Worm burdens recovered from inbred mice strains, namely C57Bl/6, C57Bl/10, CBA, BALB/c, DBA/ 2 and C3H/He, conventionally This approach intends to add new data on the helminth parasites of laboratory mice, since these investigations have arised a great interest and also, taking into account that these hosts as experimental animal models, are widely utilized in the evaluation of several biological parameters. Previously, besides the considered Swiss Webster mice, only two inbred strains (C57Bl/6, DBA/2) were investigated for the presence of helminths in Brazil (Pinto et al. 1994).Thus, the present findings ratify those reported for these strains, as well as complement the evaluation of worm burden in the other commonly referred inbred mice.The modification of the anal swab technique proposed herein aims to avoid unnecessary necropsies to investigate the spectrum of intestinal parasites in a rodent colony, since oxyurid eggs are of difficult detection during conventional stool examination procedures.
MATERIALS AND METHODSTwo hundred and fifty Mus musculus (Linnaeus, 1758) inbred mice from two animal houses in the State of Rio de Janeiro, RJ, Brazil, were divided in two groups (A, B) according to their source. The suppliers were not identified by name due to ethical reasons. In group A, were included mice of the strains C57Bl/6, C57Bl/10, CBA, BALB/c, DBA/2 and C3H/He, with 25 animals each. The group B was represented by the strains C57Bl/6, CBA, BALB/c and C3H/He, with 25 mice each. Mice were male, 30 days old, weighting 20g each.Mice were sacrificed, helminths were recovered and processed for study as described elsewhere (Pinto et al. 1994).As for the swab anal procedures, the technique of Hall (1937) was modified and the device consists of a plastic rod (Fig. 1), with appropriate dimensions, for the examination of mice weighting at least 18g. One hundred and twelve mice were tested by this method. Animals are maintained in the proper position (Hofman's position), in order to avoid stress to the animals during the procedure. The rod is moistened in a 0.85% NaCl solution (Fig. 2) and after, introduced into the anus of the mouse, with carefully induced rotatory movements (Fig. 3), to avoid bleeding. The collected feces sample is transferred to a drop (20 µl) of saline physiological solution (0.85% NaCl) on a slide with a coverslip and examined under light microscope.