Pardon P, Popoff M Y, Coynault C, Marly J, Miras I
INRA, Centre de Tours-Nouzilly, Pathologie de la Reproduction, Monnaie, France.
Ann Inst Pasteur Microbiol (1985). 1986 Jul-Aug;137B(1):47-60. doi: 10.1016/s0769-2609(86)80093-x.
The growth pattern of Salmonella enterica subsp. enterica serotype Typhimurium (Typhimurium) was studied in mice to examine the role of the 60-Mdal virulence-associated plasmid in the pathogenesis of mouse typhoid. After repeated subcultures at 45 degrees C, isogenic variants harbouring the virulence-associated plasmid (strains C52, TM122 and TM332) or having lost this large plasmid (strains C53, TM123 and TM333) were obtained from three parental strains (strains C5, TM12 and TM33, respectively). Plasmid pIP1350, present in strain C52, was tagged by Tn10 and transferred by successive conjugations to strains C53, TM123 and TM333. The behaviour of these three Typhimurium lines was studied in C57BL/6, DBA2, B6D2 (C57BL/6 X DBA2 F1 hybrid) and OF1 mice after oral infection, subcutaneous injection into the hind footpad or intravenous inoculation. The kinetics of organ colonization were followed at intervals after injection by enumeration of viable bacteria in caecum, mesenteric or popliteal lymph node, spleen, liver, kidney and lung depending on the route of infection. Strains harbouring virulence plasmid and their cured derivatives did not differ significantly in their ability to colonize caecal content and to translocate to draining lymph nodes. Elimination of the virulence plasmid was correlated with a significant reduction in the ability of cured variants to colonize spleen and liver. Reintroduction of the virulence plasmid into plasmidless variants restored the virulence to the level originally observed. These data demonstrate that a 60-Mdal plasmid in Typhimurium strains is necessary to ensure colonization of spleen and liver of experimentally infected mice.
研究了肠炎沙门氏菌肠炎亚种鼠伤寒血清型(鼠伤寒沙门氏菌)在小鼠中的生长模式,以检验60-Mdal毒力相关质粒在小鼠伤寒发病机制中的作用。在45℃反复传代培养后,从三个亲本菌株(分别为菌株C5、TM12和TM33)获得了携带毒力相关质粒的同基因变体(菌株C52、TM122和TM332)或丢失了该大质粒的变体(菌株C53、TM123和TM333)。菌株C52中存在的质粒pIP1350用Tn10进行标记,并通过连续的接合转移到菌株C53、TM123和TM333中。在口服感染、后足垫皮下注射或静脉接种后,在C57BL/6、DBA2、B6D2(C57BL/6×DBA2 F1杂交种)和OF1小鼠中研究了这三个鼠伤寒沙门氏菌品系的行为。根据感染途径,在注射后每隔一段时间通过计数盲肠、肠系膜或腘窝淋巴结、脾脏、肝脏、肾脏和肺中的活菌来跟踪器官定殖的动力学。携带毒力质粒的菌株及其治愈衍生物在定殖盲肠内容物和转移至引流淋巴结的能力上没有显著差异。毒力质粒的消除与治愈变体定殖脾脏和肝脏的能力显著降低相关。将毒力质粒重新引入无质粒变体可使毒力恢复到最初观察到的水平。这些数据表明,鼠伤寒沙门氏菌菌株中的60-Mdal质粒对于确保实验感染小鼠的脾脏和肝脏定殖是必要的。