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首页> 外文期刊>Applied and Environmental Microbiology >Comparison of Four Different Culture Media for Isolation and Growth of Type II and Type I/III Mycobacterium avium subsp. paratuberculosis Strains Isolated from Cattle and Goats
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Comparison of Four Different Culture Media for Isolation and Growth of Type II and Type I/III Mycobacterium avium subsp. paratuberculosis Strains Isolated from Cattle and Goats

机译:两种不同培养基分离和生长II型和I / III型鸟分枝杆菌亚种的比较。牛和山羊分离的副结核菌菌株

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Culture is considered the definitive technique for Johne's disease diagnosis, and it is essential for later applications of certain molecular typing techniques. In this study, we have tested four solid media (Herrold's egg yolk medium [HEYM] with sodium pyruvate and mycobactin [HEYMm-SP], HEYM with mycobactin and without sodium pyruvate [HEYMm], Middlebrook 7H11 with mycobactin [Mm], and L?wenstein-Jensen with mycobactin [LJm]) for isolation of Mycobacterium avium subsp. paratuberculosis strains in 319 tissue samples from cattle herds and goat flocks. We have shown that each of the two main groups of M. avium subsp. paratuberculosis (type II and type I/III) has different requirements for growth in the culture media studied. The recommended solid media for isolation of type I/III strains are LJm and Mm, since the combination of both media allowed the recovery of all these strains. The most widespread culture medium, HEYM, is not suitable for the isolation of this group of M. avium subsp. paratuberculosis strains. Regarding the type II strains, HEYMm-SP was the medium where more strains were isolated, but the other three media are also needed in order to recover all type II strains. The incubation period is also related to the strain type. In conclusion, because the type of strain cannot be known in advance of culture, coupled with the fact that cattle and goats can be infected with both groups of strains, we recommend the use of the four solid media and the prolongation of the incubation period to more than 6 months to detect paratuberculous herds/flocks and to determine the true prevalence of the infection.
机译:文化被认为是诊断约翰内氏病的权威技术,对于某些分子分型技术的后续应用来说必不可少。在这项研究中,我们测试了四种固体培养基(带有丙酮酸钠和分枝杆菌素[HEYMm-SP]的Herrold蛋黄培养基[HEYM],没有分枝杆菌素和无丙酮酸钠[HEYMm]的HEYM,带有分枝杆菌素[Mm]的Middlebrook 7H11和L温斯坦-詹森与分枝杆菌素(LJm))用于分离鸟分枝杆菌亚种。牛群和山羊群的319个组织样本中的副结核病菌株。我们已经显示了鸟分枝杆菌亚种的两个主要组。副结核病(II型和I / III型)对所研究培养基的生长有不同的要求。推荐的用于分离I / III型菌株的固体培养基是LJm和Mm,因为两种培养基的组合可以回收所有这些菌株。最广泛使用的培养基HEYM不适合于分离该组鸟分枝杆菌亚种。副结核菌株。关于II型菌株,HEYMm-SP是分离出更多菌株的培养基,但是还需要其他三种培养基以回收所有II型菌株。潜伏期也与菌株类型有关。总之,由于菌株的类型无法在培养前得知,再加上牛和山羊都可能感染两组菌株,因此我们建议使用四种固体培养基并延长孵育时间,需超过6个月的时间才能检测出结核旁群/羊群,并确定感染的真实发生率。

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