Hunt M E, Brown D R
Department of Pathobiology, College of Veterinary Medicine, University of Florida, Gainesville, FL 32610-0880, USA.
Clin Diagn Lab Immunol. 2005 Dec;12(12):1370-7. doi: 10.1128/CDLI.12.12.1370-1377.2005.
Mycoplasma alligatoris causes acute lethal primary infection of susceptible hosts. A genome survey implicated sialidase and hyaluronidase, potential promoters of CD95-mediated eukaryotic cell death, as virulence factors of M. alligatoris. We used immunofluorescence imaging and flow cytometry to examine the effects of M. alligatoris infection in vitro on CD95 expression and apoptosis by alligator cardiac fibroblasts, a major cell type of a target organ of M. alligatoris infection in vivo. A uniform distribution of CD95 in primary cultured cardiac, skeletal muscle, and embryonic fibroblasts was demonstrated by using polyclonal antibodies against the N or C terminus of mouse or human CD95. Anti-CD95 antibodies reacted on Western blots of fibroblast lysates with a band with the predicted apparent molecular weight of CD95, but soluble CD95 was not detected in plasma from control or M. alligatoris-infected alligators. The proportion of CD95-gated cardiac fibroblasts increased threefold (P<0.01) 48 h after inoculation with M. alligatoris. Infection induced morphological changes in cardiac fibroblasts, including translocation of CD95 characteristic of apoptosis and an eightfold increase (P<0.16) in 5-bromo-2'-deoxyuridine (BrdU) incorporation measured in a terminal deoxynucleotide transferase dUTP nick end-labeling apoptosis assay. The proportion of BrdU-gated controls activated with agonistic immunoglobulin M against human CD95 also increased threefold (P<0.03 for muscle). Heat-inactivated M. alligatoris and sterile M. alligatoris-conditioned culture supernatant had no effect. This is the first report of a CD95 homolog in the class Reptilia and establishes a new model that can be used to test the direct bacterial interaction with upstream components of the CD95 signal transduction pathway.
扬子鳄支原体可引起易感宿主的急性致死性原发性感染。一项基因组调查表明,唾液酸酶和透明质酸酶这两种潜在的CD95介导的真核细胞死亡促进因子是扬子鳄支原体的毒力因子。我们利用免疫荧光成像和流式细胞术,在体外检测了扬子鳄支原体感染对扬子鳄心脏成纤维细胞(体内扬子鳄支原体感染靶器官的主要细胞类型)CD95表达和凋亡的影响。通过使用针对小鼠或人CD95的N端或C端的多克隆抗体,证明了CD95在原代培养的心脏、骨骼肌和胚胎成纤维细胞中呈均匀分布。抗CD95抗体在成纤维细胞裂解物的蛋白质印迹上与预测的CD95表观分子量的条带发生反应,但在对照或扬子鳄支原体感染的扬子鳄血浆中未检测到可溶性CD95。接种扬子鳄支原体48小时后,CD95门控的心脏成纤维细胞比例增加了三倍(P<0.01)。感染诱导心脏成纤维细胞发生形态变化,包括凋亡特征性的CD95易位,以及在末端脱氧核苷酸转移酶dUTP缺口末端标记凋亡试验中测得的5-溴-2'-脱氧尿苷(BrdU)掺入量增加了八倍(P<0.16)。用抗人CD95的激动性免疫球蛋白M激活的BrdU门控对照的比例也增加了三倍(肌肉组P<0.03)。热灭活的扬子鳄支原体和无菌的扬子鳄支原体条件培养上清液没有影响。这是关于爬行动物纲中CD95同源物的首次报道,并建立了一个新模型,可用于测试细菌与CD95信号转导途径上游成分的直接相互作用。