Lamine-Khemiri Hela, Martínez Remigio, García-Jiménez Waldo Luis, Benítez-Medina Jose Manuel, Cortés Maria, Hurtado Inés, Abassi Mohammed Salah, Khazri Imed, Benzarti Mohammed, Hermoso-de-Mendoza Javier
Laboratory of Animal Health, Institute of Veterinary Research of Tunisia, Tunis, Tunisia.
Trop Anim Health Prod. 2014 Feb;46(2):305-11. doi: 10.1007/s11250-013-0488-y. Epub 2013 Oct 25.
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.
这项工作是针对突尼斯牛结核分枝杆菌复合群(MTBC)牛感染的分子流行病学研究方法。从突尼斯不同地区屠宰的牛的双侧咽后淋巴结样本中总共分离出35株MTBC菌株,通过间隔寡核苷酸分型(spoligotyping)和可变数目串联重复序列分型(VNTR)进行基因分型。间隔寡核苷酸分型鉴定出两个以前未记录的图谱,即来自纳布勒地区(突尼斯东北部)的山羊分枝杆菌分离株SB2024,这是该国对该物种的首次描述,以及来自斯法克斯地区(突尼斯南部)的SB2025(牛分枝杆菌)。还从斯法克斯地区的一头牛中分离出另一株具有欧洲大陆先前描述的间隔寡核苷酸分型图谱SB0418的山羊分枝杆菌。这两株分离株表明该物种在该国可能广泛分布。主要的间隔寡核苷酸分型图谱是SB0120,除纳布勒外,在所选择用于研究的所有突尼斯地区均有出现。分子分型还描述了同一动物中由两种不同的牛分枝杆菌分离株(SB0120和SB0848)引起的混合感染。通过检测一组六个位点,VNTR分型具有高度鉴别力。位点QUB3232和QUB11b鉴别力最强,而ETR-D和QUB11a的多样性指数较低。等位基因多样性的值在不同国家之间可能有很大差异;因此,标准化一组位点以便将来进行实验室间比较很重要。尽管VNTR分型被证明对有效鉴别MTBC分离株很有用,特别是与间隔寡核苷酸分型结合使用时,但仍需要进一步研究以评估突尼斯MTBC的遗传多样性。