Nathues H, Oliveira C J B, Wurm M, Grosse Beilage E, Givisiez P E N
Field Station for Epidemiology, University of Veterinary Medicine Hannover, Foundation, Hannover, Germany.
J Vet Med A Physiol Pathol Clin Med. 2007 Nov;54(9):532-8. doi: 10.1111/j.1439-0442.2007.00995.x.
Diarrhoea in growing and finishing pigs is usually caused by infectious agents and laboratory diagnosis is a prerequisite for efficient therapy. Cultivation of Brachyspira hyodysenteriae or Brachyspira pilosicoli and detection of Lawsonia intracellularis by means of immunofluorescence tests (IFT) are time-consuming and in some cases lack sensitivity. A multiplex-PCR was designed to detect simultaneously these three pathogens in faeces and tissue samples, allowing the differential diagnosis of dysentery, intestinal spirochaetosis and proliferative enteropathy. Detection limits for B. hyodysenteriae, B. pilosicoli and L. intracellularis were 10(4), 10(2) and 10(3) copies respectively. Agreement between multiplex-PCR and nested-PCR or cultivation was considered substantial to almost perfect. Agreement between multiplex-PCR and IFT in detecting L. intracellularis was only moderate, which was probably related to false-positive results given by IFT. The multiplex-PCR described herein is a valuable tool for the rapid and simultaneous detection of three different pathogens in porcine samples causing enteric diseases.
生长育肥猪的腹泻通常由感染因子引起,实验室诊断是有效治疗的前提条件。培养猪痢疾短螺旋体或毛样短螺旋体以及通过免疫荧光试验(IFT)检测胞内劳森菌耗时且在某些情况下缺乏敏感性。设计了一种多重PCR来同时检测粪便和组织样本中的这三种病原体,以便对痢疾、肠道螺旋体病和增生性肠炎进行鉴别诊断。猪痢疾短螺旋体、毛样短螺旋体和胞内劳森菌的检测限分别为10⁴、10²和10³拷贝。多重PCR与巢式PCR或培养之间的一致性被认为是高度一致到几乎完美。多重PCR与IFT在检测胞内劳森菌方面的一致性仅为中等,这可能与IFT给出的假阳性结果有关。本文所述的多重PCR是一种用于快速同时检测猪样本中引起肠道疾病的三种不同病原体的有价值工具。