Duncan J L
Infect Immun. 1983 May;40(2):501-5. doi: 10.1128/iai.40.2.501-505.1983.
Streptococcal growth in vivo was studied with inoculated micropore filter chambers which were implanted into the peritoneal cavities of mice. Eight of nine group A strains and one group B strain grew in vivo, achieving concentrations of 10(7) to 10(9) CFU/ml in the chambers. Experiments with the Richards strain showed that the number of viable organisms remained high at 5 and 8 weeks after infection. The use of specific inhibitors and appropriate toxin-negative strains demonstrated that both cytolytic toxins produced by group A streptococci, streptolysin S and streptolysin O, were present in the culture fluids harvested from the chambers. This finding represents the first evidence that streptolysin S is produced in vivo. The host response to streptococci growing in vivo was examined by following the increase in serum antistreptolysin O levels. The response was first detected 2 weeks after chamber implantation and appeared to be maximal after 5 weeks. In addition, the production of antibody to streptococcal cell surface antigens was demonstrated indirectly with fluorescein-labeled anti-mouse immunoglobulin G.
通过将接种的微孔滤器小室植入小鼠腹腔来研究体内链球菌生长情况。9株A组菌株中的8株和1株B组菌株在体内生长,小室内细菌浓度达到10⁷至10⁹CFU/ml。对理查兹菌株进行的实验表明,感染后5周和8周时活菌数量仍维持在较高水平。使用特异性抑制剂和合适的毒素阴性菌株证明,从这些小室收获的培养液中存在A组链球菌产生的两种细胞溶解毒素,即链球菌溶血素S和链球菌溶血素O。这一发现首次证明了链球菌溶血素S可在体内产生。通过追踪血清抗链球菌溶血素O水平的升高来检测宿主对体内生长的链球菌的反应。该反应在小室植入后2周首次检测到,5周后似乎达到最大值。此外,用荧光素标记的抗小鼠免疫球蛋白G间接证明了针对链球菌细胞表面抗原的抗体产生。