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用于区分引起强毒、中度或良性绵羊足腐病的结节拟杆菌菌株的基因探针的开发。

Development of gene probes of Dichelobacter nodosus for differentiating strains causing virulent, intermediate or benign ovine footrot.

作者信息

Liu D

机构信息

Department of Agriculture, Pastoral and Veterinary Institute, Hamilton, Victoria, Australia.

出版信息

Br Vet J. 1994 Sep-Oct;150(5):451-62. doi: 10.1016/S0007-1935(05)80196-4.

Abstract

Seven Dichelobacter nodosus genomic DNA clones including six specific for virulent and one for benign strains were identified. A collection of 96 footrot isolates, which in turn comprised 27 virulent isolates showing elastase activity at 7 days, 25 high intermediate isolates with elastase activity at 14 days, 24 low intermediate isolates with elastase activity at 21-28 days and 20 benign isolates with no elastase activity at up to 28 days, were used to assess these clones. Of the six virulent specific clones, five (pV238-83, pV405-239, pV470-65, pV470-145 and pV470-178) reacted with 27 virulent isolates, and 12 of 25 high intermediate isolates, but none of 24 low intermediate isolates and 20 benign isolates in dot blot hybridization. The other virulent-specific clone (pV470-13) recognized all 27 virulent and 25 intermediate isolates, and 22 of 24 low intermediate isolates and three of 20 benign isolates in dot blot hybridization. By contrast, the benign-specific clone (pB645-335) detected all 20 benign isolates and 24 low intermediate isolates, and also 13 of 25 high intermediate isolates, but none of 27 virulent isolates in dot blot hybridization. Southern hybridization analysis indicated that whereas clones pV238-83, pV405-239 and pV470-178 bound a Sau3A band of 0.5 kb, clones pV470-65 and pV470-145 recognized two Sau3A bands of 0.7 and 0.5 kb in virulent strains of serogroups A to I. However, clone pV470-13 detected a Sau3A band pattern in virulent strains different from those recognized by the other five virulent specific-clones. Besides showing a distinct Sau3A band pattern in intermediate strains, pV470-13 also reacted with three benign strains that showed binding with it in dot blot hybridization. The benign-specific clone pV645-335 detected a Sau3A band of 0.5 kb in both intermediate and benign strains of serogroups A to I. Thus the combination of pV470-13 and pB645-335, or any other virulent-specific clone, would clearly differentiate among D. nodosus strains causing virulent, intermediate or benign footrot.

摘要

鉴定出7个结节拟杆菌基因组DNA克隆,其中6个针对强毒株,1个针对良性菌株。收集了96株腐蹄病分离株,这些分离株又包括27株在7天时表现出弹性蛋白酶活性的强毒株、25株在14天时具有弹性蛋白酶活性的高中间型分离株、24株在21 - 28天时具有弹性蛋白酶活性的低中间型分离株以及20株在长达28天时无弹性蛋白酶活性的良性分离株,用于评估这些克隆。在6个强毒特异性克隆中,5个(pV238 - 83、pV405 - 239、pV470 - 65、pV470 - 145和pV470 - 178)与27株强毒株以及25株高中间型分离株中的12株发生反应,但在斑点印迹杂交中与24株低中间型分离株和20株良性分离株均无反应。另一个强毒特异性克隆(pV470 - 13)在斑点印迹杂交中识别出所有27株强毒株和25株中间型分离株,以及24株低中间型分离株中的22株和20株良性分离株中的3株。相比之下,良性特异性克隆(pB645 - 335)在斑点印迹杂交中检测到所有20株良性分离株和24株低中间型分离株,以及25株高中间型分离株中的13株,但未检测到27株强毒株中的任何一株。Southern杂交分析表明,克隆pV238 - 83、pV405 - 239和pV470 - 178与0.5 kb的Sau3A条带结合,而克隆pV470 - 65和pV470 - 145在A至I血清群的强毒株中识别出0.7 kb和0.5 kb的两条Sau3A条带。然而,克隆pV470 - 13在强毒株中检测到的Sau3A条带模式与其他5个强毒特异性克隆所识别的不同。除了在中间型菌株中显示出独特的Sau3A条带模式外,pV470 - 13还与3株良性菌株发生反应,这些良性菌株在斑点印迹杂交中与它结合。良性特异性克隆pV645 - 335在A至I血清群的中间型和良性菌株中均检测到0.5 kb的Sau3A条带。因此,pV470 - 13和pB645 - 335的组合,或任何其他强毒特异性克隆,都能清楚地区分引起强毒、中间型或良性腐蹄病的结节拟杆菌菌株。

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