Abstract
Acclimations of Oreochromis mossambicus to elevated salinity were
conducted with multiple rates of salinity increase and durations of
exposure to determine the rate-independent maximum salinity limit and
the incipient lethal salinity. Quantitative proteomics of over 3000 gill
proteins simultaneously was performed to analyze molecular phenotypes
associated with treatments representative of key zones in the
salinity-level x duration matrix. For this purpose, a species- and
tissue-specific data-independent acquisition (DIA) assay library of MSMS
spectra was created. From these DIA data, protein networks representing
complex molecular phenotypes associated with salinity acclimation were
generated. Organismal performance indicators of salinity tolerance were
then correlated with salinity-regulated protein networks. O.
mossambicus was determined to have a wide “zone of resistance” from
approximately 75g/kg salinity to 120g/kg, which fish survive for a
limited period with eventual loss of function. Crossing the critical
threshold salinity into the zone of resistance corresponds with blood
osmolality increasing beyond 400 mOsm, significantly reduced body
condition factor, and cessation of feeding. Gill protein networks
impacted at extreme salinity levels both above and below the critical
salinity threshold include increased energy metabolism, especially
upregulation of electron transport chain proteins, and regulation of
specific osmoregulatory proteins. Cytoskeletal, cell adhesion, and
extracellular matrix proteins are enriched in regulation network
patterns that are sensitive to the critical salinity threshold. Network
analysis of these patterns provides deep insight into specific
mechanisms of energy homeostasis during salinity stress.