The aim of the presentation is to elucidate recent studies carried out with the extensive use of genetic markers as operational species descriptors. lsozyme analysis at 19-24 loci was carried out on anisakid nematodes of the genera Anisaki!. Pseudoferranova and Confracaecum from. various intermedtate/paratenic (squid, fish) andr,efimttve ( marme mammals) hosts from vartous parts of the A relevant
result
was
the
detection
of a number
of
and pathogenesity has
damaged
to
be
status therely
to be taken against these parasites.
by endoscope
and
27
MOLECULAR NEMATODES
Paggi L Instttute of Parasitology. Rome, Italy
***Hajime
characteristics
47 (Suppl.) (1998) 23-48
S-E2-6
ANISAKID
PATIENTS
Medicme,
caused
The biological
in order
and
However, difficult
to
parasite,
we
by microscopic techniques. an application
of
genomic
the second internal
these
chain
Japan
measures of control
clarified of
University
decipens
species
parasites
identify
Hospital,
OF
HUMAN
1
Pseudoterranova of
FROM
**Syuj~
lHokkaido
Pathology
IDENTIFICATION
REMOVED
International
two
parasites
reaction-based
( PCR-RFLP)
of ITS2
method
transcribed
and
Indicated
restriction
to
spacer the
fragment
identi@
these
of ribosomal
( ITS2
the
polymelase
polymrophism
technique
usefulness length
)
DNA
of
A.;iphidarum within genus Anisakis and of C.mirounga and C.radiarum within enus Conrrucaecum were also defined. Higher values of genetic d’tstance between A.schu akovi, A.zi hidarum. A.physeferis, genetically and morphologica Ply well dt.R erentiated taxa and sibling spectes of the Anisakis sim lex complex were observed ranging from DN~,= 1.30 to f. 09 and between Cmiroungu, Crad~atum and members of the C oscula~um complex ranging from !I,,,,= 0.83 to 1.35. Data on genetic variability and diversity, gene flow and genetic relationships between populations and species of the genera Anisakr.$, Psrudoterranova and C’on~racaecum so far studied arc discussed