STRONGYLOIDES-STERCORALIS - HISTOPATHOLOGY OF UNCOMPLICATED AND HYPERINFECTIVE STRONGYLOIDIASIS IN THE MONGOLIAN GERBIL, A RODENT MODEL FORHUMAN STRONGYLIODIASIS
Rl. Kerlin et al., STRONGYLOIDES-STERCORALIS - HISTOPATHOLOGY OF UNCOMPLICATED AND HYPERINFECTIVE STRONGYLOIDIASIS IN THE MONGOLIAN GERBIL, A RODENT MODEL FORHUMAN STRONGYLIODIASIS, International journal for parasitology, 25(4), 1995, pp. 411-420
Tissues from corticosteroid-treated gerbils hyperinfected with Strongy
loides stercoralis were compared grossly and microscopically to simila
r tissues from animals with uncomplicated strongyloidiasis. Gerbils wi
th hyperinfection developed severe pulmonary alveolar haemorrhage with
a variable degree of subacute eosinophilic interstitial pneumonia ass
ociated with numerous alveolar, vascular and interstitial larvae. Hype
rinfection induced by corticosteroids, given either before inoculation
of S. stercoralis larvae or after a chronic Strongyloides infection w
as established, produced similar lesions, In contrast, lungs from gerb
ils with uncomplicated Strongyloides infection had severe eosinophilic
perivasculitis and vasculitis with very little haemorrhage, no pneumo
nia and no larvae, Sections of adult worms were present in the proxima
l part of the intestinal tract, lodged in spaces between mucosal epith
elial cells. Adult worms were not associated with inflammation and wer
e more common in the corticosteroid-treated gerbils. In corticosteroid
-treated gerbils only, there were numerous larvae in the distal intest
inal tract, throughout the intestinal wall and adjacent mesentery, wit
hin interstitial tissues and in lymphatic vessels. Significant inflamm
ation with associated larvae was only present In the caecum and mesent
eric lymph nodes, suggesting that the caecum was the main site for ini
tiation of parenteral migration with subsequent invasion of the lympha
tic system and lungs. The lesions in these gerbils were similar to tho
se found in humans. Infection of gerbils with S. stercoralis is the be
st rodent model of human strongyloidiasis.