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. 1979 Dec;26(3):1111-5.
doi: 10.1128/iai.26.3.1111-1115.1979.

Strain-dependent differences in murine susceptibility to coccidia

Strain-dependent differences in murine susceptibility to coccidia

P H Klesius et al. Infect Immun. 1979 Dec.

Abstract

Differences in susceptibility of strains of mice to Eimeria ferrisi were observed by infecting eight strains of mice with six infectious dose levels and comparing the mortality rate among the strains for a period of 12 days. Mice of the C57BL/6 and HA/ICR strains were susceptible, and those of A/He, AKR, BALB/c, CBA, C3H/Anf, and DBA/2 strains were resistant to coccidial infection. Resistance was a dominant genetic expression, as indicated by the resistant response of F(1) hybrids of susceptible C57BL/6 and resistant CBA, C3H/Anf, or DBA/2 strains. An E. ferrisi infection in congenitally athymic nu/nu mice and phenotypically normal heterozygous nu/+ mice was used to determine how thymus-dependent immunoincompetence in cell-mediated immunity of the nu/nu mouse affected resistance to infection in a genetic background of the resistant BALB/c mouse. Results of primary and challenge infections in these two strains of mice suggested that resistance is thymus dependent. Furthermore, impairment of thymus-dependent cell-mediated immunity in resistant AKR mice by treatment with mouse antithymus serum led to partial susceptibility. However, susceptible C57BL/6 and HA/ICR strains are phenotypically normal mice, and previous evidence showed that C57BL/6 mice are not completely immunoincompetent in cell-mediated reactivity to coccidia. Collectively, our data show that cell-mediated immunity is necessary for resistance but may be subjected to modification by genetic expression of the host. The possible role of immune response genes in the control of coccidial immunity is discussed.

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References

    1. Science. 1964 Sep 18;145(3638):1318 - PubMed
    1. J Protozool. 1964 Feb;11:46-51 - PubMed
    1. Cornell Vet. 1958 Apr;48(2):127-33 - PubMed
    1. Exp Parasitol. 1978 Aug;45(2):160-8 - PubMed
    1. Infect Immun. 1978 Dec;22(3):657-64 - PubMed

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