8.1.1.2 Shock treatment

8.1.1.2 Shock treatment

The term ploidy induction is multiplication of the chromosome set by manipulating events during embryonic development, such as insemination, release of polar body and first-cell division.

  • Chromosome sets can be manipulated by the application of thermal or temperature (cold and heat), pressure or chemical shock.
  • Shocking of a freshly inseminated fish egg causes depolymerization of tubulin polymers that form microtubules, which are essential for the formation of the spindle apparatus.
  • Therefore, shock treatment results in the inhibition of spindle formation and aster movement.
  • When applied shortly before first cleavage, the shock treatment inhibit cytokinesis and cause zygotes to undergo two genomic replications with only one cytoplasmic division.
  • This is necessary for diploidizing gynogenetic and androgenetic offspring and in inducing triploidyand tetraploidy.

1. Thermal Shock

  • Cold shocks are usually applied near 0°C for cold water species such as salmonids and somewhat at higher temperature (8-12° C) for warm water species like Common carp, Tilapia and Indian major carps.
  • Heat shock is applied at a higher temperature (around 26-28°C) in the case of cold water than in warm water fishes (39-42°C).

2. Pressure shock

This method is simple to administer.

  • The pressure range varies between 7000 to 9000 pascals (Psi).
  • The hydrostatic pressure is applied by a specialised instrument (French Cell Press) designed by mechanical engineering method.
  • Pressure shock is supposed to have less side effect than the thermal shock.

3. Chemical shock

  • Colchicine and cytochalasin-B have the potential to disrupt cell division and induce ploidy induction.
  • Anaesthetics such as nitrous oxide and Freon 22 have also been tried to induce triploidy. But the results are inconsistent and unsatisfactory.
Last modified: Thursday, 24 November 2011, 7:06 AM