Given the widespread concern that chemical contaminants may be associated with infectious
disease outbreaks in marine fish populations, work has been undertaken with the aim of developing
a suite of non-specific and specific assays of marine fish immune function and the application of
these techniques in a variety of field and laboratory investigations. Most of the work focused on
dab, Limanda limanda (L.) in view of the importance of this species in several North Sea fish
disease monitoring programmes, and was also supplemented with investigations of specific
immune function in turbot, Scopthalmus maximus (L.).
Initial field studies examined non-specific immune function in terms of lymphoid organ
morphology in dab sampled along a North Sea gradient of chemical contamination during the
March 1990 ICES/IOC Bremerhaven workshop. Significant differences were observed in the
kidney and spleen cell populations from dab, and these observations were considered in view of
the various other physico-chemical and biological results generated during the Bremerhaven
workshop. Following the valuable experience gained of the practical aspects of the field
monitoring approach, laboratory investigations were initiated with the aim of developing a suite of
immune function assays for deployment in either laboratory or field studies of marine fish health.
Assays for non-specific immune functions were considered, including serum protein and lysozyme
levels, methods of phagocyte collection, phagocyte chemiluminescence, calorimetric detection of
individual reactive oxygen species and in vitro cell migration assays. Additional field work was
undertaken, with the monitoring of serum total protein levels and lysozyme activity in dab sampled
from Lyme Bay, UK This study provided evidence of a marked seasonal variation in non-specific
immune function, which appeared to be associated with environmental factors (e.g. water
temperature) and the reproductive cycle.
Selected non-specific assays were applied to dab and turbot exposed under controlled laboratory
conditions to a variety of important marine contaminants, including cadmium, polycyclic aromatic
hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs), and the biological data integrated
with appropriate chemical characterisation of the exposure matrix. Using cultured turbot as a test
species, the non-specific assays were also supplemented with the assay of specific immune function
in fish exposed to PCB contaminated sediments. In brief, there was evidence of significant
impairment of immune function in fish exposed to either individual contaminants (viz. cadmium
and PAHs) or contaminant mixtures (viz. PAHs and PCBs) under the laboratory conditions
described. In summary, the project was successful in its primary aims of developing a suite of
techniques for evaluating both cellular and humoral immune functions in marine flatfish, and
applying these techniques in the laboratory to assess the impact of important classes of
environmental contaminants on fish health. Selected techniques were also used in field monitoring
studies of marine fish immune function, illustrating the potential of such techniques for use in
future laboratory and field studies of fish health.
Date of Award | 1996 |
---|
Original language | English |
---|
Awarding Institution | |
---|
THE EFFECTS OF ENVIRONMENTAL CONTAMINANTS ON THE IMMUNE FUNCTIONS OF MARINE FLATFISH
Hutchinson, T. (Author). 1996
Student thesis: PhD