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Non-invasive three-dimensional imaging of Escherichia coli K1 infection using diffuse light imaging tomography combined with micro-computed tomography

机译:利用漫射光成像断层扫描结合微型计算机断层扫描技术对大肠杆菌K1感染进行无创三维成像

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摘要

In contrast to two-dimensional bioluminescence imaging, three dimensional diffuse light imaging tomography with integrated micro-computed tomography (DLIT-μCT) has the potential to realise spatial variations in infection patterns when imaging experimental animals dosed with derivatives of virulent bacteria carrying bioluminescent reporter genes such as the lux operon from the bacterium Photorhabdus luminescens. The method provides an opportunity to precisely localise the bacterial infection sites within the animal and enables the generation of four-dimensional movies of the infection cycle. Here, we describe the use of the PerkinElmer IVIS SpectrumCT in vivo imaging system to investigate progression of lethal systemic infection in neonatal rats following colonisation of the gastrointestinal tract with the neonatal pathogen Escherichia coli K1. We confirm previous observations that these bacteria stably colonize the colon and small intestine following feeding of the infectious dose from a micropipette; invading bacteria migrate across the gut epithelium into the blood circulation and establish foci of infection in major organs, including the brain. DLIT-μCT revealed novel multiple sites of colonisation within the alimentary canal, including the tongue, oesophagus and stomach, with penetration of the non-keratinised oesophageal epithelial surface, providing strong evidence of a further major site for bacterial dissemination. We highlight technical issues associated with imaging of infections in new born rat pups and show that the whole-body and organ bioburden correlates with disease severity.
机译:与二维生物发光成像相比,带有集成微计算机断层扫描(DLIT-μCT)的三维漫射光成像层析成像在对实验动物进行剂量为带有生物发光报告基因的强毒细菌衍生物的成像实验时,有可能实现感染模式的空间变化如来自光致发光菌的勒克斯操纵子。该方法提供了在动物内精确定位细菌感染部位的机会,并使得能够产生感染周期的三维电影。在这里,我们描述了PerkinElmer IVIS SpectrumCT体内成像系统的使用,以调查在胃肠道中新生病原体大肠杆菌K1定殖后新生大鼠致命性全身感染的进程。我们确认以前的观察结果,即从微量移液管中喂入感染剂量后,这些细菌稳定地定居在结肠和小肠中。入侵的细菌穿过肠道上皮迁移进入血液循环,并在包括大脑在内的主要器官中建立了感染灶。 DLIT-μCT显示出消化道内新的多个定居点,包括舌头,食道和胃,并且未角化的食道上皮表面渗透,为进一步的主要细菌传播位点提供了有力的证据。我们重点介绍了与新生大鼠幼崽感染成像相关的技术问题,并显示了全身和器官的生物负荷与疾病严重程度相关。

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