Mouse interstitial lung disease and pleuritis induction by human Mollicute-like organisms.

E Wirostko, L A Johnson, W J Wirostko
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Abstract

Mollicute-Like Organisms (MLO) are cell-wall deficient intracellular bacterial pathogens. As MLO are non-cultivable, detection is based on finding typical Mollicute bodies within the host cell using a transmission electron microscope. Extracellular Mollicutes cause disease by a variety of mechanisms. MLO cause disease by similar mechanisms, and in addition directly alter the host cell nucleus, replace the cytoplasm, and destroy the organelles. MLO parasitization of plant cells causes a well studied chronic vascular disease reversible by tetracycline antibiotics. Recently similar MLO were reported to cause human chronic ocular vasculitis. As it parasitizes, lyses, and destroys leucocytes, it has been termed Leucocytoclastic MLO. Inoculation of this MLO into mouse eyelids produced delayed onset chronic ocular and lethal cardiac vasculitis. All lesions demonstrated tissue lysis with leucocytic infiltrates and MLO parasitized leucocytes. MLO-caused human and mouse disease responds to Rifampin. This report describes the 40 interstitial lung disease lesions in 21 of 100 of those MLO inoculated mice vs 0 in 200 controls (P less than 0.05) and 27 pleuritis lesions in 17 mice vs 0 control mice (P less than 0.05). The lung and pleural disease were associated in 13 lesions and unassociated in 41 lesions. MLO parasitized leucocytes were found in both the lung and pleural lesions from six of six MLO inoculated mice versus none of six controls. As most human interstitial lung and pleural diseases are idiopathic and closely resemble this mouse disease, they may be induced by MLO and treatable by Rifampin.

人分子样生物诱导小鼠间质性肺疾病和胸膜炎。
mollicute -样生物(MLO)是细胞壁缺陷的细胞内细菌病原体。由于MLO是不可培养的,检测是基于使用透射电子显微镜在宿主细胞内寻找典型的Mollicute体。细胞外分子通过多种机制引起疾病。MLO致病机制类似,并直接改变宿主细胞核,取代细胞质,破坏细胞器。MLO寄生于植物细胞引起的慢性血管疾病已被充分研究,可被四环素类抗生素逆转。最近也有类似的MLO引起人慢性眼部血管炎的报道。由于它寄生、溶解和破坏白细胞,因此被称为白细胞破溃性MLO。将这种MLO接种到小鼠眼皮上可产生迟发性慢性眼部和致死性心脏血管炎。所有病变均表现为组织溶解伴白细胞浸润和MLO寄生白细胞。mlo引起的人和小鼠疾病对利福平有反应。本报告描述了100只接种MLO的小鼠中有21只出现40个间质性肺病变,而200只对照组中0个(P < 0.05); 17只小鼠出现27个胸膜炎病变,而对照组中0个(P < 0.05)。肺和胸膜病变相关13例,非相关41例。在6只接种了MLO的小鼠中,有6只在肺和胸膜病变中发现了MLO寄生的白细胞,而6只对照组中没有发现。由于大多数人类间质性肺和胸膜疾病都是特发性的,与这种小鼠疾病非常相似,它们可能是由MLO诱导的,利福平可以治疗。
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