Hookworms are gut-dwelling, blood-feeding nematodes that infect hundreds of
millions of people, particularly in the tropics. As part of a program aimi
ng to define novel drug targets and vaccine candidates for human parasitic
nematodes, genes expressed in adults of the human hookworm Necator american
us were surveyed by the expressed sequence tag approach. In total 161 new h
ookworm genes were identified. For the majority of these, a function could
be assigned by homology. The dataset includes proteases, protease inhibitor
s, a lipid binding protein, C-type lectins, an anti-bacterial factor, globi
ns and other genes of interest from a drug or vaccine development viewpoint
. Three different classes of small, secreted proteins were identified that
may be involved in the host-parasite interaction, including potential potas
sium channel blocking peptides. One third of the genes were novel. These in
cluded highly expressed, secreted (glyco)proteins which may be part of the
excretory-secretory products of these important pathogens. Of particular in
terest are a family of 9 genes with similarity to the immunomodulatory prot
ein, neutrophil inhibitory factor, that may play a role in establishing an
immunocompromised niche for this successful parasite.