Neyrolles Olivier, Brenner Catherine, Prevost Marie-Christine, Fontaine Thierry, Montagnier Luc, Blanchard Alain
Unité d'Oncologie Virale28, rue du Dr Roux, 75724 Paris Cedex 15, France.
Laboratoire des Aspergillus Institut Pasteur, 28, rue du Dr Roux, 75724 Paris Cedex 15, France.
Microbiology (Reading). 1998 May;144 ( Pt 5):1247-1255. doi: 10.1099/00221287-144-5-1247.
Among the wall-less mycoplasmas only a few species have been identified with a capsule at their cell surface. Mycoplasma penetrans is a recently identified mycoplasma with unique morphology, isolated from HIV-infected patients. Using transmission electron microscopy, it was found that M. penetrans is surrounded by capsular material 11 nm (strain GTU-54-6A1) to 30 nm (strain HF-2) thick, which can be stained with ruthenium red and labelled with cationized ferritin. The polysaccharide composition of this capsule was indicated by its staining with periodic acid-thiocarbohydrazide silver proteinate and the abolition of ruthenium red staining of the cell surface by neuraminidase treatment. In addition, proteinase K treatment of the M. penetrans cells resulted in removal of the capsule, suggesting that polypeptides may contribute in anchoring it to the membrane or in its stability. Two different types of glycosylated material were detected in mycoplasma extracts by SDS-PAGE and periodic acid-Schiff staining. The first component was a high-molecular-mass material, which was heat- and proteinase-K-labile and which probably constitutes the capsular polymer. The other component was a low-molecular-mass glycolipid fraction, which was proteinase-K-, heat- and EDTA-resistant. The identification of a capsule at the M. penetrans cell surface is of particular interest for a mycoplasma which has been shown to adhere to various host cells and to penetrate into their intracellular compartments. The capsule may have significance in the pathogenesis of disease associated with infection by this organism.
在无细胞壁的支原体中,只有少数几种在其细胞表面被鉴定出有荚膜。穿透支原体是一种最近鉴定出的具有独特形态的支原体,从感染HIV的患者中分离得到。通过透射电子显微镜发现,穿透支原体被厚度为11纳米(GTU-54-6A1株)至30纳米(HF-2株)的荚膜物质所包围,这种物质可用钌红染色并用阳离子铁蛋白标记。该荚膜的多糖成分通过其过碘酸 - 硫代碳酰肼银蛋白染色以及神经氨酸酶处理后细胞表面钌红染色的消失得以表明。此外,用蛋白酶K处理穿透支原体细胞会导致荚膜去除,这表明多肽可能有助于将其锚定在膜上或维持其稳定性。通过SDS - PAGE和过碘酸 - 希夫染色在支原体提取物中检测到两种不同类型的糖基化物质。第一种成分是高分子量物质,对热和蛋白酶K敏感,可能构成荚膜聚合物。另一种成分是低分子量糖脂部分,对蛋白酶K、热和EDTA具有抗性。对于已被证明能粘附于各种宿主细胞并穿透进入其细胞内区室的支原体而言,在穿透支原体细胞表面鉴定出荚膜具有特别的意义。该荚膜可能在与这种生物体感染相关的疾病发病机制中具有重要意义。