A method, based on the disruption of eimerian oocysts in a French pres
sure cell in the presence of guanidine isothiocyanate, has been develo
ped to isolate large quantities of high quality total RNA efficiently.
This procedure results in a 12.5-fold greater number of oocysts broke
n, and a 22-fold greater yield of total RNA than from disruption by co
nventional grinding in liquid N-2. In addition, the RNA isolated by th
e French pressure cell method was of equal or superior quality when co
mpared to RNA isolated by grinding. This procedure provides a signific
ant improvement in RNA extraction from eimerian oocysts and will great
ly facilitate the study of gene expression in this important group of
parasites.