Voelker L L, Weaver K E, Ehle L J, Washburn L R
Department of Microbiology, University of South Dakota School of Medicine, Vermillion 57069-2390, USA.
Infect Immun. 1995 Oct;63(10):4016-23. doi: 10.1128/iai.63.10.4016-4023.1995.
Mycoplasma arthritidis causes a severe polyarthritis under natural conditions in rats and under experimental conditions in both rats and mice. Although the disease itself has been extensively studied, M. arthritidis virulence factors remain uncharacterized. Comparison of relative arthritogenicity of 20 strains of M. arthritidis revealed that the strains tended to fall into two groups, a highly arthritogenic group, inducing maximum arthritis scores of > or = 11 in rats, and a low-virulence group, inducing maximum scores of < 6. Chromosomal DNA from the more highly arthritogenic strains possessed sequences that hybridized by Southern analysis with a probe prepared from lysogenic M. arthritidis bacteriophage MAV1, while DNA from low-virulence strains did not. One of the low-virulence strains, 158, was experimentally lysogenized with MAV1. Lysogenized 158 showed a significant increase in arthritogenicity over nonlysogenized 158. These data suggest that MAV1 carries a factor that is important in pathogenesis of M. arthritidis-induced arthritis of rats.
关节炎支原体在自然条件下可使大鼠患严重的多关节炎,在实验条件下可使大鼠和小鼠都患上该病。尽管对这种疾病本身已进行了广泛研究,但关节炎支原体的毒力因子仍未得到鉴定。对20株关节炎支原体的相对致关节炎性进行比较发现,这些菌株倾向于分为两组,一组是高致关节炎性组,在大鼠中诱导的最大关节炎评分≥11,另一组是低毒力组,诱导的最大评分<6。来自高致关节炎性菌株的染色体DNA具有通过Southern分析与由溶原性关节炎支原体噬菌体MAV1制备的探针杂交的序列,而低毒力菌株的DNA则没有。其中一株低毒力菌株158,经实验用MAV1进行了溶原化处理。溶原化的158与未溶原化的158相比,致关节炎性显著增加。这些数据表明,MAV1携带一种对大鼠关节炎支原体诱导的关节炎发病机制很重要的因子。