEW PDF]
- Laurie Connell and Scott Hamilton (2007) Determination of a naturally
occurring sodium channel gene mutation in eastern Maine populations
of softshell clam, Mya arenaria. MDIBL Bulletin. 2007
- Connell LB, MacQuarrie SP, Twarog BM, Iszard M, Bricelj VM (2006)
Population differences in nerve resistance to paralytic shellfish toxins
in softshell clam, Mya arenaria, associated with sodium channel
mutations. Marine Biology . [ABSTRACT]
- Bricelj, V. M., L. B. Connell, et al. (2005). Sodium channel mutation
leading to saxitoxin resistance in clams increases risk of PSP. Nature.
434: 763-767.
- Connell, L. B., B. M. Twarog, et al. (2004). Development of resistance
to paralytic shellfish toxins in the softshell clam, Mya arenaria,
via a single mutation in the sodium channel pore region: II. Molecular
identification of a mutation associated with the resistant phenotype
in multiple populations, Cape Town South Africa.
- Trainer, V. L., K. Konoki, et al. (2004). Development of resistance
to paralytic shellfish toxins in the softshell clam, Mya arenaria,
via a single mutation in the sodium channel pore region: III. Electrophysiological
studies, Cape Town South Africa.
- Connell, L. B., V. L. Trainer, et al. (2002). A molecular basis for
variation in resistance to paralytic shellfish toxins in bivalve molluscs.
Tenth International Conference on Harmful Algal Blooms, St Pete Beach
FL. [ABSTRACT]
- Connell, L. B., V. M. Bricelj, et al. (2000). Cloning and identification
of a sodium channel gene from the clam Mya arenaria. Symposium on Harmful
Marine Algae in the US, Woods Hole MA, USA, Woods Hole MBL.
- More Connell Lab publications [READ
MORE]
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Project funded by:
NOAAs ECOHAB Research Program |
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