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用于可能的啮齿动物疫苗的肺炎支原体温度敏感突变体的生物学评价。

Biological evaluation of Mycoplasma pulmonis temperature-sensitive mutants for use as possible rodent vaccines.

作者信息

Lai W C, Bennett M, Lu Y S, Pakes S P

机构信息

Division of Comparative Medicine, University of Texas Southwestern Medical Center, Dallas 75235.

出版信息

Infect Immun. 1990 Jul;58(7):2289-96. doi: 10.1128/iai.58.7.2289-2296.1990.

Abstract

Temperature-sensitive mutants (TSMs) of Mycoplasma pulmonis were produced by treating the wild-type strain with N-methyl-N'-nitro-N-nitrosoguanidine. Three TSMs were selected at 38 degrees C, as a restrictive temperature, and at 34 degrees C, as a permissive temperature. Two TSMs, UTCMI and UTCMII, were proven to be nonpathogenic but immunogenic. In addition, they did not induce pneumonia, tracheitis, or tympanitis but did induce mild rhinitis. They were stable after 10 passages in vitro and in vivo. They elicited excellent antibody production and cell-mediated immunity in vaccinated rats. They also were not mitogenic to rat lymphocytes. Rats immunized intranasally with these TSMs were significantly protected against challenge with wild-type organisms. These mutants were morphologically and serologically indistinguishable from the wild-type organisms. The growth characteristics and antibiotic sensitivities were similar to those of wild-type organisms, except that they grew only at 34 degrees C. In contrast to wild-type organisms, they did not bind to or lyse sheep erythrocytes. Thus, these TSMs may qualify as a vaccine to prevent M. pulmonis infection in rats.

摘要

通过用N-甲基-N'-硝基-N-亚硝基胍处理肺炎支原体的野生型菌株,获得了温度敏感突变体(TSM)。在38℃(作为限制温度)和34℃(作为允许温度)下筛选出三个TSM。已证实两个TSM,UTCMI和UTCMII无致病性但具有免疫原性。此外,它们不会诱发肺炎、气管炎或鼓膜炎,但会诱发轻度鼻炎。它们在体外和体内传代10次后仍保持稳定。它们在接种疫苗的大鼠中能引发良好的抗体产生和细胞介导的免疫。它们对大鼠淋巴细胞也没有促有丝分裂作用。用这些TSM经鼻免疫的大鼠在受到野生型病原体攻击时得到了显著保护。这些突变体在形态学和血清学上与野生型生物体无法区分。其生长特性和抗生素敏感性与野生型生物体相似,只是它们仅在34℃下生长。与野生型生物体不同,它们不与绵羊红细胞结合或使其裂解。因此,这些TSM可能有资格作为预防大鼠肺炎支原体感染的疫苗。

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