This study was undertaken to determine the effects of induced molt on basal
functional activities of heterophils from aging hens. For this purpose, he
terophils from both molted and unmolted hens were examined by in vitro bioa
ssays for functional responsiveness and efficiency. We evaluated the abilit
y of the heterophils to migrate to chemotactic stimuli, phagocytize opsoniz
ed and nonopsonized Salmonella enteritidis (SE), and generate an oxidative
burst in response to inflammatory agonists. A significant (P < 0.001) heter
ophilia was found in the molted hens within 2 days after feed withdrawal an
d remained throughout the length of the experimental feed withdrawal period
. No significant differences were found in the random migration of heteroph
ils from either group. The chemotactic movement of heterophils from molted
hens was not affected until 8 days after feed withdrawal when compared with
heterophil chemotaxis from unmolted hens. A significant decrease in chemot
axis by the heterophils from molted hens was observed days 8-12 after feed
withdrawal (P < 0.05). Significantly (P < 0.05) fewer heterophils from molt
ed hens were able to phagocytize opsonized (59% vs. 38%) and nonopsonized (
26% vs. 15%) SE within 2 days after feed withdrawal. Likewise, significantl
y (P < 0.05) fewer bacteria were phagocytized per heterophil from the molte
d hens when compared with the number of bacteria per heterophil from the un
molted hens. The oxidative burst of heterophils stimulated by either opsoni
zed zymosan A or phorbol myristate acetate of heterophils from molted hens
was significantly (P < 0.05) reduced when compared with that generated by h
eterophils from the unmolted hens. These results indicate that feed withdra
wal to induce molt alters the number and function of peripheral blood heter
ophils. This decreased efficiency of heterophil functional activity appears
to play a role in the increased susceptibility of molting hens to SE infec
tions.