首页> 外文期刊>Tropical Animal Health and Production >Genotypic characterization by spoligotyping and VNTR typing of Mycobacterium bovis and Mycobacterium caprae isolates from cattle of Tunisia
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Genotypic characterization by spoligotyping and VNTR typing of Mycobacterium bovis and Mycobacterium caprae isolates from cattle of Tunisia

机译:突尼斯牛的牛分枝杆菌和卡普拉分枝杆菌分离物的Spoligotyping和VNTR分型进行基因型鉴定

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This work is an approach to the molecular epidemiology of Mycobacterium tuberculosis complex (MTBC) bovine infections in Tunisia. A total of 35 MTBC isolates from both lateral retropharyngeal lymph node samples of cattle slaughtered in different Tunisian regions were genotyped by spoligotyping and variable number tandem repeat typing (VNTR)-typing. Spoligotyping allowed to identify two profiles not previously registered, namely SB2024, a Mycobacterium caprae isolate from Nabeul Region (North East Tunisia), the first description of this species in the country, and SB2025 (Mycobacterium bovis) from Sfax Region (Southern Tunisia). A second M. caprae isolate with a spoligotyping profile previously described in Europe mainland, SB0418, was also isolated from a bovine of Sfax region. Both isolates suggest the possibility of a widespread distribution of this species in the country. The predominant spoligotype was SB0120, present in all Tunisian regions selected for the study but Nabeul. Molecular typing also allowed to describe a mixed infection caused by two different M. bovis isolates (SB0120 and SB0848) in the same animal. VNTR typing was highly discriminant by testing a panel of six loci. Loci QUB3232 and QUB11b were the most discriminant, whereas ETR-D and QUB11a had the lower diversity index. The value of allelic diversity can significantly vary among countries; thus, it is important to standardize a panel of loci for future inter-laboratory comparisons. Although VNTR typing proved to be useful for an efficient discrimination among MTBC isolates, especially in combination with spoligotyping, further studies are needed in order to assess the genetic diversity of the MTBC in Tunisia.
机译:这项工作是突尼斯结核分枝杆菌复合体(MTBC)牛感染的分子流行病学研究方法。通过突击分型和可变数目串联重复重复分型(VNTR)分型对来自在突尼斯不同地区屠宰的牛的两个侧咽后咽淋巴结样本中的总共35个MTBC分离株进行基因分型。盲目的分型可以识别两个以前未注册的谱图,即SB2024,一种来自Nabeul地区(突尼斯东北部)的卡普拉分枝杆菌分离株,该物种在该国的第一个描述;以及SB2025(牛分枝杆菌),来自Sfax地区(突尼斯南部)。还从斯法克斯地区的牛中分离出了第二个先前在欧洲大陆描述过的具有血型分型特征的卡普拉斯分枝杆菌。两种分离物都表明该物种在该国广泛分布的可能性。突尼斯的主要血吸虫型为SB0120,出现在所有突尼斯地区,但纳布勒尔除外。分子分型还可以描述由同一动物中两种不同的牛分枝杆菌分离株(SB0120和SB0848)引起的混合感染。通过测试一组六个基因座,VNTR分型具有很高的判别力。位点QUB3232和QUB11b最具判别力,而ETR-D和QUB11a具有较低的多样性指数。等位基因多样性的价值在不同国家之间可能存在很大差异。因此,标准化一个基因座小组对于将来的实验室间比较非常重要。尽管VNTR分型已被证明可用于有效区分MTBC分离株,尤其是与Spoligotyping结合使用,但仍需要进一步研究以评估突尼斯MTBC的遗传多样性。

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