A microsporidium Nosema portugal n. sp. was isolated from gypsy moths, Lyma
ntria dispar L, collected near Lisbon, Portugal, in 1985. The Life cycle in
cludes two sequential developmental cycles, a primary and a secondary cycle
. The primary cycle occurs in midgut epithelial cells, where primary spores
are produced within 48 h. The primary spores immediately extrude their pol
ar filaments, presumably to infect other cells. In the target tissues (sali
vary glands and fat body) the secondary development cycle is followed by th
e formation of environmental spores. Primary spores were also sometimes pre
sent in target tissues. Fresh unfixed and unstained primary spores have a l
arge posterior vacuole and measured 4.8 x 2.7 mu m. Ultrastructurally, they
have 5-8 polar filament coils, a large posterior vacuole, abundant endopla
smic reticulum, and were binucleate. Mature unfixed and unstained environme
ntal spores were highly refractive and the posterior vacuole and nuclei cou
ld not be seen through the spore coat. Fresh environmental spores measured
4.5 x 1.9 mu m. Ultrastructurally, environmental spores were binucleate, wi
th a typical polaroplast, 10-11 isofilar polar filament coils, and a series
of 4-6 thin polar filament-like tubules situated at the posterior end of t
he row of typical polar filament coils. The ssu rRNA sequences strongly sug
gest that this species is more closely related to the Vairimorpha subgroup
within the Nosema/Vairimorpha clade than to the Nosema subgroup. (C) 1999 A
cademic Press.