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Characterization of pathogenesis of and immune response to Burkholderia pseudomallei K96243 using both inhalational and intraperitoneal infection models in BALB/c and C57BL/6 mice

机译:使用吸入和腹膜内感染模型在BALB / c和C57BL / 6小鼠中表征假性伯克霍尔德氏菌K96243的发病机理和免疫应答

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摘要

Burkholderia pseudomallei, the etiologic agent of melioidosis, is a Gram negative bacterium designated as a Tier 1 threat. This bacterium is known to be endemic in Southeast Asia and Northern Australia and can infect humans and animals by several routes. Inhalational melioidosis has been associated with monsoonal rains in endemic areas and is also a significant concern in the biodefense community. There are currently no effective vaccines for B. pseudomallei and antibiotic treatment can be hampered by non-specific symptomology and also the high rate of naturally occurring antibiotic resistant strains. Well-characterized animal models will be essential when selecting novel medical countermeasures for evaluation prior to human clinical trials. Here, we further characterize differences between the responses of BALB/c and C57BL/6 mice when challenged with low doses of a low-passage and well-defined stock of B. pseudomallei K96243 via either intraperitoneal or aerosol routes of exposure. Before challenge, mice were implanted with a transponder to collect body temperature readings, and daily body weights were also recorded. Mice were euthanized on select days for pathological analyses and determination of the bacterial burden in selected tissues (blood, lungs, liver, and spleen). Additionally, spleen homogenate and sera samples were analyzed to better characterize the host immune response after infection with aerosolized bacteria. These clinical, pathological, and immunological data highlighted and confirmed important similarities and differences between these murine models and exposure routes.
机译:类鼻疽病的病原体伯克霍尔德氏菌是一种革兰氏阴性细菌,被指定为第1级威胁。已知这种细菌在东南亚和北澳大利亚是地方性的,可以通过几种途径感染人类和动物。吸入类li虫病与流行地区的季风降雨有关,也是生物防御界的重大关切。目前尚无用于假疟原虫的有效疫苗,非特异性症状以及高比率的天然抗生素抗性菌株均无法阻碍抗生素治疗。当在人类临床试验之前选择新颖的医学对策进行评估时,特征明确的动物模型将至关重要。在这里,我们进一步表征当通过腹膜内或气溶胶暴露途径,以低剂量的低通量和界限分明的B. pseudomallei K96243小剂量攻击时,BALB / c和C57BL / 6小鼠的反应之间存在差异。攻击前,将小鼠植入应答器以收集体温读数,并记录每日体重。在选定的日子对小鼠实施安乐死,以进行病理分析和确定选定组织(血液,肺,肝和脾)中的细菌负荷。另外,对脾匀浆和血清样品进行了分析,以更好地表征气溶胶化细菌感染后的宿主免疫反应。这些临床,病理学和免疫学数据突显并证实了这些鼠模型和暴露途径之间的重要异同。

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