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单核细胞增生李斯特菌F5817对正常与免疫受损C57B1/6J小鼠感染剂量的比较。

Comparison of Infectious Dose of Listeria monocytogenes F5817 as Determined for Normal Versus Compromised C57B1/6J Mice.

作者信息

Golnazarian Cecilia A, Donnelly Catherine W, Pintauro Stephen J, Howard Diantha B

机构信息

University of Vermont, Burlington, Vermont 05405.

出版信息

J Food Prot. 1989 Oct;52(10):696-701. doi: 10.4315/0362-028X-52.10.696.

DOI:10.4315/0362-028X-52.10.696
PMID:31003349
Abstract

The infectious dose of Listeria monocytogenes F5817, a serotype 4b human patient isolate, was determined following oral challenge in normal and compromised C57B1/6J mice. In an attempt to mimic human populations previously shown to be at risk to ingestion of L. monocytogenes , groups of mice used in this study consisted of the following: mice pretreated with hydrocortisone acetate or cimetidine; pregnant mice (12-14 d gestation); or beige mutants of C57B1/6J mice (deficient in lysosome production within monocytes and granulocytes). Mice were gavaged with varying levels of L. monocytogenes suspended in sterile 11% non-fat milk solids (NFMS). Upon expiration, the spleen, liver, lung, and brain were aseptically removed from mice. Organs were plated on LPM agar, and colonies were enumerated and biochemically confirmed as L. monocytogenes . Mice were considered infected if L. monocytogenes was recovered from at least one of the examined organs. In normal resistant C57B1/6J mice, the infectious dose (ID) ranged from 3.24-4.55 log CFU. In comparison, the ID for mice treated with 2.5 mg hydrocortisone acetate/day for 3d prior to infection decreased to 0.41 log CFU (range -1.91-2.74 log CFU). Administration of 0.25 mg hydrocortisone acetate/day for 3d prior to infection resulted in an ID similar to that calculated for normal mice. The ID calculated for pregnant mice was 2.48 log CFU, a value not significantly different from that of normal control mice. The response of beige mutants and cimetidine treated mice was comparable to that of normal controls, with ID values of 4.00 and 3.30 log CFU, respectively.

摘要

对血清型4b的人类患者分离株单核细胞增生李斯特菌F5817,在正常和免疫受损的C57B1/6J小鼠经口攻毒后测定其感染剂量。为了模拟先前显示有摄入单核细胞增生李斯特菌风险的人群,本研究中使用的小鼠组包括以下几种:用醋酸氢化可的松或西咪替丁预处理的小鼠;怀孕小鼠(妊娠12 - 14天);或C57B1/6J小鼠的米色突变体(单核细胞和粒细胞内溶酶体产生缺陷)。给小鼠灌胃悬浮于无菌11%脱脂乳固体(NFMS)中的不同水平的单核细胞增生李斯特菌。处死小鼠后,无菌取出脾脏、肝脏、肺和脑。将器官接种于LPM琼脂平板上,计数菌落并通过生化方法确认为单核细胞增生李斯特菌。如果从至少一个检测器官中分离到单核细胞增生李斯特菌,则认为小鼠被感染。在正常有抵抗力的C57B1/6J小鼠中,感染剂量(ID)范围为3.24 - 4.55 log CFU。相比之下,在感染前3天每天用2.5 mg醋酸氢化可的松处理的小鼠,其ID降至0.41 log CFU(范围 -1.91 - 2.74 log CFU)。在感染前3天每天给予0.25 mg醋酸氢化可的松,其ID与正常小鼠计算值相似。怀孕小鼠计算的ID为2.48 log CFU,该值与正常对照小鼠的ID无显著差异。米色突变体和西咪替丁处理小鼠的反应与正常对照相当,ID值分别为4.00和3.30 log CFU。

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