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首页> 外文期刊>Applied and Environmental Microbiology >Determination of virulence of different strains of Listeria monocytogenes and Listeria innocua by oral inoculation of pregnant mice.
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Determination of virulence of different strains of Listeria monocytogenes and Listeria innocua by oral inoculation of pregnant mice.

机译:通过口服接种妊娠小鼠确定单核细胞增生李斯特菌和无毒李斯特菌不同菌株的毒力。

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A pregnant mouse model was developed to follow the course of infection after peroral inoculation with six different strains of Listeria monocytogenes and one strain of Listeria innocua. Tissues were sampled and analyzed by microbiologic and histologic methods for 5 days postinoculation. In gnotobiotic pregnant BALB/c mice, L. monocytogenes Scott A (SA), serotype 4b, colonized the gastrointestinal tract, translocated to the livers and spleens of mice by day 1 postinoculation, and multiplied in these tissues until day 4. Infection of the placental tissues occurred by days 3 and 4 and was followed by infection of the fetuses. Little damage of colonic and cecal tissues was evident by histologic examination. Livers and spleens showed a cellular immune response; a similar immune response was not detected in the placentas or fetuses. A rough variant of L. monocytogenes SA which was as virulent as the parent strain in mice when injected intraperitoneally was less virulent perorally and did not consistently infect the fetuses. L. monocytogenes ATCC 19113, serotype 3a, did not colonize the gastrointestinal tract, nor was it isolated from any internal tissue. L. monocytogenes strains of serotypes 1/2a and 1/2b behaved like the SA strain in this mouse model. L. innocua colonized the gastrointestinal tract and translocated to the livers and spleens but did not survive in these organs and rapidly disappeared without infecting placental and fetal tissues. In comparison with gnotobiotic mice, conventional pregnant mice inoculated with L. monocytogenes strains showed less consistent infection. These results suggest that the gnotobiotic pregnant mouse is a useful model for detecting differences in virulence relating to colonization, invasiveness, and uteroplacental infection which cannot be detected by intraperitoneal inoculation of mice.
机译:经口接种六种不同单核细胞增生李斯特菌和一种无毒李斯特菌经口接种后,开发了一种怀孕小鼠模型。接种后5天,通过微生物学和组织学方法对组织取样并分析。在致癌生物怀孕的BALB / c小鼠中,血清单核细胞增生李斯特菌Scott A(SA)(血清型4b)在胃肠道定植,在接种后第1天转移到小鼠的肝脏和脾脏,并在这些组织中繁殖直至第4天。胎盘组织发生在第3和4天,随后是胎儿感染。组织学检查显示结肠和盲肠组织几乎没有损伤。肝和脾显示出细胞免疫反应。在胎盘或胎儿中未检测到类似的免疫反应。腹膜内注射时,单核细胞增生李斯特氏菌SA的粗变体与小鼠的亲本菌株一样具有毒性,经口的毒性较小,并且不能始终如一地感染胎儿。单核细胞增生李斯特菌ATCC 19113,血清型3a,未在胃肠道定植,也未从任何内部组织中分离出来。在此小鼠模型中,血清型1 / 2a和1 / 2b的单核细胞增生李斯特氏菌菌株的行为类似于SA菌株。无害乳杆菌在胃肠道中定居并转移至肝脏和脾脏,但在这些器官中不能存活,并且在不感染胎盘和胎儿组织的情况下迅速消失。与gnotobiotic小鼠相比,接种单核细胞增生李斯特菌菌株的常规妊娠小鼠表现出较少的一致感染。这些结果表明,致癌的妊娠小鼠是用于检测与定植,侵袭性和子宫胎盘感染有关的毒力差异的有用模型,这些差异不能通过小鼠腹膜内接种来检测。

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