Inactivation of Pasteurella multocida within the mouse peritoneal cavity.

F M Collins, W H Woodruff
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Abstract

Normal ICR mice were injected intraperitoneally with 0.5 ml of thioglycollate broth or 5 x 10(8) heat-killed Pasteurella multocida vaccine and the number of polymorphs, lymphocytes and macrophages in the peritoneal washout suspensions were determined at intervals up to 72 hours. The stimulated mice were challenged intraperitoneally with opsonized or unopsonized P. multocida at increasing time intervals and the rate of growth by the organisms in the washout suspension was determined up to 60 minutes later. The opsonized bacilli were taken up by the 6 hr. exudate cells (50-60% PMNs) and their growth inhibited more effectively than when the 72 hr exudate cells were tested (only 10% PMNs). When the challenge inoculum was introduced into the peritoneal cavities of mice stimulated 6 hrs previously with 5 x 10(8) heat-killed P. multocida vaccine, up to 80% of the bacilli were inactivated over a 30 minute period. However, when 72 or 250 hr peritoneal exudate cells were tested, the inoculum was not inactivated, but showed an increasingly lethal effect.

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小鼠腹腔内多杀性巴氏杆菌的灭活。
对正常ICR小鼠腹腔注射0.5 ml巯基乙酸酯肉汤或5 × 10(8)热杀多杀性巴氏杆菌疫苗,每隔72小时测定腹膜冲洗悬浮液中多形细胞、淋巴细胞和巨噬细胞的数量。以增加的时间间隔向受刺激的小鼠腹腔注射多杀假单胞菌或非多杀假单胞菌,并在冲洗悬浮液中测定生物体的生长速度,直至60分钟后。在6小时内对调理杆菌进行吸收。泌出细胞(50-60% PMNs)和它们的生长受到抑制比72h时的泌出细胞(仅10% PMNs)更有效。6小时前,用5 × 10(8)热灭活多杀假单胞杆菌疫苗刺激小鼠腹膜腔,将攻毒接种物引入小鼠腹膜腔,在30分钟内,高达80%的杆菌灭活。然而,当对72或250小时腹膜渗出细胞进行检测时,接种物并未灭活,但显示出越来越致命的效果。
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