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蓝狐实验性脑胞内原虫病。患病幼狐的临床和血清学检查。

Experimental encephalitozoonosis in the blue fox. Clinical and serological examinations of affected pups.

作者信息

Mohn S F

出版信息

Acta Vet Scand. 1982;23(4):503-14. doi: 10.1186/BF03546769.

Abstract

Two groups of blue fox pups about 1½— 2 and 2½—3 months old, respectively, suffering from experimental encephalitozoonosis, were examined clinically and serologically. Antibodies to Encephalitozoon cuniouli were detected in all pups, the titres varying within the range 10–12,800. In addition to unspecific signs of disease the pups showed various neurological disturbances including ataxia, posterior weakness, lameness and circling behaviour, terminaiting in recumbency, paralysis or convulsions. Reduced sight or blindness was observed occasionally. Some of the pups appeared thirsty. Haematological examinations revealed pronounced leukocytosis without any conspicuous shift within the various groups of leukocytes. Biochemical examinations of serum showed significant elevated values of urea nitrogen, creatinine, and magnesium concentrations, reflecting renal dysfunction. Alanine aminotransferase was found significantly depressed in both groups. Raised levels of total protein were demonstrated due to pronounced hyperglobulinaemia. This finding, together with the common occurrence of generalized polyarteritis nodosa and proliferations of plasma cells in clinically affected pups, is probably a result of autoimmune disturbances initiated directly or indirectly by the protozoan infection.

摘要

分别对两组患实验性脑胞内原虫病的蓝狐幼崽进行临床和血清学检查,两组幼崽年龄分别约为1.5 - 2个月和2.5 - 3个月。在所有幼崽中均检测到针对兔脑胞内原虫的抗体,抗体效价在10 - 12,800范围内变化。除了非特异性疾病体征外,幼崽还表现出各种神经功能障碍,包括共济失调、后肢无力、跛行和转圈行为,最终发展为侧卧、瘫痪或抽搐。偶尔观察到视力下降或失明。一些幼崽表现出口渴。血液学检查显示明显的白细胞增多,各白细胞亚群无明显偏移。血清生化检查显示尿素氮、肌酐和镁浓度显著升高,反映肾功能障碍。两组中丙氨酸转氨酶均显著降低。由于明显的高球蛋白血症,总蛋白水平升高。这一发现,连同在临床患病幼崽中普遍出现的结节性多动脉炎和浆细胞增生,可能是原生动物感染直接或间接引发的自身免疫紊乱的结果。

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Encephalitozoonosis in the blue fox--morphological identification of the parasite.蓝狐的脑胞内原虫病——寄生虫的形态学鉴定
Acta Pathol Microbiol Scand B. 1981 Apr;89(2):117-22. doi: 10.1111/j.1699-0463.1981.tb00162_89b.x.

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