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首页> 外文期刊>Pesquisa Veterinaria Brasileira >Detection of virulence-associated genes of Pasteurella multocida isolated from cases of fowl cholera by multiplex-PCR
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Detection of virulence-associated genes of Pasteurella multocida isolated from cases of fowl cholera by multiplex-PCR

机译:多重PCR检测禽霍乱病例中多杀性巴斯德氏菌的毒力相关基因

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> face="Verdana, Arial, Helvetica, sans-serif" size="2">The current systems of breeding poultry, based on high population density, increase the risk of spreading pathogens, especially those causing respiratory diseases and those that have more than one host. Fowl Cholera (FC) is one such pathogen, and even though it represents one of several avian diseases that should be considered in the differential diagnosis of notifiable diseases that present with sudden death, the pathogenesis and virulence factors involved in FC are still poorly understood. The objective of this study was to investigate twelve genes related to virulence in 25 samples of Pasteurella multocida isolated from FC cases in the southern region of Brazil through the development of multiplex PCR protocols. The protocols developed were capable of detecting all of the proposed genes. The ompH, oma87, sodC, hgbA, hgbB, exBD-tonB and nanB genes were present in 100% of the samples (25/25), the sodA and nanH genes were present in 96% (24/25), ptfA was present in 92% (23/25), and pfhA was present in 60% (15/25). Gene toxA was not identified in any of the samples studied (0/25). Five different genetic profiles were obtained, of which P1 (negative to toxA) was the most common. We concluded that the multiplex-PCR protocols could be useful tools for rapid and simultaneous detection of virulence genes. Despite the high frequency of the analyzed genes and the fact that all samples belonged to the same subspecies of P. multocida, five genetic profiles were observed, which should be confirmed in a study with a larger number of samples.
机译:> face =“ Verdana,Arial,Helvetica,sans-serif” size =“ 2”>基于高人口密度的当前家禽育种系统增加了传播病原体的风险,特别是引起呼吸道疾病和具有多个主机的主机。禽霍乱(FC)是一种这样的病原体,尽管它代表了在对突然死亡的应报告疾病进行鉴别诊断时应考虑的几种禽类疾病之一,但对FC的发病机理和致病性因素仍知之甚少。这项研究的目的是通过开发多重PCR方案,调查从巴西FC病例中分离出的25株多杀巴斯德氏菌样品中的十二种与毒力相关的基因。开发的协议能够检测所有提出的基因。 ompH , oma87 , sodC , hgbA , hgbB , exBD -tonB 和 nanB 基因存在于100%的样本中(25/25), sodA 和 nanH 基因是含量为96%(24/25), ptfA 含量为92%(23/25), pfhA 含量为60%(15/25)。在任何研究的样品中(0/25)未鉴定出基因 toxA 。获得了五种不同的遗传特征,其中P1(与 toxA 负)是最常见的。我们得出的结论是,多重PCR规程可能是快速且同时检测毒力基因的有用工具。尽管分析基因的频率很高,而且所有样品都属于 P的相同亚种。多杀菌,观察到五个遗传图谱,应在大量样本研究中予以证实。

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