Zierdt C H, Peterson D L, Swan J C, MacLowry J D
J Clin Microbiol. 1982 Jan;15(1):74-7. doi: 10.1128/jcm.15.1.74-77.1982.
Thirteen representative pathogenic bacterial species were used to create septicemia in rabbits, by injecting 10(6) colony-forming units into the marginal ear vein. At a selected time, usually 30 to 60 min after injection, heart blood was drawn into heparin and dispensed in 5.0-,0.5-, and 0.1-ml volumes into duplicate bottles of commercial brain heart infusion broth with sodium polyanetholesulfonate, and into duplicate bottles of a newly developed blood-lysing solution. Lysed blood was filtered, and the filter membranes were cultured in brain heart infusion broth. At the 5.0-ml blood inoculum level, of 126 total culture bottles (63 rabbits) for each system, 83 conventional cultures versus 109 lysis-filtration cultures were positive. At the 0.5-ml blood inoculum, 20 of 126 conventional culture bottles were positive, versus 66 of 126 lysis-filtration cultures. At the 0.1-ml blood inoculum, 2 of 126 conventional culture bottles were positive, versus 30 of 126 lysis-filtration cultures. Overall, 105 of 378 conventional cultures and 205 of 378 lysis-filtration cultures were positive. The advantage of the lysis-filtration system was striking for both gram-positive and gram-negative organisms at all inoculum concentrations, but was greater for gram-positive organisms. Most significant was the rate of recovery by this new system, when the number of bacteria in the blood was reduced to the point where recovery by conventional culture was unlikely. It is postulated that the superiority of lysis-filtration culture may be due to release of bacteria by lysis of phagocytes, preventing continued loss of pathogens by intracellular destruction during the first hours of blood culture.
选用13种具有代表性的致病细菌,通过向兔耳缘静脉注射10⁶菌落形成单位来制造败血症。在选定的时间,通常是注射后30至60分钟,将心脏血液抽入含肝素的容器中,并分别以5.0毫升、0.5毫升和0.1毫升的体积分装到两瓶含有聚茴香脑磺酸钠的市售脑心浸液肉汤中,以及分装到两瓶新研制的血液裂解溶液中。裂解后的血液经过过滤,滤膜在脑心浸液肉汤中培养。在每个系统126个总培养瓶(63只兔子)的5.0毫升血液接种水平下,83份传统培养物呈阳性,而109份裂解过滤培养物呈阳性。在0.5毫升血液接种量时,126个传统培养瓶中有20个呈阳性,而126个裂解过滤培养物中有66个呈阳性。在0.1毫升血液接种量时,126个传统培养瓶中有2个呈阳性,而126个裂解过滤培养物中有30个呈阳性。总体而言,378份传统培养物中有105份呈阳性,378份裂解过滤培养物中有205份呈阳性。在所有接种浓度下,裂解过滤系统对革兰氏阳性菌和革兰氏阴性菌的优势都很显著,但对革兰氏阳性菌的优势更大。最显著的是,当血液中的细菌数量减少到传统培养难以恢复的程度时,这种新系统的恢复率。据推测,裂解过滤培养的优越性可能是由于吞噬细胞裂解释放出细菌,从而防止了在血培养的最初几个小时内病原体因细胞内破坏而持续损失。