Prior immunity to Ureaplasma urealyticum protects against respiratory infection in immunosuppressed mice.

IF 3.7 2区 生物学 Q2 MICROBIOLOGY
Maha Y Al-Jabri, Robin Patel, Derek Fleming
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Abstract

Ureaplasma species can cause systemic infections in immunocompromised hosts, including lung transplant recipients. Here, we investigated the impact of prior exposure to Ureaplasma urealyticum on the risk of U. urealyticum and Ureaplasma parvum infection in mice subjected to an immunosuppression regimen similar to that administered to solid organ transplant recipients. Mice were immunized with three intramuscular injections of U. urealyticum, with control mice injected with adjuvant only. Following immunization, mice received tacrolimus, mycophenolate mofetil, and methylprednisolone, and then were challenged with U. urealyticum or U. parvum intraperitoneally and intratracheally over 6 days. Relative U. urealyticum antibody levels in plasma were assessed over time, and lungs were harvested at sacrifice for bacterial load quantification, assessed using a color-changing unit assay. U. urealyticum antibody levels were higher in immunized compared with control animals (P < 0.0001), even when animals were immunosuppressed. U. urealyticum and U. parvum lung burden was reduced in immunized compared with control mice (~6 log10 reduction for U. urealyticum and <1 log10 reduction for U. parvum; P = 0.008 and 0.046, respectively). In summary, this study shows that prior exposure to live U. urealyticum provides some protection against infection with U. urealyticum.IMPORTANCEUreaplasma-induced hyperammonemia syndrome is a rare but potentially deadly complication of solid organ transplantation, especially lung transplantation. The pathophysiology of this relatively recently recognized condition is poorly understood, and it is unclear what factors may influence patient susceptibility. This study investigates the possible protective effects of prior exposure to Ureaplasma urealyticum in a mouse model subjected to an immunosuppression regimen similar to that given to lung transplant recipients. The findings show that prior exposure could provide protection against Ureaplasma lung infection.

对尿解脲原体的先期免疫可保护免疫抑制小鼠免受呼吸道感染。
解脲支原体可引起免疫功能低下宿主(包括肺移植受者)的全身感染。在这里,我们研究了之前接触过尿解解脲脲原体对小鼠感染尿解解脲脲原体和副猪脲原体风险的影响,小鼠接受的免疫抑制方案与实体器官移植受者接受的方案类似。小鼠肌肉注射三次尿解脲原体进行免疫,对照组小鼠只注射佐剂。免疫后,小鼠接受他克莫司、霉酚酸酯和甲基强的松龙治疗,然后在 6 天内腹腔和气管内接受 U. urealyticum 或 U. parvum 的挑战。评估血浆中U. urealyticum抗体的相对水平,并在牺牲时采集肺部进行细菌负荷定量,采用变色单位检测法进行评估。与对照组相比,免疫动物的 U. urealyticum 抗体水平更高(P < 0.0001),即使动物受到免疫抑制也是如此。与对照组相比,免疫小鼠的 U. urealyticum 和 U. parvum 肺负荷减少(U. urealyticum 减少约 6 log10,U. parvum 减少 10;P = 0.008 和 0.046)。重要意义解脲脲原体诱导的高氨血症综合征是一种罕见但可能致命的实体器官移植并发症,尤其是肺移植。人们对这种最近才认识到的疾病的病理生理学知之甚少,也不清楚哪些因素会影响患者的易感性。本研究调查了在小鼠模型中预先暴露于尿解脲支原体可能产生的保护作用,该小鼠模型接受的免疫抑制方案与肺移植受者接受的方案类似。研究结果表明,事先接触尿解支原体可为肺部感染提供保护。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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