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人类类支原体样微生物诱导小鼠间质性肺病和胸膜炎

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

作者信息

Wirostko E, Johnson L A, Wirostko W J

机构信息

Edward S. Harkness Eye Institute, Columbia-Presbyterian Medical Center, New York, NY 10032.

出版信息

Br J Exp Pathol. 1988 Dec;69(6):891-902.

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.

摘要

类支原体生物(MLO)是细胞壁缺陷的细胞内细菌病原体。由于MLO不可培养,检测基于使用透射电子显微镜在宿主细胞内发现典型的支原体小体。细胞外支原体通过多种机制致病。MLO通过类似机制致病,此外还直接改变宿主细胞核、取代细胞质并破坏细胞器。MLO对植物细胞的寄生会引发一种经充分研究的慢性血管疾病,可用四环素抗生素逆转。最近有报道称,类似的MLO会导致人类慢性眼部血管炎。由于它寄生、裂解并破坏白细胞,因此被称为白细胞破碎性MLO。将这种MLO接种到小鼠眼睑会导致延迟发作的慢性眼部和致命性心脏血管炎。所有病变均表现为组织溶解,伴有白细胞浸润以及MLO寄生的白细胞。MLO引起的人类和小鼠疾病对利福平有反应。本报告描述了在100只接种MLO的小鼠中有21只出现40处间质性肺病病变,而200只对照小鼠中为0处(P<0.05),以及17只小鼠出现27处胸膜炎病变,对照小鼠中为0处(P<0.05)。肺部和胸膜疾病在13处病变中相关,在41处病变中不相关。在6只接种MLO的小鼠的肺部和胸膜病变中均发现了MLO寄生的白细胞,而6只对照小鼠中均未发现。由于大多数人类间质性肺病和胸膜疾病是特发性的,且与这种小鼠疾病极为相似,它们可能由MLO诱发,可用利福平治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ab8/2013284/9591d2256e56/brjexppathol00006-0134-a.jpg

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