We previously reported that genes within the major histocompatibility
complex influence the intensity of Taenia crassiceps murine cysticerco
sis. This genetic control, readily apparent in mice of BALE background
, was further studied in H-2 congenic and recombinant B10 mice as well
as in BALB/c substrains differing in expression of Qa-2 antigens. Sim
ilarly low parasite numbers were found in all B10-derived strains infe
cted, regardless of H-2 haplotype, indicating that the effect of H-2 g
enes in controlling susceptibility is overridden in mice of B10 backgr
ound. BALB/c substrains differed significantly in susceptibility. BALB
/cAnN was highly susceptible, whereas BALB/cJ, in contrast, was highly
resistant and BALB/cByJ showed intermediate susceptibility. Susceptib
ility or resistance in BALB/c substrains may be associated to differen
ces known to distinguish them, such as serum testosterone levels and Q
a-2 protein expression. In bidirectional F1 hybrids of C57BL/6J and BA
LB/cAnN resistance to cysticercosis was inherited as a dominant autoso
mal trait. In F1 hybrids of BALB/cJ with BALB/cAnN, BALB/cByJ and BALB
.K resistance was also inherited as a dominant trait. However, in (BAL
B/cAnN x BALB/cByJ)F1 and (BALB/cAnN x BALB.K)F1 hybrids, dominant sus
ceptibility to cysticercosis was observed.