Mendoza-Espinoza Alfredo, Koga Ysabel, Zavaleta Amparo I
Laboratorio de Biología Molecular, Facultad de Farmacia y Bioquímica, Universidad Nacional Mayor de San Marcos, Lima 1, Peru.
Avian Dis. 2008 Mar;52(1):54-8. doi: 10.1637/8036-062507-Reg.
A molecular technique based on the restriction fragment length polymorphism of the 16S ribosomal genes amplified by a polymerase chain reaction (PCR), referred to as amplified 16S ribosomal DNA restriction analysis (ARDRA), was designed to identify 19 Avibacterium paragallinarum strains isolated from infraorbital sinus and nasal turbinate bone samples of broiler chickens, breeders, and laying hens from different regions of Peru. The 16S rDNA was amplified by PCR using a pair of bacterial universal primers and restriction analysis of 16S rDNA sequences was done to select endonucleases with the highest number of cutting points inside the 16S rDNA. The DNA patterns with DdeI and RsaI endonucleases were identical for the 19 A. paragallinarum strains, but differed from those obtained for Ornithobacterium rhinotracheale, a bacterium with a high genetic and phenotypic resemblance to A. paragallinarum, as well as from Escherichia coli, a bacterium associated with infectious coryza. The ARDRA method could prove to be valuable for molecular identification of A. paragallinarum, a microorganism implicated in respiratory diseases in commercial birds.
一种基于聚合酶链反应(PCR)扩增的16S核糖体基因限制性片段长度多态性的分子技术,称为扩增16S核糖体DNA限制性分析(ARDRA),旨在鉴定从秘鲁不同地区的肉鸡、种鸡和蛋鸡的眶下窦和鼻甲骨样本中分离出的19株副鸡禽杆菌菌株。使用一对细菌通用引物通过PCR扩增16S rDNA,并对16S rDNA序列进行限制性分析,以选择在16S rDNA内切割点数量最多的内切酶。19株副鸡禽杆菌菌株用DdeI和RsaI内切酶得到的DNA图谱相同,但与鼻气管鸟杆菌(一种在遗传和表型上与副鸡禽杆菌高度相似的细菌)以及与传染性鼻炎相关的大肠杆菌所得到的图谱不同。ARDRA方法可能被证明对副鸡禽杆菌的分子鉴定有价值,副鸡禽杆菌是一种与商业禽类呼吸道疾病有关的微生物。