An. Jha et al., DEVELOPMENT OF AN IN-VIVO GENOTOXICITY ASSAY USING THE MARINE WORM PLATYNEREIS-DUMERILII (POLYCHAETA, NEREIDAE), Mutation research. Section on environmental mutagenesis and related subjects, 359(2), 1996, pp. 141-150
An in vivo genotoxicity test system has been developed using the embry
o-larval stages of the marine annelid, Platynereis dumerilii (Polychae
ta: Nereidae). This species is representative of an ecologically impor
tant group of marine invertebrates, it is amenable to laboratory cultu
re and has a well defined and stable karyotype (2n = 28) which is suit
able for the analysis of a range of cytogenetic endpoints, including c
hromosomal aberrations (CAs) and sister chromatid exchanges (SCEs). An
evaluation of the cell cycle kinetics using the embryo-larval stages
allowed selection of exposure times for cytogenetic work. Subsequently
, la-h-old embryos were exposed to reference mutagens, dissolved in se
a water, in the presence of 5-bromodeoxyuridine (BrdU) for 12 h (SCE a
nalysis) or 8 h (CA analysis) at 15 +/- 1 degrees C, by which time the
y had reached the first larval stage (20-24 h). Dose response-relation
ships for cytotoxicity, SCEs and CAs were observed for both direct act
ing mutagens (methyl methanesulfonate, mitomycin C) and mutagens which
require metabolic activation (cyclophosphamide, benzo[a]pyrene). The
sensitivity of the embryo-larval stages of P. dumerilii to both direct
and indirect acting mutagens, their suitability for laboratory cultur
e, together with the presence of a good karyotype and chromosome morph
ology for cytogenetic analyses, makes this species a potentially valua
ble in vivo model for marine genotoxicity testing.