Prieur D J, Olson H M, Young D M
Am J Pathol. 1974 Nov;77(2):283-98.
A genetic disorder of rabbits consisting of a deficiency of the enzyme lysozyme is characterized. The condition appears to be inherited as an autosomal recessive trait. Most of the tissues of lysozyme-deficient rabbits including bone marrow, liver, lung. spleen and bone had levels of lysozyme which were 1% or less of the levels in the corresponding tissues of normal rabbits when measured with the lysoplate method. Levels of lysozyme in the kidney and serum were 6% of controls, but the thymus of the lysozyme-deficient rabbits had normal levels of the enzyme. All leukocytes of the lysozyme-deficient rabbits were negative for lysozyme when examined by a histobacterial technic. No morphologic lesions could be detected in any of the tissues of the lysozyme-deficient rabbits. Although several species of animals have been reported to be lysozyme deficient, this appears to be the first report of lysozyme deficiency occurring as a mutant condition. It is suggested that these mutant rabbits may be useful as a resource for experiments designed to delineate the biologic role of lysozyme.
一种由溶菌酶缺乏引起的兔子遗传性疾病被加以描述。这种病症似乎作为常染色体隐性性状遗传。用溶菌酶平板法测定时,溶菌酶缺乏的兔子的大多数组织,包括骨髓、肝脏、肺、脾脏和骨骼,其溶菌酶水平仅为正常兔子相应组织中溶菌酶水平的1%或更低。肾脏和血清中的溶菌酶水平为对照的6%,但溶菌酶缺乏的兔子的胸腺中该酶水平正常。用组织细菌学技术检查时,溶菌酶缺乏的兔子的所有白细胞对溶菌酶均呈阴性。在溶菌酶缺乏的兔子的任何组织中均未检测到形态学病变。虽然已有报道几种动物存在溶菌酶缺乏,但这似乎是溶菌酶缺乏作为一种突变状况出现的首次报道。有人提出,这些突变兔子可作为一种资源,用于旨在阐明溶菌酶生物学作用的实验。