Xl. Zhao et al., BIOCHEMICAL PATHWAY OF MELANOTIC ENCAPSULATION OF BRUGIA-MALAYI IN THE MOSQUITO, ARMIGERES SUBALBATUS, Developmental and comparative immunology, 19(3), 1995, pp. 205-215
The mosquito, Armigeres subalbatus, is naturally resistant to the fila
rial worm, Brugia malayi, and microfilariae (mf) penetrating the midgu
t are killed by melanotic encapsulation reactions in the hemocoel with
in 48 h following ingestion. This vector-parasite system was used to a
ssess changes in hemolymph tyrosine, tyrosine derivatives, and catecho
lamine-metabolizing enzyme activities using high pressure liquid chrom
atography with electrochemical detection (HPLC-ED) during melanotic en
capsulation reactions against mf. Tyrosine and dopa were detected in t
he hemolymph of both control and immune-activated (mf-exposed) mosquit
oes, but not dopamine or N-acetyl dopamine (NADA). Tyrosine was signif
icantly increased in immune-activated mosquitoes at 6 and 12 h post bl
ood feeding, but was depleted following intrathoracic inoculation of m
f in the absence of a blood meal. Dopa also was elevated in immune-act
ivated mosquitoes at 6, 12, and 24 h post-exposure to mf. There were s
ignificant increases in phenol oxidase (PO) and dopa decarboxylase (DD
C) activities in immune-activated mosquitoes as compared to controls,
and these elevated activities were correlated with changes in tyrosine
and dopa levels in the hemolymph. No significant differences in N-ace
tyl transferase (NAT) and dopachrome conversion enzyme (DCE) activitie
s between control and immune-activated mosquitoes were observed. The p
ossible roles these molecules play in melanotic encapsulation reaction
s of A. subalbatus against mf are discussed.