Marks Stanley L, Kather Elizabeth J
Department of Medicine and Epidemiology, University of California at Davis, School of Veterinary Medicine, Davis, CA 95616, USA.
Vet Clin North Am Small Anim Pract. 2003 Sep;33(5):1029-60. doi: 10.1016/s0195-5616(03)00091-3.
The clinical documentation of enteropathogenic bacteria causing diarrhea in dogs is clouded by the presence of many of these organisms existing as normal constituents of the indigenous intestinal flora. The diagnosis of a putative bacterial enteropathogen(s) in dogs should be made based on a combination of parameters, including signalment and predisposing factors, clinical signs, serologic assays for toxins, fecal culture, and PCR. Relying on results of fecal culture alone is problematic, because C perfringens, C difficile, Campylobacter spp, and pathogenic and non-pathogenic E coli are commonly isolated from apparently healthy dogs [10,13,33]. Nevertheless, culture may be useful in procuring isolates for the application of molecular techniques, such as PCR, for detection of specific toxin genes or molecular typing of isolated strains to establish clonality in suspected outbreaks. The oversimplistic attempt to characterize bacterially associated diarrhea by anatomic localization of clinical signs should be discouraged, because most of the previously mentioned bacteria have been associated with small and large intestinal diarrhea. Accurate diagnosis of infections may require diagnostic laboratories to incorporate PCR-based assays using genus- and species-specific primers to facilitate detection of toxin genes and differentiation of species that appear phenotypically and biochemically similar. There has been tremendous interest in the application of microarray technology for the simultaneous detection of thousands of genes or target DNA sequences on one glass slide. This powerful tool could be used for detection of specific pathogenic bacterial strains in fecal specimens obtained from dogs in the future.
许多作为肠道固有菌群正常组成部分的微生物的存在,使得犬肠道致病菌引起腹泻的临床记录变得模糊不清。犬疑似细菌性肠道病原体的诊断应基于多种参数的综合判断,包括品种特征和诱发因素、临床症状、毒素血清学检测、粪便培养及聚合酶链反应(PCR)。仅依靠粪便培养结果存在问题,因为产气荚膜梭菌、艰难梭菌、弯曲杆菌属以及致病性和非致病性大肠杆菌通常可从看似健康的犬只中分离出来[10,13,33]。然而,培养对于获取分离株以应用分子技术(如PCR)检测特定毒素基因或对分离菌株进行分子分型以确定疑似暴发中的克隆性可能是有用的。应避免通过临床症状的解剖定位来简单地对细菌性腹泻进行特征描述,因为上述大多数细菌都与小肠和大肠腹泻有关。感染的准确诊断可能需要诊断实验室采用基于PCR的检测方法,使用属特异性和种特异性引物,以促进毒素基因的检测以及对表型和生化特征相似的菌种进行区分。人们对微阵列技术在一张载玻片上同时检测数千个基因或靶DNA序列的应用产生了浓厚兴趣。这个强大的工具未来可用于检测从犬只粪便样本中分离出的特定致病细菌菌株。