The quick-freeze, freeze-fracture, deep-etching and rotary replication
techniques were used to analyze the structural organization of Giardi
a duodenalis. The surface of the flagella was rugous, in contrast to t
he cell body surface which was smooth. The ventral region was characte
rized in more detail, exposing the layer of sub-pellicular microtubule
s bonded to the microribbon sheet which appears as an open flat helico
id structure where the two free ends overlap and adhere close to the f
rontal part of the protozoan. The microribbon appears as 18-nm thick p
arallel (35 nm interval) filaments connected by short bridges. A flatt
ened structure with a highly organized array of particles was seen clo
se to the microribbons.