Corney B G, Diallo I S, Wright L, Hewitson G, De Jong A, Tolosa X, Burrell P, Duffy P, Rodwell B, Boyle D B, Blackall P J
Animal Research Institute, Queensland Department of Primary Industries and Fisheries, Yeerongpilly, Queensland, Australia.
Avian Pathol. 2008 Dec;37(6):599-604. doi: 10.1080/03079450802449139.
A 5' Taq nuclease assay specific for Avibacterium paragallinarum was designed and optimized for use in diagnosing infectious coryza. The region chosen for assay design was one of known specificity for Av. paragallinarum. The assay detected Av. paragallinarum reference strains representing the three Page and the eight Kume serovars, and field isolates from diverse geographical locations. No cross-reactions were observed with other Avibacterium species, with other bacteria taxonomically related to Av. paragallinarum nor with bacteria and viruses likely to be present in swabs collected from suspected infectious coryza cases. The detection limit for the assay was 6 to 60 colony-forming units per reaction. Twenty-two out of 53 swabs collected from sick birds reacted in the 5' Taq nuclease assay, whereas Av. paragallinarum was not isolated from any of the swabs. All of the 22 swabs yielded other bacteria in culture. The presence of Av. paragallinarum in the swabs was also demonstrated by sequencing, thereby confirming the ability of the assay to detect Av. paragallinarum in the presence of other bacteria. The ability to quantify bacterial load in the swabs using the 5' Taq nuclease assay was demonstrated.
设计并优化了一种针对副鸡禽杆菌的5' Taq核酸酶检测方法,用于诊断传染性鼻炎。用于检测方法设计的区域是已知对副鸡禽杆菌具有特异性的区域之一。该检测方法可检测代表三个Page血清型和八个Kume血清型的副鸡禽杆菌参考菌株,以及来自不同地理位置的田间分离株。未观察到与其他禽杆菌属物种、与副鸡禽杆菌在分类学上相关的其他细菌,以及从疑似传染性鼻炎病例采集的拭子中可能存在的细菌和病毒发生交叉反应。该检测方法的检测限为每个反应6至60个菌落形成单位。从患病鸡采集的53份拭子中有22份在5' Taq核酸酶检测中呈阳性反应,而在任何拭子中均未分离到副鸡禽杆菌。所有22份拭子在培养中均产生了其他细菌。通过测序也证实了拭子中存在副鸡禽杆菌,从而证实了该检测方法在存在其他细菌的情况下检测副鸡禽杆菌的能力。证明了使用5' Taq核酸酶检测方法对拭子中细菌载量进行定量的能力。