Dziva Francis, Muhairwa Amandus P, Bisgaard Magne, Christensen Henrik
Division of Microbiology, Institute for Animal Health, Compton, Newbury, Berkshire, UK.
Vet Microbiol. 2008 Apr 1;128(1-2):1-22. doi: 10.1016/j.vetmic.2007.10.018. Epub 2007 Oct 23.
Pasteurella multocida is responsible for major animal diseases of economic significance in both developed and developing countries whereas human infections related to this bacterium are infrequent. Significantly, development of a carrier status or latent infections plays a critical role in the epidemiology of these diseases. Aiming at increased knowledge of these infections, we examine potential diagnostic and selected typing systems for investigating diseases caused by P. multocida. Detection of P. multocida from clinical specimen by; (i) isolation and identification, (ii) polymerase chain reaction (PCR), iii) specific hybridisation probes, (iv) serological tests and (v) other alternative methods is critically evaluated. These detection systems provide a wide spectrum of options for rapid diagnosis and for detecting and understanding of latent infections in herd/flock health control programmes, though PCR methods for detecting P. multocida in clinical specimen appear increasingly preferred. For establishing the clonality of outbreak strains, we select to discuss macromolecular profiling, serotyping, biotyping, restriction enzyme analysis, ribotyping and multiplex PCR typing. Although P. multocida infections can be rapidly diagnosed with molecular and serological tests, isolation and accurate species identification are central to epidemiological tracing of outbreak strains. Our review brings together comprehensive and essential information that may be adapted for confirming diagnosis and determining the molecular epidemiology of diseases associated with P. multocida.
多杀性巴氏杆菌在发达国家和发展中国家均引发具有重大经济意义的主要动物疾病,而与该细菌相关的人类感染则较为罕见。重要的是,携带状态或潜伏感染的发展在这些疾病的流行病学中起着关键作用。为了增加对这些感染的了解,我们研究了用于调查由多杀性巴氏杆菌引起的疾病的潜在诊断方法和选定的分型系统。对通过以下方法从临床标本中检测多杀性巴氏杆菌进行了严格评估:(i)分离和鉴定,(ii)聚合酶链反应(PCR),(iii)特异性杂交探针,(iv)血清学检测和(v)其他替代方法。这些检测系统为快速诊断以及在畜群/禽群健康控制计划中检测和了解潜伏感染提供了广泛的选择,尽管用于检测临床标本中多杀性巴氏杆菌的PCR方法似乎越来越受到青睐。为了确定暴发菌株的克隆性,我们选择讨论大分子谱分析、血清分型、生物分型、限制性酶切分析、核糖体分型和多重PCR分型。尽管可以通过分子和血清学检测快速诊断多杀性巴氏杆菌感染,但分离和准确的菌种鉴定对于暴发菌株的流行病学追踪至关重要。我们的综述汇集了全面且必要的信息,这些信息可用于确诊以及确定与多杀性巴氏杆菌相关疾病的分子流行病学。