Peters Iain R, Helps Chris R, Gruffydd-Jones Timothy J, Day Michael J, Tasker Séverine
School of Clinical Veterinary Science, University of Bristol, Langford, Bristol, United Kingdom.
Clin Vaccine Immunol. 2010 Aug;17(8):1238-43. doi: 10.1128/CVI.00136-10. Epub 2010 Jun 2.
The aim of the present study was to characterize the antigenic specificity of the humoral immune response made by cats infected with the feline hemoplasma, Mycoplasma haemofelis. A crude M. haemofelis antigen preparation was prepared from red blood cells (RBCs) collected from a cat at the time of a high level of bacteremia. Plasma samples were collected from six cats before and after experimental infection with M. haemofelis, with regular sampling being performed from 15 to 149 or 153 days postinfection (dpi). Preinfection RBC membrane ghosts were prepared from these six cats and used to identify erythrocyte proteins that may have contaminated the M. haemofelis antigen preparation. The M. haemofelis antigen preparation comprised 11 protein bands. The immunodominant bands on Western blotting with infected cat plasma had molecular masses of 78, 68, 60, 48, and 38 kDa. Most cats (n = 5) had plasma antibody that reacted with at least one band (always including the one of 68 kDa) at 15 dpi, and all cats were seroreactive by 29 dpi. The maximum number of antibodies from an individual animal specific for an antigen was identified in plasma collected from 57 to 99 dpi. Contamination of the M. haemofelis antigen preparation with RBC membrane proteins was observed. The contaminating RBC proteins had molecular masses of from 71 to 72 kDa (consistent with band 4.2) and 261 and 238 kDa (consistent with spectrin), and these were recognized by all plasma samples. A range of M. haemofelis antigens is recognized by cats infected experimentally with the organism. These represent possible targets for immunoassays, but care must be taken to prevent false-positive results due to host protein contamination.
本研究的目的是表征感染猫血支原体(Mycoplasma haemofelis)的猫所产生的体液免疫反应的抗原特异性。从一只处于高菌血症水平的猫采集的红细胞(RBC)制备了粗制的猫血支原体抗原制剂。在实验性感染猫血支原体之前和之后,从六只猫采集血浆样本,并在感染后15至149或153天(dpi)进行定期采样。从这六只猫制备感染前的红细胞膜空泡,并用于鉴定可能污染猫血支原体抗原制剂的红细胞蛋白。猫血支原体抗原制剂包含11条蛋白带。用感染猫血浆进行蛋白质印迹时的免疫显性带的分子量为78、68、60、48和38 kDa。大多数猫(n = 5)在15 dpi时血浆抗体与至少一条带(总是包括68 kDa的那条带)发生反应,并且所有猫在29 dpi时均呈血清反应阳性。在感染后57至99 dpi采集的血浆中鉴定出个体动物针对一种抗原的抗体的最大数量。观察到猫血支原体抗原制剂被红细胞膜蛋白污染。污染的红细胞蛋白的分子量为71至72 kDa(与带4.2一致)以及261和238 kDa(与血影蛋白一致),并且所有血浆样本均能识别这些蛋白。实验感染该病原体的猫能识别一系列猫血支原体抗原。这些代表了免疫测定的可能靶点,但必须注意防止由于宿主蛋白污染导致的假阳性结果。