首页> 美国卫生研究院文献>Immunology >The in vivo division and death rates of Salmonella typhimurium in the spleens of naturally resistant and susceptible mice measured by the superinfecting phage technique of Meynell.
【2h】

The in vivo division and death rates of Salmonella typhimurium in the spleens of naturally resistant and susceptible mice measured by the superinfecting phage technique of Meynell.

机译:用Meynell的超感染噬菌体技术测量了自然抵抗力和易感小鼠脾脏中鼠伤寒沙门氏菌的体内分裂和死亡率。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Salmonella typhimurium appears to divide faster in the spleen of naturally susceptible BALB/c than in resistant (B10 x A/J)F1 mice. S. typhimurium M526 is an LT2 derivative lysogenic for a non-excluding P22 mutant which allows superinfection with a second, non-replicating, P22 phage so that the proportion of superinfected organisms halves at each division. The true in vivo division and death rates can be calculated from successive determinations of the proportion of superinfected organisms and the viable count. It was found that the division time was 2.86 h in BALB/c and 5.02 h in (B10 x A/J)F1; the death rate was low and actually greater in the susceptible BALB/c strain. These results suggest that the gene controlling in vivo salmonella net growth rate, which is very important in natural resistance to salmonella infection, acts very early by regulating the division rate, perhaps inside macrophages. The actual mechanism remains unknown.
机译:鼠伤寒沙门氏菌似乎在自然易感的BALB / c脾脏中的分裂要快于抗性(B10 x A / J)F1小鼠。鼠伤寒沙门氏菌M526是LT2衍生物,对非排他性P22突变体具有致溶性,可通过第二个非复制性P22噬菌体进行超级感染,从而使每次感染时超级感染生物的比例减半。真正的体内分裂和死亡率可以通过连续测定超级感染生物的比例和存活数来计算。结果表明,BALB / c的分裂时间为2.86 h,(B10 x A / J)F1的分裂时间为5.02 h。在易感的BALB / c菌株中,死亡率很低,实际上更高。这些结果表明,控制体内沙门氏菌净生长速率的基因在沙门氏菌感染的天然抗性中非常重要,它通过调节分裂速度(可能在巨噬细胞内部)非常早地起作用。实际机制仍然未知。

著录项

  • 期刊名称 Immunology
  • 作者

    C E Hormaeche;

  • 作者单位
  • 年(卷),期 2014(41),4
  • 年度 2014
  • 页码 973–979
  • 总页数 7
  • 原文格式 PDF
  • 正文语种
  • 中图分类 免疫学;
  • 关键词

相似文献

  • 外文文献
  • 中文文献
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号