Liu D, Roycroft C, Samuel J, Webber J
Department of Agriculture, Pastoral and Veterinary Institute, Hamilton, Victoria, Australia.
Res Vet Sci. 1995 Sep;59(2):102-5. doi: 10.1016/0034-5288(95)90040-3.
A total of 141 Dichelobacter nodosus isolates from 46 merino sheep farms with various clinical forms of footrot was examined by the gelatin gel test and the polymerase chain reaction (PCR) using virulent (Vf2 and Vr2) and benign (Bf and Br) specific primers. Isolates from sheep with virulent and high intermediate footrot usually produced relatively thermostable proteases, but a decreasing proportion of the isolates from sheep with medium and low intermediate or benign footrot had thermostable proteases, as determined by the gelatin gel test. The amplification by PCR of a major band of 857 bp by Vf2 and Vr2 was often associated with isolates from the more virulent forms of footrot whereas the presence of a major band of 1300 bp by Vf2 and Vr2 and/or a band of 609 bp by Bf and Br was associated with isolates from less virulent forms of footrot. Nevertheless, the virulent and benign gene regions represented by Vf2 and Vr2 and Bf and Br are only two of the many factors involved in determining the virulence of D nodosus. As a result the relationship observed between the clinical manifestations of footrot and specific DNA products amplified by PCR was not complete.
使用毒力(Vf2和Vr2)及良性(Bf和Br)特异性引物,通过明胶凝胶试验和聚合酶链反应(PCR)对来自46个患有各种临床型腐蹄病的美利奴绵羊场的141株结节拟杆菌分离株进行了检测。明胶凝胶试验表明,来自患有强毒和高中度腐蹄病绵羊的分离株通常产生相对耐热的蛋白酶,但来自中低度或良性腐蹄病绵羊的分离株中,产生耐热蛋白酶的比例逐渐降低。通过Vf2和Vr2对一条857 bp的主要条带进行PCR扩增,通常与来自腐蹄病强毒型的分离株相关,而通过Vf2和Vr2出现一条1300 bp的主要条带和/或通过Bf和Br出现一条609 bp的条带,则与来自腐蹄病弱毒型的分离株相关。然而,由Vf2和Vr2以及Bf和Br所代表的毒力和良性基因区域只是决定结节拟杆菌毒力的众多因素中的两个。因此,观察到的腐蹄病临床表现与PCR扩增的特定DNA产物之间的关系并不完全。